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SLC23A1 and KRTAP10-7
Number of citations of the paper that reports this interaction (PMID
25416956
)
0
Data Source:
BioGRID
(two hybrid)
SLC23A1
KRTAP10-7
Gene Name
solute carrier family 23 (ascorbic acid transporter), member 1
keratin associated protein 10-7
Image
No pdb structure
No pdb structure
Gene Ontology Annotations
Cellular Component
Cytoplasm
Plasma Membrane
Integral Component Of Plasma Membrane
Brush Border
Basal Plasma Membrane
Membrane
Apical Plasma Membrane
Intracellular Organelle
Extracellular Vesicular Exosome
Keratin Filament
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
12 interactors:
ADAMTSL4
AHCYL1
KRT31
KRTAP10-1
KRTAP10-3
KRTAP10-5
KRTAP10-7
KRTAP10-8
KRTAP10-9
KRTAP4-2
MTUS2
NOTCH2NL
215 interactors:
AEN
AES
ALDH3B1
ANKRD36BP1
AP1M1
APP
AQP1
AVPI1
B4GALT7
BAHD1
BCL6B
BMP7
BUD31
BYSL
C16orf59
C19orf57
C19orf66
C8orf33
C9orf9
CARHSP1
CARKD
CATIP
CBX2
CCDC185
CCDC26
CCNG1
CDCA7L
CHIC2
CHRD
CHRNG
CLK1
CLK4
COL8A1
CRCT1
CREB5
CSNK1G1
CSNK1G2
CTNNBIP1
CTRC
CXCL16
DAAM2
DERL2
DHX57
DMRT3
E2F6
E4F1
EHHADH
FAM124B
FAM161A
FAM27E3
FAM74A4
FAM76B
FARS2
GABARAPL1
GABARAPL2
GEM
GLIDR
GLP1R
GNE
GOLGA8EP
GRN
GSTP1
GUCD1
HBZ
HHEX
HPCAL1
HSBP1
HSD3B7
IGSF8
ING5
INPP5D
IQUB
KLHL38
KRT20
KRT83
KRTAP10-3
KRTAP10-5
KRTAP10-8
KRTAP10-9
KRTAP12-1
KRTAP4-2
KRTAP5-6
KRTAP5-9
KRTAP9-2
LCE1B
LCE2A
LCE3E
LCE4A
LIMS2
LINC00242
LMNA
LMO2
LRCH4
MAPKBP1
MCM5
MOBP
MRGBP
MXD3
MXI1
NAA10
NOL12
NOTCH2NL
NPBWR2
NPDC1
NUBP2
NUDCD3
NUFIP2
P2RY6
PCED1A
PCSK5
PDIA5
PDLIM5
PFKL
PIN1
POLL
POM121L8P
PPARD
PRKAB2
PRM2
PRR13
PTGDS
PTGER3
PTPMT1
PVR
PVRL2
PVRL3
RNF175
RPF1
RPL11
RPL36AL
RPS28
RPUSD3
RSPO2
RTN4RL1
RWDD2B
SCNM1
SDCBP
SLC23A1
SLC25A48
SLC6A20
SMCO4
SMCP
SPATA3
SPATA8
SPG7
SPRY1
SSX2IP
STK16
SUV39H1
TAPBPL
TCEA2
TCEANC
THAP1
THAP6
TMA16
TMEM8A
TNP2
TNS2
TOR1A
TREX1
TRIM42
TULP3
TXNDC5
TYRO3
UCP2
UXT
VTI1B
WDYHV1
WNT11
ZBTB24
ZBTB38
ZBTB9
ZFYVE26
ZNF101
ZNF124
ZNF133
ZNF155
ZNF165
ZNF169
ZNF175
ZNF180
ZNF2
ZNF20
ZNF223
ZNF250
ZNF26
ZNF266
ZNF32
ZNF320
ZNF329
ZNF337
ZNF41
ZNF417
ZNF418
ZNF419
ZNF425
ZNF433
ZNF439
ZNF490
ZNF543
ZNF555
ZNF564
ZNF572
ZNF578
ZNF581
ZNF587
ZNF625
ZNF670
ZNF697
ZNF707
ZNF778
ZNF792
ZNF846
ZNHIT1
ZSCAN26
Entrez ID
9963
386675
HPRD ID
04810
11193
Ensembl ID
ENSG00000170482
ENSG00000205441
Uniprot IDs
Q9UHI7
P60409
PDB IDs
Enriched GO Terms of Interacting Partners
?
RNA Biosynthetic Process
Transcription, DNA-templated
RNA Metabolic Process
Gene Expression
Cellular Macromolecule Biosynthetic Process
Nucleobase-containing Compound Metabolic Process
Macromolecule Biosynthetic Process
Regulation Of RNA Metabolic Process
Heterocycle Metabolic Process
Cellular Aromatic Compound Metabolic Process
Cellular Nitrogen Compound Metabolic Process
Regulation Of Transcription, DNA-templated
Biosynthetic Process
Regulation Of Nucleic Acid-templated Transcription
Regulation Of RNA Biosynthetic Process
Regulation Of Nitrogen Compound Metabolic Process
Nitrogen Compound Metabolic Process
Regulation Of Gene Expression
Cellular Metabolic Process
Cellular Process
Regulation Of Metabolic Process
Regulation Of Cellular Process
Susceptibility To T Cell Mediated Cytotoxicity
Transepithelial Transport
Negative Regulation Of Transcription, DNA-templated
Negative Regulation Of Nucleic Acid-templated Transcription
Negative Regulation Of RNA Biosynthetic Process
Negative Regulation Of Biosynthetic Process
Metabolic Process
Keratinization
Susceptibility To Natural Killer Cell Mediated Cytotoxicity
Developmental Process
Regulation Of Transcription From RNA Polymerase II Promoter
Negative Regulation Of Smoothened Signaling Pathway Involved In Ventral Spinal Cord Patterning
Negative Regulation Of Mesenchymal Cell Proliferation
Positive Regulation Of Natural Killer Cell Mediated Cytotoxicity Directed Against Tumor Cell Target
Cellular Response To Hypoxia
Cellular Response To Decreased Oxygen Levels
Negative Regulation Of Gene Expression
Cellular Response To Oxygen Levels
Cellular Response To Topologically Incorrect Protein
Cellular Response To Stress
Penetration Of Zona Pellucida
Negative Regulation Of Transcription From RNA Polymerase II Promoter
Spinal Cord Dorsal/ventral Patterning
Positive Regulation Of Immune Response To Tumor Cell
Multicellular Organismal Development
Spinal Cord Patterning
Negative Regulation Of Cellular Metabolic Process
Respiratory Tube Development
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