About: RDH12

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

Attributes	Values
type	aapp gngm RDH12 Semmed Gene
label	RDH12 RDH12 gene\|RDH12 RDH12 protein, human\|RDH12 rdh12
sameAs	RDH12 (NIH - Gene)
http://semmed.demo...ms#interacts_with	Retinaldehyde
terms:part_of	C0030705 Family photoreceptor inner segment Human Persons Mus Photoreceptors Retinal dystrophy
terms:causes	Retinal dystrophy Retinal Degeneration Leber's amaurosis
terms:produces	Vitamin A
terms:interacts_with	Retinaldehyde 11-cis-Retinal
terms:affects	Retina
terms:inhibits	11-cis-Retinal
terms:stimulates	ranpirnase ranpirnase\|CENPV RDH11
terms:associated_with	Retinal Diseases Retinal dystrophy Retinal Degeneration Eye Manifestations Leber's amaurosis
terms:neg_affects	Gene Expression
terms:augments	Fetal Tissue
terms:neg_part_of	Cells
NEG_AFFECTS	Gene Expression
ASSOCIATED_WITH	Retinal Diseases Retinal Degeneration Eye Manifestations Leber's amaurosis
schema:identifier	145226 C1426577\|145226 C1506218\|145226
PART_OF	Family Persons Retinal dystrophy
STIMULATES	ranpirnase RDH11
is type of	RDH12
is sameAs of	RDH12 gene\|RDH12
is terms:process_of of	Mutation Mutation, Missense
is terms:location_of of	C0030705 Family Retina photoreceptor inner segment Individual Canis familiaris Human tissue network Family member Pinealocyte
is terms:compared_with of	SULT2A1
is terms:associated_with of	Pathogenesis
is LOCATION_OF of	Family Retina
is PROCESS_OF of	Mutation

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