ZMP
si:ch211-89f7.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2BIR1]
Human Orthologue:
TCTN2
Human Description:
tectonic family member 2 [Source:HGNC Symbol;Acc:25774]
Mouse Orthologue:
Tctn2
Mouse Description:
tectonic family member 2 Gene [Source:MGI Symbol;Acc:MGI:1915228]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33549 | Nonsense | Available for shipment | Available now |
| sa40369 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40370 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa8441 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa8615 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33550 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33549
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 |
|---|---|---|---|---|---|
| ENSDART00000051669 | None | None | 597 | None | 16 |
| ENSDART00000135921 | Nonsense | 131 | 709 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 14609197)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 12906634 |
| GRCz11 | 5 | 13406851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCGCAGTCTCCAGCTGTGTGGGAATGAAACCTCCATCTCGGACTGCTG[T/A]CTGGAGTTGCTTTGTGTCCAGGAGACTCTGCTTGTGTCTGCTTGTGTGGA
Long Flanking Sequence:
TGTATTTATGTCTGCACTGTCTGCACTGTTTGTACTCTCTGTACTGGAAGCTCCTGTCACTAAGACAAGTTGTTTGTGCAAACACACTTGGCAATAAAGCTCTTTCTGATTCTAATTTCTGTTTTGTGGAAAGATTTGTAAATCAATTTTAAATAAAGTGTCTGGTAAATCAGCGTTTCCAAACCCTGTTCCTGGAGGCACACCAGCAATATTTTGGCTGTCTTACTTGACCCATTAAGTTTAGATTTTGAAGTTCTGATGAATTGATTCAGTTGTGTTTTTGATTTTGTGTGCCTCCAGGAGCTTGGTTGGGAAATGAATGAATAAATATGTAAATTGATTCAAAACACTTCAAAACGCCATACTTGAATGCTGCAATTCTGATATCATATATATTCTTTCTGTTGAATGTCAATCTATCAGAATGCCTTTCTGGTGCACGTGAGTCTGAACCGCAGTCTCCAGCTGTGTGGGAATGAAACCTCCATCTCGGACTGCTG[T/A]CTGGAGTTGCTTTGTGTCCAGGAGACTCTGCTTGTGTCTGCTTGTGTGGATGAAACACCTAAAGCCTCCCTCATCATACAGACCCAGATTTATGCCCAGATCCACCCCAGTAAACCTCCATCTGGTCAGTGTTTCTCGTAATATTACTGAATGAAGTGTTGTAGGACAACCTAGTTATCTTAAAATATGCTGTGGTTCATGAATATTCCTTTCTATCTTACATGTTTTGCATTTATTTCTTTAGCGGACATAAACTCAAAAATGAGAAACATCAAGTAGTCAAGCTTAAAGATTGCAAAAGTCATAGGTTTGATTAGCAGAGAATGTATGACTTTAGAAAATGTATTGTGAATCTTGAATTTAAATTGTCCGGTTGGCATTTGTAAAAAAAAACAAAACAAAACAAAACAAAAAAAAAAACCGCCACCATAAACCATTAGACTATTAATCCTACCTGTGATTTTATTTATTTATTTAGCCTATTTTAATTACTTTTCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40369
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 |
|---|---|---|---|---|---|
| ENSDART00000051669 | Nonsense | 46 | 597 | 2 | 16 |
| ENSDART00000135921 | Nonsense | 181 | 709 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 14612352)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 12909789 |
| GRCz11 | 5 | 13410006 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCATCATATCTTTTTGTGTTTTGCAGTAAATAAAACAGTCATTCCCAAC[C/T]AAGTATTTCAGCCGCTCGGCCAGTGCCCGTGTGACGTTTCTCCAGGCGAG
Long Flanking Sequence:
TAATAAATAATAAATAAATAAATAAACAAATAAGGGAGCGTTCACTCAAAAATGTACATTTTCTCACAATTTCCTCAACTTTTATTTGTTCAAACCCTTTATGATTTTATTTCTTCTGTTGAACACAAAATAAGATATTTTGAGGAAAGCTGAAAACCTGCAACCTTTGACTTCCATAGTAGGAAAATTATATACTATGTAAGTCAATGGTTACTTTCAGCATTCTTCAAACTATCTTCTTTTGTGTTTAACAGAAAAAAGAAACCCATAGGTTTGGAACAAGTAAAGGTTGAGTAAATGATGACAGAATTCTCATTTTTGGGTGAACTATCACTTTAATTCATTGTTTACTCAGACTGCTTTTTTTCTCATTTTTTCGAACCACAAGGAGAAATAAAATAAATAGTTCATGTATATGAATATAAGGGCGAATTAATAAAAATACATTATATCATCATATCTTTTTGTGTTTTGCAGTAAATAAAACAGTCATTCCCAAC[C/T]AAGTATTTCAGCCGCTCGGCCAGTGCCCGTGTGACGTTTCTCCAGGCGAGTGTGACATACGCTGCTGCTGTGATCAGGTAATAATTCAAATTCTGAGAGAGTTTAAACACATTTATTTATGATAGTTGGAGGTGACACGGTGGCTCAGTGGTTAGCACTGTCACCTAACAGCAAGAAGGTTGCTGGTTCGATGGTTGCTGGACCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCATGTTGGTGTGGGTTTCCTCTGGGTGCTCCGATTTCCCCTACAGTCCAAAGACATGCACTATAGGTGAATTGAATAAACTAAATTGGCCGTAGTGTATGACTGTGTGTGTAAATGAGTGTGTATGAATGTTACCTTGTACTGTGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATGCACAAATAGTTGGCAGTTCATTCCGCAGTGGCAACCTCTGAAATAGAGACTAAGCTGAAGGAAAATAAATGAATGAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40370
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 |
|---|---|---|---|---|---|
| ENSDART00000051669 | Essential Splice Site | 252 | 597 | 6 | 16 |
| ENSDART00000135921 | Essential Splice Site | 387 | 709 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 14617518)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 12914955 |
| GRCz11 | 5 | 13415172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGACAACATCAGATTATTTGTGTCAAATTCTCCTGAGGTCACTTCAGG[T/C]CAGTTATTCAGGTTAACATTTTGAGCAGTCACCAATTTTAAAATCTATAT
Long Flanking Sequence:
AAAATCCAAATATTGCTTGATACAGTAGATATTAAACATAACATCTGTTTGAATAACTTGTACTGGTCTTTGAACAACATAACATTCAGATTTGTTTAGAAAGATTTCACAAAAAATGAATGTCCATGAAATTCCACAAAAGCAAATTGATTTAAATGGATTCATTTAAGAAAATGTAATTCACTTCATGCCACAGAGGTTAATCAGATATATTTAAAAGTGCCCTTTAGCCATTTGGCAGTGTTTAAGAATTCAACATTATGCATTTGAAGGAATGGCTTGCGAGAAGTGAGTTTGCCCTCAATTGTAGACTTCTTATATATAAATATAGCTTTCAGTTCACTGACTGTGTTTTCTGCCAGTATATGCATGCAAATATGTGTATGTGTGACTGTGCATATGTTTGCTTGCTTTCCAGGTGTGATAGCGGTCAGTGTTGTGGATGATGTAGCTGACAACATCAGATTATTTGTGTCAAATTCTCCTGAGGTCACTTCAGG[T/C]CAGTTATTCAGGTTAACATTTTGAGCAGTCACCAATTTTAAAATCTATATAAAAATAAATAAATAAATACACATTTAAGTATATAATTTTACATACCTAAATAAAATATATATAAGCATATGTACTAAATAATTTTATTTAATGGAGTAAAGGCTGTTAAAATACATGTTATATTAGTAACAATATTTCTGTTTTTGGTCGCACTTTATTTTAAGGTACAACTCTCTGTATTAAAAAACCATTAACCATGAATTTGATCTCAATAAGCTACTATTGCTTTTTGTTAATAGTTAGTAAGATAGTAGTTGGGATTAGGCTAGGTTTAAAGATGAATAAGAGCATGCTTCATAAGAACTTTAAAAAAGTGCCAATTTCTTAATAAAAGGCAGGTAATAAGCCAGTAGTATGATTACTACTGGCTATTAGTATAATAGCATTAACATGACTTTTTCTTTTTGATTAATTAGATTTTTAATTAGTATTCCTTCTAATAACATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8441
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 |
|---|---|---|---|---|---|
| ENSDART00000051669 | Essential Splice Site | 290 | 597 | 7 | 16 |
| ENSDART00000135921 | Essential Splice Site | 425 | 709 | 10 | 18 |
| ENSDART00000051669 | Essential Splice Site | 290 | 597 | 7 | 16 |
| ENSDART00000135921 | Essential Splice Site | 425 | 709 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 14618819)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 12916256 |
| GRCz11 | 5 | 13416473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCACCGCCATTGCTGTGACACGAACCACWGCAAACATCACTGTACCTGG[T/C]GAATATCACTCTCTCAATATAAAATACAGCTTTACTGCAYSTGCTTGTCW
Long Flanking Sequence:
CCCTTTAAGCTATATTTTTTTCAATAGTCAAACCATCATTATACAATAACTTGCTTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAGTATCTATTCAAATATTATTTACTGTCATCATGACAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATGTTTAAAAATGTGTTGAAAAAAATCTTCTCTCCGTTAAACAGAACTTGGGGAAAAATAAACAGAGGGGCTAATAATTCTGACTTCAACTGTATGCATATTAAGGGTAAAGTTCGATCTTTTCTTCTTGGTGTAATTGCAATGTTGTTGTTTTCTATTTAAGAGCCACAACAGTGTGATAATGTCGTTGTGTCCTTGCGTTACACTTTTTACTGGAGAGAGAACGGTCTCACCGCCATTGCTGTGACACGAACCACTGCAAACATCACTGTACCTGG[T/C]GAATATCACTCTCTCAATATAAAATACAGCTTTACTGCACCTGCTTGTCTTATGAGCTGCCTCTCAGTCATGCTTAACAGTTTTTTTTTCTTCAGTAACTTTGACAAGTAGATATTCTGCTGTGTTTGTGAATGGAAACGAGACCTCTCAGTCGTACTCCGGTAAGCCAACACAAATGATGTGAATTTGTATTTAGGAATGTAATGATATTTTTTATAATATTCTAAAAGTTGAAAAGGAAAGTTGCTGTTTTTAGGCTGATATGACTAGAAATTATTCTCTCATTCTGGTGTAATAGTCAAGGAACTTTGTTACCAAACCATGGCTACAGCAGGAGCAGTGATATTACGGAGCATCTGAAAATCAGCTAACTTCCATCCGTATAATCAACATGACAACCTGCTTGCATAGAGAGCACATGTGAGAGATTATTCAGAGCATATTTACTTTGGTGCAGATCATCAGCCTGCTTTAGCCATGGTACAACAGCAAAGTTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8615
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 |
|---|---|---|---|---|---|
| ENSDART00000051669 | Essential Splice Site | 290 | 597 | 7 | 16 |
| ENSDART00000135921 | Essential Splice Site | 425 | 709 | 10 | 18 |
| ENSDART00000051669 | Essential Splice Site | 290 | 597 | 7 | 16 |
| ENSDART00000135921 | Essential Splice Site | 425 | 709 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 14618819)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 12916256 |
| GRCz11 | 5 | 13416473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCACCGCCATTGCTGTGACACGAACCACWGCAAACATCACTGTACCTGG[T/C]GAATATCACTCTCTCAATATAAAATACAGCTTTACTGCAYSTGCTTGTCW
Long Flanking Sequence:
CCCTTTAAGCTATATTTTTTTCAATAGTCAAACCATCATTATACAATAACTTGCTTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAGTATCTATTCAAATATTATTTACTGTCATCATGACAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATGTTTAAAAATGTGTTGAAAAAAATCTTCTCTCCGTTAAACAGAACTTGGGGAAAAATAAACAGAGGGGCTAATAATTCTGACTTCAACTGTATGCATATTAAGGGTAAAGTTCGATCTTTTCTTCTTGGTGTAATTGCAATGTTGTTGTTTTCTATTTAAGAGCCACAACAGTGTGATAATGTCGTTGTGTCCTTGCGTTACACTTTTTACTGGAGAGAGAACGGTCTCACCGCCATTGCTGTGACACGAACCACTGCAAACATCACTGTACCTGG[T/C]GAATATCACTCTCTCAATATAAAATACAGCTTTACTGCACCTGCTTGTCTTATGAGCTGCCTCTCAGTCATGCTTAACAGTTTTTTTTTCTTCAGTAACTTTGACAAGTAGATATTCTGCTGTGTTTGTGAATGGAAACGAGACCTCTCAGTCGTACTCCGGTAAGCCAACACAAATGATGTGAATTTGTATTTAGGAATGTAATGATATTTTTTATAATATTCTAAAAGTTGAAAAGGAAAGTTGCTGTTTTTAGGCTGATATGACTAGAAATTATTCTCTCATTCTGGTGTAATAGTCAAGGAACTTTGTTACCAAACCATGGCTACAGCAGGAGCAGTGATATTACGGAGCATCTGAAAATCAGCTAACTTCCATCCGTATAATCAACATGACAACCTGCTTGCATAGAGAGCACATGTGAGAGATTATTCAGAGCATATTTACTTTGGTGCAGATCATCAGCCTGCTTTAGCCATGGTACAACAGCAAAGTTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33550
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051669 | Essential Splice Site | 316 | 597 | 8 | 16 |
| ENSDART00000135921 | None | None | 709 | None | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 14618990)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 12916427 |
| GRCz11 | 5 | 13416644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTTTGTGAATGGAAACGAGACCTCTCAGTCGTACTCCGGTAAGCCAA[C/A]ACAAATGATGTGAATTTGTATTTAGGAATGTAATGATATTTTTTATAATA
Long Flanking Sequence:
ATGACAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATGTTTAAAAATGTGTTGAAAAAAATCTTCTCTCCGTTAAACAGAACTTGGGGAAAAATAAACAGAGGGGCTAATAATTCTGACTTCAACTGTATGCATATTAAGGGTAAAGTTCGATCTTTTCTTCTTGGTGTAATTGCAATGTTGTTGTTTTCTATTTAAGAGCCACAACAGTGTGATAATGTCGTTGTGTCCTTGCGTTACACTTTTTACTGGAGAGAGAACGGTCTCACCGCCATTGCTGTGACACGAACCACTGCAAACATCACTGTACCTGGTGAATATCACTCTCTCAATATAAAATACAGCTTTACTGCACCTGCTTGTCTTATGAGCTGCCTCTCAGTCATGCTTAACAGTTTTTTTTTCTTCAGTAACTTTGACAAGTAGATATTCTGCTGTGTTTGTGAATGGAAACGAGACCTCTCAGTCGTACTCCGGTAAGCCAA[C/A]ACAAATGATGTGAATTTGTATTTAGGAATGTAATGATATTTTTTATAATATTCTAAAAGTTGAAAAGGAAAGTTGCTGTTTTTAGGCTGATATGACTAGAAATTATTCTCTCATTCTGGTGTAATAGTCAAGGAACTTTGTTACCAAACCATGGCTACAGCAGGAGCAGTGATATTACGGAGCATCTGAAAATCAGCTAACTTCCATCCGTATAATCAACATGACAACCTGCTTGCATAGAGAGCACATGTGAGAGATTATTCAGAGCATATTTACTTTGGTGCAGATCATCAGCCTGCTTTAGCCATGGTACAACAGCAAAGTTTCTTGATTATTACACCAGAATGAGAGTATAGCTCCTAGCCACATCGACTTAGAACAATGCAACTTTTAATTTACTGTCAGTCTTAGAGTGAAGCTTTAAATAGGAGAATCATCAAAACTCTTTGTGACAAATGAGCAAAAGCATTTTGTTCTGCTTTGAAGCATAATTGTTATAT
Associated Phenotype:
Not determined