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KRTAP4-2 and SLC23A1
Number of citations of the paper that reports this interaction (PMID
25416956
)
0
Data Source:
BioGRID
(two hybrid)
KRTAP4-2
SLC23A1
Gene Name
keratin associated protein 4-2
solute carrier family 23 (ascorbic acid transporter), member 1
Image
No pdb structure
No pdb structure
Gene Ontology Annotations
Cellular Component
Keratin Filament
Cytoplasm
Plasma Membrane
Integral Component Of Plasma Membrane
Brush Border
Basal Plasma Membrane
Membrane
Apical Plasma Membrane
Intracellular Organelle
Extracellular Vesicular Exosome
Molecular Function
Protein Binding
L-ascorbate:sodium Symporter Activity
Sodium Ion Transmembrane Transporter Activity
Nucleobase Transmembrane Transporter Activity
L-ascorbic Acid Transporter Activity
Dehydroascorbic Acid Transporter Activity
Sodium-dependent L-ascorbate Transmembrane Transporter Activity
Biological Process
Nucleobase-containing Compound Metabolic Process
Vitamin Metabolic Process
Water-soluble Vitamin Metabolic Process
Sodium Ion Transport
Brain Development
Response To Toxic Substance
Nucleobase Transport
L-ascorbic Acid Transport
L-ascorbic Acid Metabolic Process
Lung Development
Vitamin Transmembrane Transport
Sodium Ion Transmembrane Transport
Small Molecule Metabolic Process
Dehydroascorbic Acid Transport
Transepithelial L-ascorbic Acid Transport
Pathways
Metabolism of vitamins and cofactors
Defective CD320 causes methylmalonic aciduria
Defective GIF causes intrinsic factor deficiency
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
Defective HLCS causes multiple carboxylase deficiency
Defective MMAB causes methylmalonic aciduria type cblB
Defective BTD causes biotidinase deficiency
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
Vitamin C (ascorbate) metabolism
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
Defective MMAA causes methylmalonic aciduria type cblA
Defective CUBN causes hereditary megaloblastic anemia 1
Defective AMN causes hereditary megaloblastic anemia 1
Defective MUT causes methylmalonic aciduria mut type
Metabolism of water-soluble vitamins and cofactors
Defects in biotin (Btn) metabolism
Defective TCN2 causes hereditary megaloblastic anemia
Defects in cobalamin (B12) metabolism
Defects in vitamin and cofactor metabolism
Drugs
Vitamin C
Diseases
GWAS
Protein-Protein Interactions
72 interactors:
ADAMTSL4
ALDH3B1
AMOTL2
AQP1
ATG9A
BYSL
C19orf66
CHIC2
CHRD
CRCT1
CREB5
DLGAP2
DOCK2
FAM74A4
GLRX3
GNMT
HOXA1
HPCAL1
HSD3B7
KRTAP10-1
KRTAP10-11
KRTAP10-3
KRTAP10-5
KRTAP10-7
KRTAP10-8
KRTAP10-9
KRTAP26-1
KRTAP5-6
KRTAP5-9
KRTAP9-2
KRTAP9-4
LASP1
LCE1B
LCE2A
LCE3C
LCE3E
LCE4A
LNX1
MEOX2
NLK
NOTCH2NL
NR1D2
NUFIP2
OTX1
PDE9A
PGLS
PIN1
PLSCR1
POM121L8P
PRKAB2
PRKAG1
PSMA6
PVRL3
RASSF5
RGS20
SLC23A1
SLC25A10
SPATA24
SPATA3
SPRY1
TCEANC
TINAGL1
TRIM42
TXNDC5
TYRO3
WDYHV1
ZBTB24
ZNF124
ZNF20
ZNF417
ZNF559
ZNF581
12 interactors:
ADAMTSL4
AHCYL1
KRT31
KRTAP10-1
KRTAP10-3
KRTAP10-5
KRTAP10-7
KRTAP10-8
KRTAP10-9
KRTAP4-2
MTUS2
NOTCH2NL
Entrez ID
85291
9963
HPRD ID
13944
04810
Ensembl ID
ENSG00000244537
ENSG00000170482
Uniprot IDs
Q9BYR5
Q9UHI7
PDB IDs
Enriched GO Terms of Interacting Partners
?
Keratinization
Keratinocyte Differentiation
Epidermal Cell Differentiation
Epidermis Development
Transcription, DNA-templated
Epithelium Development
Skin Development
RNA Biosynthetic Process
Organ Development
Tissue Development
Transepithelial Transport
Cellular Process
Cellular Nitrogen Compound Metabolic Process
Gene Expression
Biosynthetic Process
RNA Metabolic Process
Nucleobase-containing Compound Metabolic Process
Cellular Macromolecule Biosynthetic Process
Macromolecule Biosynthetic Process
Multicellular Organismal Development
Nitrogen Compound Metabolic Process
Heterocycle Metabolic Process
Cellular Aromatic Compound Metabolic Process
Apoptotic Cell Clearance
BMP Signaling Pathway Involved In Spinal Cord Dorsal/ventral Patterning
Metanephric Descending Thin Limb Development
Metanephric Proximal Straight Tubule Development
Metanephric Proximal Convoluted Tubule Segment 2 Development
Abducens Nerve Formation
Maintenance Of Symbiont-containing Vacuole By Host
Transepithelial Water Transport
Optokinetic Behavior
Transepithelial L-ascorbic Acid Transport
Organic Anion Transport
Tagcloud
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Tagcloud (Difference)
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Tagcloud (Intersection)
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