Protein Sost

URN urn:agi-llid:8149
Total Entities 0
Connectivity 275
Name Sost
Description sclerostin
Notes Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease. [provided by RefSeq]

Ariadne Ontology Secreted proteins
Biofluids assayable substances

GO Molecular Function transcription factor binding
heparin binding

GO Cellular Component extracellular matrix
extracellular region
Golgi apparatus
extracellular space

GO Biological Process negative regulation of Wnt receptor signaling pathway
negative regulation of canonical Wnt receptor signaling pathway
negative regulation of Wnt receptor signaling pathway involved in dorsal-ventral axis specification
negative regulation of BMP signaling pathway
Wnt receptor signaling pathway
positive regulation of transcription, DNA-dependent
cellular response to parathyroid hormone stimulus
response to mechanical stimulus
negative regulation of ossification
negative regulation of protein complex assembly
ossification

Pathway Dexamethasone-Induced Neurotoxicity
Dexamethasone-Induced Diabetes
Dexamethasone-Induced Osteoporosis
BMP2-BMPR2 Expression Targets
Wnt signaling, canonical pathway
altered Wnt signaling, canonical pathway
Wnt signaling, canonical pathway

Group negative regulation of Wnt receptor signaling pathway
negative regulation of canonical Wnt receptor signaling pathway
negative regulation of Wnt receptor signaling pathway involved in dorsal-ventral axis specification
negative regulation of BMP signaling pathway
Wnt receptor signaling pathway
positive regulation of transcription, DNA-dependent
cellular response to parathyroid hormone stimulus
response to mechanical stimulus
negative regulation of ossification
negative regulation of protein complex assembly
ossification
transcription factor binding
heparin binding
extracellular matrix
extracellular region
Golgi apparatus
extracellular space
Secreted proteins
Biofluids assayable substances

MedScan ID 8149

Hugo ID 13771

Human chromosome position 17q11.2

GenBank ID NC_000017
NM_025237
NP_079513
NG_008078
NC_018928
AC_000149
AC055813
AF326736
AAK13451
CH471178
EAW51669
CQ986736
CAI46877
AF170491
AAQ13601
AF184211
AAQ13694
AF326739
AAK13454
AF331844
AAK16158
AY358203
AAQ88570
AY358627
AAQ88990
BC101086
AAI01087
BC101087
AAI01088
BC101088
AAI01089
BC101089
AAI01090
Q9BQB4
NC_000077
NM_024449
NP_077769
AC_000033
AF326737
AAK13452
AL591145
CAM23242
CH466558
EDL34073
AF326740
AAK13455
AK017295
BAB30678
AK041382
BC137832
AAI37833
BC137833
AAI37834
Q99P68
NC_005109
NM_030584
NP_085073
AC_000078
CH473948
EDM06161
AF326741
AAK13456
Q99P67
NT_010783
NW_001838437
NW_926839
AC_000060
Q7Z2R3
Q7Z4G0
NT_165773
NW_001030434
NW_047339
NW_001084656

LocusLink ID 8149
50964
74499
80722

Alias CDD
VBCH
UNQ2976/PRO7455/PRO7476
sclerostin
5430411E23Rik
RP23-398F7.2
sclerosteosis
5430411E23
van buchem disease gene
SOST
sclerosteosis protein
sclerosteosis gene
OTTMUSP00000002060
LOC629951

Organism Homo sapiens
Mus musculus
Rattus norvegicus

OMIM ID 605740
122860
239100
269500

Unigene ID Hs.349204
Mm.265602
Rn.95369

KEGG ID hsa:50964
mmu:74499
rno:80722

Swiss-Prot Accession Q9BQB4
B1AQF2
Q99P68
Q99P67
Q495N9
Q9D3L7
Q7Z2R3
Q7Z4G0

GO ID 0008201
0008134
0016055
0071374
0030514
2000054
0090090
0030279
0031333
0001503
0045893
0009612
0031012
0005615
0030178
0005794
0005576

Swiss-Prot ID SOST_HUMAN
SOST_MOUSE
SOST_RAT
B1AQF2_MOUSE
B2RQA5_MOUSE

Cell Localization Secreted

IPI ID IPI00019272
IPI00410101
IPI00321910
IPI00200398
IPI00896590
IPI00384900
IPI00385104

Mouse chromosome position 11

Rat chromosome position 10q32.1

Homologene ID 11542

MGI ID 1921749

RGD ID 69358