ZMP
CHRM1 (1 of 2)
Ensembl ID:
Description:
cholinergic receptor, muscarinic 1 [Source:HGNC Symbol;Acc:1950]
Human Orthologue:
CHRM1
Human Description:
cholinergic receptor, muscarinic 1 [Source:HGNC Symbol;Acc:1950]
Mouse Orthologue:
Chrm1
Mouse Description:
cholinergic receptor, muscarinic 1, CNS Gene [Source:MGI Symbol;Acc:MGI:88396]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22472 | Nonsense | Available for shipment | Available now |
sa6343 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa4557 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa22472
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 |
---|---|---|---|---|---|
ENSDART00000106074 | Nonsense | 163 | 479 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 25258714)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 23961805 |
GRCz11 | 14 | 24259050 |
KASP Assay ID:
2260-7528.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACCATCTCGTTTGTGATTTGGGCTCCAGCAATTTTGTTTTGGCAGTA[T/A]ATAGTTGGGGAACGGACTGTTCAGGAAAATGAGTGTTCAATACAGTTTCT
Long Flanking Sequence:
CTTCAGTTCATCATGAATCTCTCCAGTTTCATCAATGGGACAGATAGTCCCATCCCTGGTTTCATCTCATGGAAGACAGCCATGATCACCTTCATAACTGTTCCCCTGTCCCTCATCACCATCACAGGTAACGTCCTGGTCATGATCTCCTTTCGGGTCAACCCACTCCTGAGGACAGTAAGCAACTACTTTCTCTTAAGCTTGGCGGTGGCTGATGTAATTTTGGGCTCCATCTCGATGAACCTCTATACTACATACATCTTGCTTAATGGGTGGACTTTAGGCAATCTTGCCTGTGATGTGTGGTTGGCTGTGGACTATGTGGCAAGCAACGCCTCTGTTATGAACCTGCTGGCCATCAGTATTGACCGCTACCTTTCTGTCATGCGACCTCTGACCTATCGAGCTAAAAGAACACCCAAAAGAGCCATGATAATGATTTCTCTAGCGTGGACCATCTCGTTTGTGATTTGGGCTCCAGCAATTTTGTTTTGGCAGTA[T/A]ATAGTTGGGGAACGGACTGTTCAGGAAAATGAGTGTTCAATACAGTTTCTGTCAGAGCCTGTGATCACCTTTGGAACAGCCATCGCTGCATTTTACCTGCCAGTAAGTGTGATGGTGGCATTGTACTGGCGTGTGTATCGTGAGACAGAGAAGCGCTCTCAGAAGCTGGCTGGACTGATGGCGTCACAGGGAGGACGAACTGGAAATGCATCTCAGGTGGGTTTTACAGTAAAGACCTTGTCCATTATTTATTTTTTTCCTTTAGTTTGCATCACAGTGGGTAAAGCATGACATAAAATGCTGTTGTTGAACACTTAAAATGCTTTTTGTTTTCATTACAGATCACATTCAAACAAATGTTAAGTTATTTCAAATACAAACAAGCCTAAATTTGGGTGTTAAAAAAAGATTTGTTTATTAAAAGGTTCCTTAGGGAATCTGAAATCATTCTGGTTCTTCTTGCTCCCTCTGTTGGCTACATTTTTTCCTTGTTTATTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6343
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 |
---|---|---|---|---|---|
ENSDART00000106074 | Nonsense | 195 | 479 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 25258810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 23961901 |
GRCz11 | 14 | 24259146 |
KASP Assay ID:
554-4122.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCTGTCAGAGCCTGTGATCACCTTTGGAACAGCCATCGCTGCATTTTA[C/A]CTGCCAGTAAGTGTGATGGTGGCATTGTACTGGCGTGTGTATCGTGAGAC
Long Flanking Sequence:
ACTGTTCCCCTGTCCCTCATCACCATCACAGGTAACGTCCTGGTCATGATCTCCTTTCGGGTCAACCCACTCCTGAGGACAGTAAGCAACTACTTTCTCTTAAGCTTGGCGGTGGCTGATGTAATTTTGGGCTCCATCTCGATGAACCTCTATACTACATACATCTTGCTTAATGGGTGGACTTTAGGCAATCTTGCCTGTGATGTGTGGTTGGCTGTGGACTATGTGGCAAGCAACGCCTCTGTTATGAACCTGCTGGCCATCAGTATTGACCGCTACCTTTCTGTCATGCGACCTCTGACCTATCGAGCTAAAAGAACACCCAAAAGAGCCATGATAATGATTTCTCTAGCGTGGACCATCTCGTTTGTGATTTGGGCTCCAGCAATTTTGTTTTGGCAGTATATAGTTGGGGAACGGACTGTTCAGGAAAATGAGTGTTCAATACAGTTTCTGTCAGAGCCTGTGATCACCTTTGGAACAGCCATCGCTGCATTTTA[C/A]CTGCCAGTAAGTGTGATGGTGGCATTGTACTGGCGTGTGTATCGTGAGACAGAGAAGCGCTCTCAGAAGCTGGCTGGACTGATGGCGTCACAGGGAGGACGAACTGGAAATGCATCTCAGGTGGGTTTTACAGTAAAGACCTTGTCCATTATTTATTTTTTTCCTTTAGTTTGCATCACAGTGGGTAAAGCATGACATAAAATGCTGTTGTTGAACACTTAAAATGCTTTTTGTTTTCATTACAGATCACATTCAAACAAATGTTAAGTTATTTCAAATACAAACAAGCCTAAATTTGGGTGTTAAAAAAAGATTTGTTTATTAAAAGGTTCCTTAGGGAATCTGAAATCATTCTGGTTCTTCTTGCTCCCTCTGTTGGCTACATTTTTTCCTTGTTTATTTATGGTCACATTTTATTATTTCCCTTATCTTGAGGTTTGTTTAAAAGACTACAATGTTCCTAAAAAGGAAATGTTTTACAGGCAACAATGTTGCTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4557
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000106074 | Nonsense | 229 | 479 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 25258910)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 23962001 |
GRCz11 | 14 | 24259246 |
KASP Assay ID:
554-3505.1 (used for ordering genotyping assays)
KASP Sequence:
CAGAGAAGCGCTCTCAGAAGCTGGCTGGACTGATGGCGTCACAGGGAGGA[C/T]GAACTGGAAATGCATCTCAGGTGGGTTTTACAGTAAAGACCTTGTCCATT
Long Flanking Sequence:
TAAGCTTGGCGGTGGCTGATGTAATTTTGGGCTCCATCTCGATGAACCTCTATACTACATACATCTTGCTTAATGGGTGGACTTTAGGCAATCTTGCCTGTGATGTGTGGTTGGCTGTGGACTATGTGGCAAGCAACGCCTCTGTTATGAACCTGCTGGCCATCAGTATTGACCGCTACCTTTCTGTCATGCGACCTCTGACCTATCGAGCTAAAAGAACACCCAAAAGAGCCATGATAATGATTTCTCTAGCGTGGACCATCTCGTTTGTGATTTGGGCTCCAGCAATTTTGTTTTGGCAGTATATAGTTGGGGAACGGACTGTTCAGGAAAATGAGTGTTCAATACAGTTTCTGTCAGAGCCTGTGATCACCTTTGGAACAGCCATCGCTGCATTTTACCTGCCAGTAAGTGTGATGGTGGCATTGTACTGGCGTGTGTATCGTGAGACAGAGAAGCGCTCTCAGAAGCTGGCTGGACTGATGGCGTCACAGGGAGGA[C/T]GAACTGGAAATGCATCTCAGGTGGGTTTTACAGTAAAGACCTTGTCCATTATTTATTTTTTTCCTTTAGTTTGCATCACAGTGGGTAAAGCATGACATAAAATGCTGTTGTTGAACACTTAAAATGCTTTTTGTTTTCATTACAGATCACATTCAAACAAATGTTAAGTTATTTCAAATACAAACAAGCCTAAATTTGGGTGTTAAAAAAAGATTTGTTTATTAAAAGGTTCCTTAGGGAATCTGAAATCATTCTGGTTCTTCTTGCTCCCTCTGTTGGCTACATTTTTTCCTTGTTTATTTATGGTCACATTTTATTATTTCCCTTATCTTGAGGTTTGTTTAAAAGACTACAATGTTCCTAAAAAGGAAATGTTTTACAGGCAACAATGTTGCTGAAAAAATCCCTTCTTCACTTAAAATGCTGTATTTCCAGTAGGCCAGGGGTGTCCAAACTCAGTCCTGAAGGGCTGGTGTCCTGCATATTTTTGTTTCAACCCC
Associated Phenotype:
Not determined