Overview

Variant ID 26412
Entrez Gene ID 10512
Gene SEMA3C (GeneCards)
Location hg19 7:80607196-80607196
hg38 7:80977880-80977880
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000007.13:g.80607196 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 159138663

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.3901
CADD Raw score (version 1.3) -0.027199 (Deleterious)
FATHMM raw prediction score 0.06401 (Tolerated)
Deleterious probability by DeFine 0.1067 (Neutral)
Entrez Gene ID 10512 (NCBI Gene)
Official Gene Symbol SEMA3C (GeneCards)
Number of variants in SEMA3C in this database 8 (view all the variants)
Full name semaphorin 3C
Band 7q21.11
Other IDs Vega: OTTHUMG00000023447
OMIM: 602645
HGNC: HGNC:10725
Ensembl: ENSG00000075223
Other names SemE, SEMAE
Summary This gene encodes a secreted glycoprotein that belongs to the semaphorin class 3 family of neuronal guidance cues. The encoded protein contains an N-terminal sema domain, integrin and immunoglobulin-like domains, and a C-terminal basic domain. Homodimerization and proteolytic cleavage of the C-terminal propeptide are necessary for the function of the encoded protein. It binds a neuropilin co-receptor before forming a heterotrimeric complex with an associated plexin. An increase in the expression of this gene correlates with an increase in cancer cell invasion and adhesion. Naturally occurring mutations in this gene are associated with Hirschsprung disease. [provided by RefSeq, May 2017]

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