ZMP
chrna7
Ensembl ID:
ZFIN ID:
Description:
neuronal acetylcholine receptor subunit alpha-7 [Source:RefSeq peptide;Acc:NP_957513]
Human Orthologues:
CHRFAM7A, CHRNA7
Human Descriptions:
CHRNA7 (cholinergic receptor, nicotinic, alpha 7, exons 5-10) and FAM7A (family with sequence simila
cholinergic receptor, nicotinic, alpha 7 [Source:HGNC Symbol;Acc:1960]
cholinergic receptor, nicotinic, alpha 7 [Source:HGNC Symbol;Acc:1960]
Mouse Orthologue:
Chrna7
Mouse Description:
cholinergic receptor, nicotinic, alpha polypeptide 7 Gene [Source:MGI Symbol;Acc:MGI:99779]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21086 | Essential Splice Site | Available for shipment | Available now |
sa21087 | Nonsense | Available for shipment | Available now |
sa2371 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21086
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 |
---|---|---|---|---|---|
ENSDART00000051931 | Essential Splice Site | 199 | 509 | 6 | 10 |
ENSDART00000134733 | Essential Splice Site | 200 | 510 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 55674791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 53379719 |
GRCz11 | 7 | 53649371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGCCGACATCACAGGATACATTGCTAATGGAGAGTGGGACCTTGTGG[G/A]TAGGGTGACCGACTTCATTAAATACCAATGCTTGAACAGAAGATAATGAA
Long Flanking Sequence:
TTCAAATATATTATGCTAACCAGTTAGCATTTAGGCAGATCACTTCCTGCACCTTTAAGCCTTTAAAAAGTACTTTACCCTGAATACTAGTATCTTGAAAAATATCTAATAAATTATAATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACAACTATGTTTGGAAATATGTCGAAAAAAATCTTTCCATTAAACAGAAATTGGGAAATAAAATAAACAGGGAGGCTAATATTTCTGGCTTCAACTGTATATGTGCAGCTGGAGGACTTGTTTTACAACCCTCCACTGAAACTGTTGCACTGCAGTTATAACACATTTCTGTTTATAGGGATCTTCAAAAGCACCTGCTACATTGACGTTCGCTGGTTCCCCTTTGATCTTCAGAGGTGTGATCTGAAATTTGGCTCCTGGACGTATGGAGGATGGTCTCTGGACCTGCAGATGATTGATGCCGACATCACAGGATACATTGCTAATGGAGAGTGGGACCTTGTGG[G/A]TAGGGTGACCGACTTCATTAAATACCAATGCTTGAACAGAAGATAATGAAAGACCACTTAAAGAGAGTGCACGTTCATGACTTTCAATATAAGTCAGACTGTTCGATGTGAATTGATTTCGTTTCAATTATATTTTGAAAAATGTTTTTAAGTACACTTGATGTTGTTGACAGATTTCTTAAAAGTGCATATAAAGTACTAAAAATTTTAAGTGTAACTAGTCTTTCTATAGTTCACTTTTTAAAAATAGGAAAACTGCAGCTTCATCACTGAAAATGTGCAATGAAATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATTGCAGAAGTTCCAGGTAGACGGAATGAGAGGTTCTACGACTGCTGCAAGGAGCCGTACCCAGATGTGACTTTTACGGTGGTGATGCGGAGACGAACACTGTATTACGGTCTTAATCTACTTATTCCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21087
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 |
---|---|---|---|---|---|
ENSDART00000051931 | Nonsense | 233 | 509 | 7 | 10 |
ENSDART00000134733 | Nonsense | 234 | 510 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 55675268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 53379242 |
GRCz11 | 7 | 53648894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCCAGATGTGACTTTTACGGTGGTGATGCGGAGACGAACACTGTATTA[C/A]GGTCTTAATCTACTTATTCCCTGTGTGCTCATCTCTACTCTGGCCCTGCT
Long Flanking Sequence:
TAATGGAGAGTGGGACCTTGTGGGTAGGGTGACCGACTTCATTAAATACCAATGCTTGAACAGAAGATAATGAAAGACCACTTAAAGAGAGTGCACGTTCATGACTTTCAATATAAGTCAGACTGTTCGATGTGAATTGATTTCGTTTCAATTATATTTTGAAAAATGTTTTTAAGTACACTTGATGTTGTTGACAGATTTCTTAAAAGTGCATATAAAGTACTAAAAATTTTAAGTGTAACTAGTCTTTCTATAGTTCACTTTTTAAAAATAGGAAAACTGCAGCTTCATCACTGAAAATGTGCAATGAAATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATTGCAGAAGTTCCAGGTAGACGGAATGAGAGGTTCTACGACTGCTGCAAGGAGCCGTACCCAGATGTGACTTTTACGGTGGTGATGCGGAGACGAACACTGTATTA[C/A]GGTCTTAATCTACTTATTCCCTGTGTGCTCATCTCTACTCTGGCCCTGCTGGTGTTCCTGCTACCTGCTGACTCAGGAGAAAAGATCTCGCTCGGTGAGCTACACATTGAAGGCTTTTGCCATAATTTTAAGATGTTAATATATATTAGGGGTGTAACAGTTCACAAAAATCACGGTTCGGTTCGATACGATACAGTGGTGTCACGGTTTGGTACGTTTTTGATACAGCAAAAAAAGAAAAAAGCCGGAGGATTTCTCTGGTTTTTATTTTTTAATGTATTAAAAATACCATCATAAAAGTATGATCCTGTTTTTGATCCTGATCCTGAGCTATGCTTCTGGGGTTTCTGCTTAGCAGCAAATAAAACAAATCCTTCTTTATACTCAAAACCAAAAAGCTTCCTAAAAAAATAAATGTAATATTGTAGTAGTTAAACAAATAAAAATAAAAGAACAATCTATAGTCTATTTTCAAGTATTTTTTTTTTCAGAAAGATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2371
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 |
---|---|---|---|---|---|
ENSDART00000051931 | Nonsense | 448 | 509 | 10 | 10 |
ENSDART00000134733 | Nonsense | 449 | 510 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 55682640)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 53371870 |
GRCz11 | 7 | 53641522 |
KASP Assay ID:
554-3029.1 (used for ordering genotyping assays)
KASP Sequence:
AGCGGCCCTGGAGAAACCGAACTKTCCAAGATCTTGGATGAGGTGCGGTA[C/A]ATTTCCAAGCGCTTTCGGGACCAAGACGAGGAAGACACTGTGTGTAATGA
Long Flanking Sequence:
TGAAGGAGGAAAAATGCCAAAATGGGTGAGATCCTCATTTCTGCATTGATTTTTATTACTTTATAAACCAATCAGGTTGAATTCATCAGTATTTCATATTTTTTAATGTCAGCGCTTTGCCATTTAACAGCTATTTTTGTGTGTTAGACACGTGTGGTGCTGTTGAACTGGTGTGCCTGGTTCCTGCGGATGAAGAGACCTGGCGAAGACAAAGTTCGCCCAGCTTGTCACAACAAGCAGCCGCGCAGCAGCCTCTCCAGCGTGGATCTAAACATCAGCCCTGGAGTCGCACAGTCCACCAATGGAAACCTGCTGTACATCGGCTTCCGCGGGATGGACACTATTCACTATGCTACTTCACCTGATTCTGGGGTGATCTGCAGCCGGCTTGTGGCGACCGGAGAGGAGGATGTGCTGCTCCCCGGAGCCCAGGCATCTTCAGTTAGTAGTAGCGGCCCTGGAGAAACCGAACTGTCCAAGATCTTGGATGAGGTGCGGTA[C/A]ATTTCCAAGCGCTTTCGGGACCAAGACGAGGAAGACACTGTGTGTAATGAGTGGAAGTTTGCAGCGTCTGTGATTGACCGTCTCTGTCTCATGGCTTTTTCCCTGTTCACCATCCTCTGCACCATTGGTATCTTAATGTCTGCCCCTAACTTTGTTGAGGCCATATCAAAAGATTTTTTCACCTGAAGCCTTCACTTACCCTTATATTGTAGCTATATCTACTTCTCAGAGTCTCCTAAAGGCACAGTATGTATGGCTTTTGCACTGAAATATCCAAAAAACCCTTTATTTTGTTGACTTACTTGTATTGTACCAAAAGGAAGAAAGGATGTATATAAGAGCCCAGCCAGATCATCCTGTAGCCCAAAACTGATAAAGGTAAGCAGAGCCAAAGTCATATTACCCTGTAGCTAAGCAGGATTGAGCCTGGTCAGTACTTACAAGGAAGACCACCAGGGAGAAACCTGCTAGATCTATTGCTAATGAGGCCAGCAGGTGGC
Associated Phenotype:
Not determined