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- cadherin 1, type 1, E-cadherin (epithelial): CDH1
- cadherin-like 23: CDH23
- calcium channel, voltage-dependent, beta 4 subunit: CACNB4
- calcium channel, voltage-dependent, L type, alpha 1C subunit: CACNA1C
- calcium channel, voltage-dependent, L type, alpha 1S subunit: CACNA1S
- calcium channel, voltage-dependent, P/Q type, alpha 1A subunit: CACNA1A
- CAP-GLY domain containing linker protein 2: CLIP2
- carbamoyl-phosphate synthetase 1, mitochondrial: CPS1
- carnitine palmitoyltransferase 1A (liver): CPT1A
- carnitine palmitoyltransferase II: CPT2
- cartilage associated protein: CRTAP
- cartilage oligomeric matrix protein: COMP
- catechol-O-methyltransferase: COMT
- catenin (cadherin-associated protein), delta 2 (neural plakophilin-related arm-repeat protein): CTNND2
- CCHC-type zinc finger, nucleic acid binding protein: CNBP
- CD40 ligand: CD40LG
- cerebral cavernous malformation 2: CCM2
- ceruloplasmin (ferroxidase): CP
- CHK2 checkpoint homolog (S. pombe): CHEK2
- chloride channel 1, skeletal muscle (Thomsen disease, autosomal dominant): CLCN1
- choroideremia (Rab escort protein 1): CHM
- chromodomain helicase DNA binding protein 7: CHD7
- clarin 1: CLRN1
- claudin 14: CLDN14
- coagulation factor C homolog, cochlin (Limulus polyphemus): COCH
- coagulation factor II (thrombin): F2
- coagulation factor IX (plasma thromboplastic component, Christmas disease, hemophilia B): F9
- coagulation factor V (proaccelerin, labile factor): F5
- coagulation factor VIII, procoagulant component (hemophilia A): F8
- collagen, type I, alpha 1: COL1A1
- collagen, type I, alpha 2: COL1A2
- collagen, type II, alpha 1: COL2A1
- collagen, type III, alpha 1: COL3A1
- collagen, type IV, alpha 3 (Goodpasture antigen): COL4A3
- collagen, type IV, alpha 4: COL4A4
- collagen, type IV, alpha 5 (Alport syndrome): COL4A5
- collagen, type IX, alpha 1: COL9A1
- collagen, type IX, alpha 2: COL9A2
- collagen, type IX, alpha 3: COL9A3
- collagen, type V, alpha 1: COL5A1
- collagen, type V, alpha 2: COL5A2
- collagen, type VII, alpha 1 (epidermolysis bullosa, dystrophic, dominant and recessive): COL7A1
- collagen, type XI, alpha 1: COL11A1
- collagen, type XI, alpha 2: COL11A2
- coproporphyrinogen oxidase: CPOX
- CREB binding protein (Rubinstein-Taybi syndrome): CREBBP
- cullin 7: CUL7
- cyclic nucleotide gated channel alpha 3: CNGA3
- cyclic nucleotide gated channel beta 3: CNGB3
- cyclin-dependent kinase inhibitor 1C (p57, Kip2): CDKN1C
- cyclin-dependent kinase-like 5: CDKL5
- cystathionine-beta-synthase: CBS
- cystatin B (stefin B): CSTB
- cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7): CFTR
- cystinosis, nephropathic: CTNS
- cytochrome P450, family 1, subfamily B, polypeptide 1: CYP1B1
- cytochrome P450, family 21, subfamily A, polypeptide 2: CYP21A2
- cytochrome P450, family 27, subfamily A, polypeptide 1: CYP27A1
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