ENSG00000236320
Homo sapiens | |
Features
| Gene ID: | ENSG00000236320 | | | | | Biological name : | SLFN14 | | | | | Synonyms : | P0C7P3 / schlafen family member 14 / SLFN14 | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | 17 | | Strand: | -1 | | Band: | q12 | | Gene start: | 35548125 | | Gene end: | 35558098 | | | | | Corresponding Affymetrix probe sets: | | | | | | Cross references: | Ensembl peptide - ENSP00000391101
NCBI entrez gene - 342618
See in Manteia.
OMIM - 614958
RefSeq - XM_017024579
RefSeq - NM_001129820
RefSeq - XM_017024577
RefSeq - XM_017024578
RefSeq - XM_017024576
RefSeq Peptide - NP_001123292
swissprot - P0C7P3
Ensembl - ENSG00000236320
| | | | | Related genetic diseases (OMIM): | 616913 - Bleeding disorder, platelet-type, 20, 616913 |
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed
Ortholog prediction (from Ensembl)
Paralog prediction (from Ensembl)
Protein motifs (from Interpro)
Gene Ontology (GO)
Pathways (from Reactome)
No match
Phenotype (from MGI, Zfin or HPO)
| HP:0000006 | Autosomal dominant inheritance | "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators] |
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| | HP:0000132 | Menorrhagia | |
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| | HP:0000421 | Epistaxis | |
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| | HP:0000978 | Ecchymoses | |
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| | HP:0001873 | Thrombocytopenia | |
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Interacting proteins (from Reactome)
No match
0 s.
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