Overview

Variant ID 25603
Entrez Gene ID 11086
Gene ADAM29 (GeneCards)
Location hg19 4:175992271-175992271
hg38 4:175071120-175071120
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000004.11:g.175992271 C>A (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 -0.4053
CADD Raw score (version 1.3) -0.19738 (Deleterious)
FATHMM raw prediction score 0.06208 (Tolerated)
Deleterious probability by DeFine 0.132 (Neutral)
Entrez Gene ID 11086 (NCBI Gene)
Official Gene Symbol ADAM29 (GeneCards)
Number of variants in ADAM29 in this database 51 (view all the variants)
Full name ADAM metallopeptidase domain 29
Band 4q34.1
Other IDs Vega: OTTHUMG00000160764
OMIM: 604778
HGNC: HGNC:207
Ensembl: ENSG00000168594
Other names CT73, svph1
Summary This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene is highly expressed in testis and may be involved in human spermatogenesis. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Jul 2008]

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