ENSG00000153487
 Homo sapiens | |
Features
| Gene ID: | ENSG00000153487 | | | | | Biological name : | ING1 | | | | | Synonyms : | ING1 / inhibitor of growth family member 1 / Q9UK53 | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | 13 | | Strand: | 1 | | Band: | q34 | | Gene start: | 110712736 | | Gene end: | 110723339 | | | | | Corresponding Affymetrix probe sets: | 208415_x_at (Human Genome U133 Plus 2.0 Array) 209808_x_at (Human Genome U133 Plus 2.0 Array) 210350_x_at (Human Genome U133 Plus 2.0 Array) 244177_at (Human Genome U133 Plus 2.0 Array) | | | | | Cross references: | Ensembl peptide - ENSP00000480985 Ensembl peptide - ENSP00000345202 Ensembl peptide - ENSP00000364929 Ensembl peptide - ENSP00000364930 Ensembl peptide - ENSP00000328436 NCBI entrez gene - 3621
See in Manteia.
OMIM - 601566 RefSeq - NM_005537 RefSeq - NM_001267728 RefSeq - NM_198217 RefSeq - NM_198218 RefSeq - NM_198219 RefSeq Peptide - NP_937862 RefSeq Peptide - NP_005528 RefSeq Peptide - NP_937860 RefSeq Peptide - NP_937861 RefSeq Peptide - NP_001254657 swissprot - Q9UK53 swissprot - A0A0C4DFW2 swissprot - A0A087WXF7 Ensembl - ENSG00000153487
| | | | | Related genetic diseases (OMIM): | 275355 - Squamous cell carcinoma, head and neck, somatic, 275355 | 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:0000007 | Autosomal recessive 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 homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators] |
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| | HP:0002860 | Squamous cell carcinoma | |
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Interacting proteins (from Reactome) No match
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