ABCC9 H60Y

Stable Identifier
R-HSA-5678818
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
SUR2, ATP-binding cassette sub-family C member 9, ABCC9_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
ABCC9, SUR2
Chain
chain:1-1549
Other Identifiers
0006350114
10060
11742433_a_at
11758382_s_at
16762154
208561_at
208562_s_at
3446921
3446922
3446923
3446924
3446925
3446926
3446927
3446928
3446929
3446930
3446931
3446935
3446936
3446940
3446944
3446947
3446948
3446949
3446950
3446951
3446952
3446953
3446954
3446955
3446956
3446957
3446958
3446960
3446961
3446962
3446963
3446964
3446965
3446966
3446971
3446972
3446974
3446976
3446977
3446979
3446980
3446981
3446982
3446983
3446984
3446985
3446986
3446987
3446988
3446989
3446993
3446994
3446997
3446999
37260_at
37261_g_at
7279
75176_at
7961710
A0A024RAV7
A_23_P204194
A_23_P368691
A_24_P178503
AAC16057
AAC16058
ABCC9
ABCC9-201
ABCC9-202
AC008250
AC084806
AF061289
AF061290
AF061291
AF061292
AF061293
AF061294
AF061295
AF061296
AF061297
AF061298
AF061299
AF061300
AF061301
AF061302
AF061303
AF061304
AF061305
AF061306
AF061307
AF061308
AF061309
AF061310
AF061311
AF061312
AF061313
AF061314
AF061315
AF061316
AF061317
AF061318
AF061319
AF061320
AF061321
AF061322
AF061323
AF061324
CCDS8693
CCDS8694
CH471094
EAW96453
EAW96456
ENSG00000069431
ENSP00000261200
ENSP00000261201
ENST00000261200
ENST00000261201
EntrezGene:10060
g10947121_3p_a_at
G3V1N6
GE81542
GE85858
GO:0000166
GO:0002376
GO:0003013
GO:0003674
GO:0004871
GO:0005215
GO:0005267
GO:0005524
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005886
GO:0006810
GO:0006813
GO:0006950
GO:0007165
GO:0008150
GO:0008281
GO:0008282
GO:0010107
GO:0015459
GO:0016020
GO:0016021
GO:0016887
GO:0022857
GO:0030017
GO:0042383
GO:0042493
GO:0042626
GO:0043167
GO:0043225
GO:0043226
GO:0043234
GO:0044325
GO:0051607
GO:0055085
GO:0065009
GO:0099133
GO:1903779
HGNC:60
HPA007279
ILMN_1673243
ILMN_1751453
ILMN_2366473
IPR000388
IPR001475
IPR003439
IPR003593
IPR011527
IPR017871
IPR027417
IPR036640
LRG_377
MIM:239850
MIM:601439
MIM:608569
MIM:614050
NM_005691
NM_020297
NP_005682
NP_064693
PF00005
PF00664
PH_hs_0022557
PR01092
PR01094
Q8N4N7
SM00382
TC12001300.hg
uc001rfh.4
uc001rfi.2
UPI000013D13F
UPI000013D141
XM_005253284
XM_005253286
XM_005253287
XM_005253288
XM_005253289
XM_005253290
XM_006719025
XM_011520545
XP_005253341
XP_005253343
XP_005253344
XP_005253345
XP_005253346
XP_005253347
XP_006719088
XP_011518847
Participant Of
Other forms of this molecule
Modified Residues
Name
L-histidine 60 replaced with L-tyrosine
Coordinate
60
PsiMod HEY
A protein modification that effectively removes or replaces an L-histidine.
A protein modification that effectively converts a source amino acid residue to L-tyrosine.
Disease
Name Identifier Synonyms
osteochondrodysplasia 2256 Unspecified anomaly of cartilage (disorder), chondrodystrophy, Congenital anomaly of cartilage (disorder), Osteochondrodysplasia syndrome (disorder), Cartilage Development disorder
hypertrichosis 420 hypertrichosis NOS (disorder), hypertrichosis (disorder)
Cross References
ZINC - World Drugs
ZINC - Substances
GeneCards
ZINC target
PRO
Orphanet
ZINC - Predictions - Purchasable