|
2021
|
|
|
Carboxypeptidase B2 |
CPU, PCPB, TAFI |
|
|
2022
|
|
|
Collagen type XXVI alpha 1 chain |
EMI6, EMID2, EMU2, SH2B |
|
|
2023
|
|
|
KLF transcription factor 14 |
BTEB5 |
|
|
2024
|
|
|
Carboxypeptidase E |
BDVS, CPH, IDDHH |
|
|
2025
|
|
|
Ankyrin repeat and SOCS box containing 10 |
GLC1F |
|
|
2026
|
|
|
Claudin 4 |
CPE-R, CPER, CPETR, CPETR1, WBSCR8, hCPE-R |
|
|
2027
|
|
|
Claudin 3 |
C7orf1, CPE-R2, CPETR2, HRVP1, RVP1 |
|
|
2028
|
|
|
Claudin 7 |
CEPTRL2, CLDN-7, CPETRL2, Hs.84359, claudin-1 |
|
|
2029
|
|
|
M-phase specific PLK1 interacting protein |
ABHS, C7orf11, ORF20, TTD4 |
Amish brittle hair brain syndrome, Anemia, Astigmatism, Breast cancer, Bronchospasm, Carcinoma, Cardiomyopathy, Cerebral cortical atrophy, Clastothrix, Congenital epicanthus, Congenital exfoliative erythroderma, Congenital exomphalos, Craniosynostosis, Cryptorchidism, Dental enamel hypoplasia, Developmental delay, Dysarthria, Ectropion, Eczema, Esotropia, Gonadal dysgenesis, Hypoplasia of mandible relative to maxilla, Ichthyosis, Impaired social reciprocity, Keratoconjunctivitis sicca, Macrotia, Age-related macular degeneration, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Myopia, Nervous system diseases, Neutropenia, Nystagmus, Osteopenia, Osteosclerosis, Paraplegia, Partial agenesis of corpus callosum, Periventricular leukomalacia, Seizure, Sensorineural hearing loss, Trichorrhexis nodosa syndrome, Trichothiodystrophy, Ventricular septal defectView all (30 more) |
|
2030
|
|
|
Carboxypeptidase M |
- |
|
