Busch Lab

ZMP

cnn3b

Ensembl ID:
ENSDARG00000029856
ZFIN ID:
ZDB-GENE-050522-263
Description:
calponin 3, acidic b [Source:RefSeq peptide;Acc:NP_001019244]
Human Orthologue:
CNN3
Human Description:
calponin 3, acidic [Source:HGNC Symbol;Acc:2157]
Mouse Orthologue:
Cnn3
Mouse Description:
calponin 3, acidic Gene [Source:MGI Symbol;Acc:MGI:1919244]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa8801 Nonsense Mutation detected in F1 DNA Not yet available
sa18722 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa8801
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
ENSDART00000058484 Nonsense 266 331 7 7
ENSDART00000145893 Nonsense 225 290 6 6
ENSDART00000058484 Nonsense 266 331 7 7
ENSDART00000145893 Nonsense 225 290 6 6
Genomic Location (Zv9):
Chromosome 2 (position 14894973)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15405800
GRCz11 2 15074390
KASP Assay ID:
2259-1739.1 (used for ordering genotyping assays)
KASP Sequence:
YCAACAAAGTGGCCTCTCAAAAGGGCATGAGCGTGTACGGGCTGGGCAGA[C/T]AGGTGTATGACCCCAAATACTGCTCCTCACCCACTGAGCCCACTATCCAC
Long Flanking Sequence:
TGAATGCTCAAATAACGTAGCGTAGTTTACAGCAAGCATCACGTGTGTAGTGAGATTGTGTCGTCTGTCATATACAATAGGTCTGTTATTTTTACTAAAGACGATACATCATTTGAGTTTTTGATTAGCAGATATAGAAACTACATGTGAAACAAAATCGGATCTGTATTGGTCAACTGTATTGAGCTTGGTTCCAAAAAATGGCAGCGGTGCATCCGTATTGAGTATTCTGGCATGTGAACACAATCCAGTGGGGAAAGAGACCATGAACAAACACTGTTTTGGGTCTGTCAATCAAACTAAGTGTGAAGCACTCCTCGTTAACTATCTATTCACCTTTTCTTCTCCCTCAGGCTGGCATGTCAGCACCCGGCACCAGAAGAGACATTTTCGACCAGAAAGTGGCCGTTCAGCCTTTGGACAACTCCACCATCTCTCTTCAGATGGGCACCAACAAAGTGGCCTCTCAAAAGGGCATGAGCGTGTACGGGCTGGGCAGA[C/T]AGGTGTATGACCCCAAATACTGCTCCTCACCCACTGAGCCCACTATCCACAGCAACGGCAGTCAGGGCACTGGCACCAACGGCTCCGAGATCAGCGACAGCGACTACCAGGCTGAATACCACGGCGAATATCAGGACGAATACCAGGCAGACTACCATGATGAATACAGAGGCCAATATGACCATGGCATTGACTATTAAACCACAAGATCGTGGCGCAAATGAATATTTTTGGGATCCTGGCTTCAACAGAGCAAGGTTGTTGTTGTTTATTTTTCCTCGTTGGCCTTTTTTATATGACAAGAAACAGATGTTAAGAGGAGTTTCCTCTGTTGATTATACAGTATTTTAATAGGCAGATAGATGATTAGATTTTAGCTTGGGCTTAAAATATTGGTCCTATTTTAAATTTCGAGACTGATTTGGAGACATTTGTGAAATTTTAAACATAATTGTTTGGTAAGATTATATTGGATACCAGACTCTGGCTTGGTTTTGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18722
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
ENSDART00000058484 Nonsense 266 331 7 7
ENSDART00000145893 Nonsense 225 290 6 6
ENSDART00000058484 Nonsense 266 331 7 7
ENSDART00000145893 Nonsense 225 290 6 6
Genomic Location (Zv9):
Chromosome 2 (position 14894973)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 15405800
GRCz11 2 15074390
KASP Assay ID:
2259-1739.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAACAAAGTGGCCTCTCAAAAGGGCATGAGCGTGTACGGGCTGGGCAGA[C/T]AGGTGTATGACCCCAAATACTGCTCCTCACCCACTGAGCCCACTATCCAC
Long Flanking Sequence:
TGAATGCTCAAATAACGTAGCGTAGTTTACAGCAAGCATCACGTGTGTAGTGAGATTGTGTCGTCTGTCATATACAATAGGTCTGTTATTTTTACTAAAGACGATACATCATTTGAGTTTTTGATTAGCAGATATAGAAACTACATGTGAAACAAAATCGGATCTGTATTGGTCAACTGTATTGAGCTTGGTTCCAAAAAATGGCAGCGGTGCATCCGTATTGAGTATTCTGGCATGTGAACACAATCCAGTGGGGAAAGAGACCATGAACAAACACTGTTTTGGGTCTGTCAATCAAACTAAGTGTGAAGCACTCCTCGTTAACTATCTATTCACCTTTTCTTCTCCCTCAGGCTGGCATGTCAGCACCCGGCACCAGAAGAGACATTTTCGACCAGAAAGTGGCCGTTCAGCCTTTGGACAACTCCACCATCTCTCTTCAGATGGGCACCAACAAAGTGGCCTCTCAAAAGGGCATGAGCGTGTACGGGCTGGGCAGA[C/T]AGGTGTATGACCCCAAATACTGCTCCTCACCCACTGAGCCCACTATCCACAGCAACGGCAGTCAGGGCACTGGCACCAACGGCTCCGAGATCAGCGACAGCGACTACCAGGCTGAATACCACGGCGAATATCAGGACGAATACCAGGCAGACTACCATGATGAATACAGAGGCCAATATGACCATGGCATTGACTATTAAACCACAAGATCGTGGCGCAAATGAATATTTTTGGGATCCTGGCTTCAACAGAGCAAGGTTGTTGTTGTTTATTTTTCCTCGTTGGCCTTTTTTATATGACAAGAAACAGATGTTAAGAGGAGTTTCCTCTGTTGATTATACAGTATTTTAATAGGCAGATAGATGATTAGATTTTAGCTTGGGCTTAAAATATTGGTCCTATTTTAAATTTCGAGACTGATTTGGAGACATTTGTGAAATTTTAAACATAATTGTTTGGTAAGATTATATTGGATACCAGACTCTGGCTTGGTTTTGAGC
Associated Phenotype:
Not determined