Gene

fstl5

Species
Danio rerio
Symbol
fstl5
Name
follistatin-like 5
Synonyms
  • drMahya-1
Biotype
protein coding gene
Automated Description
Predicted to enable calcium ion binding activity. Predicted to be involved in cell differentiation and regulation of BMP signaling pathway. Predicted to be active in extracellular region. Is expressed in corpus cerebelli and dorsal telencephalon. Orthologous to human FSTL5 (follistatin like 5).
ZFIN Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR10913
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensFSTL510 of 10YesYes  
Mus musculusFstl510 of 10YesYes  
Rattus norvegicusFstl58 of 9YesYes   
Xenopus tropicalisfstl54 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
fstl4178574555 of 8  
fstl1b228244273 of 8  
fstl1a329844272 of 8  
fsta416938253 of 8  
fstb516038282 of 8  
fstl368848392 of 8  
agrn78847392 of 8  
tmeff1b86949392 of 8  

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
None
Phenotype Term
Annotation details
References
whole organism quality, normal
Showing 1 - 1 of 1 rows
per page

Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume

Alleles and Variants

Genome location
Assembly version
GRCz11
Viewer Help
47.05M47.10M47.15M47.20M47.25M47.30M
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
uab431allele
la019072Tg
  • la019072
allele
sa1377allele with one associated variant
point mutation
  • stop gained
Yes
sa22550allele with one associated variant
point mutation
  • stop gained
sa22551allele with one associated variant
point mutation
  • stop gained
sa11024allele with one associated variant
point mutation
  • stop gained
sa19099allele with one associated variant
point mutation
  • stop gained
sa12250allele with one associated variant
point mutation
  • stop gained
sa35761allele with one associated variant
point mutation
  • stop gained
sa35762allele with one associated variant
point mutation
  • splice acceptor variant
Showing 1 - 10 of 11 rows
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Transgenic Alleles

No data available

Models

Model name
Experimental condition
Associated Human Diseases
Associated Phenotypes
Modifier
Source
fstl5sa1377/sa1377 (TL)
has condition:
standard conditions
  • whole organism quality, normal
ZFIN
fstl5uab431/+ (AB)ZFIN
Showing 1 - 2 of 2 rows
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Sequence Feature Viewer

Genome location
Assembly version
GRCz11
Viewer Help
47.05M47.10M47.15M47.20M47.25M47.30M

Sequence Details

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Expression

Primary Sources
Other Sources
Must provide at least one subject
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

No data available

Genetic Interactions

No data available