TTC19 and RBP1

Data Source:
BioGRID (two hybrid)

		TTC19	RBP1
Description		tetratricopeptide repeat domain 19	retinol binding protein 1
Image		No pdb structure
GO Annotations	Cellular Component	Mitochondrion Mitochondrial Inner Membrane Centrosome Midbody Respirasome	Nucleoplasm Lipid Droplet Cytosol
	Molecular Function	Protein Binding	Retinoid Binding Protein Binding Retinal Binding All-trans-retinol Binding
	Biological Process	Mitotic Cytokinesis Mitochondrial Respiratory Chain Complex III Assembly	Retinoid Metabolic Process Retinoic Acid Biosynthetic Process Vitamin A Metabolic Process Lipid Homeostasis
Pathways			Retinoid cycle disease events The canonical retinoid cycle in rods (twilight vision) Retinoid metabolism and transport
Drugs			Acitretin
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
Interacting Genes		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	18 interacting genes: BRMS1 BRMS1L CYTOR DHPS HDAC1 HDAC2 IKBKG ING1 LRAT LRP2 MED26 RBBP4 RBBP7 SAP30 SIN3A TNFRSF10D TTC19 UBE2J2
Entrez ID		54902	5947
HPRD ID		07899	07036
Ensembl ID		ENSG00000011295	ENSG00000114115
Uniprot IDs		A0A024RD83 Q6DKK2	A0A0A0MQT0 P09455
PDB IDs			5H8T 5H9A 5HA1 5HBS 5LJB 5LJC 5LJD 5LJE 5LJG 5LJH 5LJK 6E5L 6E5T 6E6M
Enriched GO Terms of Interacting Partners?
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