ZMP
mybpc2a
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC751793 [Source:RefSeq peptide;Acc:NP_001039324]
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 |
---|---|---|---|
sa20031 | Essential Splice Site | Available for shipment | Available now |
sa31336 | Nonsense | Available for shipment | Available now |
sa10086 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20031
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103457 | Essential Splice Site | 111 | 822 | 8 | 26 |
ENSDART00000103461 | Essential Splice Site | 100 | 1120 | 6 | 29 |
ENSDART00000121883 | Essential Splice Site | 100 | 1120 | 6 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30442661)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30160700 |
GRCz11 | 3 | 30291542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGACTTGTTCTCTAGAGCTGAGAGTTACCATTTATATTTCTCTGTCGC[A/G]GATTTACACCTATGAGATGACCATCGTTAAGGTCGTGGATGGAGATGCTG
Long Flanking Sequence:
CCCTTCAATCCCTATGGATGTTTCCCAGTATTGGTAAACATCCATAGACTCTCACATTTACAAACGCACTCATACACTATGGACAATTTAGTTTATTCTATTTACTTACACCGCATGTCTTTGGACTGTGTGGGAAACCGAAGTACCCAGAGGAAACCCATACAAACATGTGGAGAACATGCAAATGCCACACAGAATTGCCAACTGACCCACAAGACCCAGCCAGTAATAATTATTTAGTTTAGCATTATTTAATTTTTATTTTGGTTTATAGGGAAGGATGTCACATTTGTGGCTAAGGTGGACTCCTCTCAGATGTTAAGAAAGCCAGCCGTTAAGTGGTTTAAGGGGAAATGGCTGGATCTGGCCAGCAAGGCTGGAAAACACTTGCAGTTCAAAGAAACCTATGACAGGAACACAAAGGTGAGTAAAGGAAAGTTGTCCTCGATTAGGGACTTGTTCTCTAGAGCTGAGAGTTACCATTTATATTTCTCTGTCGC[A/G]GATTTACACCTATGAGATGACCATCGTTAAGGTCGTGGATGGAGATGCTGGAGGTTATCGCTGTGAGGTCACGTCCAAAGACAAGTGTGACACCAGCGCATTTGATGTTACTGTCGAAGGTAAGAATTCAGGCAGTTATAAAGTGGCTCAACATTGAAGTTATCAGTGCCAGCTTGAGATCCCTGATGCATAGGACATTTAAAATGCACAAAATGTAGCCTTAGATGTCTAAAGTTAACACGCATCTGGCGTGCGTGCGCACTTTGCTGCAATCTACAGCTGATTCATTATTCAGTAGGTATTTAGCTGATTAGATCGTCTGCCGCACTTAGTAAATCAGCACTACACATTTATTGGCTTTGACAGTAATCAGATTGTGGAGCAAATCAAACACTCACAGTTTCTCATCATCATCACGCATTTCATCTTCTCCTTCAGCTGCTGAGGAGACACAGCAAACAAACATTTTGGAGGCGTTCAAGCGATCGTAAGTTTGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31336
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103457 | Nonsense | 365 | 822 | 15 | 26 |
ENSDART00000103461 | Nonsense | 369 | 1120 | 13 | 29 |
ENSDART00000121883 | Nonsense | 369 | 1120 | 13 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30453969)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30172008 |
GRCz11 | 3 | 30302850 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGGATGAAGGATGGTGTGGAACTGAGCCGAGATGGAAAGTATCGCTTT[A/T]AGAAAGATGGGACAAAGCACTGGCTCATCATCAATGAAGCAACCACAGAG
Long Flanking Sequence:
CTGATGAGTGTGTATAGGTGTTTCCCTGTACTGGGTTGCAGCTTGAAGGGCATCCGCTGCATCAAACATATTTTGGGATAGTTGGAGGTTGATTTCGTTGTGGCGACCCCTAATAAATAAGGTACTAAGCTGAAGGAAAATGAATGAATGAATTATTTTGTCTCCAGTAGAATCCAGCCTCTTAAGTATCTTAAGGATCCTAGTTTAGTTCTAAACTGATCCATCCCTAAAGTGTTTTCCTGTATCAAAGACCTGCACAGACTTTCCTCTCTCTGGCTTTGCCTCTTTCTGTCATGTCCCATTTTGTCCATCCTTGTTCCCTTTCTACGGGTCCCAGTCATTCTTTTATCTTCCTTCATCTTGGAGTAGATTGCCTTCCTCAGTTTCTTCTTATGAACATTTTTTCCAACTTAGTCTCTCTCTGTCTCGCTCTCCCTCTCTTCATCTCTCTCAGGATGAAGGATGGTGTGGAACTGAGCCGAGATGGAAAGTATCGCTTT[A/T]AGAAAGATGGGACAAAGCACTGGCTCATCATCAATGAAGCAACCACAGAGGACATCGGGACATACTATGTGTACACCAGCGGAGGGGAGTCCAAGGCAGAGCTTGAAGTGGAAGGTACTTCTTTCAAAAGAATAAAGTGACAGCTCTCCCTTCTGCCAGTTGGCCGATATTTCAGTATTATTTCTGTGCTTATTTTTAGAATCAGTTGCCTCATTGTCCTTTTGTTTTGTTCTATAGAGAGAGAACTGGAAGTTTTGCAAAGTATAGCTGATCTGACAGTGAAGGCAGCAGAACAGGCCGTCTTCAAATGTGAAGTTTCTGATGAGAAAGTGACTGGCAAGTGGTTCAAGGATGGGGTTGAGGTTGTCGCCAGTGACCGCATCAAAATGTCACACATTGGCAGGTATATCAATCCGCTTGCTTATCGATTGATGCATAAGCAAGCTCACTTCATCCTTGACCTCGCGAATATTGTTTTATACCAGGACCCTAAAACCGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10086
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103457 | Nonsense | 438 | 822 | 16 | 26 |
ENSDART00000103461 | Nonsense | 442 | 1120 | 14 | 29 |
ENSDART00000121883 | Nonsense | 442 | 1120 | 14 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30454313)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30172352 |
GRCz11 | 3 | 30303194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGCCGTCTTCAAATGTGAAGTTTCTGATGAGAAAGTGACTGGCAAGTG[G/A]TTCAAGGATGGGGTTGAGGTTGTCGCCAGTGACCGCATCAAAATGTCACA
Long Flanking Sequence:
TTTATCTTCCTTCATCTTGGAGTAGATTGCCTTCCTCAGTTTCTTCTTATGAACATTTTTTCCAACTTAGTCTCTCTCTGTCTCGCTCTCCCTCTCTTCATCTCTCTCAGGATGAAGGATGGTGTGGAACTGAGCCGAGATGGAAAGTATCGCTTTAAGAAAGATGGGACAAAGCACTGGCTCATCATCAATGAAGCAACCACAGAGGACATCGGGACATACTATGTGTACACCAGCGGAGGGGAGTCCAAGGCAGAGCTTGAAGTGGAAGGTACTTCTTTCAAAAGAATAAAGTGACAGCTCTCCCTTCTGCCAGTTGGCCGATATTTCAGTATTATTTCTGTGCTTATTTTTAGAATCAGTTGCCTCATTGTCCTTTTGTTTTGTTCTATAGAGAGAGAACTGGAAGTTTTGCAAAGTATAGCTGATCTGACAGTGAAGGCAGCAGAACAGGCCGTCTTCAAATGTGAAGTTTCTGATGAGAAAGTGACTGGCAAGTG[G/A]TTCAAGGATGGGGTTGAGGTTGTCGCCAGTGACCGCATCAAAATGTCACACATTGGCAGGTATATCAATCCGCTTGCTTATCGATTGATGCATAAGCAAGCTCACTTCATCCTTGACCTCGCGAATATTGTTTTATACCAGGACCCTAAAACCGATTAGTCATCAAAAATGTCAGCTATGCTCTTTTGTTTTCTTTCAGTAACATTTATTGATTTTTCTTGGCTACACTTCTTGTATTGTGGTAACATTAGATCTCACTCACCAAGCATGTGTATGAAAAATTAAACTATACAAATTTAAATTGGAACAGCCAAAACCACATGTGTTGGGGTGCTTAAAGGAATGGCTGAGAAGAAAGCCTTAATATGGAAATGGTTTAGGGCGTCTTTTATGCAAACAGACAATTTTGTGCAGATGGCCACTCATTTACAATACTTCAAATTCATTATTAAACAGAAACAAGCATGCTAGTGTTGTGCATACACATGTTAAGCAAAGAA
Associated Phenotype:
Not determined