ZMP
DAAM2
Ensembl ID:
Description:
dishevelled associated activator of morphogenesis 2 [Source:HGNC Symbol;Acc:18143]
Human Orthologue:
DAAM2
Human Description:
dishevelled associated activator of morphogenesis 2 [Source:HGNC Symbol;Acc:18143]
Mouse Orthologue:
Daam2
Mouse Description:
dishevelled associated activator of morphogenesis 2 Gene [Source:MGI Symbol;Acc:MGI:1923691]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11626 | Nonsense | Available for shipment | Available now |
sa23181 | Nonsense | Available for shipment | Available now |
sa36524 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23182 | Essential Splice Site | Available for shipment | Available now |
sa23183 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11626
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034563 | Nonsense | 114 | 1092 | 3 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 48999869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48761667 |
GRCz11 | 17 | 48844296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGGAACAAGAGGACCCCAACAAACTTGCCACCAGCTGGCCTGATTACTA[T/A]ATAGATCGGATCAACTCCATGGCAGCTGTAAGTATTTACTTTGTTACATT
Long Flanking Sequence:
AGGGTAATCAGGCAAGTCATTGTATAACAGTAGTTTCTTCTGCAGACCATCAAAAATACATTGCTTAAGGAGGCTAATAATATTGAGCTTAAATTGGGTTTCAAAATATTTAAACCTGCTTTTATTCTAGCCAAAATAAAACAAATCAGACTTTCTCTAGAAGACAAAATAGTAGAGGAAATACTGTTAAAGTTCCTTGCTCTGTTAAACATCATTTGGGAATTTTTTTTTATTTTTTATTTTATCAGGAGCGCTATTAATTTTGACCTTTACTGATAATCGTTTTCAATAATCGTGATAACAATTATGACCAAAATAATCATGATTATGATTTTTCCCAAAATCGAGCAGCCCTACATTATGTTTGTTTACCACTATTCTGTTATTTAACAAGAAAATATCGCATGTCTTGAAATAGAATCTGACCACCTTTATATGCTTTTCTAATTTTAGGAACAAGAGGACCCCAACAAACTTGCCACCAGCTGGCCTGATTACTA[T/A]ATAGATCGGATCAACTCCATGGCAGCTGTAAGTATTTACTTTGTTACATTACATTTTTAAATGCACAACAGACATTTGCACCTTTTGTAGCTGATTCAAGAGTTCACACTTAGACTATTAGACTGCTTGACTATTTAAGCAAGTTTGGCATGCTGTCCCTGGAGAGAACCCTGAGCTCTGAGATAGATGAGCCAAAGGCTGCCGCCTGGTCAATAAGCATTAGGAGGGATATGAGCCCTGCTGAAAAATCCAGCTTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCTGGTCAACCAGGGTGGTTTAGAGGGGTTTTGGCCATTTGCAGCCTGGTCTTAGCTGGTCAGGCTGGAAAATGACCAGCTAAAACCAGCTTGACAAGCCTGGTTTAAGCTGGACATAGCTGGTTTTGGCTGGGCTCCCAGCCTGGCTAGGCTGGTCAAGCTGGTTTTAGCTGGTCATCTCCCAGCCTGACCAGCTAAGGCCAGGCTTGAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23181
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 |
---|---|---|---|---|---|
ENSDART00000034563 | Nonsense | 376 | 1092 | 9 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 49010343)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48772141 |
GRCz11 | 17 | 48854770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGATGCATGTGGATACTAAGAGTGCTGGCCAGATGTTTGAACTGATC[A/T]AGAAGAAACTGAGCCATACAGATGCCTACCCCCACCTTCTATCTATCCTA
Long Flanking Sequence:
GTATTCAAAAGTAATGGCCTATTTATATTTGAAATAAATATTTTTTGTTCTGAATGACTCTTTTCTTTAAAATAGTTTTCAGTTAAAATAAATCATCCTTTAACTGTCATGTATAGGGAATTTACAAAGCATAAATTGTTGTCACTAGATGAGCTCCCAAAACTAGGAATTTGTTTAAAAAGCATTTCTTTATATAGGGTAATTATTATTTGCCTAAAATAAGATGTACAAATGTTAATTTAAATAGTTTATTAATATTTTTATGTACTCATTGTGAATTATCAAAAAACACCAACTCTTAAATAACTGCTTCAGTAATGAAAAATAATCATTAACAAAGTATGAAGATAAAATCATTAAGCACATTATATATGTGCTTGTAAGTCGAGTGCAACATTTGCAGCTGTTAGATGCCTTTTTCATGACTTTTAACATGTGTGTCTTTTTGTGTTCAGATGCATGTGGATACTAAGAGTGCTGGCCAGATGTTTGAACTGATC[A/T]AGAAGAAACTGAGCCATACAGATGCCTACCCCCACCTTCTATCTATCCTACAGCACTGTCTCAAAATGCCATGTAAGTAATCATGAGGGGGAAAGTCTGGGGTTGTCTGATGCAAGTCATCCTACAACAGTGGTTTGTTCTGTAGCCAATTGAATGAGGAGGCAAAGCAACGGGCAAAACACAGCAAGGCAAGGAAAATGTGTCTTAATGTTCACAATACAGCATAACAAGACTCAGCAAAGTCTGTGTGTTTGTGTGCTGTATAAAAAGTCCATCTTATCAGTTCATGAGCAACTCCCATAGACTGTAAAATATATGGACGTAGTATCCGTGACGTCACCTATTGGTTTCTAAAGAGCGCAAAAGAAGCCACAAGTAGGCGCGGCCAACCGTCAGCATTTTGTTCGCGCGTCATCACACCCATGGCGGGATACCAAACAAGGGCAAAGAGGCGGAGAGTGAGCGGAGCTACAGACACCTGCTAGCATTTTGCTTGGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36524
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034563 | Essential Splice Site | 743 | 1092 | 23 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 49029798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48791304 |
GRCz11 | 17 | 48873933 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTATAAGCAAATGCTCTGCACGTGTAAATGTTTGTTGGTTTTATTTTAC[A/T]GCTGCTTAAGTTTGTTCCTGAAAAAAGTGATATGGACCTTCTGGAGGAAC
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATATCTCTATATATCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTAATAAAGACAGCACTTTCTTTTAATACAGGCTAAAAATGAGCAATGAAGAACTAAAAAGAGCTGTTCTAGAGATGGACGAGAGGGAAGAACTGGCTAAAGACATGTTAGAACAGGTGAGTGCTATATAATAATGTCAGTCGTTGGTCATGAACAATAGAACTACTAAGTTTTTGATTAGTACAACTAATACTTATAAGCAAATGCTCTGCACGTGTAAATGTTTGTTGGTTTTATTTTAC[A/T]GCTGCTTAAGTTTGTTCCTGAAAAAAGTGATATGGACCTTCTGGAGGAACACAAGCATGAGCTTGAGCGTATGGCCCGGGCTGACCGCTTTCTGTTTGAGATGAGCAGGTACTGCTAAATAATTAAGGTTTAGATTAAAAAAACAGTGTGATTATTTGATGATTTTAGAACAAAATCTTCTTTAGATCAGTGGTTTCCAAAGTGGAGGTCGGGGGACAATGTGAGGGGGTTGCTTGGTGATTTAAAAAAATAATAATAAATCAAATCAATTAGATTTTTTTTTGATTATTTAATTTAAAACTATTAGAATTACTTTTTTATCTATAACGTACAGGAAGTAGTGTTTAATAGTTACATAAAAACAACAGCAACATGCAAATAAAAACCCATTTCCTTTGGATTGTGATCCCTGTTGTGTTTATGTTACGCTTATGCTACTGACACGCACCTCTCAAAAAATTTAACTACACGTCGCAACAATGCGTAACGCAAGCTCTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23182
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 |
---|---|---|---|---|---|
ENSDART00000034563 | Essential Splice Site | 864 | 1092 | 25 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 49039326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48800832 |
GRCz11 | 17 | 48883461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGTGTCCAGTCTTAACAAGATCATAGACACCAAGTCAAGTATAGACAG[G/A]TCAGGAGTCATCGAAAATGGTTTTATTAGCTTGCTCATCCAAATGCAATA
Long Flanking Sequence:
GTTAAATCCCTAATATATATATATATATATATATATATATATGTAAAGACCTATATAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTCTGCGTGTGTGTGTTTGGGAGGAGGGGGGCGCCAATGGATAAGTTGTGTCAAAAGGGAGGCCCACTGTCTTAGACTTTGAAAAACCCTGCCCTACATGAAGCAAAACAGGCCAAAATCTGGGGGAAAAAAGTGTAATCTTAATGGGGCTACTTTCATTACAAACCCCAACATGGGGGCTACAGTAAGCATCAGTAACCATCTTTGATTTTGTTTTTTCTTGTTTCATTTCTAGCTATTCTGTGCGCATCACGTGAGGTGATGAGAAGTAAGCTCCTGAGACAGGTTCTAGAAGTGGTTTTGGCGTTCGGGAACTTCATGAACAAAGGACAGAGGGGCAATGCATACGGTTTCAAAGTGTCCAGTCTTAACAAGATCATAGACACCAAGTCAAGTATAGACAG[G/A]TCAGGAGTCATCGAAAATGGTTTTATTAGCTTGCTCATCCAAATGCAATATTTACTGTCACTATTTTCAGCCTAACACAACTTTTTCTTACAAGTTTAATAGAATAAATGTTTCTCTGTTGAATGAACCGTTCTGAAAGAATGATCGTCTGAATGATTGTGGCATGACAGTCTCTAAATTTGGATGACACTGTCATATTTTAATCTTACCATTTTAACAGAAACATCACCATGCTGCATTACCTGATCATGATCTTTGAAAAGAATTACCCTGACATCCTCAGTATTCAACAGGACTTGTGCAGTGTATCAGAAGCCGCCAAAGTCAAGTGAGTCATATCCAGCATTATGATGAACATGAATATTTACCAATTATTATCAGTTGTTTTTTGGTATGCTTAAGCTGTTATGTTTAGTTAGTTAGAGCCATTTTTGATTGCTGTTATTTCCAGTCTAGCTGAGCTGGAGAAAGAAGTTTCCAGCATCAGGAGTGGCCTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23183
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034563 | Nonsense | 1067 | 1092 | 30 | 30 |
Genomic Location (Zv9):
Chromosome 17 (position 49048566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48810072 |
GRCz11 | 17 | 48892701 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTGTCAGCTCTTCGCTCAGGTGAAGTCTTCGACAAGGACTCTAAACTT[A/T]AACGCAACCGCAAGCGCTCTGTAAACCAGTTGGCTGATGCCGGAGGTCGA
Long Flanking Sequence:
CACAGCGTCTTTAAGCAGACAGATACATCACTCTCGTGCACACATGAACCACGCATCCACCGCTGACAGAGAGACGTCACCAGGCAAACTTTGCATCAACCTGAACTTCTTTCTAAAAGACCAATGTGGCCTTGTATGCATGAAAAGAAAAATTGTTTCTGAAAAGGCTTCTGCCAAAAACGCAGCATCAAAACTTTTCTGAACCCTGAATCAATATCCGAATTACTTTTTCACGTTGAATGATGTTATGCAGTTCAAAACAACGATCTGAAGGAAGACACCACGGCTGAAGTATTTCTTTTAGACAGGTCTGTTAAACTATTTTAGCCACGCATGACTTATGTCTGTAAATTTGTCCATCGCAGCTCAAGGACCAGCGTGAACGAGAGAGACGAGCAAAGAAAGGCACCAAAGGCAGTGTGTCAGAGGAGGTGGGAGAGTTTGATGATCTCGTGTCAGCTCTTCGCTCAGGTGAAGTCTTCGACAAGGACTCTAAACTT[A/T]AACGCAACCGCAAGCGCTCTGTAAACCAGTTGGCTGATGCCGGAGGTCGAGAAAGATCAGTCACCAAGATGAACTATTGACCACATTGAACACAGTCAAGGAGGCCAGGCTTTTATATTCGCACACTGATGAGGAACTCTCATTAATAGGATAATACTCACTATTTACTCACCATTGGTTCCTTTACGACTTTCTTTTTTTTTTTTTTTTTTTCAAAAGAGGATATTTCAAAGCAACCATAACAATTGATCCTTCACTAAACCCCGCCCTCCTTAGTTACTGTTGCTACACCTGTCAAGCTTTCGTGCCTGGCACGTCTATTATAATGTGTATGCGCCAATGTCAGACATCGCCTGGTATATAACTAATGTTAGGTGAGGTATCAGGTGAGGTATCTGAGAAAGCCAGACAAAAAAGGACTGCAGTATGCATTGCAGGGGTATATTCACCACATAATAGGCATCCGATTGAAAATAATTTAAGAAAAATAGAAGCTAGGT
Associated Phenotype:
Not determined