ITM2B

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

Integral membrane protein 2B (ITM2B or BRI2) is a protein that in humans is encoded by the ITM2B gene.[5][6]

AliasesITM2B, ABRI, BRI, BRI2, BRICD2B, E25B, E3-16, FBD, imBRI2, RDGCA, integral membrane protein 2B
End48,270,357 bp[1]
Quick facts Identifiers, Aliases ...
ITM2B
Identifiers
AliasesITM2B, ABRI, BRI, BRI2, BRICD2B, E25B, E3-16, FBD, imBRI2, RDGCA, integral membrane protein 2B
External IDsOMIM: 603904; MGI: 1309517; HomoloGene: 7388; GeneCards: ITM2B; OMA:ITM2B - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_021999

NM_008410

RefSeq (protein)

NP_068839

NP_032436

Location (UCSC)Chr 13: 48.23 – 48.27 MbChr 14: 73.6 – 73.62 Mb
PubMed search[3][4]
Wikidata
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ITM2B or BRI2 is a gene located on chromosome 13. The gene is connected to familial Danish dementia and familial British dementia causing amyloid and pre-filbrillar effects similar to those seen in Alzheimer's.

References

Further reading

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