ZMP

ENSDARG00000070174

Ensembl ID:

ENSDARG00000070174

Human Orthologue:

MYO15B

Human Description:

myosin XVB pseudogene [Source:HGNC Symbol;Acc:14083]

Mouse Orthologues:

Myo15b, Myo3b

Mouse Descriptions:

myosin IIIB Gene [Source:MGI Symbol;Acc:MGI:2448580]
myosin XVB Gene [Source:MGI Symbol;Acc:MGI:2685534]

Alleles

There are 6 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12019	Nonsense	Available for shipment	Available now
sa12795	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa12019

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
ENSDART00000102784	Nonsense	295	634	6	10

Genomic Location (Zv9):

Chromosome 3 (position 37032841)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	36896201
GRCz11	3	37038059

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGAAGTGGAGAGCTAYGCGTCCTTCATTGGCCAGGCTCTAGAGAAGACC[C/T]GAGGCAGAGAGTGTGTGCCCTCGTGGGAGGAGATTCAAGGGCTGATGGGA

Long Flanking Sequence:

ACTGTCTGACTGTCTTTTTGGGAAAGGCTATGAGGAGTCCATTACAGTAATCCACCCTGGTGCTGATAAAAGCATGAACAACTTTCTCTAAGTCTTCACTAAAAACAAAGCATGTAATTCTTGCAATGTTTTTGAGATGATAGTATGATGATTTAGTTACTGCTTTTGCTGTGCATTGTATAATCAGGTAAACTATGTTTGAAGATATTTCTCCGTGAATCAGACTTTAAATATATGTATTGTGATTAAAATCTCCCAACACAAATTGATGAAGTGTGTGACAAAAGAATGACTTGAAAGTACATTTTGGATATTTTCTTCACATTAAACTGAAAAGATAAAAACGCTTCATGAAAAGCCCAACATCTAAAAACAGTGCCTTTGCTTGTATTGTAAACTTTGTTTTTTGTTTTCCTCCATGTTTCAGGGTTCAGAGTTTGAGTGTGGACCCAGAAGTGGAGAGCTATGCGTCCTTCATTGGCCAGGCTCTAGAGAAGACC[C/T]GAGGCAGAGAGTGTGTGCCCTCGTGGGAGGAGATTCAAGGGCTGATGGGAAGACAGGAGATACTGTGTACTGTGCATTACCCTGGACCAGGCTGCTGCCAGATACCCATCACCTCACACACCACAGCTAATGAGGTTCGGTTTCAATCCTTTCCTACAACTCTGACTCACTAAAAAGTTATTTAGTTATTTTATGATGAATTATACTATACTATTATAGATGCATAAACATTTTGAGAATTGTGAGATTTTTATTCTGAGTAGAAAATTCTGAATTCTATGATAAAAAAAAATCACAATTCCAAGACTTAAAGGTCCCATGTAGTGCATTTTTATTCAATGTTTAATTAAATTTCAACCAAAACACGAAGAGGGTGGGACATAGTGTAGCTCCTCCCCTTTAAAAAAAACAGGCAGTAGCATTTTGTTTTATCACAGCTCAGCCAGTGAGAGGGGTTGAGCTCAAGTGCATAAAATGAGAACTGGCTTGAAAGGGGTGGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa12795

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000102784	Nonsense	452	634	9	10

Genomic Location (Zv9):

Chromosome 3 (position 37038969)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	36902329
GRCz11	3	37044187

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCAGCTTGTGAGGAAGATCTTCTTTCACTGGCGGCGCTGAGGCTGCAGTA[T/G]CTGCTGGGGGATTTCAGCGCCCTYTCTCCGTACCCGGCGCTAGAGCAGCT

Long Flanking Sequence:

TTGCTTGTACATATTTAGGGCTGGTGTTCTCAAGTCAAGCGAGCCCAAACATAACATGAAAATGCAAGCTGGCTTTTATCTAGATTTATCGAGATTATTGTACACATAGCTCACTATAAACACTTGTAGTTCACTTAAAACTTTCCTAACTTTATAAATCATTATTAAAGGTTCTAGTGGTATTTGTAAGGAATTGGATGCAAGCTGTTTTGTGAATCATTCAACGCCATCTGCTTTAAAAATTAAGCTCTAAATTTAAGAGAGAATAGCAATGCATTTTGAAAATATCAGAACTAATTCCTGGAATAATTTTTCACCACAAATACTTTAGCTGTGTTCATCAGCTAATTAAATAGTGTTAAAACAGCCTTGTAGTGAACTTTATAAATTGAAGCCGGCTTCTTCCCTTCTCTCTGCCAGTGTCATGAGATGGTGGTGCGAGGGCAGCTGCCAGCTTGTGAGGAAGATCTTCTTTCACTGGCGGCGCTGAGGCTGCAGTA[T/G]CTGCTGGGGGATTTCAGCGCCCTCTCTCCGTACCCGGCGCTAGAGCAGCTCTTTCCAGCAGAGGTGGTGGAGGCCCGAGCCCTGCTGGCCCCCGTCGATCCCCCCGGCTGCCCGTCCTTCCCTGGGGGTCTGCTGGCTGGGACGCTGTGGGGGCACAAGCGACGACAGGAACAGGACCAAAGGCTGCGGGCCAGGCTGAGGGAGGAGGGGGCTGTGGTGATGTCCACTATTCTAGAGCGCTGGAAAGCCCTGGTGGGATACAGTGGCAGGGACAGCATGGCTGCTTATCTTACCATTGCCCGGCAATGGTCAGGGTTCGGCTGCACACTCTATGAAGTGGACTTTTATATAGTAAGTTGGCAAACTTTTGGAATAATTAATTTTTTGTATTTGAAAAAATTACTTTATTTTCACCAAAGGTGCATTAAACATGTGGTATATACATAAATTATATGTAAATAGAGTAGTCAGATATATGAACTGTACCTTTATTTGACCTG

Associated Phenotype:

Not determined