about
P688
Localization to mature melanosomes by virtue of cytoplasmic dileucine motifs is required for human OCA2 functionOrganization and sequence of the human P gene and identification of a new family of transport proteinsA gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinismMutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in OCA2 melanosomal transmembrane protein
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
OCA2 melanosomal transmembrane protein
@en
OCA2 melanosomal transmembrane protein
@nl
type
label
OCA2 melanosomal transmembrane protein
@en
OCA2 melanosomal transmembrane protein
@nl
altLabel
OCA2
@en
P protein
@en
P-protein
@en
eye color 2 (central brown)
@en
eye color 3 (brown)
@en
hair color 3 (brown)
@en
melanocyte-specific transporter protein
@en
oculocutaneous albinism II (pink-eye dilution homolog, mouse)
@en
pink-eyed dilution protein homolog
@en
total brown iris pigmentation
@en
prefLabel
OCA2 melanosomal transmembrane protein
@en
OCA2 melanosomal transmembrane protein
@nl
P637
P680
P681
P682
P705
P352
P637
P31
P352
P361
P637
NP_001287913
XP_011519942
XP_016877744
XP_016877745
XP_016877746
XP_016877747
XP_016877748
XP_016877749
XP_016877750
P681
P682
P702
P703
P705
ENSP00000261276
ENSP00000346659
ENSP00000414425
ENSP00000415431
ENSP00000484219
ENSP00000488119
ENSP00000488215
ENSP00000488458
ENSP00000488768
P7260
2.A.45.2.1