Variant ID | 25383 |
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Entrez Gene ID | 1739 |
Gene | DLG1 (GeneCards) |
Location | hg19 3:196881920-196881920
hg38 3:197155049-197155049 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000003.11:g.196881920 T>A (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 | 198022430 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.4578 |
CADD Raw score (version 1.3) | -0.133688 (Deleterious) |
FATHMM raw prediction score | 0.04565 (Tolerated) |
Deleterious probability by DeFine | 0.0608 (Neutral) |
Entrez Gene ID | 1739 (NCBI Gene) |
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Official Gene Symbol | DLG1 (GeneCards) |
Number of variants in DLG1 in this database | 5 (view all the variants) |
Full name | discs large MAGUK scaffold protein 1 |
Band | 3q29 |
Other IDs | Vega: OTTHUMG00000047972 OMIM: 601014 HGNC: HGNC:2900 Ensembl: ENSG00000075711 |
Other names | hdlg, DLGH1, SAP97, SAP-97, dJ1061C18.1.1 |
Summary | This gene encodes a multi-domain scaffolding protein that is required for normal development. This protein may have a role in septate junction formation, signal transduction, cell proliferation, synaptogenesis and lymphocyte activation. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene, but the full-length nature of some of the variants is not known. [provided by RefSeq, Feb 2011] |
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 |