Variant ID | 23264 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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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; |