Overview

Variant ID 26155
Entrez Gene ID 7164
Gene TPD52L1 (GeneCards)
Location hg19 6:125553767-125553767
hg38 6:125232621-125232621
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000006.11:g.125553767 T>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 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 1.1706
CADD Raw score (version 1.3) 1.870405 (Deleterious)
FATHMM raw prediction score 0.93609 (Tolerated)
Deleterious probability by DeFine 0.6084 (Deleterious)
Entrez Gene ID 7164 (NCBI Gene)
Official Gene Symbol TPD52L1 (GeneCards)
Number of variants in TPD52L1 in this database 3 (view all the variants)
Full name tumor protein D52 like 1
Band 6q22.31
Other IDs Vega: OTTHUMG00000015505
OMIM: 604069
HGNC: HGNC:12006
Ensembl: ENSG00000111907
Other names D53
Summary This gene encodes a member of a family of proteins that contain coiled-coil domains and may form hetero- or homomers. The encoded protein is involved in cell proliferation and calcium signaling. It also interacts with the mitogen-activated protein kinase kinase kinase 5 (MAP3K5/ASK1) and positively regulates MAP3K5-induced apoptosis. Multiple alternatively spliced transcript variants have been observed. [provided by RefSeq, Jan 2016]

Individual #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID