Property talk:P4196

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Documentation

cytogenetic location
cytogenetic location of the gene or region

Description

Cytogenetic location of the gene or region.

Represents

locus (Q106227)

Data type

Domain

gene (Q7187)

Example

ABO (Q14839826) → 9q34.2
DMD (Q14864292) → Xp21.2-p21.1

Source

According to this template:

Entrez (ABO) https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=retrieve&dopt=default&list_uids=28&rn=1
OMIM (ABO) https://omim.org/entry/110300
OMIM list (ABO) https://omim.org/geneMap/9?start=520&limit=100&highlight=523
HGNC (ABO) https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:79
Entrez (Dystrophin) https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=retrieve&dopt=default&list_uids=1756&rn=1
OMIM (Dystrophin) https://omim.org/entry/300377
OMIM list (Dystrophin) https://omim.org/geneMap/X/144?start=-3&limit=10&highlight=144
HGNC (Dystrophin) https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:2928

According to statements in the property:
https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=retrieve&dopt=default&list_uids=28&rn=1
https://omim.org/entry/110300
https://omim.org/geneMap/9?start=520&limit=100&highlight=523
https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:79
https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=retrieve&dopt=default&list_uids=1756&rn=1
https://omim.org/entry/300377
https://omim.org/geneMap/X/144?start=-3&limit=10&highlight=144
https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:2928

When possible, data should only be stored as statements

Tracking: usage

Category:Pages using Wikidata property P4196 (Q126375091)

See also

genomic end (P645), genomic start (P644), chromosome (P1057)

Lists

Proposal discussion

Proposal discussion

Current uses

Total	185,559
Main statement	185,557	>99.9% of uses
Qualifier	2	<0.1% of uses

Search for values

[create Create a translatable help page (preferably in English) for this property to be included here]

Type “gene (Q7187)”: item must contain property “instance of (P31)” with classes “gene (Q7187)” or their subclasses (defined using subclass of (P279)). (Help)

Exceptions are possible as rare values may exist. Exceptions can be specified using exception to constraint (P2303).
List of violations of this constraint: Database reports/Constraint violations/P4196#Type Q7187, SPARQL

Scope is as main value (Q54828448): the property must be used by specified way only (Help)

List of violations of this constraint: Database reports/Constraint violations/P4196#Scope, hourly updated report, SPARQL

This property is being used by:

eu:Txantiloi:Gene infotaula automatikoa

Please notify projects that use this property before big changes (renaming, deletion, merge with another property, etc.)

v t e Wikidata properties related to genetics (Q7162)

Basic	subclass of genomic start genomic end molecular function ortholog encodes encoded by found in taxon chromosome strand orientation cytogenetic location chromosome count

Optional	regulates (molecular biology) biological process Gene Atlas image mode of inheritance ploidy increased expression in gene deletion association with gene duplication association with gene insertion association with gene inversion association with gene substitution association with posttranslational modification association with altered regulation leads to genome size genetic association positive therapeutic predictor for negative therapeutic predictor for positive diagnostic predictor for negative diagnostic predictor for positive prognostic predictor for negative prognostic predictor for biological variant of antisense inhibitor of mtDNA haplogroup Y-DNA Haplogroup recognition sequence cutting site of restriction enzyme produces cohesive end isoschizomer neoschizomer isocaudomer expressed in

Databases	Entrez Gene ID UniProt protein ID HGNC gene symbol HGNC ID OMIM ID EC enzyme number HomoloGene ID Ensembl gene ID RefSeq protein ID PDB structure ID RefSeq RNA ID KEGG ID GeneReviews ID Mouse Genome Informatics ID Gene Ontology ID Ensembl transcript ID Ensembl protein ID ClinVar Variation ID RefSeq genome ID NCBI locus tag UCSC Genome Browser assembly ID mirTarBase ID CIViC variant ID HGVS nomenclature FAO 2007 genetic resource ID GeneDB ID Saccharomyces Genome Database ID Pfam ID Human Phenotype Ontology ID REBASE Enzyme Number CIViC gene ID

Qualifiers	RefSeq genomic assembly

See also: Wikidata:WikiProject Molecular biology - Wikidata:WikiProject Medicine - Wikidata:WikiProject Haplogroups

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Hidden category:

Property with duplicated source