Busch Lab

ZMP

accn2b

Ensembl ID:
ENSDARG00000008329
ZFIN ID:
ZDB-GENE-040513-2
Description:
Amiloride-sensitive cation channel 2-B, neuronal [Source:UniProtKB/Swiss-Prot;Acc:Q708S7]
Human Orthologue:
ACCN2
Human Description:
amiloride-sensitive cation channel 2, neuronal [Source:HGNC Symbol;Acc:100]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa21190 Nonsense Available for shipment Available now
sa14670 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21190
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004588 Nonsense 9 501 2 11
ENSDART00000105541 Nonsense 9 501 1 10
Genomic Location (Zv9):
Chromosome 8 (position 7539368)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 6926171
GRCz11 8 6969719
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTTCCCAGTGGAGGAACAAGTCAATGAAGACATCAGTGATGGATCTT[A/T]AAGTGGAACCAATGGACATTGATTTCGACCAGCCTCCGCCTCTCCAAGTG
Long Flanking Sequence:
GGGTAAAACATATGCTGGATAAATTGATGGTTCATTCCGCTGTGGTGACCCCAGATTAATAAAAGGACTAAGCCGAAAAGAAAATGAATGAATGAATAATCTTTGTTAAAGTGGCAAACATTATGATTTCTTGTGTCAAAATGGTTTAAATTCACTTGAAAATGCTCGACATTCTGAGACGATCGATGTTGAAGCGATATATTGTGCAGCCCTAGTATAAATACTGTAACAATAGATGACATTTTACTGGCAATCTGCTCTAAATCACGTTAAACACAGTGACATTTAGTGCCTCGACCCTCATGGGATTTGAACACACAGCCTTTCAGCTATAATCCCAGCTCAGTAGACTTGCATCCCAAAATGACGTCGTCTTTGCTGAATGATGACTCATTTATAAAAATATAACTCTCTCTCTCTCTCTCTCTCTCTTTGTTTACCATCTCTCCCAGCTTTCCCAGTGGAGGAACAAGTCAATGAAGACATCAGTGATGGATCTT[A/T]AAGTGGAACCAATGGACATTGATTTCGACCAGCCTCCGCCTCTCCAAGTGTTCGCTCACACCTCAACTCTACACGGCATCTCTCACATCTTCTCCTATGAGAAGATCACGGCTAAATGCTGCCTCTGGGTGGTGTTTTTCCTCAGCTCTTTGACTTTTCTCATGTACGTCTGCATTGATCGCATTCAGTTCTACCTGGAATATCCTCATGTCACCAAGCTGGATGAGATCACCACGCCGGTGATGGTGTTTCCGGCTGTGACCATTTGCAATCTGAACTCCATTCGCTTCAGCAGGATCACGCGCAACGACCTGTACCATGCAGGAGAGCTGCTGGCGCTGCTCAACTCCAGGTTGGTGGAACTTTCCTTACTGTTTTCTCAGACTTTGATGATTTTTTTTTCAAACACAAACAAGATAATTTAAAGAATGTTTAGAATATACACACACACACACACACACACACATATTTTCACATAAGCTCACATTATATATATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14670
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
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000004588 Nonsense 64 501 2 11
ENSDART00000105541 Nonsense 64 501 1 10
Genomic Location (Zv9):
Chromosome 8 (position 7539535)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 6926338
GRCz11 8 6969886
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTGCCTCTGGGTGGTGTTTTTCCTCAGCTCTTTGACTTTTCTCATGTA[C/A]GTCTGCATTGATCGCATTCAGTTCTACCTGGAATATCCTCATGTCACCAA
Long Flanking Sequence:
GACATTCTGAGACGATCGATGTTGAAGCGATATATTGTGCAGCCCTAGTATAAATACTGTAACAATAGATGACATTTTACTGGCAATCTGCTCTAAATCACGTTAAACACAGTGACATTTAGTGCCTCGACCCTCATGGGATTTGAACACACAGCCTTTCAGCTATAATCCCAGCTCAGTAGACTTGCATCCCAAAATGACGTCGTCTTTGCTGAATGATGACTCATTTATAAAAATATAACTCTCTCTCTCTCTCTCTCTCTCTTTGTTTACCATCTCTCCCAGCTTTCCCAGTGGAGGAACAAGTCAATGAAGACATCAGTGATGGATCTTAAAGTGGAACCAATGGACATTGATTTCGACCAGCCTCCGCCTCTCCAAGTGTTCGCTCACACCTCAACTCTACACGGCATCTCTCACATCTTCTCCTATGAGAAGATCACGGCTAAATGCTGCCTCTGGGTGGTGTTTTTCCTCAGCTCTTTGACTTTTCTCATGTA[C/A]GTCTGCATTGATCGCATTCAGTTCTACCTGGAATATCCTCATGTCACCAAGCTGGATGAGATCACCACGCCGGTGATGGTGTTTCCGGCTGTGACCATTTGCAATCTGAACTCCATTCGCTTCAGCAGGATCACGCGCAACGACCTGTACCATGCAGGAGAGCTGCTGGCGCTGCTCAACTCCAGGTTGGTGGAACTTTCCTTACTGTTTTCTCAGACTTTGATGATTTTTTTTTCAAACACAAACAAGATAATTTAAAGAATGTTTAGAATATACACACACACACACACACACACACATATTTTCACATAAGCTCACATTATATATATATATATATATATATATATATATATATATATATATTAAAGGTGTCACGATCCTCCAAATCCTTGATTCGATTACATTTTCGATTCTAAAGGCACGATTCGATTCGATTTTCGATTATGAATAATTAATTAATTAATGACCAATTAATTATTTGTTGCCTACCGTTTAAACTA
Associated Phenotype:
Not determined