Overview

Variant ID 4443
Entrez Gene ID 79582
Gene SPAG16 (GeneCards)
Location hg19 2:215095699-215095699
hg38 2:214230975-214230975
Disease Xeroderma Pigmentosum (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000002.11:g.215095699 A>G (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 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.0165
CADD Raw score (version 1.3) 0.087698 (Deleterious)
FATHMM raw prediction score 0.09331 (Tolerated)
Deleterious probability by DeFine 0.3484 (Neutral)
Entrez Gene ID 79582 (NCBI Gene)
Official Gene Symbol SPAG16 (GeneCards)
Number of variants in SPAG16 in this database 12 (view all the variants)
Full name sperm associated antigen 16
Band 2q34
Other IDs Vega: OTTHUMG00000133015
OMIM: 612173
HGNC: HGNC:23225
Ensembl: ENSG00000144451
Other names PF20, WDR29
Summary Cilia and flagella are comprised of a microtubular backbone, the axoneme, which is organized by the basal body and surrounded by plasma membrane. SPAG16 encodes 2 major proteins that associate with the axoneme of sperm tail and the nucleus of postmeiotic germ cells, respectively (Zhang et al., 2007 [PubMed 17699735]).[supplied by OMIM, Jul 2008]

Individual #1

Individual ID 29217584.22 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Xeroderma Pigmentosum (view all the variants in this disease)
OMIM ID 278700

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;