C6orf10

C6orf10
Identifiers
Aliases C6orf10, TSBP, chromosome 6 open reading frame 10
External IDs HomoloGene: 81753 GeneCards: C6orf10
Genetically Related Diseases
liver cirrhosis, hepatitis C, obesity, atopic dermatitis, multiple sclerosis, asthma[1]
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

10665

n/a

Ensembl

n/a

n/a

UniProt

Q5SRN2

n/a

RefSeq (mRNA)

NM_001286474
NM_001286475
NM_006781

n/a

RefSeq (protein)

NP_001273403.1
NP_001273404.1
NP_006772.3

n/a

Location (UCSC) Chr 6: 32.29 – 32.37 Mb n/a
PubMed search [2] n/a
Wikidata
View/Edit Human

Uncharacterized protein C6orf10 is a protein that in humans is encoded by the C6orf10 gene.[3][4]

References

  1. "Diseases that are genetically associated with C6orf10 view/edit references on wikidata".
  2. "Human PubMed Reference:".
  3. Stammers M, Rowen L, Rhodes D, Trowsdale J, Beck S (May 2000). "BTL-II: a polymorphic locus with homology to the butyrophilin gene family, located at the border of the major histocompatibility complex class II and class III regions in human and mouse". Immunogenetics. 51 (4–5): 373–82. doi:10.1007/s002510050633. PMID 10803852.
  4. "Entrez Gene: C6orf10 chromosome 6 open reading frame 10".

Further reading


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