ZMP
accn2c
Ensembl ID:
ZFIN ID:
Human Orthologue:
ACCN3
Human Description:
amiloride-sensitive cation channel 3 [Source:HGNC Symbol;Acc:101]
Mouse Orthologues:
Accn2, Accn3
Mouse Descriptions:
amiloride-sensitive cation channel 2, neuronal Gene [Source:MGI Symbol;Acc:MGI:1194915]
amiloride-sensitive cation channel 3 Gene [Source:MGI Symbol;Acc:MGI:2159339]
amiloride-sensitive cation channel 3 Gene [Source:MGI Symbol;Acc:MGI:2159339]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44171 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37929 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24532 | Nonsense | Available for shipment | Available now |
sa24531 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44171
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050602 | Nonsense | 256 | 501 | 5 | 10 |
ENSDART00000131708 | Nonsense | 4 | 249 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 24 (position 35135818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 33987267 |
GRCz11 | 24 | 33873442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGCTTTATCCTGGCAGTAATGAATATGGCTTTATTGCAGCTGCTGTA[T/A]CTTCCTCCGCCGTGGGGCGACTGCAGATCCGCACCGATGGACTCGGAGTA
Long Flanking Sequence:
TTACAAACTGATCAGTGAGATAGTTCATTCATTCATTTTTGGCTAAGTCCCTTTATTCATCAGGGGTCGCCACAGCAGAGCTGCGGCCCTCCAGCAATTGAGTTTGATACCTACGCTTTACATGCTCAGGGTTCCCTCCCGGGACAGCATGCCAAACCTGCTAATATCTTCAAGCATTATCTACGTGTGAACTCTTGAAAATAAATATAAAAACAACATTCATTTTTATGTGGCTCTCTATAAAGTCGGAGTTAGAAACAGTAGCCGGTTCGGGTTCACATCTCTGGTTTTCTTCAGGTTTGAACTAACACTGATTTCCAGCATGTTCTCTGCATTCACTGGCTTTTGTACGCTGTGAAAAGTTTCTGATTGCGCTGTGGGTTTTATTATACTCCGCAGTTTGATTGCTGCGCTCTGGGGCTCGGTGTGGTGTGTTTTGATTTGTTATTGAACAGCTTTATCCTGGCAGTAATGAATATGGCTTTATTGCAGCTGCTGTA[T/A]CTTCCTCCGCCGTGGGGCGACTGCAGATCCGCACCGATGGACTCGGAGTATTTCTCCACTTACAGCATCACTGCCTGCCGGATCGACTGCGAGACCCGATACCTGCTGGAGAACTGCAACTGCAGGATGGTGCACATGCCAGGTGCTGAGGGGAAAACATTCACACGCTTCAACTAGCTATACTGTTTAAATATGTTGGAGGTAGAAGTAGGGCACTTTTATTTCAGGGGTCAATTTGTAATGTTTTTTTCTTAACTGTGTGTTTTTATTTCAAATATGAAGGAGGTTTTATTTAATTAATTAATTTATTTATTTTTCTAATACTTATTCAGACCCACAAAACTTTGTCTGATCTATCCTATTTTTTTGTGATTTTAAATATGTTTTCTGCATTTTATATACTTACTCTGTTGTACTCATTCATTTTTTATTAATTTTTTAAATTTTAAAAAATTTATTAAGTGTCAAGCATAATCAAACCCACAACAGTTTATATAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37929
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050602 | Nonsense | 290 | 501 | 5 | 10 |
ENSDART00000131708 | Nonsense | 38 | 249 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 24 (position 35135716)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 33987165 |
GRCz11 | 24 | 33873340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCCACTTACAGCATCACTGCCTGCCGGATCGACTGCGAGACCCGATA[C/A]CTGCTGGAGAACTGCAACTGCAGGATGGTGCACATGCCAGGTGCTGAGGG
Long Flanking Sequence:
TTTGATACCTACGCTTTACATGCTCAGGGTTCCCTCCCGGGACAGCATGCCAAACCTGCTAATATCTTCAAGCATTATCTACGTGTGAACTCTTGAAAATAAATATAAAAACAACATTCATTTTTATGTGGCTCTCTATAAAGTCGGAGTTAGAAACAGTAGCCGGTTCGGGTTCACATCTCTGGTTTTCTTCAGGTTTGAACTAACACTGATTTCCAGCATGTTCTCTGCATTCACTGGCTTTTGTACGCTGTGAAAAGTTTCTGATTGCGCTGTGGGTTTTATTATACTCCGCAGTTTGATTGCTGCGCTCTGGGGCTCGGTGTGGTGTGTTTTGATTTGTTATTGAACAGCTTTATCCTGGCAGTAATGAATATGGCTTTATTGCAGCTGCTGTATCTTCCTCCGCCGTGGGGCGACTGCAGATCCGCACCGATGGACTCGGAGTATTTCTCCACTTACAGCATCACTGCCTGCCGGATCGACTGCGAGACCCGATA[C/A]CTGCTGGAGAACTGCAACTGCAGGATGGTGCACATGCCAGGTGCTGAGGGGAAAACATTCACACGCTTCAACTAGCTATACTGTTTAAATATGTTGGAGGTAGAAGTAGGGCACTTTTATTTCAGGGGTCAATTTGTAATGTTTTTTTCTTAACTGTGTGTTTTTATTTCAAATATGAAGGAGGTTTTATTTAATTAATTAATTTATTTATTTTTCTAATACTTATTCAGACCCACAAAACTTTGTCTGATCTATCCTATTTTTTTGTGATTTTAAATATGTTTTCTGCATTTTATATACTTACTCTGTTGTACTCATTCATTTTTTATTAATTTTTTAAATTTTAAAAAATTTATTAAGTGTCAAGCATAATCAAACCCACAACAGTTTATATAATGAAACTTTTTTTTTTCATTTTAAATATATATTTCGATATTTTATACATTTACTCTGCTGTCTTCATCCATTTATTTTATTTTATTTTTTTCATTTATTTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24532
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050602 | Nonsense | 423 | 501 | 9 | 10 |
ENSDART00000131708 | Nonsense | 171 | 249 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 24 (position 35132065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 33983514 |
GRCz11 | 24 | 33869689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCGGTGGTCAGATGGGTCTGTTTATAGGAGCCAGTGTATTGACTATAT[T/A]GGAGATATTTGATTATTTGTATGAGGTTTGTTGTGGATTTGCTTTTTCTA
Long Flanking Sequence:
TTAATACACTTTGAAAGAAAAAAAAGAGTAATAAAAACAATACAGAAACAACATATTGGTCGCATCTATATCTCTACTCTCCAAAAAGACAAAGAATGTTTTCCAATTAGACCAATTAGCTTTTCAAAAAATAGTTAATCTGTTCTAAGTCAAGCCAAGAGGTCATGCTTTTTATCCACTGAGATACACCAGGACTGTCTTCTTTTAACCAGGAACACACAATTGCATGTTTATATTTATATATTTAATGTGTATTCCACAGGGACAATATACTTGTACTGGATATCTTTTTTGAGGCTCTGAATTATGAGAAAATTGAACAAAAGAAAGCATACGAAGTCGCTGGGTTACTTGGTAAGTGTATGCTATTGTGAAAGTAATATTGTTTTTCTTTTATTGACTTTAGTTTTCTGCTTTAATGTTATTATTATTTTGCATTGTTTCAGGTGATATCGGTGGTCAGATGGGTCTGTTTATAGGAGCCAGTGTATTGACTATAT[T/A]GGAGATATTTGATTATTTGTATGAGGTTTGTTGTGGATTTGCTTTTTCTACTTCTCCTGTAATGTGCTGATGGTTTTATTATTATATTTTTTATTAATATCTTTAATGGGCGAAGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTAGTTCGAGCCTCGGCTCAGTTGGGGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGTTTCCTCCTGGTGCTTCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATAAGTGTGTGTGTGAATGTGTGTGTGGATGTTACCCAGAGATGGGTTGTGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGATGGATAAATTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCCGAAAAGAATATGAATGAATAAATATCTTTAATTTCCTTATTCACACTGTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24531
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050602 | Essential Splice Site | 431 | 501 | 9 | 10 |
ENSDART00000131708 | Essential Splice Site | 179 | 249 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 24 (position 35132039)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 33983488 |
GRCz11 | 24 | 33869663 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGAGCCAGTGTATTGACTATATTGGAGATATTTGATTATTTGTATGAG[G/A]TTTGTTGTGGATTTGCTTTTTCTACTTCTCCTGTAATGTGCTGATGGTTT
Long Flanking Sequence:
AGTAATAAAAACAATACAGAAACAACATATTGGTCGCATCTATATCTCTACTCTCCAAAAAGACAAAGAATGTTTTCCAATTAGACCAATTAGCTTTTCAAAAAATAGTTAATCTGTTCTAAGTCAAGCCAAGAGGTCATGCTTTTTATCCACTGAGATACACCAGGACTGTCTTCTTTTAACCAGGAACACACAATTGCATGTTTATATTTATATATTTAATGTGTATTCCACAGGGACAATATACTTGTACTGGATATCTTTTTTGAGGCTCTGAATTATGAGAAAATTGAACAAAAGAAAGCATACGAAGTCGCTGGGTTACTTGGTAAGTGTATGCTATTGTGAAAGTAATATTGTTTTTCTTTTATTGACTTTAGTTTTCTGCTTTAATGTTATTATTATTTTGCATTGTTTCAGGTGATATCGGTGGTCAGATGGGTCTGTTTATAGGAGCCAGTGTATTGACTATATTGGAGATATTTGATTATTTGTATGAG[G/A]TTTGTTGTGGATTTGCTTTTTCTACTTCTCCTGTAATGTGCTGATGGTTTTATTATTATATTTTTTATTAATATCTTTAATGGGCGAAGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTAGTTCGAGCCTCGGCTCAGTTGGGGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGTTTCCTCCTGGTGCTTCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATAAGTGTGTGTGTGAATGTGTGTGTGGATGTTACCCAGAGATGGGTTGTGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGATGGATAAATTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCCGAAAAGAATATGAATGAATAAATATCTTTAATTTCCTTATTCACACTGTTATTTTATTCTTTTTTATTTTTATTTTATTT
Associated Phenotype:
Not determined