ZMP

hesx1

Ensembl ID:

ENSDARG00000054509

ZFIN ID:

ZDB-GENE-990415-130

Description:

hesx homeobox 1 [Source:RefSeq peptide;Acc:NP_571424]

Human Orthologue:

HESX1

Human Description:

HESX homeobox 1 [Source:HGNC Symbol;Acc:4877]

Mouse Orthologue:

Hesx1

Mouse Description:

homeobox gene expressed in ES cells Gene [Source:MGI Symbol;Acc:MGI:96071]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35157	Nonsense	Mutation detected in F1 DNA	Not yet available
sa14173	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa35157

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076711	Nonsense	34	72	1	2

Genomic Location (Zv9):

Chromosome 11 (position 43713993)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	42344129
GRCz11	11	42633475

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTATTGATATACGTGAAGAACTTGCGAAGAAGCTTCATTTAGATGAGGAC[A/T]GAATCCAGGTGAACACTGATTTAAAATCTCAAATATTGCATCATTTACTG

Long Flanking Sequence:

TCAAGCAAGGAATAAACTTAGATACTTTTACAAACTTTATATAATTTATATATACATTACAAAAGAATAAACATGAATTAATTCTTGCTAAACATTTGGTTCTGTTTTATTCTTTGTATATGTATATTTTTATATATATATTTTTAAATAGTGGATACTTTAATATTTTCTTCACCTTAAAATATATTTTGAAATATGTTTTGGATTAAATGAAATGTATCTTCAATTAAAAAAAAAATAAATTAAGTTTAAGTGAACATCACAGATACAACATGTATTTAGCATGTATTTCAAATATATTTTGGCCAGGAAAAAAATATATTTTTACCATATGCAAATGCTTAAGACAAAATGTGTTTTTAAATGTACTTTTACTCATTATTATTTTTTTTGTCGTTTACCTCCAGATCAAGATATTAGAGAGTGTTTTCCAAGTGAACTCATACCCAGGTATTGATATACGTGAAGAACTTGCGAAGAAGCTTCATTTAGATGAGGAC[A/T]GAATCCAGGTGAACACTGATTTAAAATCTCAAATATTGCATCATTTACTGTAAACATATCATTTTGTCTGATTTTTTATGTCTGATTTATTATTATATATTTTAATCCAATATTAATGTGTAAAAATTCTAAGTAAAATAATGTAAAAAGTCCAATTTTGCACAAAAGTCTTATATTTTGTGGACAAGAATATATTTTAGCAGTACTGTAGCTATAGCCAAAAATAGACAGATTTTTCTTTTATGGCAAAATTATTAGAAATATAAGATAATATGACGTCCCATGAAGATGTTTAGTTCATTTTCTACTGTAAATATATCAAAACGTAATTTTTCATTAGTAATATTAATTGAAGAACTCAACTTGTTCAACTTTAAAGGTGATTTTCTCAATGTTTACATTTTAGGATTCCAGACAAAATATTGATCCAACCAATTTCTGTTTAACAGAGAGCAGATTTTTTTCAGCACATTTCTAATCATAATATTTTTAATAACTCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa14173

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076711	Nonsense	69	72	2	2

Genomic Location (Zv9):

Chromosome 11 (position 43715021)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	42345157
GRCz11	11	42634503

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGTCCCAGTTCCTCATGGTGAAAAACGTCCTCAGCGATTTACAAACCGGC[A/T]GAGAAGAACACTGAGAGTAGAACTACATTTCTNNNNNNNNNNNNNNNTTM

Long Flanking Sequence:

TGCCATGATGACAGTAAATAATATTTGACTACATATTCTTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGGTTAACTAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAATGATGGTTTGTTCTGTAGACTATTGAAAAGAAATATAGCTTAATGGGGCTAATAATATTGACCTTAAAATGGTGTTTAAAAAATTTAAAACTGCTTTTATTCAACAAAAAAAGACTTTCTCTAGAAGAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGGTAAACATCATTTGGAAAATATTTAGAAAAGAAAAAAAAAATCAAAGGGGGCTAATAATTCTGACTTTAACTGTGTGTTTTATATTTTTTCTTTAGATTTGGTTCCAGAACAGAAGAGCAAAGCTGAAGCGTTCGCACAGAGAGTCCCAGTTCCTCATGGTGAAAAACGTCCTCAGCGATTTACAAACCGGC[A/T]GAGAAGAACACTGAGAGTAGAACTACATTTCTTTATTATTATTATTATTATTATTATTATTATTATTATCATCATTATTATTTCTCTGTTACCAAATTGTAATTTATTAAATGTCTTTATTAGTTATGTCTTTTTATGATTTAAATGATAAAAATACCTATTGTTATTTTTTATTGTGTGTGTTTGGTCAAAATATAAATAAATAATTCTAAAACTTATTCTAACGTTTTAAGTGAAATCTTTAAACTTTCCCTGGGTCTGAATGAAGGAAAGTTAACATTATTTTCTGCCAGCTGTTAAGCAAACACATCACCCCCACCTACAAATTAATTAGCGCCTTGTAACGAGTGCTCAGTAAGCCTATTAGGTATTGATTGGGTCACAAAGGGGCTGCACTGAGGGGGGCTTTCATACAGGACAGCATTTGCATTTGAGTCACTTGTTGGATTCCAGCAACATTTGCAGGTTTTTTTTTACATGTTATTTTTCTGACATACTAT

Associated Phenotype:

Not determined