BAT2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Large proline-rich protein BAT2 is a protein that in humans is encoded by the BAT2 gene.[5][6][7]

AliasesPRRC2A, BAT2, D6S51, D6S51E, G2, proline rich coiled-coil 2A
End31,637,771 bp[1]
Quick facts PRRC2A, Identifiers ...
PRRC2A
Identifiers
AliasesPRRC2A, BAT2, D6S51, D6S51E, G2, proline rich coiled-coil 2A
External IDsOMIM: 142580; MGI: 1915467; HomoloGene: 10567; GeneCards: PRRC2A; OMA:PRRC2A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004638
NM_080686

NM_001199044
NM_020027

RefSeq (protein)

NP_004629
NP_542417

NP_001185973
NP_064411

Location (UCSC)Chr 6: 31.62 – 31.64 MbChr 17: 35.37 – 35.38 Mb
PubMed search[3][4]
Wikidata
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Function

A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for TNF alpha and TNF beta. These genes are all within the human major histocompatibility complex class III region. This gene has microsatellite repeats which are associated with the age-at-onset of insulin-dependent diabetes mellitus (IDDM) and possibly thought to be involved with the inflammatory process of pancreatic beta-cell destruction during the development of IDDM. This gene is also a candidate gene for the development of rheumatoid arthritis. There are two alternatively spliced transcripts encoding different isoforms described for this gene.[7]

Interactions

BAT2 has been shown to interact with:

References

Further reading

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