Busch Lab

ZMP

mybpc2b

Ensembl ID:
ENSDARG00000021265
ZFIN ID:
ZDB-GENE-050320-80
Description:
myosin-binding protein C, fast-type [Source:RefSeq peptide;Acc:NP_001013529]
Human Orthologue:
MYBPC2
Human Description:
myosin binding protein C, fast type [Source:HGNC Symbol;Acc:7550]
Mouse Orthologue:
Mybpc2
Mouse Description:
myosin binding protein C, fast-type Gene [Source:MGI Symbol;Acc:MGI:1336170]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa10810 Nonsense Available for shipment Available now
sa19351 Nonsense Mutation detected in F1 DNA Not yet available
sa37954 Nonsense Mutation detected in F1 DNA Not yet available
sa24551 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa10810
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
ENSDART00000105672 Nonsense 259 1111 10 29
ENSDART00000143184 Nonsense 240 1092 7 26
ENSDART00000105672 Nonsense 259 1111 10 29
ENSDART00000143184 Nonsense 240 1092 7 26
Genomic Location (Zv9):
Chromosome 24 (position 39813470)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 38431605
GRCz11 24 38319476
KASP Assay ID:
554-6218.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTGGAGGTGGCAGATCCTAATGCCGAGGTCAAATGGCTGAGGAACGGA[C/T]AAGAGATCAAACCCTCTGCCAAGTAATAATGCAAATAATRTRTTCAAATG
Long Flanking Sequence:
TTTTAAACCATTTCAAGGTCAATATTATTAGCCCCCTTAAGCAATATTTGTTTTTCGATTGCTTTAGAACAAACCAATGTTATACAATGACTTGGCTAATTACTTTAACTTGCCAAATTAACCTAATTAAGCCTTTAAATGTCACTTTAAGCTGATTACTAGTATCCTGAAAAATATCTAGTTGAATATTATTAACTGTCATCATAGCAAAGATAAAATAAATCAGTTATTAGAGATGAGCTATTAAAACTATTATGATTAGAAAATCATTTTTGCGTTAAACGGAAATTGGGGAAGAATATACAGGAAGGCAAATAATTCTGACTTCAAATGTAAGCACGCAAGTCTTCTGTTTGTGATCGTGTGTGTAAATGTGGGATGTTTCTGCAGCTTTCCTGAGGCGTTTGGAGTCAGCGTACTCTGTTAATAAGGGAAAGAAGATCGTCATGTCTGTGGAGGTGGCAGATCCTAATGCCGAGGTCAAATGGCTGAGGAACGGA[C/T]AAGAGATCAAACCCTCTGCCAAGTAATAATGCAAATAATGTGTTCAAATGAATTCAGCTTTAGTGTGAAATGGATGAGAAATGCTCATTTGGGGAAAATCTTTTTTAAAGTTTGCATGAACCTGAATCTGGAACTGCTTTTTTTGCGTATGGTATGAATTAAACCGTGAGCTAACTGTATTGTTGCATCCCTATTAATTAAATAAACAGTGGGCGTGGCTTGTTTTTTTTCTGCTAGCTGATTGGATATTGTAAAGTAGGCGTTTCATTCAAACTAACAGACTCCTTCTGCTCACCATTTCTGTTTGCTGTCAAAACTGACAGCTGTTGGGGGTGTGGTTAAGTGTGTTAGCCACGTGGTTCATGTGACTTTAATATTGTAAGAAGGCATCCATCAGATATTTCTATGATTTACTCTGTCTTCTCTGTGTAATATATGACAGGTACATCATGGAGGCCGATGGAAACATTCGAACCCTGACAATCAACAAATGCAGTCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19351
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105672 Nonsense 259 1111 10 29
ENSDART00000143184 Nonsense 240 1092 7 26
ENSDART00000105672 Nonsense 259 1111 10 29
ENSDART00000143184 Nonsense 240 1092 7 26
Genomic Location (Zv9):
Chromosome 24 (position 39813470)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 38431605
GRCz11 24 38319476
KASP Assay ID:
554-6218.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGGAGGTGGCAGATCCTAATGCCGAGGTCAAATGGCTGAGGAACGGA[C/T]AAGAGATCAAACCCTCTGCCAAGTAATAATGCAAATAATGTGTTCAAATG
Long Flanking Sequence:
TTTTAAACCATTTCAAGGTCAATATTATTAGCCCCCTTAAGCAATATTTGTTTTTCGATTGCTTTAGAACAAACCAATGTTATACAATGACTTGGCTAATTACTTTAACTTGCCAAATTAACCTAATTAAGCCTTTAAATGTCACTTTAAGCTGATTACTAGTATCCTGAAAAATATCTAGTTGAATATTATTAACTGTCATCATAGCAAAGATAAAATAAATCAGTTATTAGAGATGAGCTATTAAAACTATTATGATTAGAAAATCATTTTTGCGTTAAACGGAAATTGGGGAAGAATATACAGGAAGGCAAATAATTCTGACTTCAAATGTAAGCACGCAAGTCTTCTGTTTGTGATCGTGTGTGTAAATGTGGGATGTTTCTGCAGCTTTCCTGAGGCGTTTGGAGTCAGCGTACTCTGTTAATAAGGGAAAGAAGATCGTCATGTCTGTGGAGGTGGCAGATCCTAATGCCGAGGTCAAATGGCTGAGGAACGGA[C/T]AAGAGATCAAACCCTCTGCCAAGTAATAATGCAAATAATGTGTTCAAATGAATTCAGCTTTAGTGTGAAATGGATGAGAAATGCTCATTTGGGGAAAATCTTTTTTAAAGTTTGCATGAACCTGAATCTGGAACTGCTTTTTTTGCGTATGGTATGAATTAAACCGTGAGCTAACTGTATTGTTGCATCCCTATTAATTAAATAAACAGTGGGCGTGGCTTGTTTTTTTTCTGCTAGCTGATTGGATATTGTAAAGTAGGCGTTTCATTCAAACTAACAGACTCCTTCTGCTCACCATTTCTGTTTGCTGTCAAAACTGACAGCTGTTGGGGGTGTGGTTAAGTGTGTTAGCCACGTGGTTCATGTGACTTTAATATTGTAAGAAGGCATCCATCAGATATTTCTATGATTTACTCTGTCTTCTCTGTGTAATATATGACAGGTACATCATGGAGGCCGATGGAAACATTCGAACCCTGACAATCAACAAATGCAGTCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37954
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105672 Nonsense 291 1111 11 29
ENSDART00000143184 Nonsense 272 1092 8 26
Genomic Location (Zv9):
Chromosome 24 (position 39813988)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 38432123
GRCz11 24 38319994
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCGAACCCTGACAATCAACAAATGCAGTCTGGCAGATGATGCTGCGTA[T/G]GAATGCGTGGTCGGGACTGATAAATGCTTCACTGAAGTTTTTGTTAAAGG
Long Flanking Sequence:
GCCAAGTAATAATGCAAATAATGTGTTCAAATGAATTCAGCTTTAGTGTGAAATGGATGAGAAATGCTCATTTGGGGAAAATCTTTTTTAAAGTTTGCATGAACCTGAATCTGGAACTGCTTTTTTTGCGTATGGTATGAATTAAACCGTGAGCTAACTGTATTGTTGCATCCCTATTAATTAAATAAACAGTGGGCGTGGCTTGTTTTTTTTCTGCTAGCTGATTGGATATTGTAAAGTAGGCGTTTCATTCAAACTAACAGACTCCTTCTGCTCACCATTTCTGTTTGCTGTCAAAACTGACAGCTGTTGGGGGTGTGGTTAAGTGTGTTAGCCACGTGGTTCATGTGACTTTAATATTGTAAGAAGGCATCCATCAGATATTTCTATGATTTACTCTGTCTTCTCTGTGTAATATATGACAGGTACATCATGGAGGCCGATGGAAACATTCGAACCCTGACAATCAACAAATGCAGTCTGGCAGATGATGCTGCGTA[T/G]GAATGCGTGGTCGGGACTGATAAATGCTTCACTGAAGTTTTTGTTAAAGGTGTGTGCAAATTAATTAACATTTATTTCCTTTTAAACTGACCTTTTCTTTCCCATCAAAACTCAGCTTATCTGTAGAGGTGTCACCTAACTCCACCACTTAAACCATTCACTAACTATTTACAACCTAAAACAAACCCAAATCTTTCAAAGCAAAAGATTGATCATGTCTTTTTTAAGTGAATTAGTATCAAATTCATTCTAAAGCTTTATAGTTTCTCACAATAAACCTAAAGTTAACTGTAAAACTCATCTGATGGTTCTGACATTATTGTTTTGTTATTATGTTGTTTAATATATTGTTTAATTGACCATATTTAATTTGTGCATTGCAGAACCACCAATCACCATCACTAAACTTCTGGATGATTATCATGTCGTGGTTGGAGAACGAGTGGAGTTTGAGATTGAAGTGTCTGAGGAGGGAGCTCACGTCATTTGGTAAACAATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24551
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105672 Nonsense 638 1111 20 29
ENSDART00000143184 Nonsense 619 1092 17 26
Genomic Location (Zv9):
Chromosome 24 (position 39824971)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 38443106
GRCz11 24 38330977
KASP Assay ID:
2261-9041.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATGTGAATGAGAAAGTTGAATCAGTTCTGCTTGTGTTTTCCAGGCTA[T/A]CTGATGGAGAGGAAGAAGAAAGGATCATCTAGATGGACGAAACTGAACTT
Long Flanking Sequence:
AGCAACGCGCCAGCGGTCCGCCTCAGAACGCCTTCCTTTTTAGACCAGAACGCCTATGGGCGCACAAATGAGCGCTAATGCATTTGCTATTTAAACAGCGCAGCGCAACGCCTCAAAACGACTCTTGCGCCAAGCTGAAACTACCAAAAGACTACTGCGCTGCGCCTTGCGCCACACTGCGCCGGGTGTATGATAGGGCGTCTAAAGAAGTGAGTTTTTGGGAGCCTGAATTTTTCTAAGAGATAGGAAAAGGTTACACAAGTGTTCTCATAAAAAAAAAAGATCATTATTATTTAAAATTCGTCCTCTAAAACATAATACAAATGCTCCATGAATGTTTTTTTTAATGGAATACATTTTTTTAATGCTCCAGCTAAGGAGACACGAAAATAAAACGAATAAAGTTTAGACGTACTCTATTGTGAAATAATGAGGAAAAATGTTGATTGCATTATGTGAATGAGAAAGTTGAATCAGTTCTGCTTGTGTTTTCCAGGCTA[T/A]CTGATGGAGAGGAAGAAGAAAGGATCATCTAGATGGACGAAACTGAACTTTGACGTCTACGAGAGCACCACATACGAGGCCAAGCGCATGATTGAGGGCATCTTGTATGAAATGAGGGTGTTTGCTGTCAACGGCATCGGCATTTCAGCTCCCAGCCTCAACTCGAAACCGTTCATGCCGATTGGTGAGAACACTGGACTGTTTCTTTATTTAACACATTTATAAGCTTGGTTTCCATCCACCTGTTCGCAGTGTGGGTAGAGTATCCATAATCTGTACTGTAGGATAAGTACAAGTATTGGAGAGATATTATATACTTGTGAATTGCTTTATGGTATGTTGATCTCTGTTCTGTCCACTTTTGGTGTTGAGAATTCAACTCTACAATTTAACAACGTGACTTTTATTGACATTTTAGTAGTTTGAAATGATATAATGTATAAGAAATAAGCCTGCAAAATAACAGGAAATGTGCTGGCAGTTTATTAAAGGTTTTTGTA
Associated Phenotype:
Not determined