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SCP2 and TRIP13
Data Source:
BioGRID
(two hybrid, two hybrid)
SCP2
TRIP13
Description
sterol carrier protein 2
thyroid hormone receptor interactor 13
Image
GO Annotations
Cellular Component
Nucleoplasm
Mitochondrion
Peroxisome
Peroxisomal Matrix
Cytosol
Membrane
Protein-containing Complex
Intracellular Membrane-bounded Organelle
Male Germ Cell Nucleus
Nucleus
Chromosome
Molecular Function
Fatty-acyl-CoA Binding
Acetyl-CoA C-acyltransferase Activity
Signaling Receptor Binding
Protein Binding
Cholesterol Binding
Sterol Binding
Propanoyl-CoA C-acyltransferase Activity
Long-chain Fatty Acyl-CoA Binding
Propionyl-CoA C2-trimethyltridecanoyltransferase Activity
Acetyl-CoA C-myristoyltransferase Activity
Oleic Acid Binding
Transcription Coregulator Activity
Protein Binding
ATP Binding
ATPase Activity
Identical Protein Binding
Biological Process
Protein Targeting To Peroxisome
Fatty Acid Beta-oxidation
Steroid Biosynthetic Process
Bile Acid Biosynthetic Process
Bile Acid Metabolic Process
Phospholipid Transport
Positive Regulation Of Intracellular Cholesterol Transport
Fatty Acid Beta-oxidation Using Acyl-CoA Oxidase
Alpha-linolenic Acid Metabolic Process
Lipid Hydroperoxide Transport
Oocyte Maturation
Double-strand Break Repair
Regulation Of Transcription, DNA-templated
Transcription By RNA Polymerase II
Mitotic Spindle Assembly Checkpoint
Synaptonemal Complex Assembly
Reciprocal Meiotic Recombination
Male Meiosis I
Female Meiosis I
Spermatogenesis
Spermatid Development
Oogenesis
Meiotic Recombination Checkpoint
Pathways
alpha-linolenic acid (ALA) metabolism
Peroxisomal protein import
Peroxisomal protein import
TYSND1 cleaves peroxisomal proteins
Drugs
Diseases
Peroxisomal beta-oxidation enzyme deficiency, including: Acyl-CoA oxidase (ACOX) deficiency; D-bifunctional protein (DBP) deficiency; Perrault syndrome; Sterol carrier protein X (SCPx) deficiency; 2-Methylacyl-CoA racemase (AMCR) deficiency; Hypercholanemia
Leukoencephalopathy with dystonia and motor neuropathy
GWAS
Pancreatic cancer (
25086665
)
Interacting Genes
9 interacting genes:
ACAA2
ACOX1
CACNA1A
CAV1
CREB3
EHHADH
PEX5
PITPNA
TRIP13
112 interacting genes:
ADAM15
AMDHD2
ANKRD10
ARL11
ARSA
ASB13
BUB1B
C11orf54
C19orf54
C4orf33
CARD14
CD99
CDC20
CDIN1
CEP170B
CFP
CLIP4
COMT
CRMP1
CRYBA2
CYB5R2
DCTN3
DDAH2
DIP2A
DPYSL4
DTX2
EEF2KMT
FBLN5
FBXO8
FNDC3B
GALT
GLYCTK
GPRIN2
GPSM1
HDHD3
IGFN1
IL2RB
INCA1
INTS11
KRTAP12-1
KRTAP12-2
KRTAP12-4
KRTAP26-1
KRTAP3-2
KRTAP6-1
KRTAP6-2
KYAT1
LASP1
LNX1
LOXL4
LRR1
LRRC61
M1AP
MAD2L1
MAD2L1BP
MBLAC1
MEAK7
METTL15
MGAT5B
MORN3
MPPED2
MVP
MYEOV
NIF3L1
NME4
NTAQ1
PARP11
PAX9
PBLD
PCMTD2
PCSK5
PELI1
PLAC8
PLK3
PLSCR3
PLSCR4
POLR2L
PPP2CA
PRKAA2
PRKN
PRR13
PSMB8
QARS1
RBPMS
RHOXF2
RNF4
SCP2
SDCBP
SEC24A
SELENBP1
SEMA3B
SEMA4G
SHARPIN
SIGLEC5
SMUG1
SPRYD7
SSC4D
STAMBP
STAMBPL1
SUMO2
TENT5B
TEX37
THRB
TINAGL1
TNRC6A
TPT1
UBE2I
VDR
VENTX
ZMYM5
ZNF34
ZNF655
Entrez ID
6342
9319
HPRD ID
01700
05145
Ensembl ID
ENSG00000116171
ENSG00000071539
Uniprot IDs
A0A384NY87
B2R761
E9PLD1
P22307
Q59HG9
Q15645
PDB IDs
1QND
2C0L
5VQ9
5VQA
5WC2
6F0X
6LK0
Enriched GO Terms of Interacting Partners
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Tagcloud (Intersection)
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