About: eye development

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

The process whose specific outcome is the progression of the eye over time, from its formation to the mature structure. The eye is the organ of sight.

Attributes	Values
rdf:type	Item
description	biologisch proces (nl) біологічний процес (uk) The process whose specific outcome is the progression of the eye over time, from its formation to the mature structure. The eye is the organ of sight. (en)
exact match	wds:Q5422650-E22761DF-2D0E-4FEC-868A-27BE9397006B
exact match	http://purl.obolibrary.org/obo/GO_0001654
rdfs:label	razvoj očesa (sl) Augenentwicklung (de) desenvolvimento ocular (pt) développement de l'œil (fr) eye development (en) øje-udvikling (da) күз үсеше (tt) развитие глаз (ru) розвиток ока (uk) 眼部發展 (zh)
skos:prefLabel	razvoj očesa (sl) Augenentwicklung (de) desenvolvimento ocular (pt) développement de l'œil (fr) eye development (en) øje-udvikling (da) күз үсеше (tt) развитие глаз (ru) розвиток ока (uk) 眼部發展 (zh)
name	razvoj očesa (sl) Augenentwicklung (de) desenvolvimento ocular (pt) développement de l'œil (fr) eye development (en) øje-udvikling (da) күз үсеше (tt) развитие глаз (ru) розвиток ока (uk) 眼部發展 (zh)
Freebase ID	wds:Q5422650-5BB8BBFA-B995-4236-92E0-35B54EF5DB41
Freebase ID	/m/026st9c
Gene Ontology ID	wds:Q5422650-1370B052-C264-45E2-AE13-33D0B59B9E25
Gene Ontology ID	GO:0001654
instance of	wds:Q5422650-2392C098-D4E0-4FB4-89B2-91E9BE6A9670 wds:Q5422650-9efb7378-4127-c2d2-bac1-b068ae199aa9
part of	wds:Q5422650-29D01FF8-D295-4EA9-AC08-57DDE3F16253
instance of	biological process evolutionary developmental biology
part of	visual system development
subclass of	wds:Q5422650-B94FA0AD-09B4-42C6-A226-F1237FC00F9C
subclass of	sensory organ development
anatomical location	wds:Q5422650-ea200b19-48bb-9ffe-2cc5-cc47bcc95192
anatomical location	eye
skos:altLabel	GO:0001654 (en) développement occulaire (fr)
OpenAlex ID	wds:Q5422650-C9DE2F58-D7FE-4312-AD8A-C542B676DF5A
UMLS CUI	wds:Q5422650-44138A52-E9E0-4BE7-A0A9-695FCF560682
Microsoft Academic ID	wds:Q5422650-19BF42EA-79C8-47EE-A960-7D86E8DB38CE
Microsoft Academic ID	https://makg.org/entity/114696181
OpenAlex ID	C114696181
UMLS CUI	C1517080
Microsoft Academic ID	114696181
is owl:sameAs of	eye development
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q5422650 Eye development https://pt.wikipedia.org/wiki/Desenvolvimento_ocular
is part of of	eye morphogenesis
is part of of	wds:Q15311615-568C24A4-34B9-4974-B41A-27768F173226
is subclass of of	camera-type eye development compound eye development vertebrate eye development Bolwig's organ development
is subclass of of	wds:Q21110799-56388C56-7577-4F50-A8D9-ED632F039601 wds:Q14820061-B866F5B5-5FCA-42B0-8EB1-6E3EF175D9D9 wds:Q51021887-efb74a61-4375-6ff7-e0ff-0db75fa7d722 wds:Q22298656-055EDABC-43E5-4112-B8B2-8CF84AC8046D
is main subject of	Mutations in SCO2 are associated with autosomal-dominant high-grade myopia X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development Involvement of the Hipk family in regulation of eyeball size, lens formation and retinal morphogenesis The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18 Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies Mutation of SALL2 causes recessive ocular coloboma in humans and mice Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly Glass confers rhabdomeric photoreceptor identity in , but not across all metazoans Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis Mbt/PAK4 together with SRC modulates N-Cadherin adherens junctions in the developing eye Excess caffeine exposure impairs eye development during chick embryogenesis Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis. Developmentally regulated splice variants mediate transcriptional repressor functions during eye formation Tuned polymerization of the transcription factor Yan limits off-DNA sequestration to confer context-specific repression MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome) Developmentally regulated autophagy is required for eye formation in Drosophila Arginine to Glutamine Variant in Olfactomedin Like 3 () Is a Candidate for Severe Goniodysgenesis and Glaucoma in the Border Collie Dog Breed Loss-of-function mutations in FREM2 disrupt eye morphogenesis
is main subject of	wds:Q24303793-1672CAA5-CDA9-4E45-8E29-CC9CA451CB6B wds:Q24297224-46562ECC-BF6E-4125-BD48-5E1B6D8F254D wds:Q24298949-6D42D09C-5F3C-4041-A585-43AF78972FB6 wds:Q64062115-52DDA350-38B5-41EC-8FE5-AC7ACDEEEC61 wds:Q64085498-CA8D96C4-E8F9-40CA-898E-EC15BF6CA064 wds:Q22004175-4C0DA865-ACAC-43EC-8C82-BEC278274204 wds:Q24336386-B1D6C990-121A-4882-A605-96BB5179AF43 wds:Q24311933-6208885C-B920-4B8E-BE2C-99C7F3178760

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