|
2341
|
|
|
Phospholipase B1 |
PLB, PLB/LIP |
|
|
2342
|
|
|
Zinc finger protein 385B |
ZNF533 |
|
|
2343
|
|
|
ARF like GTPase 6 interacting protein 6 |
AIP-6, AIP6, PFAAP1 |
Blue nevus, Cafe-au-lait spot, Congenital arteriovenous malformation, Cutis marmorata, Cutis marmorata telangiectatica congenita, Hypothyroidism, Impaired cognition, Leukocoria, Micrognathism, Multicystic renal dysplasia, Oral cleft, Patent ductus arteriosus, Retinal detachment, Scoliosis, Skin erosion, Strawberry nevus of skin, Stroke, Syndactyly of fingers, Syndactyly of the toesView all (4 more) |
|
2344
|
|
|
Methyltransferase 21A, HSPA lysine |
FAM119A, HCA557b, HSPA-KMT |
|
|
2345
|
|
|
Cathepsin H |
ACC-4, ACC-5, ACC4, ACC5, CPSB |
Amnesia, Autoimmune diabetes, Basal cell neoplasm, Brittle diabetes mellitus, Carcinoma, Cataplexy, Colorectal cancer, Diabetes mellitus, Hallucinations, Leukemia, Multiple sclerosis, Myeloid leukemia, Narcolepsy, Narcolepsy-cataplexy syndrome, Obesity |
|
2346
|
|
|
Kelch like family member 23 |
DITHP |
|
|
2347
|
|
|
Shugoshin 2 |
SGOL2, TRIPIN |
|
|
2348
|
|
|
Solute carrier family 23 member 3 |
E2BP3, SVCT3, Yspl1 |
|
|
2349
|
|
|
Cathepsin K |
CTS02, CTSO, CTSO1, CTSO2, PKND, PYCD |
Anemia, Arthritis, Brachycephaly, Brachydactyly, Dwarfism, Frontal bossing, Giant cell glioblastoma, Glioblastoma, Hydrocephalus, Hypodontia, Impaired cognition, Micrognathism, Osteoarthrosis deformans, Osteochondrodysplasia, Osteomyelitis, Osteosclerosis, Proptosis, Pycnodysostosis, Schizophrenia, Scoliosis, Skeletal dysplasia, Spondylolisthesis, SpondylolysisView all (8 more) |
|
2350
|
|
|
G protein-coupled bile acid receptor 1 |
BG37, GPCR19, GPR131, M-BAR, TGR5 |
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