|
81
|
|
|
Structural maintenance of chromosomes 2 |
CAP-E, CAPE, SMC-2, SMC2L1 |
|
|
82
|
|
|
Solute carrier organic anion transporter family member 1B1 |
HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 |
|
|
83
|
|
|
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 |
SAITL1, SIAT7, SIAT7B, SIATL1, ST6GalNAII, STHM |
|
|
84
|
|
|
Sperm associated antigen 5 |
DEEPEST, MAP126, hMAP126 |
|
|
85
|
|
|
STAM binding protein |
AMSH, MICCAP |
Brachydactyly, Capillary malformation-arteriovenous malformation, Capillary malformation without arteriovenous malformation, Cerebral atrophy, Clinodactyly, Congenital microcephaly, Development disorder, Epilepsy, Epileptic encephalopathy, Hypoplasia of corpus callosum, Hypoplasia of the maxilla, Microcephaly, Microcephaly-capillary malformation syndrome, Microlissencephaly, Optic atrophy, Patent foramen ovale, Ptosis, Spastic tetraparesis, Ventricular hypertrophy, Ventricular septal defectView all (5 more) |
|
86
|
|
|
Serine peptidase inhibitor, Kunitz type 2 |
DIAR3, HAI-2, HAI2, Kop, PB |
Acrania, Anaplastic carcinoma, Anencephaly, Carcinoma, Choanal atresia, Coloboma of optic disc, Congenital secretory diarrhea, Corneal erosion, Craniorachischisis, Diastematomyelia, Diverticular diseases, Hexadactyly, Intestinal epithelial dysplasia, Nasopharyngeal carcinoma, Neural tube defect, Neurenteric cyst, Polydactyly, Primary tethered cord syndrome, Prostate cancer, Spinal cord myelodysplasiaView all (5 more) |
|
87
|
|
|
Septin 14 pseudogene 21 |
SEPT14P21 |
|
|
88
|
|
|
Solute carrier family 12 member 7 |
KCC4 |
|
|
89
|
|
|
STAG3 cohesin complex component |
SA3, SPGF61 |
|
|
90
|
|
|
STAG2 cohesin complex component |
HPE13, MKMS, NEDXCF, SA-2, SA2, SCC3B, bA517O1.1 |
Alobar holoprosencephaly, Anxiety disorder, Autism, Benign neoplasm of bladder, Urinary bladder cancer, Bladder neoplasm, Bladder carcinoma, Camptodactyly of fingers, Cerebellar hypoplasia, Congenital epicanthus, Congenital heart defects, Developmental delay, Dwarfism, Dyssomnia, Encephalitis, Ewing sarcoma, Frontal bossing, Glioblastoma, Glioma, Hearing loss, Hypoplasia of corpus callosum, Leukemia, Leukemia, megakaryoblastic, of down syndrome, Leukopenia, Malocclusion, Melanoma, Mental retardation, Microcephaly, Micrognathism, Microtia, Monocytic leukemia, Myelodysplastic syndrome, Myeloid leukemia, Polydactyly, Proptosis, Respiratory failure, Scoliosis, Semilobar holoprosencephaly, Sleep disorders, Lymphoproliferative syndrome, x-linked, Xq25 duplication syndrome, Xq25 triplication syndromeView all (27 more) |
