Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
461 to 470 of 12229 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

461
Dynein axonemal light chain 4
MRMV3, PIG27
Agenesis of corpus callosum, Cerebral palsy, Congenital mirror movements, Dysgenesis of the hippocampus, Hypogonadotropic hypogonadism, Mental retardation, Mirror movements, Specific learning disorder

462
Leucine rich pentatricopeptide repeat containing
CLONE-23970, GP130, LRP130, LSFC, MC4DN5
Central nervous system demyelination, Congenital lactic acidosis, Developmental delay, Hyperglycemia, Hypoglycemia, Leigh syndrome, Mitochondrial diseases, Necrotizing encephalomyelopathy, Strabismus

463
FRY microtubule binding protein
13CDNA73, 214K23.2, C13orf14, CG003, bA207N4.2, bA37E23.1
Breast carcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Diabetes mellitus, Mental retardation, Lung carcinoma, Lung adenocarcinoma, Lung cancer, Narcolepsy, Ovarian neoplasm, Ovarian serous adenocarcinoma, Ovarian endometrioid carcinoma, Parkinson disease, Prostate cancer

464
Cadherin 15
CDH14, CDH3, CDHM, MCAD, MRD3
Mental retardation, Non-syndromic intellectual disability, Sclerocystic ovaries, Polycystic ovary syndrome

465
Protein disulfide isomerase family A member 6
ERP5, P5, TXNDC7
Schizophrenia

466
TNF receptor associated protein 1
HSP 75, HSP75, HSP90L, TRAP-1
Arthritis, Congenital anomalies of kidney and urinary tract, Crohn disease, Gastric cancer, Osteoarthrosis deformans, Stomach neoplasms, Vacterl association

467
Optineurin
ALS12, FIP2, GLC1E, HIP7, HYPL, NRP, TFIIIA-INTP
Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Anxiety disorder, Dysarthria, Dysphagia, Glaucoma, Laryngospasm, Mental depression, Mood swings, Motor neuron disease, Myopia, Open angle glaucoma, Paget disease, Respiratory failure

468
B cell receptor associated protein 31
6C6-AG, BAP31, CDM, DDCH, DELXQ28, DXS1357E, MICRODELXq28
Atrophy of corpus callosum, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Contiguous abcd1 dxs1357e deletion syndrome, Deafness, Developmental delay, Hearing loss, Mental retardation, Microcephaly, Motor and intellectual disabilities-sensorineural deafness-dystonia syndrome, Optic atrophy, Quadriplegia, Strabismus

469
Nicotinamide phosphoribosyltransferase
1110035O14Rik, PBEF, PBEF1, VF, VISFATIN
Carcinoma of the head and neck, Colitis, Colorectal cancer, Colorectal neoplasms, Dermatitis, Mouth neoplasms, Malignant neoplasm of mouth, Obesity

470
RNA binding motif protein 12
HRIHFB2091, SCZD19, SWAN
Impaired cognition, Psychosis, Schizoaffective disorder, Schizophrenia, Schizophreniform disorders