Variant ID | 29031 |
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Entrez Gene ID | 1538 |
Gene | CYLC1 (GeneCards) |
Location | hg19 X:83204566-83204566
hg38 X:83949558-83949558 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000023.10:g.83204566 C>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 | 155270560 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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CADD Raw score (version 1.3) | 0.540253 (Deleterious) |
FATHMM raw prediction score | 0.11553 (Tolerated) |
Deleterious probability by DeFine | 0.0549 (Neutral) |
Entrez Gene ID | 1538 (NCBI Gene) |
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Official Gene Symbol | CYLC1 (GeneCards) |
Number of variants in CYLC1 in this database | 3 (view all the variants) |
Full name | cylicin 1 |
Band | Xq21.1 |
Other IDs | Vega: OTTHUMG00000021922 OMIM: 300768 HGNC: HGNC:2582 Ensembl: ENSG00000183035 |
Other names | CYCL1 |
Summary | This gene encodes a sperm head cytoskeletal protein. The encoded protein is associated with the calyx of spermatozoa and spermatids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
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 |