ZMP
txlna
Ensembl ID:
ZFIN ID:
Description:
alpha-taxilin [Source:RefSeq peptide;Acc:NP_001092700]
Human Orthologue:
TXLNA
Human Description:
taxilin alpha [Source:HGNC Symbol;Acc:30685]
Mouse Orthologue:
Txlna
Mouse Description:
taxilin alpha Gene [Source:MGI Symbol;Acc:MGI:105968]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36861 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa29228 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32247 | Nonsense | Available for shipment | Available now |
sa3011 | Nonsense | Available for shipment | Available now |
sa13771 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36861
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 |
---|---|---|---|---|---|
ENSDART00000024292 | Essential Splice Site | 48 | 514 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 31098017)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 30265306 |
GRCz11 | 19 | 29852619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGCTGAAACACAGCCGGACGGCTCACCAGCCAACAAAGATGAAGGCTG[T/C]AAGGGACATGATATGATTTTGTCATTTGGAATGTGTTTTTATTTTCCAAA
Long Flanking Sequence:
ATACATATTTACAGCTATTATCAATCAGGTTAAAGTAAAACATGTTCTTTGTTTTGCACGTCTGTTAGTAATAGTTTGACAACTGCACGAAGGACTGAATGATTGACAATCGTCTGATAGCTGTAAACGTGATCTCTAGTGTTTAGTGATTAGCGTGTTTTTACCGTTGTTACCATGGTGAGTTAAAGAGTCAACTGTCGGCCTGGTTTGTTTGGTGAATTCTTTTACAAAAAGTGATTAGTAATGGCGAGGCTGAATTGAAACCGAAACCTTCAAGCTGTTTTATGATGAAGCGTGTCGTCTTGTTAGTCTTTAACTTGTGCATTGTGTGTTTTAGTATTTGCTTATAAATTAGCCATGCAGAGGCAAATGGAGGATCCTGCAGCTGATAGCAGTGCAGATGATACTGAGGAGAGCACGCCTGCATCTGAGATGACCAACAGCCCTAAAGAAGCTGAAACACAGCCGGACGGCTCACCAGCCAACAAAGATGAAGGCTG[T/C]AAGGGACATGATATGATTTTGTCATTTGGAATGTGTTTTTATTTTCCAAAGCAAAGTTTTCTCCCTTTCATATTAAAAATTAGTTTATTCTGTTCATAATACCCATTTTATTCTGCATTAATATTTTTCTTGACTGAATGTTATCAGTGTTGTACTATTCTGCACAGCATTTTGAAAATTAATATTTTTATCCATTTCTCAGTAAATATAGTCAAAATATTTTGGTGCATTTGAACAAAACAGATTTATTGAACAGATATGCTTATTTAAATTATATTTTAGTCACCAAACATATTTAGAAATGAAAAAATAAGTAAAATCAAGTTAAATATTGCAACAAAATAAATTACTACAAAACATCAACAACATTTTAGAAATGTTTTTTTTTTGTTCCCCCATATTGTATCTAACATTTTTCCCTAACATAAACTTGGGTGTACAGATGTTTTTACTGTTATCATAATTTGGTTTGTTAGTTCCAGTTTTGGCTGATTAAGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29228
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024292 | Essential Splice Site | 163 | 514 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 31094810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 30262099 |
GRCz11 | 19 | 29849412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTCCAGAGGAGAAGCTGGGTGGTCTCTGCAAGAAGTATGCTGAGCTGG[T/G]AAGAAATGATTATATTATGATCACCTCCAACAGTATTTTGTTCTTGCATA
Long Flanking Sequence:
TATTAATATTTCAGCATGTTCATAGTTGGCCAGTTTTGTTCCACTCAGTACCTTTCATGAGCTGTCACTTTCATAGTTCAGTTCAATTCATACTATCATGAACTGCTGAAGGTTTTTAAAGAACTTTGTCTTATTGTATCAATTTCTAACTAAATAGTATTTGATAAAGAGATCAATAAAGCTTTGTTAAATTATTTAGTTATTCATAAACCCTCAGAAACTTTTTCGTTTTCTATTAGTGTCATTTCACACTGCAAGGAAGTGGTAACCTGTAGTAATCGACCCAAATGGTCAATTATGACAATCAAATTGAGAGCTTTTGAATCAAAATCAAAGCATAAAATGTGTCAACTCCAGTAATAAACCCTCTTGTTAACTAAAATTTGTTTTATACTTGTGCATTGTAGGGAAGGAGATAACTCTTTTAATGCAGACCCTCAACACACTGAGCACTCCAGAGGAGAAGCTGGGTGGTCTCTGCAAGAAGTATGCTGAGCTGG[T/G]AAGAAATGATTATATTATGATCACCTCCAACAGTATTTTGTTCTTGCATACTGTCTAGATAGATGGATAGAAAAAGTAATGAATACTTATAGATATTGTATTAACTTCCTTGTTTCAAGAATAGTTTGACAAGTAGCTGTCTTCATGTTACACGTTCTTCATTGACTTATTTTTTTAAGTTTTTTGCAAGTCTTTATGAATGAGACACTGACCCGTGCTATTAAAATAATTTTTAATAGTACAAATAAATATTATTTTATTTTGAGGTGGCATGAATCCATTAATATTTTGTCAGAGGTAATTTTGTTTGAAAAAAGTTTACTATAACAAAGCATATAAAACAGAGGGTTCTCAAGCTCTACGTTAAAAGGTCCAAATTTGAATTTTATCAACAATTGATATTGCATAACTTGTTTTTAATAAACATCCATTACATGCATCACAAGTCAACACTATTTTTCTTTAAATAAAGTTGCATTTGCATTTAAATCACATTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32247
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 |
---|---|---|---|---|---|
ENSDART00000024292 | Nonsense | 293 | 514 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 31087999)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 30255288 |
GRCz11 | 19 | 29842601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAAGTATGACTTGTTTTTTTCTTTTAGCATATTGACAAGGTGTTCAAA[C/T]AGAAAGATCTGCAACAGCAGCTAGTAGATGCAAAGCTTCATCAGGCACAG
Long Flanking Sequence:
TCTGTAGCGACAACAGACCGCAAGGGATTAGGGCCAAGCCTGGGCTGATGGGAATTGTAGTTTCCGGTACCTCCCGTTCGCTTCATTCGTCTGAGCAAATTTTCTAAGAAGACCTAAAGTTTTACCGAGTCATGCGACTACGGTAATATCGAAAAACATTAATATTGCGGTATGACGGTATTTACAATACCGTTACATCCCTATTAGTTAGGCTTTAAATGTTAAGTAGAAGATAATTGTATATGTAGTGAAAGAAGATAAACAGTATTTTTATTCTCTTCAATCAATGTATCACATTAGTTTGCAATCATTCATTAAAATTGACAAAAAAAAAATCACAATAGTGGGACTAGCTTGTAGTAAAGCATAATTTTATCGACTGTTGCCTTTGGTTTTATTATTTGTATACAGTGTTATTCGTCCATTAAGACTTTTAAGTGATGAACTGATTTTAAGTATGACTTGTTTTTTTCTTTTAGCATATTGACAAGGTGTTCAAA[C/T]AGAAAGATCTGCAACAGCAGCTAGTAGATGCAAAGCTTCATCAGGCACAGGGTCTGCTCAAAGACTCAGAGGACCGGCATCAGAAAGAGAAGGACTTTGTGAGTTTCCACATCATTTTTTTAGTACTTCAATTATTTTTCGATGACTTCAGATGATACTGGTCATGGGATTTCTAGAATATCAATGAATTTAATACAAAAGTCAGGGGATATATATATATATATATATATATATATATATATATATATATATATTCCTGTCCAAGTTATGGAATATGAGGAAATTTTGTAGGGGAGGGAGAGAAAGAGGAGAGGGTTGGTTGGTTGGTATTATTGTATTTTTTTTTTCTTAGCTGGGATCTGATGTACTACCCTGTCAGTGAAAGACTGTCCAGCAAACTCACAAGCAGTGAATTGTGCATCTGCTTTTTAATTACCTTGCCATAGTAGCCATATAACGCATATGAGATTAATGACGTCAGTACAAAATAACCGGTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3011
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 |
---|---|---|---|---|---|
ENSDART00000024292 | Nonsense | 298 | 514 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 31087984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 30255273 |
GRCz11 | 19 | 29842586 |
KASP Assay ID:
554-2732.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTCTTTTAGCATATTGACAAGGTGTTCAAACAGAAAGATCTGCAA[C/T]AGCAGCTAGTAGATGCAAAGCTTCATCAGGCACAGGGTCTGCTCAAAGAC
Long Flanking Sequence:
GACCGCAAGGGATTAGGGCCAAGCCTGGGCTGATGGGAATTGTAGTTTCCGGTACCTCCCGTTCGCTTCATTCGTCTGAGCAAATTTTCTAAGAAGACCTAAAGTTTTACCGAGTCATGCGACTACGGTAATATCGAAAAACATTAATATTGCGGTATGACGGTATTTACAATACCGTTACATCCCTATTAGTTAGGCTTTAAATGTTAAGTAGAAGATAATTGTATATGTAGTGAAAGAAGATAAACAGTATTTTTATTCTCTTCAATCAATGTATCACATTAGTTTGCAATCATTCATTAAAATTGACAAAAAAAAAATCACAATAGTGGGACTAGCTTGTAGTAAAGCATAATTTTATCGACTGTTGCCTTTGGTTTTATTATTTGTATACAGTGTTATTCGTCCATTAAGACTTTTAAGTGATGAACTGATTTTAAGTATGACTTGTTTTTTTCTTTTAGCATATTGACAAGGTGTTCAAACAGAAAGATCTGCAA[C/T]AGCAGCTAGTAGATGCAAAGCTTCATCAGGCACAGGGTCTGCTCAAAGACTCAGAGGACCGGCATCAGAAAGAGAAGGACTTTGTGAGTTTCCACATCATTTTTTTAGTACTTCAATTATTTTTCGATGACTTCAGATGATACTGGTCATGGGATTTCTAGAATATCAATGAATTTAATACAAAAGTCAGGGGATATATATATATATATATATATATATATATATATATATATATATATTCCTGTCCAAGTTATGGAATATGAGGAAATTTTGTAGGGGAGGGAGAGAAAGAGGAGAGGGTTGGTTGGTTGGTATTATTGTATTTTTTTTTTCTTAGCTGGGATCTGATGTACTACCCTGTCAGTGAAAGACTGTCCAGCAAACTCACAAGCAGTGAATTGTGCATCTGCTTTTTAATTACCTTGCCATAGTAGCCATATAACGCATATGAGATTAATGACGTCAGTACAAAATAACCGGTTATGATAATTACTAAACTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa13771
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024292 | Nonsense | 337 | 514 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 31086163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 30253452 |
GRCz11 | 19 | 29840765 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTTCTTTTCCAGCTCCTGAAAGAGGCAGCAGAGTCTCAGAGGATGTA[T/A]GAGCTCATGAAACAACAGGAAGTTCATCTGAAACAGCAGGTGAGTAGCAT
Long Flanking Sequence:
ATCCAAATATATATTTTTCTTTACTGAGGGAGGTGAACGTACAGACGTTTACTGTGATACTGCCCCCAAGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTGCCTAGGCTATTTTCTCCACTACTAACATGCTGAGTTACAGACCTCGCCATCAAGGTGTCATTTTAGAGTACCTGCATGCAGAATGAATAGAACAAATACTCATTTTTTATGGTTGCCATTTAGTTACTGAACAAATCTTTTGAGGAGGAGAACATATTGGTGCTAAAAAGACTGTAAGTTGTGTAGCACACTGTGAATTTGATGTCTTAATGTTTGATTGGCCAGTATAAATGGCACTATGCTGCAACTTTAGTTACTTAAACAGCACAATAAAGTTGATTCTTAGTCTGTTGTGTGTATTCCATCTGGACAGAGCGGTCGGTTACTGAATAATATTTGTATTGTCTCGTTTCTTTCTTTTCCAGCTCCTGAAAGAGGCAGCAGAGTCTCAGAGGATGTA[T/A]GAGCTCATGAAACAACAGGAAGTTCATCTGAAACAGCAGGTGAGTAGCATATAAGACTGGTCTGATCTGGCTAACATGCTGATAGAACATCTCAATAGTTTCCCTCAAAGAGTTGTTAAGCATGATGAAATTTGGGAAAAGTTTCTGATTGAAATCTCAAGGTAGTTAGAAACAGTACTTTTACATCTCGACTGACCACTTGGTAAATGGATCAATAAAAATGCTAGTTGGAAACAGCGCCTTAGATGAGTTTTTACAAGGTCAAATGCTGCTTCCAAAACATGTTGTATTGGAATCATCTCTTTTTTTTCCAGCTTTCGTTGTACACCGAGAAGTTTGAAGAGTTCCAAAACACACTTTCCAAAAGCAACGAGGTCTTTACTACATTCAAACAAGAGATGGAAAAGGTAAATGACTTGTTTTTTTGGATGTTATGAGGTTCATGTTCCTAATTAGAAAACTGTAGCATCTGCATTTGTGCACAAAATGAAGGTCTTCTT
Associated Phenotype:
Not determined