|
691
|
|
|
Complement factor H related 1 |
CFHL, CFHL1, CFHL1P, CFHR1P, FHL-1, FHR-1, FHR1, H36, H36-1, H36-2, HFL1, HFL2 |
|
|
692
|
|
|
Complement factor H related 2 |
CFHL2, FHR2, HFL3 |
|
|
693
|
|
|
Chromosome 14 open reading frame 39 |
POF18, SPGF52, Six6os1 |
Anophthalmia/microphthalmia-esophageal atresia syndrome, Atrial fibrillation, Azoospermia, Colobomatous optic disc macular atrophy chorioretinopathy syndrome, Congenital cataract, Eye disease, Glaucoma, Hyperopia, Male infertility single gene azoospermia, Microphthalmia, Nystagmus, Open angle glaucoma, Premature ovarian failure, Prostate cancer, Retinopathy, Retinoschisis, Spermatogenic failure, Testicular azoospermiaView all (3 more) |
|
694
|
|
|
C-type lectin domain family 4 member D |
CD368, CLEC-6, CLEC6, CLECSF8, Dectin-3, MCL, MPCL |
|
|
695
|
|
|
CBY1 interacting BAR domain containing 2 |
FAM92B |
|
|
696
|
|
|
Chromosome 17 open reading frame 67 |
- |
Androgenetic alopecia, Ankylosing spondylitis, Crohn disease, Inflammatory bowel disease, Orofacial cleft, Osteoarthritis, Psoriasis, Retinal detachment, Sclerosing cholangitis, Sleep apnea, Amyotrophic lateral sclerosis, Ulcerative colitis |
|
697
|
|
|
Coiled-coil domain containing 137 |
RaRF |
|
|
698
|
|
|
C-type lectin domain family 4 member G |
DTTR431, LP2698, LSECtin, UNQ431 |
|
|
699
|
|
|
Coiled-coil domain 39 molecular ruler complex subunit |
CFAP59, CILD14, FAP59 |
|
|
700
|
|
|
Collagen type XXVIII alpha 1 chain |
COL28 |
|
