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Awaiting annotation/under development. Please contact us if you can help with annotation.
GPR143 
Family: Other 7TM proteins
Gene and Protein Information  |
| Species |
TM |
AA |
Chromosomal Location |
Gene Symbol |
Gene Name |
Reference |
| Human |
7 |
404 |
Xp22.3 |
GPR143
|
G protein-coupled receptor 143
|
|
| Mouse |
7 |
405 |
X F2-F3 |
Gpr143
|
G protein-coupled receptor 143
|
|
| Rat |
7 |
405 |
Xq21 |
Gpr143
|
G protein-coupled receptor 143
|
|
Previous and Unofficial Names  |
| MOA1 |
| OA1 |
| ocular albinism 1 (Nettleship-Falls) |
| GPR143 |
| G-protein coupled receptor 143 |
| G protein-coupled receptor 143 |
| Ocular albinism type 1 protein |
| NYS6 |
| Gpr143_predicted |
| LOC302619 |
| RGD1565799 |
| RGD1565799_predicted |
| G protein-coupled receptor 143 (predicted) |
| similar to Oa1 |
| similar to Oa1 (predicted) |
Database Links  |
|
Ensembl
|
ENSG00000101850 (Hs), ENSMUSG00000025333 (Mm), ENSRNOG00000003543 (Rn)
|
|
Entrez Gene
|
4935 (Hs), 18241 (Mm), 302619 (Rn)
|
|
GeneCards
|
GPR143 (Hs)
|
|
GenitoUrinary Development Molecular Anatomy Project
|
Gpr143 (Mm)
|
|
HomoloGene
|
230 (Hs)
|
|
Human Protein Reference Database
|
02355 (Hs)
|
|
InterPro
|
P51810 (Hs), P70259 (Mm)
|
|
KEGG Gene
|
hsa:4935 (Hs), mmu:18241 (Mm), rno:302619 (Rn)
|
|
OMIM
|
300500 (Hs)
|
|
Orphanet Gene
|
ORPHA122263 (Hs)
|
|
PhosphoSitePlus
|
P51810 (Hs), P70259 (Mm)
|
|
Protein Ontology (PRO)
|
PRO:000008186 (Hs)
|
|
RefSeq Nucleotide
|
NM_000273 (Hs), NM_010951 (Mm), NM_001103958 (Rn)
|
|
RefSeq Protein
|
NP_000264 (Hs), NP_035081 (Mm), NP_001100428 (Rn)
|
|
TreeFam
|
ENSG00000101850 (Hs), ENSMUSG00000025333 (Mm), ENSRNOG00000003543 (Rn)
|
|
UniGene Hs.
|
74124 (Hs)
|
|
UniProt
|
P51810 (Hs), P70259 (Mm)
|
|
Wikipedia
|
GPR143
|
|
Orphan and other 7TM receptors
|
Expression Datasets  |
|
Click here to show/hide data
Log average relative transcript abundance in mouse tissues measured by qPCR from Regard, J.B., Sato, I.T., and Coughlin, S.R. (2008). Anatomical profiling of G protein-coupled receptor expression. Cell, 135(3): 561-71. [PMID:18984166] [Raw data: website]
There should be a chart of expression data here, you may need to enable JavaScript!
|
|
Phenotypes, Alleles and Disease Models
|
Mouse data from MGI
|
|
Click here to show/hide data
| Gpr143tm1Inc |
Gpr143tm1Inc/Y either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
MGI:107193 |
MP:0005101 |
abnormal ciliary body pigmentation |
PMID:
11092754
|
| Gpr143tm1Inc |
Gpr143tm1Inc/Y either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
MGI:107193 |
MP:0005199 |
abnormal iris pigment epithelium |
PMID:
11092754
|
| Gpr143tm1Inc |
Gpr143tm1Inc/Y either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
MGI:107193 |
MP:0005075 |
abnormal melanosome morphology |
PMID:
11092754
|
| Gpr143tm1Inc |
Gpr143tm1Inc/Y either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
MGI:107193 |
MP:0002864 |
abnormal ocular fundus morphology |
PMID:
11092754
|
| Gpr143tm1Inc |
Gpr143tm1Inc/Y either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
MGI:107193 |
MP:0001332 |
abnormal optic nerve innervation |
PMID:
11092754
|
| Gpr143tm1Inc |
Gpr143tm1Inc/Y either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
MGI:107193 |
MP:0005200 |
abnormal pigment epithelium of the eye |
PMID:
11092754
|
| Gpr143tm1Inc |
Gpr143tm1Inc/Y either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
MGI:107193 |
MP:0005103 |
abnormal retinal pigmentation |
PMID:
11092754
|
| Gpr143tm1Inc |
Gpr143tm1Inc/Y either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6) |
MGI:107193 |
MP:0005201 |
abnormal retinal pigment epithelium morphology |
PMID:
11092754
|
|
Clinically-Relevant Mutations and Pathophysiology
|
| Disease: |
X-linked recessive ocular albinism |
| OMIM: |
300500 |
| Orphanet: |
54 |
| References: |
|
|
|
Mutations not determined
|
|
| Disease: |
Congenital idiopathic nystagmus |
| OMIM: |
300814 |
| Orphanet: |
651 |
| References: |
|
|
|
Mutations not determined
|
|
To cite this database page, please use the following:
Tom I. Bonner.
Other 7TM proteins: GPR143. Last modified on 23/02/2012. Accessed on 22/05/2013. IUPHAR database (IUPHAR-DB), http://www.iuphar-db.org/DATABASE/ObjectDisplayForward?objectId=203.
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