Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4801 to 4810 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4801
Forkhead box K1
FOXK1L
Atrial fibrillation, Gout, Hypothyroidism, Diabetes mellitus type 2

4802
Forkhead box K2
ILF, ILF-1, ILF1, nGTBP
Breast cancer, Gout, Male infertility, Psoriasis

4803
Forkhead box L1
FKH6, FKHL11, FREAC7, OTSC11
Colorectal adenoma, Colorectal cancer, Congenital heart disease, Coronary artery disease, Dental caries, Diverticular disease, Hemorrhoid, Hypertension, Multiple system atrophy, Myocardial infarction, Myocardial ischemia, Obesity, Otosclerosis, Retinopathy, Juvenile idiopathic arthritis
View all (1 more)

4804
Forkhead box L2
BPES, BPES1, PFRK, PINTO, POF3
Blepharophimosis syndrome, Blepharophimosis-ptosis-epicanthus inversus syndrome, Blepharophimosis ptosis epicanthus inversus syndrome, Colorectal neoplasms, Duane retraction syndrome, Granulosa cell tumor of ovary, Premature ovarian failure

4805
FOXL2 neighbor
C3orf72
Androgenetic alopecia, Breast cancer

4806
Forkhead box L3
-
Androgenetic alopecia, Hemorrhagic stroke, Nephrolithiasis

4807
Forkhead box M1
FKHL16, FOXM1A, FOXM1B, FOXM1C, HFH-11, HFH11, HNF-3, INS-1, MPHOSPH2, MPP-2, MPP2, PIG29, TRIDENT
Breast neoplasms, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Iga nephropathy, Leukemia, Lung neoplasms, Upper aerodigestive tract neoplasm

4808
Forkhead box N1
FKHL20, RONU, TIDAND, TLIND, WHN
Autism, Combined immunodeficiency disease, Pharyngeal disorder, Severe combined immunodeficiency

4809
Forkhead box N2
HTLF
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Schizophrenia

4810
Forkhead box N3
C14orf116, CHES1, PRO1635
Brain cancer, Brain neoplasms, Breast cancer, Color vision deficiency, Heart failure, Lewy body disease, Ovarian epithelial cancer, Ovarian cancer, Small cell lung carcinoma, Diabetes mellitus type 2