Overview

Variant ID 22886
Entrez Gene ID 8821
Gene INPP4B (GeneCards)
Location hg19 4:142990513-142990513
hg38 4:142069360-142069360
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000004.11:g.142990513 A>C (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 191154276

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1807
CADD Raw score (version 1.3) 0.207141 (Deleterious)
FATHMM raw prediction score 0.1371 (Tolerated)
Deleterious probability by DeFine 0.0753 (Neutral)
Entrez Gene ID 8821 (NCBI Gene)
Official Gene Symbol INPP4B (GeneCards)
Number of variants in INPP4B in this database 7 (view all the variants)
Full name inositol polyphosphate-4-phosphatase type II B
Band 4q31.21
Other IDs Vega: OTTHUMG00000161341
OMIM: 607494
HGNC: HGNC:6075
Ensembl: ENSG00000109452
Other names None
Summary INPP4B encodes the inositol polyphosphate 4-phosphatase type II, one of the enzymes involved in phosphatidylinositol signaling pathways. This enzyme removes the phosphate group at position 4 of the inositol ring from inositol 3,4-bisphosphate. There is limited data to suggest that the human type II enzyme is subject to alternative splicing, as has been established for the type I enzyme. [provided by RefSeq, Jul 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;