myhz1.2

Ensembl ID:

ENSDARG00000067995

ZFIN ID:

ZDB-GENE-070705-73

Description:

myosin, heavy polypeptide 1.2, skeletal muscle [Source:RefSeq peptide;Acc:NP_001154918]

Human Orthologues:

MYH6, MYH7

Human Descriptions:

myosin, heavy chain 6, cardiac muscle, alpha [Source:HGNC Symbol;Acc:7576]
myosin, heavy chain 7, cardiac muscle, beta [Source:HGNC Symbol;Acc:7577]

Mouse Orthologues:

Myh6, Myh7

Mouse Descriptions:

myosin, heavy polypeptide 6, cardiac muscle, alpha Gene [Source:MGI Symbol;Acc:MGI:97255]
myosin, heavy polypeptide 7, cardiac muscle, beta Gene [Source:MGI Symbol;Acc:MGI:2155600]

Allele Name	Consequence	Status	Availability
sa33639	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa16809	Essential Splice Site	Available for shipment	Available now
sa11919	Essential Splice Site	Available for shipment	Available now
sa33638	Nonsense	Mutation detected in F1 DNA	Not yet available
sa15463	Nonsense	Available for shipment	Available now
sa25302	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa31460	Nonsense	Available for shipment	Available now
sa10023	Nonsense	Available for shipment	Available now

Allele Name:

sa33639

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098066	None	None	446	None	11
ENSDART00000098067	None	None	1937	None	39
ENSDART00000110726	Essential Splice Site	None	945	2	24
ENSDART00000131983	Essential Splice Site	None	1937	2	41

Genomic Location (Zv9):

Chromosome 5 (position 33930330)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31692562
GRCz11	5	32292715

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCATTACAGTGTTGCAGATATTCATCAGAAGCTGTTGGAGCGTGGTAAG[G/A]TAAAGATGCAATATTGTATTATAAAATTAAGCAAAGCAAACATTGCATTA

Long Flanking Sequence:

TGCAATCTAATTAATGTTCACTTTAAATATGCGCTTCACTATTTCTGTATATTACAAAAACTTTTATTAACAAGTTATTCATGTGTTATTTCCATTTTTGTAATCCTCAATATAGACAGTGCCAAATGGTCCATCTGATCGAATTTTTAACTCCACCTTGACATGCTGTATTTGGCATAAGACACATTTAACTTCTGCATTGCTTGCAAAACAGGTACAGTATAAAGAGCATGAGCTGGACTGGAAACCTCTGCGTTCAGAAGATCAGCCAGGGTTGACTGTGGTGAGTGAAAACTTTCATTTATTTTTCAAGACACACATTTAAAAATAAATCAAATTTAAAAAAGGATGGCATCTTTTTCAATACCTATCAACTGTTTGTAATTTAGTTTACAAATTCTAATTTTTGTAAGAAAAAAAACATAATGTAACATTTAACATTTTGCTTTGTGCATTACAGTGTTGCAGATATTCATCAGAAGCTGTTGGAGCGTGGTAAG[G/A]TAAAGATGCAATATTGTATTATAAAATTAAGCAAAGCAAACATTGCATTAGAGCTATGGCCCTGTGTAGGAAAACCTGTGTGTGAATGAATGCTTTAGATTTAGAACGAAAATCCATGCTTCATTCTCTACAGGTTCACTGCCCACATAACAACATTTCTCTCGCCCAAACAATTAACCTTTGCTTGGCCCACATGCCGCAATGAATTATGCTACTGGACCAAGTCTGGCTTCTAGACAAGGGCCAATCAAATTCTAGACAACTGCCAATTTAATAACCTATAACTGTGCCTGAACGGGGCCATTTATGTCTGTGTGTCAAGACTGCTATTAAATTGATAAACCCATAAAGCATTGCACTTTAGGCATGCAATGGGTGTGCTTTTTCTCAAAGCAACCTGATTGGTAGAATTTTTTTCTTTTTTCAAAAATAATTTCAATGTGCGTCAAGGTAGGCCAAACTTATGAGGCCCACATATCAATTTTTAACATCTGGGCCAA

Associated Phenotype:

Not determined

Allele Name:

sa16809

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098066	None	None	446	None	11
ENSDART00000098067	Essential Splice Site	117	1937	2	39
ENSDART00000110726	Essential Splice Site	117	945	4	24
ENSDART00000131983	Essential Splice Site	117	1937	4	41

Genomic Location (Zv9):

Chromosome 5 (position 33928923)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31691155
GRCz11	5	32291308

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCTCTGTGCTGTATAACCTCAAAGAGCGTTATGCAGCATGGATGATCTAC[G/T]TAAGCTCTAAAACAACCTAAAGCAGCACTTCCACACATTTACATCTGTAT

Long Flanking Sequence:

AAAACATATGACAGTCTGACTTTTTTTTCTAATTGTCATTTACTTTTAGAAGTAAGCCGCCACCATGAGTACGGACGCGGAGATGGCCGTTTATGGCAAGGCTGCCATTTACCTCCGTAAGCCTGAGAAGGAGAGAATTGAAGCTCAGAACAAACCTTTTGATGCCAAAACCGCTTGTTACGTGGTTGATGACAAAGAGCTGTACGTCAAGGGAACAATCAAGAGCAGAGACGGTGGCAAAGTCACCGTTATTACACTTGACACTAAGGAGGTGAATTTTTACATTTCATAAAGATTAAATTAATTACAATTATACAGTCTTAATGAATAGATTATTGACTAGATGACTTTTATAGGAGAGAGTTGCTAAGGAGGATGACGTCCATCCAATGAATCCTCCCAAGTTTGACAAGATTGAGGACATGGCCATGATGACCCATCTCAATGAACCCTCTGTGCTGTATAACCTCAAAGAGCGTTATGCAGCATGGATGATCTAC[G/T]TAAGCTCTAAAACAACCTAAAGCAGCACTTCCACACATTTACATCTGTATTTTTGCCATTGTTGGAATTTCAAGCCAATTCCATGCATGTTCAATAAGAAAAGGTCTGGAGAGGGTTTTCTTTAATGCCAAAAATATTAGTAATTTGACCATTTCTTTCCTCATTTTAGACCTACTCTGGGCTGTTCTGCGCCACTGTGAACCCCTACAAGTGGCTCCCAGTGTATGACGCAGAAGTGGTTGCTGCCTACAGAGGCAAGAAGCGTATGGAGGCTCCACCCCACATCTTCTCTGTCTCTGACAACGCCTATCAGTTCATGTTGACTGGTGAGATCTCATTTACAAGATCTGAATTACACACAAGTTCACATTCATCATTTTAACAAAACAATTGCTAAAACATTATTACATTTGCATTTACAGACAGAGAGAACCAGTCTGTCCTGATTACGTATGTATCTACTCTAATAGAGATGCTGAGAACAGGTTTATTTTCCTCTG

Associated Phenotype:

Not determined

Allele Name:

sa11919

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098066	None	None	446	None	11
ENSDART00000098067	Essential Splice Site	654	1937	15	39
ENSDART00000110726	Essential Splice Site	654	945	17	24
ENSDART00000131983	Essential Splice Site	654	1937	17	41

Genomic Location (Zv9):

Chromosome 5 (position 33925972)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31688204
GRCz11	5	32288357

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GAGGAAAGAAGAAGGGTGGTTCCATGCAGACTGTGTCTTCCCAGTTCAGG[G/A]TRTTTRTTTTGTTTTTGTTTTGAGACCAAATGTAAACAGTTATCAAAACT

Long Flanking Sequence:

CTTATTAACAAACAACCTTCTTTTATAAACAGCCCTTAGGTATCTTCTCCATCCTTGAAGAGGAGTGCATGTTCCCCAAGGCTACAGACACTTCCTTCAAGAACAAGCTGTATGATCAGCATCTTGGCAAGTGCAATGCTTTCCAGAAACCAAAGCCTGCCAAAGGCAAGGCTGAGGCCCACTTCTCCCTGGTCCACTATGCTGGAACTGTGGACTACAACATTTCTGGCTGGCTGGACAAGAACAAGGATCCACTGAACGAGTCTGTTGTGCAGCTTTACCAGAAGTCTTCAGTCAAACTGCTGGCTACTCTCTACCCACCTGTTGTTGAGGGTAATTAGGCAACATCAGTTTAACTTTGAGTCAAATTTACAATTGTTACTCTTTCTGTTAATTACAATACATGCTTTTTTCCCATTAAATTAATAGAGACTGGCGGTGGAAAGAAGGGAGGAAAGAAGAAGGGTGGTTCCATGCAGACTGTGTCTTCCCAGTTCAGG[G/A]TATTTGTTTTGTTTTTGTTTTGAGACCAAATGTAAACAGTTATCAAAACTGAAATCAATGACATGATTTTGCCTGAAGTTAGACAAACAATACAAAGAAAAATTAAGAATGTGAAAAAAAATCTGAATTTTTTTATGACTAAACAGGAGAACTTGGGCAAGCTCATGACCAACTTGAGGAGCACTCACCCTCACTTTGTGCGTTGTCTGATTCCCAATGAGTCCAAGACTCCAGGTAAATAAATAAAGGGACATATGTGTTGACATGAACACAGCATGTAATGTAATTTTGATTATCATTATAATATAATCTTTACCAAAATCATAGAGTAAACTGTTTCTTATAGGTCTTATGGAGAACTTCCTGGTTATCCACCAGCTGAGGTGTAACGGTGTACTGGAGGGTATCAGAATCTGCAGAAAGGGTTTCCCCAGCAGAATCCTCTATGCTGACTTCAAGCAGAGGTAAATGTGACTTCATAAAAATGTAATTTACTGTAA

Associated Phenotype:

Not determined

Allele Name:

sa33638

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098066	None	None	446	None	11
ENSDART00000098067	Nonsense	1015	1937	22	39
ENSDART00000110726	None	None	945	None	24
ENSDART00000131983	Nonsense	1015	1937	24	41

Genomic Location (Zv9):

Chromosome 5 (position 33924059)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31686291
GRCz11	5	32286444

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAAAGCCCTCCAAGAGGCACATCAGCAGACTCTGGATGATCTCCAGGCT[G/T]AGGAGGACAAAGTCAACACCCTGACCAAATCTAAGACAAAGCTTGAGCAG

Long Flanking Sequence:

TCTTTATTCAAATTGGTTTGCAATAACAGAACAATGTGCTTTCTTAACAGGAATCAGAGAATCTCTCAGATGCTGAGGAAAGATGTGAGGGTCTGATCAAGAGCAAAATCCAGCTTGAGGCTAAACTCAAAGAGACAACTGAGAGACTGGAGGATGAGGAAGAAATCAATGCTGAACTGACAGCCAAGAAGAGGAAACTGGAGGACGAGTGCTCTGAGCTGAAGAAAGACATTGATGACCTGGAGCTCACCTTGGCTAAAGTGGAAAAGGAGAAACATGCCACAGAGAATAAGGTTTTTCTTTTTAGACATAATCTGTCATCTTTTAAATATGCAAATTATAAACAAAAATCTTACTAAACATATTTGATACAAATAATCACACAGGTCAAGAACTTGACAGAGGAAATGGCAGCTCAAGATGAGAGCATTGGTAAGCTTACAAAGGAGAAGAAAGCCCTCCAAGAGGCACATCAGCAGACTCTGGATGATCTCCAGGCT[G/T]AGGAGGACAAAGTCAACACCCTGACCAAATCTAAGACAAAGCTTGAGCAGCAAGTTGATGATGTAAGTTGTCATCATTAAAATGTTATTTTAATATTTTTTCATACCACAAGAAGAATGGTACGATATAAATATTAAAATATAAATGCATTAGAATGTATGGCTTATAATGTTAACCTGAATCATAAAAATATGATAACAATTAATGCACTTAATAATGTCATGTCAACTTTACAAATAACTTAGCTGGAAGGTTCCCTTGAGCAAGAGAAGAAGCTCCGTATGGACCTGGAGAGAGCCAAGAGAAAGCTTGAAGGAGACTTGAAATTGGCACAAGAGTCCATCATGGACCTGGAGAATGACAAGCAGCAGTCTGAGGAAAAGCTGAAGAAGTAGGGATTCTTTGTAAATTCTATATTAGAGTGATTGTTAATTTGGTTTTAAATCATACATAATATTTTCCCATTTTACACACAGGAAAGACTTTGAAACAAGCCAGCT

Associated Phenotype:

Not determined

Allele Name:

sa15463

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098066	None	None	446	None	11
ENSDART00000098067	Nonsense	1257	1937	26	39
ENSDART00000110726	None	None	945	None	24
ENSDART00000131983	Nonsense	1257	1937	28	41

Genomic Location (Zv9):

Chromosome 5 (position 33922889)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31685121
GRCz11	5	32285274

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTTTRTTTTTACAGGCCAATCTAGAGAAGATGTGCCGCACACTTGAGGAC[C/T]AACTTAGTGAAATTAAGTCTAAGAATGATGAGAACCTTCGCCAGTTGAAT

Long Flanking Sequence:

ACTGGAGGAAGAGATTGAGGCTGAGCGTGCTGCTCGTGCCAAGGTTGAGAAGCAGAGAGCCGATCTCTCCAGGGAACTTGAGGAGATCAGTGAGAGGCTTGAGGAGGCTGGAGGAGCCACTGCTGCTCAAATCGAGATGAATAAGAAGCGTGAAGCTGAATTCCAGAAGCTGCGTCGTGATCTTGAAGAGTCCACCCTTCAGCATGAAGCTACTGCTGCTGCCCTGCGCAAGAAGCAGGCAGACAGTGTGGCCGAGCTGGGAGAGCAAATCGACAACCTCCAGCGTGTCAAGCAGAAGCTTGAGAAAGAGAAGAGTGAATACAAAATGGAGATTGATGATCTCTCCAGCAACATGGAGGCTGTTGCCAAAGCAAAGGTTTGAGAATTGTTCAAGAATTGTAAAATAAGTATATTTTTATTGTTTGGTTAAAATTCATAATAATCAAATGACTTTGTTTTTACAGGCCAATCTAGAGAAGATGTGCCGCACACTTGAGGAC[C/T]AACTTAGTGAAATTAAGTCTAAGAATGATGAGAACCTTCGCCAGTTGAATGATCTCAGTGCTCAAAGAGCAAGACTTCAAACTGAAAATGGTAACTTATGATGAAAATGAACAACATCTATTTTACTACAAAGTTTTTTGTCAATGATTAATCAAGAATAAGGATGATTCACCAGTTTGACAAAGTCATATTTCAGCAAATACAATATTAAACAATTCAGAAGTCAACTGATAAAATATAACAAAGGATATGCTTGATATTTGATGATAGAGTTACTTAACCAATCGAAACAACAATATAATATCTCAATAATATCTCAAAAGGTGAGTTTGGCCGTCAGCTTGAGGAGAAGGAAGCTCTGGTTTCTCAGCTCACACGAGGAAAACAGGCTTTCACTCAGCAAATTGAGGAGCTTAAGAGGCAGATTGAAGAGGAGGTTAAGGTAATACAATATAAAATATACATTTATATATCCCACATTTACTATAGAGCCAGGTTAA

Associated Phenotype:

Not determined

Allele Name:

sa25302

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:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098066	None	None	446	None	11
ENSDART00000098067	Essential Splice Site	1453	1937	29	39
ENSDART00000110726	None	None	945	None	24
ENSDART00000131983	Essential Splice Site	1453	1937	31	41

Genomic Location (Zv9):

Chromosome 5 (position 33921904)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31684136
GRCz11	5	32284289

KASP Assay ID:

554-7822.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAACGCTTTGGCTGCCAACCTTGACAAAAAGCAGAGGAACTTTGACAAG[G/T]TAAAATTTGGAGTCATGTTGTGATGTGATGTTCTATTTCAGAAAGTAGTA

Long Flanking Sequence:

TATAGAGCCAGGTTAATAGTATGTGACTTTGTCTTCTAGGCTAAGAATGCACTGGCCCATGCTGTACAATCAGCCCGTCATGACTGCGACCTGCTCCGTGAGCAGTTTGAGGAAGAGCAGGAGGCAAAGGCTGAGCTGCAGCGGGGAATGTCAAAGGCCAACAGTGAGGTTGCTCAGTGGAGAACCAAATATGAAACTGATGCCATCCAGCGCACAGAAGAACTTGAAGAATCCAAGTATGAACTTTAAAAGAACTGTGTGGTTTTATTTGGGTGACAGCATGCATTTTTATTGATGATTATGAAATATTTAACAGGAAGAAGCTGGCTCAGCGTCTGCAAGAGGCAGAGGAACAAATTGAGGCAGTGAACTCCAAATGTGCATCTCTGGAGAAGACCAAACAGAGACTCCAGGGTGAAGTGGAGGACCTCATGATTGATGTGGAGAGAGCCAACGCTTTGGCTGCCAACCTTGACAAAAAGCAGAGGAACTTTGACAAG[G/T]TAAAATTTGGAGTCATGTTGTGATGTGATGTTCTATTTCAGAAAGTAGTATTAGCTTTCTTCTGGAGAATACAAGTTGAACAAACCTGATATATTCCACCCTAAAGGTCCTGGCAGAATGGAAGCAGAAATATGAGGAAGGTCAGGCAGAGCTGGAAGGTGCCCAGAAAGAAGCTCGTTCACTCAGCACTGAGCTGTTCAAGATGAAGAACTCCTATGAGGAGACTCTGGATCAGCTGGAGACCCTCAAGAGAGAGAACAAGAATCTGCAGCGTAAGAATCAAAAAATAATAAAACCTGATGAATAACCGTCTTTATGATATGATACAGATAATATTTTTTCTTTCTACAGAGGAGATTTCAGATCTGACAGAGCAGATAGGTGAGACTGGTAAGAGCATCCATGAGCTGGAAAAGTCCAAGAAGGCAGTGGAGACTGAGAAGGCAGAGATTCAGACCGCTCTGGAGGAGGCTGAAGTGAGTGGAGATGGAGATTTATAT

Associated Phenotype:

Not determined

Allele Name:

sa31460

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098066	Nonsense	33	446	2	11
ENSDART00000098067	Nonsense	1523	1937	31	39
ENSDART00000110726	None	None	945	None	24
ENSDART00000131983	Nonsense	1523	1937	33	41

Genomic Location (Zv9):

Chromosome 5 (position 33921511)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31683743
GRCz11	5	32283896

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTCTACAGAGGAGATTTCAGATCTGACAGAGCAGATAGGTGAGACTGGT[A/T]AGAGCATCCATGAGCTGGAAAAGTCCAAGAAGGCAGTGGAGACTGAGAAG

Long Flanking Sequence:

AGACCAAACAGAGACTCCAGGGTGAAGTGGAGGACCTCATGATTGATGTGGAGAGAGCCAACGCTTTGGCTGCCAACCTTGACAAAAAGCAGAGGAACTTTGACAAGGTAAAATTTGGAGTCATGTTGTGATGTGATGTTCTATTTCAGAAAGTAGTATTAGCTTTCTTCTGGAGAATACAAGTTGAACAAACCTGATATATTCCACCCTAAAGGTCCTGGCAGAATGGAAGCAGAAATATGAGGAAGGTCAGGCAGAGCTGGAAGGTGCCCAGAAAGAAGCTCGTTCACTCAGCACTGAGCTGTTCAAGATGAAGAACTCCTATGAGGAGACTCTGGATCAGCTGGAGACCCTCAAGAGAGAGAACAAGAATCTGCAGCGTAAGAATCAAAAAATAATAAAACCTGATGAATAACCGTCTTTATGATATGATACAGATAATATTTTTTCTTTCTACAGAGGAGATTTCAGATCTGACAGAGCAGATAGGTGAGACTGGT[A/T]AGAGCATCCATGAGCTGGAAAAGTCCAAGAAGGCAGTGGAGACTGAGAAGGCAGAGATTCAGACCGCTCTGGAGGAGGCTGAAGTGAGTGGAGATGGAGATTTATATGGCGTTATCTGTAGAACATTTTATACTATAAATTATTTATCTTTGTCATAGGGCACTCTGGAGCATGAGGAGTCCAAGATTCTTCGTGTCCAGCTTGAGCTAAACCAGGTCAAAAGTGAGATCGACAGGAAGCTTGCAGAGAAGGATGAGGAGATAGAGCAGATCAAGAGGAACAGTCAGAGAATTACTGATTCCATGCAGAGCACTCTGGACTCTGAAGTCAGAAGCAGGAATGATGCTCTCAGAATCAAGAAGAAGATGGAGGGAGACCTTAATGAGATGGAGATTCAGCTGAGCCATGCCAATCGCCAGGCTGCTGAGGCTCAGAAACAGCTCAGAAATGTTCAGGCACAACTCAAGGTATGACTTCTCGTCAGCTTTAGGTGCATTCAT

Associated Phenotype:

Not determined

Allele Name:

sa10023

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
ENSDART00000098066	Nonsense	176	446	4	11
ENSDART00000098067	Nonsense	1666	1937	33	39
ENSDART00000110726	None	None	945	None	24
ENSDART00000131983	Nonsense	1666	1937	35	41

Genomic Location (Zv9):

Chromosome 5 (position 33920902)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31683134
GRCz11	5	32283287

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCTGTTRTGTTCAGGATGCCCAGCTGCACCTTGATGATGCCGTGAGAGGA[C/T]AGGAAGACATGAAGGAGCAGGTGGCCATGGTGGAGCGCAGAAATACTCTG

Long Flanking Sequence:

GCGTTATCTGTAGAACATTTTATACTATAAATTATTTATCTTTGTCATAGGGCACTCTGGAGCATGAGGAGTCCAAGATTCTTCGTGTCCAGCTTGAGCTAAACCAGGTCAAAAGTGAGATCGACAGGAAGCTTGCAGAGAAGGATGAGGAGATAGAGCAGATCAAGAGGAACAGTCAGAGAATTACTGATTCCATGCAGAGCACTCTGGACTCTGAAGTCAGAAGCAGGAATGATGCTCTCAGAATCAAGAAGAAGATGGAGGGAGACCTTAATGAGATGGAGATTCAGCTGAGCCATGCCAATCGCCAGGCTGCTGAGGCTCAGAAACAGCTCAGAAATGTTCAGGCACAACTCAAGGTATGACTTCTCGTCAGCTTTAGGTGCATTCATATGTTTTTCAAATTAAAACTATGTGCTAACACACAGCACTCAAAAAGCTTACTGTAAAGCTGTTATGTTCAGGATGCCCAGCTGCACCTTGATGATGCCGTGAGAGGA[C/T]AGGAAGACATGAAGGAGCAGGTGGCCATGGTGGAGCGCAGAAATACTCTGATGCAGTCTGAGATTGAAGAGCTGAGAGCTGCTCTGGAGCAGACAGAGAGAGGACGCAAAGTGGCTGAACAAGAGCTGGTGGATGCCAGTGAGCGTGTTGGGCTGCTGCACTCTCAGGTAAAAAAGCATAATGGCTTTGTTTTTGCTTTCTGTTGCGCAATGTCATTAAGATAGTTGAAAGCATTTTTCAATACATTTATCTTGTTGCTTTCCATGTTGTAGAACACAAGTCTTCTGAACACCAAGAAGAAGCTTGAGGCTGACCTTGTTCAGATCCAGAGTGAAGTTGAAGACACTGTACAGGAAGCCAGAAATGCAGAGGACAAGGCCAAGAAGGCCATCACTGATGTGAGCAACAGAACAAAAGTTTCAAAGTGTATTTTAAAAAAAAAGTCTAATGGAGATTTGTGTTCATGTAAAAGGCTGCAATGATGGCAGAGGAGCTGAAGA

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details