ITM2B Chromosome 13

Integral membrane protein 2B
8 variants 8 Health Risk

Upload your DNA to see your personal genotypes for variants in ITM2B.

What This Gene Does
Amyloid precursor proteins are processed by beta-secretase and gamma-secretase to produce beta-amyloid peptides which form the characteristic plaques of Alzheimer disease. This gene encodes a transmembrane protein which is processed at the C-terminus by furin or furin-like proteases to produce a small secreted peptide which inhibits the deposition of beta-amyloid. Mutations which result in extension of the C-terminal end of the encoded protein, thereby increasing the size of the secreted peptide, are associated with two neurogenerative diseases, familial British dementia and familial Danish dementia. [provided by RefSeq, Oct 2009]
Gene Info
Gene Group
BRICHOS domain containing
Locus Type
gene with protein product
Location
13q14.2
Ensembl
ENSG00000136156
Associated Conditions (5)
ITM2B-related disorder
Inborn genetic diseases
ABri amyloidosis
ADan amyloidosis
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
Key Variants
All Variants (8)
RSID Category Clinical Significance Conditions
RS144217555 Health Risk Conflicting classifications of pathogenicity ITM2B-related disorder, ITM2B-related disorder
RS180832133 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201399334 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS769773974 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, ITM2B-related disorder, Inborn genetic diseases
RS2137997888 Health Risk Likely pathogenic ABri amyloidosis, ABri amyloidosis
RS104894417 Health Risk Pathogenic ABri amyloidosis, ABri amyloidosis
RS606231166 Health Risk Pathogenic ADan amyloidosis, ADan amyloidosis
RS606231283 Health Risk Pathogenic Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies, Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
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