GlyCosmos Portal

Displaying entries **251 - 275** of **10109** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
481	ATPase Na+/K+ transporting subunit beta 1	ATP1B1	essential hypertension
482	ATPase Na+/K+ transporting subunit beta 2	ATP1B2
483	ATPase Na+/K+ transporting subunit beta 3	ATP1B3
488	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2	ATP2A2	acrokeratosis verruciformis essential hypertension keratosis follicularis pulmonary hypertension
489	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3	ATP2A3
493	ATPase plasma membrane Ca2+ transporting 4	ATP2B4
496	ATPase H+/K+ transporting subunit beta	ATP4B	atrophic gastritis autoimmune gastritis stomach cancer
498	ATP synthase F1 subunit alpha	ATP5F1A	combined oxidative phosphorylation deficiency 22 mitochondrial complex V (ATP synthase) deficiency nuclear type 4A mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
501	aldehyde dehydrogenase 7 family member A1	ALDH7A1 26g turgor protein homolog EPD P6c dehydrogenase PDE alpha-AASA dehydrogenase alpha-aminoadipic semialdehyde dehydrogenase antiquitin 1 delta1-piperideine-6-carboxylate dehydrogenease	early-onset vitamin B6-dependent epilepsy 4
506	ATP synthase F1 subunit beta	ATP5F1B
509	ATP synthase F1 subunit gamma	ATP5F1C
521	ATP synthase membrane subunit e	ATP5ME
523	ATPase H+ transporting V1 subunit A	ATP6V1A V-ATPase subunit A V-type proton ATPase (V-ATPase) catalytic subunit A VA68 Vma1	autosomal recessive cutis laxa type IID developmental and epileptic encephalopathy 93
527	ATPase H+ transporting V0 subunit c	ATP6V0C	early-onset epilepsy 3 thyroid gland carcinoma
529	ATPase H+ transporting V1 subunit E1	ATP6V1E1	autosomal recessive cutis laxa type IIC
535	ATPase H+ transporting V0 subunit a1	ATP6V0A1	developmental and epileptic encephalopathy 104
537	ATPase H+ transporting accessory protein 1	ATP6AP1 16A Ac45 CF2 ORF VATPS1 X-associated protein 3 XAP-3 XAP3 vacuolar ATPase subunit S1	immunodeficiency 47
538	ATPase copper transporting alpha	ATP7A	Menkes disease X-linked distal spinal muscular atrophy 3 cutis laxa occipital horn syndrome
540	ATPase copper transporting beta	ATP7B	Wilson disease
545	ATR serine/threonine kinase	ATR	Seckel syndrome 1 adenoid cystic carcinoma colon cancer lung cancer pancreatic cancer
546	ATRX chromatin remodeler	ATRX	X-linked mental retardation-hypotonic facies syndrome-1 alpha thalassemia-X-linked intellectual disability syndrome alpha-thalassemia myelodysplasia syndrome high grade glioma lung small cell carcinoma
551	arginine vasopressin	AVP	diabetes insipidus neurohypophyseal diabetes insipidus
552	arginine vasopressin receptor 1A	AVPR1A	hypertension
553	arginine vasopressin receptor 1B	AVPR1B	autism spectrum disorder bipolar disorder mood disorder
554	arginine vasopressin receptor 2	AVPR2	X-linked nephrogenic diabetes insipidus nephrogenic diabetes insipidus nephrogenic syndrome of inappropriate antidiuresis

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