SLC23A1 and AHCYL1

Number of citations of the paper that reports this interaction (PMID 25416956)
0

Data Source:
BioGRID (two hybrid)

		SLC23A1	AHCYL1
Gene Name		solute carrier family 23 (ascorbic acid transporter), member 1	adenosylhomocysteinase-like 1
Image		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	Endoplasmic Reticulum Cytosol 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	Adenosylhomocysteinase Activity Protein Binding
	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	MRNA Polyadenylation Protein Export From Nucleus One-carbon Metabolic Process Biological_process Positive Regulation Of Sodium Ion Transport Regulation Of MRNA 3'-end Processing Regulation Of Ion Transmembrane Transporter Activity S-adenosylmethionine Cycle Regulation Of Anion 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	14 interactors: BID CDKN2C DACH1 GEM HGS ITPR1 MEOX2 PPL PSMD9 SLC23A1 SOX30 SRPK1 SRPK2 ZNF165
Entrez ID		9963	10768
HPRD ID		04810	07613
Ensembl ID		ENSG00000170482	ENSG00000168710
Uniprot IDs		Q9UHI7	O43865
PDB IDs			3MTG
Enriched GO Terms of Interacting Partners?			Positive Regulation Of Viral Genome Replication Negative Regulation Of Viral Genome Replication Regulation Of Metabolic Process Intracellular Signal Transduction Nuclear Speck Organization Transepithelial L-ascorbic Acid Transport Neuron Death Regulation Of MRNA Splicing, Via Spliceosome Regulation Of Viral Genome Replication Positive Regulation Of Viral Process Negative Regulation Of Viral Process Developmental Process Regulation Of Cell Proliferation L-ascorbic Acid Transport Molecular Hydrogen Transport Regulation Of MRNA Processing Signal Transduction In Response To DNA Damage Regulation Of RNA Splicing Regulation Of Cell Cycle Gene Expression RNA Polymerase II Transcriptional Preinitiation Complex Assembly Proteasome Regulatory Particle Assembly Multicellular Organismal Development Nucleus Organization Voluntary Musculoskeletal Movement Dehydroascorbic Acid Transport Regulation Of Cellular Localization Cell Death Death Regulation Of Gene Expression Regulation Of G1/S Transition Of Mitotic Cell Cycle Regulation Of Cell Cycle G1/S Phase Transition Negative Regulation Of Cell Proliferation Involved In Contact Inhibition Cellular Nitrogen Compound Metabolic Process Nucleobase Transport Somite Specification Regulation Of Viral Process G1/S Transition Of Mitotic Cell Cycle Epidermal Growth Factor Receptor Signaling Pathway ERBB Signaling Pathway Glial Cell Apoptotic Process Negative Regulation Of Calcium-mediated Signaling Intrinsic Apoptotic Signaling Pathway Immune Response Cellular Macromolecular Complex Assembly Negative Regulation Of Transcription By Competitive Promoter Binding Sperm Chromatin Condensation Positive Regulation Of Protein Homooligomerization Regulation Of Secretion Immune System Process
Tagcloud ?			abnormality accession attempt csf1 elicit exon exons fused fusion giant karyotypic kb nos nt p11 pathogenetic q21 replaced replacement s100a10 sole stop tag tenosynovial theme transcript tsgct untranslated utr
Tagcloud (Difference) ?			abnormality accession attempt csf1 elicit exon exons fused fusion giant karyotypic kb nos nt p11 pathogenetic q21 replaced replacement s100a10 sole stop tag tenosynovial theme transcript tsgct untranslated utr
Tagcloud (Intersection) ?