Busch Lab

ZMP

ctnnbl1

Ensembl ID:
ENSDARG00000011958
ZFIN ID:
ZDB-GENE-040426-1850
Description:
beta-catenin-like protein 1 [Source:RefSeq peptide;Acc:NP_957160]
Human Orthologue:
CTNNBL1
Human Description:
catenin, beta like 1 [Source:HGNC Symbol;Acc:15879]
Mouse Orthologue:
Ctnnbl1
Mouse Description:
catenin, beta like 1 Gene [Source:MGI Symbol;Acc:MGI:1913892]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa17860 Essential Splice Site Available for shipment Available now
sa39952 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33055 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17860
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015535 Essential Splice Site 220 563 6 16
Genomic Location (Zv9):
Chromosome 2 (position 54318983)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 54279813
GRCz11 2 53731802
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGACGAGACTGTGAAGGAGGAAGCTGATGGAGTTTACAACACTTTAGG[T/A]AAGACAGAAMKACACTCCAGCCAGCKAATTAATGCACAKGTCAATCTGAT
Long Flanking Sequence:
AAATAAATAAAATAAATAAATAAAGCGCATCAAGTATAAAAGCCTTATCCGTTTTGTGAGGTGCGCGATGTGGTGCCAGACGAAAGTATAAATCCAGCTTTACAGTATTACAGGTCAGACATAAAATCATACATAAGACAACATGGTCATCATTGTATAAAAATTAAAAATATGAATATAATATGTAACAATATCTTTGTTTTAATAGTAAGTAAATAATATAATCCTACGATGTGACTATTGCAGATATTGATGCTCAAACAATCTATTGTGCGGCCCTGCCATGAACTATTTTTATTATTAAACTTTGAACTTTTCTGTTACATTTATGGGTGACGGTCTTGGGATGTATTTAATTCATCATTAGCTTGAATAAATAGTTTTGATGTGTGTGTTTTTATTCAGTTGGAGGGTCAGGTCGTGGCTCTCATGGTGCAGAATATGGAGCGTTTGGACGAGACTGTGAAGGAGGAAGCTGATGGAGTTTACAACACTTTAGG[T/A]AAGACAGAAAGACACTCCAGCCAGCTAATTAATGCACATGTCAATCTGATTGGCTGATGGTGGGTTTGTGTAAGTTCGCTAAGAAACAAAGAGCTGTTTATACGTGCAGTTCTGTGCTTTTTAATTTTATTCAGTGTTTGTTTCTTGCTGTTTGGAAACTAGTTAATTATTAAAATGCCATTAATAATTGGCTAAATAAATAAATTCTAAAAACAAATTGTGAAAAACAAAGTGATTGATTTTAATTATTTTAAAAAATAATTAATAAACTTCTAAATAAATAAATGCATTTAATTCATGCACAGAAAAGATCAGTAATATAATTAAATGCAAATAATATATAATATAAAATAAATATTAATTTGTATTTTATATAATATTTATCATTAATAAGTAATTTAAAAATGTCATTTAAAAAAACGTATATTTATTTATTTTTTTTATTATCACTGCCTAAGTATTATCTCAAGCGCACTTCATGCCATCAAACTTTTATTCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39952
Status:
Mutation detected in F1 DNA
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
ENSDART00000015535 Essential Splice Site 344 563 10 16
Genomic Location (Zv9):
Chromosome 2 (position 54335926)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 54296756
GRCz11 2 53748745
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGTTTCCTCAGGGGGGAGGGGCTTCAGCTCATGAACCTCATGCTCAGG[T/C]AAAACTGATTTTCTTTCTTGCTGAAATTCAGGATCTGTGTCTTTATTTCT
Long Flanking Sequence:
CATTCCCTCCTTCCTTTATTTTTCTGTCATTCTGTTTTTGTCTTACTTTTTATCTGTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTCCCTCCTTTCTCTTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTTTTTCTTTCTTTTTTTCTTTCTTTCTTCCCTCCTTTCTCTTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTTTCTTTCTTTCTTCCTTCCTTCCTTCCTTTCTTTGATTGCTCCAGACTCATCCATCATCTTTTTCTCCTCCAGGTGTTTAAGCGTCATAATCCTTCCACAGCAGAGGAACAGGAAATGATGGAGAACCTGTTTGATGCTCTCTGTTCCTGCCTGATGCTTCCAGCCAATCGGGATCGTTTCCTCAGGGGGGAGGGGCTTCAGCTCATGAACCTCATGCTCAGG[T/C]AAAACTGATTTTCTTTCTTGCTGAAATTCAGGATCTGTGTCTTTATTTCTTTAATTATTTATTATTATTATTATTATTATTATTATTAATAATAATGCTATGATTATTATCATATTTAATAATTTTATATTTATAATTCATGTTCCCCGGCCACTCCCCCCCTCTCTCTGTGTGTCTCTGCTGCTCCATTTTTCTTTCTTCTGCTCTTGACATCTGCAGTATTTTCCTGCAGTGTAGATAAACTGTAGTTTGTCATTGGCAGATGAAGGAAGTGGCAGTGTGACGGACAGCTACATTTCCCTTGAGCGAGGCCATGATAGTCAGTTTGCGTCTGTACCGTCCGCTCTCGTCAAGCTGTTTCCAGCATCCAACATGCTGTTTCCTGTCTTTTATACACGTGAAGCACATATGTGAAAATGAATATGTTAAAAAAGTAGACTCCAGAGAAAAGGCTTTGTAAAAAACATTAATGTTCTCCTTTTAAACATGTGAAAATATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33055
Status:
Mutation detected in F1 DNA
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
ENSDART00000015535 Nonsense 422 563 12 16
Genomic Location (Zv9):
Chromosome 2 (position 54368798)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 54329628
GRCz11 2 53781617
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACGTGTGCTCCATCATCGCCTCCATGCTGAGGAACCTGAAAGGGCAG[C/T]AGAGAAGTCGACTGCTCAGCAAATTCACAGAGAACGACTGCGAGAAGGTA
Long Flanking Sequence:
GTTGGGGGGATGAAGCTGAGTTTCAGCATACTCAGATGCAAATGCAGCAGGAACTGGTTTTTCCCGCATACCCCCCTGGTGGGTTGTGGAGTCCATTGGCCCTGTTTTCAGCTCATGTTTTGAATTGTCAAAGACATCAAAAATATTGGTAATATTTCAATTCTTACAACATTGAGTCACAAAGTGCTTTACAATAAGAGAAAACAAGTAAAAGAAAACATATAAATAAAAGAAAACAGGTTAAAAGCTCATCATAAATCATCAGCATTGACTCTGACGGCTACAAGAGAAAGGTTTCCACTTGTTTTTAATCAGCAGGTGATTGTGTGTGTGTGTGCCGAGGATTCTCTTAAGGCTTTGTTGTATTTGTGTTCTGGGCATCACGTTCGTCTCAGTGGTTTACCGCGGTTAATAAGCACATTTTAAGTGTGGTGTTGTGTTTTTCTGCAGAACACGTGTGCTCCATCATCGCCTCCATGCTGAGGAACCTGAAAGGGCAG[C/T]AGAGAAGTCGACTGCTCAGCAAATTCACAGAGAACGACTGCGAGAAGGTAAAAATAAGACGGCTGACGCTTGGCCTTTATTATCATCTACTGCTGCTGCTAAAAACGGCAAACGAGTGACGACAAAACGGCTTTAATGCAGAGCTAATGCTGCCATCAGGAGAATGCACTGCAGACTTCTGCTCTACAGCCTGCTCTCTGACTTTACCACCTATAAATACATATATTTTAGAGGAACAATGTGGCTGATTTAGTTGTAGATGTCACTTAAATGTGTTTGCTAGGAATTATTATTTACATCTGAACAAATAGCAGGGCTCAACAATAAGGACTGCCCGGTGGCCCGGGGCCAGCGTGTGAGATGCTCGAGACAGTAGACAGGATCGTTACTGGCCCGATCGGACCAGTGATGCCTTGTCACTAAAGTTTAATTTGCCTGTGACTTTTTGTCAATTGCGTGCAAATAGTCTTAGAATTGAGAAACAGTGTTTTCAAGCCTTC
Associated Phenotype:
Not determined