About: sensory perception of sound

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

The series of events required for an organism to receive an auditory stimulus, convert it to a molecular signal, and recognize and characterize the signal. Sonic stimuli are detected in the form of vibrations and are processed to form a sound.

Attributes	Values
rdf:type	Item
description	biologisch proces (nl) біологічний процес (uk) fysiologinen prosessi (fi) The series of events required for an organism to receive an auditory stimulus, convert it to a molecular signal, and recognize and characterize the signal. Sonic stimuli are detected in the form of vibrations and are processed to form a sound. (en)
exact match	wds:Q14865145-84AC7355-C592-49C0-8308-2AF0B9F64615
exact match	http://purl.obolibrary.org/obo/GO_0007605
rdfs:label	hörande (sv) kuuleminen (fi) perception (sw) sensory perception of sound (en) senzorična zaznava zvoka (sl) smyslové vnímání zvuku (cs)
skos:prefLabel	hörande (sv) kuuleminen (fi) perception (sw) sensory perception of sound (en) senzorična zaznava zvoka (sl) smyslové vnímání zvuku (cs)
name	hörande (sv) kuuleminen (fi) perception (sw) sensory perception of sound (en) senzorična zaznava zvoka (sl) smyslové vnímání zvuku (cs)
Gene Ontology ID	wds:Q14865145-8B7969AD-DBD1-4FA2-85F3-E30F4220C4B9
Gene Ontology ID	GO:0007605
instance of	wds:Q14865145-8C6EC8F4-DF3D-4ACB-B85F-7F0A8F9F7789
instance of	biological process
subclass of	wds:Q14865145-59D5EBE4-684E-4DB9-A434-066AC2958338
subclass of	sensory perception of mechanical stimulus
skos:altLabel	hearing (en) sluh (sl) GO:0007605 (en) perception of sound (en) slišanje (sl) zaznavanje zvoka (sl)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q14865145
is instance of of	head shadow Sensory processing of sound by inner hair cells of the cochlea Sensory processing of sound
is part of of	detection of mechanical stimulus involved in sensory perception of sound vibrational conductance of sound to the inner ear
is instance of of	wds:Q106520214-83B78FCE-F555-401A-8CDF-229277ADCDD3 wds:Q5689465-96b2ff5b-4ce9-8707-e0a8-a4b53d8236bd wds:Q106520218-9B2501D6-7150-43C1-BA63-021E5DCF518C
is part of of	wds:Q14906097-DBE15E65-AF12-4519-8D41-5B22366183FF wds:Q22299505-6647EBA5-4848-4C28-B578-43C7948C211F
is facet of of	tonotopy
is facet of of	wds:Q82654-87613b8a-48f4-8b46-f48d-b8da190d088a
is main subject of	Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese A gene upregulated in the acoustically damaged chick basilar papilla encodes a novel WD40 repeat protein X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mapping Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5 Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4). Nonsyndromic hearing impairment is associated with a mutation in DFNA5 Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss Epistatic relationship between Waardenburg syndrome genes MITF and PAX3 Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4 Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13) Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness HOMER2, a stereociliary scaffolding protein, is essential for normal hearing in humans and mice. Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneity Modification of human hearing loss by plasma-membrane calcium pump PMCA2 Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79 Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1) Tricellulin is a tight-junction protein necessary for hearing The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30 Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans A frameshift mutation in GRXCR2 causes recessively inherited hearing loss GRM7 variants confer susceptibility to age-related hearing impairment Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54 Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing. Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing loss CDC14A Phosphatase is Essential for Hearing and Male Fertility in Mouse and Human. Sequence and expression patterns of a human EMAP-related protein-2 (HuEMAP-2) Molecular cloning of a zinc finger gene eZNF from a human inner ear cDNA library, and in situ expression pattern of its mouse homologue in mouse inner ear Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss
is main subject of	wds:Q22008800-2F41C738-C826-4A93-A021-8E189BAAD6E9 wds:Q24305234-CA3228F2-23E8-4DEB-971D-F43D8EEBBFA0 wds:Q24337513-C9030D52-825F-49BA-A90C-BFB1FBC3F7D6 wds:Q24337885-5D14CD96-07EF-469D-B2F6-9EB22D474BB7 wds:Q24318817-B179934C-8852-4B3E-A28E-4BDB588DAC34 wds:Q24310158-8149A2A3-FA53-4AA5-AB7A-19B0F5C5E2E7 wds:Q24300298-29929A83-0A7A-49E2-ABFB-BDE475012F0F wds:Q24315649-2C8C08A8-0BDF-435D-BD34-1A00EF37C497

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