RHO - RHODOPSIN
Family: 7TM|A|Light|Opsin
Synonyms: OPSIN 2, OPN2|RETINITIS PIGMENTOSA, RHODOPSIN-RELATED, INCLUDED|RETINITIS PIGMENTOSA 4, INCLUDED, RP4, INCLUDED|NIGHT BLINDNESS, CONGENITAL STATIONARY, RHODOPSIN-RELATED, INCLUDED
External
links: Entrez Gene ,
Omim
Summary: (from NCBI-Entrez)
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Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which co
Receptor RHO interacts with:
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OocyteDevelopment
PreEmbryoHuman
PreEmbryoMouse
PreimplantMmEmbryo
Follicle_Maturation_and_Ovulation_POnly
Castrillon_Ovary_Set
Castrillon_Soma_Set
EmbryonicOvary
Mm_Testis_Development
NormEndometrium
PituitaryAdenoma
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Preimplantation Mouse Embryo
Description :
Fields :
Experiment: Testis development
Testes of mice at days 0, 3, 6, 8, 10, 14, 18, 20, 30, 35, and 56 of age.
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Experiment: Pituitary adenoma subtypes
Normal pituitary, pituitary adenomas secreting GH, PRL, or ACTH, and non-functioning adenoma.
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{%="("+prot_type.slice(0,3)+") "+GeneSymbol%>
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Experiment: Preimplantation mouse embryo
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RHO - RHODOPSIN
Family:7TM|A|Light|Opsin
All interactions in Receptor family ( 7TM|A|Light|Opsin )
Gene Expression data