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SLC6A5 Y377* [plasma membrane]
Stable Identifier
R-HSA-5660879
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
GLYT2, Sodium- and chloride-dependent glycine transporter 2, SC6A5_HUMAN
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Disorders of transmembrane transporters (Homo sapiens)
SLC transporter disorders (Homo sapiens)
Defective SLC6A5 causes hyperekplexia 3 (HKPX3) (Homo sapiens)
Defective SLC6A5 does not cotransport Gly, Cl-, Na+ from extracellular region to cytosol (Homo sapiens)
SLC6A5 mutants [plasma membrane] (Homo sapiens)
SLC6A5 Y377* [plasma membrane] (Homo sapiens)
External Reference Information
External Reference
UniProt:Q9Y345 SLC6A5
Gene Names
SLC6A5, GLYT2, NET1
Chain
chain:1-797
Reference Genes
BioGPS Gene:9152 SLC6A5
COSMIC (genes):NET1 SLC6A5
COSMIC (genes):SLC6A5 SLC6A5
CTD Gene:9152 SLC6A5
dbSNP Gene:9152 SLC6A5
ENSEMBL:ENSG00000165970 SLC6A5
HGNC:11051 SLC6A5
KEGG:hsa:9152 SLC6A5
Monarch:9152 SLC6A5
NCBI Gene:9152 SLC6A5
OMIM:604159 SLC6A5
UCSC:Q9Y345 SLC6A5
Reference Transcript
RefSeq:NM_004211.4 SLC6A5
RefSeq:NM_001318369.1 SLC6A5
Other Identifiers
11735289_a_at
16722825
210810_PM_s_at
210810_s_at
236508_PM_at
236508_at
33028_at
3323516
3323517
3323519
3323520
3323521
3323524
3323525
3323526
3323527
3323532
3323533
3323536
3323537
3323538
3323539
3323540
3323545
3323547
3323549
3323550
3323551
3323552
3323553
3323555
7938907
80321_at
9152
A_14_P113842
A_14_P114336
A_23_P116624
GE54742
GE868385
GO:0005215
GO:0005768
GO:0005886
GO:0006836
GO:0007268
GO:0015187
GO:0015293
GO:0015375
GO:0015816
GO:0016020
GO:0022857
GO:0023052
GO:0031045
GO:0031410
GO:0035725
GO:0042734
GO:0043226
GO:0046872
GO:0055085
GO:0060012
GO:0098690
GO:1903804
HMNXSV003027987
Hs.147546.0.A1_3p_at
PH_hs_0008239
TC11000258.hg
g4689409_3p_s_at
Participates
as a member of
SLC6A5 mutants [plasma membrane] (Homo sapiens)
Other forms of this molecule
SLC6A5 S510R [plasma membrane]
SLC6A5 T425M [plasma membrane]
SLC6A5 V432F [plasma membrane]
SLC6A5 [plasma membrane]
Modified Residues
Name
Nonsense mutation at L-tyrosine 377
Coordinate
377
PsiMod
L-tyrosine removal [MOD:01649]
A protein modification that effectively removes or replaces an L-tyrosine.
Disease
Name
Identifier
Synonyms
brain disease
DOID:936
encephalopathy
Cross References
Guide to Pharmacology - Targets
936
ENSEMBL
ENSP00000434364
,
ENST00000525748
OpenTargets
ENSG00000165970
HPA
ENSG00000165970-SLC6A5
ZINC - Substances
SC6A5_HUMAN
ZINC target
Q9Y345
PRO
Q9Y345
Pharos - Targets
Q9Y345
GlyGen
Q9Y345
Orphanet
SLC6A5
ZINC - Predictions - Purchasable
SC6A5_HUMAN
HMDB Protein
HMDBP03205
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