for example to search all human alpha/beta hydrolase found in human genome enter this search in the window below:
select a, fam, nam, c from a in class Gene_locus,
spec in a->Species where spec.name like "Homo sapiens",
fam in a->Family,
nam in a->Name,
c in count(select a->Structure)
sort by: fam, :nam
for more examples from esther go to AQL esther
for examples from esther on insecticide resistance go to AQL esther resistance
for more examples from wormbase go to AQL wormbase
AQL for the supplementary material of the Pucon Poster Pucon Poster
125 rows returned| Gene_locus | | | |
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| human-AADAC | | | | | human-AADACL2 | | | | | human-AADACL3 | | | | | human-AADACL4 | | | | | human-ABHD1 | | | | | human-ABHD2 | | | | | human-ABHD3 | | | | | human-ABHD4 | | | | | human-ABHD5 | 1 | 44 | NAFLD | | human-ABHD5 | 1 | 44 | Chanarin-Dorfman syndrome | | human-ABHD6 | 1 | | | | human-ABHD8 | | | | | human-ABHD10 | | | | | human-ABHD11 | | | | | human-ABHD12 | | 18 | PHARC Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract | | human-ABHD12B | | | | | human-ABHD13 | | | | | human-ABHD14A | | | | | human-ABHD15 | | | | | human-ABHD16A | | 9 | Hereditary spastic paraplegia (HSP) ABHD16A | | human-ABHD16B | | | | | human-ABHD17A | | | | | human-ABHD17B | | | | | human-ABHD17C | | | | | human-ABHD18 | | | | | human-ACHE | 80 | 191 | | | human-ACOT1 | | | | | human-ACOT2 | 1 | | | | human-ACOT4 | 1 | | | | human-ACOT6 | | | | | human-AFMID | | | | | human-APEH | | | | | human-BAAT | | 1 | Familial hypercholanemia | | human-BCHE | 92 | 273 | | | human-BPHL | 4 | | | | human-CEL | 7 | 13 | Maturity-onset diabetes of the Young, Type8, with exocrine dysfunction, MODY8 | | human-CES1 | 19 | 34 | | | human-CES2 | | | | | human-CES3 | | | | | human-CES4A | | | | | human-CES5A | | | | | human-CIB | 1 | | | | human-CMBL | | | | | human-CPVL | | | | | human-CTSA | 9 | 25 | Galactosialidosis | | human-DAGLA | | 7 | Neuro-ocular DAGLA-related syndrome | | human-DAGLB | | 4 | Parkinson disease, autosomal recessive (ARPD) early-onset (EOPD) | | human-DPP4 | 104 | 1 | | | human-DPP6 | 9 | 5 | Ventricular fibrillation, paroxysmal familial 2 | | human-DPP6 | 9 | 5 | Gilles de la Tourette syndrome (GTS) | | human-DPP6 | 9 | 5 | Mental retardation, autosomal dominant 33 | | human-DPP7 | 3 | | | | human-DPP8 | 19 | | | | human-DPP9 | 11 | 4 | Hatipoglu syndrome | | human-DPP10 | 1 | | | | human-EPHX1 | | 6 | Lipoatrophic diabetes | | human-EPHX1 | | 6 | Familial hypercholanemia | | human-EPHX2 | 109 | 1 | | | human-EPHX3 | | | | | human-EPHX4 | | | | | human-ESD | 1 | | | | human-f172a | | | | | human-FAM135A | | | | | human-FAM135B | | | | | human-FAP | 2 | | | | human-FASN | 6 | | | | human-KANSL3 | | | | | human-LCAT | 6 | 91 | Lecithin-cholesterol acyltransferase deficiency (LCATD) and fish-eye disease (FED) | | human-LDAH | | | | | human-LIPA | 1 | 62 | Wolman disease WD, Cholesterol Ester Storage Disease, CESD | | human-LIPC | | 16 | Hypobetalipoproteinemia Familial 2 | | human-LIPC | | 16 | Hepatic triglyceride lipase Deficiency | | human-LIPE | | 8 | Lipodystrophy, familial partial, type 6 | | human-LIPF | 1 | | | | human-LIPG | | 3 | | | human-LIPH | | 32 | Hypotrichosis | | human-LIPI | | 1 | Susceptibility to Hypertriglyceridemia | | human-LIPJ | | | | | human-LIPK | | | | | human-LIPM | | | | | human-LIPN | | 1 | Late-Onset Form of Autosomal-Recessive Congenital Ichthyosis | | human-LPL | 4 | 157 | Hyperlipoproteinemia TypeI | | human-LYPLA1 | 6 | | | | human-LYPLA2 | 2 | | | | human-LYPLAL1 | 2 | | | | human-MEST | | | | | human-MGLL | 15 | | | | human-NCEH1 | | | | | human-NDRG1 | 1 | 8 | Hereditary motor and sensory neuropathy, LOM Type | | human-NDRG2 | 3 | | | | human-NDRG3 | 3 | | | | human-NDRG4 | | 1 | pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF) | | human-NLGN1 | 2 | 6 | Neuroligin 1 Alzheimer's disease (AD) Autism | | human-NLGN2 | 2 | 2 | Neuroligin 2 Suceptibility Schizophrenia, anxiety, autism, intellectual disability, hyperphagia, and obesity | | human-NLGN3 | 1 | 3 | Neuroligin 3 Autism AUTSX1 Asperger syndrome ASPGX1 | | human-NLGN4X | 3 | 8 | Neuroligin 4 Autism AUTSX2 Asperger syndrome ASPGX2 | | human-NLGN4Y | | 1 | Neuroligin 4 Autism AUTSX2 Asperger syndrome ASPGX2 | | human-NOTUM | 141 | | | | human-OLAH | 1 | | | | human-OVCA2 | | | | | human-PAFAH2 | | | | | human-PGAP1 | | 9 | Mental retardation, autosomal recessive 42 MRT42 | | human-PLA1A | | | | | human-PLA2G7 | 33 | 11 | Suceptibility to asthma and atopy, Platelet-activating factor acetylhydrolase (PLA2G7) deficiency (PAFAD) coronary artery disease risk factor | | human-PLA2G15 | 8 | | | | human-PNLIP | 4 | 8 | Congenital absence of pancreatic lipase | | human-PNLIPRP1 | 1 | | | | human-PNLIPRP2 | 2 | | | | human-PNLIPRP3 | | | | | human-PPME1 | 2 | | | | human-PPT1 | 1 | 73 | Infantile neuronal ceroid lipofuscinosis | | human-PPT2 | 1 | | | | human-PRCP | 1 | | | | human-PREP | 1 | | | | human-PREPL | 1 | 10 | Hypotonia-Cystinuria Syndrome | | human-PRSS16 | | | | | human-RBBP9 | 2 | | | | human-SCPEP1 | | | | | human-SERAC1 | | 30 | MEGDEL syndrome | | human-SERHL2 | | | | | human-SPG21 | | 7 | Mast Syndrome | | human-TEX30 | | | | | human-TG | 2 | 96 | Goiter, familial with hypothyroidism, autosomal recessive | | human-TMCO4 | | | | | human-TMEM53 | | | |
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