Gene

Inafm1

Species
Mus musculus
Symbol
Inafm1
Name
InaF motif containing 1
Synonyms
  • 2610014I16Rik
  • proline rich 24
Biotype
protein coding gene
Automated Description
Orthologous to human INAFM1 (InaF motif containing 1).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR34929
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensINAFM110 of 10YesYes  
Rattus norvegicusInafm19 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
Inafm2112444383 of 9 

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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
No data available

Alleles and Variants

Genome location
Assembly version
GRCm39
Viewer Help
16.0060M16.0062M16.0064M16.0066M16.0068M16.0070M16.0072M16.0074M
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
Inafm1em1(IMPC)Kmpcallele
NC_000073.7:g.16006165T>Avariant
SNP
  • 3 prime UTR variant
NC_000073.7:g.16006870G>Avariant
SNP
  • missense variant
NC_000073.7:g.16007548G>Cvariant
SNP
  • 5 prime UTR variant
NC_000073.7:g.16006188C>Tvariant
SNP
  • 3 prime UTR variant
NC_000073.7:g.16006377T>Cvariant
SNP
  • 3 prime UTR variant
NC_000073.7:g.16007173C>Tvariant
SNP
  • missense variant
NC_000073.7:g.16006742G>Tvariant
SNP
  • 3 prime UTR variant
NC_000073.7:g.16007576G>Avariant
SNP
  • 5 prime UTR variant
NC_000073.7:g.16006741G>Tvariant
SNP
  • 3 prime UTR variant
Showing 1 - 10 of 45 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
16.0060M16.0062M16.0064M16.0066M16.0068M16.0070M16.0072M16.0074M

Sequence Details

Transcript: Mode:

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

Genetic Interactions

No data available