ZMP
trabd
Ensembl ID:
ZFIN ID:
Description:
traB domain-containing protein [Source:RefSeq peptide;Acc:NP_997788]
Human Orthologue:
TRABD
Human Description:
TraB domain containing [Source:HGNC Symbol;Acc:28805]
Mouse Orthologue:
Trabd
Mouse Description:
TraB domain containing Gene [Source:MGI Symbol;Acc:MGI:1915226]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2982 | Essential Splice Site | F2 line generated | Not yet available |
sa36599 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15109 | Nonsense | Available for shipment | Available now |
sa32193 | Nonsense | Available for shipment | Available now |
sa13996 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2982
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008035 | Essential Splice Site | 84 | 360 | 5 | 10 |
ENSDART00000145842 | Essential Splice Site | 83 | 103 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 14482414)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14927832 |
GRCz11 | 18 | 14896344 |
KASP Assay ID:
554-3321.1 (used for ordering genotyping assays)
KASP Sequence:
TAGCAGCTGRTTGATCAAATGTTGTTTTKAATRAATGCTTYTTTTGCTTC[A/G]GACGATCCGAGCRGTCCAGCCTGATGTAGTAGTGGTGGAGCTGTGCCAGT
Long Flanking Sequence:
TTGTGGCAGGTTCGGACCCAGCGACGGCAGAAGGAGCCTGATCTGCCAGAAACTGTGACGCGTCTCACCACACCTGAGGGTAGTGTTGTGTACCTGGTTGGCACTGCCCACTTCAGTGACAGCAGTAAGAAGGATGTTGCCACTGTAAGCACTGGCTTTCTCCAAAGATATTTGTATGCACTAACAACCAGCATTTAATAGTTGAACACCTTTTTGTTCATATAGACCATTTTGAGGGATTTATACAAAAACAATGGTCCCAACGTATTTCCTGTTTCACATTTTTCATTTCTATAGCTTCCGAGAATCCAAAAAGGGACACATATTAATAAATAATGTTACGATAACTCTTAATATGAAGTTATGATTGAATTGCCTTTTGTTACATTTATGAAATAGTTTGATAACAAGCAGGAAATGTTCATGACATCACCACATTAAAATGGTCTGTAGCAGCTGATTGATCAAATGTTGTTTTGAATGAATGCTTTTTTTGCTTC[A/G]GACGATCCGAGCAGTCCAGCCTGATGTAGTAGTGGTGGAGCTGTGCCAGTACAGAGTATCCATGCTTAAAATGGATGAGAAAACGCTGCTAAAAGAGGCTAAAGACATTAACTTGGAGAAGGTCCAGCAGGCCATTAAACAGGTCAGCCATGAGACGGAAGACTGTGCTGACATAGTATTATATTGTCAAACACTTTCATCTGGATGCTTTTATCGACATGTAGTGTTACTTGTAATTACTTTCAAAGTGTAATAAAATTTCTGATCACTCTCAAATAGTAAAGGATTATTTAAATGAAATTATTTAATTATAGTTTCTTAATCTGAACTGCTAGAAGGTGCATATTTTGTTGGTCGTGACTGGAATGATGCGAGTCATTGTCCTCATTACATATTATGGGACTCCTGCAGAATTCATGTTCATGGATGAGCTAAAGTATTCTAAACTTATTATCTTGGTAGTTTGATGCAAAGTAAGGCTGTTAATTGTCGAAGCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36599
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 |
---|---|---|---|---|---|
ENSDART00000008035 | Nonsense | 121 | 360 | 5 | 10 |
ENSDART00000145842 | None | None | 103 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 14482300)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14927718 |
GRCz11 | 18 | 14896230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTAAAATGGATGAGAAAACGCTGCTAAAAGAGGCTAAAGACATTAACT[T/A]GGAGAAGGTCCAGCAGGCCATTAAACAGGTCAGCCATGAGACGGAAGACT
Long Flanking Sequence:
AGTGACAGCAGTAAGAAGGATGTTGCCACTGTAAGCACTGGCTTTCTCCAAAGATATTTGTATGCACTAACAACCAGCATTTAATAGTTGAACACCTTTTTGTTCATATAGACCATTTTGAGGGATTTATACAAAAACAATGGTCCCAACGTATTTCCTGTTTCACATTTTTCATTTCTATAGCTTCCGAGAATCCAAAAAGGGACACATATTAATAAATAATGTTACGATAACTCTTAATATGAAGTTATGATTGAATTGCCTTTTGTTACATTTATGAAATAGTTTGATAACAAGCAGGAAATGTTCATGACATCACCACATTAAAATGGTCTGTAGCAGCTGATTGATCAAATGTTGTTTTGAATGAATGCTTTTTTTGCTTCAGACGATCCGAGCAGTCCAGCCTGATGTAGTAGTGGTGGAGCTGTGCCAGTACAGAGTATCCATGCTTAAAATGGATGAGAAAACGCTGCTAAAAGAGGCTAAAGACATTAACT[T/A]GGAGAAGGTCCAGCAGGCCATTAAACAGGTCAGCCATGAGACGGAAGACTGTGCTGACATAGTATTATATTGTCAAACACTTTCATCTGGATGCTTTTATCGACATGTAGTGTTACTTGTAATTACTTTCAAAGTGTAATAAAATTTCTGATCACTCTCAAATAGTAAAGGATTATTTAAATGAAATTATTTAATTATAGTTTCTTAATCTGAACTGCTAGAAGGTGCATATTTTGTTGGTCGTGACTGGAATGATGCGAGTCATTGTCCTCATTACATATTATGGGACTCCTGCAGAATTCATGTTCATGGATGAGCTAAAGTATTCTAAACTTATTATCTTGGTAGTTTGATGCAAAGTAAGGCTGTTAATTGTCGAAGCAAAACTAGACCGCTGAAGCAATTGCTGATAAGAGATGAGCGTGACTCTGCACAAAAGCAGCAGAGCTTTTTTAGGCCACAGTCCACCACTGCTGGTTCTTTCAGTCATGATCACATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15109
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 |
---|---|---|---|---|---|
ENSDART00000008035 | Nonsense | 249 | 360 | 8 | 10 |
ENSDART00000145842 | None | None | 103 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 14477911)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14923329 |
GRCz11 | 18 | 14891841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGATGATCGGCGAGTTTCCAGCCCTCCACCGCACTATTGTWGCAGAA[C/T]GAGACATCTACCTCACACACACACTTCGACAGGCAGCGCGCTGTGTRGAG
Long Flanking Sequence:
ACAGTTCCTTTAAGATAAAAAAAATCAATGATTCCTTGTGCCTTCACATTTAACTCTGTGAAATTATGCCAGCAAATATGTAAACTTGGTCACAAATGTGGTGTGAGATTCCATTTGAATATTTATTTTATTTCATTTGGTTGACTGAATTCACTCCACTGAAAGACAGCTTCTTTTTTTACCACAACTTTACACTAATGACAAGGTTGATTTTCATTTTGCATTGCAATACTGAGAATAAAATACATTTTGATGTTTAGTTAAACCTTGATTTTAAATCATCAGTTAATTGTCATTAAAATAATGCTCCTAAATCTAGTCTTTGTTTTACCTTGGCATGTTATTGTGTAATTTACATGAATTTTTATATACATTATATAATTTTTTTTTCTATCAGTAAGGAGGACGTTGAGAAATGCAAACAAAAGGATCTTCTGGAGCAGACCATGTCAGAGATGATCGGCGAGTTTCCAGCCCTCCACCGCACTATTGTTGCAGAA[C/T]GAGACATCTACCTCACACACACACTTCGACAGGCAGCGCGCTGTGTAGAGGCGCCTCCTACTGCTGAGAGTGAGTACTGCATCCTCTGCTCATGCTCATGTCTCGTCCAGTGCTGTAATCAGTGATTGGGGAAAAAGTCTTGAGTTTTAAGGTGCACTACCAGCACTCTTATTGTTAAATGGATGGTCCACCCAAAATGATTTACTCACCGTCATGTCATTCTAGAGCTGTAAGACTTCTGTATCTGTGGAACATAACGGTAAATATTTTGAAGCACTTTGGTAACCAAATAGTTTTGTTACACTTCCAACTCACTTCCATTGTATAGTAAAAAAAATGGAACACAAAATTTACTTACTATCATATCTTTTTTTTTTTTTTTTTTTACTTTAAATAATGGAAGTCACACTTTTGGAACAGCATGAGTCAAAGCTTAAAGTTCATTAAAATAAATTTTTAATGAAATATAAAGTGTATATGAAAAGCCTAAAGTTTAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32193
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 |
---|---|---|---|---|---|
ENSDART00000008035 | Nonsense | 259 | 360 | 8 | 10 |
ENSDART00000145842 | None | None | 103 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 14477881)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14923299 |
GRCz11 | 18 | 14891811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGCACTATTGTTGCAGAACGAGACATCTACCTCACACACACACTTCGA[C/T]AGGCAGCGCGCTGTGTAGAGGCGCCTCCTACTGCTGAGAGTGAGTACTGC
Long Flanking Sequence:
ATTCCTTGTGCCTTCACATTTAACTCTGTGAAATTATGCCAGCAAATATGTAAACTTGGTCACAAATGTGGTGTGAGATTCCATTTGAATATTTATTTTATTTCATTTGGTTGACTGAATTCACTCCACTGAAAGACAGCTTCTTTTTTTACCACAACTTTACACTAATGACAAGGTTGATTTTCATTTTGCATTGCAATACTGAGAATAAAATACATTTTGATGTTTAGTTAAACCTTGATTTTAAATCATCAGTTAATTGTCATTAAAATAATGCTCCTAAATCTAGTCTTTGTTTTACCTTGGCATGTTATTGTGTAATTTACATGAATTTTTATATACATTATATAATTTTTTTTTCTATCAGTAAGGAGGACGTTGAGAAATGCAAACAAAAGGATCTTCTGGAGCAGACCATGTCAGAGATGATCGGCGAGTTTCCAGCCCTCCACCGCACTATTGTTGCAGAACGAGACATCTACCTCACACACACACTTCGA[C/T]AGGCAGCGCGCTGTGTAGAGGCGCCTCCTACTGCTGAGAGTGAGTACTGCATCCTCTGCTCATGCTCATGTCTCGTCCAGTGCTGTAATCAGTGATTGGGGAAAAAGTCTTGAGTTTTAAGGTGCACTACCAGCACTCTTATTGTTAAATGGATGGTCCACCCAAAATGATTTACTCACCGTCATGTCATTCTAGAGCTGTAAGACTTCTGTATCTGTGGAACATAACGGTAAATATTTTGAAGCACTTTGGTAACCAAATAGTTTTGTTACACTTCCAACTCACTTCCATTGTATAGTAAAAAAAATGGAACACAAAATTTACTTACTATCATATCTTTTTTTTTTTTTTTTTTTACTTTAAATAATGGAAGTCACACTTTTGGAACAGCATGAGTCAAAGCTTAAAGTTCATTAAAATAAATTTTTAATGAAATATAAAGTGTATATGAAAAGCCTAAAGTTTAAAGAATAATTAGAAAATACCAGAGCCAATTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13996
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008035 | Essential Splice Site | 304 | 360 | 9 | 10 |
ENSDART00000145842 | None | None | 103 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 14472525)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14917943 |
GRCz11 | 18 | 14886455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATCGAGAGGAACTGGGATAAAGAGCTCAACATCCATGAAATCATGAGG[T/C]GCGTATCRGTATGGTACTTTGGTGCAATGTAAYACCAGATCTGTCATAAC
Long Flanking Sequence:
GTTGTGCAATAAGTCCATATATTGATTATTGTGACAGGCCTAGTTCATACTAACAACTGAATTAAAAACAACAACAACATCTGTTTGCATTTACTCACCACAAACACATCTGCATAATCTGATTAGTTGTGTTAATCTTTTTAGCATTTGGTCCATGTTCATGATATTTTATGTATTCATTTAATTATTATTCATTTGATTGCCAGAATATAATTAGCCTTTAAATCTGGATTTGTTTTTTTTTTTAAACAGTTGGGTGATGCTTATTGTTTTATCAGCCAACGCAGTTACTCAGTATCACTATCATAGAGTATAAACAATACTAGGATAACACTGCCAGAGCTTCCTTAAGCGTTCTGTTACCTGATACATGAAACCTTTTGTTCGTACTTTGTTTCTCAGAAGTGCCTGCTGTGGTGGTTGGGGTGGTTGGCATGGGTCATGTGTCTGGCATCGAGAGGAACTGGGATAAAGAGCTCAACATCCATGAAATCATGAGG[T/C]GCGTATCGGTATGGTACTTTGGTGCAATGTAATACCAGATCTGTCATAACAACAACAAAAATCTGTTTCCTTTTCTATTAGCGTGGCTCCACCGTCTCGTCTCGGCAGGGTGGTACGCACCGTGTTAAAAGGGGCCATGTGGGGGCTTCTAGGTTATGCCTGCTACCGGGCCAGCAAGGGTGTGGGCAGAGCGTTACTTTCCTTACCAACTGTGCAATCATTGCTTCAGAATATACGAACACCTTCCGTTTGACCCTTCTTTAATCTGTACAGACTTTCAGCAGTAACCACCAATAGCCTTAACTCTACAGGATGCTGGTTGGGTGAAGAGGAAGATTTTAGAGCAAAAAGCATCTCCATCCTACAGGAAATGAAACCGTGTGGATGGAAGTCTCTCTCTTTCGCCTACTCAACCTCTGTCCATCAGCTCTGTAGACTCAGAGCTGTACTGCCAAAGAAGTGGAGCGTGCTTTCATTTCCCTTTTCGACCCATTAGGAAT
Associated Phenotype:
Not determined