Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4911 to 4920 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4911
Frizzled class receptor 10
CD350, FZ-10, Fz10, FzE7, hFz10
Metabolic syndrome

4912
Frizzled class receptor 2
Fz2, OMOD2, fz-2, fzE2, hFz2
Omodysplasia, Robinow syndrome, Colonic neoplasms, Desbuquois syndrome, Keratoconus

4913
Frizzled class receptor 3
Fz-3
Arthrogryposis multiplex congenita, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Obstructive pulmonary disease, Hydrocephalus, Schizophrenia, Williams syndrome

4914
Frizzled class receptor 4
CD344, EVR1, FEVR, FZD4S, Fz-4, Fz4, FzE4, GPCR, hFz4
Arachnodactyly, Bipolar disorder, Cleft palate, Craniofacial abnormalities, Exudative retinopathy, Exudative vitreoretinopathy, Major depressive disorder, Retinitis pigmentosa, Retinopathy of prematurity, Syndactyly

4915
Frizzled class receptor 5
C2orf31, HFZ5, MCOPCB11
Bladder exstrophy and epispadias complex, Cleft eyelid, Coloboma, Congenital iris coloboma, Congenital ocular coloboma, Microphthalmia

4916
Frizzled class receptor 6
FZ-6, FZ6, HFZ6, NDNC1, NDNC10
Non-immune hydrops fetalis

4917
Frizzled class receptor 7
FzE3
Attention deficit hyperactivity disorder, Bone fracture, Coronary artery disease, Partial epilepsy, Substance abuse, Uterine fibroid

4918
Frizzled class receptor 9
CD349, FZD3
Gout

4919
Fizzy and cell division cycle 20 related 1
CDC20C, CDH1, DEE109, FZR, FZR2, HCDH, HCDH1
Autism, Cerebellar ataxia, Developmental and epileptic encephalopathy, Global developmental delay

4920
G0/G1 switch 2
-
Carcinoma