Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
5011 to 5020 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5011
Golgi associated RAB2 interactor family member 4
FAM71A, GARI-L4, GARIL4
Tourette syndrome

5012
Golgi associated RAB2 interactor 5A
FAM71E1, GARIL5
Neurodevelopmental disorder

5013
GTPase activating Rap/RanGAP domain like 3
bA356B19.1
Astrocytoma, Bipolar disorder, Intellectual developmental disorder, Lewy body disease

5014
Granule associated Rac and RHOG effector 1
KIAA0355, MiniBAR
Colorectal cancer, Myopathy

5015
Glycyl-tRNA synthetase 1
CMT2D, DSMAV, GARS, GlyRS, HMN5, HMN5A, HMND5, SMAD1, SMAJI
Charcot-marie-tooth disease, Distal hereditary motor neuropathy, Congenital pes cavus, Dejerine-sottas disease, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Motor neuron disease, Hypertrophic neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Spinal muscular atrophy

5016
Phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase
AIRS, GARS, GARTF, PAIS, PGFT, PRGS
Rheumatoid arthritis, Psoriasis

5017
Growth arrest specific 1
-
Asthma, Cadasil, Cyclocephaly, Holoprosencephaly, Microform holoprosencephaly, Syntelencephaly, Oligodendroglioma, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Systemic lupus erythematosus

5018
Growth arrest specific 2
DFNB125, GAS-2
Adenoid cystic carcinoma, Kidney disease, Deafness, Hearing impairment, Hearing loss, Salivary gland neoplasms

5019
Growth arrest specific 2 like 1
GAR22
Myeloid leukemia

5020
Growth arrest specific 2 like 2
CILD41, GAR17
Ciliary dyskinesia, Pharyngeal disorder, Nasal disorder