Variant ID | 28690 |
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Entrez Gene ID | 4685 |
Gene | NCAM2 (GeneCards) |
Location | hg19 21:22542112-22542112
hg38 21:21169794-21169794 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000021.8:g.22542112 A>T (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 | 48129895 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.2984 |
CADD Raw score (version 1.3) | -0.207967 (Deleterious) |
FATHMM raw prediction score | 0.06641 (Tolerated) |
Deleterious probability by DeFine | 0.1351 (Neutral) |
Entrez Gene ID | 4685 (NCBI Gene) |
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Official Gene Symbol | NCAM2 (GeneCards) |
Number of variants in NCAM2 in this database | 12 (view all the variants) |
Full name | neural cell adhesion molecule 2 |
Band | 21q21.1 |
Other IDs | Vega: OTTHUMG00000078121 OMIM: 602040 HGNC: HGNC:7657 Ensembl: ENSG00000154654 |
Other names | NCAM21 |
Summary | The protein encoded by this gene belongs to the immunoglobulin superfamily. It is a type I membrane protein and may function in selective fasciculation and zone-to-zone projection of the primary olfactory axons. [provided by RefSeq, Jul 2008] |
Individual ID | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |