GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8026 - 8050** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
92255	LMBR1 domain containing 2	LMBRD2
92259	alpha-ketoglutarate dehydrogenase subunit 4	KGD4
92285	zinc finger protein 585B	ZNF585B
92293	transmembrane protein 132C	TMEM132C
92304	secretoglobin family 3A member 1	SCGB3A1
92312	mex-3 RNA binding family member A	MEX3A
92335	STE20 related adaptor alpha	STRADA
92340	proline rich 29	PRR29
92359	crumbs cell polarity complex component 3	CRB3
92369	splA/ryanodine receptor domain and SOCS box containing 4	SPSB4
92370	2-phosphoxylose phosphatase 1	PXYLP1 FLJ23751	myopia
92399	mitochondrial ribosome recycling factor	MRRF
92400	RNA binding motif protein 18	RBM18
92483	lactate dehydrogenase A like 6B	LDHAL6B LDH6B LDHL	breast cancer breast carcinoma disease of metabolism
92521	sperm antigen with calponin homology and coiled-coil domains 1	SPECC1
92579	glucose-6-phosphatase catalytic subunit 3	G6PC3 UGRP	Crohn's colitis Crohn's disease Marfan syndrome Wiskott-Aldrich syndrome acute myeloid leukemia agranulocytosis androgen insensitivity syndrome anemia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect bacterial sepsis bronchiectasis cancer cleft palate colitis congenital heart disease cryptorchidism cyclic hematopoiesis cystinuria embryoma essential thrombocythemia eunuchism galactosemia gastroenteritis glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hydronephrosis hypogonadism ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability isolated cleft palate learning disability leukopenia lymphopenia macrocytic anemia microcephaly mitral valve insufficiency mitral valve prolapse myelodysplastic syndrome neutropenia oculocutaneous albinism pancytopenia patent ductus arteriosus patent foramen ovale premature menopause primary immunodeficiency disease primary pulmonary hypertension pulmonary valve stenosis sensorineural hearing loss severe congenital neutropenia 4 severe congenital neutropenia situs inversus thrombocytopenia tuberous sclerosis ulcerative colitis varicose veins
92689	family with sequence similarity 114 member A1	FAM114A1
92737	delta/notch like EGF repeat containing	DNER
92745	solute carrier family 38 member 5	SLC38A5
92747	BPI fold containing family B member 1	BPIFB1
92749	dynein regulatory complex subunit 1	DRC1
92815	H2A clustered histone 25	H2AC25
92922	coiled-coil domain containing 102A	CCDC102A
92935	methionyl-tRNA synthetase 2, mitochondrial	MARS2
92949	ADAMTS like 1	ADAMTSL1 ADAMTSR1 FLJ35283 punctin punctin-1

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