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3651
|
|
|
Pescadillo ribosomal biogenesis factor 1 |
NOP7, PES |
|
|
3652
|
|
|
TDP-glucose 4,6-dehydratase |
CATMANS, SDR2E1, TDPGD |
Aortic coarctation, Atrial septal defect, Camptodactyly of fingers, Catel manzke syndrome, Congenital camptodactyly, Congenital clubfoot, Congenital exomphalos, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Dextrocardia, Dwarfism, Glossoptosis, High palate, Cystic hygroma, Micrognathism, Multiple congenital anomalies, Otitis media, Overriding aorta, Scoliosis, Ventricular septal defectView all (7 more) |
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3653
|
|
|
Leptin receptor overlapping transcript like 1 |
HSPC112, Vps55, my047 |
|
|
3654
|
|
|
Carboxylesterase 3 |
ES31 |
|
|
3655
|
|
|
Chromobox 7 |
- |
|
|
3656
|
|
|
Hes related family bHLH transcription factor with YRPW motif 2 |
CHF1, GRIDLOCK, GRL, HERP1, HESR2, HRT2, bHLHb32 |
Anaplastic astrocytoma, Astrocytoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Brugada syndrome, Fibrillary astrocytoma, Gemistocytic astrocytoma, Grade i astrocytoma, Hypertrophic cardiomyopathy, Intracranial astrocytoma, Marfan syndrome, Oligoastrocytoma, Pancreatic ductal carcinoma, Protoplasmic astrocytoma |
|
3657
|
|
|
TNF receptor superfamily member 13B |
CD267, CVID, CVID2, IGAD2, RYZN, TACI, TNFRSF14B |
Anemia, Brachycephaly, Bronchiectasis, Bronchitis, Common variable immunodeficiency, Conjunctivitis, Gastrointestinal stromal tumor, Immune thrombocytopenic purpura, Immunoglobulin a deficiency, Immunoglobulin deficiency, Immunologic deficiency syndromes, Imperforate anus, Lymphoma, Lymphopenia, Monoclonal gammapathies, Multiple myeloma, Neoplasms, Otitis media, Paraproteinemia, Selective immunoglobulin a deficiency, Sinusitis, VasculitisView all (7 more) |
|
3658
|
|
|
3-hydroxyanthranilate 3,4-dioxygenase |
3-HAO, HAO, VCRL1, h3HAO |
Abnormal spinal segmentation, Allanson pantzar mcleod syndrome, Aortic valve sclerosis, Atrial septal defect, Congenital malformation syndrome, Congenital vertebral-cardiac-renal anomalies syndrome, Developmental delay, Dwarfism, Hearing loss, Hypoplastic left heart syndrome, Hypospadias, Laryngeal web, Microcephaly, Mitral valve stenosis, Multiple congenital anomalies, Otitis media, Primary tethered cord syndrome, Renal hypoplasia, Sacral agenesis, Sensorineural hearing loss, Spina bifida, Submucosal cleft palate, Talipes, Vesicoureteral refluxView all (9 more) |
|
3659
|
|
|
Microtubule actin crosslinking factor 1 |
ABP620, ACF7, KIAA0754, LIS9, Lnc-PMIF, MACF, OFC4 |
Breast cancer, Cerebellar hypoplasia, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Developmental delay, Diabetes mellitus, Dysphagia, Hypoplasia of corpus callosum, Lissencephaly, Lissencephaly with complex brainstem malformation, Mental retardation, Pachygyria, Strabismus, Vascular diseases |
|
3660
|
|
|
Folate receptor beta |
BETA-HFR, FBP, FBP/PL-1, FOLR1, FR-BETA, FR-P3, FRbeta |
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