about
P688
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosisAIPL1, a protein implicated in Leber's congenital amaurosis, interacts with and aids in processing of farnesylated proteinsThe inherited blindness associated protein AIPL1 interacts with the cell cycle regulator protein NUB1
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Aryl hydrocarbon receptor interacting protein like 1
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Aryl hydrocarbon receptor interacting protein like 1
@en
Aryl hydrocarbon receptor interacting protein like 1
@nl
type
label
Aryl hydrocarbon receptor interacting protein like 1
@en
Aryl hydrocarbon receptor interacting protein like 1
@nl
altLabel
AIPL1
@en
aryl-hydrocarbon-interacting protein-like 1
@en
prefLabel
Aryl hydrocarbon receptor interacting protein like 1
@en
Aryl hydrocarbon receptor interacting protein like 1
@nl
P527
P637
P680
P681
P682
P705
P352
P31
P352
P527
P637
NP_001028226
NP_001028227
NP_001272328
NP_001272329
NP_001272330
NP_001272331
NP_001272332
P680
P682
P702
P703
P705
ENSP00000250087
ENSP00000370520
ENSP00000370521
ENSP00000458456
ENSP00000459522
ENSP00000459673
ENSP00000460134
ENSP00000460672
ENSP00000460827
ENSP00000461287