16598 GENES FOUNDi
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Genei Gene descriptioni x Evidencei x Tissuei Cell typei Pathologyi Braini Bloodi Celli
ALG13ALG13, UDP-N-acetylglucosaminyltransferase subunit
ALG14ALG14, UDP-N-acetylglucosaminyltransferase subunit
ALG2ALG2, alpha-1,3/1,6-mannosyltransferase
ALG3ALG3, alpha-1,3- mannosyltransferase
ALG5ALG5, dolichyl-phosphate beta-glucosyltransferase
ALG6ALG6, alpha-1,3-glucosyltransferase
ALG8ALG8, alpha-1,3-glucosyltransferase
ALG9ALG9, alpha-1,2-mannosyltransferase
ALKALK receptor tyrosine kinase
ALKAL2ALK and LTK ligand 2
ALKBH1AlkB homolog 1, histone H2A dioxygenase
ALKBH2AlkB homolog 2, alpha-ketoglutarate dependent dioxygenase
ALKBH3AlkB homolog 3, alpha-ketoglutaratedependent dioxygenase
ALKBH4AlkB homolog 4, lysine demethylase
ALKBH5AlkB homolog 5, RNA demethylase
ALKBH6AlkB homolog 6
ALKBH7AlkB homolog 7
ALKBH8AlkB homolog 8, tRNA methyltransferase
ALLCAllantoicase
ALMS1ALMS1, centrosome and basal body associated protein
ALOX15Arachidonate 15-lipoxygenase
ALOX15BArachidonate 15-lipoxygenase, type B
ALOX5Arachidonate 5-lipoxygenase
ALOX5APArachidonate 5-lipoxygenase activating protein
ALPK1Alpha kinase 1
ALPLAlkaline phosphatase, liver/bone/kidney
ALPPL2Alkaline phosphatase, placental like 2
ALS2ALS2, alsin Rho guanine nucleotide exchange factor
ALS2CR12Amyotrophic lateral sclerosis 2 chromosome region 12
ALX1ALX homeobox 1
ALX3ALX homeobox 3
ALX4ALX homeobox 4
ALYREFAly/REF export factor
AMACRAlpha-methylacyl-CoA racemase
AMBNAmeloblastin
AMBRA1Autophagy and beclin 1 regulator 1
AMD1Adenosylmethionine decarboxylase 1
AMDHD1Amidohydrolase domain containing 1
AMDHD2Amidohydrolase domain containing 2
AMELXAmelogenin, X-linked
AMER1APC membrane recruitment protein 1
AMER2APC membrane recruitment protein 2
AMER3APC membrane recruitment protein 3
AMFRAutocrine motility factor receptor
AMHAnti-Mullerian hormone
AMHR2Anti-Mullerian hormone receptor type 2
AMIGO1Adhesion molecule with Ig like domain 1
AMIGO2Adhesion molecule with Ig like domain 2
AMIGO3Adhesion molecule with Ig like domain 3
AMMECR1Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
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