11781
|
|
|
SET domain containing 5 |
MRD23, SETD5A |
Attention deficit hyperactivity disorder, Autism, Congenital heart disease, Developmental disability, Global developmental delay, Hearing impairment, Hyperphosphatasia with intellectual disability syndrome, Intellectual developmental disorder, Intellectual developmental disorder dysmorphic facial, Irritable bowel syndrome, Metabolic syndrome, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Polymicrogyria, Diabetes mellitus type 2, UranostaphyloschisisView all (1 more) |
11782
|
|
|
SET domain containing 6, protein lysine methyltransferase |
- |
|
11783
|
|
|
SET domain containing 7, histone lysine methyltransferase |
KMT7, SET7, SET7/9, SET9 |
|
11784
|
|
|
SET domain containing 9 |
C5orf35 |
|
11785
|
|
|
SET domain bifurcated histone lysine methyltransferase 1 |
ESET, H3-K9-HMTase4, KG1T, KMT1E, TDRD21 |
|
11786
|
|
|
SET domain bifurcated histone lysine methyltransferase 2 |
C13orf4, CLLD8, CLLL8, KMT1F |
|
11787
|
|
|
SET and mariner transposase domain methyltransferase |
METNASE, Mar1 |
|
11788
|
|
|
SET like protein |
SETP18 |
|
11789
|
|
|
Senataxin |
ALS4, AOA2, SCAN2, SCAR1, STEX, Sen1, bA479K20.2 |
Alzheimer disease, Amyotrophic lateral sclerosis, Ataxia with oculomotor apraxia, Distal hereditary motor neuropathy, Cerebellar ataxia, Cerebellar atrophy, Cerebral palsy, Charcot-marie-tooth disease, Dementia, Distal spinal muscular atrophy, Frontotemporal dementia, Hereditary motor and sensory neuropathies, Motor neuron disease, Nystagmus, Proximal spinal muscular atrophy, Spastic ataxia, Spastic paraplegia, Hereditary spastic paraplegia, Spinocerebellar ataxia, Tay-sachs diseaseView all (5 more) |
11790
|
|
|
Seizure related 6 homolog |
BSRPC |
|
