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SERINC1 and CYP39A1
Number of citations of the paper that reports this interaction (PMID
21988832
)
14
Data Source:
BioGRID
(two hybrid)
SERINC1
CYP39A1
Gene Name
serine incorporator 1
cytochrome P450, family 39, subfamily A, polypeptide 1
Image
No pdb structure
No pdb structure
Gene Ontology Annotations
Cellular Component
Endoplasmic Reticulum Membrane
Plasma Membrane
Integral Component Of Membrane
Extracellular Vesicular Exosome
Endoplasmic Reticulum Membrane
Intracellular Membrane-bounded Organelle
Molecular Function
Protein Binding
L-serine Transmembrane Transporter Activity
Iron Ion Binding
Steroid 7-alpha-hydroxylase Activity
Oxysterol 7-alpha-hydroxylase Activity
Heme Binding
24-hydroxycholesterol 7alpha-hydroxylase Activity
Biological Process
Phosphatidylserine Metabolic Process
Sphingolipid Metabolic Process
Phospholipid Biosynthetic Process
L-serine Transport
Positive Regulation Of Transferase Activity
Bile Acid Biosynthetic Process
Cholesterol Catabolic Process
Xenobiotic Metabolic Process
Digestion
Bile Acid Metabolic Process
Sterol Metabolic Process
Bile Acid Catabolic Process
Small Molecule Metabolic Process
Oxidation-reduction Process
Pathways
Bile acid and bile salt metabolism
Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B)
Metabolism of lipids and lipoproteins
Metabolic disorders of biological oxidation enzymes
Phase 1 - Functionalization of compounds
Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A)
Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4)
Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56)
Cytochrome P450 - arranged by substrate type
Endogenous sterols
Biological oxidations
Synthesis of bile acids and bile salts
Synthesis of bile acids and bile salts via 24-hydroxycholesterol
Defective FMO3 causes Trimethylaminuria (TMAU)
Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD)
Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR)
Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX)
Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4)
Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA)
Defective CYP1B1 causes Glaucoma
Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5)
Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3)
Defective CYP19A1 causes Aromatase excess syndrome (AEXS)
Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5)
Defective CYP24A1 causes Hypercalcemia, infantile (HCAI)
Defective MAOA causes Brunner syndrome (BRUNS)
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency)
Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
Drugs
Diseases
GWAS
Protein-Protein Interactions
4 interactors:
CYP39A1
MAK
PAX8
ZMYND10
4 interactors:
GLUL
ORM2
SERINC1
SMYD3
Entrez ID
57515
51302
HPRD ID
15480
07067
Ensembl ID
ENSG00000111897
ENSG00000146233
Uniprot IDs
Q9NRX5
B7Z786
Q9NYL5
PDB IDs
Enriched GO Terms of Interacting Partners
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Regulation Of Thyroid-stimulating Hormone Secretion
Positive Regulation Of Metanephric DCT Cell Differentiation
Pronephric Field Specification
Negative Regulation Of Apoptotic Process Involved In Metanephric Collecting Duct Development
Negative Regulation Of Apoptotic Process Involved In Metanephric Nephron Tubule Development
Negative Regulation Of Mesenchymal Cell Apoptotic Process Involved In Metanephric Nephron Morphogenesis
Positive Regulation Of Thyroid Hormone Generation
Bile Acid Catabolic Process
Kidney Rudiment Formation
Positive Regulation Of Mesenchymal To Epithelial Transition Involved In Metanephros Morphogenesis
Negative Regulation Of Mesenchymal Cell Apoptotic Process Involved In Nephron Morphogenesis
Thyroid-stimulating Hormone Signaling Pathway
Metanephric Nephron Tubule Formation
Metanephric Comma-shaped Body Morphogenesis
Metanephric Tubule Formation
Regulation Of Thyroid Hormone Generation
Comma-shaped Body Morphogenesis
Inner Dynein Arm Assembly
Negative Regulation Of Mesenchymal Cell Apoptotic Process Involved In Metanephros Development
Metanephric S-shaped Body Morphogenesis
Metanephric Distal Convoluted Tubule Development
Metanephric Nephron Tubule Morphogenesis
Pronephros Development
S-shaped Body Morphogenesis
Outer Dynein Arm Assembly
Motile Cilium Assembly
Metanephric Distal Tubule Development
Regulation Of Mesenchymal To Epithelial Transition Involved In Metanephros Morphogenesis
Regulation Of Metanephric Nephron Tubule Epithelial Cell Differentiation
Cholesterol Catabolic Process
Mesenchymal To Epithelial Transition Involved In Metanephros Morphogenesis
Metanephric Tubule Morphogenesis
Distal Tubule Development
Negative Regulation Of Mesenchymal Cell Apoptotic Process
Axonemal Dynein Complex Assembly
Metanephric Renal Vesicle Morphogenesis
Renal Vesicle Morphogenesis
Otic Vesicle Development
Mesenchymal To Epithelial Transition
Positive Regulation Of Branching Involved In Ureteric Bud Morphogenesis
Metanephric Nephron Tubule Development
Nephron Tubule Formation
Regulation Of Nephron Tubule Epithelial Cell Differentiation
Regulation Of Branching Involved In Ureteric Bud Morphogenesis
Regulation Of Epithelial Cell Differentiation Involved In Kidney Development
Bile Acid Biosynthetic Process
Steroid Catabolic Process
Specification Of Organ Identity
Cellular Response To Gonadotropin Stimulus
Metanephric Nephron Morphogenesis
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Tagcloud (Intersection)
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