About: SLC26A4

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An Entity of Type : http://semmed.demo.openlinksw.com/schemas/Gene#this, within Data Space : semmed.demo.openlinksw.com associated with source document(s)

Attributes	Values
type	aapp gngm SLC26A4 Semmed Gene Semmed Gene Class
label	SLC26A4 SLC26A4 gene\|SLC26A4 ptgds SLC26A4\|PTGDS SLC26A4\|MPZL2 slc26a4 mpzl2
sameAs	MPZL2 (NIH - Gene) prostaglandin R2 D-isomerase\|PTGDS MPZL2 SLC26A4 (NIH - Gene) PTGDS (NIH - Gene)
http://semmed.demo...com/terms#part_of	C0030705 Human Mus
http://semmed.demo...s#associated_with	hearing impairment Sensorineural Hearing Loss Pendred's syndrome
http://semmed.demo....com/terms#causes	hearing impairment Deafness
http://semmed.demo...terms#location_of	Mutation
http://semmed.demo...ms#interacts_with	Doxycycline ATP6V1B1\|ATP6V1B2
http://semmed.demo...com/terms#affects	Deafness Renal Excretion
http://semmed.demo.../terms#stimulates	Interleukin-13
http://semmed.demo...terms#predisposes	Disease
http://semmed.demo...terms#neg_part_of	Entire membranous labyrinth
terms:part_of	Kidney C0030705 DNA Sequence Family Ovum Human Child Adult Individual Mothers Persons Mus Infant cohort Infant, Newborn sibling Family member parent father husband Ethnic group Han Chinese Unmarried person Chromosomes, Human, Pair 7 wife Vestibular Aqueduct Motor area luminal membrane
terms:causes	Disease Hypertensive disease Asthma Congenital Abnormality hearing impairment Sensorineural Hearing Loss Autosome Disorders Goiter acidification Deafness Alkalosis Endolymphatic Hydrops chloride transport Pendred's syndrome HEARING LOSS CONGENITAL iodide transport
terms:location_of	Mutation Transcription, Genetic Transcriptional Activation Hypermethylation Mutation, Missense Point Mutation mRNA Expression
terms:produces	SNW1 Gene Bicarbonates Mucous body substance KCNJ10
terms:interacts_with	Cells Human Cell Line Epithelial Cells Cations Anions Xenopus oocyte Bicarbonates Iodine Chlorides Iodides Doxycycline Short Tandem Repeat

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