Busch Lab

ZMP

si:dkey-45h18.1

Ensembl ID:
ENSDARG00000019753
ZFIN ID:
ZDB-GENE-100921-56
Human Orthologue:
KCNN3
Human Description:
potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3 [Source:HG
Mouse Orthologue:
Kcnn3
Mouse Description:
potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3 Gene [Sour

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa42716 Nonsense Mutation detected in F1 DNA Not yet available
sa39099 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36115 Nonsense Mutation detected in F1 DNA Not yet available
sa22833 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa42716
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
ENSDART00000103211 Nonsense 208 771 1 9
ENSDART00000131627 Nonsense 208 771 2 10
Genomic Location (Zv9):
Chromosome 16 (position 25839955)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 23685630
GRCz11 16 23600662
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCAAAGAGGGTGGTGCGAGCACAAGCCAGGTGACCGCGGCCTCCTCT[C/T]AGCACAGCCAGCCCCAACCCCAGAACCCCCCAGAGATCGTTATCTCCTCG
Long Flanking Sequence:
CCAACCACTCGAATCACACGGGAGGGAACAGCAGCCTGGAGCGTCTCAATGGCACTCCATCGCCCACCACGCCAAACCTTCCCCCAGCGTCACTGCCCAAGTTGCCCCTGTCCACAACACCCCAGCTTTCCACACCAATCCCCAACGCTCTTCACCCGACCAGTACGCCACTCTCCTCCTGCTTGGGAAGCCAACACAGCTTAAGCGGGGAGACTTCACCCGTCTACAATGCTCTGTTTTACTCTTCTCATTCACCTTCCACTGAGCGGGAACGGGAGCGAGAGAGGGGATGTAAGCACAGGCAGGCCAGTCCCCTGGTGCACAGGCGGGACAGTAATCCTTTTACAGAGATCGCCATGAGCTCGTGCAAGTACAGCGGTGGTGTGATGAAGCCACTTAGCCGCCTTAGCGCCTCCCGCCGGAATCTCATCGAGTCCGACAGCGGAAGTGACACCAAAGAGGGTGGTGCGAGCACAAGCCAGGTGACCGCGGCCTCCTCT[C/T]AGCACAGCCAGCCCCAACCCCAGAACCCCCCAGAGATCGTTATCTCCTCGAAAGAGGATCCGCCTTATGGACATGCTTACGAACTTGAGGCCTCAGCCAATCAAATGTCCATCTACCACCAGAACCACGCCCTCTCTGAGAGCAGGAGTGTGCTCGGTGGGGCGGCAGGGGGCGGGACTAATGGAAGGAGGGGCGGTGCTGCGGGAGGGCCTGGAAGGACCGCTTCTAAAGCTCCTAAACGTAAGAATCAGAACATTGGCTACAAACTAGGCCACAGGAGGGCACTGTTCGAAAAGAGGAAGAGACTTAGTGACTATGCCCTCATATTCGGCATGTTTGGCATTGTTGTCATGGTGATTGAGACCGAGCTGTCCTGGGGTGTCTACAGTAAGGTGAGGACTTTGTGTACAGGGGACTGAATGGTTGGGCACGAGGACACATCCGGCTGGTCCTGCTCTGTGTGTATGAAATTGAATGAGAGTATGTGCATGTTTCGGATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39099
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103211 Essential Splice Site 510 771 4 9
ENSDART00000131627 Essential Splice Site 510 771 5 10
Genomic Location (Zv9):
Chromosome 16 (position 25916406)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 23762081
GRCz11 16 23677113
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATCTCCCTGTGGATCATCGCTGCCTGGACCGTACGAGTGTGTGAGAGG[T/G]AAGAAAGAGAAAACGAATGAACAAATGAATCATTGTGTTTGGAGCTGCGC
Long Flanking Sequence:
TTTATAGCAAGTGGAATAATTGGCTAAAAAGTTGTGAAACTGTACATTTTTGCTGTCAATTCAGTTAGTAACTACCCATAAGGATTTTTCTTGCTATGATTTATTGTTATTTCTACACATTACTAAATTCATCCATGACATCCATTTATTTATTTGAACTGTTTGTATTTGTTTTTAGCAAAGGAGGCTCTTTTTCCATGTAGCATTTAAGTGCATTTTCTTGTCAATGAAGTATTACTGGACCATTTTAAAGCTTTTAAAGATAAGACTCATTAGAGCTTCTCTTATCCATCAGTAAAAGCACTAAAAAAAATCTTTTATGATGATGAAATCCGGTCTGAAAGGAATCACACGGCTGCTTGTTTTCCTCTTTTCAGGTGCACTTTAACACACGCTTTGTGATGAAGACCCTGATGACCATATGCCCGGGCACGGTGCTGCTAGTCTTCAGTATCTCCCTGTGGATCATCGCTGCCTGGACCGTACGAGTGTGTGAGAGG[T/G]AAGAAAGAGAAAACGAATGAACAAATGAATCATTGTGTTTGGAGCTGCGCCGTGCTGTCTAGACGCTGTCAAGTTTCTTATGCTTAATGAGGACTCACCTGAATCCCCACCAATAAGTGACAGAAGCTGGATGAAAACACGCCGCCTGAGGTGTGCAAACGCTCGCTCTACACGTCCGGGAGGCGCAGAGACCAGAGAGAAAGAGAGAGCTGGAAAGAGAGAGCACTTTCATTCACACCCTTGTCTATCTAACATCGTTCCTCCTTTTCTAGGCACACATTCAGGCATCACTACGTGTATTAACAGATTTCCCATGTTGCATCCTAAAAGGGGTCGATGGGATAAACTAGTGGGTGTTTCCCACTCTTCCAGGCACGTTGTCATGGTTACAAATTCTGGATGCGTGTTAGACGCTGTATAATATTGAGGGTTCCCCATGGCAAGGATTTAAGGTTTGATTATTGTTTTGATAGCGGCAGGCTGGAGCAGTGAGTTTTGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36115
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103211 Nonsense 626 771 7 9
ENSDART00000131627 Nonsense 626 771 8 10
Genomic Location (Zv9):
Chromosome 16 (position 25946325)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 23792000
GRCz11 16 23707032
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACAAGCACACCAAGCTGATGAAGAAAATCGACCACTCCCGTGTGCGC[A/T]AACATCAGAGGAAGTTCCTTCAAGCCATTCACCAGTGAGAGAAACAAACA
Long Flanking Sequence:
ATTAACTGAGCTTTCTCATATGGTATAGATATGGCATACAAAGCTCTGATTATCTGTTCACCATTCTATTGTCTGAGATGGTGAAAGAGCTTCTTTCTTCTTTTGTCCTTTAAAACTTTATCACAAAGGCATAAAAGTATTTTGTAGCAGCTCTGCAGTTGACCCTTTCTTATTGCACATCACTGGTCTGAGGCCAGAATTCTGAATTGATCAGATGACAGAATTATAGGCTGCAAAGTCTGTTGTCAGGTCATTCTGGAAAAACTCCCAAGAGAACCTTTCATTTGGCAGAAGCTTATAGGCTTGTGTGCGTGTATTGGCAAAGCAGAGCTTATACTTGTGATTACTCTCTCCTAAGGTGCTTTTCCTGTTGTTAATATTGTTGTTATGGTGACTTGTCCCCTCAGATAAAGAACGCAGCAGCGAATGTTCTCAGAGAGACTTGGCTGATTTACAAGCACACCAAGCTGATGAAGAAAATCGACCACTCCCGTGTGCGC[A/T]AACATCAGAGGAAGTTCCTTCAAGCCATTCACCAGTGAGAGAAACAAACACACATCTGTACACAGCAAATTCACTCAAATCCTCATCTACACACTTTAGAAAATCACTTGGAAAAATGAACAGCCAAAGTGCTAAGTGAGCTTTAGCGATGTAAGCTAAAACCGCACAAAGAGCATTTGAAGTGCTTCACATTTGGGCTGAGTGGCTAGTTGTGCGCTAAGTGTGATTGGGGTAGTTAGGATGTCTGACCTGGCCACAGAGACAATACCTAAGAGGAACCATGACAAATGCATCAACAGGCAGCAGCTTTTATTGACAACATTTAACTGTTTCTCAAGCTTTTTATATGCTCAAGTACTGTATGCCGATGCTCAGGTTTCTTTCTTGTGTTTGTTAGGTCACTTCTTGAACTGTGAAACTTAAACTTGAGGTTTATGATATAATTCAGTTTGCAACATCCAAATACAATTTACTTTTTTTTTTTGTTGGGACTTATATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22833
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103211 Nonsense 655 771 8 9
ENSDART00000131627 Nonsense 655 771 9 10
Genomic Location (Zv9):
Chromosome 16 (position 25949259)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 23794934
GRCz11 16 23709966
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGAAGCGTAAAAATGGAGCAGAGAAAACTCAGTGATCAAGCCAATACAT[T/A]GGTGGACTTATCAAAGGTAAGACTATTGTACATGTACACAAATCACAGAC
Long Flanking Sequence:
GAGAACATCTTATTTTTTTTCCAACTGTCATTATGCATGTAGTTCCCCTGTTAGCTCAGTAAGTCTGATGCGAATGCTACACACTCCTGCTGTGTGGGTGCCCATAACACACATACTCATCATTTGAAGAACTCTAATCCTTCTGTCACTGTTTTGTCAAGGCCTGTCCTCCAATTTAAAGGGTTCCTTTCAAAACCAAAGCCTTTCTTTTAAAGAAATCCCACACTTATGAAATCCTTTTAAGTCTGATGCTTTTAGGATTTACGCCGTAATTGCATATTCATCTTGGGGGATTCTCATCAACCGCAAACAAATAAAGAAAACAAGCTGATTAAGTTAATTAGCTAGTTGAGGTTTACAATTGAGGGCTAGAGAGCTTAGAAGGAGGTCTAATGGGTTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTCCCTGTTTTTGTAGATTGCGAAGCGTAAAAATGGAGCAGAGAAAACTCAGTGATCAAGCCAATACAT[T/A]GGTGGACTTATCAAAGGTAAGACTATTGTACATGTACACAAATCACAGACATGGTCGCACATCAGAGCCCACACATATGCACGTTACATCGGTTAGGAAATAGTTGACACCCACACACACTTTCAATGACATTGTGTTCCCTTTCCTGCAATTTTATCATGCCCACATACACATACACACTCTTTATAATGCCCAAGGCTGCAAGTATGTCGATGGCAGCACATAATGCCTGGTGACACACACACACACATACCTTTGCTTTCCCAAATATATCTCAGCATTCAACTGTTTCCATGCTGACCCGTTTGTTTCTGTGGCTTTGTGTCTCCTAGCAACCTGAACAAGTGTTAAAGCAGGGATGACAGTGGGAGCGAGGAGAGGGTGGGAGGGGAGAGAGACAGGAAGCTGAAGAATGATTGAAAATGTGTGCAATTCAAGAGATTTTCTTCTGATGGCTGAGTGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTCTGGTCATT
Associated Phenotype:
Not determined