ZMP
im:7136778
Ensembl ID:
ZFIN ID:
Human Orthologue:
MAPK13
Human Description:
mitogen-activated protein kinase 13 [Source:HGNC Symbol;Acc:6875]
Mouse Orthologue:
Mapk13
Mouse Description:
mitogen-activated protein kinase 13 Gene [Source:MGI Symbol;Acc:MGI:1346864]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9763 | Essential Splice Site | Available for shipment | Available now |
| sa34327 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9763
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081341 | Essential Splice Site | 146 | 362 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 11865759)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 10803365 |
| GRCz11 | 8 | 10841070 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTGTCTCCACTCCACAGTACATTCATGGCGCTGGCATCATTCACAGAG[T/C]AAGTGAGACTGGCAGTGAATAAACAGCATCTGCTCAKAATTATCATTTCC
Long Flanking Sequence:
GCAAGTAATTTGACTGAATTATGCAGTTTTTATTCCTAGTCATTTCTCCCATAGGCAGCAGAATCAGAAGTACTCAATCGAAAAAACGAACGCACTTCCACATCGAAGAATAAGGTCAATAATGTGAGCTCGCACATTGTTTTAACAACAATTACAGTATTGTTGAAAATAAAATTGCACAACCCTATATTAGTACACAAATTGTGCTTCAGATTGCATTCACTAACATGCACAGGCTTAGAAAAGTTGGATTCAGAACACGCATACAATATTATCCTGATGCTGAAACTGCATAAGAATGCATAAAAACAGAAGTGTCTTTTAGGCTTAAGATGTTTGCCAGTGGGAATGGTAATGCAATCTCTTAAGTTAATCCTTATTTGTGTAATACTAAAACATAAGACTGTGAGGAATAATCCTGATATTTCTTCTTTCTCTCTCTGTCCCTCTGTTTGTCTCCACTCCACAGTACATTCATGGCGCTGGCATCATTCACAGAG[T/C]AAGTGAGACTGGCAGTGAATAAACAGCATCTGCTCATAATTATCATTTCCACACAGAGCTGAATTAAAGACACATGGCATCTCTTGGGATCGCTGTAGCTTTTGCGCCGGGAGATGCAAATCTGGTCCATGGGGGAGTTTTCATCTCCACGAATTACATTTACTAATTCGCTAATATGCATTAATCAGTAGACCATCAGCAGCCATAAAAGATTAGATAGAGCAGTCACCCCTAAGTATAATTTTGTTATTTATTTTTCTTAATATATGAACTATTTTTCAACAGCTTAGATGCAGTTCTTCTAGTTGATTTTATATAATAAGGATTAAACAAGGTGGCATGGTGGCTAGCACCCTCACCACACAGCAAGGAGATTGCTGGTTCGAGCCCCGACTGGGCCAGTTGGTGGTTCTGTATGGAGTTTGCTTGTTTTCCCCGTGTTCATGTGGGGTTTTTTCGGGTGCTACAGTGTGTCACACAGTCCAAAGACATGCGGTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34327
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081341 | Nonsense | 231 | 362 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 11854674)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 10814450 |
| GRCz11 | 8 | 10852155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCATGCATTGTCTTTAACTTCTGACATTCAGACATGGATCAGCTGACT[C/T]AGATAATGAAAGTTGCAGGAACACCAGGCCCAGAATTCGTGGAGAAGCTG
Long Flanking Sequence:
AAGCTTTTCCAACTTTAAAAAATGCATGATTTACACAAGCCATTGAAATGTAGTTGGAGGCTTTTTTGATTTCCAGTGACGTAGAATATGATGCCAAGCTAAAAATGAGGTAAAGGCCAAAATATCAAGTTGTTTAGAATTTAACTGGGACCAAATCTTTGGAATCCCAAAAATGGCTACATCAGGGGATGGGTCTGTATTTACTGTATTTGCAACAGCTTAGAAAAATTTGTAGCACCGTGGTGATTTGAACCCTGGTCTCCTGTGAGCAGTTTAGCTCTCACATCATGAGCACTGACCACTAGGTCACCTGGAACTCACAGCTTAAGTCTATTTAACTGATTGTATTTTAATTACACTACAACATCGATGCTGTAAAAGAAACCTTATGAAGAAAAAAATAGTCACATTAACCTTTCATTGGAAGTTTATCATGTGCATGTAGCCTATTGCCATGCATTGTCTTTAACTTCTGACATTCAGACATGGATCAGCTGACT[C/T]AGATAATGAAAGTTGCAGGAACACCAGGCCCAGAATTCGTGGAGAAGCTGGAAAGCCCAGAGGTGAGACATTTTCATTGCAAGCAAAGATAGTATCTTTAATACATGGAGTGTCTGAAACTTGATTAAAGCCAAGACTGATCTCTGATGTTACTTGGAATGAATAGCTAATGCGATGCAAAATAAGATTGTGAAAGTAATTTTGGTCTTGACTATTTTGGAGAAAAGTTGAGCTTGAATTATTAACATCGTGTGACGGTTGCTGTTGCTTCTGTTCAGCTGTCATCCCTCATCCTGATCAATGTCAATGTGTCTTGGCTGCTGTTAAATAGGCAAAGAGTTATGTCAGATCCCTGCCCCACTACCCACACAGAGATTTCTCCACATTGTTTCCCAGAGCTAGTAAAAAAGGTAAGTAATACCCCAATGAAAAATTACTCCTTTGTCATGTTGTCACATTTCTTGCTTAGCGCGAGACTTTTTTCATTGTAAAACTTGTGA
Associated Phenotype:
Not determined