IMPDH1 Chromosome 7

Inosine monophosphate dehydrogenase 1
76 variants 76 Health Risk

Upload your DNA to see your personal genotypes for variants in IMPDH1.

What This Gene Does
The protein encoded by this gene acts as a homotetramer to regulate cell growth. The encoded protein is an enzyme that catalyzes the synthesis of xanthine monophosphate (XMP) from inosine-5'-monophosphate (IMP). This is the rate-limiting step in the de novo synthesis of guanine nucleotides. Defects in this gene are a cause of retinitis pigmentosa type 10 (RP10). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Info
Gene Group
Inosine monophosphate dehydrogenase family
Locus Type
gene with protein product
Location
7q32.1
Ensembl
ENSG00000106348
Associated Conditions (10)
Leber congenital amaurosis 11
Retinitis pigmentosa
Retinal dystrophy
Retinitis pigmentosa 10
IMPDH1-related disorder
Familial cancer of breast
Thyroid cancer
nonmedullary
1
Inborn genetic diseases
Key Variants
RS1042250
Conflicting classifications of pathogenicity
Leber congenital amaurosis 11, Retinitis pigmentosa, Leber congenital amaurosis 11
Health Risk
RS121912553
Conflicting classifications of pathogenicity
Leber congenital amaurosis 11, Retinal dystrophy, Leber congenital amaurosis 11
Health Risk
RS1238910577
Conflicting classifications of pathogenicity
Retinal dystrophy, Retinal dystrophy
Health Risk
RS1272549405
Conflicting classifications of pathogenicity
Retinitis pigmentosa 10, Retinitis pigmentosa 10
Health Risk
RS138502867
Conflicting classifications of pathogenicity
IMPDH1-related disorder, IMPDH1-related disorder
Health Risk
RS139785999
Conflicting classifications of pathogenicity
Leber congenital amaurosis 11, Retinitis pigmentosa, Leber congenital amaurosis 11
Health Risk
RS139979391
Conflicting classifications of pathogenicity
Retinitis pigmentosa 10, Leber congenital amaurosis 11, Retinitis pigmentosa 10
Health Risk
RS143796089
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Leber congenital amaurosis 11, IMPDH1-related disorder
Health Risk
RS144498273
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Leber congenital amaurosis 11, Retinal dystrophy
Health Risk
RS144587211
Conflicting classifications of pathogenicity
Health Risk
RS144659635
Conflicting classifications of pathogenicity
Leber congenital amaurosis 11, Retinitis pigmentosa, IMPDH1-related disorder
Health Risk
RS1478038443
Conflicting classifications of pathogenicity
Leber congenital amaurosis 11, Retinitis pigmentosa, Leber congenital amaurosis 11
Health Risk
All Variants (76)
RSID Category Clinical Significance Conditions
RS1354063885 Health Risk Likely pathogenic
RS1562998089 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1584728115 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1798216037 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2116601689 Health Risk Likely pathogenic Retinitis pigmentosa 10, Retinitis pigmentosa 10
RS2535731868 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2535731890 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2535761770 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS1218568607 Health Risk Pathogenic
RS121912554 Health Risk Pathogenic Leber congenital amaurosis 11, Leber congenital amaurosis 11
RS1225476931 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1282816133 Health Risk Pathogenic
RS1343867350 Health Risk Pathogenic
RS1391527038 Health Risk Pathogenic
RS1798090540 Health Risk Pathogenic Leber congenital amaurosis 11, Retinal dystrophy, Retinitis pigmentosa 10
RS1798091523 Health Risk Pathogenic
RS2116594089 Health Risk Pathogenic
RS2535751225 Health Risk Pathogenic
RS2535814033 Health Risk Pathogenic
RS754031943 Health Risk Pathogenic
RS767123748 Health Risk Pathogenic
RS886037911 Health Risk Pathogenic Retinitis pigmentosa 10, Retinitis pigmentosa 10
RS982830278 Health Risk Pathogenic
RS121912550 Health Risk Pathogenic/Likely pathogenic Retinitis pigmentosa 10, Retinal dystrophy, Retinitis pigmentosa 10
RS1238921380 Health Risk Pathogenic/Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1798086782 Health Risk Pathogenic/Likely pathogenic Leber congenital amaurosis 11, Retinitis pigmentosa 10, Leber congenital amaurosis 11
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