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3391
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Myelin transcription factor 1 like |
MRD39, NZF1, ZC2H2C2, ZC2HC4B, myT1-L |
Atrial septal defect, Autism spectrum disorder, Dermatitis, Developmental delay, Impaired cognition, Mental depression, Mental retardation, Neurodevelopmental disorders, Non-syndromic intellectual disability, Obesity, Psoriasis, Schizophrenia, Syndromic mental retardation |
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3392
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|
|
Pyridoxal dependent decarboxylase domain containing 1 |
LP8165 |
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3393
|
|
|
TRAF2 and NCK interacting kinase |
MRT54 |
Absence of septum pellucidum, Arsenic encephalopathy, Arthritis, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Dermatologic disorders, Developmental delay, Dyskinetic syndrome, Dyssomnia, Frontotemporal dementia, Hypoplasia of corpus callosum, Mental retardation, Juvenile arthritis, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Polymicrogyria, Salaam seizures, Schizophrenia, Seizure, Sleep disorders, Stereotyped behavior, Still disease, Vascular diseasesView all (14 more) |
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3394
|
|
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Kinesin family member 21B |
- |
|
|
3395
|
|
|
PDS5 cohesin associated factor B |
APRIN, AS3, CG008 |
|
|
3396
|
|
|
Formin binding protein 1 |
FBP17 |
Ankylosing spondylitis, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Celiac disease, Common variable immunodeficiency, Crohn disease, Diabetes mellitus, Lupus erythematosus, Psoriasis, Ulcerative colitis |
|
3397
|
|
|
SMG1 nonsense mediated mRNA decay associated PI3K related kinase |
61E3.4, ATX, LIP |
|
|
3398
|
|
|
Forkhead box M1 |
FKHL16, FOXM1A, FOXM1B, FOXM1C, HFH-11, HFH11, HNF-3, INS-1, MPHOSPH2, MPP-2, MPP2, PIG29, TRIDENT |
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3399
|
|
|
Zinc fingers and homeoboxes 3 |
TIX1 |
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3400
|
|
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Nuclear receptor coactivator 6 |
AIB3, ASC2, NRC, PRIP, RAP250, TRBP |
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