Busch Lab

ZMP

NP_571531.1

Ensembl ID:
ENSDARG00000036118
Description:
catenin alpha-1 [Source:RefSeq peptide;Acc:NP_571531]
Human Orthologue:
CTNNA1
Human Description:
catenin (cadherin-associated protein), alpha 1, 102kDa [Source:HGNC Symbol;Acc:2509]
Mouse Orthologue:
Ctnna1
Mouse Description:
catenin (cadherin associated protein), alpha 1 Gene [Source:MGI Symbol;Acc:MGI:88274]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa24534 Essential Splice Site Available for shipment Available now
sa39460 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24534
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
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052441 Essential Splice Site 766 907 16 18
Genomic Location (Zv9):
Chromosome 24 (position 35883603)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 34652912
GRCz11 24 34539177
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAGCCGGATCAAGAATGGACAAGCTGGGCCGCGCCATTGCAGATCAA[G/T]TAAGTTCAACTCGAGTCCGTTTCGCAGAAAACACACACGCATCATCTTTT
Long Flanking Sequence:
CCTCTTAACGCAATGGCGCATTTGTTTAACTGATACCATTAATCGGCTACAAAGCACTCTTTCGGTTAACGGTTAATCGATTATTTTGAGCATCCCTAACACAGAGAGAACATGCAAACTCCAGTGGACTTGAACCAGCCACCTTTTTGCTGTGAGGTGTCTGTGCTAACCACTGAGCCATGGTGTCGCCCCACACATAGATGTGCAGATGTGAAATGCAAGCCTGTTTTTCCCCTTTTCTTAACCTTGTAAATACAACCAGCCATTCCTATCATTGGAATGTGTTGATATCTTGACTTGTACCATCCATGCTCACACACACTGCCACATGAGACTGCACACACAGAACAGCAACTGTGAATGAAACCGCTATCTTTTTTCCCCTTATTCCCAGGGGGAAAGGACCACTCAAAAACACCTCAGATGTGATTAGTGCTGCCAAGAAGATTGCTGAAGCCGGATCAAGAATGGACAAGCTGGGCCGCGCCATTGCAGATCAA[G/T]TAAGTTCAACTCGAGTCCGTTTCGCAGAAAACACACACGCATCATCTTTTGGTGAATTATCCATGCTCTTGTGTTTCACTTAAGCATCTTAATCCTTACCGAGCACTCCAGTGATACGCAACAGTGCATAATTTATCTCCCAGCCAACTCACATCCCTGGCTTTAGCCCAGCACCTTTCGAAATCGGTGACTGAGGCCGTGATGATAAAGACTGCAATCTGGGTCTCCAAATTCAATCTCCGCAGTCCGACGTTTGTTTTCCTGGAAAGCTCCTCTTATTCCTGAAGCTGAGTGACAATGACAGGTTCACAGGCTTTTCGTGAAAATAATATGGGAACATTTCCAGTAAACGTCAACCCGCCGTATGTGCTGCAAGGGTTCTTTCAGATTTCTCTTGTTTTCTCAATAGCGCAGTTGAAAGGGATATTGTGAGCACGGGAAGGGGGTTTTGCGGGGTAGAATCATCACCCATCACTCATCCTTCCATGAAGGCCTCTCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39460
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
ENSDART00000052441 Essential Splice Site 766 907 16 18
Genomic Location (Zv9):
Chromosome 24 (position 35883602)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 34652911
GRCz11 24 34539176
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCCGGATCAAGAATGGACAAGCTGGGCCGCGCCATTGCAGATCAAG[T/C]AAGTTCAACTCGAGTCCGTTTCGCAGAAAACACACACGCATCATCTTTTG
Long Flanking Sequence:
CTCTTAACGCAATGGCGCATTTGTTTAACTGATACCATTAATCGGCTACAAAGCACTCTTTCGGTTAACGGTTAATCGATTATTTTGAGCATCCCTAACACAGAGAGAACATGCAAACTCCAGTGGACTTGAACCAGCCACCTTTTTGCTGTGAGGTGTCTGTGCTAACCACTGAGCCATGGTGTCGCCCCACACATAGATGTGCAGATGTGAAATGCAAGCCTGTTTTTCCCCTTTTCTTAACCTTGTAAATACAACCAGCCATTCCTATCATTGGAATGTGTTGATATCTTGACTTGTACCATCCATGCTCACACACACTGCCACATGAGACTGCACACACAGAACAGCAACTGTGAATGAAACCGCTATCTTTTTTCCCCTTATTCCCAGGGGGAAAGGACCACTCAAAAACACCTCAGATGTGATTAGTGCTGCCAAGAAGATTGCTGAAGCCGGATCAAGAATGGACAAGCTGGGCCGCGCCATTGCAGATCAAG[T/C]AAGTTCAACTCGAGTCCGTTTCGCAGAAAACACACACGCATCATCTTTTGGTGAATTATCCATGCTCTTGTGTTTCACTTAAGCATCTTAATCCTTACCGAGCACTCCAGTGATACGCAACAGTGCATAATTTATCTCCCAGCCAACTCACATCCCTGGCTTTAGCCCAGCACCTTTCGAAATCGGTGACTGAGGCCGTGATGATAAAGACTGCAATCTGGGTCTCCAAATTCAATCTCCGCAGTCCGACGTTTGTTTTCCTGGAAAGCTCCTCTTATTCCTGAAGCTGAGTGACAATGACAGGTTCACAGGCTTTTCGTGAAAATAATATGGGAACATTTCCAGTAAACGTCAACCCGCCGTATGTGCTGCAAGGGTTCTTTCAGATTTCTCTTGTTTTCTCAATAGCGCAGTTGAAAGGGATATTGTGAGCACGGGAAGGGGGTTTTGCGGGGTAGAATCATCACCCATCACTCATCCTTCCATGAAGGCCTCTCCTC
Associated Phenotype:
Not determined