si:dkey-90a13.6

Ensembl ID:
ENSDARG00000078191
ZFIN ID:
ZDB-GENE-090313-352
Human Orthologue:
ZBTB46
Human Description:
zinc finger and BTB domain containing 46 [Source:HGNC Symbol;Acc:16094]
Mouse Orthologue:
Zbtb46
Mouse Description:
zinc finger and BTB domain containing 46 Gene [Source:MGI Symbol;Acc:MGI:1919397]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa6730 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa6730
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112738 Nonsense 155 610 1 4
ENSDART00000142494 Nonsense 155 515 1 4
Genomic Location (Zv9):
Chromosome 23 (position 13834278)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 13966211
GRCz11 23 13722288
KASP Assay ID:
554-4868.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TTGCRGACGAACTAGCRGATATTGAAATGGGCAATGTGGTAAGCTCAATC[G/T]GAGGCGGGGCTGTTYCTGGGGTTGGYGGTGCCTCGGAGGCACTAGCKTCT
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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