ZMP
txlnbb
Ensembl ID:
ZFIN ID:
Description:
taxilin beta b [Source:RefSeq peptide;Acc:NP_001077022]
Human Orthologue:
TXLNB
Human Description:
taxilin beta [Source:HGNC Symbol;Acc:21617]
Mouse Orthologue:
Txlnb
Mouse Description:
taxilin beta Gene [Source:MGI Symbol;Acc:MGI:2671945]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa80 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa6458 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa80
Status:
Confirmed mutation in F2 line
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 |
|---|---|---|---|---|---|
| ENSDART00000026106 | Nonsense | 21 | 520 | 1 | 9 |
| ENSDART00000115389 | Nonsense | 8 | 340 | 3 | 11 |
| ENSDART00000137389 | Nonsense | 21 | 353 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 6136400)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6215336 |
| GRCz11 | 17 | 6372566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCTGTGCTCAATCTGCAAACGGAGAAATGACGGAGGATCTGTCTCAG[C/T]AGCTACAGGAGATCATCAACACATACCAGCTGAACGAACAGAAGCACGAA
Long Flanking Sequence:
GCCTACCATTGACTGGACGGTTCTCGCGGTAGTGCCGGAAAAGGGGAATGTCTTGGAAAATTAGGACATCTGATCACCCTTATGGGTGACTAAAACAGGGCTATTCAATATTATGATTGGGCAACAGCCACTCTGAGCCCTAGTTTAGCACTAGTTGTTTTTGAACAGCAGCGAACCGAAAGGAATACTTCATATTATTGATGAGAGAAAGCATAACGCAAAGAGGCATTTCCCACATCATAGCATGAATTAAAAGCTAATTAAGAGCCCCTCCTTCTTCACATCGCCCTTATGTTACTCCGGCCCTGCTCGTGACATCAATATTGTGTATTTTCATTATTGCGATATATTAACATGTTGATGAACTCCTATTTTCTACATGAGTCTGAAGATTGTGTTGTTGGATCTCTCCTATCTGGATAGCAGAATCGCCCCTCAGGATGGAGATGGAGACCTGTGCTCAATCTGCAAACGGAGAAATGACGGAGGATCTGTCTCAG[C/T]AGCTACAGGAGATCATCAACACATACCAGCTGAACGAACAGAAGCACGAAACCGAGGAGGACGAGATGGAGGAGGAAGAGGAGGAGCCGAAGAGCAGAGAGCAGAAGATGGAGAAAAAGATGCTGAAAGGCCTCGGTGAGACACAAACACACTGAACATTAGTGACCAGGGTGCGAATGGGGCATGTGCACATGGACTTTTAATTTTCAGTCAGCCAGCCCAAGCGTTTCCAAAGAATCGTCACTCTATTACAAAATTGCCACTTTGCTACTGACGGCGCTTGCGTTTACACAGCATTTCATCTTGTTTTAAGCTTTAACAGCTTAATGAATGCTCTAATCCAGTGGTTCTTAAACTGTGGTACATGTACCACTAGTGGTGCGCGGGCTTCCTTCTAGTGGTACGTGGAGGAATCAAATATGTCATTTATACATGCTACATATATTTCTAAATGTATCAAAAATGATTTATATATGAATATGATGACATATAGCCTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6458
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 |
|---|---|---|---|---|---|
| ENSDART00000026106 | Essential Splice Site | 314 | 520 | 7 | 9 |
| ENSDART00000115389 | Essential Splice Site | 301 | 340 | 9 | 11 |
| ENSDART00000137389 | Essential Splice Site | 314 | 353 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 6127912)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 6206848 |
| GRCz11 | 17 | 6364078 |
KASP Assay ID:
554-4974.1 (used for ordering genotyping assays)
KASP Sequence:
GTCTAAGAGTAATGGTGTTTATGCCAGCTTCAAACAGGAYATGGACAAGG[T/C]GTGTATCCACAGYACATTACAGGTTATTCTTTTAGAGGTTAAAAKGGTCA
Long Flanking Sequence:
ACCTTCTTGCTCTTAAGTAAAACAAATAATTCATTCATTCATTCATTTTATTTTTGGCTTGGTCCCTTTATTAATCGGGGTCGCTACAGCGGAATGGACCGCCAACTTATCCAGCATATGTTTTACGCAGTGGATGCCCTTCCAGCTGCAACCCAAGACTGAGAAATAAAACACATAATATCTGTATTATTTATTGTTGTTTTGTTGTACTGGCCTGTATTAATTACAACTTCTGGCCTGTATTAATCCCTAGTTACTGAAGCAAGCCGCGGAGGCCAAACTGCACGTTAAACTTCTGAAAGAGCAAGAGGTTGACATGAAGGCTCAGGTAAAGTTACGTCAGATATTTCAGTTTTTTTCTCAAATCATATCTGTTCATAGATTAACCTACATTTTTTTCTGTCAGCTTGCTGTATATTCCGAGAAGTTTGATGAACTACAAGGATCGGTGTCTAAGAGTAATGGTGTTTATGCCAGCTTCAAACAGGACATGGACAAGG[T/C]GTGTATCCACAGCACATTACAGGTTATTCTTTTAGAGGTTAAAAGGGTCATTAATATACAGTTGAAGTCAGAATTATTAGCCCCCCTGAATTATTCGCCCCCCTGTTTATTTTTTCTTCAATTTCTATTTAACGAAGAGAACAATTTTTCAGCACATTACTAATCATAATAGTTTTAATAGCTCATCTCTAATAACTGATTTATTTTTTCTTTGCCATGATGTCAGTAAATAATATTTGACTAGATATTTTTCAAGACACTACTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTCAACTAGGCAGGTTAGGGGAATTAGGCAAGTTATTGTTTATCAGTGGTTTGTTTTGTAGACTATCGAAAAAAATATAGCATAAAGGGGCTAATAATATTGACCTTTAAAATGGCTTTTAACATTTTTACATTTCAATTCCAATTTTTAATTTTCTACCCAAAATAAAACAAATAAGCGTTTCTACAGGAG
Associated Phenotype:
Not determined