ENSG00000067082
Homo sapiens | |
Features
| Gene ID: | ENSG00000067082 | | | | | Biological name : | KLF6 | | | | | Synonyms : | KLF6 / Kruppel like factor 6 / Q99612 | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | 10 | | Strand: | -1 | | Band: | p15.2 | | Gene start: | 3775996 | | Gene end: | 3785281 | | | | | Corresponding Affymetrix probe sets: | 1555832_s_at (Human Genome U133 Plus 2.0 Array) 208960_s_at (Human Genome U133 Plus 2.0 Array) 208961_s_at (Human Genome U133 Plus 2.0 Array) 211610_at (Human Genome U133 Plus 2.0 Array) 224606_at (Human Genome U133 Plus 2.0 Array) | | | | | Cross references: | Ensembl peptide - ENSP00000419079
Ensembl peptide - ENSP00000419923
Ensembl peptide - ENSP00000445301
NCBI entrez gene - 1316
See in Manteia.
OMIM - 602053
RefSeq - NM_001160125
RefSeq - NM_001160124
RefSeq - NM_001300
RefSeq Peptide - NP_001153596
RefSeq Peptide - NP_001153597
RefSeq Peptide - NP_001291
swissprot - Q99612
Ensembl - ENSG00000067082
| | | | | Related genetic diseases (OMIM): | 176807 - Prostate cancer, somatic, 176807 | | | 613659 - Gastric cancer, somatic, 613659 |
This gene has been taged as a transcription factor by TFT
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:0001428 | Somatic mutation | |
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| | HP:0012125 | Prostate cancer | "A cancer of the `prostate` (FMA:9600)." [HPO:probinson] |
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| | HP:0012126 | Stomach cancer | "A cancer arising in any part of the stomach." [HPO:probinson] |
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| | HP:0410067 | Increased level of L-fucose in urine | "An increase in the level of L-fucose in the urine." [PMID:2311216] |
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Interacting proteins (from Reactome)
No match
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