ZMP
daam1b
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa32288 | Nonsense | Available for shipment | Available now |
sa23682 | Essential Splice Site | Available for shipment | Available now |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa23682
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:
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