Q9H321 (VCX3B_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
December 14, 2011.
Version 58.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Variable charge X-linked protein 3B Alternative name(s): Variably charged protein X-C Short name=VCX-C | ||||
| Gene names |
| ||||
| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 216 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | May mediate a process in spermatogenesis or may play a role in sex ratio distortion. |
| Tissue specificity | Expressed exclusively in testis. |
| Sequence similarities | Belongs to the VCX/VCY family. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Polymorphism |
| Domain | Repeat |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular component | nucleolus Inferred from sequence or structural similarity. Source: UniProtKB |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 216 | 216 | Variable charge X-linked protein 3B | PRO_0000184662 | |||||
Regions | |||||||||
| Repeat | 104 – 113 | 10 | 1 | ||||||
| Repeat | 114 – 123 | 10 | 2 | ||||||
| Repeat | 124 – 133 | 10 | 3 | ||||||
| Repeat | 134 – 143 | 10 | 4 | ||||||
| Repeat | 144 – 153 | 10 | 5 | ||||||
| Repeat | 154 – 163 | 10 | 6 | ||||||
| Repeat | 164 – 173 | 10 | 7 | ||||||
| Repeat | 174 – 183 | 10 | 8 | ||||||
| Repeat | 184 – 193 | 10 | 9 | ||||||
| Repeat | 194 – 203 | 10 | 10 | ||||||
| Repeat | 204 – 213 | 10 | 11 | ||||||
| Region | 104 – 213 | 110 | 11 X 10 AA tandem repeats of L-S-Q-E-S-[EQ]-V-E-E-P | ||||||
Natural variations | |||||||||
| Natural variant | 15 | 1 | K → T. Ref.1 Corresponds to variant rs5934423 [ dbSNP | Ensembl ]. | VAR_037644 | |||||
Experimental info | |||||||||
| Sequence conflict | 98 – 102 | 5 | GTQHD → VEE in AAH98143. Ref.2 | ||||||
| Sequence conflict | 109 – 110 | 2 | EL → QV in AAH98143. Ref.2 | ||||||
| Sequence conflict | 120 | 1 | V → M in AAH98143. Ref.2 | ||||||
Sequences
| ||||||||||||||||||
References
| « Hide 'large scale' references | |
| [1] | "A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation." Fukami M., Kirsch S., Schiller S., Richter A., Benes V., Franco B., Muroya K., Rao E., Merker S., Niesler B., Ballabio A., Ansorge W., Ogata T., Rappold G.A. Am. J. Hum. Genet. 67:563-573(2000) [PubMed: 10903929] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT THR-15. |
| [2] | "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: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF167080 mRNA. Translation: AAG41766.2. BC098143 mRNA. Translation: AAH98143.1. |
| IPI | IPI00385888. |
| RefSeq | NP_001001888.3. NM_001001888.3. |
| UniGene | Hs.279737. Hs.534814. |
3D structure databases | |
| ProteinModelPortal | Q9H321. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q9H321. |
Polymorphism databases | |
| DMDM | 166215027. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000434876; ENSP00000391767; ENSG00000205642. ENST00000444481; ENSP00000414780; ENSG00000205642. |
| GeneID | 425054. |
| KEGG | hsa:425054. |
| UCSC | uc010ndo.1. human. |
Organism-specific databases | |
| CTD | 425054. |
| GeneCards | GC0XP008393. |
| HGNC | HGNC:31838. VCX3B. |
| neXtProt | NX_Q9H321. |
| PharmGKB | PA134866686. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | maNOG18775. |
| GeneTree | ENSGT00440000034745. |
| InParanoid | Q9H321. |
Gene expression databases | |
| CleanEx | HS_VCX3B. |
| Genevestigator | Q9H321. |
| GermOnline | ENSG00000205642. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| NextBio | 108691. |
Entry information
| Entry name | VCX3B_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9H321 Secondary accession number(s): Q4KN12 | ||||||||
| Entry history |
| ||||||||
| 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 X Human chromosome X: 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