ZMP
CTNNB1
Ensembl ID:
Description:
catenin (cadherin-associated protein), beta 1, 88kDa [Source:HGNC Symbol;Acc:2514]
Human Orthologue:
CTNNB1
Human Description:
catenin (cadherin-associated protein), beta 1, 88kDa [Source:HGNC Symbol;Acc:2514]
Mouse Orthologues:
AC165274.1, Ctnnb1
Mouse Description:
catenin (cadherin associated protein), beta 1 Gene [Source:MGI Symbol;Acc:MGI:88276]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43353 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23605 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43353
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081675 | Nonsense | 77 | 742 | 2 | 17 |
ENSDART00000123771 | Nonsense | 77 | 741 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 19 (position 49732440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 48336525 |
GRCz11 | 19 | 47986984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGCTGTACGAGTGGGAGCAGGGCTTCAGCCAGCCCTTCACACCTGAG[C/T]AGGTGGCAGGTACGCCAATGCCTTCGCCACAGCACACTGACTATAATACA
Long Flanking Sequence:
AGTCTCTAAAAGTGACAGTTCTCATCTAGAAGATGTAAACAAATGTTTGCGGTTTGTCTCTTACGCTTAAATCAATGATTTATGTTGTCTCATTTGCCTTTAATTCGATGCGCTTGTTTAACCAATCACTAGCAGAGCTGTGATAAACTAAACCCTATTGGTGGTTTTTCAAGAACAGGGCAGGACGTACTGTAGCTCCGCCCCTTTATTCAGTTGAGAAACATTGAATAATGCATGTTTCAGAGCACTTGGCGGGATCTTTAATGTTCTGTGTGTGTGCTGCAGCTGACCTGATGGAGCTGGACATGGCCATGGAGCAGGACCGTAAGGCTGCAGTGAGCCACTGGCAGCAGCAGTCCTACCTGGATTCAGGGATTCACTCGGGCGCCACCACCACTGCGCCCTCGCTCTCAGGCAAAGGAAACCCAGAGGAAGAGGATCTGGACAACCAGGTGCTGTACGAGTGGGAGCAGGGCTTCAGCCAGCCCTTCACACCTGAG[C/T]AGGTGGCAGGTACGCCAATGCCTTCGCCACAGCACACTGACTATAATACATATGGAGTATACGTTTATTAACCACAGCAGAACTTATCCTTTTCATATATGTTTGACCTTTTTTTATGTACATTATAATACTATATAATAACTAATGTTTAATTACCAGCAACATTTCAGAAACTATTATAAATGTTTGCTAGACGTTTCCTAACCTGTCTGTTTATTCATGTTAATTGATGAACATTAATTGAGATAAATGTCTCTTGTTTGTTATTACATTCGATGATTTGAGTCGCGTGTTTCTTATTTCGTGCTTCCTGAAAATACACCATGCGTCCTTAACAGGTGTGAACATTTCAGTGCAATAAGAGTTTAGCCATTGAGATGGCATTTAAAATGGTTTGTGACCTGATGAGTGCACTGACTAGTAAACAATAGAGCTGATTGACACTGTAGTCCTTTATTTCTCCTTCCTGTCTGGATAATCACTCTTCCTCCTGTAGATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23605
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081675 | Essential Splice Site | 713 | 742 | 16 | 17 |
ENSDART00000123771 | Essential Splice Site | 712 | 741 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 19 (position 49722938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 48327023 |
GRCz11 | 19 | 47978261 |
KASP Assay ID:
2261-3759.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCTGGATATCGGTGCTCCAGGAGAGACACTCGCATACAGAGCAGACGG[T/C]ACCTCATTACATCAATACATTACCGCTGTATAGAGATATTATACATCACT
Long Flanking Sequence:
GATTTATGTGCAGGTTTTGTTGAAATATTCGGGATATTTGATGTTGTTGTTTATTTTTGTATTGAGATTGAGAACCTGCGCATCAGCATGTCTCTAACAAACAGCCTTTTTATTCAATATAATAAGAGCAGAGTTTTACACTGCTTACAGGAGGAGATATTCGGTGCACGGTGTGTGTTTAACTCCTGAATGTAAATGCACAGTAGTTTTGTCTGACTTCTGCTGTTCATCTCTGCAGCCACATACGCCGCAGCCGTGCTCTTCCGCATGTCTGAGGACAAACCACAGGACTATAAGAAGCGTCTGTCAGTGGAGCTCACCAGCTCACTCTTCAGAACCGAGCCCATGGCCTGGAATGAGGTACAGAGAGACCGATATTACCACATGATGATCTGAACACTGATTATAGCTGACACTGAGTCTCCTCTTCTGTCTCAGACTGCTGATCTAGGTCTGGATATCGGTGCTCCAGGAGAGACACTCGCATACAGAGCAGACGG[T/C]ACCTCATTACATCAATACATTACCGCTGTATAGAGATATTATACATCACTGCAATATAGCAGATGTTGTGCATTACAGAGCTTTAGAGGATATTAATATGGCTATATTGAGGATATGTTTATATTAGGGCTCCATAGAGGATATATGTATATTACTGCTGCAGAGTGGACATCACTGTTATACTGTTGCATGACATTTCCACATCATCCAGACTGGAAAAACCTGAAGGCAGTTAGAATTAATACATTTAATTGGCCTTACTTTAGATTAAGTGGCTCTAATTACTGTGTGCTATAATGTTTAATCATTAAGTACAGTGTGTTTATGCATGGTTTCTGAAAAAGTATAAAAATCATCTGCATGCATCTGTATTATCAGTATTTTGTAGTTTATAATTAACCCGGCCCGTTCCCCACATCCAGAGCAGCGGCAGTGTTGAGCAATACAAGCAAGTGCTTCATGTGCTCGTGTTTATATAAAGGCAGCTTAATATAAAGAGG
Associated Phenotype:
Not determined