Genes | GeDiPNet - Gene Disease Pathway & Associations

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3591 to 3600 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
3591	23352	UBR4	Ubiquitin protein ligase E3 component n-recognin 4	RBAF600, ZUBR1, p600	Breast cancer, Episodic ataxia, Melanoma
3592	23353	SUN1	Sad1 and UNC84 domain containing 1	UNC84A	Atrial fibrillation, Paroxysmal atrial fibrillation
3593	23355	VPS8	VPS8 subunit of CORVET complex	KIAA0804	Arthrogryposis multiplex congenita
3594	23358	USP24	Ubiquitin specific peptidase 24	-	Chronic obstructive pulmonary disease
3595	23360	FNBP4	Formin binding protein 4	FBP30	Microphthalmia with limb anomalies
3596	23362	PSD3	Pleckstrin and Sec7 domain containing 3	EFA6D, EFA6R, HCA67	Amyotrophic lateral sclerosis, Glioma, Impaired cognition, Lateral sclerosis, Pterygium, Schizophrenia
3597	23363	OBSL1	Obscurin like cytoskeletal adaptor 1	-	3m syndrome, Camptodactyly of fingers, Developmental dysplasia of the hip, Dolichocephaly, Dwarfism, Frontal bossing, High palate, Hypospadias, Macrocephaly, Micromelia, Scoliosis, Vertical talus
3598	23365	ARHGEF12	Rho guanine nucleotide exchange factor 12	LARG, PRO2792	Coronary artery disease, Glaucoma
3599	23368	PPP1R13B	Protein phosphatase 1 regulatory subunit 13B	ASPP1, p53BP2-like, p85	Development disorder, Schizophrenia
3600	23370	ARHGEF18	Rho/Rac guanine nucleotide exchange factor 18	P114-RhoGEF, RP78, SA-RhoGEF, p114RhoGEF	Cataract, Congenital hypoplasia of penis, Cystoid macular edema, Diabetes mellitus, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Leukemia, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa View all (1 more)

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