SLC22A18AS and TTC19

Data Source:
BioGRID (two hybrid)

		SLC22A18AS	TTC19
Description		solute carrier family 22 member 18 antisense	tetratricopeptide repeat domain 19
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component		Mitochondrion Mitochondrial Inner Membrane Centrosome Midbody Respirasome
	Molecular Function		Protein Binding
	Biological Process		Mitotic Cytokinesis Mitochondrial Respiratory Chain Complex III Assembly
Pathways
Drugs
Diseases			Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (MT-C1D); Complex II deficiency (MT-C2D); Complex III deficiency (MT-C3D); Complex IV deficiency (MT-C4D); Complex V deficiency (MT-ATPSD); Leigh syndrome (LS); Kearns-Sayre Syndrome (KSS); LCHD deficiency (LCHD); Leber Hereditary Optic Neuropathy (LHON); Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); NARP; MELAS; ACAD9 deficiency; HADH deficiency; HIBCH deficiency; GRACILE syndrome
GWAS		Autism spectrum disorders (repetitive sensory-motor behaviour) ( 32624584) Gout ( 22179738) Malaria ( 31844061)
Interacting Genes		6 interacting genes: DTX2 FRS3 INCA1 MTDH NRF1 TTC19	44 interacting genes: AGXT APRT ATXN1 C20orf85 CCDC33 CHMP4A COA6 CYSLTR2 DMRT3 EIF4ENIF1 FAM136A FAM217B FH FTO GORASP2 GPANK1 HOXD12 HPS6 IHO1 L3MBTL3 LDB2 MLN MXRA8 NAB2 NME4 POU6F2 PRR35 RBP1 REL RUSC1 RXFP3 SH2D4A SHISA6 SLC22A18AS SMG9 SPRED1 TBX2 TCAP UBA1 UPF3B USP20 USP54 WASHC1 ZNF688
Entrez ID		5003	54902
HPRD ID		09127	07899
Ensembl ID		ENSG00000254827	ENSG00000011295
Uniprot IDs		Q8N1D0	A0A024RD83 Q6DKK2
PDB IDs
Enriched GO Terms of Interacting Partners?
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