ZMP
tada2b
Ensembl ID:
ZFIN ID:
Description:
Transcriptional adapter 2-beta [Source:UniProtKB/Swiss-Prot;Acc:Q503N9]
Human Orthologue:
TADA2B
Human Description:
transcriptional adaptor 2B [Source:HGNC Symbol;Acc:30781]
Mouse Orthologue:
Tada2b
Mouse Description:
transcriptional adaptor 2B Gene [Source:MGI Symbol;Acc:MGI:3035274]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34134 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40969 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34134
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004365 | Essential Splice Site | 90 | 486 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 7 (position 41131567)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39467824 |
| GRCz11 | 7 | 39738841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGCAGTCGCTGCTCGATGCCATCGAGCAATATGGATTTGGAAATTGG[G/A]TACGACTCTCAAAATAATTACACATGGATGCAGCTCATAAAAAGCTGCCT
Long Flanking Sequence:
TATCAAGATTAGTTCGATGTAGTTTCTCTTGAGCTCTTGAAGAAGCGCTGGCATCAACTATTTTGTGTTCGTACGTGTTGCCATGGACACCTATAGCAAGAGCCAATCACAAGCATTCGCTGCGCCGCTTTTAATATTAATGAGACGCAGCGGCGTGAGCAGAGATACTCCACTGCGCATGCTCTGCCCCGCGCCACTGCTGCTTCCAACAACAAGCGGTAGTAAGCAATATGGCCGACCTAGGGAAGAAGTACTGCGTGAACTGCTTGGCAGATGTTACGAATTTGCGGATTCGCTGTGCTGAATGTCAAGATATTGAACTTTGCCCGGAGTGCTTCTCGGCGGGCGCCGAAATCGGCAACCACAGACGATGGCACGGCTATCAGCAAGTGGACGGCGGGCGCTTCTCGCTCTGGGGTCCCGAAGCAGAGGGAGGATGGACCAGCAGGGAAGAGCAGTCGCTGCTCGATGCCATCGAGCAATATGGATTTGGAAATTGG[G/A]TACGACTCTCAAAATAATTACACATGGATGCAGCTCATAAAAAGCTGCCTTTGCCTTGCCTAATTGTGCACGTCAACATAAACTAGCCATATCTAACCTTAGTCTGCAACACAAAATGCACTTCTTAGTATAGAAACTTAAACTATTTTCGTAAGGCAGCTTTCCTTGGTTTGTGATGCCTATAAATTTAATAGAATATGTAACCCAAAATACAACTCATTTATAGTTTTTGTCAATCATAACAACTGCATTCTGTAGATAATTCATACAGAAAACTATTGAAAACAGCTGCTTTTGCTATTGCATTAATATTAGCATTGCACATTATTGTATATTTGCATAATAAAAAGGGAGTATTGTTTCCATTTAAGTAAATAATATTAAGCAGTTATTGCATTTTCATTGCAGTTATTCTTAATGCTTCTGCCAAGCTTTGTTTGACAACAGTTCTTTTCATCCCTTTTTAAATGATCACGTTGGAAGACGTTTGCTGTGGTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40969
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004365 | Nonsense | 422 | 486 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 7 (position 41134005)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39470262 |
| GRCz11 | 7 | 39741279 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAGCTATTGAGAACCTGTCCGGATTTGAGCTGCTATCCGATAGGGAG[A/T]AAGTACTGTGCAACTCCATGAACCTCAGTCCCATGCGTTATCTGACAGTC
Long Flanking Sequence:
GTGGAGCTGTGGGATCGGGGAGCGGTGCCACCGTCGTTCCAGCTGGGCCGCTGGGTTCCTCTACAGCAGCGACACCGAAACGAAAAATCACCAAGGAGGAGAAGGAGCAGCGGACCAAACTACGTGCCCTTTGTCAGTTCATGCCACAACGTGAGTTTGAAGAGTTTTTCGATAACATGCACAAAGAGCGGATGCTCCGAGCGAAGGTTCGGGAGCTTCAGCGGTATCGGCGGAATGGCATTACAAGACTTGACGAGTCAGCAGAGTATGAGGCAGCACGCCACAAACGGGAAAAGCGGAAAGAGAATAAAAGTATTGCCGGGTCAAAGAGAGGAAGCAGTGGTGGAGGAGGAGGAACAGCTGGTCTTGGAGGAGGTGTTGGAGCAGGAGGTGGGCTTGGCGGAGGCGGCGGAGTCAGTACCATCAAAGAGGAAGGGAAAGACAGTGAGTTTTCAGCTATTGAGAACCTGTCCGGATTTGAGCTGCTATCCGATAGGGAG[A/T]AAGTACTGTGCAACTCCATGAACCTCAGTCCCATGCGTTATCTGACAGTCAAGACTATCATAATCAAAGATCATCTACAGAAAAGGCAAGGCATTCCCTCCAAAAGCCGCTTGCCCAGTTACCTGGACAAGGTGCTGAAAAAACGGATTCTGAATTTTCTTTCGGAGAGTGGCTGGATATCTCGAGATGCCTCCTAATGACACTGTCTAAAGAGCTGGCTGTATGAATAATGACTGTAAATATATTTTTCTAATGTTTTATACTGAGACTATGAAAAGCATGTGAGAACAAAATGGCTGTTGGTGCCGCACTACTGGATGTGGTCTAAATTGTCTGTCTTTAATCTCGAATCTCATCATAGGAATGGAAACATGGAAAAATTGTACATCAGTACTTAAAGGGAACTTTGCAGTATGTTGTTCTGTGTAATACATCATAATGCAACAACAACAACAAACATTTCCCAGTTTTATAATGCCTTTGGTTTGAATGTGTTTTTT
Associated Phenotype:
Not determined