Species

Danio rerio

Symbol

si:ch1073-126c3.2

Name

si:ch1073-126c3.2

Synonyms

fd36h06
wu:fd36h06

Biotype

protein coding gene

Automated Description

Not Available

ZFIN Description

Not Available

Cross References

Additional Information

Literature

Orthology

Gene tree: Not Available

No data available

Links to orthology data in JBrowse by filter level: Stringent, Moderate, No filter, Best and Best Reverse

Paralogy

No paralogs for the gene.

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources: None
Other Sources: None

No data available

Disease Associations

	all annotations		all disease by infectious agent	bacterial infectious disease	fungal infectious disease	parasitic infectious disease	viral infectious disease		all disease of anatomical entity	cardiovascular system disease	central nervous system disease	endocrine system disease	gastrointestinal system disease	hematopoietic system disease	immune system disease	integumentary system disease	musculoskeletal system disease	peripheral nervous system disease	reproductive system disease	respiratory system disease	sensory system disease	thoracic disease	urinary system disease		all disease of cellular proliferation	benign neoplasm	cancer	pre-malignant neoplasm		all genetic disease	chromosomal disease	monogenic disease	polygenic disease		all other disease	disease of mental health	disease of metabolism	physical disorder	syndrome
si:ch1073-126c3.2 (Dre)

Cell color indicative of annotation volume

Gene	Association	Disease Qualifier	Disease	Evidence	Source	Based On	References
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Alleles and Variants

Genome location

Chr13:20535159...20540790 (5.63 kb)

Assembly version

GRCz11

Viewer Help

Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.

Allele/Variant Symbol	Allele Synonyms	Category	Variant	Variant type	Molecular consequence	Has Disease Annotations	Has Phenotype Annotations
sa42180		allele with one associated variant	NC_007124.7:g.20535907T>A point mutation 3 prime UTR variant

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View detailed Alleles/Variants information

Download all Alleles/Variants for all genes of the species

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location

Chr13:20535159...20540790 (5.63 kb)

Assembly version

GRCz11

Viewer Help

Sequence Details

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Expression

Primary Sources

None

Other Sources

	all annotations		all anatomical structures	alimentary part of gastrointestinal system	chemosensory system	circulatory system	endocrine system	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mechanosensory system	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system	vestibulo-auditory system	visual system	endoderm	ectoderm	mesoderm	mesenchyme	adipose tissue	appendage	entire extraembryonic component	imaginal precursor	pharyngeal arch	other		all stages	embryo stage	post embryonic, pre-adult	post-juvenile adult stage		all cellular components	extracellular region	plasma membrane	synapse	cell junction	cell projection	cytoplasmic vesicle	endosome	vacuole	golgi apparatus	endoplasmic reticulum	cytosol	mitochondrion	nucleus	chromosome	cytoskeleton	protein-containing complex	other locations

Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

No data available

Genetic Interactions

si:ch1073-126c3.2 role	si:ch1073-126c3.2 genetic perturbation	Interactor gene	Interactor species	Interactor role	Interactor genetic perturbation	Interaction type	Phenotype or trait	Source	Reference
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