GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8926 - 8950** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
778	calcium voltage-gated channel subunit alpha1 F	CACNA1F
777	calcium voltage-gated channel subunit alpha1 E	CACNA1E
776	calcium voltage-gated channel subunit alpha1 D	CACNA1D
775	calcium voltage-gated channel subunit alpha1 C	CACNA1C
774	calcium voltage-gated channel subunit alpha1 B	CACNA1B
773	calcium voltage-gated channel subunit alpha1 A	CACNA1A
57685	cache domain containing 1	CACHD1
26256	calcium binding tyrosine phosphorylation regulated	CABYR
81928	Cdk5 and Abl enzyme substrate 2	CABLES2
91768	Cdk5 and Abl enzyme substrate 1	CABLES1
23523	calcineurin binding protein 1	CABIN1
768	carbonic anhydrase 9	CA9
765	carbonic anhydrase 6	CA6
11238	carbonic anhydrase 5B	CA5B
762	carbonic anhydrase 4	CA4 CAIV Car4	Behcet's disease Zollinger-Ellison syndrome achromatopsia acquired color blindness blindness blue color blindness brain cancer cancer cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease diabetes mellitus dissociated nystagmus eye disease fundus albipunctatus glaucoma hyperinsulinism hypogonadism intellectual disability keratoconus large intestine cancer learning disability lung cancer lung non-small cell carcinoma myocarditis night blindness nonpapillary renal cell carcinoma obesity obsolete asthenopia ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus red color blindness red-green color blindness renal carcinoma renal cell carcinoma retinitis pigmentosa 17 retinitis pigmentosa sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus type 2 diabetes mellitus
23632	carbonic anhydrase 14	CA14
771	carbonic anhydrase 12	CA12
770	carbonic anhydrase 11	CA11
759	carbonic anhydrase 1	CA1
203228	C9orf72-SMCR8 complex subunit	C9orf72
735	complement C9	C9
157773	chromosome 8 open reading frame 48	C8orf48
65265	chromosome 8 open reading frame 33	C8orf33
732	complement C8 beta chain	C8B
731	complement C8 alpha chain	C8A