Busch Lab

ZMP

ENSDARG00000090514

Ensembl ID:
ENSDARG00000090514
Human Orthologue:
MYOM2
Human Description:
myomesin (M-protein) 2, 165kDa [Source:HGNC Symbol;Acc:7614]
Mouse Orthologue:
Myom2
Mouse Description:
myomesin 2 Gene [Source:MGI Symbol;Acc:MGI:1328358]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa30368 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45869 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30368
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
ENSDART00000130478 Essential Splice Site 165 345 5 9
Genomic Location (Zv9):
Chromosome Zv9_scaffold3535 (position 30599)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6842317
GRCz11 13 6970695
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGATGCTGAGAAAACCCACACTCGTACCCTGGATCTTTCTGGACAACG[T/C]GAGTTGTTTGAATGTGTCACTTCTTAATATGAAGCTTAAGCTTTTTAAAG
Long Flanking Sequence:
TAGCCTATATTATTTTAATTCATTTCTTTTGTCTCTGTTACTTGCAGTTCAATACACGTGCGCTGCACGAAATAAGAGAGAACAGGGCAATATTGATCTTTTTTATCATTAATATTTATTGTGAACAGTGTCTTGAAGATATTATAGTAGTAAGGTAGTAAGGTATTATGTACTGTCATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACCATTATGTTTAGAAATGTGTTGATAAATATTCTCTCTGTTAAACAGAAATTCTGACTTCAACTTGAATTAATGGGCGTTTTAAATTTGATTGCTCTTTGTGTTTAAAGGGAAGCTAAAATCAGTGCATCAGAAAGAATGCGAATTGGTGGCAACCCAGCAATGGCAACCCTGGAAGTAGTCGAACCTACTGATAAAGATAAAGGCATGTACACGTTTGAGATTGTGGATGCTGAGAAAACCCACACTCGTACCCTGGATCTTTCTGGACAACG[T/C]GAGTTGTTTGAATGTGTCACTTCTTAATATGAAGCTTAAGCTTTTTAAAGTTGCCAAAGGTAGCCTGATATGATTTGTTATTTGTTCTCCGATATCTGCATAGTATGTATGTGGCTTAAGTAAGAGAGAAAAATACTCCAGAAACTGTTTTAGAAGCACATTTTGAATCATAGATTTTATCTCTAAAAATCTGCAAATAAGCATTTTATATATCTTGTGATTCATGTTTTTTTTCACCCGTTTATTTATGCTTTAGAATTGTATTATGTGACCTTATTCTTTTAATCCTGAAAGGTTTGAAAAAAGTGACTTTTATTAATATTTTAATAGTTTAAAGTGATATATCGTTAGAGTTGGTGTTGTATATTATGGTACAAAAGCCTTGTAATTGACTGACAGTACATTTTGTGTTATTTTACAGACTTTTTTCCCTACAGTATATATTATTTTTGTAACACTTTACAATAAGGTTCATTAGTTAATGCATTTACTAACATGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45869
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130478 Essential Splice Site 165 345 6 9
Genomic Location (Zv9):
Chromosome Zv9_scaffold3535 (position 35681)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 6837235
GRCz11 13 6965613
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTGTTCTTAACTTTTATTTATTCGTTCATTCACTTTGTTTCCCCCAT[A/C]GTCTACGACAACGCCTATGCAGAATTCCAGAGACTCAAGTAAGATATCTG
Long Flanking Sequence:
ATCACATCAACGCAATATGGAATGACATGACGGACTGTCATATTTGTAATTTTCTATCAACACACATAAAATGTCATCTATAACACGTGTTCTGGCATTGATCCTGTGTGGATGTAGTCAAAAAGGCCAGCACTGCAGCTGCACACACTGGGAGATCCAGGCATGAAAAAGAGCAGTTATAGTATCAAAGGTGCAGATACTGGCAGCGGTTTCAGTTAGTCAACAGACTGTTTGATGACAAACATAATCAAGGGCTGGCATCTGACAGGTCATGCGATTTGCCGAATGGTGACAGTAATGAGTATAGGGGAAGTAGAGCTATTTCCAGCAAAGCAGGAAAACAATGCTATTAAAATAATGAGGGCTGATTTTCCTTTTATGCTATGCCTCAGGGACAAAACGCAACGAACTGAAAGACAGTGAAATTTTTTTCTTTAAAAAAAAAATTTATTTGTGTTCTTAACTTTTATTTATTCGTTCATTCACTTTGTTTCCCCCAT[A/C]GTCTACGACAACGCCTATGCAGAATTCCAGAGACTCAAGTAAGATATCTGGTTCCACCACATGGGTATCCACATCCTAAATGTTTTGAGATGCAAAGCATGTGAGCTGTGTGTCAGTGTTTGGGTAAAATATTAAGGTCTGCTAATGAACTCAACTATGCTATTCTTCTTTTGCCCTTCAGAGCGGAAGCATATGCTGAAAAGAGTGAGTATACTCAATCAGTACCAGCACTCTTGGGGGTCCTGCTTTGATATGTAATTAAATTCTCTTAAATTAACTTTGTGATGTTTTTTAATTGTCAGATCGTGGCAAAGTGGTTGGCGGTCTTCCTGATGTTGTGACTATCATGGAAAAGAAGGTTTGTTTCAGCCATAGCGTTTTGAATAATACATCACAAGCCACACAAAAATGATTTGTGATATAAGTTAGCACTATATTTATTTGTCTATCTGTATATGTGCGCTTGAAATATAAGAGTGTATTTATACAAAACTAATTTA
Associated Phenotype:
Not determined