ZMP
si:ch73-34b5.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
MAP9
Human Description:
microtubule-associated protein 9 [Source:HGNC Symbol;Acc:26118]
Mouse Orthologue:
Mtap9
Mouse Description:
microtubule-associated protein 9 Gene [Source:MGI Symbol;Acc:MGI:2442208]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32682 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32681 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38267 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1974 | Essential Splice Site | F2 line generated | Not yet available |
| sa11352 | Nonsense | Available for shipment | Available now |
| sa8871 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32682
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054225 | Essential Splice Site | 269 | 678 | 3 | 13 |
| ENSDART00000133937 | Essential Splice Site | 269 | 678 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 24605406)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25057177 |
| GRCz11 | 1 | 25748006 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGTTCCTCAACCCAGGGAAAGAACTGTTAAATCAAAATCGTCAGCAG[G/A]TTAGACCAGACATTTTAAAATTTTGCTAATTTTTTTATTTAAAATTAAGT
Long Flanking Sequence:
CAAAAAAGTCTCTTTCATGAAAACCAAAAGGACCAGCTCACCTCTACACTTTGAACAGTCAAACTCAGCGGGAAGTGCAGACGGCCAGTGTAGTTCTGTTCATTCCAGCCAGCCCAGGAATTCATCTCAAAGCCCAAGCAACTCTTACACTCCAGAGAAAAATCAACAGTCAGATTCCCCTTTTTCCTCTTTATCTGATAAATATCTACCTGAGTCCACTTTACTCAAGAATGATGAACAGTCGAAATCAGCAGTGCGGCTGAGGAACCAGACAGAATCTTCTATGGTGAGGAAGAGCCTATCAGAATCTCCACTGCCACTAAACTCTGAGAACAGTCAGTGGGATTCGTCCATACCTTTTACATCAGAAGGCTCACAGTGGGACAGTCCAGTGCCATTGCCTTCAGAAAAACATGAAGACAACCAGAAGATTGAGAAAGATGATGAAGTGCCTGTTCCTCAACCCAGGGAAAGAACTGTTAAATCAAAATCGTCAGCAG[G/A]TTAGACCAGACATTTTAAAATTTTGCTAATTTTTTTATTTAAAATTAAGTTTTCAACCGTGTTTGTGTGTTTTTTTCAATAGAACAGCATTTATTTTTTCAATAATTTAAAATCATTTTGTACAGTATGACTAGTGTTTACGATCACTGTTTAACAATTGAATGTAGTTTTGCTGAATTAAAGAATCCTTTATTTCTTTTTTTGTTCTTTATTTTCAAACGGCGGTAACATCAAAGCAAAAAAATAAGATTTTTTAAATTAAAAATGCTATCACAAAGTGTGTAGCGTTTCAAGCACACCGGCTTTTTATCAAACAGTATTCATCATAGCAAGTTACTCTTTTTATACACTCTTTTTATACACAACGGATCACATGATCTCAAACAGTATCTCACAACAAAAAATGTAAAAATACGCATTAGTATATTACACAACTTACATATTCAAAACGAAAATACAAAAACAAATCCTAATAATACAAACAGAATATAAAAAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32681
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 |
|---|---|---|---|---|---|
| ENSDART00000054225 | Nonsense | 377 | 678 | 6 | 13 |
| ENSDART00000133937 | Nonsense | 377 | 678 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 24603397)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25055168 |
| GRCz11 | 1 | 25745997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGGATTTTTCATTATAGCTGCCACAGAAGAGAGCAAAGAGAGAAATTA[T/A]TCTACATCCTTTGAAGAAAAGCCTGTAAGTCAGATGAAGTGTGAAAATGT
Long Flanking Sequence:
CTCTGAGAAGAGTCAAGCCTCTACCAATGAATGTACAAGTGTACAGGTAAAAAATATAGTAAATCAGAGAAATAGAAGACATACAATTAAAGAAAATGCATTTAAACTGTTTAAAATACTAAAACACAAGTGAGAGATCTGTTTTACAATTTCCAAGAATTAATAAATCTGGTTCAAGCTGATGTTTTGACAGACCCTTTCTTTTTTTTAACTGTGCTTTAGGGTCCAGATGGAGACCAAGCCATGACAGAAAGATCGTTTTTATCATCAGAGCAACTATCTGAAAATCTAGCCACTGCTGGCAGTGGTATGTAAAAAAAAAACTACAACAAAAAAAAGCGTTTTATTGTTTAGAATAGTATTGAGATTATATTTTGGTTTTAGGTATTGGTGACCTGTGACAGATGACAATTTATAATAGTTAAACAGTTATTAATAACTTTGTATGTCTATGGATTTTTCATTATAGCTGCCACAGAAGAGAGCAAAGAGAGAAATTA[T/A]TCTACATCCTTTGAAGAAAAGCCTGTAAGTCAGATGAAGTGTGAAAATGTTTTATTATTATTAATATTATGATTCTTATTATTAAAGATCCCCTATTACGGGTTTTGAAAATGACCTTCCATGCAGTGTGTAACACATCTCTTCAAGAGTTCACACTTAGCTGATGATTGATTATAAAGCTTGTTTGGCATGCTGTCCCATGAAAGAGCCCTGAGCTCATAAAATCCTCGAGCCGTTTGCAAAGCGAGAGGGGAGTTTAAGCTCAGGAAGATCTCAAGAACTCCCCTGCTGTAGTAGCTAATGAACAGATAGTGATTGCTCTTAAGAGATAAATACTTACTAGGAGCATGTCTATGGTGCCAATTTGGATTAGCCAATTAACATAAGTTAATGTTAACATAAGTTGGATGTAATTGGATGGTGGGAGGAAACCAGGGGAGCATGGGGAGAACGTATAAACTCTGCACATAAACGTCGGCTGGCTTGGTAAGGACTAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38267
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 |
|---|---|---|---|---|---|
| ENSDART00000054225 | Nonsense | 423 | 678 | 8 | 13 |
| ENSDART00000133937 | Nonsense | 423 | 678 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 24600415)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25052186 |
| GRCz11 | 1 | 25743015 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTTTAGGCCTTCAAGCTCTCAGTCAACCAGTTCCAGAAAGTCCAAGTG[T/A]TCTTATAAAGCAGAGTCCAAATACTTGGGAACACTGAAAATTTTGGATCA
Long Flanking Sequence:
TCTCAGTGCATTGACAACAGAAATAAAACATTTTAATCTTTAAATTTGAGTTAAACAGGACCTTTGAATTTTTAAACACTTTAAAAATAAACATCAAACCTGTAACATTTTTATTTGACTAATAACTCAATTAAAGACATTTTATTGAAATCAGAGATATTTCTAGACAATATGCAAAGTAGTTATATTAATCAAGCAATACATTTAGTTTTTTAAATGTAACCATTAGACTGTCAGCAAGATATCACTGCTATAAAATTTATAATATCATAAACATGCTGTATTGAAACCATATTAAACTAACAACTATCTGTTTTTAACTATTCTGCTAAATACTACAGTATGTTAATTGTTTAAAATGTTTTAAAGATGAAAAAATCCTCACTTTACATGTAACTATAGAGTGTTACTGAAATTCATTCAATAAACATTGTAAACTGAAATATTTTGGGCTTTAGGCCTTCAAGCTCTCAGTCAACCAGTTCCAGAAAGTCCAAGTG[T/A]TCTTATAAAGCAGAGTCCAAATACTTGGGAACACTGAAAATTTTGGATCAGAGAACACAGAAGGCCCAACAGGTTCCAGAAGCAGCAGATTCACTAAGAGCAGCTGTCTACCAGGTTAGACGCTTACTAAAACATTATTACTTTAAAGGACATGTAGAGACTGGCCGTTATTGTTTTAATGGGGAAAAAGATTTTAATGCATCTAACATTTGTTTGAAAAATAACAGGAATGGCTGAAAAAGAAAGAAGAAACCTTGGAAATTACTAGGAGGGCAAAAAAGCAGGAACAGAAAATGAAAGAGGAGAAAATGCAAGAGGTAATTAAGATGTTCAATATAAATTTCTTCTCTAGATCATTCATTCATTCATTTTCTTTTCGGCTTAGTCTCTTTATTAATTCGGGGTCGCCATAGCGGAATGAACCGCCAACTTATCCAGCACGTTTTTTGCGCAGCAAATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACAATCACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1974
Status:
F2 line generated
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054225 | Essential Splice Site | 462 | 678 | 9 | 13 |
| ENSDART00000133937 | Essential Splice Site | 462 | 678 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 24600189)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25051960 |
| GRCz11 | 1 | 25742789 |
KASP Assay ID:
554-2676.1 (used for ordering genotyping assays)
KASP Sequence:
TTAATGGGGAAAAAGATTTTAATGCATCTAACATTTGTTTGAAAAATAAC[A/T]GGAATGGCTGAAAAAGAAAGAAGAAACCTTGGAAATTACTAGGAGGGCAA
Long Flanking Sequence:
TAGACTGTCAGCAAGATATCACTGCTATAAAATTTATAATATCATAAACATGCTGTATTGAAACCATATTAAACTAACAACTATCTGTTTTTAACTATTCTGCTAAATACTACAGTATGTTAATTGTTTAAAATGTTTTAAAGATGAAAAAATCCTCACTTTACATGTAACTATAGAGTGTTACTGAAATTCATTCAATAAACATTGTAAACTGAAATATTTTGGGCTTTAGGCCTTCAAGCTCTCAGTCAACCAGTTCCAGAAAGTCCAAGTGTTCTTATAAAGCAGAGTCCAAATACTTGGGAACACTGAAAATTTTGGATCAGAGAACACAGAAGGCCCAACAGGTTCCAGAAGCAGCAGATTCACTAAGAGCAGCTGTCTACCAGGTTAGACGCTTACTAAAACATTATTACTTTAAAGGACATGTAGAGACTGGCCGTTATTGTTTTAATGGGGAAAAAGATTTTAATGCATCTAACATTTGTTTGAAAAATAAC[A/T]GGAATGGCTGAAAAAGAAAGAAGAAACCTTGGAAATTACTAGGAGGGCAAAAAAGCAGGAACAGAAAATGAAAGAGGAGAAAATGCAAGAGGTAATTAAGATGTTCAATATAAATTTCTTCTCTAGATCATTCATTCATTCATTTTCTTTTCGGCTTAGTCTCTTTATTAATTCGGGGTCGCCATAGCGGAATGAACCGCCAACTTATCCAGCACGTTTTTTGCGCAGCAAATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACAATCACACACGTTCATTTATACTCCTACACAACGGACAATTTAGCCTACCCAATTCACCTGTACCACATCTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGAACGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGACCCAGCTGAGGCTCGAACCAGCGACTTTCTTGCTGTGAGGTGACAGCACTACCTACTACGCCACTGCAGCGCCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11352
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 |
|---|---|---|---|---|---|
| ENSDART00000054225 | Nonsense | 510 | 678 | 10 | 13 |
| ENSDART00000133937 | Nonsense | 510 | 678 | 11 | 14 |
| ENSDART00000054225 | Nonsense | 510 | 678 | 10 | 13 |
| ENSDART00000133937 | Nonsense | 510 | 678 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 24599558)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25051329 |
| GRCz11 | 1 | 25742158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTTCTAAAACTRCAGATGCAAAGGCCTCTTATGATGCCTGGAAAGAG[A/T]AAAAACGTGACGTCATAAGAAAGAAACTCAGCGAAAAACAGAAGCTAATC
Long Flanking Sequence:
TTCATTCATTCATTTTCTTTTCGGCTTAGTCTCTTTATTAATTCGGGGTCGCCATAGCGGAATGAACCGCCAACTTATCCAGCACGTTTTTTGCGCAGCAAATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACAATCACACACGTTCATTTATACTCCTACACAACGGACAATTTAGCCTACCCAATTCACCTGTACCACATCTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGAACGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGACCCAGCTGAGGCTCGAACCAGCGACTTTCTTGCTGTGAGGTGACAGCACTACCTACTACGCCACTGCAGCGCCCTCTTTTCCACTTAATACAGTGAAAGTTTTCAGAATCCTTTGTAAGGTTTATTAAATATGCATATTGTTTCCCTTCTAGGAAAAGCTTTCTAAAACTGCAGATGCAAAGGCCTCTTATGATGCCTGGAAAGAG[A/T]AAAAACGTGACGTCATAAGAAAGAAACTCAGCGAAAAACAGAAGCTAATCAACCAACAACAAGTGGAAATGGATAAAAAACAAGAAAAAAAGGAAACAGCAAAACAGGTCTGCGTTTTCATAAAAAATATTTACAAATACAATTATTAGAAATACTTTATTAAAACAAATATGAAAGGGATCTACTTATTTATCCACTACACATTTATACATTTCCAAAAGCAGGTTTTTGAGAAGTGGAAAGAGGAGCACGACAGTATCCTTAAAGACAAGATCAGGGAAAAGAAACAGGCTGAAAGAAAGCTGAAACTACAGAAGGTCACAGAGAAAGAAGAGAGAAAGAAGGACTGCTCCTCTGCTTTCACTAAATGGTAAGAAAGACACATTTGAAATATACGGAACTTTAATTTTAGTCTTTCTCTTTTGTTAAACAGCTCTCATTTGGTTATGCTCAAGCCACTCAGCAATTATGTATTGATTAAAATGTAAATGAGCTCTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8871
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:
A > C
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054225 | Nonsense | 510 | 678 | 10 | 13 |
| ENSDART00000133937 | Nonsense | 510 | 678 | 11 | 14 |
| ENSDART00000054225 | Nonsense | 510 | 678 | 10 | 13 |
| ENSDART00000133937 | Nonsense | 510 | 678 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 24599558)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 25051329 |
| GRCz11 | 1 | 25742158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTTCTAAAACTRCAGATGCAAAGGCCTCTTATGATGCCTGGAAAGAG[A/C]AAAAACGTGACGTCATAAGAAAGAAACTCAGCGAAAAACAGAAGCTAATC
Long Flanking Sequence:
TTCATTCATTCATTTTCTTTTCGGCTTAGTCTCTTTATTAATTCGGGGTCGCCATAGCGGAATGAACCGCCAACTTATCCAGCACGTTTTTTGCGCAGCAAATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACAATCACACACGTTCATTTATACTCCTACACAACGGACAATTTAGCCTACCCAATTCACCTGTACCACATCTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGAACGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGACCCAGCTGAGGCTCGAACCAGCGACTTTCTTGCTGTGAGGTGACAGCACTACCTACTACGCCACTGCAGCGCCCTCTTTTCCACTTAATACAGTGAAAGTTTTCAGAATCCTTTGTAAGGTTTATTAAATATGCATATTGTTTCCCTTCTAGGAAAAGCTTTCTAAAACTGCAGATGCAAAGGCCTCTTATGATGCCTGGAAAGAG[A/C]AAAAACGTGACGTCATAAGAAAGAAACTCAGCGAAAAACAGAAGCTAATCAACCAACAACAAGTGGAAATGGATAAAAAACAAGAAAAAAAGGAAACAGCAAAACAGGTCTGCGTTTTCATAAAAAATATTTACAAATACAATTATTAGAAATACTTTATTAAAACAAATATGAAAGGGATCTACTTATTTATCCACTACACATTTATACATTTCCAAAAGCAGGTTTTTGAGAAGTGGAAAGAGGAGCACGACAGTATCCTTAAAGACAAGATCAGGGAAAAGAAACAGGCTGAAAGAAAGCTGAAACTACAGAAGGTCACAGAGAAAGAAGAGAGAAAGAAGGACTGCTCCTCTGCTTTCACTAAATGGTAAGAAAGACACATTTGAAATATACGGAACTTTAATTTTAGTCTTTCTCTTTTGTTAAACAGCTCTCATTTGGTTATGCTCAAGCCACTCAGCAATTATGTATTGATTAAAATGTAAATGAGCTCTCTT
Associated Phenotype:
Not determined