about
P688
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosaLocalization of extracellular matrix receptors in ICGN mice, a strain of mice with hereditary nephrotic syndromeIdentification and subcellular localization of the RP1 protein in human and mouse photoreceptors
P921
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
RP1 axonemal microtubule associated
@en
RP1 axonemal microtubule associated
@nl
type
label
RP1 axonemal microtubule associated
@en
RP1 axonemal microtubule associated
@nl
altLabel
RP1
@en
doublecortin domain containing 4A
@en
oxygen-regulated protein 1
@en
retinitis pigmentosa 1 (autosomal dominant)
@en
retinitis pigmentosa 1 protein
@en
retinitis pigmentosa RP1 protein
@en
prefLabel
RP1 axonemal microtubule associated
@en
RP1 axonemal microtubule associated
@nl
P637
P681
P682
P705
P352
P279
P31
P352
P637
NP_001362583
XP_016869210
XP_016869211
XP_016869646
XP_016869647
P681
P682
P702
P703
P705
ENSP00000220676
ENSP00000489857
ENSP00000490104