Q969T3 (SNX21_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 29, 2013.
Version 98.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Sorting nexin-21 Alternative name(s): Sorting nexin L Short name=SNX-L | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 373 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | May be involved in several stages of intracellular trafficking By similarity. |
| Subcellular location | Cytoplasmic vesicle membrane; Peripheral membrane protein; Cytoplasmic side By similarity. |
| Tissue specificity | Highly expressed in fetus liver, but only weakly expressed in brain, skeleton muscle, smooth muscle, and cardiac muscle, kidney, and adrenal gland. Ref.2 |
| Domain | The PX domain mediates specific binding to membranes enriched in phosphatidylinositol 3-phosphate (PtdIns(P3)) By similarity. |
| Sequence similarities | Belongs to the sorting nexin family. Contains 1 PX (phox homology) domain. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Protein transport Transport |
| Cellular component | Cytoplasmic vesicle Membrane |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Ligand | Lipid-binding |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | cell communication Inferred from electronic annotation. Source: InterPro protein transportInferred from electronic annotation. Source: UniProtKB-KW |
| Cellular_component | cytoplasmic vesicle membrane Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular_function | phosphatidylinositol binding Inferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q969T3-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q969T3-2) The sequence of this isoform differs from the canonical sequence as follows: 197-199: RKR → QSH 200-373: Missing. | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 373 | 373 | Sorting nexin-21 | PRO_0000213870 | |||||
Regions | |||||||||
| Domain | 129 – 246 | 118 | PX | ||||||
Sites | |||||||||
| Binding site | 171 | 1 | Phosphatidylinositol 3-phosphate By similarity | ||||||
| Binding site | 173 | 1 | Phosphatidylinositol 3-phosphate; via amide nitrogen and carbonyl oxygen By similarity | ||||||
| Binding site | 198 | 1 | Phosphatidylinositol 3-phosphate By similarity | ||||||
| Binding site | 212 | 1 | Phosphatidylinositol 3-phosphate By similarity | ||||||
Natural variations | |||||||||
| Alternative sequence | 197 – 199 | 3 | RKR → QSH in isoform 2. | VSP_045048 | |||||
| Alternative sequence | 200 – 373 | 174 | Missing in isoform 2. | VSP_045049 | |||||
| Natural variant | 154 | 1 | A → T. Ref.5 Corresponds to variant rs4638862 [ dbSNP | Ensembl ]. | VAR_052482 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "A new member (SNX21) of the sorting nexin protein family." Hong W. Submitted (JUN-2001) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1). |
| [2] | "Expression of a novel member of sorting nexin gene family, SNX-L, in human liver development." Zeng W., Yuan W., Wang Y., Jiao W., Zhu Y., Huang C., Li D., Li Y., Zhu C., Wu X., Liu M. Biochem. Biophys. Res. Commun. 299:542-548(2002) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), TISSUE SPECIFICITY. |
| [3] | Stavrides G.S., Huckle E.J., Deloukas P. Submitted (MAY-2001) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1). |
| [4] | "The DNA sequence and comparative analysis of human chromosome 20." Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L., Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M., Beasley O.P., Bird C.P., Blakey S.E. Rogers J.Nature 414:865-871(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [5] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), VARIANT THR-154. Tissue: Kidney. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF395845 mRNA. Translation: AAK73126.1. AF523834 mRNA. Translation: AAM77915.1. AL591562 mRNA. Translation: CAC39140.1. AL008726 Genomic DNA. Translation: CAI20243.1. AL008726 Genomic DNA. Translation: CAI20244.1. BC019823 mRNA. Translation: AAH19823.1. |
| IPI | IPI00056503. IPI00335868. |
| RefSeq | NP_219489.1. NM_033421.2. NP_690857.1. NM_152897.1. |
| UniGene | Hs.472854. |
3D structure databases | |
| ProteinModelPortal | Q969T3. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q969T3. 1 interaction. |
| STRING | 9606.ENSP00000418593. |
PTM databases | |
| PhosphoSite | Q969T3. |
Polymorphism databases | |
| DMDM | 20140138. |
Proteomic databases | |
| PaxDb | Q969T3. |
| PRIDE | Q969T3. |
Protocols and materials databases | |
| DNASU | 90203. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000342644; ENSP00000344586; ENSG00000124104. ENST00000491381; ENSP00000418593; ENSG00000124104. |
| GeneID | 90203. |
| KEGG | hsa:90203. |
| UCSC | uc002xps.1. human. uc002xpv.1. human. |
Organism-specific databases | |
| CTD | 90203. |
| GeneCards | GC20P044462. |
| HGNC | HGNC:16154. SNX21. |
| HPA | HPA046359. |
| neXtProt | NX_Q969T3. |
| PharmGKB | PA25703. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG299779. |
| HOGENOM | HOG000118351. |
| HOVERGEN | HBG056464. |
| InParanoid | Q969T3. |
| OMA | RRNFTAE. |
| PhylomeDB | Q969T3. |
Enzyme and pathway databases | |
| SignaLink | Q969T3. |
Gene expression databases | |
| ArrayExpress | Q969T3. |
| Bgee | Q969T3. |
| CleanEx | HS_SNX21. |
| Genevestigator | Q969T3. |
| GermOnline | ENSG00000124104. Homo sapiens. |
Family and domain databases | |
| Gene3D | 1.25.40.10. 1 hit. 3.30.1520.10. 1 hit. |
| InterPro | IPR001683. Phox. IPR011990. TPR-like_helical. [Graphical view] |
| Pfam | PF00787. PX. 1 hit. [Graphical view] |
| SMART | SM00312. PX. 1 hit. [Graphical view] |
| SUPFAM | SSF64268. PX. 1 hit. |
| PROSITE | PS50195. PX. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 90203. |
| NextBio | 76589. |
Entry information
| Entry name | SNX21_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q969T3 Secondary accession number(s): Q5JZH5 Q9BR16 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any 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. | ||||||||
Relevant documents
| Human chromosome 20 Human chromosome 20: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| SIMILARITY comments Index of protein domains and families |

Clusters with
