F2RL1 - New-wiki

Interactant Symbol	Name	Associated Pathways Hide	Binding Drugs Hide	Associated Diseases Hide
R3HDM1	R3H domain containing 1
RGR	retinal G protein coupled receptor	G alpha (i) signalling events Opsins		Retinitis pigmentosa (RP)
RTN1	reticulon 1
RTN4	reticulon 4	Axonal growth inhibition (RHOA activation)
SCN1B	sodium voltage-gated channel beta subunit 1	Interaction between L1 and Ankyrins Phase 0 - rapid depolarisation	Ranolazine Phenytoin Valproic acid Oxcarbazepine Cocaine Zonisamide Brivaracetam Dichlorobenzyl alcohol Fish oil	Febrile seizures, including: Febrile convulsions; Generalized epilepsy with febrile seizure plus (GEFS+); Dravet syndrome/ Severe myoclonic epilepsy in infancy (SMEI) Brugada syndrome (BRS)
SDHD	succinate dehydrogenase complex subunit D	Respiratory electron transport Citric acid cycle (TCA cycle)	Hexachlorophene 2-Hexyloxy-6-Hydroxymethyl-Tetrahydro-Pyran-3,4,5-Triol Ubiquinone Q1	Carcinoid
SLC12A5	solute carrier family 12 member 5	Cation-coupled Chloride cotransporters	Potassium chloride Bumetanide
SLC18B1	solute carrier family 18 member B1
SLC1A4	solute carrier family 1 member 4	Amino acid transport across the plasma membrane	Alanine
SLC31A2	solute carrier family 31 member 2
SLC32A1	solute carrier family 32 member 1	Transport of inorganic cations/anions and amino acids/oligopeptides GABA synthesis, release, reuptake and degradation
SLC35A1	solute carrier family 35 member A1	Sialic acid metabolism Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) Transport of nucleotide sugars		Congenital disorders of glycosylation (CDG) type II
SLC39A13	solute carrier family 39 member 13			Ehlers-Danlos syndrome (EDS), including: EDS classical type (EDS1/2); EDS hypermobility type (EDS3); EDS vascular type (EDS4); EDS kyphoscoliosis type (EDS6); EDS arthrochalasia type (EDS7A/7B); EDS dermatospraxis type (EDS7C); EDS autosomal recessive cardiac valvular form (EDSCV); EDS musculocontractural type (EDSMC); EDS progeroid form (EDSP); Tenascin-X deficiency (TNXD); Brittle cornea syndrome (EDS6B); EDS-like spondylocheiro dysplasia (SCD-EDS)
SLC43A2	solute carrier family 43 member 2	Amino acid transport across the plasma membrane
ST14	ST14 transmembrane serine protease matriptase	Formation of the cornified envelope Formation of the cornified envelope	Urokinase Benzamidine Camostat	Ichthyosis with hypotrichosis
SYNGR2	synaptogyrin 2
TMBIM1	transmembrane BAX inhibitor motif containing 1	Neutrophil degranulation
TMED1	transmembrane p24 trafficking protein 1
TMEM161A	transmembrane protein 161A
TMEM62	transmembrane protein 62

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