Busch Lab

ZMP

daam1a

Ensembl ID:
ENSDARG00000015059
ZFIN ID:
ZDB-GENE-030911-6
Human Orthologue:
DAAM1
Human Description:
dishevelled associated activator of morphogenesis 1 [Source:HGNC Symbol;Acc:18142]
Mouse Orthologue:
Daam1
Mouse Description:
dishevelled associated activator of morphogenesis 1 Gene [Source:MGI Symbol;Acc:MGI:1914596]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa18124 Essential Splice Site Available for shipment Available now
sa9001 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39153 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6462 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18124
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024726 Essential Splice Site 148 1060 4 24
Genomic Location (Zv9):
Chromosome 17 (position 14383925)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14501025
GRCz11 17 14508958
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAAAACCATAGAGAGCCTGAAAACTGCTCTCCGCACACAGCCCATGAGG[T/C]ACTATCTTGAGCAATCACATTTACTGTTCCTCATTTCATACCTRTGGCAT
Long Flanking Sequence:
TTTTTAATTTTATTTATTTAATTAATTAATTTTGTTTGGTTGTTTTTTGTTTATTATTTGTTTATTTATTTGTTTATTTTGGATTTTTTACTTTATTTATTTATTTTTTGTTTAATTTGTGTTAGATTTTTTACTTCTTTGTTTACTGTTTGTTTACTGTCATATTTATTTGTTTGTTTCTTTTGGTTTTATTTATTTTTTATTAATTGTATTTATTTGTTTTTGTTTGGTTGTTTAGTTTATTACTTTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTCTGTTTGTTTACTGTTACAAACTTTACCAAAACTCTGGTATTGTAAACTTTGGTCAGTCCATTAATTATTTGCATCTGTGTTAAATCTCACCAGAGGAAGTCTTTGCTAGCTCTGGAGAAGGAGGATGAGGAGGAGAGGAATAAAACCATAGAGAGCCTGAAAACTGCTCTCCGCACACAGCCCATGAGG[T/C]ACTATCTTGAGCAATCACATTTACTGTTCCTCATTTCATACCTGTGGCATTAGTTTCAAATACTGATAAAAAAAAGTGTTTCATTAGTGCTAAGTGTATTTATATAGTGCTTGCAGTATGTTGACTTTGCAGACTATTAAATCTGCTACTCAGTTCTTCACAGCAGAGTGATTCAGTTTTATTTGCGTGAAGAAATCTTTGCATCATATATAAAGAAGCAGACCACATCAAATATACAGCAACAGTATGTAGTTAAATACTTTAACATAATTAATAGGGCTGCATGATTTATCGTTTCTGCATCTATATAGCAATATGCTCATCTGCAATATTCACATAGCAGGAATTGGTTTTATAGCTGACCAGGAGCCACATTTAGAACACATAGGATTTTTTGGTGTCACTGCAGAGTTTAATCATGGAAAGTTTATTATTTGCATGATAACATTTGTAACCATGATAAAGAGCAATCTTGTTCATTTTTTCGCTATAAAATAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9001
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
ENSDART00000024726 Essential Splice Site 296 1060 6 24
Genomic Location (Zv9):
Chromosome 17 (position 14379071)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14496171
GRCz11 17 14504104
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCATCATGTCCTTCATCAACGCCGTCCTCAGTCAAGGAGCAGGGGAGG[T/C]AARCGCTACTTTCCNCCCCACACATCTGYCTCTCATTACATTCAAATCATC
Long Flanking Sequence:
CAAAAAAGATTGAATAAAAAGTCTAATAATATTGACTTTAAAACGGTTTAAAAATAAAAAAATAAAAACGTTTATTCTAGACAAAATAAAACAAATAAAACTTTCTACAGGAGAAAAAATATTATCGGAAATACTGTGAAAAATTCCTTGCTTTGTTAAGCATCATTTGGGAAATATTTGTAAAAGAAAAAGAAGTGTACACGAGGGCGAATAATTCTTCAACTGTATACATTATTAGTTCTCCCTTTAAATCGAATGCAACGTCCAAATTGGCCCTTCTTGTTCTTCTGAAATAAGACCCTTGAGATTTGTGAATGAAATACGAAGAGCTTGTTCTCCTTTGTAGTTCTCATTCCTTCTCCTCATCTTGTTTTTTTTCCACACACAGACTCTCCTGAATGACTTGGACAGGAGTACGGGCCGCTACAGAGATGAGGTGAACCTCAAGACGGCCATCATGTCCTTCATCAACGCCGTCCTCAGTCAAGGAGCAGGGGAGG[T/C]AAGCGCTACTTTCCCCCCACACATCTGCCTCTCATTACATTCAAATCATCCAAGAGTTTTTCTTTGACTTCCAATATTTTGTGCACAGACCAGTTTGGAGTTCAGAATTCATTTGCGGTATGAGTTTCTAATGCTGGGCATCCAACCAGTGATTGATAAATTACGGTCCCATGAAAACTCCACGTTAGATCGGTAAGTGCTGTATTTCGAGACACTGCAGGCCTCAAGTGCTTGGCTGAGTTTAACGTGTGCTCTTTCATTACTCGTCAGGCATTTGGACTTCTTTGAGATGCTACGAAATGAAGATGAATTAGCTCTCGCTAAGCGGTTTGAAAACGTACGATTGGGGTTTAAATGGGTTTGTAAATACAGCTACTTTGTTTTGGGAGTCGTTTCATGTTTGTTTGTTTGTTTGTTTGGTTGGTTGGTTCAGGTTCATGTAGATACTAAAAGTGCCACTCAGATGTTCGAGCTCATCCGGAAGAGGATAAACCACACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39153
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024726 Essential Splice Site 458 1060 11 24
Genomic Location (Zv9):
Chromosome 17 (position 14371864)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14488964
GRCz11 17 14496897
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAACGAGGTGAAACAATGGAAAGAGCAAGCGGAAAAAATGAGGAAAG[G/A]TACAGTACATGACCTCTCTACGACCCCAATATTGATTAAAGCGACTGATT
Long Flanking Sequence:
AGTTGGCTTCATTACACAACCAGTGGCTTTTGAAATAAAGGAATAAAGCTTGCACATTTTAAAAACAATTCTGCTATTATCATTGACTATAAATATCATGCATTTCAAGTTTGTAATGATATGAAAGAGAATAAATAATGACGATGACAGAATTTAGACTATTAGTAACACTTTACAATATGGTTGTATTTGTTATTGATAATGTATTTACTAGCATAAACAATGAACAATACTTTAACAAAAGATGGATAATAATGTATTCATTAAAGTTAGTTCATGGAAATAAATTTGTTGAAGTTGGATTGTAATAGCACATTAGTAAATGTTAAGTAAATGTTGCACGAGTGTTCCTTATTAGTTCATGTTAGTAAATCTATTGTGTGAATGATCTCTTTAACCATTCCTAATAGTCTAACACTGCTCTCTTGTTCGATTCTACAGGCTGGTCAATGAGAACGAGGTGAAACAATGGAAAGAGCAAGCGGAAAAAATGAGGAAAG[G/A]TACAGTACATGACCTCTCTACGACCCCAATATTGATTAAAGCGACTGATTCCCTTCAGAAGGCCTTGAATGTGTTTGCATGTGCCTTCATCAGCATGGGAATCAGCGATGACATTGCTGATGTTGTCAAATATTAATGCGCTTGTGCATTTTTTTGACACACACTTTCTTCTTTGTTTTCTCTGGCTTGAATCGTAGAACATAATGAACTTCAGCAGAAGCTGGAAAAGAAAGAAAGGGAGTGTGATGCTAAAGCCCAAGAGAAGGAAGAAATGATGCAAACGCTCAATAAGATGAAAGAGAAGCTGGAAAAGGAAAGCAGTGAACATAAGCTTGTTAAGCAGCAAGTGGCTGACCTTTCTGCCCGGCTACATGAGATGAGTAATGTATGTTAAATACGCAGATCCGCACACACTGCCTCTTCCAAAACCCACTGAACTGTATTTTAAGGCAAAGTCTAAATAAATGGAGCCAAATAAGTCCCTGAATTGGAAGGAGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6462
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024726 Nonsense 673 1060 15 24
Genomic Location (Zv9):
Chromosome 17 (position 14363313)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14480413
GRCz11 17 14488346
KASP Assay ID:
554-5126.1 (used for ordering genotyping assays)
KASP Sequence:
ACGAYACTGTCACTTCTAAAAAGGTCAAAGAACTGTCTGTCATCGATGGA[C/T]GACGTGCRCAAAACTGCAACATCCTTCTCTCCAAGTGAGTCTGCAGCTTA
Long Flanking Sequence:
TCAAACTGTAGAGCGTCCTGCTTCTCGACTAAAAAAAAGCCTAAAAAGTACATTATGTTGTCCAACAGCAGCCATATTTGTCAAACTGTAGAGCGTCCTGCTTGTTGCTGTATGTGGGCGGAGTAATACACAAGGGTGAAGAGGCGGTACAAGTGCTATAACTGTCAGAAAATTGAACAGCTATCAACCAATCAGATTTAAGAACCAGACAGAACAGTTGTATAAAGTACAATAAAGAATACATTTTAAAATGAAGCAGTAGAAAAGACTATTAAAATAATATTCAATGGCCAAGCTGAACAGGAAAGTTTTTAGGAGTGATTTAAAAAAAGGGATTTGAGAACTTCATCAACTCTGAAATCAACATTAGCCTTCTCATAGTATTTGTGTTCCTCCTCTCACATGATGTTGACCTTCTCTATGTTTATCTTTTTCAGAAAGAGTCCGAGGACGACACTGTCACTTCTAAAAAGGTCAAAGAACTGTCTGTCATCGATGGA[C/T]GACGTGCGCAAAACTGCAACATCCTTCTCTCCAAGTGAGTCTGCAGCTTAAAAAAACTCCTAGATTGCATCTTTGAGCCTTTAAGATTGATTCACAGTATAAAGCTTCCTGCATGACTCATTGTAGAGCCATTCTTTGTTTACTTCAGCCATTTTGTTAACGGTTGGTGATGTGTTTAAAACACTATTGCAGCCGAGCGTTTTATTCATAAGATGATCCTGGCCTGGATTTCTTTCCTGTTGCGTCACAAGTCACCATAGCAACAGTGATAAACAAAGATGCCTGTGATCTTTCCCATAAGCTCACTTCTTCTGTTTGAATGAACAGTAAAGCTGGAAGTAAATCTAACATCTATTAAAACTAAAGCCTTTAATTCAGGCATTTTAGATTTGCGTTGAGAATTTTTTTCACTGTTATTTTAGAACTGATTGCAAAGTTTGGTGGAAAAAAACAACAACAACAACAAAAATGGAATTGAAATAGATTGAACTGGGACAAAA
Associated Phenotype:
Not determined