SLC7A7 Y457*

Stable Identifier
R-HSA-5660952
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
L-tyrosine 457 replaced with unknown
Coordinate
457
PsiMod HEY
A protein modification that effectively removes or replaces an L-tyrosine.
Disease
Name Identifier Synonyms
amino acid metabolic disorder 9252 inborn errors of amino acid metabolism
Cross References
GeneCards
PRO
Orphanet
HMDB Protein