B1WB97_DANRE

Ensembl ID:
ENSDARG00000078233
Description:
LOC556726 protein [Source:UniProtKB/TrEMBL;Acc:B1WB97]
Human Orthologue:
CTNND1
Human Description:
catenin (cadherin-associated protein), delta 1 [Source:HGNC Symbol;Acc:2515]
Mouse Orthologue:
Ctnnd1
Mouse Description:
catenin (cadherin associated protein), delta 1 Gene [Source:MGI Symbol;Acc:MGI:105100]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa31222 Nonsense Mutation detected in F1 DNA During 2016
sa14184 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa31222
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000106048 Nonsense 390 904 7 18
Genomic Location (Zv9):
Chromosome 1 (position 44641742)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 43507767
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATGCATTTGATGCCCCGTCTCTGTGTTTGCAGGTGAAGTCAGAAGTTAGA[C/T]GACTGAAGGGAATCCCTGCCCTGGTGTCCATGCTGGATAACCCAAAGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14184
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000106048 Nonsense 877 904 17 18
Genomic Location (Zv9):
Chromosome 1 (position 44627448)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 43522061
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TAATGCGATGGCTGTGCTAATTCTAATGTGTGTGTGGTGGCAGACGCTTA[T/A]TCAACAATAGACCAGCGAGGACGKAGAAACACTTTAGATGACACTCTGGA
Associated Phenotype:
Not determined

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