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Q9H321 (VCX3B_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified December 14, 2011. Version 58. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
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Names and origin

Protein namesRecommended name:
Variable charge X-linked protein 3B
Alternative name(s):
Variably charged protein X-C
Short name=VCX-C
Gene names
Name:VCX3B
Synonyms:VCXC
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length216 AA.
Sequence statusComplete.
Protein existenceEvidence 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 diversityPolymorphism
   DomainRepeat
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular componentnucleolus

Inferred from sequence or structural similarity. Source: UniProtKB

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 216216Variable charge X-linked protein 3B
PRO_0000184662

Regions

Repeat104 – 113101
Repeat114 – 123102
Repeat124 – 133103
Repeat134 – 143104
Repeat144 – 153105
Repeat154 – 163106
Repeat164 – 173107
Repeat174 – 183108
Repeat184 – 193109
Repeat194 – 2031010
Repeat204 – 2131011
Region104 – 21311011 X 10 AA tandem repeats of L-S-Q-E-S-[EQ]-V-E-E-P

Natural variations

Natural variant151K → T. Ref.1
Corresponds to variant rs5934423 [ dbSNP | Ensembl ].
VAR_037644

Experimental info

Sequence conflict98 – 1025GTQHD → VEE in AAH98143. Ref.2
Sequence conflict109 – 1102EL → QV in AAH98143. Ref.2
Sequence conflict1201V → M in AAH98143. Ref.2

Sequences

Sequence LengthMass (Da)Tools
Q9H321 [UniParc].

Last modified January 15, 2008. Version 3.
Checksum: E484B89804562E95

FASTA21623,494
        10         20         30         40         50         60 
MSPKPRASGP PAKAKEAGKR KSSSQPSPSD PKKKTTKVAK KGKAVRRGRR GKKGAATKMA 

        70         80         90        100        110        120 
AVTAPEAESG PAAPGPSDQP SQELPQHELP PEEPVSEGTQ HDPLSQESEL EEPLSQESEV 

       130        140        150        160        170        180 
EEPLSQESQV EEPLSQESEV EEPLSQESQV EEPLSQESEV EEPLSQESQV EEPLSQESEM 

       190        200        210 
EEPLSQESQV EEPLSQESEM EEPLSQESEM EELPSV 

« Hide

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.
IPIIPI00385888.
RefSeqNP_001001888.3. NM_001001888.3.
UniGeneHs.279737.
Hs.534814.

3D structure databases

ProteinModelPortalQ9H321.
ModBaseSearch...

Protein-protein interaction databases

STRINGQ9H321.

Polymorphism databases

DMDM166215027.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000434876; ENSP00000391767; ENSG00000205642.
ENST00000444481; ENSP00000414780; ENSG00000205642.
GeneID425054.
KEGGhsa:425054.
UCSCuc010ndo.1. human.

Organism-specific databases

CTD425054.
GeneCardsGC0XP008393.
HGNCHGNC:31838. VCX3B.
neXtProtNX_Q9H321.
PharmGKBPA134866686.
GenAtlasSearch...

Phylogenomic databases

eggNOGmaNOG18775.
GeneTreeENSGT00440000034745.
InParanoidQ9H321.

Gene expression databases

CleanExHS_VCX3B.
GenevestigatorQ9H321.
GermOnlineENSG00000205642. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

NextBio108691.

Entry information

Entry nameVCX3B_HUMAN
AccessionPrimary (citable) accession number: Q9H321
Secondary accession number(s): Q4KN12
Entry history
Integrated into UniProtKB/Swiss-Prot: November 16, 2001
Last sequence update: January 15, 2008
Last modified: December 14, 2011
This is version 58 of the entry and version 3 of the sequence. [Complete history]
Entry statusReviewed (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.

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