ZMP
accn1
Ensembl ID:
ZFIN ID:
Human Orthologue:
ACCN1
Human Description:
amiloride-sensitive cation channel 1, neuronal [Source:HGNC Symbol;Acc:99]
Mouse Orthologue:
Accn1
Mouse Description:
amiloride-sensitive cation channel 1, neuronal (degenerin) Gene [Source:MGI Symbol;Acc:MGI:1100867]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40123 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6906 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31347 | Nonsense | Available for shipment | Available now |
sa18762 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11288 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40123
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084803 | Nonsense | 70 | 564 | 1 | 10 |
ENSDART00000137038 | None | None | 271 | None | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 38349386)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 38212746 |
GRCz11 | 3 | 38354604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGAACACCACGAGACGATCTGTCCCGCCTCACCGTGGCCCTCCTCTCA[C/T]GAACTCGCCTCCATGGATTGCGGCATATCTGCTCTCCATCAAACTCTCTC
Long Flanking Sequence:
AGAAAATAGCCTGGGGATTTTGCCTGAGGCATTATAGAGAGTTGCCAGCGGGTATGAGGACACATGCTGTGTTTTTGACACCTTAGGGAGCAGTGTGCTTGTACGTGAATGTGTTTATTCGATCCCGAATTGAAGTTTGCATACATTTAACAGCATATTAAAGTGAAAGTCGAAGGAGAGTTGGGGTTTTAGACTTCAATTGAATTTGGAGTAGTAGTCTGAAGGTGTGACTTTGCTACAAATTAGTATTCCAGAAGTCAGTGTTGTGGCTTTCCCGGTGCTTTTGGAGCCCCATGAGGGCCCCGGCTGTGGAGGCCTGGCTGGGAGATGAAGCCGTCCGCCCTGCTGCTCTAGCAGCTCTGTGGGCCCTAATGGCTCTGGAAGGTCGCTGTCTGCGCCCTGCTTCGCCCACACCGGGCCAACGCAGGGCCCGCCGTCGCCACACTAGACCAGGAACACCACGAGACGATCTGTCCCGCCTCACCGTGGCCCTCCTCTCA[C/T]GAACTCGCCTCCATGGATTGCGGCATATCTGCTCTCCATCAAACTCTCTCAGTCGTCGGGCCTTTTGGATGATAGCATTCTGTACTTGTCTGGGTCTTCTGTTGTCTTGGTCCTCAAATCGGTTACTTCACTGGCTGGCCTTCCCCACTCACACGCGAGTCCACACAGAGTGGGCGAAAGAACTTGCTTTTCCCACAGTCACCATCTGCAACAATAACCCTGTGCGTTTGTATCACCTCACTAAAAGTGATCTGTACTTTGCGGGTCACTGGCTTGGACTGTTGCTGGCTAACCGCACAGCTAGGCCCCTGGTTCTGGACCTGCTTCAAGATGATAGGCGTGGATGGTTTAGCAAGCTGTCAGATTTCCGTCTTTTCCTGCCTCCACGGCGCTTTGAGGGCACCAGCTTGGAGTTCATGGACCGACTGGGCCACCAGCTGGAGGATATGCTACTGGCCTGCAAGTACCGCGGCGAGCCCTGTGGAGCCCATAACTTCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6906
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084803 | Nonsense | 106 | 564 | 1 | 10 |
ENSDART00000137038 | None | None | 271 | None | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 38349496)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 38212856 |
GRCz11 | 3 | 38354714 |
KASP Assay ID:
554-5321.1 (used for ordering genotyping assays)
KASP Sequence:
GCCTTTTGGATGATAGCATTCTGTACTTGTCTGGGTCTTCTKTTGTCTTG[G/A]TCCTCAAATCGGTTACTTCACTGGCTGGCCTTCCCCACTCACACGMGAGT
Long Flanking Sequence:
GTGTTTATTCGATCCCGAATTGAAGTTTGCATACATTTAACAGCATATTAAAGTGAAAGTCGAAGGAGAGTTGGGGTTTTAGACTTCAATTGAATTTGGAGTAGTAGTCTGAAGGTGTGACTTTGCTACAAATTAGTATTCCAGAAGTCAGTGTTGTGGCTTTCCCGGTGCTTTTGGAGCCCCATGAGGGCCCCGGCTGTGGAGGCCTGGCTGGGAGATGAAGCCGTCCGCCCTGCTGCTCTAGCAGCTCTGTGGGCCCTAATGGCTCTGGAAGGTCGCTGTCTGCGCCCTGCTTCGCCCACACCGGGCCAACGCAGGGCCCGCCGTCGCCACACTAGACCAGGAACACCACGAGACGATCTGTCCCGCCTCACCGTGGCCCTCCTCTCACGAACTCGCCTCCATGGATTGCGGCATATCTGCTCTCCATCAAACTCTCTCAGTCGTCGGGCCTTTTGGATGATAGCATTCTGTACTTGTCTGGGTCTTCTGTTGTCTTG[G/A]TCCTCAAATCGGTTACTTCACTGGCTGGCCTTCCCCACTCACACGCGAGTCCACACAGAGTGGGCGAAAGAACTTGCTTTTCCCACAGTCACCATCTGCAACAATAACCCTGTGCGTTTGTATCACCTCACTAAAAGTGATCTGTACTTTGCGGGTCACTGGCTTGGACTGTTGCTGGCTAACCGCACAGCTAGGCCCCTGGTTCTGGACCTGCTTCAAGATGATAGGCGTGGATGGTTTAGCAAGCTGTCAGATTTCCGTCTTTTCCTGCCTCCACGGCGCTTTGAGGGCACCAGCTTGGAGTTCATGGACCGACTGGGCCACCAGCTGGAGGATATGCTACTGGCCTGCAAGTACCGCGGCGAGCCCTGTGGAGCCCATAACTTCTCCACTGTGAGTCAGAACAAATGACCTCTATCCCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCACACACACAAACACACTCTCTCTCTCTCTCTTTCTCTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31347
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084803 | Nonsense | 246 | 564 | 2 | 10 |
ENSDART00000137038 | Nonsense | 9 | 271 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 38500417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 38363777 |
GRCz11 | 3 | 38505635 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTTTTTCTTCTTGGTTTCAGGTGTTTACCCGTTACGGGAAATGCTA[C/A]ATGTTTAACGCTGCCGAAGAGGGGAAGACTTTGAGGACTACAATGAAAGG
Long Flanking Sequence:
GTAATATAATAACTCTTGCCATGACCATGTAAAATATACATTTGGTTTTTTATCTGTGCAAGGAATGCCAGGAGGGCACACGTGGGAGATAAATATTGTATGTGATATGTAAACCACAGCGGGGCTGCATGCGTTCAGTAAACTCCAGCCAGAGGAATTATATCAATATATTATAAGCACCACCTAGAGAGAATGTTTCTCTCAGGAGGATGAAACAGACATCTTTACAGCTCAATAAATATACATTTTTGATACTGAATTATTTATGTACACTTCATATTAATGCTTTCAAAGTCTGCGGCCAACTTGCCTGCTAAGGCAAATGCTTTATTAGGAGTGTTGCTGTACATGTATTTGATGGTCTTTATACATATTCAGAATGCCTGTAGCTATCACAACCTTGATATGAATGCATAGATTTATAAAGAATTCAGTCAAGTGACATTCCTTCTCTCTTTTTCTTCTTGGTTTCAGGTGTTTACCCGTTACGGGAAATGCTA[C/A]ATGTTTAACGCTGCCGAAGAGGGGAAGACTTTGAGGACTACAATGAAAGGAGGCACAGGAAATGGCCTGGAGATCATGTTGGACATCCAGCAAGATGAATACCTGCCTGTATGGGGAGAAACAGGTACACTAACATTGAATACTTTACCGTTTTGTGTGGAATCTTCATTGATATTATGGATTTTACTGTACAAACTTTACATCCTATCCCCTAAACATAGCCCTTAGGCAGTGTGCCTACCAAATCATTTTACCCCCCTGAAAATTTCTAGTTCTTTTCTAAAAAATTCCCAGCCGTGGGCACTTTTTGAGGCACAGAGTTTTTATTTATTTTTTTATTTGTATTTTATTTATTTTTGAGCTGGGTGATGCAGAATCGGTATGGTAATGTTTCCAGGTATTTTGTTTATTTTTATCTATTTATTTATTTTGACTAAAAGTGTTGACTCAGTCTAGTGCAATATTAATGTCTTCTCCACTTTTTTCTTTGCTGTTCAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18762
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 |
---|---|---|---|---|---|
ENSDART00000084803 | Nonsense | 543 | 564 | 10 | 10 |
ENSDART00000137038 | None | None | 271 | None | 7 |
ENSDART00000084803 | Nonsense | 543 | 564 | 10 | 10 |
ENSDART00000137038 | None | None | 271 | None | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 38619539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 38482899 |
GRCz11 | 3 | 38624757 |
KASP Assay ID:
2259-3865.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTATTTCTCTTAGAGTACCTGTGATCCAGTAGTGAACCATTCAGAAT[C/A]GATAAGCCACACTGTCAGTGTTCCCCTTCAGACAACACTGGGCACCCTAG
Long Flanking Sequence:
TAGGCCCACACACAATCTGCACAGATATCCGCTGATTTTTAGCCTGTTATTGAGTCTATGTATTTATTTGTGTTAATGTAATAAATTGATATTTATTTAGATTTTAAATTAATTTTGCTAATATTATTGTAATATAATGATAGTAATAATAAAATGTTCATATGATTTATTTACAATACAGTTTGTAAAGTAATATTTTCTGTCTTTTAGTAGATATATTACATGAGAGACTTGCTTTGTTTACCAAATAGTGGATCTCATTGCATTTGCACTTTAAAGATTTAATAAAACTTAAAAATGTATAATTTTTATTTCTTATTTTAAGCTTATAGTCATATTTTAAAATCATTCAACATAAATCCACAGATTTTTTTTTTTTTTTTTACAAAATTCTCAGCAGAAAAAGCAAAAAATGTCAGCAGGTTCTGTCTGGCCTTACTAATAACATGTGTGTTATTTCTCTTAGAGTACCTGTGATCCAGTAGTGAACCATTCAGAAT[C/A]GATAAGCCACACTGTCAGTGTTCCCCTTCAGACAACACTGGGCACCCTAGAGGAGATCGCCTGCTGAGTGCCCTAACCCTCCATGCCACCAGGGGGAACAGAGACACTCCATTTCAATGGGAGAAGAACAGAGTAAAGAGAGCCTGTTTTTCTAGACATGTCATCATTTGGCACAGACATGCAAACTAGAAGCCAAGAAGCTTCTTGAGGAACACAAGGACCCCAAAATTTTCTCACAAACACCATCTGTTTGTTCTGGACTTGCGAAGGAAAGCAGACGCTTGTGGACCTGTCAGGACGGTCAGTTGTAAACATGAGACACAAAACACAAAAACACAAGAATAAGAGGAACTGCAAAATGCACATGGCCTCAACGTGCTCTCGCATTCGTTCTTTATCTCTCTACCCCAGCCACTGTTTTGAAGTCTACTGCCAAAACACTGTAAATTATTAACGGAGAAAATGTTGTGAAACTGTTCTAACTGTGCATGTGTCAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11288
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084803 | Nonsense | 543 | 564 | 10 | 10 |
ENSDART00000137038 | None | None | 271 | None | 7 |
ENSDART00000084803 | Nonsense | 543 | 564 | 10 | 10 |
ENSDART00000137038 | None | None | 271 | None | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 38619539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 38482899 |
GRCz11 | 3 | 38624757 |
KASP Assay ID:
2259-3865.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTTATTTCTCTTAGAGTACCTGTGATCCRGTAGTGAACCATTCAGAAT[C/A]GATAAGCCACACTGTCAGTGTTCCCCTTCAGACAACACTGGGCACCCTAG
Long Flanking Sequence:
TAGGCCCACACACAATCTGCACAGATATCCGCTGATTTTTAGCCTGTTATTGAGTCTATGTATTTATTTGTGTTAATGTAATAAATTGATATTTATTTAGATTTTAAATTAATTTTGCTAATATTATTGTAATATAATGATAGTAATAATAAAATGTTCATATGATTTATTTACAATACAGTTTGTAAAGTAATATTTTCTGTCTTTTAGTAGATATATTACATGAGAGACTTGCTTTGTTTACCAAATAGTGGATCTCATTGCATTTGCACTTTAAAGATTTAATAAAACTTAAAAATGTATAATTTTTATTTCTTATTTTAAGCTTATAGTCATATTTTAAAATCATTCAACATAAATCCACAGATTTTTTTTTTTTTTTTTACAAAATTCTCAGCAGAAAAAGCAAAAAATGTCAGCAGGTTCTGTCTGGCCTTACTAATAACATGTGTGTTATTTCTCTTAGAGTACCTGTGATCCAGTAGTGAACCATTCAGAAT[C/A]GATAAGCCACACTGTCAGTGTTCCCCTTCAGACAACACTGGGCACCCTAGAGGAGATCGCCTGCTGAGTGCCCTAACCCTCCATGCCACCAGGGGGAACAGAGACACTCCATTTCAATGGGAGAAGAACAGAGTAAAGAGAGCCTGTTTTTCTAGACATGTCATCATTTGGCACAGACATGCAAACTAGAAGCCAAGAAGCTTCTTGAGGAACACAAGGACCCCAAAATTTTCTCACAAACACCATCTGTTTGTTCTGGACTTGCGAAGGAAAGCAGACGCTTGTGGACCTGTCAGGACGGTCAGTTGTAAACATGAGACACAAAACACAAAAACACAAGAATAAGAGGAACTGCAAAATGCACATGGCCTCAACGTGCTCTCGCATTCGTTCTTTATCTCTCTACCCCAGCCACTGTTTTGAAGTCTACTGCCAAAACACTGTAAATTATTAACGGAGAAAATGTTGTGAAACTGTTCTAACTGTGCATGTGTCAGTTT
Associated Phenotype:
Not determined