Variant ID | 23414 |
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Entrez Gene ID | 1539 |
Gene | CYLC2 (GeneCards) |
Location | hg19 9:105775232-105775232
hg38 9:103012950-103012950 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000009.11:g.105775232 T>C (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 | 141213431 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3587 |
CADD Raw score (version 1.3) | -0.149003 (Deleterious) |
FATHMM raw prediction score | 0.07896 (Tolerated) |
Deleterious probability by DeFine | 0.4753 (Neutral) |
Entrez Gene ID | 1539 (NCBI Gene) |
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Official Gene Symbol | CYLC2 (GeneCards) |
Number of variants in CYLC2 in this database | 6 (view all the variants) |
Full name | cylicin 2 |
Band | 9q31.1 |
Other IDs | Vega: OTTHUMG00000020396 OMIM: 604035 HGNC: HGNC:2583 Ensembl: ENSG00000155833 |
Other names | None |
Summary | Cylicin II (CYCL2) is specifically expressed in testis and is part of the cytoskeletal calyx of mammalian sperm heads. Cylicin II may play a role in the morphogenesis of the sperm head. [provided by RefSeq, Jul 2008] |
Individual ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
Journal | Science |
Publication date | 2018.02 |
Disease | Asymptomatic |
Number of cases | cases of unknown sex: 3; |