ZMP

LOC100149598

Ensembl ID:

ENSDARG00000071298

Human Orthologue:

CHRM3

Human Description:

cholinergic receptor, muscarinic 3 [Source:HGNC Symbol;Acc:1952]

Mouse Orthologue:

Chrm3

Mouse Description:

cholinergic receptor, muscarinic 3, cardiac Gene [Source:MGI Symbol;Acc:MGI:88398]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35376	Nonsense	Mutation detected in F1 DNA	Not yet available
sa30967	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35376

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105331	Nonsense	292	502	1	1

Genomic Location (Zv9):

Chromosome 12 (position 48725012)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	47432422
GRCz11	12	47430280

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGAATGTGGAGGAAGAATCTGTGGTGGTCGTTCCTCAAACGGGAAGTTCT[C/T]GAAGTCACAGCAGCTACGAGCTCCAACCGGCAGCTCCGATGAGGAAAACT

Long Flanking Sequence:

TGAATCTATACACCACCTACATCATCATGGACCAGTGGGCGCTGGGAAACTTCGCTTGTGATCTATGGCTGGCTATTGATTACGTAGCCAGCAATGCATCAGTTATGAATCTGCTGGTTATCAGTTTCGACCGCTATTTTTCAGTCACGCGTCCGCTTACTTACAGAGCAAAGCGGACTACTAAGCGCGCAATGACTATGATTGGTTTAGCCTGGTCCATTTCGTTCATCCTATGGGCTCCTGCTATTCTCTTCTGGCAGTATTTTGTCGGAGAGCGGACGGTTGAGCCGGATAAGTGTTACATACAGTTCATTTCAGAGCCGATAACTACGTTTTGCACAGCTATCGCTGCGTTTTACCTGCCGGTGACCATCATGACGGTGCTTTACTGGAGGATCTATAAGGAAACGGAAAACCGTTCTAGAGAATTAGCCGGATTGAAAGCATCTGGGAATGTGGAGGAAGAATCTGTGGTGGTCGTTCCTCAAACGGGAAGTTCT[C/T]GAAGTCACAGCAGCTACGAGCTCCAACCGGCAGCTCCGATGAGGAAAACTAAAACAAGACGACTGTGGTTTTGGAGCCGTGGAGATGTGGAGCGCAGCAGTAGCGACAGCTGGAATAACAACGAAACTGCCATCTCTATCGATCAATCCGATGACGACGAGGAAGAGGATGCCGAACACATCTACACAATCGAGAAGCAAGATTTAGAGGCGAAACCATCTAAATTCGGAGTTTCAAAATCATCCACTCTGGACTCCAAAGATCAACCTGTTAAATCCGCACGCAAGACAAACAAGCGGAAGAAGCTCTCGCTGGTGAAAGAGAAAAAAGCAGCGCAGACTTTAAGCGCCATCTTGTTGGCTTTCATCATCACGTGGACGCCGTATAATATTATGGTGCTTCTGAATGCTTTCTGCGACGGATGCATCCCGGAGACGCTGTGGGCTTTGGGGTATTGGCTGTGCTACGTCAATAGTACGGTAAACCCCATGTGTTACGCG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30967

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105331	Nonsense	368	502	1	1

Genomic Location (Zv9):

Chromosome 12 (position 48724784)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	47432650
GRCz11	12	47430508

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACATCTACACAATCGAGAAGCAAGATTTAGAGGCGAAACCATCTAAATTC[G/T]GAGTTTCAAAATCATCCACTCTGGACTCCAAAGATCAACCTGTTAAATCC

Long Flanking Sequence:

TCCTATGGGCTCCTGCTATTCTCTTCTGGCAGTATTTTGTCGGAGAGCGGACGGTTGAGCCGGATAAGTGTTACATACAGTTCATTTCAGAGCCGATAACTACGTTTTGCACAGCTATCGCTGCGTTTTACCTGCCGGTGACCATCATGACGGTGCTTTACTGGAGGATCTATAAGGAAACGGAAAACCGTTCTAGAGAATTAGCCGGATTGAAAGCATCTGGGAATGTGGAGGAAGAATCTGTGGTGGTCGTTCCTCAAACGGGAAGTTCTCGAAGTCACAGCAGCTACGAGCTCCAACCGGCAGCTCCGATGAGGAAAACTAAAACAAGACGACTGTGGTTTTGGAGCCGTGGAGATGTGGAGCGCAGCAGTAGCGACAGCTGGAATAACAACGAAACTGCCATCTCTATCGATCAATCCGATGACGACGAGGAAGAGGATGCCGAACACATCTACACAATCGAGAAGCAAGATTTAGAGGCGAAACCATCTAAATTC[G/T]GAGTTTCAAAATCATCCACTCTGGACTCCAAAGATCAACCTGTTAAATCCGCACGCAAGACAAACAAGCGGAAGAAGCTCTCGCTGGTGAAAGAGAAAAAAGCAGCGCAGACTTTAAGCGCCATCTTGTTGGCTTTCATCATCACGTGGACGCCGTATAATATTATGGTGCTTCTGAATGCTTTCTGCGACGGATGCATCCCGGAGACGCTGTGGGCTTTGGGGTATTGGCTGTGCTACGTCAATAGTACGGTAAACCCCATGTGTTACGCGCTCTGCAATAAAGCTTTCCGCACCACCTTCAGGTCTATCCTGCTGTGTCAGTGGAGGAAGAAGAAACTCAACAAAGCACAGATCCAGAAGAGAGCGCCGGCCGCCACGTACCGCAAACACACTCAAAGCCTAGACTAGATATATGAAAATATATGCAAATTACATCATATGACATACACACTCATATTTGGATTGCACATATATAAAGTGTATGCAACATATATTTTG

Associated Phenotype:

Not determined