ENSG00000118094
Homo sapiens | |
Features
| Gene ID: | ENSG00000118094 | | | | | Biological name : | TREH | | | | | Synonyms : | O43280 / TREH / trehalase | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | 11 | | Strand: | -1 | | Band: | q23.3 | | Gene start: | 118657316 | | Gene end: | 118679690 | | | | | Corresponding Affymetrix probe sets: | 207378_at (Human Genome U133 Plus 2.0 Array) | | | | | Cross references: | Ensembl peptide - ENSP00000264029
Ensembl peptide - ENSP00000477923
Ensembl peptide - ENSP00000381020
NCBI entrez gene - 11181
See in Manteia.
OMIM - 275360
RefSeq - NM_001301065
RefSeq - NM_007180
RefSeq Peptide - NP_001287994
RefSeq Peptide - NP_009111
swissprot - A0A087WTJ4
swissprot - O43280
Ensembl - ENSG00000118094
| | | | | Related genetic diseases (OMIM): | 612119 - Trehalase deficiency, 612119 |
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)
No match
Protein motifs (from Interpro)
| IPR001661 | Glycoside hydrolase, family 37 | | IPR008928 | Six-hairpin glycosidase superfamily | | IPR018232 | Glycoside hydrolase, family 37, conserved site |
Gene Ontology (GO)
Pathways (from Reactome)
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] |
Show
| | HP:0002014 | Diarrhea | |
Show
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Interacting proteins (from Reactome)
No match
0 s.
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