Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "F"
561 to 570 of 580 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

561
FXYD domain containing ion transport regulator 2
ATP1G1, HOMG2
Primary hypomagnesemia with hypocalciuria, Magnesium metabolism disorder, Hyperopia, Hypertension, Diabetes mellitus type 2

562
FXYD domain containing ion transport regulator 3
MAT8, PLML
Heart failure, Hodgkin lymphoma, Non-small cell lung carcinoma, Pancreatic neoplasms

563
FXYD domain containing ion transport regulator 4
CHIF
Atrial fibrillation, Hirschsprung disease

564
FXYD domain containing ion transport regulator 5
DYSAD, HSPC113, IWU1, KCT1, OIT2, PRO6241, RIC
Color vision deficiency

565
FXYD domain containing ion transport regulator 6
-
Myeloid leukemia, Schizophrenia

566
FXYD6-FXYD2 readthrough
FXYD6
Diabetes mellitus type 2

567
FYN binding protein 1
ADAP, FYB, PRO0823, SLAP-130, SLAP130, THC3
Central nervous system cancer, Congenital small-platelet thrombocytopenia, Allergic contact dermatitis, Glioblastoma, Glioma, Major depressive disorder, Mood disorder, Nonalcoholic fatty liver disease, Thrombocytopenia, Diabetes mellitus type 2, Vascular dementia

568
FYN binding protein 2
ARAP, C1orf168
Endometrial cancer, Endometrial neoplasms, Esophageal disease, Hoarding disorder, Obesity, Schizophrenia, Scoliosis, Diabetes mellitus type 2

569
FYVE and coiled-coil domain autophagy adaptor 1
CATC2, CTRCT18, RUFY3, ZFYVE7
Cataract, Congenital cataract, Congenital total cataract, Nuclear cataract, Major depressive disorder, Osteoarthritis

570
FYN proto-oncogene, Src family tyrosine kinase
SLK, SYN, p59-FYN
Alzheimer disease, Androgenetic alopecia, Eczema, Autoimmune thyroid disease, Bipolar disorder, Catalepsy, Color vision deficiency, Hypothyroidism, Inflammatory skin disease, Insomnia, T-cell leukemia-lymphoma, Premature ovarian failure, Parkinson disease, Psoriasis, Psoriasis vulgaris
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