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Entry version 152 (12 Aug 2020)
Sequence version 1 (01 Dec 2001)
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Protein

G-protein coupled receptor-associated sorting protein 2

Gene

GPRASP2

Organism
Homo sapiens (Human)
Status
Reviewed-Annotation score:

Annotation score:5 out of 5

<p>The annotation score provides a heuristic measure of the annotation content of a UniProtKB entry or proteome. This score <strong>cannot</strong> be used as a measure of the accuracy of the annotation as we cannot define the 'correct annotation' for any given protein.<p><a href='/help/annotation_score' target='_top'>More...</a></p>
-Experimental evidence at protein leveli <p>This indicates the type of evidence that supports the existence of the protein. Note that the 'protein existence' evidence does not give information on the accuracy or correctness of the sequence(s) displayed.<p><a href='/help/protein_existence' target='_top'>More...</a></p>

<p>This section provides any useful information about the protein, mostly biological knowledge.<p><a href='/help/function_section' target='_top'>More...</a></p>Functioni

May play a role in regulation of a variety of G-protein coupled receptors.1 Publication

<p>The <a href="http://www.geneontology.org/">Gene Ontology (GO)</a> project provides a set of hierarchical controlled vocabulary split into 3 categories:<p><a href='/help/gene_ontology' target='_top'>More...</a></p>GO - Molecular functioni

Enzyme and pathway databases

Pathway Commons web resource for biological pathway data

More...
PathwayCommonsi
Q96D09

<p>This section provides information about the protein and gene name(s) and synonym(s) and about the organism that is the source of the protein sequence.<p><a href='/help/names_and_taxonomy_section' target='_top'>More...</a></p>Names & Taxonomyi

<p>This subsection of the <a href="http://www.uniprot.org/help/names%5Fand%5Ftaxonomy%5Fsection">Names and taxonomy</a> section provides an exhaustive list of all names of the protein, from commonly used to obsolete, to allow unambiguous identification of a protein.<p><a href='/help/protein_names' target='_top'>More...</a></p>Protein namesi
Recommended name:
G-protein coupled receptor-associated sorting protein 2
Short name:
GASP-2
<p>This subsection of the <a href="http://www.uniprot.org/help/names%5Fand%5Ftaxonomy%5Fsection">Names and taxonomy</a> section indicates the name(s) of the gene(s) that code for the protein sequence(s) described in the entry. Four distinct tokens exist: 'Name', 'Synonyms', 'Ordered locus names' and 'ORF names'.<p><a href='/help/gene_name' target='_top'>More...</a></p>Gene namesi
Name:GPRASP2
<p>This subsection of the <a href="http://www.uniprot.org/help/names%5Fand%5Ftaxonomy%5Fsection">Names and taxonomy</a> section provides information on the name(s) of the organism that is the source of the protein sequence.<p><a href='/help/organism-name' target='_top'>More...</a></p>OrganismiHomo sapiens (Human)
<p>This subsection of the <a href="http://www.uniprot.org/help/names%5Fand%5Ftaxonomy%5Fsection">Names and taxonomy</a> section shows the unique identifier assigned by the NCBI to the source organism of the protein. This is known as the 'taxonomic identifier' or 'taxid'.<p><a href='/help/taxonomic_identifier' target='_top'>More...</a></p>Taxonomic identifieri9606 [NCBI]
<p>This subsection of the <a href="http://www.uniprot.org/help/names%5Fand%5Ftaxonomy%5Fsection">Names and taxonomy</a> section contains the taxonomic hierarchical classification lineage of the source organism. It lists the nodes as they appear top-down in the taxonomic tree, with the more general grouping listed first.<p><a href='/help/taxonomic_lineage' target='_top'>More...</a></p>Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
<p>This subsection of the <a href="http://www.uniprot.org/help/names%5Fand%5Ftaxonomy%5Fsection">Names and taxonomy</a> section is present for entries that are part of a <a href="http://www.uniprot.org/proteomes">proteome</a>, i.e. of a set of proteins thought to be expressed by organisms whose genomes have been completely sequenced.<p><a href='/help/proteomes_manual' target='_top'>More...</a></p>Proteomesi
  • UP000005640 <p>A UniProt <a href="http://www.uniprot.org/manual/proteomes%5Fmanual">proteome</a> can consist of several components.<br></br>The component name refers to the genomic component encoding a set of proteins.<p><a href='/help/proteome_component' target='_top'>More...</a></p> Componenti: Chromosome X

Organism-specific databases

Eukaryotic Pathogen Database Resources

More...
EuPathDBi
HostDB:ENSG00000158301.18

Human Gene Nomenclature Database

More...
HGNCi
HGNC:25169, GPRASP2

Online Mendelian Inheritance in Man (OMIM)

More...
MIMi
300969, gene

neXtProt; the human protein knowledge platform

More...
neXtProti
NX_Q96D09

<p>This section provides information on the location and the topology of the mature protein in the cell.<p><a href='/help/subcellular_location_section' target='_top'>More...</a></p>Subcellular locationi

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionGraphics by Christian Stolte & Seán O’Donoghue; Source: COMPARTMENTS

<p>This section provides information on the disease(s) and phenotype(s) associated with a protein.<p><a href='/help/pathology_and_biotech_section' target='_top'>More...</a></p>Pathology & Biotechi

<p>This subsection of the 'Pathology and Biotech' section provides information on the disease(s) associated with genetic variations in a given protein. The information is extracted from the scientific literature and diseases that are also described in the <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?db=omim">OMIM</a> database are represented with a <a href="http://www.uniprot.org/diseases">controlled vocabulary</a> in the following way:<p><a href='/help/involvement_in_disease' target='_top'>More...</a></p>Involvement in diseasei

Deafness, X-linked, 7 (DFNX7)1 Publication
The disease is caused by mutations affecting the gene represented in this entry.
Disease descriptionA congenital form of bilateral mixed or conductive hearing loss, which is progressive in some patients. Additional clinical features include ear anomalies and facial dysmorphism with bilateral ptosis.
Related information in OMIM
Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the 'Sequence' section describes natural variant(s) of the protein sequence.<p><a href='/help/variant' target='_top'>More...</a></p>Natural variantiVAR_081645573A → N in DFNX7; requires 2 nucleotide substitutions. 1 Publication1

<p>UniProtKB Keywords constitute a <a href="http://www.uniprot.org/keywords">controlled vocabulary</a> with a hierarchical structure. Keywords summarise the content of a UniProtKB entry and facilitate the search for proteins of interest.<p><a href='/help/keywords' target='_top'>More...</a></p>Keywords - Diseasei

Deafness, Disease mutation

Organism-specific databases

DisGeNET

More...
DisGeNETi
100528062
114928

MalaCards human disease database

More...
MalaCardsi
GPRASP2
MIMi301018, phenotype

Open Targets

More...
OpenTargetsi
ENSG00000158301

Orphanet; a database dedicated to information on rare diseases and orphan drugs

More...
Orphaneti
500188, X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome

The Pharmacogenetics and Pharmacogenomics Knowledge Base

More...
PharmGKBi
PA134976848

Miscellaneous databases

Pharos NIH Druggable Genome Knowledgebase

More...
Pharosi
Q96D09, Tbio

Polymorphism and mutation databases

BioMuta curated single-nucleotide variation and disease association database

More...
BioMutai
GPRASP2

Domain mapping of disease mutations (DMDM)

More...
DMDMi
74751808

<p>This section describes post-translational modifications (PTMs) and/or processing events.<p><a href='/help/ptm_processing_section' target='_top'>More...</a></p>PTM / Processingi

Molecule processing

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the 'PTM / Processing' section describes the extent of a polypeptide chain in the mature protein following processing or proteolytic cleavage.<p><a href='/help/chain' target='_top'>More...</a></p>ChainiPRO_00002390531 – 838G-protein coupled receptor-associated sorting protein 2Add BLAST838

Amino acid modifications

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the 'PTM / Processing' section specifies the position and type of each modified residue excluding <a href="http://www.uniprot.org/manual/lipid">lipids</a>, <a href="http://www.uniprot.org/manual/carbohyd">glycans</a> and <a href="http://www.uniprot.org/manual/crosslnk">protein cross-links</a>.<p><a href='/help/mod_res' target='_top'>More...</a></p>Modified residuei282PhosphoserineBy similarity1
Modified residuei284PhosphoserineBy similarity1

Keywords - PTMi

Phosphoprotein

Proteomic databases

Encyclopedia of Proteome Dynamics

More...
EPDi
Q96D09

jPOST - Japan Proteome Standard Repository/Database

More...
jPOSTi
Q96D09

MassIVE - Mass Spectrometry Interactive Virtual Environment

More...
MassIVEi
Q96D09

MaxQB - The MaxQuant DataBase

More...
MaxQBi
Q96D09

PaxDb, a database of protein abundance averages across all three domains of life

More...
PaxDbi
Q96D09

PeptideAtlas

More...
PeptideAtlasi
Q96D09

PRoteomics IDEntifications database

More...
PRIDEi
Q96D09

ProteomicsDB: a multi-organism proteome resource

More...
ProteomicsDBi
76244

PTM databases

iPTMnet integrated resource for PTMs in systems biology context

More...
iPTMneti
Q96D09

Comprehensive resource for the study of protein post-translational modifications (PTMs) in human, mouse and rat.

More...
PhosphoSitePlusi
Q96D09

<p>This section provides information on the expression of a gene at the mRNA or protein level in cells or in tissues of multicellular organisms.<p><a href='/help/expression_section' target='_top'>More...</a></p>Expressioni

<p>This subsection of the 'Expression' section provides information on the expression of a gene at the mRNA or protein level in cells or in tissues of multicellular organisms. By default, the information is derived from experiments at the mRNA level, unless specified 'at protein level'.<br></br>Examples: <a href="http://www.uniprot.org/uniprot/P92958#expression">P92958</a>, <a href="http://www.uniprot.org/uniprot/Q8TDN4#expression">Q8TDN4</a>, <a href="http://www.uniprot.org/uniprot/O14734#expression">O14734</a><p><a href='/help/tissue_specificity' target='_top'>More...</a></p>Tissue specificityi

Expressed in the brain.1 Publication

Gene expression databases

Bgee dataBase for Gene Expression Evolution

More...
Bgeei
ENSG00000158301, Expressed in endothelial cell and 212 other tissues

Genevisible search portal to normalized and curated expression data from Genevestigator

More...
Genevisiblei
Q96D09, HS

Organism-specific databases

Human Protein Atlas

More...
HPAi
ENSG00000158301, Tissue enhanced (brain)

<p>This section provides information on the quaternary structure of a protein and on interaction(s) with other proteins or protein complexes.<p><a href='/help/interaction_section' target='_top'>More...</a></p>Interactioni

<p>This subsection of the <a href="http://www.uniprot.org/help/interaction%5Fsection">'Interaction'</a> section provides information about the protein quaternary structure and interaction(s) with other proteins or protein complexes (with the exception of physiological receptor-ligand interactions which are annotated in the <a href="http://www.uniprot.org/help/function%5Fsection">'Function'</a> section).<p><a href='/help/subunit_structure' target='_top'>More...</a></p>Subunit structurei

Interacts with cytoplasmic tails of a variety of G-protein coupled receptors such as muscarinic acetylcholine receptor M1/CHRM1 and calcitonin receptor/CALCR.

1 Publication

<p>This subsection of the '<a href="http://www.uniprot.org/help/interaction%5Fsection">Interaction</a>' section provides information about binary protein-protein interactions. The data presented in this section are a quality-filtered subset of binary interactions automatically derived from the <a href="https://www.ebi.ac.uk/intact/">IntAct database</a>. It is updated at every <a href="http://www.uniprot.org/help/synchronization">UniProt release</a>.<p><a href='/help/binary_interactions' target='_top'>More...</a></p>Binary interactionsi

Hide details

GO - Molecular functioni

Protein-protein interaction databases

The Biological General Repository for Interaction Datasets (BioGRID)

More...
BioGRIDi
125399, 72 interactors
1529361, 1 interactor

Protein interaction database and analysis system

More...
IntActi
Q96D09, 69 interactors

Molecular INTeraction database

More...
MINTi
Q96D09

STRING: functional protein association networks

More...
STRINGi
9606.ENSP00000437872

Miscellaneous databases

RNAct, Protein-RNA interaction predictions for model organisms.

More...
RNActi
Q96D09, protein

<p>This section provides information on the tertiary and secondary structure of a protein.<p><a href='/help/structure_section' target='_top'>More...</a></p>Structurei

3D structure databases

SWISS-MODEL Repository - a database of annotated 3D protein structure models

More...
SMRi
Q96D09

Database of comparative protein structure models

More...
ModBasei
Search...

<p>This section provides information on sequence similarities with other proteins and the domain(s) present in a protein.<p><a href='/help/family_and_domains_section' target='_top'>More...</a></p>Family & Domainsi

<p>This subsection of the 'Family and domains' section provides information about the sequence similarity with other proteins.<p><a href='/help/sequence_similarities' target='_top'>More...</a></p>Sequence similaritiesi

Belongs to the GPRASP family.Curated

Phylogenomic databases

evolutionary genealogy of genes: Non-supervised Orthologous Groups

More...
eggNOGi
ENOG502S6CE, Eukaryota

Ensembl GeneTree

More...
GeneTreei
ENSGT00940000162726

The HOGENOM Database of Homologous Genes from Fully Sequenced Organisms

More...
HOGENOMi
CLU_017437_0_0_1

InParanoid: Eukaryotic Ortholog Groups

More...
InParanoidi
Q96D09

Identification of Orthologs from Complete Genome Data

More...
OMAi
WPREEAN

Database of Orthologous Groups

More...
OrthoDBi
860703at2759

Database for complete collections of gene phylogenies

More...
PhylomeDBi
Q96D09

TreeFam database of animal gene trees

More...
TreeFami
TF335652

Family and domain databases

Integrated resource of protein families, domains and functional sites

More...
InterProi
View protein in InterPro
IPR006911, ARM-rpt_dom
IPR016024, ARM-type_fold
IPR043374, BHLHb9/GASP-1/GASP-2

The PANTHER Classification System

More...
PANTHERi
PTHR46414, PTHR46414, 1 hit

Pfam protein domain database

More...
Pfami
View protein in Pfam
PF04826, Arm_2, 1 hit

Superfamily database of structural and functional annotation

More...
SUPFAMi
SSF48371, SSF48371, 1 hit

<p>This section displays by default the canonical protein sequence and upon request all isoforms described in the entry. It also includes information pertinent to the sequence(s), including <a href="http://www.uniprot.org/help/sequence%5Flength">length</a> and <a href="http://www.uniprot.org/help/sequences">molecular weight</a>. The information is filed in different subsections. The current subsections and their content are listed below:<p><a href='/help/sequences_section' target='_top'>More...</a></p>Sequencei

<p>This subsection of the <a href="http://www.uniprot.org/help/sequences%5Fsection">Sequence</a> section indicates if the <a href="http://www.uniprot.org/help/canonical%5Fand%5Fisoforms">canonical sequence</a> displayed by default in the entry is complete or not.<p><a href='/help/sequence_status' target='_top'>More...</a></p>Sequence statusi: Complete.

Q96D09-1 [UniParc]FASTAAdd to basket
« Hide
        10         20         30         40         50
MTGAEIEPSA QAKPEKKAGE EVIAGPEREN DVPLVVRPKV RTQATTGARP
60 70 80 90 100
KTETKSVPAA RPKTEAQAMS GARPKTEVQV MGGARPKTEA QGITGARPKT
110 120 130 140 150
DARAVGGARS KTDAKAIPGA RPKDEAQAWA QSEFGTEAVS QAEGVSQTNA
160 170 180 190 200
VAWPLATAES GSVTKSKGLS MDRELVNVDA ETFPGTQGQK GIQPWFGPGE
210 220 230 240 250
ETNMGSWCYS RPRAREEASN ESGFWSADET STASSFWTGE ETSVRSWPRE
260 270 280 290 300
ESNTRSRHRA KHQTNPRSRP RSKQEAYVDS WSGSEDEASN PFSFWVGENT
310 320 330 340 350
NNLFRPRVRE EANIRSKLRT NREDCFESES EDEFYKQSWV LPGEEANSRF
360 370 380 390 400
RHRDKEDPNT ALKLRAQKDV DSDRVKQEPR FEEEVIIGSW FWAEKEASLE
410 420 430 440 450
GGASAICESE PGTEEGAIGG SAYWAEEKSS LGAVAREEAK PESEEEAIFG
460 470 480 490 500
SWFWDRDEAC FDLNPCPVYK VSDRFRDAAE ELNASSRPQT WDEVTVEFKP
510 520 530 540 550
GLFHGVGFRS TSPFGIPEEA SEMLEAKPKN LELSPEGEEQ ESLLQPDQPS
560 570 580 590 600
PEFTFQYDPS YRSVREIREH LRARESAESE SWSCSCIQCE LKIGSEEFEE
610 620 630 640 650
FLLLMDKIRD PFIHEISKIA MGMRSASQFT RDFIRDSGVV SLIETLLNYP
660 670 680 690 700
SSRVRTSFLE NMIHMAPPYP NLNMIETFIC QVCEETLAHS VDSLEQLTGI
710 720 730 740 750
RMLRHLTMTI DYHTLIANYM SGFLSLLTTA NARTKFHVLK MLLNLSENPA
760 770 780 790 800
VAKKLFSAKA LSIFVGLFNI EETNDNIQIV IKMFQNISNI IKSGKMSLID
810 820 830
DDFSLEPLIS AFREFEELAK QLQAQIDNQN DPEVGQQS
Length:838
Mass (Da):93,773
Last modified:December 1, 2001 - v1
<p>The checksum is a form of redundancy check that is calculated from the sequence. It is useful for tracking sequence updates.</p> <p>It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low.</p> <p>However UniProtKB may contain entries with identical sequences in case of multiple genes (paralogs).</p> <p>The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x<sup>64</sup> + x<sup>4</sup> + x<sup>3</sup> + x + 1. The algorithm is described in the ISO 3309 standard. </p> <p class="publication">Press W.H., Flannery B.P., Teukolsky S.A. and Vetterling W.T.<br /> <strong>Cyclic redundancy and other checksums</strong><br /> <a href="http://www.nrbook.com/b/bookcpdf.php">Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993)</a>)</p> Checksum:i2D30515916B7EACE
GO

Natural variant

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_049265173R → S. Corresponds to variant dbSNP:rs6616421Ensembl.1
Natural variantiVAR_081645573A → N in DFNX7; requires 2 nucleotide substitutions. 1 Publication1

Sequence databases

Select the link destinations:

EMBL nucleotide sequence database

More...
EMBLi

GenBank nucleotide sequence database

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GenBanki

DNA Data Bank of Japan; a nucleotide sequence database

More...
DDBJi
Links Updated
AL035427 Genomic DNA No translation available.
CH471190 Genomic DNA Translation: EAW54727.1
CH471190 Genomic DNA Translation: EAW54728.1
CH471190 Genomic DNA Translation: EAW54729.1
BC013576 mRNA Translation: AAH13576.1
BC036772 mRNA Translation: AAH36772.1
AK092981 mRNA No translation available.

The Consensus CDS (CCDS) project

More...
CCDSi
CCDS14501.1

NCBI Reference Sequences

More...
RefSeqi
NP_001004051.1, NM_001004051.3
NP_001171803.1, NM_001184874.2
NP_001171804.1, NM_001184875.2
NP_001171805.1, NM_001184876.2
NP_001186747.1, NM_001199818.1
NP_612446.1, NM_138437.5

Genome annotation databases

Ensembl eukaryotic genome annotation project

More...
Ensembli
ENST00000332262; ENSP00000339057; ENSG00000158301
ENST00000535209; ENSP00000437394; ENSG00000158301
ENST00000543253; ENSP00000437872; ENSG00000158301

Database of genes from NCBI RefSeq genomes

More...
GeneIDi
100528062
114928

KEGG: Kyoto Encyclopedia of Genes and Genomes

More...
KEGGi
hsa:100528062
hsa:114928

UCSC genome browser

More...
UCSCi
uc004ejm.3, human

Keywords - Coding sequence diversityi

Polymorphism

<p>This section provides links to proteins that are similar to the protein sequence(s) described in this entry at different levels of sequence identity thresholds (100%, 90% and 50%) based on their membership in UniProt Reference Clusters (<a href="http://www.uniprot.org/help/uniref">UniRef</a>).<p><a href='/help/similar_proteins_section' target='_top'>More...</a></p>Similar proteinsi

<p>This section is used to point to information related to entries and found in data collections other than UniProtKB.<p><a href='/help/cross_references_section' target='_top'>More...</a></p>Cross-referencesi

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AL035427 Genomic DNA No translation available.
CH471190 Genomic DNA Translation: EAW54727.1
CH471190 Genomic DNA Translation: EAW54728.1
CH471190 Genomic DNA Translation: EAW54729.1
BC013576 mRNA Translation: AAH13576.1
BC036772 mRNA Translation: AAH36772.1
AK092981 mRNA No translation available.
CCDSiCCDS14501.1
RefSeqiNP_001004051.1, NM_001004051.3
NP_001171803.1, NM_001184874.2
NP_001171804.1, NM_001184875.2
NP_001171805.1, NM_001184876.2
NP_001186747.1, NM_001199818.1
NP_612446.1, NM_138437.5

3D structure databases

SMRiQ96D09
ModBaseiSearch...

Protein-protein interaction databases

BioGRIDi125399, 72 interactors
1529361, 1 interactor
IntActiQ96D09, 69 interactors
MINTiQ96D09
STRINGi9606.ENSP00000437872

PTM databases

iPTMnetiQ96D09
PhosphoSitePlusiQ96D09

Polymorphism and mutation databases

BioMutaiGPRASP2
DMDMi74751808

Proteomic databases

EPDiQ96D09
jPOSTiQ96D09
MassIVEiQ96D09
MaxQBiQ96D09
PaxDbiQ96D09
PeptideAtlasiQ96D09
PRIDEiQ96D09
ProteomicsDBi76244

Protocols and materials databases

Antibodypedia a portal for validated antibodies

More...
Antibodypediai
351, 190 antibodies

The DNASU plasmid repository

More...
DNASUi
114928

Genome annotation databases

EnsembliENST00000332262; ENSP00000339057; ENSG00000158301
ENST00000535209; ENSP00000437394; ENSG00000158301
ENST00000543253; ENSP00000437872; ENSG00000158301
GeneIDi100528062
114928
KEGGihsa:100528062
hsa:114928
UCSCiuc004ejm.3, human

Organism-specific databases

Comparative Toxicogenomics Database

More...
CTDi
100528062
114928
DisGeNETi100528062
114928
EuPathDBiHostDB:ENSG00000158301.18

GeneCards: human genes, protein and diseases

More...
GeneCardsi
GPRASP2
HGNCiHGNC:25169, GPRASP2
HPAiENSG00000158301, Tissue enhanced (brain)
MalaCardsiGPRASP2
MIMi300969, gene
301018, phenotype
neXtProtiNX_Q96D09
OpenTargetsiENSG00000158301
Orphaneti500188, X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
PharmGKBiPA134976848

GenAtlas: human gene database

More...
GenAtlasi
Search...

Phylogenomic databases

eggNOGiENOG502S6CE, Eukaryota
GeneTreeiENSGT00940000162726
HOGENOMiCLU_017437_0_0_1
InParanoidiQ96D09
OMAiWPREEAN
OrthoDBi860703at2759
PhylomeDBiQ96D09
TreeFamiTF335652

Enzyme and pathway databases

PathwayCommonsiQ96D09

Miscellaneous databases

BioGRID ORCS database of CRISPR phenotype screens

More...
BioGRID-ORCSi
100528062, 2 hits in 65 CRISPR screens
114928, 5 hits in 498 CRISPR screens

The Gene Wiki collection of pages on human genes and proteins

More...
GeneWikii
GPRASP2
PharosiQ96D09, Tbio

Protein Ontology

More...
PROi
PR:Q96D09
RNActiQ96D09, protein

The Stanford Online Universal Resource for Clones and ESTs

More...
SOURCEi
Search...

Gene expression databases

BgeeiENSG00000158301, Expressed in endothelial cell and 212 other tissues
GenevisibleiQ96D09, HS

Family and domain databases

InterProiView protein in InterPro
IPR006911, ARM-rpt_dom
IPR016024, ARM-type_fold
IPR043374, BHLHb9/GASP-1/GASP-2
PANTHERiPTHR46414, PTHR46414, 1 hit
PfamiView protein in Pfam
PF04826, Arm_2, 1 hit
SUPFAMiSSF48371, SSF48371, 1 hit

ProtoNet; Automatic hierarchical classification of proteins

More...
ProtoNeti
Search...

MobiDB: a database of protein disorder and mobility annotations

More...
MobiDBi
Search...

<p>This section provides general information on the entry.<p><a href='/help/entry_information_section' target='_top'>More...</a></p>Entry informationi

<p>This subsection of the 'Entry information' section provides a mnemonic identifier for a UniProtKB entry, but it is not a stable identifier. Each reviewed entry is assigned a unique entry name upon integration into UniProtKB/Swiss-Prot.<p><a href='/help/entry_name' target='_top'>More...</a></p>Entry nameiGASP2_HUMAN
<p>This subsection of the 'Entry information' section provides one or more accession number(s). These are stable identifiers and should be used to cite UniProtKB entries. Upon integration into UniProtKB, each entry is assigned a unique accession number, which is called 'Primary (citable) accession number'.<p><a href='/help/accession_numbers' target='_top'>More...</a></p>AccessioniPrimary (citable) accession number: Q96D09
Secondary accession number(s): D3DXA0, Q8NAB4
<p>This subsection of the 'Entry information' section shows the date of integration of the entry into UniProtKB, the date of the last sequence update and the date of the last annotation modification ('Last modified'). The version number for both the entry and the <a href="http://www.uniprot.org/help/canonical%5Fand%5Fisoforms">canonical sequence</a> are also displayed.<p><a href='/help/entry_history' target='_top'>More...</a></p>Entry historyiIntegrated into UniProtKB/Swiss-Prot: May 30, 2006
Last sequence update: December 1, 2001
Last modified: August 12, 2020
This is version 152 of the entry and version 1 of the sequence. See complete history.
<p>This subsection of the 'Entry information' section indicates whether the entry has been manually annotated and reviewed by UniProtKB curators or not, in other words, if the entry belongs to the Swiss-Prot section of UniProtKB (<strong>reviewed</strong>) or to the computer-annotated TrEMBL section (<strong>unreviewed</strong>).<p><a href='/help/entry_status' target='_top'>More...</a></p>Entry statusiReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

<p>This section contains any relevant information that doesn't fit in any other defined sections<p><a href='/help/miscellaneous_section' target='_top'>More...</a></p>Miscellaneousi

Keywords - Technical termi

Reference proteome

Documents

  1. Human chromosome X
    Human chromosome X: entries, gene names and cross-references to MIM
  2. Human entries with polymorphisms or disease mutations
    List of human entries with polymorphisms or disease mutations
  3. Human polymorphisms and disease mutations
    Index of human polymorphisms and disease mutations
  4. MIM cross-references
    Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot
  5. SIMILARITY comments
    Index of protein domains and families
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