ENSG00000154646
Homo sapiens | |
Features
| Gene ID: | ENSG00000154646 | | | | | Biological name : | TMPRSS15 | | | | | Synonyms : | P98073 / TMPRSS15 / transmembrane serine protease 15 | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | 21 | | Strand: | -1 | | Band: | q21.1 | | Gene start: | 18269116 | | Gene end: | 18485879 | | | | | Corresponding Affymetrix probe sets: | 207638_at (Human Genome U133 Plus 2.0 Array) 217269_s_at (Human Genome U133 Plus 2.0 Array) | | | | | Cross references: | Ensembl peptide - ENSP00000474811
Ensembl peptide - ENSP00000284885
Ensembl peptide - ENSP00000398253
NCBI entrez gene - 5651
See in Manteia.
OMIM - 606635
RefSeq - XM_011529659
RefSeq - NM_002772
RefSeq - XM_011529656
RefSeq - XM_011529657
RefSeq - XM_011529658
RefSeq - XM_011529654
RefSeq - XM_011529655
RefSeq Peptide - NP_002763
swissprot - P98073
swissprot - E9PG70
Ensembl - ENSG00000154646
| | | | | Related genetic diseases (OMIM): | 226200 - Enterokinase deficiency, 226200 |
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)
| IPR000082 | SEA domain | | IPR000859 | CUB domain | | IPR000998 | MAM domain | | IPR001190 | SRCR domain | | IPR001254 | Serine proteases, trypsin domain | | IPR001314 | Peptidase S1A, chymotrypsin family | | IPR002172 | Low-density lipoprotein (LDL) receptor class A repeat | | IPR009003 | Peptidase S1, PA clan | | IPR011163 | Peptidase S1A, enteropeptidase | | IPR013320 | Concanavalin A-like lectin/glucanase domain superfamily | | IPR017448 | SRCR-like domain | | IPR018114 | Serine proteases, trypsin family, histidine active site | | IPR023415 | Low-density lipoprotein (LDL) receptor class A, conserved site | | IPR033116 | Serine proteases, trypsin family, serine active site | | IPR035914 | Spermadhesin, CUB domain superfamily | | IPR036055 | LDL receptor-like superfamily | | IPR036364 | SEA domain superfamily | | IPR036772 | SRCR-like domain superfamily |
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:0001508 | Failure to thrive | |
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| | HP:0002014 | Diarrhea | |
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| | HP:0003075 | Hypoproteinemia | |
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| | HP:0007609 | Hypoproteinemic edema | "An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body because of decreased osmotic pressure of plasma (hypoproteinemia)." [HPO:curators] |
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Interacting proteins (from Reactome)
No match
0 s.
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