ZMP
ctnnd2b
Ensembl ID:
ZFIN ID:
Description:
catenin delta-2 [Source:RefSeq peptide;Acc:NP_001180580]
Human Orthologue:
CTNND2
Human Description:
catenin (cadherin-associated protein), delta 2 (neural plakophilin-related arm-repeat protein) [Sour
Mouse Orthologue:
Ctnnd2
Mouse Description:
catenin (cadherin associated protein), delta 2 Gene [Source:MGI Symbol;Acc:MGI:1195966]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6847 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19788 | Nonsense | Available for shipment | Available now |
sa32942 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6847
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 |
---|---|---|---|---|---|
ENSDART00000087270 | Nonsense | 185 | 1207 | 5 | 22 |
ENSDART00000090292 | Nonsense | 185 | 1210 | 6 | 22 |
ENSDART00000110798 | Nonsense | 185 | 794 | 6 | 14 |
ENSDART00000142500 | None | None | 268 | None | 5 |
ENSDART00000145405 | None | None | 114 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 30332945)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30634580 |
GRCz11 | 2 | 30618113 |
KASP Assay ID:
554-4420.1 (used for ordering genotyping assays)
KASP Sequence:
GCCTCTCARCCGCCTCGCAGTGGTCAGGTGGGAGGAGCCTTACATAGCTA[T/A]AATCAGGTGGGGATTCATYGCTTYGGAAAAACNCTGACACTTTTAAAGGAA
Long Flanking Sequence:
GGGACATGTCATCGGCCAGAAAAACACGTGAAATGGTTCATGTCTGAAAATAAATAGCCTATAAATTCTTTTTAGTATTTGCCGCTGTGCACATCTCTACAAAAAGAAAATCTGAATAGCCCTAAAAGGCATTCTAAAAGTGTCTAGTTACGTTAGATATCACGTCTAGTGTAAATGCTAATTAAACCATAACCAAATGTATAACTTCTATTACTTTTTTGGGTCCAGATCAAACGAAACAAGTAAAGGAATTGATGATTGTAAACACACCCTAAGAGTTCAAATCTTAGCTGATCAGTTTCAATCATGTGTTTCTTTCTCCCTAATTTCCCCTTCACAGGACCAGGCATCCTCTCTCAGAGTGCTCTGCAGCTCAATAATCAGGAGGGCACCTTTCCCTATCCAGTCAGTTACCATAGCAACCAGACCCTGGCCCTCGGCGACCTGTCGGCCTCTCAGCCGCCTCGCAGTGGTCAGGTGGGAGGAGCCTTACATAGCTA[T/A]AATCAGGTGGGGATTCATCGCTTTGGAAAAACCTGACACTTTTAAAGGAATAGTTCACCCAAAAATGAAAAATTTACACCATTAATTGACTTGCCCTTTACTTGACTTGCTATTTAAACATAGGCAATTCTTTTTCTGTAGTATAACAGATTTTTAGGTGAATTGGTTATACATATAATGCAAGTTAACACTGTGAGAGTCAAAACTTATAATAAATAAATAAACAAATACATTTATATATAAATAAAATTAATTAATAAAATTTTTGGGTGAACTATCTCTTTGAACCAGAGGTGTCAAACTCAGGTCCTGGAGGGACGCAGCCCTATACAGTTTAGTTCCAACCTTGCTCCAACATGCTTACCTGTAGGTTTCAAACCAGCCTGAAGGACTTAATTAGTTTGATCAGGTATGTTTAATTAGAGTTGGAACTAAACTGTTTAGAGCTGCATCCCTACATGAACTGAGTTTGACACCTGTGTTTTAAACCATATGAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19788
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087270 | Nonsense | 258 | 1207 | 6 | 22 |
ENSDART00000090292 | Nonsense | 258 | 1210 | 7 | 22 |
ENSDART00000110798 | Nonsense | 258 | 794 | 7 | 14 |
ENSDART00000142500 | None | None | 268 | None | 5 |
ENSDART00000145405 | None | None | 114 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 30329104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30630739 |
GRCz11 | 2 | 30614272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGAGCTCTCCCTTTTCCATGCAGGCTTTGGGCTCCCCCTCCAAACTG[C/T]AGAGGCTGGGCTCAGCCTCTGACATGCCCAGCTATGCCACTCTGGCGCGG
Long Flanking Sequence:
TCAAAAGTTATCTTATGTAGTCAGAAATTTAAGCATGGAAGACGATACAGTGTTGTGGCATCTTTGATCTATGACGATTTGTTGAGCGTTCCAAGAAGGCAGAAGCTACGATGTGTCCCCACACCTAAAAGTGTCTACCAAATGTAAATAAAAGTGACGCAATAGTTTAGCGAATTCACCCCCCCCCCTTCCCCAATTCCCCTTAAAAATATGATGTGGGTCTCCATCACTTAGCTCAAAGCTGGTAGAGTGAGTGAAATGCTAGCTCTTTACGTGTCACTTACCTCCAGGTGACGTCTAATCGTGTTGCCCAGCTGGCTGCCAGAGAGACAGCCGCCCGGGCCCATTCTCGAGACTCCTATGCCCAGAGTCATGGCAGTGCATTCCACATGCCTGACGATCAGCCAACAGTCCCTGTAAACTATTCCTGCGCCACTCTACCAGCTCAGCGAGTGAGCTCTCCCTTTTCCATGCAGGCTTTGGGCTCCCCCTCCAAACTG[C/T]AGAGGCTGGGCTCAGCCTCTGACATGCCCAGCTATGCCACTCTGGCGCGGGTGTCGTCGCCCAAGCAGTCCCCCAGCCGGCTGGCCAAATCCTACAGCACGAGCTCTCCCATCAACATGGCGGCGGGAGGAGGGTCGTCTTCTTCACCACTACACATGGCCGGAGCGGGCAATGTCTCCAACTCGTCTCCGCTGCACCAGCTCAGTGCCGCCGTAGGAAGCTACGCCACTCTGTCACCCACCAAGCGTATGCTGCACACCACCGACCAGTACAAGATCTCTCATGATTTGTACGCCAACGCCACACTTCAGAGACCGGGCAGTCTAGCAGGTCAGTACGCCTTCAAAAACACATAAGCACTGGTCATTTTCACACATCGTGCTTGTTTGATATCATCAGAATCCAACACTGTTGTTTTTAAGTGTATTTGTAGCACTTTTGTTCTGGTTAATGGTGCTTGCAAATTCTCAACGATACAGGTTCCAGGGGTTCGTACAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32942
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 |
---|---|---|---|---|---|
ENSDART00000087270 | Nonsense | 276 | 1207 | 6 | 22 |
ENSDART00000090292 | Nonsense | 276 | 1210 | 7 | 22 |
ENSDART00000110798 | Nonsense | 276 | 794 | 7 | 14 |
ENSDART00000142500 | None | None | 268 | None | 5 |
ENSDART00000145405 | None | None | 114 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 30329049)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30630684 |
GRCz11 | 2 | 30614217 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGGCTCAGCCTCTGACATGCCCAGCTATGCCACTCTGGCGCGGGTGT[C/A]GTCGCCCAAGCAGTCCCCCAGCCGGCTGGCCAAATCCTACAGCACGAGCT
Long Flanking Sequence:
TGGCATCTTTGATCTATGACGATTTGTTGAGCGTTCCAAGAAGGCAGAAGCTACGATGTGTCCCCACACCTAAAAGTGTCTACCAAATGTAAATAAAAGTGACGCAATAGTTTAGCGAATTCACCCCCCCCCCTTCCCCAATTCCCCTTAAAAATATGATGTGGGTCTCCATCACTTAGCTCAAAGCTGGTAGAGTGAGTGAAATGCTAGCTCTTTACGTGTCACTTACCTCCAGGTGACGTCTAATCGTGTTGCCCAGCTGGCTGCCAGAGAGACAGCCGCCCGGGCCCATTCTCGAGACTCCTATGCCCAGAGTCATGGCAGTGCATTCCACATGCCTGACGATCAGCCAACAGTCCCTGTAAACTATTCCTGCGCCACTCTACCAGCTCAGCGAGTGAGCTCTCCCTTTTCCATGCAGGCTTTGGGCTCCCCCTCCAAACTGCAGAGGCTGGGCTCAGCCTCTGACATGCCCAGCTATGCCACTCTGGCGCGGGTGT[C/A]GTCGCCCAAGCAGTCCCCCAGCCGGCTGGCCAAATCCTACAGCACGAGCTCTCCCATCAACATGGCGGCGGGAGGAGGGTCGTCTTCTTCACCACTACACATGGCCGGAGCGGGCAATGTCTCCAACTCGTCTCCGCTGCACCAGCTCAGTGCCGCCGTAGGAAGCTACGCCACTCTGTCACCCACCAAGCGTATGCTGCACACCACCGACCAGTACAAGATCTCTCATGATTTGTACGCCAACGCCACACTTCAGAGACCGGGCAGTCTAGCAGGTCAGTACGCCTTCAAAAACACATAAGCACTGGTCATTTTCACACATCGTGCTTGTTTGATATCATCAGAATCCAACACTGTTGTTTTTAAGTGTATTTGTAGCACTTTTGTTCTGGTTAATGGTGCTTGCAAATTCTCAACGATACAGGTTCCAGGGGTTCGTACAGCAGTCAGCACAGTCACCTGGGCTCCGAGCTCAGACCCCTGCAGTCTCCCGAGCACCA
Associated Phenotype:
Not determined