ZMP
si:ch211-247j9.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
MAPK9
Human Description:
mitogen-activated protein kinase 9 [Source:HGNC Symbol;Acc:6886]
Mouse Orthologue:
Mapk9
Mouse Description:
mitogen-activated protein kinase 9 Gene [Source:MGI Symbol;Acc:MGI:1346862]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23984 | Nonsense | Available for shipment | Available now |
sa37352 | Nonsense | Available for shipment | Available now |
sa18329 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23984
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 |
---|---|---|---|---|---|
ENSDART00000112550 | Nonsense | 172 | 421 | 6 | 12 |
The following transcripts of ENSDARG00000077364 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 31122287)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 32321757 |
GRCz11 | 21 | 32355015 |
KASP Assay ID:
2261-5832.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTGGTGAAGTCCGACTGCACTTTAAAGATCTTAGACTTTGGACTGGCC[A/T]GAACCGCCTGCACTAATTTTATGATGACACCTTATGTAGTGACCAGATAC
Long Flanking Sequence:
CAAAAAGAAATTTACTTCCGTATTTGCTTCACGAGGGAGAGCAGGAGGTTGCTGCTTGATTTTAACATGTAGAGAGATAAGTGATCCAAAATGATTGTAACAATCATTGACCCCTAAATCTATTTATGTCTTAGAACTGTAAAAATAAAAATAAATAAATAAATAAATAATGCCAACCAGAACAATTGTTTAAACCTTAAATTAAAAGCCTGGTCACATGAGCTGTCACAGTAGGAAAGAATGTAAAAATAATTATCATCCAGAGAGTACAAAATTCCATATATTCAAGGAGAGAACCCCACATTTCCTAATAAAGTCTAATAATTTGATTTAATAAGTGAATTTTAAACTACTGAGACCTTTCATTGTGTTAATGTGTGAGATTGTCTTTCAGCATGACAGTATGGGATTGCATTCTCTTTGCTATTCAGGATCTGAAGCCCAGTAATATAGTGGTGAAGTCCGACTGCACTTTAAAGATCTTAGACTTTGGACTGGCC[A/T]GAACCGCCTGCACTAATTTTATGATGACACCTTATGTAGTGACCAGATACTACAGAGCGCCAGAGGTCATCCTGGGCATGAAATACAAGGAGAATGGTAATGCTGTTTTTTTTTTTTGGCGGTAATGCCCTTCAGAGCCAATGAAGATATTGAAATGGAATTGTGTTATTAATATTTGATTGTCTTTTTGCAGTGGATATCTGGTCTGTAGGCTGCATCATGGGCGAAATGGTTAAAGGGAGCGTCATATTCCAGGGCACTGATCGTATCCACTTAATTCTAAAACCTGAAAAATAAGCAGTTAAGCTTGCATTTTTTGCAATGCTATTTTTAAATGTCAGTTTTATGTTTTAGTTTTTCAAATATGCTCTTCAAATATATATTCACCTGCATTTATTTGATCAAAAATACAATAAAAACTTTTTTAAAAAATTAAAAAACTGAATTTTTATTTTATTTTATTTTTTTTACATTTAGAGTAACTGTTTTCAACTTGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37352
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 |
---|---|---|---|---|---|
ENSDART00000112550 | Nonsense | 322 | 421 | 9 | 12 |
The following transcripts of ENSDARG00000077364 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 31119926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 32319396 |
GRCz11 | 21 | 32352654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCGTATCTCTGTGCAGGAGGCTCTTAATCACCCCTACATTCATGTGTG[G/A]TACGACCCAGCTGAGGCTGATGCGGTCAGTGCACCTCTGTCTATCTATGT
Long Flanking Sequence:
GGGAACCCCCTCTCTGGAGTTTATGAACCGTTTGATGGAGACTGTAAGGAACTATGTGATGAACAAACCCCAGTTTCCTGGAGTCAGTTTTAATGAGCTTTTTCCCGACTGGGCCTTCCCATCAGAGACGGAGCATGACAAGATCAAAAGTAAAACCATCCTCGCTTTTCTTTCATGTCTGTTTCTTTTTCTACTTTACACTAGCACACTCCTAAAGGCATAGTCCACCCAAGAATGAAATTTCTGTCATTTAATCACTCTCCACTTGTATCAAATCTGGTCAACTCATAAAGGTTTAGAACTGAATGAGGGAAGGCTGAGTAAATTATCATTTTTGGGATAACAATGCCGTTAACTGTAAACTTTACTTGACACCCGATTTCTATTCTTTCCAATGTAGCAAGTCAAGCACGAGATCTGCTTTCCAAGATGCTGGTAATCGACCCTGAATGCCGTATCTCTGTGCAGGAGGCTCTTAATCACCCCTACATTCATGTGTG[G/A]TACGACCCAGCTGAGGCTGATGCGGTCAGTGCACCTCTGTCTATCTATGTCACTTTGTCCTGCCCAGACTAGCACAAACTGTTTTACAGGGGACGTTTTTACGATGTCAGGGAGGTCTTGGGCCTTGAATTTGTACTGATTGTTTTATGTGTTCAGCCTCCTCCACAGATCTCAGACAAGCAGCTTGAGGAGCGGGAACACAGCATCGAGCAGTGGAAAGGTACAGTCGCCCTCTGCTGTCAACATCTTCCGTTAAAAGCTACCTGTAGATGTAAATAAATGTCTACAGCAGAAATGATCATTGTGGTGTATTGGTTAAATGATTCCAAGGTCATTTGTGTTCTCATTTTAATAAACAGTAATCGGGTTGATTTTGTGTCATTAAAAGATTTTGACATTAAAAGTTCATAATCCTAATGTTTGCTAAAGGGTTTGTAAAAAAATAAAAAACATAGAAATCCACTGAACTCTGTTAATGATTTCTTGGGGTGGGGTTTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18329
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112550 | Nonsense | 334 | 421 | 10 | 12 |
The following transcripts of ENSDARG00000077364 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 31119760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 32319230 |
GRCz11 | 21 | 32352488 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTGGGCCTTGAATTTGTACTGATTRTTTTATGTGTTCWGCCTCCTCCA[C/T]AGATCTCAGACAAGCAGCTTGAGGAGCGSGAACACAGCAYYGAGCAGTGG
Long Flanking Sequence:
TTTCTTTCATGTCTGTTTCTTTTTCTACTTTACACTAGCACACTCCTAAAGGCATAGTCCACCCAAGAATGAAATTTCTGTCATTTAATCACTCTCCACTTGTATCAAATCTGGTCAACTCATAAAGGTTTAGAACTGAATGAGGGAAGGCTGAGTAAATTATCATTTTTGGGATAACAATGCCGTTAACTGTAAACTTTACTTGACACCCGATTTCTATTCTTTCCAATGTAGCAAGTCAAGCACGAGATCTGCTTTCCAAGATGCTGGTAATCGACCCTGAATGCCGTATCTCTGTGCAGGAGGCTCTTAATCACCCCTACATTCATGTGTGGTACGACCCAGCTGAGGCTGATGCGGTCAGTGCACCTCTGTCTATCTATGTCACTTTGTCCTGCCCAGACTAGCACAAACTGTTTTACAGGGGACGTTTTTACGATGTCAGGGAGGTCTTGGGCCTTGAATTTGTACTGATTGTTTTATGTGTTCAGCCTCCTCCA[C/T]AGATCTCAGACAAGCAGCTTGAGGAGCGGGAACACAGCATCGAGCAGTGGAAAGGTACAGTCGCCCTCTGCTGTCAACATCTTCCGTTAAAAGCTACCTGTAGATGTAAATAAATGTCTACAGCAGAAATGATCATTGTGGTGTATTGGTTAAATGATTCCAAGGTCATTTGTGTTCTCATTTTAATAAACAGTAATCGGGTTGATTTTGTGTCATTAAAAGATTTTGACATTAAAAGTTCATAATCCTAATGTTTGCTAAAGGGTTTGTAAAAAAATAAAAAACATAGAAATCCACTGAACTCTGTTAATGATTTCTTGGGGTGGGGTTTCCCTCCTTGCAGAGTTGATTTATAAAGAAGTAATGGACTGGGAGGAGCGGAACAAGAATGGGGTACTGAAAGAGGAGTGTTTAGGTGAGTCACATATTTTCTTTAATAGTTATTCTTTTATTATTTAAATAATCTGTATTATGCTGCTACTTTTATTCCAAAGCAGATT
Associated Phenotype:
Not determined