Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
661 to 670 of 12229 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

661
Teashirt zinc finger homeobox 1
CAA, NY-CO-33, SDCCAG33, TSH1
Aural atresia, congenital, Congenital absence, atresia and stricture of auditory canal, Hearing loss, Prostate cancer, Prostate cancer, hereditary

662
ALG3 alpha-1,3- mannosyltransferase
CDG1D, CDGS4, CDGS6, D16Ertd36e, NOT56L, Not56, not
Arthrogryposis multiplex congenita, Cerebellar atrophy, Cerebral atrophy, Clinodactyly, Congenital clubfoot, Congenital coloboma of iris, Congenital disorder of glycosylation, Congenital epicanthus, Developmental delay, Food intolerance, High palate, Macrotia, Microcephaly, Nail diseases, Nail dysplasia
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663
Long intergenic non-protein coding RNA 970
-
Leukemia

664
M-phase phosphoprotein 9
MPP-9, MPP9
Arthritis, Development disorder, Diabetes mellitus, Multiple sclerosis, Schizophrenia

665
ADAM metallopeptidase domain 10
AD10, AD18, CD156c, CDw156, HsT18717, MADM, RAK, kuz
Alzheimer disease, Breast cancer, Mammary neoplasms, Breast carcinoma, Dowling-degos disease, Hyperkeratosis, Marfan syndrome, Reticulate acropigmentation of kitamura, Schizophrenia, Senile dementia, Skin melanoma

666
Cyclin dependent kinase 5
LIS7, PSSALRE
Agenesis of corpus callosum, Agyria, Arthrogryposis multiplex congenita, Cerebellar hypoplasia, Developmental delay, Lissencephaly, Lissencephaly with cerebellar hypoplasia, Microcephaly, Micrognathism, Schizophrenia, Tauopathies

667
Dehydrogenase/reductase 2
HEP27, SDR25C1
Colorectal cancer

668
Calcitonin receptor like receptor
CGRPR, CRLR, LMPHM8
Dermatitis

669
Nuclear transport factor 2
NTF-2, NTF2, PP15
Coronary heart disease

670
Myelin protein zero like 2
DFNB111, EVA, EVA1
Deafness, Lung adenocarcinoma, Lung carcinoma, Non-syndromic sensorineural deafness