ZMP
si:dkey-158b13.2
Ensembl ID:
ZFIN ID:
Description:
Triple functional domain protein [Source:UniProtKB/Swiss-Prot;Acc:Q1LUA6]
Human Orthologue:
TRIO
Human Description:
triple functional domain (PTPRF interacting) [Source:HGNC Symbol;Acc:12303]
Mouse Orthologue:
Trio
Mouse Description:
triple functional domain (PTPRF interacting) Gene [Source:MGI Symbol;Acc:MGI:1927230]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32258 | Nonsense | Available for shipment | Available now |
sa12039 | Nonsense | Available for shipment | Available now |
sa23586 | Nonsense | Available for shipment | Available now |
sa12333 | Nonsense | Available for shipment | Available now |
sa11605 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32258
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087055 | Nonsense | 213 | 3087 | 5 | 57 |
ENSDART00000144275 | Nonsense | 154 | 3028 | 4 | 56 |
Genomic Location (Zv9):
Chromosome 19 (position 43482543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 42361591 |
GRCz11 | 19 | 41946730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTGACGGCTGACTTTGAGGGCAGCCTGGACTACAACCATGAAGAGTG[G/A]ATTGAAATCCGCGTGGCCTTCGAAGACTTTACAGGCAATGCTCGGCACCT
Long Flanking Sequence:
AAAACTTTACATAAAAACTGTACATGTATTTGTGCAAAAGCAATGCAGTGCCTATAGAAAATCATCGTATCCTGTGAATATATACTCGCAATACACCCTGCTTCCAAAAGACCTTCTGGATAAAGTTTGAAAATGTACAGGTTAGAAGAAGACTACAAAAACATTTCAAAGGCTGGAAAATGTGATTTGATTTCAGGCTGTATGACAAATAAAGTAATTAATTCAAAGGGGTGTTATGATTGTTGTGCAGAAAAGAGATGAAGTAAATGTATATTATCATATTAAGTAGCACAGAGTCTGTGCCAAAAGTCACTAATGTACATATAGGGGGATAAGTGTGTTGCTGTTGGTGGTTTGTACAACCAACTCACCTGTGTTCACCTGTATCATGTCTTCTTTCAGACCACAATGGTTTCTTTGGAGGGCTTATCGAAGGTGGTGGACCCATCCCAGTTGACGGCTGACTTTGAGGGCAGCCTGGACTACAACCATGAAGAGTG[G/A]ATTGAAATCCGCGTGGCCTTCGAAGACTTTACAGGCAATGCTCGGCACCTGCTCGCCCGGCTAGAAGAGATGCATGAAACGGTGACGCGTAAAGACTTACCGCAGGACTTAGATGGAGCCCGACGGATGATAGAGGAGCACGCGGCTTTGAAGAAGAGGGTGATAAAGGCTCCGGTGGAGGAGGTGGACAATGAGGGCCAAAGGCTCCTGCAAAGGATCCAGAGCAGTGAGAGCTACGCCAACCGAACTGTGCCTGTGCCGCCTGGTCAGAGGGAAGGGCAGGGGCAGCCCAACGCCGACACCCAGGGCCTGGTGCCCCGTATTACAGCTCTGCTGGAGAAACTGCACAGCACCAGGCAGAACCTGCACCAGTCCTGGCACATCCGCAAGCTGCAGCTGGACCAGTGCTTCCAGCTCAGGCTGTTCGAGCAGGACGCTGAGAAGGTAAGAACCATACCCTGCTAAAATATCCAGCTCAAACCAGCCTAGGCTAGTTTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12039
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 |
---|---|---|---|---|---|
ENSDART00000087055 | Nonsense | 836 | 3087 | 14 | 57 |
ENSDART00000144275 | Nonsense | 777 | 3028 | 13 | 56 |
Genomic Location (Zv9):
Chromosome 19 (position 43450714)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 42329762 |
GRCz11 | 19 | 41914901 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCGCAGCAGATGAATGAGTTTGATACAGAAGACCTGACGCTGGCTGAA[C/T]AGAGACTGCAGCACCAYGCTGATAAAGCCCTGACCATGAACAACCTGGCC
Long Flanking Sequence:
TTTACCCATGAAGACCTCAATTTTGGTCCTCACAGTGACACAAGTCCCCATGAGTCTGTGTGCATTCAGGTTTAAGTCCCCACCAGGATATAAAAACAAGTGCACACACACAGACTTGTTCTTGTCATAGACATAATGATATTTCTACTACAAACCACATATACTATCCCCTGACCCCTAAACCCAACCCTTACAGGAAGCAATCTGCATTTTAAAATACTTCATTCTGTGTGATTTATTAGCGCGTTTACCTGTCAGTTTTGGTCCCCACGAGTCTGTGTACATTCAGGTTCAAGTCTGTACCGGGATATAAAAGAAGTACAAACACATTAACTTTTATATATAAGAGCGTGTCAAGTCAGGTCTCTCTTTTTCTTGTCCTGGGTGATCTCATACTGTTGTATCTTCTTTTGCAGATTATCTCAGATCTGGACTCGTGGAATGAGGAGCTGTCGCAGCAGATGAATGAGTTTGATACAGAAGACCTGACGCTGGCTGAA[C/T]AGAGACTGCAGCACCATGCTGATAAAGCCCTGACCATGAACAACCTGGCCTTCCACGTCATCCACCAGGGCCAGGAACTGCTGCAGTACGTCAACGAGGTGCAGGCGTCTGGTGAGTCAATAATGAAGCACACCTATTATCAAACGTCTGTTTTCCAATGTACTATAAACATTCCTCAGAGATTCATTCCTCCTGGAAGCTTGAACTATTGATTCATGGCAGGATAGATCCATGCGTTAAGGTTGTTTACTCCAAATTTTGATGCTAACATCTTAAAGTCGAAACAAAAAGAGATATGTCGGACCTGGGAACAGTTATCTTTAATCTTCTGTTGTCAGGAGCGTCAGTTTGCTTTTGTTCTTCTGCTGCTGTAGCTTATCTTCTTCAAGGTTTGATGTGTAGTTGCTGTTTGAGATTTTAGTACTTTTCTATTAACTACTTCTTAGCCCATAGAATGGCCTCTTGGTGGAAATTTTCCCCTATTTCAGACCACTGGCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23586
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 |
---|---|---|---|---|---|
ENSDART00000087055 | Nonsense | 1355 | 3087 | 25 | 57 |
ENSDART00000144275 | Nonsense | 1296 | 3028 | 24 | 56 |
Genomic Location (Zv9):
Chromosome 19 (position 43430029)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 42309077 |
GRCz11 | 19 | 41894216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCCCACCAGGCATCGTCAACAAAGAGCACATCATTTTTGGTAACATG[C/T]AAGATCTGTACGAGTTCCATCACAAGTGAGTTCAATCTTTCAGCCTGAAT
Long Flanking Sequence:
TTATAGAATTTACAGTTTGTGGTCATACCTCTGTTTTGTTTTGTTAATATGTGATCCAATGATGACTGGGGCTCTGCTGCATTTTTATGGACAGCCCAGTACAGCTGCCATTATGGCCCAATGTTTCGTTTTTTTGCCCGCCGGATCTCCGCAAAGGTCGCGTGACTGAAAATTATCAATATGATATAATGATCCTATAATTTTGACTTTGTGACTTTCTCACAATCCAGATCTAATATATAACAATTTTTAACAATTATTATTATTATTAGTTAAATTGCAACTTATTTGTCATGGTTGCAGTTTCTTATATCTTTATTTCTCCATACTGTGTCTTTATTTCTCACAATCCTGAGTTTATATCTTACAATTTTATTATATCTCACTAATAACATTCTTTCTTTTCCTTCCTGCAGACGTATCTGTGGGAGATGACCAGCGGCGTGGAGGAGATCCCACCAGGCATCGTCAACAAAGAGCACATCATTTTTGGTAACATG[C/T]AAGATCTGTACGAGTTCCATCACAAGTGAGTTCAATCTTTCAGCCTGAATCAATCCTGCCGTCCAGCATTCATTCAATCATTCATCCAGGCGCTATAATCAGAGACTCTTCTCATGTGTATCTTCATCTATCTCCAGTATATTCCTCAAAGAGCTGGAGAAATACGAGCAGCTTCCTGAAGATGTGGGCCACTGTTTTGTGACTTGGGTGAGTAAATTGTAATTGTATATACAGTTGAAGTCAGAATTATTAGACCCCTGTTTATTTTTTCCCCGATTTCTGTTAAACAGAGAAGATTTCTTTCAACACATTTCTAAACATAACAGTTTTAATAACTCATCTCTAATAACTGATTTATTTTATCTTTGTCTTGATGACAGTAAATAATATTTTACTACATAATTTTCAAGACAATTCTATACAGCTTAAAGTGACATTTAAAGGCTTTACTAGGTTAATTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAACGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12333
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 |
---|---|---|---|---|---|
ENSDART00000087055 | Nonsense | 2160 | 3087 | 45 | 57 |
ENSDART00000144275 | Nonsense | 2101 | 3028 | 44 | 56 |
Genomic Location (Zv9):
Chromosome 19 (position 43399345)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 42278393 |
GRCz11 | 19 | 41863532 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGRTCATGTGCATTGTACCAAAAAGATGCAACGACATGATGAATGTTGGT[C/T]GACTCCAGGGGTTTGATGTAAGNNNNTGGTATTTTTCATACCAGTRGATC
Long Flanking Sequence:
CCAATTTCTGCAGCGAGCAACGCCACTGAAGCTGCGCCGACGGATCCACAATGCAGTTCGGAAACGCCTGACGTCACCCATTCAAAGTGAATGGGAAGCGCTGACGCCCCGTGTGAATGGTGTGTTATTCACTTGTGGTCAAGGGGATTCTCAGTTCTTGAATGAGCCTGTGTTATTTAGCGGTTGTTATCTCTGAATAACAATCCTTGAAATGTCACAACTGACCAATCAGAATAGAGTATTCCAGACTGCCGCGTAATAACAACTTTATTTCCATTAGCTGCCATTAACAAATATGTATAAATACATTAATAAATGTAATGTTCATTGTTTATTCATGTAAGGAAATGCATTAACTAACATTAACTATTACAGGCTTTTATAGCCTTTATAGCCTTTTATTCTCTTCTATTTGTGCTGATGATGTTCTTGTGTTGTAGAAAGCGGTTGAGGTCATGTGCATTGTACCAAAAAGATGCAACGACATGATGAATGTTGGT[C/T]GACTCCAGGGGTTTGATGTAAGACTGTGGTATTTTTCATACCAGTAGATCATTATCAGAAATAATGACAGTATATTATATTCGAGTTCATGATTAAATCTGGTCTCTCACAGGGAAAGATTGTTGCTCAGGGGCGTCTCCTACTCCAGGACACCTTCATGGTGGCCGAACCAGAGGGAGGCCTGCTGAACAGGATGAAGGAGAGGAGAGTCTTCCTCTTTGAGCAGATCGTCATCTTCAGTGAACCTCTAGATAAAAAGAGGGGCTTCTCCATGCCTGGCTATTTGTACAAATACAGCATCAAGGTACAGGCGTCATTCTCTTTCTTTGATTTTATCATGCACAGGGTACCTGCGGGGCCTTAAAAAGTCTTACATTTCAAAAAAAAAAATTGCGCCTTAAAAATATTGACTTGTAGGTCTAAAAAGGGGACCTCTTATGCCCCTTTTACCTCTTGTAAAATAAGATGTTCCTAGAGTGTGTATATGAAGTTTCAGCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11605
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 |
---|---|---|---|---|---|
ENSDART00000087055 | Nonsense | 2320 | 3087 | 48 | 57 |
ENSDART00000144275 | Nonsense | 2261 | 3028 | 47 | 56 |
Genomic Location (Zv9):
Chromosome 19 (position 43393641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 42272689 |
GRCz11 | 19 | 41857828 |
KASP Assay ID:
2261-3645.1 (used for ordering genotyping assays)
KASP Sequence:
AGGGTCCTGGTGTGWCAGGCAGCGGTGTACAGRCTGGAGGCAGCGGGGGG[C/T]AGATGATGGCCCCTGGAGGAGGAGTAGGGGTCYCGGCTGGGCCGGGTTCC
Long Flanking Sequence:
ATGATGACAGCACATAAAATTTGACTAGATGTTTTTTTTAAATACTAGTATTTAGCTTATAGTGACATTTAAAGGCTTAACTAGGCTAATTAGGCATTTATAATGATGGTTTGTTCTGTAGACAATTTAAAATGAATGCTAATAATATTAACCTGAAAATGGTTTTATAAAAAATTAAAAACTGCTTTAATTCTAGCCGAAATAAAACAAATAAGACTTTCTCCAGAAGAACAAATACTGTGAAAAATTCCTTGCTCTGTTAAACATCATTTGGGAAATGCTGAAAAATTCACAGGAGGACTAATCATTTTGATTGTTTATTATATCAAAACAAACTTTTATTATGTATGCGATTACTTTTGCCCAGCACTAAATAATAGATCATCTCACCACGTGCCTTTCCTCCTGTAGCACTTACATCTCCTATAGACTACCAGAGGAACCACGTGGAGGGTCCTGGTGTGTCAGGCAGCGGTGTACAGGCTGGAGGCAGCGGGGGG[C/T]AGATGATGGCCCCTGGAGGAGGAGTAGGGGTCCCGGCTGGGCCGGGTTCCCGTTCTCGTCCGTCCCGTATCCCCCAGCCCTCGCGCTTGCCTCAACCGCTCCGTCATCACTCTCCTGCCCTGGGGCCTGGAGCCCACGAGCATGACGGCCCCGACAAACTATCAGGTATGTCCCCAAGACCTCTCTCCAGGGGTCCCTCACCCTCATGCACCACAGAGCCCGAGCCAAAGGTGAAGCTTCCTGCGAGCCCTCACCCCAAACAGACGGACTCCCAACAGACAGAAAGCCCAGCCAAAGAGATCCCACGAGCCACTGTGGCCCCGCTGGCTCTTGTCAAACCCAGACCTGGAACGGTTTCACCAATGGCCTCTCCGTTAGCCACACCGGCTTTCAAAGACTCCATTCCACCCTGTAGTCCAGGCCCGAAGACTGGCAGCAGCTCGTTTTGGAGCTCAGTGCCCGCGTCCCCCGCCAGCAGGCCTGCTTCCTTCACCTTCCCC
Associated Phenotype:
Not determined