ZMP
si:dkey-37m8.10
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate microtubule-associated protein 1B (MAP1B) [Source:UniProtKB/TrEM
Human Orthologue:
MAP1S
Human Description:
microtubule-associated protein 1S [Source:HGNC Symbol;Acc:15715]
Mouse Orthologue:
Mtap1s
Mouse Description:
microtubule-associated protein 1S Gene [Source:MGI Symbol;Acc:MGI:2443304]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37570 | Nonsense | Available for shipment | Available now |
| sa11714 | Nonsense | Available for shipment | Available now |
| sa17845 | Nonsense | Available for shipment | Available now |
| sa29837 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43883 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37570
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 |
|---|---|---|---|---|---|
| ENSDART00000086064 | Nonsense | 384 | 1311 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 39685570)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 36862203 |
| GRCz11 | 22 | 36802948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTGACCCTAGGGTCCTCAGAAGTTCTGATCAGGTTTCTCTAACATTA[C/T]AGCATTTAGAAAAGTTGTCGATATTTCCAGAACGGCTCAGTCGATCTGCC
Long Flanking Sequence:
TGCTCCCCGAGATGGAGGGCCTTCAGGAGTTCACCGAGTATCTCTCAGAGTCTCTTGAACCTCAGTCGCCATTTGACCTGCTTGTGCCTCCCAGTACAGTAGGCTTTCTGAAACTGTCCCGTCCCTGCTGCTATGTGTTCCCCGGAGGAAGAGGCGACAGTGCCTTCTTCGCTGTGAATGGTTTTAATGTCTTAGTCAATGGCGGGTCTGATGCTCGATCCTGTTTTTGGAAACTGGTGAGGCATCTAGACCGAGTTGACTCCGTATTGCTCACCCATGCAGGTGTAGATAATTTACCTGGTATAAACAGCCTACTTTACAGAAAAGTGGCTGAACATGAAGAAGAACAGTCCGCTGGATCACAGAGCAGTGACGACTGGCAGAAGAATCTTATATCTCCAGAAATAGGTGTTGTATTTTTCAATGCATCAGAAAGACTCAAGAAATTGCAGAGTGACCCTAGGGTCCTCAGAAGTTCTGATCAGGTTTCTCTAACATTA[C/T]AGCATTTAGAAAAGTTGTCGATATTTCCAGAACGGCTCAGTCGATCTGCCGGGCCAACTATTGAGCCGGTAATTCTTTTCCAGAAAATGGGTGTAGGTCGACTAGATCTTTATGTGCTCAATCCAGTCAAAGGTAGCAAAGAACTAGAGGCTTTCTTGCAAACTTGGCCTGCAAGTCCTCCAAATATAAAACCCACAGATATTCCTCTTGAGAGTATAGTGTCTATATGTGCGCTGTTGGTGTGGCATCCAGCTAATCCTCGAGAAAAGATCATCAGGGTTTTGTTTCCTGGGTGCACTCCACAGTCCAAGATCTTTGAAGGTTTAGAGAGACTAAAACATCTGGAGTTCCTCAAACACTCAGTAGTTAGTTTGAAGGACCTTGAGGCATCCAAATTGGATAAACAGCCAAAGCACACCGGGAGCAAGGAAAGCCTTAAGAGTATTTCCAAAGAATCTCGACCTGGCAGTGCCTTACTCAAAGACAAGGTAGTCAAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11714
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086064 | Nonsense | 712 | 1311 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 39684586)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 36861219 |
| GRCz11 | 22 | 36801964 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCTAAAAAGGATCCTGTAACTAAAGGGAAACCAAAGCCAGACAAAAAG[G/T]AGCCTGACAATGTGAAGTCCTCAAGTGGRGACAAWTCAAAGACWTCCACG
Long Flanking Sequence:
ACAAGGTAGTCAAAGTAGATCCGAAAAAGCAAGACACTAAAACAAAGACTAAACCCACTAATGAAAGTGAAGAAAAGGCAAAGCCAAAAGATGATGTGAAGCTGAGACCTAAGACTGCTGAAAAGCAAGTAGCTAAGAAAGAACCTGCAAAAGATGAGAAAAAGGAAGTGAGGAAGAAAGAGGAAAAGCCGCCGACAAGTATTGCAAAGAAAGATGAGCATGTGGAGAAAAAGAAAGAACCCTTGAAAAAAGATCTTGGTGCAAAGCCCAAGAAAGATATTGTTAAACCTGATCTAAAAAAGGAGATTAAGAAAGAGGTCAAACCAGAAAACAAAAAAACTACCAAACCTCCTGTCAAGGAGGTTAAAAAACCTGCTGGAAGTTTGCCTGGGAATACAGAGTCTAGAAAGTCAGTTGGCAAGAATGGCTCTCTAAAAAAAGACGTATTGGTCTCTAAAAAGGATCCTGTAACTAAAGGGAAACCAAAGCCAGACAAAAAG[G/T]AGCCTGACAATGTGAAGTCCTCAAGTGGGGACAAATCAAAGACATCCACGCCTGAGGACATTTCTAAACAATTAGAGAAGTTGAAGTTGGATAATGAACATGGGTCACTGCAGGATGCTGAGGGAAACAATATGAGCTCAAGAACTGCCTCTGACTGCAGCGCTGGGCAAGTGAACGGCTCTAAAACTGGTACTGAGGAAAGTCCAGAGAAGTTTCGGAGTATGGATGGAACTCCCGGCTCAAACAACCCCTCACCACTTACCAAGACTCCAAAGAGTGAGAGAAGTGTTAATTTTGATCTCACACCAACAGAGCTTGATGGATGCCTCAAAGAGGATGCCTGTACAAGCTCGGATGAAAAAACTCTTGAGTTAGTTTCTCCTGCAGACTCCGGGAAGAACAGTTCATGGCATACCCGTTACCCACAATCCCCGGACAATGCTTGTCTAGATTCTAGTGAAGATTGTAAGGTAGGCATCAGGAAGTCTGGTCTTGCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17845
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 |
|---|---|---|---|---|---|
| ENSDART00000086064 | Nonsense | 768 | 1311 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 39684418)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 36861051 |
| GRCz11 | 22 | 36801796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CWGAGGGAAACAATATGAGCTCAAGAACTGCCTCTGACWGCAGCGCTGGG[C/T]AAGTGAACGGCTCTAAAACTGGTACTGAGGAAAGTCCAGAGAAGTTTCGG
Long Flanking Sequence:
TGAGGAAGAAAGAGGAAAAGCCGCCGACAAGTATTGCAAAGAAAGATGAGCATGTGGAGAAAAAGAAAGAACCCTTGAAAAAAGATCTTGGTGCAAAGCCCAAGAAAGATATTGTTAAACCTGATCTAAAAAAGGAGATTAAGAAAGAGGTCAAACCAGAAAACAAAAAAACTACCAAACCTCCTGTCAAGGAGGTTAAAAAACCTGCTGGAAGTTTGCCTGGGAATACAGAGTCTAGAAAGTCAGTTGGCAAGAATGGCTCTCTAAAAAAAGACGTATTGGTCTCTAAAAAGGATCCTGTAACTAAAGGGAAACCAAAGCCAGACAAAAAGGAGCCTGACAATGTGAAGTCCTCAAGTGGGGACAAATCAAAGACATCCACGCCTGAGGACATTTCTAAACAATTAGAGAAGTTGAAGTTGGATAATGAACATGGGTCACTGCAGGATGCTGAGGGAAACAATATGAGCTCAAGAACTGCCTCTGACTGCAGCGCTGGG[C/T]AAGTGAACGGCTCTAAAACTGGTACTGAGGAAAGTCCAGAGAAGTTTCGGAGTATGGATGGAACTCCCGGCTCAAACAACCCCTCACCACTTACCAAGACTCCAAAGAGTGAGAGAAGTGTTAATTTTGATCTCACACCAACAGAGCTTGATGGATGCCTCAAAGAGGATGCCTGTACAAGCTCGGATGAAAAAACTCTTGAGTTAGTTTCTCCTGCAGACTCCGGGAAGAACAGTTCATGGCATACCCGTTACCCACAATCCCCGGACAATGCTTGTCTAGATTCTAGTGAAGATTGTAAGGTAGGCATCAGGAAGTCTGGTCTTGCTGTGGAAGACGGTCAATTGGGAATCTGCAAGAACTCTAGAAGCAATATTGAAAACAGCTCCATATCGTCACAAGATCGACAATCAAGCTTTCTCTCCTCAACTTCATTTAAAGACGGCTCTACCAGCATCACTTCCTTCCCCGCGGAAGTAGGCTCTCCACACTCCACTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29837
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 |
|---|---|---|---|---|---|
| ENSDART00000086064 | Nonsense | 1076 | 1311 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 39683492)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 36860125 |
| GRCz11 | 22 | 36800870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTATTTCGGTTTCTGATTCTGACGTGCCGCCAGCCACTGAAGAGTG[T/A]CCTTCTATTAGTGAGGAGTTGGACTCTGAAGAGGACACTACTAGTGATTT
Long Flanking Sequence:
TCAACTTCATTTAAAGACGGCTCTACCAGCATCACTTCCTTCCCCGCGGAAGTAGGCTCTCCACACTCCACTGAAGTAGAGGACTCTTTATCGGTTTCCTTCGAACAAGTGCCTGTTTGTCATCCTCAAGAGGAGATGGGTAGTCTAGCGTACACTAATGGACATCTAGCAGACCGTGACCCAAAAGCAGATATGTCTTTACCTTTAAAAACATCTCACAATAGTCACCATGCATACGATGACTCTGAAAATCACCTTTATGGACTACAGGGTGACGTTCTGCCTCATGATGTCGATCTATGTCTGGTTTCACCTTGTGAGTTTAAGCACCACAAATCTCTGGAGAACCAACAAGGATTGTCTTCGGAGGTTGCCGCCCCGAGTCCTGACCTTTCTCAGGAGCCACTTAGAGATCACCAATCACAGGAGACCACATCATCTGTAAGCGTCTCTCTTATTTCGGTTTCTGATTCTGACGTGCCGCCAGCCACTGAAGAGTG[T/A]CCTTCTATTAGTGAGGAGTTGGACTCTGAAGAGGACACTACTAGTGATTTGTTTCCACCTCACCATCCAAGCAGTCACTCGTTACACCACAATTCCCAAGACCCTCCGCCTGCCCCAATGAAGGATTTACCACCGCTGCCACCCCAACGCGGTGCCTGCATGGCTGACCCTGAGGCTGACAGTCAGGGAAAGTCTTCCAAGAATGTAACTGCAAAGACCAAAAAAACTGCAGCAGCAGCTCCCACAAAGACGGGATCTGCTAATGTTGTAGCACAGACTGGGAAGACAAAGATTGGTGGTCCGGTGTCTGCAACTGGGACTATTCGGGTAACATCGAGTTTGGACACCAGACCTCCGTCCCGCAGTGCTATTGGTGGATCTAGGCCAACGTCTTCCAAGTCCTCATCCAGTAAGTGGCCTTTTGTGCTGGGACATTCATTAGTATATATTTGTGGCCTAAAATGATTTTGTGACACTTTTTTTTAAAACGTATGACATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43883
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086064 | Essential Splice Site | 1213 | 1311 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 39683081)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 36859714 |
| GRCz11 | 22 | 36800459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCAGTGCTATTGGTGGATCTAGGCCAACGTCTTCCAAGTCCTCATCCAG[T/C]AAGTGGCCTTTTGTGCTGGGACATTCATTAGTATATATTTGTGGCCTAAA
Long Flanking Sequence:
GATCACCAATCACAGGAGACCACATCATCTGTAAGCGTCTCTCTTATTTCGGTTTCTGATTCTGACGTGCCGCCAGCCACTGAAGAGTGTCCTTCTATTAGTGAGGAGTTGGACTCTGAAGAGGACACTACTAGTGATTTGTTTCCACCTCACCATCCAAGCAGTCACTCGTTACACCACAATTCCCAAGACCCTCCGCCTGCCCCAATGAAGGATTTACCACCGCTGCCACCCCAACGCGGTGCCTGCATGGCTGACCCTGAGGCTGACAGTCAGGGAAAGTCTTCCAAGAATGTAACTGCAAAGACCAAAAAAACTGCAGCAGCAGCTCCCACAAAGACGGGATCTGCTAATGTTGTAGCACAGACTGGGAAGACAAAGATTGGTGGTCCGGTGTCTGCAACTGGGACTATTCGGGTAACATCGAGTTTGGACACCAGACCTCCGTCCCGCAGTGCTATTGGTGGATCTAGGCCAACGTCTTCCAAGTCCTCATCCAG[T/C]AAGTGGCCTTTTGTGCTGGGACATTCATTAGTATATATTTGTGGCCTAAAATGATTTTGTGACACTTTTTTTTAAAACGTATGACATTATTTGCTTGGATTCTAGTGCTTTCCTGTAAATATACAAAAAACTTGTGATCTTAAGAACCATTGTACTCGCAAAATTCTGGAGGGACTGATGAATCTTATGATCTCAAGTAGGGCTGCATGACATTGGGAAATCTGACAATGCGTGATTTAGTTTTTCTGCAAAAGTTTAATTGGTATAAAATGGATAAAATGTAATAAACTAATTTCAATCATTGAATAAATAAGTTCTTAACCATTTTCTAGGGAGTCCTAATAGTATTCAGGTAAAGAAATTAAATAATGAAATGTAAAACAGCGCTGTACAGTCTATAGTCTGTATGGTCATATTAATAATTCTATCAAATTAACCTTCACTAAAGTTTCAAACTATAAACTTTCTAGTTCCTAGATGCTTTAAATCAGAGGTCACCA
Associated Phenotype:
Not determined