|
741
|
|
|
THAP domain containing 9 |
hTh9 |
|
|
742
|
|
|
Transcription elongation factor, mitochondrial |
C17orf42, COXPD58 |
|
|
743
|
|
|
Thioredoxin domain containing 15 |
BUG, C5orf14, MKS14, TMX5, UNQ335 |
|
|
744
|
|
|
Tissue factor pathway inhibitor 2 |
PP5, REF1, TFPI-2 |
Arthritis, Breast cancer, Mammary neoplasms, Breast carcinoma, Colorectal cancer, Colorectal neoplasms, Liver carcinoma, Marfan syndrome, Melanoma, Osteoarthrosis deformans, Pancreatic neoplasm, Pancreatic cancer, Rheumatoid arthritis |
|
745
|
|
|
Tetratricopeptide repeat domain 21B |
ATD4, CFAP60, FAP60, FLA17, IFT139, IFT139B, JBTS11, NPHP12, Nbla10696, SRTD4, THM1 |
Asphyxiating thoracic dystrophy, Brachydactyly, Ciliopathies, Congenital hepatic fibrosis, Disorder of eye, Dwarfism, Finnish congenital nephrotic syndrome, Foot polydactyly, Jeune syndrome, Jeune thoracic dystrophy, Kidney disease, Liver cyst, Majewski syndrome, Micromelia, Nephronophthisis, Osteochondrodysplasia, Polydactyly, Renal insufficiency, Scoliosis, Senior-loken syndrome, Short rib-polydactyly syndrome, Short-rib thoracic dysplasia with polydactyly, Skeletal dysplasia, Syndactyly of the toes, Postaxial hand polydactylyView all (10 more) |
|
746
|
|
|
TLE family member 6, subcortical maternal complex member |
GRG6, OZEMA15, PREMBL |
|
|
747
|
|
|
Transmembrane channel like 5 |
- |
|
|
748
|
|
|
Transmembrane 4 L six family member 20 |
PRO994, SLI5, TCCE518 |
|
|
749
|
|
|
Tectonic family member 2 |
C12orf38, JBTS24, MKS8, TECT2 |
Anencephaly, Cataract, Cerebellar hypoplasia, Cerebellar vermis agenesis, Ciliopathies, Asplenia, Congenital cerebral hernia, Congenital clubfoot, Congenital coloboma of iris, Congenital hepatic fibrosis, Cryptorchidism, Cystic liver disease, Dandy-walker syndrome, Developmental delay, Disorder of eye, Double ureter, Fibrosis of pancreas, Foot polydactyly, Hirschsprung disease, Hydrocephalus, Hyperopia, Joubert syndrome, Lobar holoprosencephaly, Male pseudohermaphroditism, Meckel syndrome, Meckel-gruber syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Oral cleft, Pachygyria, Pancreatic cyst, Polycystic liver disease, Polydactyly, Polydactyly of toes, Polymicrogyria, Ptosis, Sclerocornea, Scoliosis, Situs inversus, Strabismus, Syndromic microphthalmia, Talipes, True hermaphroditism, Postaxial hand polydactyly, Urethral atresiaView all (38 more) |
|
750
|
|
|
Thrombospondin type 1 domain containing 4 |
AAT12, ADAMTSL-6, ADAMTSL6, FVSY9334, PRO34005 |
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