ZMP
si:ch211-254e15.1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100034581 [Source:RefSeq peptide;Acc:NP_001137526]
Human Orthologue:
CTNNAL1
Human Description:
catenin (cadherin-associated protein), alpha-like 1 [Source:HGNC Symbol;Acc:2512]
Mouse Orthologue:
Ctnnal1
Mouse Description:
catenin (cadherin associated protein), alpha-like 1 Gene [Source:MGI Symbol;Acc:MGI:1859649]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43314 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36874 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa36875 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43314
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 |
|---|---|---|---|---|---|
| ENSDART00000016057 | Nonsense | 498 | 754 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 36314296)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 35178816 |
| GRCz11 | 19 | 34765936 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAAAGAGAACCTGGATGTATTTTGTGAGGCCTGGGAGTCCCAGCTCTG[C/A]GACATGGCGATCCTATTGAAGGAGATTAATGATGTGTTTGAGGGCCGCAG
Long Flanking Sequence:
ATTAGTTGAATGAGTTTTGAGTAGCCATAACTCCTGTCATCAGTTTTACATGATGCTTCAGAAATTTTTCTAATATGATAATGAAAATTTCTTAATTTATGCAATGTTGTAAACAGTTATGCTTTTTTATGGAAACATTTATACATTTTTATAATATATTGATGAATAGAAGTTACAATATGGCATTAATATGCCTTTTGAAGCTTTTTTTTTATTGTTCTTGTTTTAGTCCTTGGAACATGTTCATGACTGAGTTCATAAGAAAATGAAATTCGCTTTGGTCACACTTTATTTTGATAGTTTGTTCGTTTTGTTTAAGTTTGTTCCTTTTTATTTTCCGGGACTTTTCAAAAGCTTGTCTAATTAAATCAAATCATGAATTTCTCAAATTTCTCCTGTCAGATCATCTCAGCGGCACAGACTCTTGCTCTGCACCCCACCAGCAAGATAGCCAAAGAGAACCTGGATGTATTTTGTGAGGCCTGGGAGTCCCAGCTCTG[C/A]GACATGGCGATCCTATTGAAGGAGATTAATGATGTGTTTGAGGGCCGCAGAGGTACGTCAATCGGGTTTAGTCATCACATTAGATTTAAGGCCAAGTTTTATGATTACAAATCCCAACACCTCCCTTTTCCAAGCCAACATATGAACTCACTTTACATCATCAATGATATGCATTTAGAATAGAACAATATATACTTTTATAATCAAAATTATTATGTTAGTCAGCAAGACATCTTGGTGCCATCAGATTGAAAACATCAGTGAACTTTTATGAATTTATTGTGTCCGATTTTGTAGAAAATATTATACCATTTTTTCTTCATAATCTGTTATTAATCAACCTCAGTCTTGATAAAATTAATAAATGTTTTTTTTTTAAATACAGGATTTTGACTCTTTAATTGCCAAGTTAATAAGTCTTTTCAGAAATTAAGTCATTTTGTGTGTGTTTTTCACCAAATCAGTGACATCATTTATAAACTTGGCAGAGTTATTAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36874
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016057 | Essential Splice Site | 528 | 754 | 12 | 19 |
| ENSDART00000016057 | Essential Splice Site | 528 | 754 | 12 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 36311583)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 35176103 |
| GRCz11 | 19 | 34763223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTTTAGGTGATAAGAAAACATATCTGTCTTTACCAAGGCCAGGGG[T/C]GAGTGTGATGAGGAACTATGATTTTATTACAAATTTGATTTACCATATTA
Long Flanking Sequence:
GGTAAATCTCTGTAGGCAAGGTTAGGGGGGGTGCATTTCGACAGTCCCACAGAGATTACAGGTCTGTGAAAAAAGCATTTGCTTATCTGTATTTGGGCTCAAGGATGTGTTTGAGTGATTTCGACTTCTCTGGGTGAAAGTGTGTTTTCTCACAGCGATGTATGAGGAGCTTTATGTGGCAGCGATATTTGTCAGTCTGAGGGAAAAGGCATCAGTAACATGACAGAAACCCGACGCCTGGGGAAATGTTTTTGTTCTAGATGAGAGGCTCTCGGTCATCAACCGTGCCAGTCCAGATCTTTCCCAGAAACCAAGTGTCATCCTCCAAGATCCTGCCTTTGTTTCTGTTCATCCTCATTATCATCTAAAGACATTTGTTTTAGGCTGGGCGAAGCAAGCTTGTAAATTGAAATGTTGTTAATATTAAGTAAAATGGTTGTCTCTCTCTTTTTTTTTTTTAGGTGATAAGAAAACATATCTGTCTTTACCAAGGCCAGGGG[T/G]GAGTGTGATGAGGAACTATGATTTTATTACAAATTTGATTTACCATATTAATTGTGTTGTTATTTTCTGATTGATCTTTTTCCTAGAAACACTCTGCTAACCTGAAGACAGTCAAGGCTGCCAAACTTGATGCTGAGGTACTCATGATAAAATGATGTGTGACAGTATATTTGAGTAATAATAATTAATACCTGTCATTTTTTAAATCATCATTGTTCTTGTTCTTAGTTGTTATTCCTTTTAAAAAAAATTATATACAGTATGTATTTGCAATATAATTGTCGTATTTGCCATTCCACAAAATCCAAAAACCAAATCACTTTCAAGATAATATCTAAAATAACCTGGACTTGACAAAACATAATCTGCAACAGAAGATTAAAGCCTCTTTTCCACTGCACACGACAATCGACAAGCGACAGACCGGAAGTCATTCATTTCCAATGGAGAGCAGTCTGGGAGCTGCGCTGAGTTTAGATCATCTCCGTATGCGGAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36875
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016057 | Essential Splice Site | 528 | 754 | 12 | 19 |
| ENSDART00000016057 | Essential Splice Site | 528 | 754 | 12 | 19 |
Genomic Location (Zv9):
Chromosome 19 (position 36311583)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 35176103 |
| GRCz11 | 19 | 34763223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTTTAGGTGATAAGAAAACATATCTGTCTTTACCAAGGCCAGGGG[T/C]GAGTGTGATGAGGAACTATGATTTTATTACAAATTTGATTTACCATATTA
Long Flanking Sequence:
GGTAAATCTCTGTAGGCAAGGTTAGGGGGGGTGCATTTCGACAGTCCCACAGAGATTACAGGTCTGTGAAAAAAGCATTTGCTTATCTGTATTTGGGCTCAAGGATGTGTTTGAGTGATTTCGACTTCTCTGGGTGAAAGTGTGTTTTCTCACAGCGATGTATGAGGAGCTTTATGTGGCAGCGATATTTGTCAGTCTGAGGGAAAAGGCATCAGTAACATGACAGAAACCCGACGCCTGGGGAAATGTTTTTGTTCTAGATGAGAGGCTCTCGGTCATCAACCGTGCCAGTCCAGATCTTTCCCAGAAACCAAGTGTCATCCTCCAAGATCCTGCCTTTGTTTCTGTTCATCCTCATTATCATCTAAAGACATTTGTTTTAGGCTGGGCGAAGCAAGCTTGTAAATTGAAATGTTGTTAATATTAAGTAAAATGGTTGTCTCTCTCTTTTTTTTTTTTAGGTGATAAGAAAACATATCTGTCTTTACCAAGGCCAGGGG[T/C]GAGTGTGATGAGGAACTATGATTTTATTACAAATTTGATTTACCATATTAATTGTGTTGTTATTTTCTGATTGATCTTTTTCCTAGAAACACTCTGCTAACCTGAAGACAGTCAAGGCTGCCAAACTTGATGCTGAGGTACTCATGATAAAATGATGTGTGACAGTATATTTGAGTAATAATAATTAATACCTGTCATTTTTTAAATCATCATTGTTCTTGTTCTTAGTTGTTATTCCTTTTAAAAAAAATTATATACAGTATGTATTTGCAATATAATTGTCGTATTTGCCATTCCACAAAATCCAAAAACCAAATCACTTTCAAGATAATATCTAAAATAACCTGGACTTGACAAAACATAATCTGCAACAGAAGATTAAAGCCTCTTTTCCACTGCACACGACAATCGACAAGCGACAGACCGGAAGTCATTCATTTCCAATGGAGAGCAGTCTGGGAGCTGCGCTGAGTTTAGATCATCTCCGTATGCGGAAAATT
Associated Phenotype:
Not determined