ZMP
dtna
Ensembl ID:
ZFIN ID:
Description:
dystrobrevin alpha [Source:RefSeq peptide;Acc:NP_001074050]
Human Orthologue:
DTNA
Human Description:
dystrobrevin, alpha [Source:HGNC Symbol;Acc:3057]
Mouse Orthologue:
Dtna
Mouse Description:
dystrobrevin alpha Gene [Source:MGI Symbol;Acc:MGI:106039]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31102 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa670 | Nonsense | F2 line generated | Not yet available |
sa19346 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44175 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37940 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37939 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31102
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042290 | Nonsense | 128 | 710 | 4 | 21 |
ENSDART00000105680 | Nonsense | 128 | 714 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 24 (position 37246336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 35861762 |
GRCz11 | 24 | 35749859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGACTTTAACATCTTTTTTTTTTTTTAGGGAAGGTGTGGGGAAGATCT[C/A]GGCTTTTGTGATGAAGATGGCTCTGGCTACTCTTTGTGGAGGGAAGATTT
Long Flanking Sequence:
AACAAATCACTGATAGTTGTGTAAATATTGTCATACTAACAGCTGTCTGTATTATTTTTGGATGGATGTAATCAATTACATACTGTAGCATTCTATCAAAGTTATCTGACATCATTAAAATGCATTTTGAAGAACTGAATGAATCCTTTATTAAAGGGATAGTTCACCCCAAAATGAAAATGTACTCATTATTTACTCTCTCACAAATGGTTCCAAACCTTTATGAGTTTTTATGTTCTGTTGAATGAGAAAGAAGACAATTTGAAGCATGCTGGAAACCTGTAACCATTGACTAACATAGTATTTATTCACCCTACTGTGGAAGTCAATGGTTACAGGTTTCTATCATCCTTCACAATATTTTGTGTTCAACTCCACCATCTGAGTGGGAGTAAATAATGAGTAATTATTATTTTGGGGGGGTGAACTATCCCTTTAGGAATATTTTAGTTAGACTTTAACATCTTTTTTTTTTTTTAGGGAAGGTGTGGGGAAGATCT[C/A]GGCTTTTGTGATGAAGATGGCTCTGGCTACTCTTTGTGGAGGGAAGATTTTGGACAAACTAAGATGTAAGTTTCACTTTGGATTTGCCTTTGAACTGATGAGCGCTCAATGGTTTGATGCTGATTAATGGACGCATAAGTGAATGGACTGGATTAATCATTCTATCATCATCATTTTAAAGGTCAGAGCAGCTGTCGTTACTTGAAAGTCACTTCTTAGCAAGCATTACACTCGCCTCTCATGACCTTGTCAGTGTGGGGAAAACTTTTCGATTCATTCTTAGCGATGAAACTTTAGTTGGGGGTTGAGAAGATTTTGAATTTGCTGTTCGAATGGTCTTTCGCATATCGAGACTTCATTTATTTGATGAAAACATACAGTAAAGCAGTGTTTCTCAACCATGTTCCCGGAGGACCACCAACACTGCATGTTTTGGATGTCTCCTTTGTCTGTTACAACCATTACAGTACAGATCTTTCAGTCTCTGCTAATGAGCTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa670
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042290 | Nonsense | 289 | 710 | 7 | 21 |
ENSDART00000105680 | Nonsense | 289 | 714 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 24 (position 37239151)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 35854577 |
GRCz11 | 24 | 35742674 |
KASP Assay ID:
554-0578.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGGCCACGCATCGGGCAGCCACAGYAACCAGCACCAGATGAAGGAGTA[C/A]ATGTCATGGGTAGGTGAACGTCAGAGCCTCGTCATACAGACTACTCACAG
Long Flanking Sequence:
AAATCTTGTTTGGCATGCTGTCCCGGGAGAGAGCGAACGAAGATAAAGTGAACTGAAAACTGTGGCTATTTATAGTAGCTTAGGGCTCATATGATTGGAAGATAGTGATTAGCAAATGCAAGACCGGCCGTGATAAATCATAAAGCACGTGATTCTCTTGAAATTAGTTTATGAATAAACTTCACTTAGTTCATGTTAAACTATTATTAATACAAGCTTTACAAGATAATTCACACTTAGTTAATGTTATTAAATACATTAACTAATGGAGCATTATTATATAGTGTTGTTACTATACAACCAGATTGTAAAGTGTACCAATTTTATCTGGTCTCCTCTGTAGTTTTTCATCCAGTGGAGTGTTCATACTGCCACAGCCAGAGTATGATGGGATTTCGCTACCGATGCCAGCAGTGTGATAATTACCAGCTCTGCCAGGAGTGTTTCTGGAGAGGCCACGCATCGGGCAGCCACAGTAACCAGCACCAGATGAAGGAGTA[C/A]ATGTCATGGGTAGGTGAACGTCAGAGCCTCGTCATACAGACTACTCACAGTCCAATCACTTCTTACAGAATGTCATGACACATGTTTGTGTGTGTCATATTGGCAGCTTCTTTAGATTTTTTTTTCTTTTTAGCTGAGTTTACTTAGAGTTGATAGCAAATTTATGGACCATTTTCACGTTTACGGGTTTGTTAGTAGAGTAAGTCATCATAGTCAGATAAACATAGAGCGCAGTAAATTTTATTCAATGAAGTTTATTCCCCACTTCATTTAAGCAGGCTAGGGTAACCCAACTGCTAAAGAAACCCAACCTGGACCATACGCTACTTGAAAACTACAGACCAGTATCCCTGCTTCCATTCATGGCCAAGATTCTGGAGAAAGTAGTGTTCAATCAAGTCCTGGACTTTCTTACTCAAAACAATCTCATGGACAACAAGCAATCCGGCTTTAAGAAAGGCCACTCAACTGAGACTGCCCTGCTCTCGGTCGTGGAGGAT
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:
sa19346
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042290 | Essential Splice Site | 334 | 710 | 8 | 21 |
ENSDART00000105680 | Essential Splice Site | 334 | 714 | 8 | 22 |
Genomic Location (Zv9):
Chromosome 24 (position 37235059)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 35850485 |
GRCz11 | 24 | 35738582 |
KASP Assay ID:
554-6213.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGTTCTCGGATACACCTGAGAAAACACTCAACCTCAATCACATTGTG[T/A]ACGTGAACTCCAACATCCAACACAGAAAAAAAATCACCAGCCTTATTACT
Long Flanking Sequence:
TTCTGTTGACAGTCGCAAATACAGCTTAAGGGGGCTAATAATATTATTAACCTTGAAATGGTTTTAAAAAATTAAAAAACTTTTTTTCTCTAGCTGAAATAAAACAAATAAGACTTTATCCAGAGGAAAAAATATTATCAGACATACTGTGGAAAGATTTCTTGCTCTATTGAACATCATTTTTGAAAAAAAAAAAAAAAAAAAAAGTAAATAATTCACAGGAAGGCGAATAATTCTGACTTTAACTGTATATTAAAAATGAATTTTATTATTAATTATTTAATGTTTTCTATAAAACAACTCTATTAAAAACATGCAAATGTGTTCTTGTTCTTTATTCTTCTGCTTGTTTTCTGTCATGTGTTTTTGTGCAGAAATCTCCAGCTAAGAAGCTGTCGGACGCTCTCAGTAAATCTCTGAGCTGTGCGGCGAGTCGAGAGCCTGCGTATCCACAGTTCTCGGATACACCTGAGAAAACACTCAACCTCAATCACATTGTG[T/A]ACGTGAACTCCAACATCCAACACAGAAAAAAAATCACCAGCCTTATTACTTTACAATGAATGTGACATAAACTGTGCAATCTAACATTTCCCTCCTTTTTTTTCACTTTTTTTCTGCAAAACAGGGGCACATGGTGAGTAATGTGAAATGCAGAGTCAGATATCATCATATATTTCAGCATTCATTTGATGTGTAAAACTATTTTTAGACGACTTTATGTGTGTGTGTTTGCTGAAGGCCGCCCAGACCTGTGGCCACTGGAAATGAGTACATGCTTTCTCACTCCATGCCTTCCTCAGGAAACCCTTACTCCAGCAAAGCGTGAGTTTAACACTGCACAATAATTAGTGTTTACATGCCTAGTTCAGAGCATTCAAGCCTCACATCAGCTCATGAAGACATTCTTTCCTTTTTAAATAGGGTTAATAATGCTTTTTTAATTTAAAATGTCATTCTGTGTACTTGTGTTGATACTGTATACATTCACCGGCCACTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44175
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042290 | Essential Splice Site | 362 | 710 | 9 | 21 |
ENSDART00000105680 | Essential Splice Site | 365 | 714 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 24 (position 37234737)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 35850163 |
GRCz11 | 24 | 35738260 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTTTCTCACTCCATGCCTTCCTCAGGAAACCCTTACTCCAGCAAAGC[G/T]TGAGTTTAACACTGCACAATAATTAGTGTTTACATGCCTAGTTCAGAGCA
Long Flanking Sequence:
TGTTCTTGTTCTTTATTCTTCTGCTTGTTTTCTGTCATGTGTTTTTGTGCAGAAATCTCCAGCTAAGAAGCTGTCGGACGCTCTCAGTAAATCTCTGAGCTGTGCGGCGAGTCGAGAGCCTGCGTATCCACAGTTCTCGGATACACCTGAGAAAACACTCAACCTCAATCACATTGTGTACGTGAACTCCAACATCCAACACAGAAAAAAAATCACCAGCCTTATTACTTTACAATGAATGTGACATAAACTGTGCAATCTAACATTTCCCTCCTTTTTTTTCACTTTTTTTCTGCAAAACAGGGGCACATGGTGAGTAATGTGAAATGCAGAGTCAGATATCATCATATATTTCAGCATTCATTTGATGTGTAAAACTATTTTTAGACGACTTTATGTGTGTGTGTTTGCTGAAGGCCGCCCAGACCTGTGGCCACTGGAAATGAGTACATGCTTTCTCACTCCATGCCTTCCTCAGGAAACCCTTACTCCAGCAAAGC[G/T]TGAGTTTAACACTGCACAATAATTAGTGTTTACATGCCTAGTTCAGAGCATTCAAGCCTCACATCAGCTCATGAAGACATTCTTTCCTTTTTAAATAGGGTTAATAATGCTTTTTTAATTTAAAATGTCATTCTGTGTACTTGTGTTGATACTGTATACATTCACCGGCCACTTTATTAGGTACACCTGTCAACCGTTTGTTAAAACAAATTTCTAATCAGCCAATCACATGGCAGCAACTCAAAGCATTTAGGCATGTAGACACGGTCAAGACGATCTGCTGCAGTTTAAATCGAGCATCAGAATGGGGAAGAGCACGGCAATGAGTTCACTGTACTCAAATGGCCTCCACAGTCACCAGAATTCAATCTAATAGAGCACCTTTGGGATGTGGTGGAATGGGAGATTCACATCATGGATGTGCAGCTGACAAATCTGCAGCAACTGCATGATGCTATTATGTCCATATGGAGCAAAATCTCTGAGGAATATTTCCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37940
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042290 | Nonsense | 462 | 710 | 13 | 21 |
ENSDART00000105680 | Nonsense | 466 | 714 | 14 | 22 |
Genomic Location (Zv9):
Chromosome 24 (position 37223025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 35838451 |
GRCz11 | 24 | 35726548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGGGCAGAGTGCCGACAGACATCTCTCTCTGCTTGGACTCTAATAAA[C/T]AGCAGCGACAACTCATTGCTGAGCTGGAAAACAAAAACAAGTGAGTTCGA
Long Flanking Sequence:
ATTTTTGAAACACCATTTTAAGGTCAGATTTGGCTTCAGATCTGACTAATCTAATGTATATGAACAAATATTATTTAGCGTCCTTTAGAAAATATTGATTTGCATGTGAGATTTGTGTAGGAAATATACAAAAATGTACATAAAATACAGAAATATACAAAATAAATATTTTTAAATGTGTATTTATATATGATTTGTGTATAGATTTGTACTATATAGTATGAGATATTTGTTCATATTTAAATATATATATATATTTAAATATGAACAAATATCTTATACTATATAGTAATGCATTTATTTATATACACAAAAATATAAACAGTACGCACAAATATATTTCGCAAATATGAACTTTTATTTTTTGGATGCAGTTAATGGGGATTAATTGTTTGACATCCAGTGAATAAGTAAATGAGCTGTTTCTCTGTGATCTGCCAACTGATCAGCAGAAGGGCAGAGTGCCGACAGACATCTCTCTCTGCTTGGACTCTAATAAA[C/T]AGCAGCGACAACTCATTGCTGAGCTGGAAAACAAAAACAAGTGAGTTCGAGCCTGTTTGCTTTGCTGTTGCACACTGATTTGATGCAGAATTCATATTTAAATGAACAAAAAATATATTGTTTATTATTAGGGAGATTTTGCAAGAGATTCAGCGCCTGAGACAACAACATGAGGAAGCCTCTCAGCCTCCATTAGACAAGAACCAACAAAATCCAATGTTACTGGCTGAACTGAGATTGCTGAGGTAAACACACACACGGACACACACGTTTGTTTGTGTGAATTACGTAGGTGTCTATTGTTTTTATTCTGTACAAACTTTATTTTGTATTTTTTTTTTTTTTGAGAAATTGTTTTAACTTTTCTTGAAAGTCAAGTTTACATACAATAAGATTATTCTGCCTCTGAAAAAGCTCAGATGATGGTGTCGAGGTTTTGAAAGTTTCTGATTGGCTAATTGACAACATTTGAGTTAATTGGAGGCACAACTGTAGAATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37939
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 |
---|---|---|---|---|---|
ENSDART00000042290 | Nonsense | 698 | 710 | 19 | 21 |
ENSDART00000105680 | Nonsense | 702 | 714 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 24 (position 37214847)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 35830273 |
GRCz11 | 24 | 35718370 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAGGATCTGGAGAAGCAGCTGAAGATGGAGGAACGGCTCAGACACTCG[C/T]AGGAACCCGACAAGAACCTCCTGGTGAGGCATTACACAGATTCGGAAGCA
Long Flanking Sequence:
GAATGAATGAATGTATTTTTTACTACTAATAAATATTCTATCATTTGATTTATTTGTGAAGGCTCTAGAAGGAACTTAAGAAGCGATCTCCTGGTAGCTGCAGACTCCATAACCAACACAATGTCCTCACTGGTCAAAGAACTCAACTCAGGTTGTACTCTGCTGTTATGTTTTTTCTGATCAATCTCATGTCCACAAACTGTGTGTACACTTTGTGAATCACTGCCATCTAAACTTCCTCTTCACAAATGTTTAGAGGCTGGAAATGAAAGCAACAGCATCTCAGACTTCATGTTTCCAGAGTCAGACGTTCGCCACACACGCAGCTCATCTAGATCAGGGTAACAGAAGCGAATCTCCTGCTGGTTTCTGATCTCCTGGACTGGTTTTGATGGTGTTTCTTATTTCACAGGGCAGCTAGTAAACTGGAGCCGGGAGATTTCTATGGCCACGAGGATCTGGAGAAGCAGCTGAAGATGGAGGAACGGCTCAGACACTCG[C/T]AGGAACCCGACAAGAACCTCCTGGTGAGGCATTACACAGATTCGGAAGCAAAAGCATCACATATTTAAAGGGACACTTCACCTAAAAATCATTTTGTGAGCTTTTTGTGTCTTCTGTTGAACACAAAGGAAGATATTCTGAAGAAGGTCTTTTTAAAAGCAGTATTTTGTTCCTACCAAGTCAAAATTATGAGCGCTCCTGTGAATGTTTTTTATTTTTTGAAGATTTGGCAAATGATCTTTAATAGAGCAAAGAATTTTTCACAGTATTTTCTATATATATTTTTTTCTGGAGAAAGTCTTATTTTTGTTATTTTGGCTAGAATAAAAGCAGTTTTTGATTTTTTTAAAAAACATTTTAAAGTCAATATTATTAGCCCGCTTAAACATCTGAACATTCTCCAGAATATCTTCCTTTTTGCTCAACAGAATAAAGAAAATAAAATATTCCGAACCACTTGAGTGCCAGTAAATGATGAGAAAATAAAAAATTTGGGTTAA
Associated Phenotype:
Not determined