Busch Lab

ZMP

wu:fd60h05

Ensembl ID:
ENSDARG00000074852
ZFIN ID:
ZDB-GENE-030131-4797
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 7 alleles of this gene:

Allele Name Consequence Status Availability
sa22145 Nonsense Available for shipment Available now
sa35341 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa22145
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
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111897 Nonsense 65 1612 4 41
Genomic Location (Zv9):
Chromosome 12 (position 35195988)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 33600097
GRCz11 12 33701080
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCCCATTTGTTAAATCAGTTATTTGGTGTTTTGTTGATTAGGATGGAT[G/A]GTGCCAAGCACAGGGTTATCCACTTCAGAGGCCTTTGACGTCCCTTGACC
Long Flanking Sequence:
TTTACCAGATTTATCTAAAATAACTCACAAATGAAGAAGTACTTCAGATCTTATATAAAATGTATAGACGCTATGACAAATGGAAGTTAGTTTAGCACCTTATTTATTTTCTTATTTTTTATTATCGAATCCTTTTCACAGGGTGTTTTAAGAGGAAAAAGCAAAGAGTGTGTTTCCTACAGGTGGTTTGTAAACCCCACTCACCAGTGTAAAGCACACTCAGAATCACACAGTGTTTTCCTAGGAACATGGAGAGTTTATACGAAGGTGTTTGGTGCATATGGAGAGTAAAAAGGAAAGAGTTTGTTTTCTATAGGTGGTTTGTAAACACCACTTACCTGTGAGAAGCACATTAAGAATCGCACAATGTTTTTTTTTTTTTGAAGTATGTATTAGAGTGTCTGGTGCATATGGAGAGGAAATACTGTCTTTTCTATATGTGGTTTTGTCGAGCCCATTTGTTAAATCAGTTATTTGGTGTTTTGTTGATTAGGATGGAT[G/A]GTGCCAAGCACAGGGTTATCCACTTCAGAGGCCTTTGACGTCCCTTGACCATGAGGATGCCCGTACAGCTTTGGAAATCTACAAACTGGTCAGTACGAAATTTAAAGGCATTTGTTCATACATAATTTGCCTGATTATGTACAACATTTTATTCTACAAAAAATATGTTAGAATGTGTTTATTTTCTGGCTCTTTGCAGTATTTATTAAATTATTAAGTGAAACTATCTCCTTTGACTTTAATAGTATGTCAAAAATGTAAATAAGAGCTTTTAAAGTCGACTTCATCCAATGTTTAAATCGTTGTTCTAGAAATGTATGCTAATTAGTGCATATTTAATTTGATGCCTCATTAGAATATGTAAACATAACATTTTAGAAAGCTTGTAATACAAGAAATCATAACATAATCAATTAAACTGGGTAGGTATGATGATAATCAGTTAATCTTGTTTACCCAATATTTACCTGCTGTGTCTTGCTTTAACATAAACCTTCAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35341
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
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111897 Nonsense 1471 1612 38 41
Genomic Location (Zv9):
Chromosome 12 (position 35161526)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 33565635
GRCz11 12 33666618
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGGATGGATGGACTCAACTCTACTGATGAAAGACTCCTTGCTACGATA[C/T]GAGCGCAGTTTTCAACCTTAGGCCCCATCAGCCCTCTTGATGCCAAAGCT
Long Flanking Sequence:
TATCTTTGCCATGATGACAGTAAATAATATTTGACACTTCTTAAAGTGACATTTAAAGGCTTAACTTGGTTGATTAGGTTAACTGGGCAGGATAGGAACTATAGCACTATAGAAAACATTATAAAGTGGCTAATAATATTGACCTTAAAATGTTTAAATGTGTAACATTTCACAATATTACTGTTTTCCGTTTTTCAGCTTGTGGCCAGTTATCTGGAAGGGAAAATGTTTCTGTCCATGAACAGTTCTACAGTTTACCAGCAGGTGGCAGAACTGACCGCTCTTCAACACCTTGCGCTTGGACTAAATAATCTGCCCTCAAAGTAATTTCATACATCTCACACAGACGGATTTCTAAAATATCAAATGAAACCTGCATCCATTAATTGTTTCCCCATCTGACACTCTTATTTCTAAACCCGGCCAGTGCTGAGATAAAGCAGTATCATCCCCGGATGGATGGACTCAACTCTACTGATGAAAGACTCCTTGCTACGATA[C/T]GAGCGCAGTTTTCAACCTTAGGCCCCATCAGCCCTCTTGATGCCAAAGCTCGGTTTATCAGTGAGTGAACAAATCTGTCCAAACATGCTCCCAGGTTATTGTTACACAATTATAATGAATGATTTTACATCCAAAACAAACTCTTAAAACAGATGTGGGGTAAGTTACTTAAAAAAACTCATTAATTACTGATGAAAATTAAAGGAATAGTTCACCAAAAAATAAAAAATGTTCATAATTTACTCACCCTCCACTTCTTCAAAACCTGTTTGAGTTTATTTCCTCTGTTGAACACAAAACAATATATACTTAAGAATGCCGGAAAAAGTAGCCTTTGACTTCCATAGTGGTACATTTGTATTTAATTTACTTCACTCAATACATACATTTCAGTGCATAGTAAACCAAATTTAAGATTGTAATTATTCAAATTTGAGTCACTTTTGGTCTTATTTTTATAATATTTTAAGCTTTTTAAAGAGTTTACTCCAAAATGTTAT
Associated Phenotype:
Not determined