Busch Lab

ZMP

DHX32 (1 of 2)

Ensembl ID:
ENSDARG00000077461
Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 32 [Source:HGNC Symbol;Acc:16717]
Human Orthologue:
DHX32
Human Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 32 [Source:HGNC Symbol;Acc:16717]
Mouse Orthologue:
Dhx32
Mouse Description:
DEAH (Asp-Glu-Ala-His) box polypeptide 32 Gene [Source:MGI Symbol;Acc:MGI:2141813]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa9632 Nonsense Available for shipment Available now
sa35374 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9632
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
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112750 Nonsense 97 727 2 11
Genomic Location (Zv9):
Chromosome 12 (position 45884529)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 44779467
GRCz11 12 45157889
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTGCAGATCCCGCAGTGGTGTGCAGAGTTCTGTCTGTCTGCGCAGTA[T/A]CAGCACGGTGTGGTTGTGTGCAGTCAGATCCAGAGACGGCAGGCTGTAGA
Long Flanking Sequence:
TGTTATCTCTAATCTGATAATTAGTTTTAGTTTTTTCCTCTGTCAGTTGCTCGAGTGCTTTAGTTAAGATTGTGTAGATTCGATTTCTGTAGTAAGCAAGGTCTGACAAAATGTGTGTCTTTAATGCAAATCAAAATGCTCTGTGTAATGCATGAAATTGTAAAACTTCTTTAATTGTGTGTTTGTTGGTTTGTTTGTTTTTTGCATGTACAGCAGGGGTGTCCACACTCCTGGAGTGCCAGTGTCCTGGAGAGTTTAGCTCCAACCCTAATCAAACACACCTTAACCAGCTAATCAAGCTCTTACTAGATATACTAAAAAACTTCCTGGCAGGTGTGTTAAAGCTAGGACACCGGCCCTCCAGGACTGAGTTTGGACACCCCTTATGTTCAGTATAGTGCTGTTTGACCGGAATGCTTTAGCACAGGCAGTTATAATAACGCTGGTGTTTTTGTGCAGATCCCGCAGTGGTGTGCAGAGTTCTGTCTGTCTGCGCAGTA[T/A]CAGCACGGTGTGGTTGTGTGCAGTCAGATCCAGAGACGGCAGGCTGTAGATTTGGCTCTCCGGGTTGCAGACGAGATGGACGTAAACATCGGGCATGAGATTGGCTACAGTATCCCGCTGGAGACGTGCTGCTCCAACGACACTATCCTCAGGTGTGTGTGAAAACCTCACTCTGATGCTCACGGATATACCAAAGGCTTTCACATTGGTTGGTTTGCTCAGCTAAAGTATGTGGCAACTTCTCAAATTCTTGACATTTTTGAGGCCTTTTTGTTTTATGATCTGGCATTTTTAATATTTGTGACATTTCTACCAGTGTAGATTTGGAAAATAATGATGAGCGCATTACTGGATAATCTATGCCAGTATTTTCTAACGTAATAGTTTTTTTTTTTTTTAATCAAACCTTTGTTTTGTATAATGTATATTAAATTTAATCTCTCACCGGCCACTTTATTAGGTACACCTTACTAGTACCGGGTTGGACTCCCTATCTGCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35374
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112750 Nonsense 416 727 6 11
Genomic Location (Zv9):
Chromosome 12 (position 45892802)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 44787740
GRCz11 12 45165762
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTCGTATTCTGGAGTCTAACATCACGTCCACGGCGCTGTTTCTGAAG[C/T]GAATGGAGGCAGCCGGCGTCACACATTGCCACTTCATCAACAGACCCGGT
Long Flanking Sequence:
ATAGCTACATAATATTTGACTAGATATTTTTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAAGCTTAACTAGGTTAATTAGGTTAAACTTGGTTTGTTCTGTAGACAAATGGAAAAAAAAAACTGCTTAAGGGGCTAATTATATTGATCTTAAAATGGTTTTAAAATAATTAAAAACTGCATTTATTGTAGCCAAAATAAAACAAATAAGACTTTCTCCTGCAGAAAAAATATTATAGGAAATACTGTGAAAAATGTATTGCTCTGTTAAAAATAATTTGGGAAATATTTGATTTATATTTTATTATTATTTTTACTTGAACTGTAAATGCGTTGCTTGAGTTCCAGTCAGTGCTGAATCACTGTTGAATCTTGAATCACTGTTCATTTGAAGGAAAGTGCTTCTGTTTGTATCCCGAGGACGTTCAGCTTCCCGCTGAGATACATCCTCGTATTCTGGAGTCTAACATCACGTCCACGGCGCTGTTTCTGAAG[C/T]GAATGGAGGCAGCCGGCGTCACACATTGCCACTTCATCAACAGACCCGGTGCGTACACTATATAGAGGTGCATATTCAATGGCCATAACACTCACACACTAACACAGTGGTGTCAAACTCAGCTTCTGAAGGGCTGTATTTCTGCAAAGTTTATTTCCAACCCTGATTAAACACACCTGAGAATTTTCTCCAATTTAAATATACAATGTGAAACTTGTCTTTTTTTTTTTTTTAATAATTATTTTTTAGGGGTTTTGCCTTTCATTTGATAGGAGTGTAGAGAATTGACAGGAAAGCATGGGGAGCAGAGAGAGGGGAAGGATCGGCATAGGACCGCAAGGCGGAATTAAACTCAGGTCGCCGCAAGCACCGGAGTACATGTGTCAACTGTTACGAACCCCAGTTTTTTAAGGCTCGTCTAGGGAAGGGGTTAGCAACATAAAAGGACACAGAAACCAGAATTACAATTCTCTATTTATTTAGAGACCAGAAGATACGTG
Associated Phenotype:
Not determined