Busch Lab

ZMP

daam1b

Ensembl ID:
ENSDARG00000009689
ZFIN ID:
ZDB-GENE-030131-4212
Description:
si:ch211-87i20.1 [Source:RefSeq peptide;Acc:NP_001025307]
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 6 alleles of this gene:

Allele Name Consequence Status Availability
sa45695 Nonsense Mutation detected in F1 DNA Not yet available
sa32288 Nonsense Available for shipment Available now
sa300 Nonsense F2 line generated Not yet available
sa23682 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa45695
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
ENSDART00000004984 Nonsense 93 1079 3 25
ENSDART00000109084 Nonsense 93 1069 3 24

The following transcripts of ENSDARG00000009689 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 21955186)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 21983353
GRCz11 20 21883026
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTATTCTTTATTTTTTTAATCGCATACACTTTACGTTTCTTTTTAGGAA[C/T]AAGAGGAGAATAAAGGTGCTACTAGCTGGCCGGAGTTCTACATCGACCAG
Long Flanking Sequence:
CAAAAGCAGCAACAGAATAAATAAATGCCTTTCAGATAAGCCAATTCACACTTCAGTCAGCTGAATATTTGGTTTCACACAACTGGTCGGTATCAAAATAAGATCATTTTCAAGATAATGATCATTTTTCATCGCTGTTGAGTTGGGAAAGTTTCATTCCCATCGAAGCGTCCAAATTATGTCATTACTAATAACATTCCGAAACCACACTTTCTTTCCCTGCTCAGTCCTGATATGTTGTTTCACATTCCTCTATTCCCAGCGCCATGTTGGTGTTGTTTGCTCTCAGATCAGTGTGAACGCGTCTCATGTGGGCCGCGTGGATTAATGGCGTGTGACTGAAATGAAAACAAGAGCCATGTTTATATTTGTTTTTCAGTCTTCTCATGCTGACATTTTTAGACCAGTGTTCAATCCAAAGAAATAAAAACAAAGATATTATTTAGGTGTGTTATTCTTTATTTTTTTAATCGCATACACTTTACGTTTCTTTTTAGGAA[C/T]AAGAGGAGAATAAAGGTGCTACTAGCTGGCCGGAGTTCTACATCGACCAGCTTAATTCAATGGCAGCTGTAAGTATGACACTTTTGAAAACATTTTCTTTATCCTTTAACACCTGGACCATGAGCTTGTTCAGTTTGACCTGTTTTGATTTTTAAATTGTTGCAAATACTACACTGTAAAAAATGTTGGGTTCCACACAATTCCTTCATGTTATACTAACACAAATCGATTAAGTTAACTTAATCGTTTTTACAAACTTTTTTAGTGGATTAAACATAAAATCCCCCAAAAAACTTTTAAATAAGTAGTTTGAACAGGCAGCAAAATGTTTTTTTAGTTTATTTAAAGAGCACACTCCCACCCCAAAAAACCCCAAGAGACTGTTATTTTGTTAAACAAAAGAAGATATTTGGAAGAATGTTGGTAACCAGACTCTGCTATCAATTGACTTCAGAATCAAAGTGCACCATCACAAGTTTGGTTAGCAACTTTCTTTATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32288
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004984 Nonsense 132 1079 4 25
ENSDART00000109084 Nonsense 132 1069 4 24

The following transcripts of ENSDARG00000009689 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 21951975)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 21980142
GRCz11 20 21879815
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGAAGACTCTGTTGGCCTTGGAGAAGGAAGAAGAGGAGGAACGCAAC[A/T]AGACCATTGAAAGCCTTAAAACGGCACTGCGAACACAACCCATGAGGTCT
Long Flanking Sequence:
AGTTTATTTAACTGATTGTATTGTAATTACATTACAACATCGATGCTAGAAAAGGAATAGTATAAAATGGAAAAAAGTCACATTACCCCTTCACAGGAAGTTTATCTTTATGGGTAGAAACATTAGCTCCCCGTACACCCTATAGTCAAGCTTTAAATAGGAAAATTGTCAATACTCGTTTGTCATTTTTCTATAGATGCTTATTGTCGAATCTGATTTAAGAATTTATGTTAAGCTAACCTTAGCTAAACTCTAGACTGACGTTGATATCAGCTGAATGGATTCAAAAATTGTAAAACTCAACTGTTTACCACTTAGGGAGTTGTAAAATGAGCCTGTTTACAAAAAATGTGGTGTTCTTTAAGCCAATAGCACAAAAAAAGAAAGTTTTGGTTTTGTGTCTAGTCCTCGGTTGTCAGTTTGTAAGTATGACATGTCATTATATTTTACAGAGGAAGACTCTGTTGGCCTTGGAGAAGGAAGAAGAGGAGGAACGCAAC[A/T]AGACCATTGAAAGCCTTAAAACGGCACTGCGAACACAACCCATGAGGTCTGTATACTGTTACAACAAACACTCTTTCAAGGAAATCCTGTTTACTTGGCAGCCATGTTTGCAACACCCTCAAGCATATATATCAGGGATACAAGACAAAGCCCTGTCTATTTATATGAGGAAATGCTGGATTGCCAAAAAACTTTTGACAAACTCACAATTAAATGCGTAGTTTACACAAAACTGAAAATTCTGTTATCATATACTCATCTTCCACTTGTTTCAAACCTGTTTGAGCTTCTCTTTTCTGTTGAACAAAAAGAAAGATATACTGAAGAACTTTGGAAAAAACTGCCATTGACCTCCATAGTATTTTTGTCAATGACTGCTTTTCTTCAATGTTTGTTTTACCGATGTTTTGTTAATATTTAACAAAAGAAAGAAATGTATAAAAGTTTAGAATGTACCATTTGAGGGTGAATAAGTAGTAAGCAAATGGTAATTTTTAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa300
Status:
F2 line generated
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
ENSDART00000004984 Nonsense 485 1079 12 25
ENSDART00000109084 Nonsense 485 1069 12 24
ENSDART00000004984 Nonsense 485 1079 12 25
ENSDART00000109084 Nonsense 485 1069 12 24

The following transcripts of ENSDARG00000009689 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 21937474)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 21965641
GRCz11 20 21865314
KASP Assay ID:
554-3271.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAGGAGCGAGAGTGTGACGCCAAAACACAGGAGAAGGAGGAGATGATG[C/T]AGACCCTCAACAAGATGAAAGAGAAGTTAGAAAGAGAAATGGGGGAACAT
Long Flanking Sequence:
ATTTATATAACCTGCTACAAAGCATATTTCTCTTGTTGAACCAAGTCAGTTTTTTTTATCTAAAAAAGATATACCTTTAATCATACACAATTGAAGTCTTATAAGCCCCCCTGAATTATTACAACAAAATACAAAATAAAACAAATATTGTCAGACATACTGTTAAAATGTCCTTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAAAGAAAAAAAATCAAAGGGGGGCTAATAATTCTGACTTCAACTGTACATACATATACATAACGATTGTAAAAAATTTTTAAATAAAGTCTCTTTTGACTTTACCTGATTGCAGCCTATTTATGGATTCATTGTGCAGTGCAGACTTTTAGAAATGGCTGAAATGGAAACACTGTGTATAATATTTGACCTGTAAGCTGTTTGTCCTGCAGACCACCATGAGCTTCAACAGAAAATGGAGAAGAAGGAGCGAGAGTGTGACGCCAAAACACAGGAGAAGGAGGAGATGATG[C/T]AGACCCTCAACAAGATGAAAGAGAAGTTAGAAAGAGAAATGGGGGAACATAAACTCGTCAAGCAGCAAGTGGCAGAAATGACCACCAGACTACATGAGCTCAGCACGGTACGCTAATGATGTCACACATACAGTCATGGTCAAAATGATTGGCACCCTTGGTAAATATGAGTAAAGAAGAAGACCGTGGCTAGAATTTTTCAAATGTTTTATTGATGTAAAACAATTGAAAACATTAAAGTGTCTTATTATATATATTAATTAAGTGTCTTATTCTAAAAAAATATTGATTAAAATTATTGACACCCATTTATACAATACATTCTGCTCTAAATTGTCTCCCATAATGTCTGATGAGGTTGGCGGAAACCTAGAAGGATATTAGACAGATTTTTTTTCATAAAAGTCTCTCCAGATCCTTCATGTTCTCTGGTCCGTGTTTATGCTCTTTCCTCATTTTCTAGAGGATTCCTGACAGGAGACTGGCCATGGCTAAACTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23682
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004984 Essential Splice Site 953 1079 24 25
ENSDART00000109084 Essential Splice Site 943 1069 23 24

The following transcripts of ENSDARG00000009689 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 21891309)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 21919476
GRCz11 20 21819149
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATTTATGTTGAAAATGGCTCTCATACGAGTTCTGCTTCTGTTCTCTA[G/A]TTCATCAAGACAGTCAAGCACTTCGGTGAGGACGCTGATAAGATGCAGCC
Long Flanking Sequence:
CACCACTTATTAAACTTTATTAATGTTAGTTTAAAAAACAGCATTTACAGTAGTTTACGTTTGATTGGCTAATTATTGTTAATCAAGTTTATTAATCTAGGTAAATAATGAAGGGTCTAATAAACTAATGAAATGTTACCAATAGTTATATTTCACTTTTTCAAATACTTCTAAAATGCAATACATTTTTCGAGCAATTTTATTACTTTTTGAACAGTTACATTTTCTCTCGGATGCATTTGTGAGCAGTAACCACAATGTATATTTCCCCGAAATCTCAGAAACCACAAATGGACTAAAATTATAAATAAACCAGTAATTTAGGGTTATTTAAAAAAAAAAAAGCACGTATAGAATATGCTCCAAGAAAAAAACAAAGAATTTCATTGTTATTCCTTGTTGTGTCTATAAAACATTTGAAAAGTGTTTTGGCATTAAATAAGTTTTTTCAGGATTTATGTTGAAAATGGCTCTCATACGAGTTCTGCTTCTGTTCTCTA[G/A]TTCATCAAGACAGTCAAGCACTTCGGTGAGGACGCTGATAAGATGCAGCCTGATGAGTTCTTTGGGATTTTCGACCAGTTCTTGCAATCCTTTGCAGAGGCTCGTCAAGAGAACGAGAACATACGCCGGCGCAAAGAGGAGGAGGAGCGCAGGGCACGAATGGAGGCTCAGGTCTGACATTTAACATGTTTTTTTGGAAAACATAAATGATAATAATAATAATAATAAATTATGTATTAAAGGCACAGTATATAAGTTTCGGCTGTAGAGGCTCTGTATTCACAACAAAAACAAAGGTATTTATTTTGTACTTAGGTACTTAATAAGTACTTAAAATGACACAGTGACTGAGTGTTGCAATCATGGGAGTTGTGGTCTTCATTACATTCTGTGGGACTCTGACTGCAGAAATCATATTTATGAATAAGCTGATGTAGAGTAACAAGGAGTTGATGTGAAATGAGATGAAGCTATTGCTGATGTAAAACAAGTAAGACACA
Associated Phenotype:
Not determined