ZMP

HDX

Ensembl ID:

ENSDARG00000079382

Description:

highly divergent homeobox [Source:HGNC Symbol;Acc:26411]

Human Orthologue:

HDX

Human Description:

highly divergent homeobox [Source:HGNC Symbol;Acc:26411]

Mouse Orthologue:

Hdx

Mouse Description:

highly divergent homeobox Gene [Source:MGI Symbol;Acc:MGI:2685226]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa17613	Nonsense	Available for shipment	Available now
sa35629	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa17613

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111681	Nonsense	326	649	4	13

Genomic Location (Zv9):

Chromosome 14 (position 6223768)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	5910765
GRCz11	14	6217599

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GAAGGGATGCAAAACCAGCAGCTTCTTGCWGAACAGATCAKCGTCCCCTA[T/A]YAGCTTACCATTAAAACTGATCTCCCAGGCATCGTCCAGAATTCCCTGTC

Long Flanking Sequence:

AGACTCTGCAGTAATCGCTCCCAGTTGGGCCAAGCCATGCAGAACATCTCAACCTCCATCATGGAATCTTACCTCCCCCCTAAAAACGTCTGTGGCTCATCGGGGTCCTGTAGACAGCGGTGCTCAGGTTCAGCAAGCTTTGACCGTGGCTGGATTAGGAGAGCGACCTCCCACAGGAAACGCTCCAGAAACCGTGGTGAGAAAATCGAGGCCGGTCGATGCATCGGAGATCTTCTCGATTGCCATGGAAACGGCAGACGCTGATGACGAATATTCCAGAGAAGAGGAGCTGGCGAACATGGCGGTGCAGATGCAGTGCAGTAAAGGATCTGTGGATGGTGGGCGGAGATCCAGCGCAGGTTCCTCTGCCTTGGTTGACAGCCCAGGACTATCAGAAAAGAGCCAGTCAGCCTGTGCGCTCAACCTCTCAAACTCTGCTCTTTTTGGAGAGAAGGGATGCAAAACCAGCAGCTTCTTGCTGAACAGATCATCGTCCCCTA[T/A]CAGCTTACCATTAAAACTGATCTCCCAGGCATCGTCCAGAATTCCCTGTCTCAAGGTATGCAATGTTTAGTTTATGATATATAGTGGTCCCTTATTAATCGTGGGAGTTACGTTCTAAAAATAACCTGCAGTAGGTGAAATCTGTAAAGTAGTCAGCTATATTTTTTACCATTTTAATAGATGTTTTAAGGCTGTAAAACCCCTCACTACACACTTTTCTCAGACAGGCATTAACATTTTCACACTTTTCTCTCTTGTTTAAGCACTCTCAAAGTCCAAACTTTTGTAGAAAAATAAGTCACGTATTATAGAATGAAACCAAAGCTCAAAACCTGTTGTCAGGCGCAAATATTCATCGCTGTCAGCAAAAAGTTCATAAAGCTTTTAGGCCTTTTTGTGGATAATGTTGGCATCCAGCGTAATGTTGTTTTTCCTGCAGTCACTGATCTACAAAGCAAAAGCAGACTCCATCTTTAAGTGGTTCGCACAACCAATATGTC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35629

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111681	Essential Splice Site	508	649	9	13

Genomic Location (Zv9):

Chromosome 14 (position 6219987)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	5906984
GRCz11	14	6213818

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATGACGCAATGTCACTTTGTTTGTCTGACGGTGGGAGGGATTTTCAAGC[T/A]GTTGACTAATCAGATTACATTCTTTTTTATAATAAATAATAATAATAGTT

Long Flanking Sequence:

ATGAATAAGTTGGGGGTTCATTCCACTGTGGCGACCCCTGATTAATAAAGGGACTAAGCTGAAAAGAAAATAAATGAATAAATCTTGTCCTTAGATATCTTATTTGCAGAAATATGTATCTTTATTCATTTATTTTCATTCAGCTAAGTCTCTGATTAGCTGCTGTTGCCACAGCACAGCACATATTACATGGTTTCTCAATAATGAGACATATTTTTTACTTAATTTGGTTTATAAATGCTTAATTTTATGTAGTTTTAAGACCTTTCTAAAATCTCTATTTGACAGACGTGGATTGGTAACCGCAGACGGAAGTACCGTCTCATGGGCATTGAAATTCCACCACCTAAAGGAGGACCAATCATGTTCTCAAATCAGCCAGCGCCGCATTCACCTCACATCCCTGAAGATGACTTTCAGACTGCAGATCTAGGAGAGGCCAGCGAACACAATGACGCAATGTCACTTTGTTTGTCTGACGGTGGGAGGGATTTTCAAGC[T/A]GTTGACTAATCAGATTACATTCTTTTTTATAATAAATAATAATAATAGTTTCCTTTTTAAGATGCCAGTGATTTATATCTGAAAGAAAATGACGTTAATGATGAATCGGATGGTTCCACCCCTGCTAAACATGTGGTATGAGCGCATTAACAATTTGCTTCATTGAATGGTTTAATGATAACTCAAATTTAAAGTCACTCAAACATGAAACTTTATTCTAGAAAATTGAAATCGTCGAAGATGAAGATGATGACGACGGTGACATGTTGACCACAGAGATGGAACACATGCAAAACCTCCTAGAGTTCAAGGTAAGCTGAGCTGATTGAAACAGAGGTCAGTTTTTTTGTAAGTCTCTTTAAGGCAAGTCATTTCACTTGGCAGCCATCTTTAAAATGCTTCTTTGGCAGTATGCTCGGGCATTCTGTCTGAAAGGGAAAACATCAAATTCTTCAAAACTGTTTTTCAAGCTTACAATTAAATTACATATTTGGAAGCAC

Associated Phenotype:

Not determined