Overview

Variant ID 28900
Entrez Gene ID 154796
Gene AMOT (GeneCards)
Location hg19 X:112121970-112121970
hg38 X:112878742-112878742
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000023.10:g.112121970 G>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 155270560

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
CADD Raw score (version 1.3) 0.40666 (Deleterious)
FATHMM raw prediction score 0.75673 (Tolerated)
Deleterious probability by DeFine 0.5337 (Deleterious)
Entrez Gene ID 154796 (NCBI Gene)
Official Gene Symbol AMOT (GeneCards)
Number of variants in AMOT in this database 2 (view all the variants)
Full name angiomotin
Band Xq23
Other IDs Vega: OTTHUMG00000022216
OMIM: 300410
HGNC: HGNC:17810
Ensembl: ENSG00000126016
Other names None
Summary This gene belongs to the motin family of angiostatin binding proteins characterized by conserved coiled-coil domains and C-terminal PDZ binding motifs. The encoded protein is expressed predominantly in endothelial cells of capillaries as well as larger vessels of the placenta where it may mediate the inhibitory effect of angiostatin on tube formation and the migration of endothelial cells toward growth factors during the formation of new blood vessels. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

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