Transient receptor potential cation channel subfamily M member 1
about
sameAs
P527
P688
Chromosomal localization and genomic characterization of the mouse melastatin gene (Mlsn1)Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humansMutations in TRPM1 are a common cause of complete congenital stationary night blindnessMetabotropic glutamate receptor 6 signaling enhances TRPM1 calcium channel function and increases melanin content in human melanocytes
P921
Transient receptor potential cation channel subfamily M member 1
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Transient receptor potential cation channel subfamily M member 1
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Transient receptor potential cation channel subfamily M member 1
@en
Transient receptor potential cation channel subfamily M member 1
@nl
type
label
Transient receptor potential cation channel subfamily M member 1
@en
Transient receptor potential cation channel subfamily M member 1
@nl
altLabel
LTrpC1
@en
TRPM1
@en
long transient receptor potential channel 1
@en
melastatin-1
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transient receptor potential cation channel subfamily M member 1
@en
transient receptor potential melastatin family
@en
prefLabel
Transient receptor potential cation channel subfamily M member 1
@en
Transient receptor potential cation channel subfamily M member 1
@nl
P361
P637
P680
P681
P682
P705
P352
P31
P352
P361
P637
NP_001238949
NP_001238953
NP_001238959
P681
P682
P702
P703
P705
ENSP00000256552
ENSP00000380897
ENSP00000437849
ENSP00000452946
ENSP00000453119
ENSP00000453477
ENSP00000453644
ENSP00000453851
ENSP00000454077
ENSP00000479390