161
|
|
|
HemK methyltransferase 1, mitochondrial release factors N(5)-glutamine |
HEMK, MPRMC, MTQ1 |
|
162
|
|
|
HemK methyltransferase 2, ETF1 glutamine and histone H4 lysine |
C21orf127, KMT9, MTQ2, N6AMT, N6AMT1, PRED28, PrmC, m.HsaHemK2P |
|
163
|
|
|
HEN methyltransferase 1 |
C1orf59, HEN1 |
|
164
|
|
|
Hepatic and glial cell adhesion molecule |
GlialCAM, HEPN1, MLC2A, MLC2B |
|
165
|
|
|
HEPACAM family member 2 |
MIKI |
|
166
|
|
|
Hephaestin |
CPL, Hp |
|
167
|
|
|
Hephaestin like 1 |
HJDD, ZP |
|
168
|
|
|
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 |
MDFPMR, p532, p619 |
Atrial fibrillation, Attention deficit hyperactivity disorder, Obstructive pulmonary disease, Dental caries, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Neurodevelopmental disorder, Neurotic disorder, Substance abuse, Diabetes mellitus type 2 |
169
|
|
|
HECT and RLD domain containing E3 ubiquitin protein ligase 2 |
D15F37S1, MRT38, SHEP1, jdf2, p528 |
Alzheimer disease, Asthma, Eczema, Cerebellar atrophy, Basal cell carcinoma, Eye neoplasms, Cataract, Ulcerative colitis, Colorectal cancer, Conjunctivitis, Corneal astigmatism, Melanoma, Macular and posterior pole degeneration, Developmental delay with autism spectrum disorder, Erythematosquamous dermatosis, Eye disease, Glaucoma, Global developmental delay, Intellectual developmental disorder, Keratinocyte carcinoma, Macular degeneration, Multiple myeloma, Non-melanoma skin carcinoma, Non-small cell lung carcinoma, Open angle glaucoma, Osteoarthritis, Prader-willi syndrome, Primary angle closure glaucoma, Rosacea, Sebaceous gland disease, Seborrheic dermatitis, Intellectual disability, Skin cancer, Skin disease, Skin neoplasms, Skin hair eye pigmentation variation, Squamous cell carcinoma, Diabetes mellitus type 2, Uveal melanoma, Uveitis, VitiligoView all (26 more) |
170
|
|
|
HECT and RLD domain containing E3 ubiquitin protein ligase 3 |
- |
|
