ARSB G144R

Stable Identifier
R-HSA-2314612
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Arylsulfatase B, ARSB_HUMAN, p.Gly144Arg ARSB
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
ARSB
Chain
signal peptide:1-36, chain:37-533
Other Identifiers
0006840133
11731767_at
11731768_x_at
11732739_a_at
11732740_at
1554030_at
16997519
1FSU
206129_s_at
232197_3p_x_at
232197_x_at
2863980
2863981
2863982
2863983
2863984
2863991
2863992
2863996
2864000
2864002
2864003
2864004
2864005
2864006
2864007
2864008
2864009
2864010
2864011
37770
37771
37795_at
411
79310_r_at
8112807
85876_at
A0A024RAJ9
A_24_P205213
ARSB
ARSB-201
ARSB-202
ARSB-206
CCDS4043
CCDS43334
ENSG00000113273
ENSP00000264914
ENSP00000379455
ENSP00000456339
ENST00000264914
ENST00000396151
ENST00000565165
EntrezGene:411
g4557332_3p_a_at
GE57934
GO:0003824
GO:0003943
GO:0004065
GO:0005576
GO:0005739
GO:0005764
GO:0005788
GO:0005791
GO:0005794
GO:0006687
GO:0006914
GO:0007040
GO:0007041
GO:0007417
GO:0007584
GO:0008152
GO:0008484
GO:0009268
GO:0009986
GO:0010632
GO:0010976
GO:0016787
GO:0030207
GO:0035578
GO:0043202
GO:0043312
GO:0043627
GO:0043687
GO:0046872
GO:0051597
GO:0061580
GO:0070062
GO:1904813
HGNC:714
HPA037770
HPA037771
Hs2.1256.2.A1_3p_at
ILMN_1668727
ILMN_1683312
ILMN_1712587
ILMN_1722045
M32373_at
MIM:253200
MIM:611542
NM_000046
NM_198709
NP_000037
NP_942002
PF00884
PH_hs_0022654
TC05001519.hg
uc003kfq.5
uc003kfr.5
uc063evm.1
UPI00000728C3
UPI00001260A3
XM_011543390
XM_011543391
XM_011543392
XM_011543393
XM_017009471
XP_011541692
XP_011541693
XP_011541694
XP_011541695
XP_016864960
Participant Of
Other forms of this molecule
Modified Residues
Name
glycine 144 replaced with L-arginine
Coordinate
144
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to an L-arginine.
A protein modification that effectively removes or replaces an glycine.
Disease
Name Identifier Synonyms
mucopolysaccharidosis VI 12800 Maroteaux-Lamy syndrome, arylsulfatase B deficiency, Maroteaux - Lamy syndrome, Maroteaux-Lamy syndrome (disorder), deficiency of N-acetylgalactosamine-4-sulfatase (disorder)
Cross References
Brenda
GeneCards
DOCK Blaster
PRO
Orphanet
PDB
HMDB Protein