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Protein

Putative uncharacterized protein LRRC75A-AS1, mitochondrial

Gene

LRRC75A-AS1

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

Functioni

Caution

Product of a dubious CDS prediction. Probable non-coding RNA.Curated

Names & Taxonomyi

Protein namesi
Recommended name:
Putative uncharacterized protein LRRC75A-AS1, mitochondrial
Alternative name(s):
FAM211A antisense RNA 1
LRRC75A antisense RNA 1
Putative uncharacterized protein FAM211A-AS1, mitochondrial
Gene namesi
Name:LRRC75A-AS1
Synonyms:C17orf45, C17orf76-AS1, FAM211A-AS1, NCRNA00188
OrganismiHomo sapiens (Human)
Taxonomic identifieri9606 [NCBI]
Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
Proteomesi
  • UP000005640 Componenti: Unplaced

Organism-specific databases

HGNCiHGNC:28619 LRRC75A-AS1
neXtProtiNX_Q8N1F1

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; Source: COMPARTMENTS

Keywords - Cellular componenti

Mitochondrion

Pathology & Biotechi

Organism-specific databases

PharmGKBiPA165432227

PTM / Processingi

Molecule processing

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Transit peptidei1 – 36MitochondrionSequence analysisAdd BLAST36
ChainiPRO_000028656437 – 130Putative uncharacterized protein LRRC75A-AS1, mitochondrialAdd BLAST94

Proteomic databases

PRIDEiQ8N1F1
ProteomicsDBi71592

Expressioni

Gene expression databases

CleanExiHS_C17orf45

Interactioni

Binary interactionsi

WithEntry#Exp.IntActNotes
RBPMSQ930623EBI-2872544,EBI-740322

Protein-protein interaction databases

IntActiQ8N1F1, 4 interactors
MINTiQ8N1F1

Structurei

3D structure databases

ProteinModelPortaliQ8N1F1
ModBaseiSearch...
MobiDBiSearch...

Family & Domainsi

Keywords - Domaini

Transit peptide

Phylogenomic databases

InParanoidiQ8N1F1

Sequencei

Sequence statusi: Complete.

Sequence processingi: The displayed sequence is further processed into a mature form.

Q8N1F1-1 [UniParc]FASTAAdd to basket

« Hide

        10         20         30         40         50
MFPGSLSRGR RAAVEMAWLP GSCARVAFAA GAAARYWTAW QGSAGPNPAA
60 70 80 90 100
VAEAHGSLFC GRATSARAWS LRRPGPGSPA HSGGVQTREN WIAYPLQSAE
110 120 130
DGVATRLQIR EESASCLAAE YWSQEPAMRF
Length:130
Mass (Da):13,824
Last modified:October 1, 2002 - v1
Checksum:i1F4AAFED1A7FBC04
GO

Natural variant

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_03212036Y → C. Corresponds to variant dbSNP:rs35517418Ensembl.1
Natural variantiVAR_03212178S → T. Corresponds to variant dbSNP:rs35752829Ensembl.1

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
BC027986 mRNA Translation: AAH27986.1
BC040159 mRNA Translation: AAH40159.1
UniGeneiHs.368934

Keywords - Coding sequence diversityi

Polymorphism

Similar proteinsi

Entry informationi

Entry nameiC1AS1_HUMAN
AccessioniPrimary (citable) accession number: Q8N1F1
Entry historyiIntegrated into UniProtKB/Swiss-Prot: May 15, 2007
Last sequence update: October 1, 2002
Last modified: June 20, 2018
This is version 89 of the entry and version 1 of the sequence. See complete history.
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.

Miscellaneousi

Keywords - Technical termi

Complete proteome, Reference proteome

Documents

  1. Human chromosome 17
    Human chromosome 17: 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

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