SLC7A7 T299Ifs*10

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
36227
7977786
9056
A0A0S2Z502
A_23_P99642
CCDS9574
ENSG00000155465
ENSP00000285850
ENSP00000380662
ENSP00000380663
ENSP00000380666
ENSP00000451881
ENST00000285850
ENST00000397528
ENST00000397529
ENST00000397532
ENST00000555702
EntrezGene:9056
g4507054_3p_a_at
GE55209
GO:0000821
GO:0003333
GO:0005886
GO:0005887
GO:0006461
GO:0006520
GO:0006810
GO:0006865
GO:0015171
GO:0015174
GO:0015179
GO:0015297
GO:0015807
GO:0016020
GO:0016021
GO:0016323
GO:0050900
GO:1902475
GO:1990822
HGNC:11065
HPA036227
Hs.513147
ILMN_1810275
LRG_695
LRG_695t1
LRG_695t2
MIM:222700
MIM:603593
NM_001126105
NM_001126106
NP_001119577
NP_001119578
NR_040448
PF13520
PH_hs_0011505
SLC7A7
SLC7A7-201
SLC7A7-202
SLC7A7-203
SLC7A7-204
SLC7A7-215
TC14000936.hg
TC14001926.hg
uc001wgr.5
uc001wgs.5
uc001wgt.5
uc001wgu.5
uc001wgv.5
UPI000000CC04
XM_006720302
XM_011537298
XM_011537299
XP_006720365
XP_011535600
XP_011535601
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
Cross References
GeneCards
PRO
Orphanet
HMDB Protein