ZMP
si:rp71-39b20.3
Ensembl ID:
ZFIN ID:
Description:
small conductance calcium-activated potassium channel protein 1 [Source:RefSeq peptide;Acc:NP_00112
Human Orthologue:
KCNN1
Human Description:
potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1 [Source:HG
Mouse Orthologue:
Kcnn1
Mouse Description:
potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1 Gene [Sour
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19745 | Nonsense | Available for shipment | Available now |
sa11915 | Nonsense | Available for shipment | Available now |
sa12321 | Nonsense | Available for shipment | Available now |
sa13213 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19745
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033922 | Nonsense | 12 | 890 | 1 | 9 |
ENSDART00000135104 | None | None | 538 | None | 8 |
ENSDART00000147885 | None | None | 261 | None | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 23401978)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24806517 |
GRCz11 | 2 | 24462168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCGGATATTGAGGGGATGCGGCATCGGCACGCGGGAGCTGTCCACCAG[C/T]AGCACAGCAACGACGCGGACGCTCGTGACAGTCCAAAAGAAGCATCTTGT
Long Flanking Sequence:
CTGGCTAGTTTAGTCTTCCTGTAGGTACTGAATGTGCGCGTATGATATTGCTTTATTGTCTTCAACTCATCACATTACGCCATCACAAAATAAGCCATTTCTTCCAGCGGTGCACCTGTTCCGCAAGTATTTGATTTGATGCTGTTTTTATTTTTATTTTTTGTAATCGACCTGCAATGGCACAGGCTTGAAAATGTCAATCCTGCCAGGACATTGAGCTTTCGACGCGCGCATGACCTTGCTAATACCCAATTCGCATCTCAGGTTTAATCTTATCCACTGTAAACATAAAGCGGTTTTCACACGAGGGCGGCGTTCATCTCGGCGATGACGTCACGAGGCAGGTCTCGCTCGAGTCCACCAATGAGACGAGGCAGCTCGGTTCTTTTGGGGCACATCGCAATGAATGGGTGTCGGTGCTTTACAAGGCAAAGGAGCAACCACAACAAGACGCGGATATTGAGGGGATGCGGCATCGGCACGCGGGAGCTGTCCACCAG[C/T]AGCACAGCAACGACGCGGACGCTCGTGACAGTCCAAAAGAAGCATCTTGTCCAGTCGCCCCGCTCTTTAGTCTGCCGCCCCCACCGCCATCGATAAAGGAGCGATCCACCTCCTCACATAACAACCGACATGTACAGTCCTGTCCGGACCGCGGCACCAGGAACGACGAGTGCCTGCCTTTGACCGGCCACTGCAGCCTCGCGCAGGGAGCGCGCACCGACCGTCAGCCTTACGACAACCTGCCGCATCCGTTTCCAGGGGCCTCATCTGGCTATCAGTGTCATTCAGAGGGGAGCCATTCTCCTCAGCAGAGATCTTCCGTTTCCCCGCAGCCCTCCCCATCTGAACTGCTGCCGCCGCCTCTGCCTTCGCACATTTCTAATACGCGGGATACGCGCCAAAAGAGTGCTAATTACAAACAAGACATCGTACAGCGTCGCGTCGGGGAGGGGGGGCGTCGAGACCAATACCAGTTGCTGCAGCAACCTTGTTATAATCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11915
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033922 | Nonsense | 169 | 890 | 1 | 9 |
ENSDART00000135104 | None | None | 538 | None | 8 |
ENSDART00000147885 | None | None | 261 | None | 4 |
ENSDART00000033922 | Nonsense | 169 | 890 | 1 | 9 |
ENSDART00000135104 | None | None | 538 | None | 8 |
ENSDART00000147885 | None | None | 261 | None | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 23402449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24806046 |
GRCz11 | 2 | 24461697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGACATCGTACAGCGTCGCGTCGGGGAGGGGGGGCGTCGAGACCAATAC[C/T]AGTTGCTGCAGCAACCTTGTTATAATCAAYAAAGGGACCCCTCCTTTRAG
Long Flanking Sequence:
GGCATCGGCACGCGGGAGCTGTCCACCAGCAGCACAGCAACGACGCGGACGCTCGTGACAGTCCAAAAGAAGCATCTTGTCCAGTCGCCCCGCTCTTTAGTCTGCCGCCCCCACCGCCATCGATAAAGGAGCGATCCACCTCCTCACATAACAACCGACATGTACAGTCCTGTCCGGACCGCGGCACCAGGAACGACGAGTGCCTGCCTTTGACCGGCCACTGCAGCCTCGCGCAGGGAGCGCGCACCGACCGTCAGCCTTACGACAACCTGCCGCATCCGTTTCCAGGGGCCTCATCTGGCTATCAGTGTCATTCAGAGGGGAGCCATTCTCCTCAGCAGAGATCTTCCGTTTCCCCGCAGCCCTCCCCATCTGAACTGCTGCCGCCGCCTCTGCCTTCGCACATTTCTAATACGCGGGATACGCGCCAAAAGAGTGCTAATTACAAACAAGACATCGTACAGCGTCGCGTCGGGGAGGGGGGGCGTCGAGACCAATAC[C/T]AGTTGCTGCAGCAACCTTGTTATAATCAACAAAGGGACCCCTCCTTTAAGCCACTCTTGCCAAACTCTAGTCAAGGACACGTAAATGAGCGCGAGGAAGCCGAGAAGGAGAGGCAATTAATTGAGCCTCAGGCTCAGTTACTGTTGGGCAGCAGCTTGCCGATCAACTACTGCATCGGCGGATCGGGGCAAGTGTGCAGAAACAAGCAGGCGCCGCTGTTGCAGCATCAGCATCAGCAGGCTCGCGCGCAGGAGCACAGCCTCCAGCAGCAGCACAGTGACCGAGACAGCAGGTACCAGGAGGGGAAAATCGCGCTCTGTCAGCCGTATCGATGCGAGCGCGCGCTGGAGAGAAACTCGTCCGTGTCTAGTAGTGAAGCCAGCAGCCCCCCGTACGGCTCCAGCAGTCAACTGTGGCCAGAGCCCCACGACAAGGAGGAGAAGAAAAATCGGGCTGGCAAACACAAGGTATTTATGTATGGACAGCAGCACAGCTTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12321
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033922 | Nonsense | 169 | 890 | 1 | 9 |
ENSDART00000135104 | None | None | 538 | None | 8 |
ENSDART00000147885 | None | None | 261 | None | 4 |
ENSDART00000033922 | Nonsense | 169 | 890 | 1 | 9 |
ENSDART00000135104 | None | None | 538 | None | 8 |
ENSDART00000147885 | None | None | 261 | None | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 23402449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24806046 |
GRCz11 | 2 | 24461697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGACATCGTACAGCGTCGCGTCGGGGAGGGGGGGCGTCGAGACCAATAC[C/T]AGTTGCTGCAGCAACCTTGTTATAATCAAYAAAGGGACCCCTCCTTTRAG
Long Flanking Sequence:
GGCATCGGCACGCGGGAGCTGTCCACCAGCAGCACAGCAACGACGCGGACGCTCGTGACAGTCCAAAAGAAGCATCTTGTCCAGTCGCCCCGCTCTTTAGTCTGCCGCCCCCACCGCCATCGATAAAGGAGCGATCCACCTCCTCACATAACAACCGACATGTACAGTCCTGTCCGGACCGCGGCACCAGGAACGACGAGTGCCTGCCTTTGACCGGCCACTGCAGCCTCGCGCAGGGAGCGCGCACCGACCGTCAGCCTTACGACAACCTGCCGCATCCGTTTCCAGGGGCCTCATCTGGCTATCAGTGTCATTCAGAGGGGAGCCATTCTCCTCAGCAGAGATCTTCCGTTTCCCCGCAGCCCTCCCCATCTGAACTGCTGCCGCCGCCTCTGCCTTCGCACATTTCTAATACGCGGGATACGCGCCAAAAGAGTGCTAATTACAAACAAGACATCGTACAGCGTCGCGTCGGGGAGGGGGGGCGTCGAGACCAATAC[C/T]AGTTGCTGCAGCAACCTTGTTATAATCAACAAAGGGACCCCTCCTTTAAGCCACTCTTGCCAAACTCTAGTCAAGGACACGTAAATGAGCGCGAGGAAGCCGAGAAGGAGAGGCAATTAATTGAGCCTCAGGCTCAGTTACTGTTGGGCAGCAGCTTGCCGATCAACTACTGCATCGGCGGATCGGGGCAAGTGTGCAGAAACAAGCAGGCGCCGCTGTTGCAGCATCAGCATCAGCAGGCTCGCGCGCAGGAGCACAGCCTCCAGCAGCAGCACAGTGACCGAGACAGCAGGTACCAGGAGGGGAAAATCGCGCTCTGTCAGCCGTATCGATGCGAGCGCGCGCTGGAGAGAAACTCGTCCGTGTCTAGTAGTGAAGCCAGCAGCCCCCCGTACGGCTCCAGCAGTCAACTGTGGCCAGAGCCCCACGACAAGGAGGAGAAGAAAAATCGGGCTGGCAAACACAAGGTATTTATGTATGGACAGCAGCACAGCTTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13213
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033922 | Nonsense | 179 | 890 | 1 | 9 |
ENSDART00000135104 | None | None | 538 | None | 8 |
ENSDART00000147885 | None | None | 261 | None | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 23402479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24806016 |
GRCz11 | 2 | 24461667 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGGGCGTCGAGACCAATACYAGTTGCTGCAGCAACCTTGTTATAATCAA[C/T]AAAGGGACCCCTCCTTTRAGCCACTCTTGCCAAACTCTAGTCAAGGACAC
Long Flanking Sequence:
AGCACAGCAACGACGCGGACGCTCGTGACAGTCCAAAAGAAGCATCTTGTCCAGTCGCCCCGCTCTTTAGTCTGCCGCCCCCACCGCCATCGATAAAGGAGCGATCCACCTCCTCACATAACAACCGACATGTACAGTCCTGTCCGGACCGCGGCACCAGGAACGACGAGTGCCTGCCTTTGACCGGCCACTGCAGCCTCGCGCAGGGAGCGCGCACCGACCGTCAGCCTTACGACAACCTGCCGCATCCGTTTCCAGGGGCCTCATCTGGCTATCAGTGTCATTCAGAGGGGAGCCATTCTCCTCAGCAGAGATCTTCCGTTTCCCCGCAGCCCTCCCCATCTGAACTGCTGCCGCCGCCTCTGCCTTCGCACATTTCTAATACGCGGGATACGCGCCAAAAGAGTGCTAATTACAAACAAGACATCGTACAGCGTCGCGTCGGGGAGGGGGGGCGTCGAGACCAATACCAGTTGCTGCAGCAACCTTGTTATAATCAA[C/T]AAAGGGACCCCTCCTTTAAGCCACTCTTGCCAAACTCTAGTCAAGGACACGTAAATGAGCGCGAGGAAGCCGAGAAGGAGAGGCAATTAATTGAGCCTCAGGCTCAGTTACTGTTGGGCAGCAGCTTGCCGATCAACTACTGCATCGGCGGATCGGGGCAAGTGTGCAGAAACAAGCAGGCGCCGCTGTTGCAGCATCAGCATCAGCAGGCTCGCGCGCAGGAGCACAGCCTCCAGCAGCAGCACAGTGACCGAGACAGCAGGTACCAGGAGGGGAAAATCGCGCTCTGTCAGCCGTATCGATGCGAGCGCGCGCTGGAGAGAAACTCGTCCGTGTCTAGTAGTGAAGCCAGCAGCCCCCCGTACGGCTCCAGCAGTCAACTGTGGCCAGAGCCCCACGACAAGGAGGAGAAGAAAAATCGGGCTGGCAAACACAAGGTATTTATGTATGGACAGCAGCACAGCTTTCAAATGTCACTCAAATGTATAGAATGCGCTGCG
Associated Phenotype:
Not determined