ZMP
LOC793956
Ensembl ID:
Human Orthologue:
MKL2
Human Description:
MKL/myocardin-like 2 [Source:HGNC Symbol;Acc:29819]
Mouse Orthologue:
Mkl2
Mouse Description:
MKL/myocardin-like 2 Gene [Source:MGI Symbol;Acc:MGI:3050795]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35271 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35272 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44760 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22081 | Nonsense | Available for shipment | Available now |
sa10017 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35271
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127655 | Essential Splice Site | 46 | 986 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 21088579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19870423 |
GRCz11 | 12 | 19992297 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTGCACCCCAGCCAGAGGCTTCCTCCTCTCAATGAGCGCAAAAATGG[T/G]AAGTCTTGCTGAGATGAACTAATCAAAACTGTTGGTTTGAGTCTTCTAAA
Long Flanking Sequence:
CTATTCATTCACCGTCTGTGGAGAGGCTCATTTTTATTATTTGTTGGCGCTGTGATCTATATATGCAACAGCAGCAACTGTATATGCTGTAGATTCAACACATCTTCAGTGTTTATAAAGGCTAAAGTGAAATTACAGACTCCACCACATCCTTGACCTATTACATCATCCCCAAACTCTCCATTTCAACTATGATCGCTAATACACAGCCTGCAAACCTTGGACCAAGTTCCTTTGCTAACTTTTTGCAGACCTGTAATGCATATTAACATTGTCTTTTGCAGAAATTGAAGTGACGAGCTTCCTGTGTCCGCTTCTCCTGCTGATCCCCCAAGAGACCCTTGACTCCTCAACTGAGGAGACATGGAGGAACAGGGGGATGCTGCGATTGGGGGACTGTTGGCACCCAGCCCACAGAGTGAGGCTGTGACCCATGAGATGGGTGAACTGTCCCTGCACCCCAGCCAGAGGCTTCCTCCTCTCAATGAGCGCAAAAATGG[T/G]AAGTCTTGCTGAGATGAACTAATCAAAACTGTTGGTTTGAGTCTTCTAAAGACAGTTGGGATTCACAACATATCATTGGATTATTGGTTACTGGCCACTAAAGAATATGCATTCATAAAAGGGATAGAATCAGAATCTGTTTTATTATGTGCTTCACACACACAAGGAATTTGTTTTGGCTACAGAAGCTTCCAGTGTACATCAAGTGACAACACAAAATAAATGTGAAAAAAGACGATAAACATTAAACAGAGATGCAGTCAGTCAAGAAATCTGGATGTTGAGTTGTATAGATTTGTTATATATAAACAGGTTATAAGGTGCTGTGTACAAATGGGAATGTAGAAAGTATTGCATTGTATATTGATATGGTGTGCTGTGTACAAGTGCGTATGAGAAAGTATTGCACATATTTATTGCACAGTTGGTGGATATTTAACTGTTCATGAGGTTGATGGCCAGAGGAAAATAAACTTTTCCTGTGTCTGGCTGTTTTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35272
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127655 | Nonsense | 181 | 986 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 21114968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19896812 |
GRCz11 | 12 | 20018686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTAGATGGTCAGATGCAGTACCCTAGAACTCTAGAAGATCTAATAGAT[G/T]AAGACAGTGGAGATGCTTTTTCACCAGAGCAGCCAGCCAGTCAGGAGTCC
Long Flanking Sequence:
AACGAATTGTAATATAAGCATTGTAATAAGCAGTAGTTTATGGACCTAATTCTTTTTAGGAAAGAAGTAATGGATTTATAAGTATGAATTTTAAATTCTTATGCATTAAAAAGCTGTTGTTGTTGTTGTTGTTGTAAAAACAAGTGTTGGTTTGGGTGATTGCTGTTCAAATTGTCAATAATTTTTGGTGGTTTGGCAGAGACCTTGGCAGAGCCTTCACTGCAGGCCACCCAGTTGAGACTAAAGAGAGCTCGACTGGCTGATGACCTCAATGAGAAGATTGCACAGCGCCCCGGCCCAATGGAGCTGGTGGAAAAGAACATCCTGCCAGTGGACTCCAGCCTCAAGGAGGCCATAATTGGTGAACATTCACACTATTGTAGCTTAATTACATTGGCGTAAGGGATAAACATTTATGAAATATTGTCATTTGTGTAATTTGTGTTCTTTGTGTAGATGGTCAGATGCAGTACCCTAGAACTCTAGAAGATCTAATAGAT[G/T]AAGACAGTGGAGATGCTTTTTCACCAGAGCAGCCAGCCAGTCAGGAGTCCCAGGGATCTGCAGCCTCACCTGCAGAGGTCAGGACTATGGAGGAGACCTCACCGCTGCCCAATAACTTGCTACAGGTAGTTCTAATTACTTCCTTTGACTTTTGACAGAACATTTAAGCCCAATGTATTCTTTAGGTTTCATACTTTTGTGACGATTTGCATAAATGCATGATGCAAAATTCAGCACCAGCATAGTACTCACATACTGTCCACGCATTGCCTGATTTTTTTAACCAAGTTTACAAAGTAGGGGTCTGTACACTGGTCTTAGAGTTTGGCTTGATTACAATTATAATATCATTGGTACAGTTCAATTCAATACCACAGTGCTTTCCACAAACAAGTTCACCTATGATTGGCCATTGTGTTTACACGTTTAACAGAAACGTCTGTGATTGCACTTGAACAGCGGTGATCAATAGTGCCAAACACAGATACATAAACACTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44760
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127655 | Nonsense | 317 | 986 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 21122220)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19904064 |
GRCz11 | 12 | 20025938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCCAGATCAGAAACAAGAACCCGACCAAGCCCCGATGGACTCCTCGTA[T/A]GCTCGTTTACTACAACAACAGCAGCTATTTTTGCAGCTACAGATCCTGAG
Long Flanking Sequence:
TTTTTACAACAGTTTTCTTTCCGGTTTTGAATTACATTCTCAATGTGAAGACACTCTTTGAATTTCTGTGTGGAATTTGGTCTTTCAATTTTAGCAGAAAGTCTGAAATTCATTGTTTATTTTTTTTCAGCACTTTCCTGCAGTCACCACTACTTCGACAGATTTCCTCAAGCCCTTTTCCACCGTTGAACAATCCGTTAGCCCTCCAGCTCCCATACCACAACTAGTCACAGTAGCCCCTGTGAAGTCGGGGCCCACCCTTGTAAAGGTCAGTAAAGATCTGCCTTCTGTGGCTTCAACAAAAATGTATTAAATTCAATAACTTTAGATGTCAAACCTCTGTTTGATCTACAGCAGAGTCAGCCCAAGTTACCTGGAGACAAGAGCCGCAGCAAGAAGAGCAAGGAGTCCAAGCCACGTGTGAAAAAGTTGAAATATCATCAGTACATTCCCCCAGATCAGAAACAAGAACCCGACCAAGCCCCGATGGACTCCTCGTA[T/A]GCTCGTTTACTACAACAACAGCAGCTATTTTTGCAGCTACAGATCCTGAGCCAACAGCAACAGCAGCACTACAACTACCAGACCATCCTTCCTGCACCTCTCAAGTAAGCAAGAAGATCCGGATCTTGTGTTTAGAACTGCATTGCCAGTTTGGTGGATGCAAACCATTTGGCATTTGTCTTTCTTAATTTGATAAATGTCTTCTTTTGCTTTTGAAGCTCCCCATTAGGATGAGTTTAGTTGACTGCATATGAATGATTTTAGCTGGAAAATGTCTAAACCCTTTTGTTGCCCTGAGGACCATTACCTATTTTCCAATAACAAATCTTGTTTAGAGATTTTTCTTAATGGCAGGAAGTTGATGAGGTTAGTCCTCCGCTTCCTTTTCCATCTTTTATTCTGCATTATTTATTTTCCTACGACGCCTGTTGTTTTCTGCCTCTGCATTGTTTGATCATGTTTATTTATTGAGATTGGGTGAGCGAACGAATAGTTCCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22081
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127655 | Nonsense | 416 | 986 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 21125819)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19907663 |
GRCz11 | 12 | 20029537 |
KASP Assay ID:
2260-5301.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACTAATAATGTGTTTATTTTGGCAGGTGGCAGAGCTGAAAATGGAGT[T/A]GAAGTTGCGTGGTCTTCCAGTATCAGGAACAAAAACTGACCTTATTGAAC
Long Flanking Sequence:
TGATCACTCATGCCCCCACGCATCATTTACCTCTTCACGTGTTGTAATCATCTGCTGATGAGCTCAAGTGTGTCTTCGTCTGTGTGTAAACTCATAAACAAACAGTCGCAATCGGTTCATGAGATCAGCCAGATTGACAAGTACCAATCGAGTCATAAAATGTTATTATCAGCCAATCGAGTGGAGTATCCCTACTATTGACTATTACTTTTAATCAATGAAATGCATCTTTGGTGTGTAAGTTTTCTTTTTTTTTTTTTTTTTTTTCAGAAAAAAAATTGTTAATGTTAAATGTTTATCAGGTGTTGTTTAATGTTAAAAAATAGTGGTGTATAAAACTAAATAAACAAGGAAATAATATTACTCTAAAATTAAGTAAGCATCCTATTCATTAAGTTTGAGTGACATCAATTGTTAGTAATAGACCCAGAAATTACTTTATTTGTTAATTTTACTAATAATGTGTTTATTTTGGCAGGTGGCAGAGCTGAAAATGGAGT[T/A]GAAGTTGCGTGGTCTTCCAGTATCAGGAACAAAAACTGACCTTATTGAACGGCTCAAGCCTTTCCAAGAAAATCCTATCACTACTGCACCCAACAACTCCTCCACAGGACCTAAAACACAGCCCTGCGGTACACCTATGGAAGTTTCCAGCACCACTACAACCATCTCCCCCATCCAACTCCCCTCTAATACTCTGAGTTCCACTCCACCAGTGTCTCCCAGTTCCTCAGAGCTTCTCAGCAGGGAGGACATGTCCGTGGAAGGACAAGCAGAGACTCAAAACCGCTGTTTAATTAAAGCAAATGCTGTTCCTGAGGAACAAGATCGGAGACTGCACGAAAAGGAGCGACAGATTGAGGAATTGCTGCGTAAATTGGAGCAGGAGCAGAAACTGGTGGAAGAACTAAAGATGCAGCTAGAAGTGGAGAAACGAAGTGGAGTTGTTCCATCTGTGGAAAATAACAACGTTTCTGGCCCAAGCATCATGTTGGCATCTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10017
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127655 | Nonsense | 758 | 986 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 21131073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 19912917 |
GRCz11 | 12 | 20034791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTAGCTCCCCAGAGAACAGAACCTCACCTCAGACGTCCCCCATCCCAT[C/A]ATCCCTTATCAATGGACAACTAAACAAGGTAGAACTTTTTGTTTTTATTA
Long Flanking Sequence:
ACTCCACAACTTCAGCCCAGCATTTTAAATAAAGAGATGATTCCATAGACGTTTAATTATTAGTCATGTTGAATCAATGAAAGCAGTTAAATCTTCTGTTTATTCAACAACTGCTGGGGAGTTTGGCGTTTCCTTGTGTGAGAGTGCTCTCTGGCCTTTGGAGAACATTTACTACAGATCACAGAACCATGCTTTCCTGACAAGATGAACATGATAACCACAACAAGTTGCGATTTAATTTTAATTAAATTTTTTTTAATTGTCCTAGTCATGAAATTATGTCACAAAATTGCACCGATGGCTTAGGATAGAAGTGGCTGATTTTGGAGTCTGAAGTTCTTTTGGTTTTCTCTTAACACAGACCCTGTCTGTGGGCACCACTGAGAGGTCAGGTTTCCAGCACAGTACCAGTGAGAACCAGGCAGGCCTGGAGATTCCTCAGTGTTTCCTCAGTAGCTCCCCAGAGAACAGAACCTCACCTCAGACGTCCCCCATCCCAT[C/A]ATCCCTTATCAATGGACAACTAAACAAGGTAGAACTTTTTGTTTTTATTATCTTTGTGGCAATGGTTGTTCTGCATTGAGGCCCCGTATACACTGATATGTTTTACTTTTAAAACGCATAAGTTTTGCTACGGTTACACCTTCCGTCCACACTACCCTGGAGTTTTCCAGCCCTGAAAACAGAGCTTTTTGAAAACGCAAAGAGGCCACTTTTATTTTAAACACTGCTGCTGTGTCAGTGTGGATGGGGGAAAACAAAGACATCGGAAAACAAAGACAAACGGAGGTGCGGCTGCAGATGTTTGACAATCAGATTGGGGCTTTTTCCTCAATATGAAGTACCCAAATTTCAGTCTTGAATTTTTTCCTTAAGTTCTGAATAAATATTGGAAAACAAACTTTTGGGGACACGTTGGGTAAAAACAGTGTAGTTTATAACCTCATTCGCATTACCCTGGCTATGTTGTTATAGTTTCTTAACAATAAAATGAAAACCTGATA
Associated Phenotype:
Not determined