ZMP
zgc:103474
Ensembl ID:
ZFIN ID:
Description:
Novel protein containing tubulin-binding domains (Zgc:103474) [Source:UniProtKB/TrEMBL;Acc:B0UXK7]
Human Orthologue:
MAP2
Human Description:
microtubule-associated protein 2 [Source:HGNC Symbol;Acc:6839]
Mouse Orthologue:
Mtap2
Mouse Description:
microtubule-associated protein 2 Gene [Source:MGI Symbol;Acc:MGI:97175]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14807 | Nonsense | Available for shipment | Available now |
sa8917 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21548 | Nonsense | Available for shipment | Available now |
sa21549 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14807
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 |
---|---|---|---|---|---|
ENSDART00000059736 | None | None | 248 | None | 5 |
ENSDART00000077358 | None | None | 291 | None | 5 |
ENSDART00000112298 | Nonsense | 305 | 1710 | 6 | 16 |
ENSDART00000134294 | None | None | 374 | None | 8 |
ENSDART00000135581 | None | None | 169 | None | 3 |
ENSDART00000135902 | None | None | 248 | None | 6 |
ENSDART00000140436 | None | None | 591 | None | 9 |
ENSDART00000144893 | None | None | 154 | None | 4 |
ENSDART00000148306 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 40012124)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 39150020 |
GRCz11 | 9 | 38959815 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATTAATAATTCAATACAATGCAGACTACTTGAGATTTGCTTTCAGCTT[T/A]GAAGATGGAAGCAGAGAGGCCAGAGAGTGAGAGGACAGATCCAATTGGCA
Long Flanking Sequence:
TATTTTATCTAGAAGTGTATTTTAAACCTAGTTAATGCACAAAATATAGGAATAATCAACAAGTAGCTTGCATATTGTCTTATATGTGTTTACTAGTACTTGTTTATCTACTGAAAATGAGAACCACTGTGCATTTTCCATAATCTCTGTATATGTATTTGGCAGAAGTTTTTAAATCAGCCATTTCATCTTGCTGCTGGTGTACTGAAGTCACCATCGTCTTTGGACCACCGTCTTGGATATTTCATCCTCATTTTCTGGACTTCATCCACGCAACATTAATTGTTCTGGGTCTGCATGCTGGTCCTTGTCATATCCATGCTATCACTCCATCACTGAATTGGTATGTGTGTCTCATCGGCTGCTGGTATTTGAAAATGGATGTTCATTTTACCAAGAGCTTTGCCTGTCTGTGTGGTGGTTGGCCTGGCAAACAAGTTGTACTTTGAATTATTAATAATTCAATACAATGCAGACTACTTGAGATTTGCTTTCAGCTT[T/A]GAAGATGGAAGCAGAGAGGCCAGAGAGTGAGAGGACAGATCCAATTGGCATGGACTTCACTGAATCTGCAATGCATCTCGATGATGATCTCCCATCTTACCAGAGTCTTGCCAGAGATGCAGATATGCCAGAAAGCCCCTTTGCTCTAACATGCCCCATGGAGGATTTTGAAGTGCCTCCAAGAGATCAGGGTTATGCCAAAGAACCTTGTGAGGCTCCAACTGAAAATCCTGATGGACAATGTGGTGCTGTGAAACAGCCTTCAATCGAATTATGTGTCTCAAGCAACATTAATGAGGTCAAATTAGAGCAGATTCAAGAAAAACAAGTGGACATAACAGCAGCAGAGGGAGACATGAAGGACAAATCTGGCATGTCTGCTTACTTTGAGACCACAACAATTAAAACCGATGCTGTTGGATCTCAAGGAGAAGGATATTATGAGCTGAGTAATACATCAGAGGAACAAAAGGACTTTACTGGTAACATGCCACTTCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8917
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 |
---|---|---|---|---|---|
ENSDART00000059736 | None | None | 248 | None | 5 |
ENSDART00000077358 | None | None | 291 | None | 5 |
ENSDART00000112298 | Nonsense | 522 | 1710 | 6 | 16 |
ENSDART00000134294 | None | None | 374 | None | 8 |
ENSDART00000135581 | None | None | 169 | None | 3 |
ENSDART00000135902 | None | None | 248 | None | 6 |
ENSDART00000140436 | None | None | 591 | None | 9 |
ENSDART00000144893 | None | None | 154 | None | 4 |
ENSDART00000148306 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 40012774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 39150670 |
GRCz11 | 9 | 38960465 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGAAGAGATGACTGCAGATTGTCTCCTGGGAAATTGGCTCTGGAGCAG[C/T]GAAGTTACTCTTTGAATATTACTATTGGGGCAATGGATCATGGAGATGCC
Long Flanking Sequence:
CATGCCCCATGGAGGATTTTGAAGTGCCTCCAAGAGATCAGGGTTATGCCAAAGAACCTTGTGAGGCTCCAACTGAAAATCCTGATGGACAATGTGGTGCTGTGAAACAGCCTTCAATCGAATTATGTGTCTCAAGCAACATTAATGAGGTCAAATTAGAGCAGATTCAAGAAAAACAAGTGGACATAACAGCAGCAGAGGGAGACATGAAGGACAAATCTGGCATGTCTGCTTACTTTGAGACCACAACAATTAAAACCGATGCTGTTGGATCTCAAGGAGAAGGATATTATGAGCTGAGTAATACATCAGAGGAACAAAAGGACTTTACTGGTAACATGCCACTTCCTGAAATCAGCTACAGCACATTGGCTCAAACACAATCTTTGGAAGTCCAACCAGATCTTCCGAAAAGTAGTGCAAACACACTAGATACCACTTCACCAGCAGACAGAAGAGATGACTGCAGATTGTCTCCTGGGAAATTGGCTCTGGAGCAG[C/T]GAAGTTACTCTTTGAATATTACTATTGGGGCAATGGATCATGGAGATGCCCAAGGGCGTCCCAGAAATTTCTCTCCATTGGCCACTGACATCATGTCTCATACTAGTGGGAGCCTTGATGAATCAGCTGATTACCTTCCTGTCACAACCCCCTCAGTGGAGAAACTCCCTCCGTTTCCCCCACTAATCCTGGAGGCAACTACCTCTGTTACAACTGCATCATCTTCACCTCCCCAAGCAACAGTCACTGATGTAAAGACCAGTCCACTGACAGAATCTCCAGAATCACCCATCCAAGCTAAGTGCTGTTATAAGAATGGCACCGTCATGGCCCCAGACCTACCTGAAATGTTGGACCTGGCAGGTACTCGTTCAAGGCTGACGTCTGACAACACGGATCAGGAGATGATGAGGAGAAAGTCTGTCCCAATGGACATGTCTTCTCTTGTGAGTGATTCTTTTGCACATTTGTTCAAAGGTGACCAGGCCCAAACTGCTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21548
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 |
---|---|---|---|---|---|
ENSDART00000059736 | None | None | 248 | None | 5 |
ENSDART00000077358 | None | None | 291 | None | 5 |
ENSDART00000112298 | Nonsense | 823 | 1710 | 6 | 16 |
ENSDART00000134294 | None | None | 374 | None | 8 |
ENSDART00000135581 | None | None | 169 | None | 3 |
ENSDART00000135902 | None | None | 248 | None | 6 |
ENSDART00000140436 | None | None | 591 | None | 9 |
ENSDART00000144893 | None | None | 154 | None | 4 |
ENSDART00000148306 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 40013677)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 39151573 |
GRCz11 | 9 | 38961368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTCCAACTTTACCAGATAATGAGAAAGAGTTGCCTGACAAACCAGCT[G/T]AAATCTTTATCACACCAAAGGTGACGGTTACTCTTGAGGAAGCAAAGCCT
Long Flanking Sequence:
AGATGATGAGGAGAAAGTCTGTCCCAATGGACATGTCTTCTCTTGTGAGTGATTCTTTTGCACATTTGTTCAAAGGTGACCAGGCCCAAACTGCTACAAAAAGAGAAATGCAATTGGAGGAGCAAGGATATTGTGTTTTTAGTGAATACTCTGGTCCCATGCCATCCCCTGCAGATGTGCACAGTCCAATAGACACTTCTTCTCAGATCTTCAACACTGTGATATCAGAAGAGAAAGAAACTGGCCTTGTTGCATTTGGCCAACAGAAGAGCCAATCAACTGAAGATGTAAAAGCAATAGAAGTTATTTTGCCACAAGCAAAATCAGAAGAAGAAAAGCCACAAAACCAAGACTCATTTGAAAATGAAAGTGCACCTTTTGGAAAACCTTCTACAGATAATGCGAAAGATAAGTCTGGTCTTTTGACAACTGAACCTTTGGAAGAAATCAAGAGTCCAACTTTACCAGATAATGAGAAAGAGTTGCCTGACAAACCAGCT[G/T]AAATCTTTATCACACCAAAGGTGACGGTTACTCTTGAGGAAGCAAAGCCTGATCTTGATGCAGATACTAAACTTGCAGCTGAAACTGAAGCTGAAATAGCTGCTTATGAGAGGCAAATTCGCAAATTGGAGATGGAAGACCGGCCACTGAGTGTAGAGGAGGAACGGGAGCTCCAGGAACTCAGGGAGAAAGTAAAGAATAAACCAGACCTTGTCCACCAAGAAGCCTATGAGGAGGTGGATGCAGAGGACGTGTATCAGCTCACTGGAGCTGCGAAGGACAGAATTGCCCGACCCCTCAGACCATCCCCTGCATCTTCTGTAGAAAGCGCCACAGATGAGGAGAAACCTAGATCACCAGGCGAGAAAGAAGCTCTCAAAACAGATCCTAACAGGTTATCTCCTGTTGGGTCTTTTGAGAAATATTTTAGAGAAGAGAGACCTTCTGAGCAGGAGGTAAAGATGAAAGACTCAGCGGAGCCTGTCAAAGAGAAGGTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21549
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059736 | None | None | 248 | None | 5 |
ENSDART00000077358 | None | None | 291 | None | 5 |
ENSDART00000112298 | Essential Splice Site | 1338 | 1710 | 9 | 16 |
ENSDART00000134294 | Essential Splice Site | 173 | 374 | 4 | 8 |
ENSDART00000135581 | None | None | 169 | None | 3 |
ENSDART00000135902 | None | None | 248 | None | 6 |
ENSDART00000140436 | Essential Splice Site | 300 | 591 | 4 | 9 |
ENSDART00000144893 | None | None | 154 | None | 4 |
ENSDART00000148306 | Essential Splice Site | 147 | 179 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 40019198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 39157094 |
GRCz11 | 9 | 38966889 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCGACTGCCTTTCAGTGTGGCCAGGCACTCAAGAGACCGAGCATCTG[T/A]AAGAACCATATCAGATTTACGTCTTATACAAGTATATTAAAGTAATAGTA
Long Flanking Sequence:
ATGTACTTTTATGGTAAACACTTATGGTGCTATTGAGGTGGAACACTGTTAAGGTTAGGGACAGGTTTTTTGGTATGGGTAGGCTTAAAGGTGGAATAAGGTGTCAAAGTATGGCTTAACAGTGTAATTTTTGTTCATTTGAAAGAATATGAGTACAATTTAAAATCATGTACAATATGTACATAAAAAGTGTATCGTACCAAGAGATTAACATAAATGTAAGTATATAGCGGTTAAGGCCTTTTAATACAAAGTGGGACTGTTTATTCTGTTGTGCATTTGGGTGATAACTGTAAGTACCTTGCGTTTAAGGTTCCAGTGTGTTTGCTTGACTGTACAATCTGTTTAATTTCATCGGAGCACATATAAGTCAGTGGTCATTGTCACAGTATGTATTTTCTTTTTGACTCTCATTTTGAATCTTTTCTGTCTTTTTGCAGTGTCTGCAGATGGTCGACTGCCTTTCAGTGTGGCCAGGCACTCAAGAGACCGAGCATCTG[T/A]AAGAACCATATCAGATTTACGTCTTATACAAGTATATTAAAGTAATAGTAAATAATTAGAGAGTAGACTGTGTACTACAGATCAACTTAAAGGGACAGTTCATCCTTGCATTTAAATCTGCTGTTAACTTGATCATCTCCAGGCCATACATATATCAGTACACTGTAAATCCCAACAGTCAACTTTATTAAATGAAATGAATGTAGTTAACTCAAAATTGACTGAAAGTTAATTCTACCCATTTGAAAAGAGTTTTAAACTCAGTGTTGAAAGTAATGAGATAATTAAATACCCCATCACCTCAACTTTAATGCAGGTAGTTCACCGTACTCATATAGATTAGTTTTTTTAAACTCAAATGGTTAGTAGCAATTGGTTTCCTTAAACAGTTTGAGTTGCCTTAACTTATTGGGTTTTACAGTACTCAGTTGGTTTGAGTTTTCTTCATTTATTAGGTTTTACTGTGCTCAAATTGCTTTGTTTAAAATCTTAAAGGGATT
Associated Phenotype:
Not determined