Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4611 to 4620 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4611
Ferredoxin 2
FDX1L, MEOAL
Mitochondrial myopathy, Psoriasis, Systemic lupus erythematosus

4612
Ferredoxin reductase
ADR, ADXR, ANOA, MMDS9B
Auditory neuropathy, Auditory neuropathy with optic atrophy, Optic atrophy

4613
Ferrochelatase
EPP, EPP1, FCE
Erythropoietic protoporphyria, Bile duct disease, Metabolic syndrome, Migraine, Porphyria

4614
Fem-1 homolog A
EPRAP
Alzheimer disease

4615
Fem-1 homolog B
F1A-ALPHA, F1AA, FEM1-beta, NEDBES
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

4616
Fem-1 homolog C
EUROIMAGE686608, EUROIMAGE783647, FEM1A
Asthma, Neurodevelopmental disorder, Conotruncal cardiac defect, Non-specific syndromic intellectual disability

4617
Flap structure-specific endonuclease 1
FEN-1, MF1, RAD2
Colorectal cancer, Colorectal neoplasms, Crohn disease, Non-immune hydrops fetalis, Inflammatory bowel disease, Lung neoplasms, Ulcerative colitis

4618
FER tyrosine kinase
PPP1R74, TYK3, p94-Fer
Asthma, Coronary artery disease, Duane retraction syndrome, Dupuytren contracture, Major depressive disorder, Psoriasis, Psychiatric disorders, Schizophrenia, Hypertension

4619
Fer3 like bHLH transcription factor
N-TWIST, NATO3, NTWIST, PTFB, bHLHa31
Amyotrophic lateral sclerosis, Aortic stenosis, Aortic valve disease, Asthma, Atrial fibrillation, Brain aneurysm, Cancer, Central nervous system cancer, Colorectal cancer, Coronary artery disease, Diabetes mellitus, Glioblastoma, Glioma, Heart failure, Major depressive disorder
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4620
FERM domain containing kindlin 1
C20orf42, DTGCU2, KIND1, UNC112A, URP1
Crohn disease, Inflammatory bowel disease, Kindler epidermolysis bullosa, Skin disease, Ulcerative colitis