Busch Lab

ZMP

si:dkeyp-69b9.3

Ensembl ID:
ENSDARG00000088881
ZFIN ID:
ZDB-GENE-100922-275
Human Orthologue:
MYOCD
Human Description:
myocardin [Source:HGNC Symbol;Acc:16067]
Mouse Orthologue:
Myocd
Mouse Description:
myocardin Gene [Source:MGI Symbol;Acc:MGI:2137495]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa14150 Nonsense Available for shipment Available now
sa31001 Nonsense Mutation detected in F1 DNA Not yet available
sa42681 Nonsense Mutation detected in F1 DNA Not yet available
sa44842 Nonsense Mutation detected in F1 DNA Not yet available
sa36066 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14150
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
ENSDART00000122111 Nonsense 140 757 6 14
ENSDART00000145410 Nonsense 4 621 1 9
Genomic Location (Zv9):
Chromosome 16 (position 15268157)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 13626616
GRCz11 16 13516736
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATGTCTTTGAAGATGACAACTCCTCTTCTGCCTCTGCATCTCCCGAG[C/T]AACTCGGGATGCACCAATCTCCCGGCTTCTCCTYATCATCACCTGGGCAA
Long Flanking Sequence:
TTGAGAAATACGATCATTTTAGAAGAAAGTTTAAGATGTAACTTGTATCTGAATTCTTTAATTGCTTTTTGTATCGTTATATCAGCTTAGTGTGACTAGTGGTTTAACAGTATCTATATTTTTCGGAGCTTGCAGTGCTCAGACATGCAGCATGGTTGCGGTTTGGGTTACCAAACTTCTAGAATCGTCACCACCCACCACATTTACTCCCCAACCCATCCCTGCTCTCCTCCGTTTTTGCTTTCTGTCAGCTCTTCAACTATCCTGTCTAACTGAAGCCAAAAATAAAACAAAATAAATTCATAGGGGAAAAATAACCTCACAAATATATAAAAAACTTTAGTTGCACATTTTGCACATAACATTTAATCTATAACTAGGGTTGCTGCAGAGAAATTGATACATTTCACCATTTCACCATTTCCTTTGCCTCAGCTGCTTTATTGCCATCAGATGTCTTTGAAGATGACAACTCCTCTTCTGCCTCTGCATCTCCCGAG[C/T]AACTCGGGATGCACCAATCTCCCGGCTTCTCCTCATCATCACCTGGGCAAGGAGGTGACCAATCACTGAGTGATGTGTCACCTGTTGCTACGCCTATCAGTCCAAACAATGTACAGGTATAATGGGCATATAACACCTACACAGTTTTAAAACTAAGTCTATCAATTTAATTTGTCCTTTTATTCTCTTTTATTCAAAATTAAACTGTTTAATTAAAAAAAAAGTGGTCACACTTTTTAATGGTACAGTTCTCACTAATAATAAAACATTAACTATGCCTTTTTAGCTCAATAAACTCTTAATTGGCTTCTTTTTATTCGTTAATAAGGTAGCTATGTTTATGTATTTGGTAGGCCTGAGAATTTAAAATAATATAATGCAGAATATGTACTTTATAAGAATTAATCATAACCCCAAAAGAATCATTCTTCTTTAATTTAAGTACTGAAGCAAATAAAATAGCCTCTGTTTTACCTAGGTATAAAGAAAGTGTATTACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31001
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
ENSDART00000122111 Nonsense 314 757 8 14
ENSDART00000145410 Nonsense 178 621 3 9
ENSDART00000122111 Nonsense 314 757 8 14
ENSDART00000145410 Nonsense 178 621 3 9
Genomic Location (Zv9):
Chromosome 16 (position 15265456)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 13623915
GRCz11 16 13514035
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCCTCATACTCGCACCTCTTGCAACAACAGCAGGTGTTCTTACAACTA[C/T]AAATTCTCAACCAGCAACAACAACTCCCTGTGACAAACAGGTAATCCTCC
Long Flanking Sequence:
CATCAGCCAACCAATGACCATGACAGTAACGGGGTCAAACTCCATAACAACTGGGAGACCCAAAGGGATGTACATGCCCTCCCAGACACCACCACTGCTGCCAAAGGTACAGAGAATTAAAATAATGATTTGTTTTGCTTCTCGCCCCATTTCATCCTTCATTATTTCTCTCATCTACTAGATAATGTCATTTTTCCAAATTATGTTAATCACATTTTCGCTTTGTTTGCCTCAAGACCGCACAGCCTCCAGCTCCACCTTCTCATTCCATTCTGGGTGGGTCCTTAAATTCATCCCGCCCTTCACGACCACGGAAACCTCGCGATTCAAAGCCTAAAATGAGGAAACTGAAATACCATCAGTACATTCCTCCAGATCAAAGGACTGGGACTGGAAGCGGAGCTGCAAATGCTTCACAAAAAAATAACAACAGTCAGGTTCCGGCCACTGATTCCTCATACTCGCACCTCTTGCAACAACAGCAGGTGTTCTTACAACTA[C/T]AAATTCTCAACCAGCAACAACAACTCCCTGTGACAAACAGGTAATCCTCCAAACAAAACACTCATGGAAAAATGCATGATTTGTACAGCTAAAGCCCTGTGCATGCTCTATGATTGGTATTATTTTCACATTTTCCTACAATATAACTGAAATTCTAAATAAAATCCAGAATCACTATTTTATGTCAGCCTTACCGTGAAAAATATTTGGATTAGGTGGCAGCATAGAGTAAAAAGCAAGAACGTAAAATCCTCATATACAGTTTGGAAGCTGTAGTTCTCACTTGTATCAACCTGCATCACCTTTCCCCAATTCCAAATGAGAAAAGTAGAGTAATGTAATCTAGCATTAAATGAATAAAGGCCAACTGATATGTGCAATCTTTTGTGATTCTGAAATTTCTCTCAGCAAAATCACAGCCAAAATTGTATTCTTGCTACTCCTACCCCTTTTACACCAAGGTAGTTTAAGTGCTGGTTTACAGCCAGAACCTTGCTCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42681
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
ENSDART00000122111 Nonsense 314 757 8 14
ENSDART00000145410 Nonsense 178 621 3 9
ENSDART00000122111 Nonsense 314 757 8 14
ENSDART00000145410 Nonsense 178 621 3 9
Genomic Location (Zv9):
Chromosome 16 (position 15265456)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 13623915
GRCz11 16 13514035
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCCTCATACTCGCACCTCTTGCAACAACAGCAGGTGTTCTTACAACTA[C/T]AAATTCTCAACCAGCAACAACAACTCCCTGTGACAAACAGGTAATCCTCC
Long Flanking Sequence:
CATCAGCCAACCAATGACCATGACAGTAACGGGGTCAAACTCCATAACAACTGGGAGACCCAAAGGGATGTACATGCCCTCCCAGACACCACCACTGCTGCCAAAGGTACAGAGAATTAAAATAATGATTTGTTTTGCTTCTCGCCCCATTTCATCCTTCATTATTTCTCTCATCTACTAGATAATGTCATTTTTCCAAATTATGTTAATCACATTTTCGCTTTGTTTGCCTCAAGACCGCACAGCCTCCAGCTCCACCTTCTCATTCCATTCTGGGTGGGTCCTTAAATTCATCCCGCCCTTCACGACCACGGAAACCTCGCGATTCAAAGCCTAAAATGAGGAAACTGAAATACCATCAGTACATTCCTCCAGATCAAAGGACTGGGACTGGAAGCGGAGCTGCAAATGCTTCACAAAAAAATAACAACAGTCAGGTTCCGGCCACTGATTCCTCATACTCGCACCTCTTGCAACAACAGCAGGTGTTCTTACAACTA[C/T]AAATTCTCAACCAGCAACAACAACTCCCTGTGACAAACAGGTAATCCTCCAAACAAAACACTCATGGAAAAATGCATGATTTGTACAGCTAAAGCCCTGTGCATGCTCTATGATTGGTATTATTTTCACATTTTCCTACAATATAACTGAAATTCTAAATAAAATCCAGAATCACTATTTTATGTCAGCCTTACCGTGAAAAATATTTGGATTAGGTGGCAGCATAGAGTAAAAAGCAAGAACGTAAAATCCTCATATACAGTTTGGAAGCTGTAGTTCTCACTTGTATCAACCTGCATCACCTTTCCCCAATTCCAAATGAGAAAAGTAGAGTAATGTAATCTAGCATTAAATGAATAAAGGCCAACTGATATGTGCAATCTTTTGTGATTCTGAAATTTCTCTCAGCAAAATCACAGCCAAAATTGTATTCTTGCTACTCCTACCCCTTTTACACCAAGGTAGTTTAAGTGCTGGTTTACAGCCAGAACCTTGCTCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44842
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122111 Nonsense 556 757 12 14
ENSDART00000145410 Nonsense 420 621 7 9
Genomic Location (Zv9):
Chromosome 16 (position 15261060)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 13619519
GRCz11 16 13509639
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATACATTTCTTTCTTTATTGTTATTCTTAATATTAGGTAAACTGCTG[T/A]CAGCTTTGTGATGCAATTGGGCAGGACTTTGATTTGCCAATGCAAATCAC
Long Flanking Sequence:
TCAAAGCTCGAACCATCAACCGTCCAGCTGTGAGGTGAACTACTACCCACTGCGCCAATGTGCAGCCCTGAATAAGACTATAATATGATTAAACATCACCACATGACACTATCCAATGTTTCCTTTAAAGTTTCACTCATCATAATTCATGTTCGTAAAGGGTACTATATGAATTTAGTATGTTTTATTTTTAGTTTATCGACACTTGAACTGCAGTTCATTTATTTAAATGAGCAAACAAATGGTGACAGATATAAATTCTCCAGCAACAGGCCTTCTCTGCTCTTTAATGGGACATATAGAGGACTACTGCACATGTCTTAATTTAATTTGTTTACTTTGATATTGACTTTTTAACTGGATCAAAGTAATCTAAAATCTGATTACATATTAGATTCTTAATCAGAGCATTATCCTAATCATATTAATGTCCACTGAAACATACTTATTGAGATACATTTCTTTCTTTATTGTTATTCTTAATATTAGGTAAACTGCTG[T/A]CAGCTTTGTGATGCAATTGGGCAGGACTTTGATTTGCCAATGCAAATCACTGCCAGTCCAGCACAAGCATCACCCACTGTCCGCAGTTTGGAAGAGGAACTACAGGAGGCCATTCAAAGAGTGCAGGTGAGTGTTTACGAGTTTATGTGCCGTCTGCTGTTGACAATTCCTTCAATATGCAACTATTGATGAATTGATCGCTGTTCATTAACAATGAGCACTGACGTTCAACTTCCTGTCCACTCTTCTTTCACCATGTAAGATGGACCCTTCTCAATCCATAGATGACATTTTGGATGTGAATATTGGTGGTTCAGGTAAGTAAAACTTGACTAGTGGATTAAAATTTAAGAGTATTTCTGAAAATTATCTGAAGAGAGACAGCAATTATGACATTTTTAAAATCACTGACAGCTGGTTGTGGATGACAAATAGGTTAAGATTAGGGGTGTGACGAGACGCATATCAACCCGAGGTAGGGCATGAGACTGGGTTCACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36066
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122111 Essential Splice Site 617 757 None 14
ENSDART00000145410 Essential Splice Site 481 621 None 9
Genomic Location (Zv9):
Chromosome 16 (position 15257801)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 13616260
GRCz11 16 13506380
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACATCTTTAACACTGAATTCACCATTAAATTATTTTGTTATCTTTTC[A/T]GATAACTCTTCGCTCGTCACAGACATCCAATCAGCCGCTCTCGTCGTCTC
Long Flanking Sequence:
AATCTGCCAATGGGGTAAGCAAAATAATCTAGTTTTTCCTTTTGACTTCAGATAATTTAGCTTTCCTCATTGGCAGATTATTTTGCTTGTTTTAGGGAAATACTCACTTAATTTTAACATATTATTTCTTAAAACAAGACAATATGTTTTGCTTGTCCAGAAAATGCTTCTTAGTTTAGAAGTTTTTAGATATTTGGACTAGAATCAAAACAAAAAAGTAAGGAAAGTATTGTTTGCAGTGCCTGCTCTCCTGACGCAAGCGGTTCTGACGCAAGCGGTTACTTCTAGCCCAGCAGTGTTTTACTGCTACTTAAGAATCACTTTTCCAAGTTCATATTGGCTATTTTGACTGTCAAAGAAAAGTAACCGATTTGGAACTGATTTCACACCAATCTCAGCCAGATATCATGAGGCTCATCAGATTTCCTCACACCCATACTTAAGATCCATCAAACATCTTTAACACTGAATTCACCATTAAATTATTTTGTTATCTTTTC[A/T]GATAACTCTTCGCTCGTCACAGACATCCAATCAGCCGCTCTCGTCGTCTCAGGCTTCTCCTCTGCCCTACAGCCTGACCAATCACAGTCCACCAAGCGGCAAAAAGATGACAACTTCCTGTCGTCTCCTTTATGCTCTTCGCTTCTTTTAGAGCTTCCTCCCTCACCTAACAACACTTCAGCCCTCTGTCCGACCCCAGCTCCGCTTCCCCCTCCCCCCATCTGCACCACTCCACCATCAACCTCCCTGTCCAGGAAAAGAAGGTCAGAGGTCCCCGCTTTTGACCCCGCTGATTGGCTGGAGACCTTGACCTCTGGTCTGCATCCACTAACGCCCCCTGCCGCCCCGTTTCTTGAGAGCGACTTTGGCCTCGACTCGGACCTAAACGTCAACAGGGTCCTGGATCTGATGGTGGAGCAATGGTGAAGAAGGGGGCGTAGTGTGTCTGTATGTGCTTGTGGCTAATTGGATGCATGATTGGAAATGAAGCACCTTTCAAA
Associated Phenotype:
Not determined