Busch Lab

ZMP

CHRM1 (1 of 2)

Ensembl ID:
ENSDARG00000037292
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.
Availability:
Order Allele From ZIRC
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.
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.
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