Busch Lab

ZMP

ENSDARG00000069964

Ensembl ID:
ENSDARG00000069964
Human Orthologue:
HARBI1
Human Description:
harbinger transposase derived 1 [Source:HGNC Symbol;Acc:26522]
Mouse Orthologue:
Harbi1
Mouse Description:
harbinger transposase derived 1 Gene [Source:MGI Symbol;Acc:MGI:2443194]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa11016 Nonsense Available for shipment Available now
sa18697 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa11016
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113431 Nonsense 137 346 3 4
ENSDART00000113431 Nonsense 137 346 3 4
Genomic Location (Zv9):
Chromosome 1 (position 27422562)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 27668649
GRCz11 1 28362363
KASP Assay ID:
2259-0650.1 (used for ordering genotyping assays)
KASP Sequence:
GATGGAAAACWCATCCGTATACAGCCTCCTGCAAAAAGTGGCAGCCTCTA[C/A]CATAATTACAAATCCAGCTTCTCTGTGATAATGATGGCTGTTGTGGATGC
Long Flanking Sequence:
CCTATAATCATTCCGCATGTATCCGCAGTTTATTTTTATTTTTTTATTTTTTACACAATTCTCCACAGGAATAACAAAAAATGTCAGCTGATTCTGTCTGGCCTATTACTCATAACTACAGTTATTTTACTTTGTAAAGGATCTTAATGCGTCTAGTATACAAAACAAGAGCATGCTATAAAAATAAGCAATATAGCTAGATCCTCTCACATTATTTGTCTTTTGAAAGCTCACTGTTTTTTGTATTTAAATGTATTAATTTCTGTAGTCAGTTAAGCCTTAAATAAGGAGTTCATATTTAGAGTGTTTTATTTTTACCCTGCGTGTAAAAATAAAATTGTTCTGTTCTAACTGTTCTTTTGCTAGACACCATCAACAGAAGCAGAATGGAGGGAAATAGCCCATGAGTTTCAATCTAAATGGCAATTCCCACATTGCCTAGGTGCACTTGATGGAAAACACATCCGTATACAGCCTCCTGCAAAAAGTGGCAGCCTCTA[C/A]CATAATTACAAATCCAGCTTCTCTGTGATAATGATGGCTGTTGTGGATGCCAATTACAAGTTCATATATGCCAGTGTGGGTACCCAAGGTAGAGTTTCTGATGCTGGACTATTCGCTCAGTCAGACTTGCGCCAAGCAATGGATCAGGGCCAGCTGAACTTTCCTCCACCCGAACCATTGCCCAGCAGTGACATAATAATGCCATACATGTTTGTGGGTGATGAGGCATATCCTTTAAGGCCTGATCTTATGAAGCCGTATCCTTACAGACAAATGGACCACAGTCAACGAATCCTGAACTATCGCCTGTCAAGAGCACGACGAGTGGTAGAAAATGCATTCGGCATTCTTGCCAACAGGCTACGAGTTTTTAGGAGCACCATATGCTTGGAGCCAGACAAGGTAGTTAAAATAACTATGGCCTCCCTATGCATCCATAACTTCCTCCGTGAGCGGAGATCTGAGGCCTACACACCTCCAGCCTTTGCAGACTGGGAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18697
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113431 Nonsense 137 346 3 4
ENSDART00000113431 Nonsense 137 346 3 4
Genomic Location (Zv9):
Chromosome 1 (position 27422562)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 27668649
GRCz11 1 28362363
KASP Assay ID:
2259-0650.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGAAAACACATCCGTATACAGCCTCCTGCAAAAAGTGGCAGCCTCTA[C/A]CATAATTACAAATCCAGCTTCTCTGTGATAATGATGGCTGTTGTGGATGC
Long Flanking Sequence:
CCTATAATCATTCCGCATGTATCCGCAGTTTATTTTTATTTTTTTATTTTTTACACAATTCTCCACAGGAATAACAAAAAATGTCAGCTGATTCTGTCTGGCCTATTACTCATAACTACAGTTATTTTACTTTGTAAAGGATCTTAATGCGTCTAGTATACAAAACAAGAGCATGCTATAAAAATAAGCAATATAGCTAGATCCTCTCACATTATTTGTCTTTTGAAAGCTCACTGTTTTTTGTATTTAAATGTATTAATTTCTGTAGTCAGTTAAGCCTTAAATAAGGAGTTCATATTTAGAGTGTTTTATTTTTACCCTGCGTGTAAAAATAAAATTGTTCTGTTCTAACTGTTCTTTTGCTAGACACCATCAACAGAAGCAGAATGGAGGGAAATAGCCCATGAGTTTCAATCTAAATGGCAATTCCCACATTGCCTAGGTGCACTTGATGGAAAACACATCCGTATACAGCCTCCTGCAAAAAGTGGCAGCCTCTA[C/A]CATAATTACAAATCCAGCTTCTCTGTGATAATGATGGCTGTTGTGGATGCCAATTACAAGTTCATATATGCCAGTGTGGGTACCCAAGGTAGAGTTTCTGATGCTGGACTATTCGCTCAGTCAGACTTGCGCCAAGCAATGGATCAGGGCCAGCTGAACTTTCCTCCACCCGAACCATTGCCCAGCAGTGACATAATAATGCCATACATGTTTGTGGGTGATGAGGCATATCCTTTAAGGCCTGATCTTATGAAGCCGTATCCTTACAGACAAATGGACCACAGTCAACGAATCCTGAACTATCGCCTGTCAAGAGCACGACGAGTGGTAGAAAATGCATTCGGCATTCTTGCCAACAGGCTACGAGTTTTTAGGAGCACCATATGCTTGGAGCCAGACAAGGTAGTTAAAATAACTATGGCCTCCCTATGCATCCATAACTTCCTCCGTGAGCGGAGATCTGAGGCCTACACACCTCCAGCCTTTGCAGACTGGGAGAA
Associated Phenotype:
Not determined