Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5031 to 5040 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5031
GRB2 associated regulator of MAPK1 subtype 2
FAM59B, GAREML
Trifunctional protein deficiency

5032
Golgi associated RAB2 interactor family member 2
C14orf54, FAM71D, GARI-L1, GARI-L2
Rhinosinusitis, Sinusitis

5033
Golgi associated RAB2 interactor family member 3
FAM71B, GARI-L3
Multiple sclerosis

5034
Golgi associated RAB2 interactor family member 4
FAM71A, GARI-L4, GARIL4
Tourette syndrome

5035
Golgi associated RAB2 interactor 5A
FAM71E1, GARIL5
Neurodevelopmental disorder

5036
GTPase activating Rap/RanGAP domain like 3
bA356B19.1
Astrocytoma, Bipolar disorder, Intellectual developmental disorder, Lewy body disease

5037
Granule associated Rac and RHOG effector 1
KIAA0355, MiniBAR
Colorectal cancer, Myopathy

5038
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

5039
Phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase
AIRS, GARS, GARTF, PAIS, PGFT, PRGS
Rheumatoid arthritis, Psoriasis

5040
Growth arrest specific 1
-
Asthma, Cadasil, Cyclocephaly, Holoprosencephaly, Microform holoprosencephaly, Syntelencephaly, Oligodendroglioma, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Systemic lupus erythematosus