Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
1291 to 1300 of 12229 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1291
Hydroxyacyl-thioester dehydratase type 2
-
Rheumatoid arthritis

1292
Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta
14-3-3, 1C5, HS1
Arthritis, Osteoarthrosis deformans

1293
KRT7 antisense RNA 1
-
Asthma

1294
Long intergenic non-protein coding RNA 2236
-
Breast carcinoma

1295
Activating signal cointegrator 1 complex subunit 3
ASC1p200, HELIC1, MRT81, RNAH
Mental retardation

1296
Cleavage factor polyribonucleotide kinase subunit 1
HEAB, hClp1
Acquired kyphoscoliosis, Cerebral cortical atrophy, Congenital kyphoscoliosis, Cryptorchidism, Developmental delay, Epileptic encephalopathy, Esotropia, High palate, Hypoplasia of corpus callosum, Mental retardation, Nystagmus, Optic atrophy, Pontoneocerebellar hypoplasia, Proptosis, Sensorimotor neuropathy
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1297
FERM domain containing kindlin 2
KIND2, MIG2, PLEKHC1, UNC112, UNC112B, mig-2
Alzheimer disease, Angle closure glaucoma, Urinary bladder cancer, Bladder neoplasm, Prostate cancer

1298
RAB32, member RAS oncogene family
PARK26
Dermatitis, Leprosy

1299
Microtubule associated protein RP/EB family member 2
CSCSC2, EB1, EB2, RP1
Congenital epicanthus, Congenital exomphalos, Congestive heart failure, Cryptorchidism, Developmental delay, Dwarfism, Hypoplasia of corpus callosum, Hypospadias, Neuroblastoma, Mental retardation, Michelin tire baby syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos
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1300
KCNQ1 opposite strand/antisense transcript 1
KCNQ1-AS2, KCNQ10T1, Kncq1, KvDMR1, KvLQT1-AS, LIT1, NCRNA00012
Adrenocortical carcinoma, Beckwith-wiedemann syndrome, Cardiomyopathy, Congenital hemihypertrophy, Congenital long qt syndrome, Congenital omphalocele, Cryptorchidism, Diabetes mellitus, Gonadoblastoma, Hemihyperplasia, Hepatoblastoma, Jervell-lange nielsen syndrome, Long qt syndrome, Macroglossia, Meningomyelocele
View all (9 more)