ZMP
dvl1a
Ensembl ID:
ZFIN ID:
Human Orthologue:
DVL1
Human Description:
dishevelled, dsh homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:3084]
Mouse Orthologue:
Dvl1
Mouse Description:
dishevelled, dsh homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:94941]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44013 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44014 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8764 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44013
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035755 | Nonsense | 179 | 729 | 5 | 15 |
ENSDART00000143583 | Nonsense | 21 | 569 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 30205106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30039996 |
GRCz11 | 23 | 29966527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGGTCACCCGAAATCGGAGCGTCTGAATCGTGACTCGGCAGTAGTTTA[T/A]GACAGTGCGTCTGTCATGAGCAGTGAACTGGAATCCAGCTCTTTTATTGA
Long Flanking Sequence:
GGGTTATTCCATAATATCAATGCTAATTCTCTTATTTACTTTGCAACTGTTTTGTTACTTTGTGCACAAAAGTGATCTAAATGACAACATTTAATTTTTTTTTTTCAATATTTGCCGGAATATGTCATCAGAAGTTTATGAAGTGGGGAAAATATGATGCTTTACTTAAACATATTACTATAAATCATGAATTTAAGGAAACAATGACACACTGTCCTCTGTTATTTGTTGAAAATGACTTGGAACTGATTTCATGATTGAATTACTTCTGAACAGTGACGATCCTTGTTACTCCATCAGCATGAAAATGCTTCACAGTCTAATAGAATTTGTTGTCAAGAACCAATATTTCTTTGCCAGAATCATTTCCTGTACTTGATGTTTTTGATGTTCTGTTGTGCTTTCTCTTCTTAAACAATGTTTTATTTGTCTCTTTCAGTCCCTCGGGTGAACGGTCACCCGAAATCGGAGCGTCTGAATCGTGACTCGGCAGTAGTTTA[T/A]GACAGTGCGTCTGTCATGAGCAGTGAACTGGAATCCAGCTCTTTTATTGACAGTGACGATGATGCCAGCAGGTCAGACACTCACTAACTTTTTTATTTCCCAGGAAGAATTAAATGAGCTCAGAGCGCAGTATTCATTTCCTCCTAAATGCTGACCGTCTTTATTTGAGGATGATTATTTTTTATATCAGGATGTTTTTCTCTTAGTCAGTTTGTAACGCTGGACAAAGTCAGCATTAGATCCTTGTTGGTTCATTTTAGGTATAATTTTTGCAGTTTTAGTTAAGTTTTATTTGATTAATATGTTTTTAGATTACAATTATAGAACTTCAGAAAATATTTATTAACAAAAGTTTTGTATTTCTGTTTAGTTTGAAACAATCTATGTAGTCTAAACGAAGTAATCTAAATGTATTCTCATTATTTTATAATCCGCAATCAATAATTACATTTGAATTATCTGTAATATCAGTAATTGTTACATCATGTTATTATTTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44014
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 |
---|---|---|---|---|---|
ENSDART00000035755 | Nonsense | 608 | 729 | 15 | 15 |
ENSDART00000143583 | Nonsense | 448 | 569 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 30230669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30065559 |
GRCz11 | 23 | 29992090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACATGGGTCACAAGAAGGGGTGAAAAAGCACCCAGTCAGCTGAGCCAC[C/T]AAAGCCACAGCCGATCGGCCGCCAGCCAGTCCCAATCCGCTTACAGTCAC
Long Flanking Sequence:
TTTAATTACTCCAAAAAACTCAAGAATTGTATTTATTTCAGCTCATTTTAAGTAGTTTGAACAGTCATTTTTATGACTGTACACATTTTATCTTCTGAAGAGCGAAGCGTTAAATAAAAAAAAATATCAAAAGTCTTTTTGAAATTTTTGAGGGAGATGCTAATGGTCTAATCCGATACAATGATTTATGCTATGCTAAGCTAAACTAAAAGTACTCATGCCAGGCCTGGATATCAGCTGAACGGATTAAAAAAAAAGTCAAACTAGAGTGTTCCTTTAAGAACAACAACAACAAAATAACACTAGTCTTTTCTAATCAATTACGTTTCTTTCTCTCCGCAGGCAGCAGAAGCAGTGGCTCAAACCCCAGCGCTGGCAAAGGACGCAGAGCCTCGCCCCGAGAGAAGGAACACAAGGCACCCTGCTGTGGGGGGAGTGAATCAGAACTGGTGACATGGGTCACAAGAAGGGGTGAAAAAGCACCCAGTCAGCTGAGCCAC[C/T]AAAGCCACAGCCGATCGGCCGCCAGCCAGTCCCAATCCGCTTACAGTCACGGCCACACACAGTGCCACCTCATCCCACAGCACAGCCTTAGCTTCAGCTACAGCCATGCTCCATTCATCCAGCCCAGTCATCTGTCATGCGCCCACAGCGAAAGGAGTCACGGCTCTTCTTATGGCCCGCCGGGTTTACCCCCTCCCTACTGCCTTGCGCATCTCGCCCCCAAAACAGCCGCAGGCAACAGCAACAGCCCGCCAGGAGCTCCTCCGATTCGGGAGATTGGAAACGTCCCACCAGAACTCACAGCAAGTCGGCAGTCTTTTCAGCACGCTATGGGCAATCCTTGTGAGTTCTTTGTGGATATTATGTGACAGGAGAGAGTGCCTTCAACATTCACTTCATAAGGTTTTGCTACTGACGATCCAATGCCTGCACTGAGAATGTACAAACTGATGCACAAATCTAAAGGGAGAGTTCACCTAATGCTGGAAATTCTGTCGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8764
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 |
---|---|---|---|---|---|
ENSDART00000035755 | Nonsense | 641 | 729 | 15 | 15 |
ENSDART00000143583 | Nonsense | 481 | 569 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 30230770)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30065660 |
GRCz11 | 23 | 29992191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RGCCACACACAGTGCCACCTCATCCCACAGCACAGCCTTAGCTTCAGCTA[C/A]AGCCATGCTCCATTCATCCAGCCCAGTCATCTGTCATGCGCCCACAGCGA
Long Flanking Sequence:
GCGAAGCGTTAAATAAAAAAAAATATCAAAAGTCTTTTTGAAATTTTTGAGGGAGATGCTAATGGTCTAATCCGATACAATGATTTATGCTATGCTAAGCTAAACTAAAAGTACTCATGCCAGGCCTGGATATCAGCTGAACGGATTAAAAAAAAAGTCAAACTAGAGTGTTCCTTTAAGAACAACAACAACAAAATAACACTAGTCTTTTCTAATCAATTACGTTTCTTTCTCTCCGCAGGCAGCAGAAGCAGTGGCTCAAACCCCAGCGCTGGCAAAGGACGCAGAGCCTCGCCCCGAGAGAAGGAACACAAGGCACCCTGCTGTGGGGGGAGTGAATCAGAACTGGTGACATGGGTCACAAGAAGGGGTGAAAAAGCACCCAGTCAGCTGAGCCACCAAAGCCACAGCCGATCGGCCGCCAGCCAGTCCCAATCCGCTTACAGTCACGGCCACACACAGTGCCACCTCATCCCACAGCACAGCCTTAGCTTCAGCTA[C/A]AGCCATGCTCCATTCATCCAGCCCAGTCATCTGTCATGCGCCCACAGCGAAAGGAGTCACGGCTCTTCTTATGGCCCGCCGGGTTTACCCCCTCCCTACTGCCTTGCGCATCTCGCCCCCAAAACAGCCGCAGGCAACAGCAACAGCCCGCCAGGAGCTCCTCCGATTCGGGAGATTGGAAACGTCCCACCAGAACTCACAGCAAGTCGGCAGTCTTTTCAGCACGCTATGGGCAATCCTTGTGAGTTCTTTGTGGATATTATGTGACAGGAGAGAGTGCCTTCAACATTCACTTCATAAGGTTTTGCTACTGACGATCCAATGCCTGCACTGAGAATGTACAAACTGATGCACAAATCTAAAGGGAGAGTTCACCTAATGCTGGAAATTCTGTCGTTTGCTCTAAACTTATTCTGTGAAACAGGAAAATCTGTTTAGTTGACCACAGTTAACTAAAACTGGGAAATTATTTAATTTATTAAATTTTCTTCGGCTTACTG
Associated Phenotype:
Not determined