ZMP

ash1l

Ensembl ID:

ENSDARG00000070981

ZFIN ID:

ZDB-GENE-030131-6101

Description:

Novel protein similar to vertebrate ash1 (Absent, small, or homeotic)-like (Drosophila) (ASH1L) [Sou

Human Orthologue:

ASH1L

Human Description:

ash1 (absent, small, or homeotic)-like (Drosophila) [Source:HGNC Symbol;Acc:19088]

Mouse Orthologue:

Ash1l

Mouse Description:

ash1 (absent, small, or homeotic)-like (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2183158]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18097	Nonsense	Available for shipment	Available now
sa43225	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa43226	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18097

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000052915	Nonsense	1526	2962	2	25
ENSDART00000127755	Nonsense	1502	2938	2	25

Genomic Location (Zv9):

Chromosome 19 (position 9670828)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	9129367
GRCz11	19	9048292

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGAACGGTACAAGCGAAAAGAGGCCTCTATGTCTTGTCTTGGGCCCTCA[C/T]GACTGTCTWTGGGCACTGCAAGTCGGGGACATCATCCTGTTGACTCCTGG

Long Flanking Sequence:

CCCACCATGTTCATTCACCATCTTTTCCTCCACCTCCACCCCCTTCTTATGTGCATCATCATCACCCATCCCACCTGCTTCTTAACCCCTCCAAATTTCACAAGAAGAAACATAAGCTACTTAGGCAAGAGTATTTAGGTGGTGGTCGTTCATCCATGCTCTATCCTGCCATGTCATCTGAGCTGTCATTTGGCTGGCACCACAAACACAAGCATAGGCACAAACACCGTGATCGCTGTGGAGAAGAGGAGGGTGATGATGGTGGTGGAGTTTTAGGTGGTATAGGAGGCAGAGGTGTTGGAGGTGAGGGCTTGGGGGCCGGAAGAGGGGAGAGAGGGAGCGTAGAGTCCCTGCAGCACTGCCGGTTTGGACGAGATGGCTCTGCTGACTCCCGAACTAACAAACAGTCAGCTTCTGCCAACTCCCCTTCCTCTTCCTCCACATCCTCTGCAGAACGGTACAAGCGAAAAGAGGCCTCTATGTCTTGTCTTGGGCCCTCA[C/T]GACTGTCTTTGGGCACTGCAAGTCGGGGACATCATCCTGTTGACTCCTGGTTCAGAATGGGAAGTTCTGATACTGATTACTCCAAGCTCTCTAGAAACCAGTCTTTTTCGGGGTCTGGTGCATTCTCTGAAGGACATGTGCAAAATCCAGTGGATTGCTCAGAGAGTGATGAGGAAGATGCTGCTTCCCCCATTGAAGAGCCAGAGATCAGCCATCACACAAACCTGTTTGCATCTGCACTATCAAGGACCTCCCTCAAAGGAAGTCGCAGCAAAAAAGGTGGACCATTAGAGAGTCCCAGTCTCTCACGGTTGGACAGGACGGTTAGAAGGGATCGTTCAACATCTTCAGAGAAAAGAGAAATTGGTGAGAAAATCAGCTTTTTTTTACATTGTCAAATGAACAAATGCAAATCTGTACTTGAGCCTTATCTGGTGAACTAGTTAATTTGATATTGCAAAGGTTGCAGAATTAATGCAGTAAATGTAGTCACTCTCCAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43225

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000052915	Essential Splice Site	1985	2962	5	25
ENSDART00000127755	Essential Splice Site	1961	2938	5	25

Genomic Location (Zv9):

Chromosome 19 (position 9673901)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	9132440
GRCz11	19	9051365

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTCCAGGTGAACATGACTATGGCCTTCTTCCTGCTCCCATTCATGTTGG[T/C]GAGTTTCTACAAATTTTAACCTGCCTAAATTTAGCCCAATATCTGTTTGC

Long Flanking Sequence:

CCAGGAAGAAGTGCACTGTTTTCGCAGGTATGCAGAACAAGTCTGATCTACAATGTCTGACTCTAGGTTGCTAGGAAAAAGATTATAATCTAAGTCAATTGATTTTATGGCCACAAACTTCTTCTTCTAATAATAAATTTTGCAGTGCACTGGAGGGAAAACCTGATGGCTCCCCTGAGCGCCCAGGCCCTGCTACTTCGGAACCAACCCCAAACCCATCAGTGACCAGCCAACGTGAGAAGAGAGTTGCTAGACCACCCAAAAAGAAGTTTCAAAAGGCGGGACTTTACTCTGATGTGTACAAGACTGATGAGTAAGAATTAGCATGTTCAGTAGGCTTGTCTTGTTATCTAATCTTTATATCTTTGGTAAATAAATGTAACCTCTCTCCATTTCCCCTTCAGTCCTCGCAGTCAGCTGCTACAGTTAAAGAAAGAGAAGCTAGAATACACTCCAGGTGAACATGACTATGGCCTTCTTCCTGCTCCCATTCATGTTGG[T/C]GAGTTTCTACAAATTTTAACCTGCCTAAATTTAGCCCAATATCTGTTTGCAGTTTGCTTGAGAGTTGGAGTTACGATCTTGTTTCAGCAATAAGGCCTATGCACACCACATCAACAGACTCTAACAAACATGGAAGACTAGCAGATCACTCCACCTGATTTCTCAGAAATTCTGCAACCCAGCAAGAGTTGATTCAGCATGTTCAGTTGGTGAAAACCAGATACTAACAGGGGAAAAACCCCCACAAAGTGTTTGCTGGTGTGGTGTGAATTGGTATTTTAAAGCACTATCGTTTCAACAAATAAAACTTGATTTGAGTGTGCAGTGTCGTTCCCAGCCAGTTCATTATGTAAGGCCTCATGGGCAATCAGGCTGATTAGTTATGGTTTATGAGTTATGAGGTGATTAGTTGATTCAATACTGGAATGGCGCAGCCTGAAGTTAAAGGACAAAGAGATTGAATTAATAACTGCAATTTGTCTTCGGTGTTTGTCCAGGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43226

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
ENSDART00000052915	Essential Splice Site	2179	2962	10	25
ENSDART00000127755	Essential Splice Site	2155	2938	10	25

Genomic Location (Zv9):

Chromosome 19 (position 9681111)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	9139650
GRCz11	19	9058575

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCGCTTTGTCAACCACAGCTGCGAGCCCAACTGTGAGATGCAGAAATGG[T/A]GAGTAAAAATGAGACCATGGATGAGTCACTCAATAAAATCCCATCAGCTT

Long Flanking Sequence:

GCAAATTGGCCACAAAACGTAATATTTACAGACATTGTTGACATGTATTTTTAGTTCCCCTCACTCCCAACAAATCCTTTAAATGTTGCAGTTTTCAGAAAAAAGGAGGAATTATAAATGTGAATTATTTTTTACCTTTTACACATTACCTAAAGCAAAACTCAGACTAGCAATTTGTGGGACATCCACTGTACAAATACTCACAATCCTCTGTCATTCAGCATGTTCACGCTTTTCACATATTATGCCGGTTTGATTATATGAATACCTTGATTGTTAACAGTTTTCTAGAATTGTATCATGTGTTTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTAGGAGTCGCATGATGGAGCAGTACTTCTCTCACAGCGGCCACTACTGCCTGAATCTGGACAGCGGCATGGTCATCGATAGCTACCGCATGGGCAACGAGGCTCGCTTTGTCAACCACAGCTGCGAGCCCAACTGTGAGATGCAGAAATGG[T/A]GAGTAAAAATGAGACCATGGATGAGTCACTCAATAAAATCCCATCAGCTTTTGATGAGTTCAGAAACCCAATGGTCATTTTTGTATGCTGAGTCACCAGGTATGTGGACAACCACCAACACTGAGCAAGCAATGACTGTATTCTTTAGAAATTGCTGTATTACTAACAAGTCATAGTCATTTCGAAAGTGTACAGAAGGTGTTCAAGGGATAGCTTAATCTAAATATAAAAGTTCTATTTTCTTTCATCACCCCTTAAATTCCTCCAAACATGAATTTCGTTCTTCGGTTGAACATAAAAAGATAAACCTGTAATCATTTTCCTACTGTGGATGTCAATGTCTATTAGTTTTCCATCATATTTTAAATGATATTATTTTGTGTTCAACAAAGAAAAGAAACTTTTATACTTAATTAAAGTAAAGATCTGTTCTTTGAAAAACTTCATACATACGTGTAGATATTACATTTTGTGCAAAATTAGCTGCACAGTTTTACAAT

Associated Phenotype:

Not determined