ENSG00000167772
Homo sapiens | |
Features
| Gene ID: | ENSG00000167772 | | | | | Biological name : | ANGPTL4 | | | | | Synonyms : | angiopoietin like 4 / ANGPTL4 / Q9BY76 | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | 19 | | Strand: | 1 | | Band: | p13.2 | | Gene start: | 8363289 | | Gene end: | 8374373 | | | | | Corresponding Affymetrix probe sets: | 221009_s_at (Human Genome U133 Plus 2.0 Array) 223333_s_at (Human Genome U133 Plus 2.0 Array) | | | | | Cross references: | Ensembl peptide - ENSP00000473090
Ensembl peptide - ENSP00000472869
Ensembl peptide - ENSP00000473025
Ensembl peptide - ENSP00000301455
Ensembl peptide - ENSP00000377534
Ensembl peptide - ENSP00000470307
Ensembl peptide - ENSP00000471345
Ensembl peptide - ENSP00000472551
NCBI entrez gene - 51129
See in Manteia.
OMIM - 605910
RefSeq - XM_005272485
RefSeq - NM_001039667
RefSeq - NM_139314
RefSeq - XM_005272484
RefSeq Peptide - NP_647475
RefSeq Peptide - NP_001034756
swissprot - M0QZ51
swissprot - M0R0N8
swissprot - M0R2X8
swissprot - M0R3A2
swissprot - M0R369
swissprot - Q9BY76
Ensembl - ENSG00000167772
| | | | | Related genetic diseases (OMIM): | 615881 - Plasma triglyceride level QTL, low, 615881 |
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)
| IPR002181 | Fibrinogen, alpha/beta/gamma chain, C-terminal globular domain | | IPR014715 | Fibrinogen, alpha/beta/gamma chain, C-terminal globular, subdomain 2 | | IPR014716 | Fibrinogen, alpha/beta/gamma chain, C-terminal globular, subdomain 1 | | IPR020837 | Fibrinogen, conserved site | | IPR028793 | Angiopoietin-related protein 4 | | IPR036056 | Fibrinogen-like, C-terminal |
Gene Ontology (GO)
Pathways (from Reactome)
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] |
Show
|
Interacting proteins (from Reactome)
No match
0 s.
|
