Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5941 to 5950 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5941
Homeobox C13
ECTD9, HOX3, HOX3G
Ectodermal dysplasia

5942
Homeobox C4
HOX3, HOX3E, cp19
Atrial fibrillation, Cardiovascular disease, Obstructive pulmonary disease, Hypertension, Gout, Osteoporosis, Diabetes mellitus type 2

5943
Homeobox C5
CP11, HOX3, HOX3D
Gout

5944
Homeobox C6
CP25, HHO.C8, HOX3, HOX3C
Obstructive pulmonary disease, Endometriosis, Gastroesophageal reflux disease, Gout, Hypertension, Osteoporosis

5945
Homeobox D1
HOX4, HOX4G, Hox-4.7
Androgenetic alopecia, Kidney disease, Colorectal neoplasms, Gout, Hyperalgesia, Ovarian neoplasms

5946
Homeobox D10
HOX4, HOX4D, HOX4E, Hox-4.4
Rheumatoid arthritis, Bilateral congenital vertical talus, Charcot-marie-tooth disease, Congenital vertical talus, Glioblastoma, Gout, Migraine, Mouth neoplasms, Amyotrophic lateral sclerosis, Squamous cell carcinoma, Vertical talus

5947
Homeobox D11
HOX4, HOX4F
Rheumatoid arthritis, Autism, Bone disease, Breast neoplasms, Glioma, Hemorrhoid, Male infertility, Kidney disease, Congenital anomaly of limb, Mouth neoplasms, Ovarian neoplasms, Squamous cell carcinoma

5948
Homeobox D12
HOX4H
Congenital clubfoot, Congenital anomaly of limb, Melanoma

5949
Homeobox D13
BDE, BDSD, HOX4I, SPD, SPD1
Anemia, Rheumatoid arthritis, Brachydactyly, Brachydactyly-syndactyly syndrome, Brachymesophalangy, Congenital clubfoot, Cryptorchidism, Desbuquois syndrome, Gout, Hematologic disease, Hemimelia of limb, Congenital anomaly of limb, Major depressive disorder, Male infertility, Neutropenia
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5950
Homeobox D3
HOX1D, HOX4, HOX4A, Hox-4.1
Ovarian epithelial cancer, Obstructive sleep apnea syndrome, Ovarian cancer, Ovarian mucinous adenocarcinoma, Ovarian serous carcinoma, Pelvic organ prolapse, Prostatic neoplasms