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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	tst Semmed Gene Class
label	tst RDS gene\|PRPH2\|TST rds gene prph2
sameAs	PRPH2 (NIH - Gene) PRPH2 TST TST (NIH - Gene)
http://semmed.demo...com/terms#part_of	Wild Type Mouse
http://semmed.demo...s#administered_to	Mus
terms:part_of	C0030705 Ganglion cell Individual House mice Lanugo Wild Type Mouse Chromosomes, Human, Pair 17
terms:causes	Degenerative abnormality physiological aspects Retinitis Pigmentosa Dystrophy Gliosis Autosomal dominant retinitis pigmentosa Pattern dystrophy of macula
terms:location_of	Mutation
terms:produces	PHEMX protein, human\|TSPAN32
terms:coexists_with	Genes ROM1 gene\|ROM1
terms:compared_with	Alleles
terms:associated_with	Disease Age related macular degeneration Retinitis Pigmentosa Dystrophy Retinal dystrophy Macular dystrophy Cone dystrophy
terms:neg_causes	Retinal dystrophy
terms:augments	Visual impairment
terms:administered_to	Mus
terms:neg_location_of	Mutation
terms:neg_coexists_with	retinal phosphodiesterase, beta subunit\|PDE6B
terms:neg_interacts_with	Opsin
NEG_LOCATION_OF	Mutation
LOCATION_OF	Mutation
ASSOCIATED_WITH	Dystrophy
schema:identifier	5961 7263 C1419329\|5961\|7263 c1419329
PART_OF	House mice Lanugo
CAUSES	physiological aspects Autosomal dominant retinitis pigmentosa
is type of	tst
is terms:process_of of	Mutation Polymorphism, Genetic Mutation, Missense Splice-Site Mutation Point Mutation Deletion Mutation
is terms:part_of of	5' Untranslated Regions Exons 5' Flanking Region
is terms:location_of of	Cells C0030705 Family Retina member Individual Population Group Mus House mice Chromosomes Family member Photoreceptors COS-7 Cells outer membrane Hispanics Neural Retina Chromosomes, Human, Pair 6
is terms:produces of	Proteins
is terms:affects of	Mutation
is terms:coexists_with of	Tryptophan Ciliary Neurotrophic Factor Arrestin TYRP1 gene\|TYRP1 CACD gene\|CACD
is terms:inhibits of	NR2E3
is terms:stimulates of	Nerve Growth Factors\|NGF EGR1 gene\|EGR1 RAB8A gene\|RAB8A
is terms:associated_with of	Dystrophy
is terms:neg_process_of of	Mutation
is LOCATION_OF of	Cells C0030705 Family Individual Population Group

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