ENSG00000143147


Homo sapiens

Features
Gene ID: ENSG00000143147
  
Biological name :GPR161
  
Synonyms : GPR161 / G protein-coupled receptor 161 / Q8N6U8
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 1
Strand: -1
Band: q24.2
Gene start: 168079543
Gene end: 168137667
  
Corresponding Affymetrix probe sets: 206971_at (Human Genome U133 Plus 2.0 Array)   206972_s_at (Human Genome U133 Plus 2.0 Array)   214104_at (Human Genome U133 Plus 2.0 Array)   230369_at (Human Genome U133 Plus 2.0 Array)   232350_x_at (Human Genome U133 Plus 2.0 Array)   235961_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000271357
Ensembl peptide - ENSP00000356809
Ensembl peptide - ENSP00000356810
Ensembl peptide - ENSP00000356812
Ensembl peptide - ENSP00000437576
Ensembl peptide - ENSP00000441039
Ensembl peptide - ENSP00000444348
NCBI entrez gene - 23432     See in Manteia.
OMIM - 612250
RefSeq - NM_001349634
RefSeq - NM_001349635
RefSeq - NM_153832
RefSeq - XM_017000862
RefSeq - NM_001267609
RefSeq - NM_001267610
RefSeq - NM_001267611
RefSeq - NM_001267612
RefSeq - NM_001267613
RefSeq - NM_001267614
RefSeq - NM_001349632
RefSeq - NM_001349633
RefSeq - XM_006711253
RefSeq - XM_011509370
RefSeq - XM_011509371
RefSeq - XM_011509372
RefSeq - XM_011509373
RefSeq - XM_011509375
RefSeq - XM_011509376
RefSeq - XM_011509377
RefSeq - XM_011509378
RefSeq - XM_017000858
RefSeq - XM_017000859
RefSeq - XM_017000860
RefSeq - XM_017000861
RefSeq - XM_005245055
RefSeq - XM_005245056
RefSeq - XM_005245057
RefSeq - XM_006711251
RefSeq Peptide - NP_001254538
RefSeq Peptide - NP_001254539
RefSeq Peptide - NP_001254540
RefSeq Peptide - NP_001254541
RefSeq Peptide - NP_001254542
RefSeq Peptide - NP_001254543
RefSeq Peptide - NP_001336561
RefSeq Peptide - NP_001336562
RefSeq Peptide - NP_001336563
RefSeq Peptide - NP_001336564
RefSeq Peptide - NP_722561
swissprot - Q8N6U8
swissprot - A0A0A0MQW8
Ensembl - ENSG00000143147
  
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)
Ortholog nameID Species
 gpr161ENSDARG00000055659Danio rerio
 si:ch211-237c6.4ENSDARG00000058903Danio rerio
 GPR161ENSGALG00000015247Gallus gallus
 B2RPY5ENSMUSG00000040836Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
GPR101 / Q96P66 / G protein-coupled receptor 101ENSG0000016537016
GPR45 / Q9Y5Y3 / G protein-coupled receptor 45ENSG0000013597315
GPR63 / Q9BZJ6 / G protein-coupled receptor 63ENSG0000011221814


Protein motifs (from Interpro)
Interpro ID Name
 IPR000276  G protein-coupled receptor, rhodopsin-like
 IPR017452  GPCR, rhodopsin-like, 7TM


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007186 G-protein coupled receptor signaling pathway ISS
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0030819 obsolete positive regulation of cAMP biosynthetic process IEA
 biological_processGO:1901621 negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0005929 cilium ISS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0030666 endocytic vesicle membrane TAS
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0055037 recycling endosome IEA
 cellular_componentGO:0060170 ciliary membrane TAS
 molecular_functionGO:0004871 obsolete signal transducer activity IEA
 molecular_functionGO:0004930 G-protein coupled receptor activity ISS


Pathways (from Reactome)
Pathway description
Hedgehog off state
Hedgehog on state


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000028 Cryptorchidism "Absence of one or both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis." [HPO:curators]
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 HP:0000786 Primary amenorrhea 
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 HP:0000821 Hypothyroidism 
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 HP:0000823 Delayed puberty 
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 HP:0000835 Adrenal hypoplasia 
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 HP:0000873 Diabetes insipidus "A state of excessive water intake and hypotonic (dilute) polyuria. Diabetes insipidus may be due to failure of vasopressin (AVP) release (central or neurogenic diabetes insipidus) or to a failure of the kidney to respond to AVP (nephrogenic diabetes insipidus)." [HPO:curators]
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001508 Failure to thrive 
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 HP:0001522 Death in infancy 
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 HP:0001943 Hypoglycemia "A lower than normal level of blood glucose." [HPO:curators]
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0008736 Hypoplasia of penis 
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 HP:0011755 Ectopic posterior pituitary "An abnormal anatomical location of the posterior lobe of the hypophysis, also known as the `neurohypophysis` (FMA:74628). The posterior pituitary is normally present in the dorsal portion of the sella turcica, but when ectopic is usually near the median eminence. This defect is likely to be due to abnormal migration during embryogenesis." [DDD:spark, HPO:probinson]
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 HP:0100842 Septo-optic dysplasia "Underdevelopment of the optic nerve and absence of the septum pellucidum." [HPO:sdoelken]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000123607 Q7Z4L5 / TTC21B / tetratricopeptide repeat domain 21B  / reaction / complex
 ENSG00000118965 WDR35 / Q9P2L0 / WD repeat domain 35  / complex / reaction
 ENSG00000163913 IFT122 / Q9HBG6 / intraflagellar transport 122  / reaction / complex
 ENSG00000187535 IFT140 / Q96RY7 / intraflagellar transport 140  / complex / reaction
 ENSG00000157796 WDR19 / Q8NEZ3 / WD repeat domain 19  / complex / reaction
 ENSG00000078246 TULP3 / O75386 / tubby like protein 3  / reaction / complex






 

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contact: otassy@igbmc.fr