Gene

Zfp804b

Species
Rattus norvegicus
Symbol
Zfp804b
Name
zinc finger protein 804B
Synonyms
  • hypothetical LOC499994
  • LOC499994
Biotype
protein coding gene
Automated Description
Predicted to enable metal ion binding activity. Predicted to be active in nucleus. Orthologous to human ZNF804B (zinc finger protein 804B).
RGD Description
Predicted to enable metal ion binding activity. Orthologous to human ZNF804B (zinc finger protein 804B); INTERACTS WITH 2,3,7,8-Tetrachlorodibenzofuran; glyphosate; valproic acid.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR17614
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensZNF804B10 of 10YesYes  
Mus musculusZfp804b9 of 9YesYes   
Xenopus tropicalisznf804b5 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
Gpatch81154241283 of 9 
Zfp804a2146940273 of 9 

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

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

Alleles and Variants

No mapped variant information available
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NC_051339.1:g.26628913G>Avariant
SNP
  • intron variant
NC_051339.1:g.26630230T>Avariant
SNP
  • intron variant
NC_051339.1:g.26661648T>Cvariant
SNP
  • intron variant
NC_051339.1:g.26670201G>Avariant
SNP
  • intron variant
NC_051339.1:g.26672179T>Cvariant
SNP
  • intron variant
NC_051339.1:g.26672711A>Gvariant
SNP
  • intron variant
NC_051339.1:g.26676620C>Tvariant
SNP
  • intron variant
NC_051339.1:g.26679869T>Cvariant
SNP
  • intron variant
NC_051339.1:g.26652321C>Tvariant
SNP
  • intron variant
NC_051339.1:g.26691775A>Gvariant
SNP
  • intron variant
Showing 1 - 10 of 4,120 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
mRatBN7.2
Viewer Help
26.65M26.70M26.75M26.80M26.85M26.90M26.95M27.00M27.05M27.10MENSRNOT00000045346.5 (Zfp804b)XM_008762730.4 (Zfp804b)ENSRNOT00000011359.5 (Tex47)NM_001077681.1 (Tex47)ENSRNOT00000096001.1 (Rnu2-34)ENSRNOT00000091433.2 (LOC120102775)

Sequence Details

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Expression

Primary Sources
None
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