|
811
|
|
|
Transmembrane O-mannosyltransferase targeting cadherins 4 |
DFNB122 |
|
|
812
|
|
|
Transmembrane protein 87B |
- |
|
|
813
|
|
|
Tensin 4 |
CTEN, PP14434 |
|
|
814
|
|
|
TOX high mobility group box family member 2 |
C20orf100, GCX-1, GCX1, dJ1108D11.2, dJ495O3.1 |
|
|
815
|
|
|
Tripartite motif containing 5 |
RNF88, TRIM5alpha |
|
|
816
|
|
|
Tubulin gamma complex component 6 |
GCP-6, GCP6, MCCRP, MCCRP1, MCPHCR |
Cataract, Cerebellar hypoplasia, Cerebral atrophy, Cerebral cortical atrophy, Chorioretinopathy-microcephaly syndrome, Developmental delay, Dwarfism, Leukemia, Malformation of cortical development, Mental retardation, Microcephaly, Microcephaly with chorioretinopathy, Microphthalmos, Nystagmus, Optic atrophy, Pachygyria, Retinal detachment, Retinal dystrophy, Scoliosis, StrabismusView all (5 more) |
|
817
|
|
|
Tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 |
ROLSB, TANC |
|
|
818
|
|
|
Thymic stromal lymphopoietin |
- |
|
|
819
|
|
|
Titin-cap |
CMD1N, CMH25, LGMD2G, LGMDR7, T-cap, TELE, telethonin |
Cardiomyopathy, Dilated cardiomyopathy, Distal lower limb amyotrophy, Hearing loss, Hypertrophic cardiomyopathy, Limb-girdle muscular dystrophy, Lipoatrophy, Lipodystrophy, Muscular dystrophy, Myopathy, Palmoplantar keratoderma |
|
820
|
|
|
THO complex subunit 5 |
C22orf19, Fmip, PK1.3, fSAP79 |
|