Overview

Variant ID 26229
Entrez Gene ID 9096
Gene TBX18 (GeneCards)
Location hg19 6:85682604-85682604
hg38 6:84972886-84972886
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000006.11:g.85682604 C>T (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 -0.2533
CADD Raw score (version 1.3) -0.151621 (Deleterious)
FATHMM raw prediction score 0.09164 (Tolerated)
Deleterious probability by DeFine 0.5209 (Deleterious)
Entrez Gene ID 9096 (NCBI Gene)
Official Gene Symbol TBX18 (GeneCards)
Number of variants in TBX18 in this database 11 (view all the variants)
Full name T-box 18
Band 6q14.3
Other IDs Vega: OTTHUMG00000015129
OMIM: 604613
HGNC: HGNC:11595
Ensembl: ENSG00000112837
Other names CAKUT2
Summary This genes codes for a member of an evolutionarily conserved family of transcription factors that plays a crucial role in embryonic development. The family is characterized by the presence of the DNA-binding T-box domain and is divided into five sub-families based on sequence conservation in this domain. The encoded protein belongs to the vertebrate specific Tbx1 sub-family. The protein acts as a transcriptional repressor by antagonizing transcriptional activators in the T-box family. The protein forms homo- or heterodimers with other transcription factors of the T-box family or other transcription factors. [provided by RefSeq, Nov 2012]

Individual #1

Individual ID 29217587.03 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID