A - Cl
ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1):
ALMS1 (Alstrom Syndrome 1):
ACCN1 (Amiloride-Sensitive Cation Channel 1, Neuronal):
ATP2B2 (ATPase, Ca++ Transporting, Plasma Membrane 2):
ATP6V1B1 (ATPase, H+ Transporting, Lysosomal 56/58kDa, V1 Subunit B1):
ATP6V0A4 (ATPase, H+ Transporting, Lysosomal V0 Subunit A4):
BARHL1 (BarH-Like Homeobox 1):
BSND (Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin)):
CACNA1D (Calcium Channel, Voltage-Dependent, L Type, alpha 1D Subunit):
CEACAM16 (Carcinoembryonic Antigen-Related Cell Adhesion Molecule 16):
CLIC5 (Chloride Intracellular Channel 5):
CHRNA10 (Cholinergic Receptor, Nicotinic, alpha 10):
CHRNA9 (Cholinergic Receptor, Nicotinic, alpha 9 (Neuronal)):
CHRNB2 (Cholinergic Receptor, Nicotinic, beta 2 (Neuronal)):
CHM (Choroideremia (Rab Escort Protein 1)):
CHD7 (Chromodomain Helicase DNA Binding Protein 7):
Co - F
COL1A1 (Collagen, Type I, alpha 1):
COL2A1 (Collagen, Type II, alpha 1):
COL11A1 (Collagen, Type XI, alpha 1):
COL11A2 (Collagen, Type XI, alpha 2):
CDKN1B (Cyclin-Dependent Kinase Inhibitor 1B (p27, Kip1)):
CDKN2D (Cyclin-Dependent Kinase Inhibitor 2D (p19, Inhibits CDK4)):
DFNA5 (Deafness, Autosomal Dominant 5):
DFNB31 (Deafness, Autosomal Recessive 31):
DIAPH1 (Diaphanous Homolog 1):
EML2 (Echinoderm Microtubule Associated Protein Like 2):
EYA1 (Eyes Absent Homolog 1):
EYA4 (Eyes Absent Homolog 4):
FBXO11 (F-Box Protein 11):
FGFR1 (Fibroblast Growth Factor Receptor 1):
FZD4 (Frizzled Family Receptor 4):
G - J
GPBAR1 (G Protein-Coupled Bile Acid Receptor 1):
Gpr98 (G Protein-Coupled Receptor 98):
GABRB3 (gamma-aminobutyric Acid (GABA) A Receptor, beta 3):
GABRA5 (gamma-aminobutyric Acid (GABA) A Receptor, alpha 5):
GABRB2 (gamma-aminobutyric Acid (GABA) A Receptor, beta 2):
GJB2 (Gap Junction Protein, beta 2, 26kDa):
GJB6 (Gap Junction Protein, beta 6, 30kDa):
GJE1 (Gap Junction Protein, epsilon 1):
GRM7 (Glutamate Receptor, Metabotropic 7):
GRXCR1 (Glutaredoxin, Cysteine Rich 1):
GPX1 - Glutathione Peroxidase 1:
HEXB (Hexosaminidase B (Beta Polypeptide)):
IFI27 (Interferon, alpha-Inducible Protein 27):
IFT88 (Intraflagellar Transport 88 Homolog):
K - O
KPTN (Kaptin (Actin Binding Protein)):
KIFAP3 (Kinesin Associated Protein 3):
LRTOMT - Leucine Rich Transmembrane and 0-Methyltransferase Domain Containing:
LHFPL5 (Lipoma HMGIC Fusion Partner-Like 5):
KIT (Mast/stem Cell Growth Factor Receptor):
MKKS (McKusick-Kaufman Syndrome):
MAP1A (Microtubule-Associated Protein 1A):
MRPS12 (Mitochondrial Ribosomal Protein S12):
MPV17 (MpV17 Mitochondrial Inner Membrane Protein):
MPV17L (MPV17 Mitochondrial Membrane Protein-Like):
MYCBPAP (MYCBP Associated Protein):
NDUFB9 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 9, 22kDa):
NAV2 (Neuron Navigator 2):
NIPBL (Nipped-B like Protein):
NDP - Norrie Disease (Pseudoglioma):
P - Si
PTH2 - Parathyroid Hormone 2:
PGAP1 (Post-GPI Attachment To Proteins 1):
KCNMA1 (Potassium Large Conductance Calcium-Activated Channel, Subfamily M, alpha Member 1):
KCNE1 (Potassium Voltage-Gated Channel, Isk-Related Family, Member 1):
KCNQ1 (Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1):
KCNQ4 (Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 4):
POU3F4 (POU Domain, Class 3, Transcription Factor 4):
POU4F2 (POU Domain, Class 4, Transcription Factor 2):
POU4F3 (POU Domain, Class 4, Transcription Factor 3):
PCDH15 (Protocadherin-15):
SLC52A3 - Solute Carrier Family 52 (Riboflavin Transporter), Member 3:
RPL38 (Ribosomal Protein L38):
SCO1 (SCO1 Cytochrome C Oxidase Assembly Protein):
SRRM4 (Serine/arginine Repetitive Matrix 4):
SOBP (Sine Oculis Binding Protein Homolog):
So - Th
SCN8A (Sodium Channel, Voltage-Gated, Type VIII, alpha):
SLC1A3 (Solute Carrier Family 1 (Glial High Affinity Glutamate Transporter), Member 3):
SLC12A2 (Solute Carrier Family 12 (Potassium-Chloride Transporter) Member 2):
SLC17A8 (Solute Carrier Family 17 (Sodium-Dependent Inorganic Phosphate Cotransporter), Member 8):
SLC26A4 (Solute Carrier Family 26, Member 4):
SLC26A5 (Solute Carrier Family 26, Member 5 (Prestin)):
SPTBN4 (Spectrin Beta, Non-Erythrocytic 4):
SPRY2 (Sprouty Homolog 2):
SOX2 (SRY (Sex Determining Region Y)-Box 2):
SOD1 (Superoxide Dismutase 1, Soluble):
SOD2 (Superoxide Dismutase 2, Mitochondrial):
TSPEAR (Thrombospondin-Type Laminin G Domain and EAR Repeats):
THRA (Thyroid Hormone Receptor, alpha):
THRB (Thyroid Hormone Receptor, beta):
Tr - Z
TFAP2A (Transcription Factor AP-2 alpha (Activating Enhancer Binding Protein 2 Alpha)):
TBL1X (Transducin (Beta)-Like 1X-Linked):
TIMM10 (Translocase of Inner Mitochondrial Membrane 10):
TIMM13 (Translocase of Inner Mitochondrial Membrane 13 Homolog):
TIMM8B (Translocase of Inner Mitochondrial Membrane 8 Homolog B):
TIMM9 (Translocase of Inner Mitochondrial Membrane 9 Homolog (Yeast)):
TMC1 (Transmembrane Channel-Like 1):
TMIE (Transmembrane Inner Ear):
TOMT (Transmembrane O-Methyltransferase):
TMPRSS3 (Transmembrane Protease, Serine 3):
Trpl (Transient Receptor Potential-Like):
TH - Tyrosine Hydroxylase:
USH1C (Usher Syndrome 1C (Autosomal Recessive, Severe)):
USH1G (Usher Syndrome 1G (Autosomal Recessive)):
USH2A (Usher Syndrome 2A (Autosomal Recessive, Mild)):
KIT (Mast/stem Cell Growth Factor Receptor):
WDR1 (WD Repeat Domain 1):
WFS1 (Wolfram Syndrome 1):
ZNF354A (Zinc Finger Protein 354A):