GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **7826 - 7850** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
84869	carbonyl reductase 4	CBR4 FLJ14431 SDR45C1 short chain dehydrogenase/reductase family 45C, member 1	biliary atresia pancreatic cancer tuberculosis
84870	R-spondin 3	RSPO3
84873	adhesion G protein-coupled receptor G7	ADGRG7
84875	poly(ADP-ribose) polymerase family member 10	PARP10 ARTD10 FLJ14464	ataxia telangiectasia bipolar I disorder bipolar disorder hepatocellular carcinoma liver cancer neurodegenerative disease pancreatic cancer pancreatic carcinoma
84876	ORAI calcium release-activated calcium modulator 1	ORAI1
84879	MFSD2 lysolipid transporter A, lysophospholipid	MFSD2A
84883	AIF family member 2	AIFM2
84886	chromosome 1 open reading frame 198	C1orf198
84888	signal peptide peptidase like 2A	SPPL2A
84889	solute carrier family 7 member 3	SLC7A3
84892	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	POMGNT2 AGO61 FLJ14566 protein O-mannose beta-1,4-N-acetylglucosaminyltransferase 2	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome acute myeloid leukemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly malaria microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type C8 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
84893	F-box DNA helicase 1	FBH1
84894	leucine rich repeat and Ig domain containing 1	LINGO1
84896	ATPase family AAA domain containing 1	ATAD1
84897	transforming growth factor beta regulator 1	TBRG1
84898	plexin domain containing 2	PLXDC2
84899	transmembrane O-mannosyltransferase targeting cadherins 4	TMTC4 FLJ14624 FLJ22153	autosomal recessive nonsyndromic deafness breast cancer idiopathic scoliosis
84901	nuclear factor of activated T cells 2 interacting protein	NFATC2IP
84910	transmembrane protein 87B	TMEM87B
84912	solute carrier family 35 member B4	SLC35B4 FLJ14697 YEA4	prostate cancer prostate carcinoma stomach cancer stomach carcinoma
84915	family with sequence similarity 222 member A	FAM222A
84916	UTP4 small subunit processome component	UTP4
84918	LDL receptor related protein 11	LRP11
84920	ALG10 alpha-1,2-glucosyltransferase	ALG10 ALG10A DIE2 FLJ14751 derepression of ITR1 expression 2 homolog (S. cerevisiae) dolichyl-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-dolichol alpha-1,2- glucosyltransferase	hepatitis C long QT syndrome 2 long QT syndrome nonsyndromic deafness sick sinus syndrome
84925	solute carrier family 49 member 4	SLC49A4

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