ZMP

dhx32

Ensembl ID:

ENSDARG00000079029

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 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18186	Nonsense	Available for shipment	Available now
sa17670	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa18186

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109015	Nonsense	308	732	4	11

Genomic Location (Zv9):

Chromosome 17 (position 32553414)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	32395145
GRCz11	17	32347656

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATCTCGCTCTGTCTCATGGAGAGCTGGTGCCCGTGTCTCTGTGCCCAAGG[C/T]AAGGTGACAGTCTCTCACYGACTGAGGAGAGCAAAAGCAGGAGAGYCTTC

Long Flanking Sequence:

CATTTTTGAATATATATTTAATATATTAATAATAATATATTTAATCAGTATAGTTTATGAATATATTTTAAAAATCTATAATATAATATAATAAATTTAAAACCTTATAGAAGTTAATGCTTTCTTTTTGTTTTATATTTTTAAATGGAGATTTATTATAAAAATTACAAAAATTATACATTTTAGAATTAAAATGGTAAATTACAAATTATAATATGTATGAATTAAATAATTGATAATATTTGATATAAAATAATATAAAAAAATTATATAATTAATTATTTATAAATAATATAAATAATTAAATAATTATAAAAATTCTTAAATCTAGTATACTGTAGAATAACAAAAATAAATAAATAAATTCTATGGTAATTAAAACTTTTGTTTCCCGTTTTATTTTCAAGGAGATTGAATGTGCCCATGCCATTTTGCGGAGAGAGGGTGCCAATCTCGCTCTGTCTCATGGAGAGCTGGTGCCCGTGTCTCTGTGCCCAAGG[C/T]AAGGTGACAGTCTCTCACTGACTGAGGAGAGCAAAAGCAGGAGAGTCTTCCTCACCTGCAGCCCCAGCGAAGATCTCTTCTGGGCCCTTCACACCATTCGCTTTGTGATTGATGCTGGAGTGCAGAAAAGATATGTACGTAGCAATTTCGTTTTTATTGTGACTTTTACAGGCTAGTCTTTCCTTTAATTGTGTTAAGTACTCTTGAGTGAAGGTCAAAATGTAGTATATGTAGTAATTATACCAAAAATACGTTGAAAGTGCTATACTTCATATAGTTCAGTACTACTTGAAATTAAATTGGCCGCTAAGTTTATAATCAGCTCCTTTTTTCTTATTTTGAATGGTGGCCATAAAACAGTGATGTTTCATTGTGACAGGTGTACAATCCCCGAATCAGAGCCAACTCAATTGTAATTCGACCAATCAGCAAGAGCCAAGCTGAGAGCCGCAAACAACTCGCAGGCCCAACAGGTAAGCACCTCTTTCTACATTTCTAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17670

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109015	Essential Splice Site	499	732	7	11

Genomic Location (Zv9):

Chromosome 17 (position 32559001)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	32400732
GRCz11	17	32353243

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GAATTTGACTGTGTGTGTGAAGTGCTGACCATCGCTGCSATGCTAACAGG[T/A]AATCCTGTCTCAGTACAATCCACTCGACAGGTGTGTCACCATGTGTCTCA

Long Flanking Sequence:

AAGCTTTGGAGACATAAAATAAATTTTGCTTTTAAATAATAATTTGCGAATGTTTGTTGGAACGATGGATTTGGGAAATGCTGAATCAATGATTTAAGTTTGTAATGACAGAACTTGCAACCTTAGTTGGCTATTGATGGTTTTCAGAAACTCACCCTGGTTAACAATAAACAATGACAACATTTGTTTTTTATCACTCAATAAACAATCAATTATTTGCAACATTTTACTTAATAAATAGCACAATTAGAAAAAAAGTATTGTTTTAAAAATAAGTGAAACATTTGTGTGTGTTCCTCCACTGTAGATCCCGAAGGCCTCATGCAAGCTTTAGAGGAACTGGACTATCTCGCCGCACTGGATGATGACGGAAATCTGTCCGAGATTGGAATTATCATGTCAGAGTTTCCTCTGGAGCCACAGATGGCTAAGACTTTGCTTGCGTCCTGTGAATTTGACTGTGTGTGTGAAGTGCTGACCATCGCTGCCATGCTAACAGG[T/A]AATCCTGTCTCAGTACAATCCACTCGACAGGTGTGTCACCATGTGTCTCACTTCCACTATGTCTTTGCTCCGTCCAGTTATATCTGGAAATCATGTCAGGTCACTATTATTGCACCAAGTGTATGTACCATTCAAGCGTATGTACAGTACCAATAAAAATATTTACAATAGAAAATTAATTACACGCACACACATAAAGTTGAATTCAGAATTATTAACCCTCCTTTGATTTTCTTTTTTAAATATTTCTCAAATGATGTTGAACAGAGCAAGGAAATGATAATATATTTTCTTCTGGAGAAAGTCTTATTAGTTTTTATTTCAGCTAGAATAAAAGCAGTTTTGAATTTTTTTTAAATTATTTTATGGTCAAAATTATTAGCCCCTTCAAGCCATTTTTTTTTCGATAGTCTACAGAACAAACCATCGTCATACAATAACTTGCCTAATTACCCTAACCTGCCTTGTCAACCTAATTAACCTAGTTAAGCCTTTAAATG

Associated Phenotype:

Not determined