Busch Lab

ZMP

ENSDARG00000043008

Ensembl ID:
ENSDARG00000043008
Human Orthologue:
KIAA0802
Human Description:
KIAA0802 [Source:HGNC Symbol;Acc:29121]
Mouse Orthologue:
1110012J17Rik
Mouse Description:
RIKEN cDNA 1110012J17 gene Gene [Source:MGI Symbol;Acc:MGI:1915867]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa15132 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa15132
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063146 Nonsense 16 592 1 3
Genomic Location (Zv9):
Chromosome 2 (position 55151769)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 54809829
GRCz11 2 54534476
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACATGAATGCTATACAAATATACTCTATTTGTTATTGTCCCCCTGATTA[T/A]CATGAAGCAGTTCTGTTCACTTTTNNNNNNNNNNNGCTGTTTCAGGCRCT
Long Flanking Sequence:
TAAAAATAAAAACCCTGATAAATCACATGTACATCAGTATTCACAGCTTTTGCCGTGAAGCTCTAAATTGAGCTCAGGTACACTCTGTTTCCACTGATCATTCTTGAGATGTTTCAGCAGCTTCATTGGAGTTCACCTGTGGTCAATTCATTGTATGAAGAATTTTGAGAAAATAAATTAATTTAATCCATTTTGGAATAAGGCTGTAGCATAAAAAAATGTGGAAAAAGTGAAGCGCTCTAAATTATTTCTGGATGCACTGTAAGTATATTCGACTTGTAGTCAATGGGTTTACTTGCTTTTTTTAGGTTAAGTAACAAATTGCTTTTTAAATTGTACGTAAACATGAGAAAGAAAGTTTTGAGTTTTTAAATCAAACAATTTTATTCTAAATATTAAGAACTTTCCTTGATATCCACCTTTTTAAACCCCTACTGACTGACTGCATTATACATGAATGCTATACAAATATACTCTATTTGTTATTGTCCCCCTGATTA[T/A]CATGAAGCAGTTCTGTTCACTTTTATTACTGTGTTGCTGTTTCAGGCACTGAATGAGATTTCTGAGATTGCGGATCCTGCCATTTACCCTGAAGAAGAGAAAAGTAGTGGCAGCTTACTCAGGTAGAGTATTAGCTTGAGTAGAATTGAGCCTTAGACGTTCTCAGAAGAAATGAAAACCTTGACACAACCTGAACAGGAATGTGACTTTATAATGTAAAATATCTCTATTTAATTTTAAGTAGCATTTTTGGATTAGTGTTTGCTCGTGGCCAAGGTGAGATACAGTACATGCCTATGATCTTCTTGTCTTTAGAAGTAGCTTGGGTTCTTTGCTAAAAAAAATGTCTTGCTTTTATCTGCTGCTAAACTCCCTTGAGTCCAGGTTATTGATCTAATGTCCATTTATCGTTGTCCTTTACAAAGATCTGGTCAGCATTGTTTCAGTTACTGCAAATAAGCTTCGGTGTCTTTCCTGACTGCCCCACCTTGAACCTTAAT
Associated Phenotype:
Not determined