Busch Lab

ZMP

KIAA0146

Ensembl ID:
ENSDARG00000086681
Description:
KIAA0146 [Source:HGNC Symbol;Acc:28971]
Human Orthologue:
KIAA0146
Human Description:
KIAA0146 [Source:HGNC Symbol;Acc:28971]
Mouse Orthologue:
2310008H04Rik
Mouse Description:
RIKEN cDNA 2310008H04 gene Gene [Source:MGI Symbol;Acc:MGI:1924834]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa37938 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa37937 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa37938
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130705 Essential Splice Site 162 539 5 11
ENSDART00000130705 Essential Splice Site 162 539 5 11
Genomic Location (Zv9):
Chromosome 24 (position 37164500)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 35781760
GRCz11 24 35669857
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAATTCAGCTTCCAAAGAGCACAGTGACTTCCTAAATCCTGCTGTGG[T/A]AAGTGTGTTTTAAAGTTTAATATCGGCCGAAGCATCTCATAAGTGTAAAG
Long Flanking Sequence:
ACATGTGTGTATATATATGTGTGTGTATATATGTGTGTGTATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATGTATATATATATATATATATATATATATATATATTCGTGTGTGTGTATATATGTATATACATATATATATATATATTATATTTATTATTATTTATACATAATACAGTATATATATATATATATATATATATATATATATATATATATATATATATATACTGTATTATGTATAATTATCAAAAACAATAATCCCGATAATACATGATATTACCTGCTGCTTGCCCTCAGACACAGATGAACTGCCCACTATTGATTCAGACAGTGAAATAGAGGAGGAGAATTCAGCTTCCAAAGAGCACAGTGACTTCCTAAATCCTGCTGTGG[T/A]AAGTGTGTTTTAAAGTTTAATATCGGCCGAAGCATCTCATAAGTGTAAAGTAATTTTGGCTTAAATTTTAGCAATTTTAGAGAAATAAAACATATGTTTTAACAATATTAAAATGCAAGACTCTTGTAAAGAGAAGGTTTTGTGTGTGGTTGTTCAGTAGGTGGCGCTGTGAGCCCTCAAGTAGCAGCTTTTTAGGTGTTCATCAGGGTTCTCAATGTTCCTGCTCCTTTTAGGACTGCCCTTTGGCCTGAATGTTTTATTTGTAACCTTTTCTTGACTTTAGTTTATTAATATTTGACATTTTGATGAGTACAGGTGTCACTCATGGCATCTGAATATAAAATCAAACGAGTCTCAGAGGGACATCCCAATCAAACGCAATATTAAGTGAAGACTTTAGTGTTAAGTTCAGTAGTAGCAATGTCAAATCTACTGTTCTGCAAATACTCTTGTATGCGTCTCATAATGGTATATTGTAGATACTGCATATTATCTAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37937
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130705 Essential Splice Site 162 539 5 11
ENSDART00000130705 Essential Splice Site 162 539 5 11
Genomic Location (Zv9):
Chromosome 24 (position 37164500)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 35781760
GRCz11 24 35669857
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAATTCAGCTTCCAAAGAGCACAGTGACTTCCTAAATCCTGCTGTGG[T/A]AAGTGTGTTTTAAAGTTTAATATCGGCCGAAGCATCTCATAAGTGTAAAG
Long Flanking Sequence:
ACATGTGTGTATATATATGTGTGTGTATATATGTGTGTGTATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATGTATATATATATATATATATATATATATATATATTCGTGTGTGTGTATATATGTATATACATATATATATATATATTATATTTATTATTATTTATACATAATACAGTATATATATATATATATATATATATATATATATATATATATATATATATATACTGTATTATGTATAATTATCAAAAACAATAATCCCGATAATACATGATATTACCTGCTGCTTGCCCTCAGACACAGATGAACTGCCCACTATTGATTCAGACAGTGAAATAGAGGAGGAGAATTCAGCTTCCAAAGAGCACAGTGACTTCCTAAATCCTGCTGTGG[T/G]AAGTGTGTTTTAAAGTTTAATATCGGCCGAAGCATCTCATAAGTGTAAAGTAATTTTGGCTTAAATTTTAGCAATTTTAGAGAAATAAAACATATGTTTTAACAATATTAAAATGCAAGACTCTTGTAAAGAGAAGGTTTTGTGTGTGGTTGTTCAGTAGGTGGCGCTGTGAGCCCTCAAGTAGCAGCTTTTTAGGTGTTCATCAGGGTTCTCAATGTTCCTGCTCCTTTTAGGACTGCCCTTTGGCCTGAATGTTTTATTTGTAACCTTTTCTTGACTTTAGTTTATTAATATTTGACATTTTGATGAGTACAGGTGTCACTCATGGCATCTGAATATAAAATCAAACGAGTCTCAGAGGGACATCCCAATCAAACGCAATATTAAGTGAAGACTTTAGTGTTAAGTTCAGTAGTAGCAATGTCAAATCTACTGTTCTGCAAATACTCTTGTATGCGTCTCATAATGGTATATTGTAGATACTGCATATTATCTAAAAA
Associated Phenotype:
Not determined