Variant ID | 22737 |
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Entrez Gene ID | 53833 |
Gene | IL20RB (GeneCards) |
Location | hg19 3:137381377-137381377
hg38 3:137662535-137662535 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000003.11:g.137381377 G>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 | -0.8557 |
CADD Raw score (version 1.3) | -0.19063 (Deleterious) |
FATHMM raw prediction score | 0.02899 (Tolerated) |
Deleterious probability by DeFine | 0.0659 (Neutral) |
Entrez Gene ID | 53833 (NCBI Gene) |
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Official Gene Symbol | IL20RB (GeneCards) |
Number of variants in IL20RB in this database | 9 (view all the variants) |
Full name | interleukin 20 receptor subunit beta |
Band | 3q22.3 |
Other IDs | Vega: OTTHUMG00000159779 OMIM: 605621 HGNC: HGNC:6004 Ensembl: ENSG00000174564 |
Other names | DIRS1, FNDC6, IL-20R2 |
Summary | IL20RB and IL20RA (MIM 605620) form a heterodimeric receptor for interleukin-20 (IL20; MIM 605619) (Blumberg et al., 2001 [PubMed 11163236]).[supplied by OMIM, Feb 2009] |
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; |