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:

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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