2,651–2,700 of 20,598 genesranked by Most Researched

#	Gene	Name	Chr	Tags	PubMed Papers
2651	OAT	ornithine aminotransferase	10	OMIM Disease GeneTrending	168
2652	PGAM1	phosphoglycerate mutase 1	10	TrendingExperimental GO Evidence	168
2653	PPP1R13L	protein phosphatase 1 regulatory subunit 13 like	19	Transcription FactorOMIM Disease Gene	168
2654	PRAME	PRAME nuclear receptor transcriptional regulator	22	Transcription FactorTrending	168
2655	PRPF4	pre-mRNA splicing tri-snRNP complex factor PRPF4	9	Highly ConstrainedHub Gene	168
2656	RAD52	RAD52 DNA repair protein	12	DNA RepairHomologous Recombination	168
2657	RANBP1	RAN binding protein 1	22	TrendingExperimental GO Evidence	168
2658	S100P	S100 calcium binding protein P	4	TrendingExperimental GO Evidence	168
2659	SFXN1	sideroflexin 1	5	TransporterTrending	168
2660	SLC12A3	solute carrier family 12 member 3	16	TransporterFDA Approved Target	168
2661	SMARCD1	SWI/SNF related BAF chromatin remodeling complex subunit D1	12	Highly ConstrainedHub Gene	168
2662	TNRC6A	trinucleotide repeat containing adaptor 6A	16	Highly ConstrainedOMIM Disease Gene	168
2663	VIP	vasoactive intestinal peptide	6	Hub GeneExperimental GO Evidence	168
2664	ACADM	acyl-CoA dehydrogenase medium chain	1	OMIM Disease GeneTrending	167
2665	ALOX12	arachidonate 12-lipoxygenase, 12S type	17	FDA Approved TargetOMIM Disease Gene	167
2666	AP1B1	adaptor related protein complex 1 subunit beta 1	22	TransporterOMIM Disease Gene	167
2667	AP1M1	adaptor related protein complex 1 subunit mu 1	19	TransporterTrending	167
2668	BGN	biglycan	X	Hub GeneOMIM Disease Gene	167
2669	DRG1	developmentally regulated GTP binding protein 1	22	OMIM Disease GeneExperimental GO Evidence	167
2670	GPS1	G protein pathway suppressor 1	17	Highly ConstrainedTrending	167
2671	IRF8	interferon regulatory factor 8	16	Transcription FactorOMIM Disease Gene	167
2672	LCT	lactase	2	OMIM Disease GeneExperimental GO Evidence	167
2673	NR0B1	nuclear receptor subfamily 0 group B member 1	X	Highly ConstrainedReceptor	167
2674	NUP133	nucleoporin 133	1	TransporterOMIM Disease Gene	167
2675	RGS2	regulator of G protein signaling 2	1	TrendingExperimental GO Evidence	167
2676	SHANK3	SH3 and multiple ankyrin repeat domains 3	22	OMIM Disease GeneTrending	167
2677	SNU13	small nuclear ribonucleoprotein 13	22	Hub GeneExperimental GO Evidence	167
2678	TNFSF4	TNF superfamily member 4	1	Clinical TrialsOMIM Disease Gene	167
2679	TPM2	tropomyosin 2	9	OMIM Disease GeneTrending	167
2680	UFD1	ubiquitin recognition factor in ER associated degradation 1	22	Hub GeneTrending	167
2681	APBB1	amyloid beta precursor protein binding family B member 1	11	Transcription FactorExperimental GO Evidence	166
2682	ATP1B1	ATPase Na+/K+ transporting subunit beta 1	1	Highly ConstrainedTransporter	166
2683	BAZ1B	bromodomain adjacent to zinc finger domain 1B	7	Highly ConstrainedKinase	166
2684	CD226	CD226 molecule	18	ReceptorTrending	166
2685	COPS2	COP9 signalosome subunit 2	15	Highly ConstrainedExperimental GO Evidence	166
2686	DOT1L	DOT1 like histone lysine methyltransferase	19	DNA RepairHighly Constrained	166
2687	GJB6	gap junction protein beta 6	13	OMIM Disease GeneExperimental GO Evidence	166
2688	GSTO1	glutathione S-transferase omega 1	10	Hub GeneTrending	166
2689	ITGA1	integrin subunit alpha 1	5	Hub GeneReceptor	166
2690	KIF4A	kinesin family member 4A	X	Highly ConstrainedHub Gene	166
2691	MASP2	MBL associated serine protease 2	1	ProteaseClinical Trials	166
2692	MFGE8	milk fat globule EGF and factor V/VIII domain containing	15	TrendingExperimental GO Evidence	166
2693	NPHS2	NPHS2 stomatin family member, podocin	1	OMIM Disease GeneVariant-Rich	166
2694	OAS1	2'-5'-oligoadenylate synthetase 1	12	Hub GeneOMIM Disease Gene	166
2695	PLRG1	pleiotropic regulator 1	4	Hub GeneExperimental GO Evidence	166
2696	PMAIP1	phorbol-12-myristate-13-acetate-induced protein 1	18	ApoptosisTrending	166
2697	RBCK1	RANBP2-type and C3HC4-type zinc finger containing 1	20	OMIM Disease GeneTrending	166
2698	RBM4	RNA binding motif protein 4	11	TrendingExperimental GO Evidence	166
2699	RECQL	RecQ like helicase	12	Homologous RecombinationOMIM Disease Gene	166
2700	SPTLC1	serine palmitoyltransferase long chain base subunit 1	9	OMIM Disease GeneTrending	166