Overview

Variant ID 23296
Entrez Gene ID 7227
Gene TRPS1 (GeneCards)
Location hg19 8:116635051-116635051
hg38 8:115622824-115622824
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000008.10:g.116635051 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 146364022

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.3042
CADD Raw score (version 1.3) 0.097561 (Deleterious)
FATHMM raw prediction score 0.21216 (Tolerated)
Deleterious probability by DeFine 0.5226 (Deleterious)
Entrez Gene ID 7227 (NCBI Gene)
Official Gene Symbol TRPS1 (GeneCards)
Number of variants in TRPS1 in this database 8 (view all the variants)
Full name transcriptional repressor GATA binding 1
Band 8q23.3
Other IDs Vega: OTTHUMG00000142829
OMIM: 604386
HGNC: HGNC:12340
Ensembl: ENSG00000104447
Other names GC79, LGCR
Summary This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III. [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;