ZMP

DMXL2 (1 of 3)

Ensembl ID:

ENSDARG00000091293

Description:

Dmx-like 2 [Source:HGNC Symbol;Acc:2938]

Human Orthologue:

DMXL2

Human Description:

Dmx-like 2 [Source:HGNC Symbol;Acc:2938]

Mouse Orthologue:

Dmxl2

Mouse Description:

Dmx-like 2 Gene [Source:MGI Symbol;Acc:MGI:2444630]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23359	Essential Splice Site	Available for shipment	Available now
sa23358	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa23359

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

Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000129387	Essential Splice Site	293	551	8	14

Genomic Location (Zv9):

Chromosome 18 (position 38121606)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	39703309
GRCz11	18	39684317

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACCTGAACAATGTGAAGAGGATGACGTCCCATCCTATCTATCAGTACTG[T/A]GAGTATTTCTTAGCAGGGACTTTGTAGTTGCCTTTTTATGGGATTAGATT

Long Flanking Sequence:

CCTATAGTTGTGTGGGCAACATTTGTATATTTACAGTATAACCACCTTAAAAAATGGGTGTCGCGTCTCGCGGGCTGTAAAGTTTGAAAAATGACTGCTTTAGATGATCGAAAAAAATATATAGCTTAAATGGAGCTAATAATTTTGACCTTAAAATGTTTTTTTTTCTTTTTTTTAATTAAAATTGCTTTTATTGAAGCCGAAATAAAACCAATAAGACTTTCTCCAGAAGAAAAAAAATATTATAAGACATTCTGTGAAAATTTCCTGACTCTGTTAAGCATCATTTGGGAAATATTTAAAAAAAAGAAAAAAAATTCAAAGGGGGGCGAATAATTCTGACTAAATGTTTGTCAAATCTGAAGAAACCGTTTGAATATCAGTGTTTTATGGGGGGTCGTGAAAATGATCTTTGTTAAACTGTGTCATTTCTCGCAGATCATGAAGAGGAACCTGAACAATGTGAAGAGGATGACGTCCCATCCTATCTATCAGTACTG[T/A]GAGTATTTCTTAGCAGGGACTTTGTAGTTGCCTTTTTATGGGATTAGATTTGTGCCAAATGAATCGAACAAAACCTGTCAAAATGCACACAAATAAATAAAACAAACAACATTTTTGTAAAACAAACAAAAATAAACAACAAACACAAATTAACAATCTCACTAACAAACTTACACTTAAGAGCTGGGGTGAAGTGTTCTTCAGGCTCAGTAGCTTCAGAAAGTGGCTGTTTCTCAATTCCAAGAATGCAGAGAACAGAGCTGCGTTCTTGTGAAGACCGGTCTTGACAGGTGTCCGCGTAGAAACGAACTGAGGAAACCACGAGAACAGAGAACGCGTCCTTTCCTTTTTGATGGAAAACTATTTAAACATTACAGCATTCATACAACGATTTACTGTTTTTCCCCCTTTTCAAAATATAAACTCTAAATAAAAATATTACAAATATACGTTGCACAATATAAATAAAACAGATTTTAATATGAATTTCAGCAAACAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23358

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

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000129387	Nonsense	387	551	11	14

Genomic Location (Zv9):

Chromosome 18 (position 38114137)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	39695840
GRCz11	18	39676848

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGTGATTTTGCCTTCATCACGTCCTCTAGTCTGATCGCCACAGCGGGA[C/T]AGTCCAACGATGGCAGGTCAGTTGAATGCTTTATCTTGTCATCACATAGA

Long Flanking Sequence:

GGCACATATCCACATATCGCCCCGCGGAGGTCGGAAGCAGTATTACTACATGTCAACATACTAATTTTACCATGCCAAACAATACACCATGCAAAAAAAAAATAATAATAAAATAAATAATTCGGAAAATGATAACAGTAACATTATCTAACTGTTACAATATAATAGTATAATAATTATAATACTACAGTATTTATGTTATAGTATAATATAATATATCATAATATATAATATAATATAATACAATATAATATAATATAATATCATATAATATCATATAATATAGTCCAATAGTAATCGCTGTGAATTGTTACTTATTGTTATCATTGAAATCAAAAAAATACAATTAGAATTGAATTACAGGTTTCTCTAATTCAGTGCTACTGTATGATATCAAAATACGCTTGTGTGTGTGTTTGTCTCAGAGCTGGCAGTGTCACAGTAAAAGCTGTGGTGATTTTGCCTTCATCACGTCCTCTAGTCTGATCGCCACAGCGGGA[C/T]AGTCCAACGATGGCAGGTCAGTTGAATGCTTTATCTTGTCATCACATAGAAACAAACTGTTCATAGTGTTTTTAAAGAAGTGTTTCTCTTTGTTCCACAGAAATGTCTGTTTATGGGACACACTGATCGCTCCTAGTAACTCCATGATACACTGTGAGTTCACAGACAGAGCAAGATATTGAAAAGAAAATAGCGAAACAATTGATTAACATAGACTATTATAATATTTCTGTTCTTTATACATGATGTGTGTGCGTTTGTGTGTGGTGGATGTGTATAGGCCTATATCAGCCCTCCTGTGGATTTTTTATTTTCAAATATTTCCAAATGATTAGTAACAGAGCAAGGAATTTTACACAGTATTTCCTATAATATTTTATCTTATTTGTTTTATTTCGGCTAGAATAAAAGCAGTGTTAATTTTTTTAAAGCCATTTTATGGTCAAGATTATTAGCCCTTTTAAGCATTTTTTTCCAATGGTCTTCAGAACAAACCATCA

Associated Phenotype:

Not determined