GlyCosmos Portal

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
154141	membrane bound O-acyltransferase domain containing 1	MBOAT1 LPEAT1 LPLAT14 MGC44669 dJ434O11.1 lysophosphatidylethanolamine acyltransferase 1 lysophospholipid acyltransferase 1 lysophospholipid acyltransferase 14	brachydactyly-syndactyly syndrome cholestasis
154197	PARN like ribonuclease domain containing exonuclease 1	PNLDC1
154313	cilia and flagella associated protein 206	CFAP206
154664	ATP binding cassette subfamily A member 13	ABCA13
154790	C-type lectin domain family 2 member L	CLEC2L FLJ32986
154796	angiomotin	AMOT
155066	ATPase H+ transporting V0 subunit e2	ATP6V0E2
155184	solute carrier family 2 member 7	SLC2A7
155435	RNA binding motif protein 33	RBM33
155465	anterior gradient 3, protein disulphide isomerase family member	AGR3
157310	phosphatidylethanolamine binding protein 4	PEBP4
157313	cell division cycle associated 2	CDCA2
157570	establishment of sister chromatid cohesion N-acetyltransferase 2	ESCO2
157680	vacuolar protein sorting 13 homolog B	VPS13B
157773	chromosome 8 open reading frame 48	C8orf48
157855	potassium calcium-activated channel subfamily U member 1	KCNU1
157869	somatomedin B and thrombospondin type 1 domain containing	SBSPON
157922	calmodulin regulated spectrin associated protein 1	CAMSAP1
158038	leucine rich repeat and Ig domain containing 2	LINGO2
158056	MAM domain containing 4	MAMDC4
158131	olfactory receptor family 1 subfamily Q member 1	OR1Q1
158234	tRNA methyltransferase 10B	TRMT10B
158326	FRAS1 related extracellular matrix 1	FREM1 C9orf143 C9orf145 DKFZp686M16108 FLJ25461 TILRR	3p deletion syndrome Angelman syndrome Baraitser-Winter syndrome CAKUT Fraser syndrome 1 Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome NFIA-related disorder Nance-Horan syndrome Potter's syndrome SATB2-associated syndrome Sakati-Nyhan syndrome Smith-Magenis syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acquired immunodeficiency syndrome anorectal stricture bilateral renal aplasia branchiootic syndrome cardiovascular system disease chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia craniosynostosis distal 10q deletion syndrome eye disease heart disease hiatus hernia human immunodeficiency virus infectious disease microphthalmia myelofibrosis omphalocele orofaciodigital syndrome I orofaciodigital syndrome X rectal prolapse renal agenesis umbilical hernia
158358	bromodomain containing 10	BRD10
158399	zinc finger protein 483	ZNF483

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