ZMP
MAPKBP1
Ensembl ID:
Description:
mitogen-activated protein kinase binding protein 1 [Source:HGNC Symbol;Acc:29536]
Human Orthologue:
MAPKBP1
Human Description:
mitogen-activated protein kinase binding protein 1 [Source:HGNC Symbol;Acc:29536]
Mouse Orthologue:
Mapkbp1
Mouse Description:
mitogen-activated protein kinase binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:1347004]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23006 | Essential Splice Site | Available for shipment | Available now |
sa11673 | Essential Splice Site | Available for shipment | Available now |
sa36331 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45595 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23006
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 |
---|---|---|---|---|---|
ENSDART00000128909 | Essential Splice Site | 273 | 961 | 7 | 23 |
Genomic Location (Zv9):
Chromosome 17 (position 9955516)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10489716 |
GRCz11 | 17 | 10645750 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGAGTTCAACGACAAAAGAATGCTGGACAAGTGGGTGGAGCTCAGGG[T/C]GAGTCACGAGGATGCTGATTGGTGGTTGTGTAAATAAACAACTTTGGCAG
Long Flanking Sequence:
ATCCAAAAATGTTAAATAACTCACCATTTACTCACCCTCACGTGGTTTTAAACCTTTATGGGTTTCATTTTTATGTTGAACACAAAAGAAGATATTTTGAAGAAAGCTGAAAACCTGCAACCATACTATGGAAGTCAATAGTTGCAGGTTTGCAACTTTCTTCCAAATATCAACCTTGTGTTCAAAAGAATAAAGGAAAACAAGGGGAACAACTGAAGGGTGAGTGAATTATGACAGAATTTTCATTTTTGGGTGAGCTATCCCTTTAATACTGTACTAAATATCATCAGAATCTCCTAATTGTCATCTCTACCAGGTGAACGCCACAGTGCCATTATCAGGCCGCTCTGGTCTTCTGGGAGAGCTAAGGAATAACTTCTTCAGCGATGTTGCGTGTGGAAAAGGCCGAAAAGCGAGCAGTACATTCTGCATCACTACGTCTGGGCTGCTCTGTGAGTTCAACGACAAAAGAATGCTGGACAAGTGGGTGGAGCTCAGGG[T/C]GAGTCACGAGGATGCTGATTGGTGGTTGTGTAAATAAACAACTTTGGCAGCTACTTATCGCAATATGAGGAGGGATGCTTCAAATTTTAAAGAGCCTTTGATTGGACAGAAAACCTGACGAGACGCTGAAGTGCAGGGTGATGTCGTCAGAAATCATTTATACATGTTTACAGAAGCTAGAGACCAGCTTTAAATGCATATATCTTGTGAATTAGAATTTTATAATCATTTTAATAGATAACATTATGGCTAAACTGTTCATTGCATATGCTAAAAAACGTCAGGTTTGATTACATGGGGTCTTTGACGATTTTGTATTAAAGGGGTGGTCCACTACGATATCATATTTTAAACTTTAGTTGATGTGTAATGTGGATGTGTGAACATAAACAGCATCTCTGAATGTAAAACGCTCAAAGTTCAATGCAAAAGGAGACATTGGCTTTTACAGAGTTAGCTTAGCAAAGCCTACAGCGAACAAAGTTTGGGGACTAAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11673
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 |
---|---|---|---|---|---|
ENSDART00000128909 | Essential Splice Site | 571 | 961 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 17 (position 9928325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10516898 |
GRCz11 | 17 | 10672932 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTWACAACWAATACTAGRAATGTTAATGTGTGACGTGTGCTTCTTTTCCA[G/A]CTAATGAAGGAAAAGTCCGAATGATCAGTTGTGGTGCTGATAAGAGCATC
Long Flanking Sequence:
GCATGTCTTTGGACTGTGGGGGAACCCGAAGCACCTGGAGGAAACCCACGGGAGCACGTGGAGAACATGCAAACTCCACACAGAAATACCAAGTGACCCAGCTGGGACTCGAACCAGCGACCTTTTTGCTGTGAGGCGACAGTGCTAACCATCGAGCCACTGTGCCCCACTTGACTTCCAGTGACTTACTATGGAAGTCAGTGGTTACCGGTTTCCAACATTTTTCAAAGTAACTTATTTTGTGATCACCTGAAAAAAAACATTTCAGTGTTGAATAAACTCTGATGTTTCCCAGTACTGGGTTGCAGCTGGACCCTTCCGCTGTGTTAACCATATGTTGGATAAGTTGGCAGATCATTCTGCCGTGGTGACCCCTGATGAATAAAGGGAGTAAGCCGAAGAAAAATGAATGAATGAATGAATGACATAGCAAAACAGCATATTACTGCGTTAACAACTAATACTAGGAATGTTAATGTGTGACGTGTGCTTCTTTTCCA[G/A]CTAATGAAGGAAAAGTCCGAATGATCAGTTGTGGTGCTGATAAGAGCATCTACTTCCGCACGGCACAGAAGGTGAGACGCTTTACTTTTACATCTTAATTCTTTACTATGACCTATTCATCATCATCATCACCATCTTTAATAATGGAGGAGTGGTGTTTCTTTCATCAGTTATGAGGGGTGAAACAGGGTCCAGATTCAGCTGTCAGATTCCTCAGGCCTCAAGAAACAGTTGCCAGAGTTTTCCAAGAGCACCTGATTTAAATAGACATGCAAGCACTTAACACCCTTCTGCAAATGAGATACCAGCGGCCAGTGATTAAGTGTGAGACTCAAACAAGCTCTTCTGATGTCCTGAATCAATCCGTCAGCGATGAAGAGTCTCTGTATGTGTCTAAATATTAAAATCTTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36331
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 |
---|---|---|---|---|---|
ENSDART00000128909 | Nonsense | 577 | 961 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 17 (position 9928307)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10516916 |
GRCz11 | 17 | 10672950 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTAATGTGTGACGTGTGCTTCTTTTCCAGCTAATGAAGGAAAAGTC[C/T]GAATGATCAGTTGTGGTGCTGATAAGAGCATCTACTTCCGCACGGCACAG
Long Flanking Sequence:
GGGGAACCCGAAGCACCTGGAGGAAACCCACGGGAGCACGTGGAGAACATGCAAACTCCACACAGAAATACCAAGTGACCCAGCTGGGACTCGAACCAGCGACCTTTTTGCTGTGAGGCGACAGTGCTAACCATCGAGCCACTGTGCCCCACTTGACTTCCAGTGACTTACTATGGAAGTCAGTGGTTACCGGTTTCCAACATTTTTCAAAGTAACTTATTTTGTGATCACCTGAAAAAAAACATTTCAGTGTTGAATAAACTCTGATGTTTCCCAGTACTGGGTTGCAGCTGGACCCTTCCGCTGTGTTAACCATATGTTGGATAAGTTGGCAGATCATTCTGCCGTGGTGACCCCTGATGAATAAAGGGAGTAAGCCGAAGAAAAATGAATGAATGAATGAATGACATAGCAAAACAGCATATTACTGCGTTAACAACTAATACTAGGAATGTTAATGTGTGACGTGTGCTTCTTTTCCAGCTAATGAAGGAAAAGTC[C/T]GAATGATCAGTTGTGGTGCTGATAAGAGCATCTACTTCCGCACGGCACAGAAGGTGAGACGCTTTACTTTTACATCTTAATTCTTTACTATGACCTATTCATCATCATCATCACCATCTTTAATAATGGAGGAGTGGTGTTTCTTTCATCAGTTATGAGGGGTGAAACAGGGTCCAGATTCAGCTGTCAGATTCCTCAGGCCTCAAGAAACAGTTGCCAGAGTTTTCCAAGAGCACCTGATTTAAATAGACATGCAAGCACTTAACACCCTTCTGCAAATGAGATACCAGCGGCCAGTGATTAAGTGTGAGACTCAAACAAGCTCTTCTGATGTCCTGAATCAATCCGTCAGCGATGAAGAGTCTCTGTATGTGTCTAAATATTAAAATCTTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACACACACACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45595
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128909 | Essential Splice Site | 698 | 961 | 18 | 23 |
Genomic Location (Zv9):
Chromosome 17 (position 9919864)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10524159 |
GRCz11 | 17 | 10680193 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTAAATTAAGCACAAATTGAAGTGTTTGTTTTTTTTTTGTACACTTTTA[G/T]AGGTTGTAACGGGAATGAAGTTTACTAATGACTGCAGACATCTGATAACT
Long Flanking Sequence:
GTTATGTCCACAGATTTTTTACAAAATTACTAAATGAGTAATTTTCATGTAGTCTCAATTTTTTTTTTCCGTAGCTTTAATGATAAAAGCATAATGATTTCTGTTCTCTGTTAACTGCAGGATCTTTAACATCGGCAATGGCAAACAGAAGAAGGTCTACAAGGGATCCCAAGGGGAGGACGGGACCGTTATCAAGGTAAACAGACCTTGAATTTCTTCAGACACTGCTTTTAACATCAGACGCACAGGTATTGATCCATCTGAATGTGGTCATCAGGTTCAGACAGATCCATCTGGTCTCTATGTTGCCACAAGCTGCTCAGACAAAAACATCAGCATCTTCGACTTCTACACTGGAGAATGTGTGGCCACCATGTTCGGCCATTCTGGTGAGATCCTGTAAAAGACAGTAATGCTCCATCTGATATAAGTAAATCTCCACAAATTCAATCTAAATTAAGCACAAATTGAAGTGTTTGTTTTTTTTTTGTACACTTTTA[G/T]AGGTTGTAACGGGAATGAAGTTTACTAATGACTGCAGACATCTGATAACTGTGTCTGGAGACAGGTGGGTTTTTGCGAATCATATTTCTCAGTTGAAGAATCAATTATTGTATCCACCATATCTCGGTCACCATATCTCGATGGTAAATATGTCTGTGCTGTGTGTGTTTAGCTGTATCTTTGTGTGGCGGCTCTCTCCTGAGTTGACCATCAATATGAGACAACGGCTCTCAGACCTGAAGCAGAACAGCAGACCTGTACAGAAGACTCCTCCAAACAAACAACACACACTTAGGTATGAAACCAGTCACACTCTTTACCCAGCTAGCTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTTTAAATGAAGTCTATTAGATGTCTAAACATAGACGTCATGGCTAAAATGAGGCTAAATTTGGGCTTTCAGTGAAAATCTTACGGAACAGAAGTTAAACAATAGACTAGTCATCAAATGAACA
Associated Phenotype:
Not determined