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Gene id 6342
Gene Summary    Protein Summary    Gene ontology    KEGG pathways    Diseases    PubMed    

Gene Summary

Gene Symbol SCP2   Gene   UCSC   Ensembl
Aliases NLTP, NSL-TP, SCP-2, SCP-CHI, SCP-X, SCPX
Gene name sterol carrier protein 2
Alternate names non-specific lipid-transfer protein, epididymis secretory sperm binding protein, propanoyl-CoA C-acyltransferase, sterol carrier protein X,
Gene location 1p32.3 (15778327: 15853231)     Exons: 8     NC_000004.12
Gene summary(Entrez) This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), as a result of transcription initiation from 2 independently regulated promoters. The transcript initiated from the proximal promoter encodes the longer S
OMIM 184755

Protein Summary

Protein general information P22307  

Name: Non specific lipid transfer protein (NSL TP) (EC 2.3.1.176) (Propanoyl CoA C acyltransferase) (SCP chi) (SCPX) (Sterol carrier protein 2) (SCP 2) (Sterol carrier protein X) (SCP X)

Length: 547  Mass: 58994

Tissue specificity: Liver, fibroblasts, and placenta.

Sequence MSSSPWEPATLRRVFVVGVGMTKFVKPGAENSRDYPDLAEEAGKKALADAQIPYSAVDQACVGYVFGDSTCGQRA
IYHSLGMTGIPIINVNNNCATGSTALFMARQLIQGGVAECVLALGFEKMSKGSLGIKFSDRTIPTDKHVDLLINK
YGLSAHPVAPQMFGYAGKEHMEKYGTKIEHFAKIGWKNHKHSVNNPYSQFQDEYSLDEVMASKEVFDFLTILQCC
PTSDGAAAAILASEAFVQKYGLQSKAVEILAQEMMTDLPSSFEEKSIIKMVGFDMSKEAARKCYEKSGLTPNDID
VIELHDCFSTNELLTYEALGLCPEGQGATLVDRGDNTYGGKWVINPSGGLISKGHPLGATGLAQCAELCWQLRGE
AGKRQVPGAKVALQHNLGIGGAVVVTLYKMGFPEAASSFRTHQIEAVPTSSASDGFKANLVFKEIEKKLEEEGEQ
FVKKIGGIFAFKVKDGPGGKEATWVVDVKNGKGSVLPNSDKKADCTITMADSDFLALMTGKMNPQSAFFQGKLKI
TGNMGLAMKLQNLQLQPGNAKL
Structural information
Protein Domains
(433..54-)
(/note="SCP2"-)
Interpro:  IPR003033  IPR036527  IPR016039  IPR020615  IPR020617  
IPR020613  IPR020616  
Prosite:   PS00098 PS00737

PDB:  
1QND 2C0L
PDBsum:   1QND 2C0L
MINT:  
STRING:   ENSP00000360569
Other Databases GeneCards:  SCP2  Malacards:  SCP2

Gene ontology

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GO accessionTerm nameEvidence codeGo category
GO:0032934 sterol binding
IBA molecular function
GO:0032385 positive regulation of in
tracellular cholesterol t
ransport
IBA biological process
GO:0015914 phospholipid transport
IBA biological process
GO:0006694 steroid biosynthetic proc
ess
IBA biological process
GO:0006635 fatty acid beta-oxidation
ISS biological process
GO:0003988 acetyl-CoA C-acyltransfer
ase activity
ISS molecular function
GO:0008206 bile acid metabolic proce
ss
ISS biological process
GO:0050633 acetyl-CoA C-myristoyltra
nsferase activity
ISS molecular function
GO:0016747 transferase activity, tra
nsferring acyl groups oth
er than amino-acyl groups
IEA molecular function
GO:0003824 catalytic activity
IEA molecular function
GO:0008289 lipid binding
IEA molecular function
GO:0016740 transferase activity
IEA molecular function
GO:0016746 transferase activity, tra
nsferring acyl groups
IEA molecular function
GO:0005777 peroxisome
IEA cellular component
GO:0005737 cytoplasm
IEA cellular component
GO:0005739 mitochondrion
IEA cellular component
GO:0006869 lipid transport
IEA biological process
GO:0033814 propanoyl-CoA C-acyltrans
ferase activity
IEA molecular function
GO:0050632 propionyl-CoA C2-trimethy
ltridecanoyltransferase a
ctivity
IEA molecular function
GO:0050632 propionyl-CoA C2-trimethy
ltridecanoyltransferase a
ctivity
EXP molecular function
GO:0005782 peroxisomal matrix
TAS cellular component
GO:0005782 peroxisomal matrix
TAS cellular component
GO:0005782 peroxisomal matrix
TAS cellular component
GO:0005782 peroxisomal matrix
TAS cellular component
GO:0005782 peroxisomal matrix
TAS cellular component
GO:0036109 alpha-linolenic acid meta
bolic process
TAS biological process
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0006625 protein targeting to pero
xisome
TAS biological process
GO:0006699 bile acid biosynthetic pr
ocess
TAS biological process
GO:0033540 fatty acid beta-oxidation
using acyl-CoA oxidase
TAS biological process
GO:0050632 propionyl-CoA C2-trimethy
ltridecanoyltransferase a
ctivity
TAS molecular function
GO:0050632 propionyl-CoA C2-trimethy
ltridecanoyltransferase a
ctivity
TAS molecular function
GO:0050632 propionyl-CoA C2-trimethy
ltridecanoyltransferase a
ctivity
TAS molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0007031 peroxisome organization
IEA biological process
GO:0005737 cytoplasm
IEA cellular component
GO:0005777 peroxisome
IEA cellular component
GO:0005739 mitochondrion
IEA cellular component
GO:0005654 nucleoplasm
IDA cellular component
GO:0005777 peroxisome
IDA cellular component
GO:0043231 intracellular membrane-bo
unded organelle
IDA cellular component
GO:0032991 protein-containing comple
x
IDA cellular component
GO:0032385 positive regulation of in
tracellular cholesterol t
ransport
IDA biological process
GO:0000062 fatty-acyl-CoA binding
IDA molecular function
GO:1901373 lipid hydroperoxide trans
port
IDA biological process
GO:0070538 oleic acid binding
IDA molecular function
GO:0005777 peroxisome
IDA cellular component
GO:0036042 long-chain fatty acyl-CoA
binding
IDA molecular function
GO:0015485 cholesterol binding
IDA molecular function
GO:0005777 peroxisome
IDA cellular component
GO:0016020 membrane
HDA cellular component
GO:0005515 protein binding
IPI molecular function
GO:0005102 signaling receptor bindin
g
IPI molecular function

KEGG pathways

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Pathway idPathway name
hsa01100Metabolic pathways
hsa04146Peroxisome
hsa03320PPAR signaling pathway
hsa01212Fatty acid metabolism
hsa01040Biosynthesis of unsaturated fatty acids
hsa00120Primary bile acid biosynthesis
Associated diseases References
Peroxisomal beta-oxidation enzyme deficiency KEGG:H00407
Leukoencephalopathy with dystonia and motor neuropathy KEGG:H00874
Peroxisomal beta-oxidation enzyme deficiency KEGG:H00407
Leukoencephalopathy with dystonia and motor neuropathy KEGG:H00874
Zellweger syndrome PMID:3555624
Aberrant CpGs in Low Motility Sperm MIK: 21674046
Cryptorchidism MIK: 28606200
Hypospermatogenesis MIK: 28361989
Teratozoospermia MIK: 17327269

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
17327269 Teratozoos
permia

19 (6 controls
, 13 cases)
Male infertility GSE6872 analyzed by GEO2R (cutoff 1.5 fold)
Show abstract
21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
Show abstract
28606200 Cryptorchi
dism

Monozgotic twin
s (1 control, I
cwith cryptorc
hidism)
Male infertility MeDIP-Seq
Show abstract
28361989 Hyposperma
togenesis

6 (3 controls,
3 Klienfelter s
yndrome
Male infertility Microarray
Show abstract