Overview

Variant ID 23264
Entrez Gene ID 3614
Gene IMPDH1 (GeneCards)
Location hg19 7:128091408-128091408
hg38 7:128451354-128451354
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000007.13:g.128091408 A>G (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 159138663

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0904
CADD Raw score (version 1.3) 0.537835 (Deleterious)
FATHMM raw prediction score 0.54783 (Tolerated)
Deleterious probability by DeFine 0.2248 (Neutral)
Entrez Gene ID 3614 (NCBI Gene)
Official Gene Symbol IMPDH1 (GeneCards)
Number of variants in IMPDH1 in this database 2 (view all the variants)
Full name inosine monophosphate dehydrogenase 1
Band 7q32.1
Other IDs Vega: OTTHUMG00000157713
OMIM: 146690
HGNC: HGNC:6052
Ensembl: ENSG00000106348
Other names IMPD, RP10, IMPD1, LCA11, IMPDH-I, sWSS2608
Summary 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]

Individual #1

Individual ID 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
Title Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis.
Journal Science
Publication date 2018.02
Disease Asymptomatic
Number of cases cases of unknown sex: 3;