Busch Lab

ZMP

txlnbb

Ensembl ID:
ENSDARG00000076241
ZFIN ID:
ZDB-GENE-070424-77
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.
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.
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