Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions About   Site Map   Contact Us
 
Home A service of the U.S. National Library of Medicine®
 
Genes >

Browse Genes by Name

1-9 | A | B | C | D | E | F | G | H | I | J-K | L | M | N | O | P | Q-R | S | T | U | V | W-Z
  • abhydrolase domain containing 5: ABHD5
  • acetyl-CoA acetyltransferase 1: ACAT1
  • achalasia, adrenocortical insufficiency, alacrimia: AAAS
  • actin, alpha 1, skeletal muscle: ACTA1
  • actin, alpha 2, smooth muscle, aorta: ACTA2
  • actin, beta: ACTB
  • actin, gamma 1: ACTG1
  • activin A receptor, type I: ACVR1
  • activin A receptor type II-like 1: ACVRL1
  • acyl-CoA dehydrogenase, C-2 to C-3 short chain: ACADS
  • acyl-CoA dehydrogenase, C-4 to C-12 straight chain: ACADM
  • acyl-CoA dehydrogenase family, member 8: ACAD8
  • acyl-CoA dehydrogenase, short/branched chain: ACADSB
  • acyl-CoA dehydrogenase, very long chain: ACADVL
  • acyl-CoA synthetase family member 3: ACSF3
  • 1-acylglycerol-3-phosphate O-acyltransferase 2: AGPAT2
  • ADAM metallopeptidase with thrombospondin type 1 motif, 2: ADAMTS2
  • ADAM metallopeptidase with thrombospondin type 1 motif, 10: ADAMTS10
  • ADAM metallopeptidase with thrombospondin type 1 motif, 13: ADAMTS13
  • ADAMTS-like 2: ADAMTSL2
  • adenine phosphoribosyltransferase: APRT
  • adenomatous polyposis coli: APC
  • adenosine deaminase: ADA
  • adenosine monophosphate deaminase 1: AMPD1
  • adenosylhomocysteinase: AHCY
  • ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited): ARFGEF2
  • age-related maculopathy susceptibility 2: ARMS2
  • aggrecan: ACAN
  • alanine-glyoxylate aminotransferase: AGXT
  • aldehyde dehydrogenase 3 family, member A2: ALDH3A2
  • aldehyde dehydrogenase 4 family, member A1: ALDH4A1
  • aldehyde dehydrogenase 5 family, member A1: ALDH5A1
  • aldehyde dehydrogenase 7 family, member A1: ALDH7A1
  • aldolase B, fructose-bisphosphate: ALDOB
  • alkaline phosphatase, liver/bone/kidney: ALPL
  • alkylglycerone phosphate synthase: AGPS
  • alpha thalassemia/mental retardation syndrome X-linked: ATRX
  • Alstrom syndrome 1: ALMS1
  • ALX homeobox 4: ALX4
  • amelogenin, X-linked: AMELX
  • aminoadipate-semialdehyde synthase: AASS
  • aminolevulinate dehydratase: ALAD
  • aminolevulinate, delta-, synthase 1: ALAS1
  • aminolevulinate, delta-, synthase 2: ALAS2
  • aminomethyltransferase: AMT
  • amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase: AGL
  • amyloid beta (A4) precursor protein: APP
  • amyotrophic lateral sclerosis 2 (juvenile): ALS2
  • anaplastic lymphoma receptor tyrosine kinase: ALK
  • androgen receptor: AR
  • angiogenin, ribonuclease, RNase A family, 5: ANG
  • ankylosis, progressive homolog (mouse): ANKH
  • ankyrin 1, erythrocytic: ANK1
  • ankyrin 2, neuronal: ANK2
  • anoctamin 5: ANO5
  • anthrax toxin receptor 2: ANTXR2
  • anti-Mullerian hormone: AMH
  • anti-Mullerian hormone receptor, type II: AMHR2
  • apolipoprotein A-I: APOA1
  • apolipoprotein B (including Ag(x) antigen): APOB
  • apolipoprotein E: APOE
  • aprataxin: APTX
  • aquaporin 2 (collecting duct): AQP2
  • arachidonate 12-lipoxygenase, 12R type: ALOX12B
  • arachidonate lipoxygenase 3: ALOXE3
  • arginase 1: ARG1
  • arginine vasopressin: AVP
  • arginine vasopressin receptor 2: AVPR2
  • argininosuccinate lyase: ASL
  • argininosuccinate synthase 1: ASS1
  • arginyl-tRNA synthetase 2, mitochondrial: RARS2
  • aristaless related homeobox: ARX
  • arylsulfatase A: ARSA
  • arylsulfatase B: ARSB
  • arylsulfatase E (chondrodysplasia punctata 1): ARSE
  • asp (abnormal spindle) homolog, microcephaly associated (Drosophila): ASPM
  • aspartoacylase: ASPA
  • aspartyl-tRNA synthetase 2, mitochondrial: DARS2
  • aspartylglucosaminidase: AGA
  • ataxia telangiectasia mutated: ATM
  • ataxin 1: ATXN1
  • ataxin 2: ATXN2
  • ataxin 3: ATXN3
  • atlastin GTPase 1: ATL1
  • ATP-binding cassette, sub-family A (ABC1), member 1: ABCA1
  • ATP-binding cassette, sub-family A (ABC1), member 3: ABCA3
  • ATP-binding cassette, sub-family A (ABC1), member 4: ABCA4
  • ATP-binding cassette, sub-family A (ABC1), member 12: ABCA12
  • ATP-binding cassette, sub-family B (MDR/TAP), member 4: ABCB4
  • ATP-binding cassette, sub-family B (MDR/TAP), member 7: ABCB7
  • ATP-binding cassette, sub-family B (MDR/TAP), member 11: ABCB11
  • ATP-binding cassette, sub-family C (CFTR/MRP), member 2: ABCC2
  • ATP-binding cassette, sub-family C (CFTR/MRP), member 6: ABCC6
  • ATP-binding cassette, sub-family C (CFTR/MRP), member 8: ABCC8
  • ATP-binding cassette, sub-family C (CFTR/MRP), member 9: ABCC9
  • ATP-binding cassette, sub-family D (ALD), member 1: ABCD1
  • ATPase, aminophospholipid transporter, class I, type 8B, member 1: ATP8B1
  • ATPase, Ca++ transporting, cardiac muscle, fast twitch 1: ATP2A1
  • ATPase, Ca++ transporting, cardiac muscle, slow twitch 2: ATP2A2
  • ATPase, Ca++ transporting, plasma membrane 2: ATP2B2
  • ATPase, Cu++ transporting, alpha polypeptide: ATP7A
  • ATPase, Cu++ transporting, beta polypeptide: ATP7B
  • ATPase, H+ transporting, lysosomal V0 subunit a2: ATP6V0A2
  • ATPase, Na+/K+ transporting, alpha 2 polypeptide: ATP1A2
  • ATPase, Na+/K+ transporting, alpha 3 polypeptide: ATP1A3
  • atrophin 1: ATN1
  • AU RNA binding protein/enoyl-CoA hydratase: AUH
  • autoimmune regulator: AIRE
  • autophagy related 16-like 1 (S. cerevisiae): ATG16L1
 
 
Published: May 13, 2013