SLC7A7 T299Ifs*10 [plasma membrane]

Stable Identifier
R-HSA-5660949
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Y+L amino acid transporter 1
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
SLC7A7
Chain
chain:1-511
Other Identifiers
0007100487
11720989_a_at
204588_s_at
33731_at
3556817
3556818
3556819
3556820
3556822
3556823
3556825
3556826
3556827
3556828
3556829
3556830
3556831
3556837
3556838
3556839
3556842
3556843
3556844
3556845
7977786
9056
A_23_P99642
GE55209
GO:0000821
GO:0002376
GO:0003674
GO:0005575
GO:0005886
GO:0005887
GO:0006520
GO:0006810
GO:0006865
GO:0008150
GO:0015174
GO:0015179
GO:0016020
GO:0016021
GO:0016323
GO:0022857
GO:0034641
GO:0040011
GO:0044281
GO:0048870
GO:0050900
GO:0055085
GO:1902475
GO:1990822
ILMN_1810275
PH_hs_0011505
TC14000936.hg
TC14001926.hg
g4507054_3p_a_at
Participant Of
Other forms of this molecule
Modified Residues
Name
Replacement of residues 299 to 307
Disease
Name Identifier Synonyms
amino acid metabolic disorder 9252 inborn errors of amino acid metabolism
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