Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4811 to 4820 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4811
Forkhead box D4 like 5
bA15J10.2
Lung neoplasms

4812
Forkhead box E1
BAMLAZ, FKHL15, FOXE2, HFKH4, HFKL5, NMTC4, TITF2, TTF-2, TTF2
Alzheimer disease, Androgenetic alopecia, Differentiated thyroid carcinoma, Thyroid cancer, Orofacial cleft, Nonmedullary thyroid cancer

4813
Forkhead box E3
AAT11, ASGD2, CATC3, CTRCT34, FKHL12, FREAC8
Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Aortic aneurysm, Congenital primary aphakia, Cataract, Congenital cataract, Congenital aneurysm of ascending aorta, Congenital aphakia, Dissection of aorta, Thoracic aortic aneurysm and aortic dissection, Retinitis pigmentosa

4814
Forkhead box F1
ACDMPV, FKHL5, FREAC1
Alveolar capillary dysplasia, Congenital alveolar capillary dysplasia, Gastrointestinal stromal tumor, Pulmonary hypertension, Lung disease, Mastocytosis, Vacterl association, Ventricular septal defect

4815
Forkhead box F2
FKHL6, FREAC-2, FREAC2
Androgenetic alopecia, Cerebrovascular disorder, Erectile dysfunction, Glioma, Major depressive disorder, Mood disorder, Ovarian cancer, Ovarian serous carcinoma, Stroke, Urinary bladder cancer

4816
Forkhead box G1
BF1, BF2, FHKL3, FKH2, FKHL1, FKHL2, FKHL3, FKHL4, FOXG1A, FOXG1B, FOXG1C, HBF-1, HBF-2, HBF-3, HBF-G2, HBF2, HFK1, HFK2, HFK3, KHL2, QIN
14q11.2 microduplication syndrome, Autism, Congenital microcephaly, Congenital neurologic anomalies, Epilepsy, Global developmental delay, Intellectual developmental disorder, Lissencephaly, Microcephaly, Nervous system disease, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Rett syndrome, Seizures, Intellectual disability
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4817
Forkhead box H1
FAST-1, FAST1
Congenital heart malformation, Conotruncal cardiac defect, Holoprosencephaly, Microform holoprosencephaly, Syntelencephaly, Noonan syndrome, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Tetralogy of fallot

4818
Forkhead box I1
FKH10, FKHL10, FREAC-6, FREAC6, HFH-3, HFH3
Distal renal tubular acidosis, Nonsyndromic hearing loss, Breast cancer, Craniofacial abnormalities, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Pendred syndrome, Triple negative breast cancer

4819
Forkhead box I2
-
Carotid artery disease, Central nervous system cancer, Dental caries, Glioma, Insomnia, Obstructive sleep apnea syndrome, Ocular hypotension

4820
Forkhead box I3
CFM2
Color vision deficiency, Craniofacial microsomia, Goldenhar syndrome, Hemifacial microsomia, Migraine, Tooth agenesis, Diabetes mellitus type 1