detection of light stimulus involved in visual perception
about
Retinol binding protein 4, plasmaCalcium voltage-gated channel subunit alpha1 FG protein subunit alpha transducin 2Calcium voltage-gated channel auxiliary subunit alpha2delta 4Cyclic nucleotide gated channel subunit beta 1G protein subunit alpha transducin 1Gap junction protein alpha 10TUB like protein 1Receptor accessory protein 6Bestrophin 1Coiled-coil domain containing 66Eyes shut homologATPase phospholipid transporting 8A2Guanylate cyclase 2F, retinalSemaphorin 5BRetinoid isomerohydrolase RPE65Regulator of G protein signaling 9 binding proteinPhotoreceptor disc componentGlutamate receptor, metabotropic 6Receptor accessory protein 6Calcium channel, voltage-dependent, beta 4 subunitCoiled-coil domain containing 66Gap junction protein, alpha 10Calcium channel, voltage-dependent, alpha 2/delta subunit 4Bestrophin 1ATPase, aminophospholipid transporter-like, class I, type 8A, member 2Guanine nucleotide binding protein, alpha transducing 1Guanine nucleotide binding protein, alpha transducing 2Voltage-dependent L-type calcium channel subunit alpha-1FGuanylate cyclase 2fRegulator of G-protein signalling 9 binding proteinRetinal pigment epithelium 65Sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5BSemaphorin-5ATubby like protein 1Photoreceptor cilium actin regulatorGuanylate cyclase 2FReceptor accessory protein 6Calcium voltage-gated channel auxiliary subunit beta 4Glutamate metabotropic receptor 6
P682
Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosaMutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsiaNight blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein traffickingTwo novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese populationMutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophyIdentification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosaThe electroretinographic diagnosis of the incomplete form of congenital stationary night blindnessp.Gln200Glu, a putative constitutively active mutant of rod alpha-transducin (GNAT1) in autosomal dominant congenital stationary night blindnessA homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markersEYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosaMutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa
P921
Q14911603-98E35EE2-9E5E-41A6-98C9-1F1BBD576411Q21102124-696A1C6C-4102-4F08-99EE-6AF8A5F8E371Q21103236-6250444C-BF24-4874-B65B-BC1598F72B8FQ21105539-1A051CAB-438E-401B-9B0A-1EED480D371CQ21105651-3A39ADD4-D602-41E0-8A11-2E53F04462DFQ21106178-95B15969-9EC2-44DE-8D3A-4BF2EBDDEE2AQ21107088-6BBB271D-40ED-43D6-83C7-9ADE59BC4D92Q21108996-FA579B5B-78B9-4631-85FE-FCA61EF46C3FQ21111217-D0124240-C01B-429F-A93C-304A982518A1Q21112809-A16C0BE0-DDAF-4A40-AE60-B37BDEBF814BQ21112962-CA7FBDCE-8C0F-4512-85B7-13DBB2F8FB8AQ21114426-E7CC990C-A7F0-46A7-82C3-4BC96D081136Q21115361-52F57AA8-351D-45B3-8922-5FE8F1888E28Q21119036-C08E3D85-05B2-4B5B-979D-5CB142B8D515Q21122813-1DDA08BA-AF72-4EF7-B4E1-A667DA486FDEQ21123400-98CFA6B0-8597-4D39-A29B-6A9796EBB738Q21125003-5D9C98F2-54A0-4D1B-9A76-0B8C7214D35AQ21441769-981BF1F0-43CF-416F-975D-62AF7DFA3995Q21495792-15928194-FB5B-4835-A0C4-D3459670598BQ21495792-DE0AFE8A-1C0D-4764-8519-39678B81E981Q21496802-B87618EE-81D5-4F6B-AE21-D9483EAB441DQ21497160-1AA812BE-9D47-4D34-A719-90DD96BA2FC5Q21497263-871599C8-F854-430F-AF68-12E067088260Q21499423-DC8A88CE-1CB7-40A6-9AD6-A2B162F27089Q21981684-AFD562E0-530B-4937-AD2C-31AAFFA368E1Q21982782-0321842C-B80E-40EC-B7DB-94AAD38EB0EAQ21983516-C60EB656-14E7-4C05-A178-610C5CBF34F2Q21984034-6675EEA2-DEC8-4B52-9C24-47D0C62EC95AQ21984036-F4007162-7311-4AB4-BD11-68FA581B5EA5Q21984383-7213B69A-6356-4D88-BF9E-830EC414CE55Q21985420-67BA16A3-4642-4752-8492-8599CFE96568Q21986349-FCEE4917-F202-4CD6-AF54-5BBE12CD3BF0Q21991011-AD1E8216-F820-4B6F-8091-9D7670876E39Q21991133-142D3B7F-CFC5-48DF-B278-11DE0A16DA05Q21991134-28699FB8-A6F1-48D9-BD2A-9D6C28F67305Q21991921-461AA3D7-58F6-48B0-A6C8-E694C9E7BFCAQ22680222-1AABF083-AC53-4CF5-8DE4-E73CFD88D6B9Q28557030-1A58B36D-85CB-42CA-A814-D79134AA0B4EQ28558428-3B68E3C8-A2A0-4EFA-9BE7-44A2EFD04E63Q28560010-93EB4E2F-1E28-4D41-96D2-0894EC1DFEB2
P682
Q24294725-CF5295C5-9E70-452D-BB6B-DC5ECA596140Q24300063-ADC80E4E-7146-4489-9708-6C431D00A89DQ24301599-E51E86A5-67F2-4B00-8FD4-23A9E35FA4CCQ24306041-0CC97C1B-2803-4816-88E1-3C9CA7439C80Q24306524-08415157-1449-4881-851D-767F1200D6BFQ24310728-90575204-FF3B-497B-A968-3DFDED7D0C12Q24312225-39E4C9C6-7057-4A3B-810A-DEEE26A76B9DQ24313069-D4E7112A-61FC-4B79-B504-3B5AFB13C7A3Q24316083-3CEF7F2D-E609-4BC5-8665-1A9FC8806DE0Q24319794-7EAB4198-4756-4EC0-BD0C-681D17D80EE8Q29147466-0486DC4A-B898-48DC-A24A-C8A6A4D6DCE0
P921
detection of light stimulus involved in visual perception
description
The series of events involved ...... erted into a molecular signal.
@en
biologisch proces
@nl
name
detection of light stimulus involved in visual perception
@en
type
label
detection of light stimulus involved in visual perception
@en
altLabel
GO:0050908
@en
sensory detection of light during visual perception
@en
sensory detection of light stimulus during visual perception
@en
sensory transduction of light during visual perception
@en
sensory transduction of light stimulus during visual perception
@en
visual perception, detection of light stimulus
@en
visual perception, sensory transduction during perception of light
@en
visual perception, sensory transduction of light stimulus
@en
prefLabel
detection of light stimulus involved in visual perception
@en
P2888
P686
GO:0050908