ZMP
mapk8ip2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens mitogen-activated protein kinase 8 interacting protein [Source:Un
Human Orthologue:
MAPK8IP2
Human Description:
mitogen-activated protein kinase 8 interacting protein 2 [Source:HGNC Symbol;Acc:6883]
Mouse Orthologue:
Mapk8ip2
Mouse Description:
mitogen-activated protein kinase 8 interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:1926555]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11080 | Essential Splice Site | Available for shipment | Available now |
sa43046 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23232 | Nonsense | Available for shipment | Available now |
sa16465 | Essential Splice Site | Available for shipment | Available now |
sa23231 | Essential Splice Site | Available for shipment | Available now |
sa23230 | Essential Splice Site | Available for shipment | Available now |
sa23229 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11080
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092033 | Essential Splice Site | 22 | 1242 | None | 13 |
The following transcripts of ENSDARG00000063157 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 7750114)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8327492 |
GRCz11 | 18 | 8285511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACTAAAGAGAGAACTGGTGTGTTCATGATTAWTTTCTGTGTTGTCTGC[A/T]GGCCGGCTCATGACATCAGTCTGGAGGAGTTTGATGATGAAGATCTGTCT
Long Flanking Sequence:
AAAACAGTACAATAGTATATATTTTGAAAAACAATTCAAATTGGAACCTGAAAATTCCAGATTTGAGCCCTTGAAATTTAAATGTATACCTTGTGAAAGGGCACCACCTCTTGTGTGATTTATTTCTGAGAGTGTGTGCATGTCAGGTGTGCGTATGTGTGTGTGCATATATATGATGTGCTAGTATGAGTGACCTTGTGGATTTCTTAGGGCCGTGACCTGTGTGTGTGGAATCAGCTAATATGTCTTGGCAGCTCATATTTCAAATCAGACATCCACAGGGACACACACACACACGCACACACGCACACACAAACACACACAGCTTTCTCTATATTAGCAAGTGCATCACGGATGCAATGAGCTGACAATATTTTCTAAACTTATGCCTCATTTAAAGCTGCTGAATTCAGTACATTTGAGGAAATTATGATTTATTTATGAGCCTTTCCACTAAAGAGAGAACTGGTGTGTTCATGATTATTTTCTGTGTTGTCTGC[A/T]GGCCGGCTCATGACATCAGTCTGGAGGAGTTTGATGATGAAGATCTGTCTGAAATCACAGATGACTGTGGTATAGGCCTCAACTATGACTCTGACCCCTATGAGAAGGTATGACACTTTTACAATGCAAATATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTGACATGTAACAATCATTCATTCATTCATTTTCTTTTTGGCTTGGTCCCTTTATTAATCTGGGGTTGCCACAGCAGAATGAACTGCCAACTTATCTGGCATGTGTTTTACGCAGCGGATGCCCTTCCAGCTGCATCCCATCATTGGAAAACATCCATACACATTCATTCACACTCATGCACTACATGCAAACTCCACACAGAAATGCCAACTGAATCAGCTGAGGCTCGAACGGGCAACCTTCTTGCTGTGAGGCAATCGTGCTACCCACTGCACCATCTTGACGCCCATGTCAGAATGATGAAAAATGGAAAAAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43046
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 |
---|---|---|---|---|---|
ENSDART00000092033 | Nonsense | 55 | 1242 | 2 | 13 |
The following transcripts of ENSDARG00000063157 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 7750013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8327391 |
GRCz11 | 18 | 8285410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAATCACAGATGACTGTGGTATAGGCCTCAACTATGACTCTGACCCCTA[T/A]GAGAAGGTATGACACTTTTACAATGCAAATATTCTATTCTATTCTATTCT
Long Flanking Sequence:
CACCACCTCTTGTGTGATTTATTTCTGAGAGTGTGTGCATGTCAGGTGTGCGTATGTGTGTGTGCATATATATGATGTGCTAGTATGAGTGACCTTGTGGATTTCTTAGGGCCGTGACCTGTGTGTGTGGAATCAGCTAATATGTCTTGGCAGCTCATATTTCAAATCAGACATCCACAGGGACACACACACACACGCACACACGCACACACAAACACACACAGCTTTCTCTATATTAGCAAGTGCATCACGGATGCAATGAGCTGACAATATTTTCTAAACTTATGCCTCATTTAAAGCTGCTGAATTCAGTACATTTGAGGAAATTATGATTTATTTATGAGCCTTTCCACTAAAGAGAGAACTGGTGTGTTCATGATTATTTTCTGTGTTGTCTGCAGGCCGGCTCATGACATCAGTCTGGAGGAGTTTGATGATGAAGATCTGTCTGAAATCACAGATGACTGTGGTATAGGCCTCAACTATGACTCTGACCCCTA[T/A]GAGAAGGTATGACACTTTTACAATGCAAATATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTATTCTGACATGTAACAATCATTCATTCATTCATTTTCTTTTTGGCTTGGTCCCTTTATTAATCTGGGGTTGCCACAGCAGAATGAACTGCCAACTTATCTGGCATGTGTTTTACGCAGCGGATGCCCTTCCAGCTGCATCCCATCATTGGAAAACATCCATACACATTCATTCACACTCATGCACTACATGCAAACTCCACACAGAAATGCCAACTGAATCAGCTGAGGCTCGAACGGGCAACCTTCTTGCTGTGAGGCAATCGTGCTACCCACTGCACCATCTTGACGCCCATGTCAGAATGATGAAAAATGGAAAAAAAAAAAAACAACAACAACATAGCAATGCATTAAATTATCACAGTTCATTAGCAATGACTGGCTGTGTTTACCCCTGACAAAGAAGGAAAAAGCAAAATAAGGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23232
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 |
---|---|---|---|---|---|
ENSDART00000092033 | Nonsense | 583 | 1242 | 6 | 13 |
The following transcripts of ENSDARG00000063157 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 7731068)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8308446 |
GRCz11 | 18 | 8266465 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCCCCCTGCCATCCCCTGTGAGGATAGCAGTTCTCAGCAGTTGTTGT[T/A]GAAGATTGAGCCTGACCACAGTCTTGAAAGCTTCAAACGCTCCTTCTACT
Long Flanking Sequence:
TAAACGCTATGCAGAGTCAGACCGCCACAGTGATGACCTTAGCTCTCCTGGATCAGACTCTGATATTGAAGGGGAACTTGAGGAAGCGTTTGCATGTGGTGGCCCACTTGCTAGTAACATGATTTCCTCCATCTCAGAGACAGAGCTAGACCTGACCAGTGAATCCAGCAGTGGGCGCTCCTCGCACCTCACCAATTCCATTGAAGAAGCCAGCTCTCCAACTTCAGACCAAGAACTGGACCAGGAGCTGGATACTGAGCAGGACAGTGGTATTGTAGGTCTAAAAGCATCTCTTCTTTTGGGCCAGCCTGACCCAATTAAACAAGACCCTTTACCAGGGTTGGACCCCAGCTCAGACATGTTGCAACTAGATGACGGGCAAGCTCTGATGGGTCTGCAGAACGTAGATGACGAACAGGATTATGAGCACCAAGCTGATCCAGATGAGACTCTTCCCCCTGCCATCCCCTGTGAGGATAGCAGTTCTCAGCAGTTGTTGT[T/A]GAAGATTGAGCCTGACCACAGTCTTGAAAGCTTCAAACGCTCCTTCTACTTGCCGGTTGGCCCAAAACTCATGCCTTCTGTGGATGACTATGATGGTAACAGTGAGGGAGACTCTGAATCAGAGTCTGAGGATGAGCTCAGTGAAAACTCTGACTCTCCTTGGCTTCTTAGTAACCTTGTCAACAGAATGATCTCAGAAGGCTCCTATCCAATCAGCTGTCCTGAAGAGTGCTTCAAACGCTCAGCCTCCATCTCTGACACCATCTCACCCTCATCTGATCTGGAAACAGATGCTTTCAATGAAACCGATGGCTGCAATTTCCAAAAACAGAAGTCAGAAGAAAAGTCACAGGAGGTGAAATCTGAGGCAAGAGTGGTGGAAGAGAAAGAGAGAGAAGCCAGTTGTGCATCTGAAGAGGGTCAAAAAGAAAGCAAGAGAACGGACTCTTGTCTGTATATGAGTAACCCCACATATGGTACGGTTACACCTGTCTTCACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16465
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092033 | Essential Splice Site | 1002 | 1242 | 6 | 13 |
The following transcripts of ENSDARG00000063157 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 7729810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8307188 |
GRCz11 | 18 | 8265207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCWAAGAAGTTCCTCAATGTGTTTGTCAATGGCACRTCACGGWCCTCCAG[T/G]AAGTGAAGATAAAACYGCACAATTWACTTAKGAGGCATTTTACCCCAAAA
Long Flanking Sequence:
GCACAGACCAATCACTGTTTCAGTCTCACTTACTCAACGGATAACGATGAAGATGAGCAAGATACCTCTCCTTTTCTGGATGATCTTCACAAGATACCTTCACCCTATGGAAACGAGACATACTTGGACAGTTCTCCACCTATTGATGAGAGTGTGCGAGAGTTGAGGAACAGAACCTCTGACCGGCCCATAGATGACTCCTTGGCATATGATTCAATGAAGTACACCCTTGTGGTGGATGAAAATACGACACTGGAGCTGGTGAGCCTTAAGCGCTGCACCTCTGTTCTCAGTGAGGACAGTGATGGACTCTCTACTATCTGTGATGATGACGTGGCTGATGAAGATGATGACATTTATGGGCGGGGTCAGATGGTACGAGGCATGAGACCCAATTTGCTATTAAGCTCCTCTGAAGAAGACTCTTCTCCTGAGGCAGATTTGCCTTTCTCAAAGAAGTTCCTCAATGTGTTTGTCAATGGCACGTCACGGTCCTCCAG[T/G]AAGTGAAGATAAAACCGCACAATTTACTTAGGAGGCATTTTACCCCAAAATTTGAATTCTGTCAACATTTGATGACTTTAATTTTCCAAAGACGGTTTTATTCAAATAGTATTTTGTTTATACAAGCGAAATCCAGTGTTGTTTTGGTCCTATTAATGAATTGACTATCATTAAATGGACAAAAAATATAAATTTAACGATGACTGTTTAACAAAATAGTAAAAAAATAGGAAAATATATTGTTATATTTTACTTACACAAATTACCAAATTAAATTCACCCCATCACAGAGCCAATCAGGCTCTTTTAATGTAGTTTAAAAGATTTAGATGATAATATTATATAATTTAGGAGGCTGTCTTGCCGAACAGAAAGTATATTTAATAATCCTAATGAGATGACATCATAAGATGAAAGGTTTTGTATGATCTGCTTCTAAATTGGTTTTGCTGTAGTGTGTGACACACACACACACACACAGAGGGTCTATCTTGGGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23231
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092033 | Essential Splice Site | 1027 | 1242 | 7 | 13 |
The following transcripts of ENSDARG00000063157 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 7729186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8306564 |
GRCz11 | 18 | 8264583 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACTATAAATGGAGAAGAAAGAGATCAGACTCACAGAGCAGTCTTCAG[G/A]TGAGTAACGCTGCCCACATGAATAGCCTAGCTCTAATGAAAATGCTCCAG
Long Flanking Sequence:
AAGCGAAATCCAGTGTTGTTTTGGTCCTATTAATGAATTGACTATCATTAAATGGACAAAAAATATAAATTTAACGATGACTGTTTAACAAAATAGTAAAAAAATAGGAAAATATATTGTTATATTTTACTTACACAAATTACCAAATTAAATTCACCCCATCACAGAGCCAATCAGGCTCTTTTAATGTAGTTTAAAAGATTTAGATGATAATATTATATAATTTAGGAGGCTGTCTTGCCGAACAGAAAGTATATTTAATAATCCTAATGAGATGACATCATAAGATGAAAGGTTTTGTATGATCTGCTTCTAAATTGGTTTTGCTGTAGTGTGTGACACACACACACACACACAGAGGGTCTATCTTGGGCTATACCAAAGTATACAGTAGAATAATGCTTATGCACTATGCGTGTTTCAGGCACAGAGTCCTTTGGGCTTTTTTCATGCACTATAAATGGAGAAGAAAGAGATCAGACTCACAGAGCAGTCTTCAG[G/A]TGAGTAACGCTGCCCACATGAATAGCCTAGCTCTAATGAAAATGCTCCAGTCTAGTTTAAAGTATCAACCCTCATTCACAAGCCCTCAAGGAAATCTTCTTTCTCAGTATATTTTAATGCTTGAAAATTGACTGCTCATGATATCTATTGCAAGCAATCCTAATGCGAGTTTTAATGCCCATGCTGTAGGTTCATCCCACGACATGCAGATGAGCTGGAGTTAGATGTTGATGATCCGTTATTCGTTGAGGAAGAAGAGGATGATTACTGGTATCGTGGGTACAACATGCGCACAGGGGCCAGGGGGATTTTCCCAGCGTACTACGCCCACGAGGTTGTTGGGCAAACAAAAGACCTGATGAGTAAGAATTGTATGATGCAATGTTTTTAGTATGTTTCCTGTTCTCATGCATAATAGTTTTTAAATTACGACAGGCCGGAAGTTCTTGCTAATCAAGCTCCTCTTTTACGCCAAATGTTGGGCTTTTTAGAGAAGACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23230
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 |
---|---|---|---|---|---|
ENSDART00000092033 | Essential Splice Site | 1027 | 1242 | 8 | 13 |
The following transcripts of ENSDARG00000063157 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 7728998)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8306376 |
GRCz11 | 18 | 8264395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATATCTATTGCAAGCAATCCTAATGCGAGTTTTAATGCCCATGCTGT[A/G]GGTTCATCCCACGACATGCAGATGAGCTGGAGTTAGATGTTGATGATCCG
Long Flanking Sequence:
GTAGTTTAAAAGATTTAGATGATAATATTATATAATTTAGGAGGCTGTCTTGCCGAACAGAAAGTATATTTAATAATCCTAATGAGATGACATCATAAGATGAAAGGTTTTGTATGATCTGCTTCTAAATTGGTTTTGCTGTAGTGTGTGACACACACACACACACACAGAGGGTCTATCTTGGGCTATACCAAAGTATACAGTAGAATAATGCTTATGCACTATGCGTGTTTCAGGCACAGAGTCCTTTGGGCTTTTTTCATGCACTATAAATGGAGAAGAAAGAGATCAGACTCACAGAGCAGTCTTCAGGTGAGTAACGCTGCCCACATGAATAGCCTAGCTCTAATGAAAATGCTCCAGTCTAGTTTAAAGTATCAACCCTCATTCACAAGCCCTCAAGGAAATCTTCTTTCTCAGTATATTTTAATGCTTGAAAATTGACTGCTCATGATATCTATTGCAAGCAATCCTAATGCGAGTTTTAATGCCCATGCTGT[A/G]GGTTCATCCCACGACATGCAGATGAGCTGGAGTTAGATGTTGATGATCCGTTATTCGTTGAGGAAGAAGAGGATGATTACTGGTATCGTGGGTACAACATGCGCACAGGGGCCAGGGGGATTTTCCCAGCGTACTACGCCCACGAGGTTGTTGGGCAAACAAAAGACCTGATGAGTAAGAATTGTATGATGCAATGTTTTTAGTATGTTTCCTGTTCTCATGCATAATAGTTTTTAAATTACGACAGGCCGGAAGTTCTTGCTAATCAAGCTCCTCTTTTACGCCAAATGTTGGGCTTTTTAGAGAAGACATAAGTCACCATGTCACCACAAATCACCATGGTTTTGGTTCTGCAAATCACAAAACTCAATCAAAGAAAGCAACCATGTCCAGCACAGGACCTAACAAAATATAAATATATTGATTTAAATTATTATTAACATACACCCATTGGGTACAGCTTGCAAGCTGGGGTCTTTTTGCCTCCAGAACTGCTCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23229
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 |
---|---|---|---|---|---|
ENSDART00000092033 | Nonsense | 1031 | 1242 | 8 | 13 |
The following transcripts of ENSDARG00000063157 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 7728986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8306364 |
GRCz11 | 18 | 8264383 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGCAATCCTAATGCGAGTTTTAATGCCCATGCTGTAGGTTCATCCCA[C/T]GACATGCAGATGAGCTGGAGTTAGATGTTGATGATCCGTTATTCGTTGAG
Long Flanking Sequence:
ATTTAGATGATAATATTATATAATTTAGGAGGCTGTCTTGCCGAACAGAAAGTATATTTAATAATCCTAATGAGATGACATCATAAGATGAAAGGTTTTGTATGATCTGCTTCTAAATTGGTTTTGCTGTAGTGTGTGACACACACACACACACACAGAGGGTCTATCTTGGGCTATACCAAAGTATACAGTAGAATAATGCTTATGCACTATGCGTGTTTCAGGCACAGAGTCCTTTGGGCTTTTTTCATGCACTATAAATGGAGAAGAAAGAGATCAGACTCACAGAGCAGTCTTCAGGTGAGTAACGCTGCCCACATGAATAGCCTAGCTCTAATGAAAATGCTCCAGTCTAGTTTAAAGTATCAACCCTCATTCACAAGCCCTCAAGGAAATCTTCTTTCTCAGTATATTTTAATGCTTGAAAATTGACTGCTCATGATATCTATTGCAAGCAATCCTAATGCGAGTTTTAATGCCCATGCTGTAGGTTCATCCCA[C/T]GACATGCAGATGAGCTGGAGTTAGATGTTGATGATCCGTTATTCGTTGAGGAAGAAGAGGATGATTACTGGTATCGTGGGTACAACATGCGCACAGGGGCCAGGGGGATTTTCCCAGCGTACTACGCCCACGAGGTTGTTGGGCAAACAAAAGACCTGATGAGTAAGAATTGTATGATGCAATGTTTTTAGTATGTTTCCTGTTCTCATGCATAATAGTTTTTAAATTACGACAGGCCGGAAGTTCTTGCTAATCAAGCTCCTCTTTTACGCCAAATGTTGGGCTTTTTAGAGAAGACATAAGTCACCATGTCACCACAAATCACCATGGTTTTGGTTCTGCAAATCACAAAACTCAATCAAAGAAAGCAACCATGTCCAGCACAGGACCTAACAAAATATAAATATATTGATTTAAATTATTATTAACATACACCCATTGGGTACAGCTTGCAAGCTGGGGTCTTTTTGCCTCCAGAACTGCTCTATTTCTTTATGACA
Associated Phenotype:
Not determined