ZMP

LOC568566

Ensembl ID:

ENSDARG00000019983

Human Orthologue:

CHRNB4

Human Description:

cholinergic receptor, nicotinic, beta 4 [Source:HGNC Symbol;Acc:1964]

Mouse Orthologue:

Chrnb4

Mouse Description:

cholinergic receptor, nicotinic, beta polypeptide 4 Gene [Source:MGI Symbol;Acc:MGI:87892]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7449	Missense	Mutation detected in F1 DNA	Not yet available
sa23392	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa7449

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 > A

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000008870	Missense	163	525	5	6

Genomic Location (Zv9):

Chromosome 18 (position 49565503)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	50634119
GRCz11	18	50630684

KASP Assay ID:

554-4185.1 (used for ordering genotyping assays)

KASP Sequence:

CTTCAACGGCAGCATCGCRTGGCTCCCGCCGGCCATCTACAAGAGCGCCT[G/A]TAAGATCGAGGTCAAGCACTTTCCCTTCGACCAGCAGAACTGCACGCTCA

Long Flanking Sequence:

TGTCTTGTTTCTAGCACAGAATATACTGTTGTGTTCAGGAGTAATGAGTCAAAATCAAGAGAGTTTCTCATTAAAGCAAGCTAAATAAAGGCCTCAAAGCAAGAAGGTCTCTGGTTCGAGTCCCGGCTGGTGTTCCCCTACAGTTTGGACAGTGGAGGACACCTGAGCACCCGGAGGAAACCCACGCCAACAGGGGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCCCGCTGGGGCTCAAACCAGAGACCTTCCTTCCGTGAGGCCACAGTGCTGACCACTGAGCCAGTGCCCTTGAATTTCATATTTTGGCGAGTTCATCTGTTTAGTCAGCAGAGTCAGGGAGTTTGGCATCTGGCTTGTGTAGTGTATCTGAAACTCTGGTGTCTCCACAGTGCTGACGGGACGTACGAGGTGACGGTGTTCACTAACGCCATCGTGCTCTTCAACGGCAGCATCGCGTGGCTCCCGCCGGCCATCTACAAGAGCGCCT[G/A]TAAGATCGAGGTCAAGCACTTTCCCTTCGACCAGCAGAACTGCACGCTCAAGTTCCGCTCCTGGACCTACGACCACACCGAGATCGACCTGCTGCTGAAGTCGGACGCCGCCAGCATGGACGACTTCACGCCCAGCGGCGAGTGGGACATCCTGGCGCTGCCAGGCCGTCGAACGGTCAGCCCGCTGGACGCCACGTACGTAGACCTGACCTACGACTTCATCATCAAGAGGAAGCCGCTGTTTTACACCATCAACCTGATCATCCCGTGTGTGCTCATCACCTCGCTGGCCATCCTGGTGTTCTACCTGCCGTCCGACTGCGGAGAGAAGATGACTCTGTGTATCTCCGTCCTACTAGCGCTCACCGTTTTCCTCTTGCTGATCTCCAAAATCGTGCCGCCCACTTCCCTGGACGTTCCTTTAATCGGGAAGTACCTGATGTTCACGATGGTTCTGGTGACCTTCTCGATTATCACTAGTGTGTGTGTGTTAAACGTGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23392

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
Order Allele From EZRC

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000008870	Nonsense	377	525	5	6

Genomic Location (Zv9):

Chromosome 18 (position 49566144)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	50634760
GRCz11	18	50631325

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGAGAGGACATTCGGCACGCCAGCGTCTGCGCCAGAACCGCCGTCTGCTT[G/T]GATTGGCTGATACTCCTGGCAGATCCGTCATGTGCTCGTCTGCGTCTGCG

Long Flanking Sequence:

AGTGGGACATCCTGGCGCTGCCAGGCCGTCGAACGGTCAGCCCGCTGGACGCCACGTACGTAGACCTGACCTACGACTTCATCATCAAGAGGAAGCCGCTGTTTTACACCATCAACCTGATCATCCCGTGTGTGCTCATCACCTCGCTGGCCATCCTGGTGTTCTACCTGCCGTCCGACTGCGGAGAGAAGATGACTCTGTGTATCTCCGTCCTACTAGCGCTCACCGTTTTCCTCTTGCTGATCTCCAAAATCGTGCCGCCCACTTCCCTGGACGTTCCTTTAATCGGGAAGTACCTGATGTTCACGATGGTTCTGGTGACCTTCTCGATTATCACTAGTGTGTGTGTGTTAAACGTGCACCATCGTTCTCCCAGTACCCACAGCATGCCGGCGTGGGTGAAGATCGTGTTTTTGGTGCGACTGCCGGCGCTGCTGTTTATGCAGAGACCGAGAGGACATTCGGCACGCCAGCGTCTGCGCCAGAACCGCCGTCTGCTT[G/T]GATTGGCTGATACTCCTGGCAGATCCGTCATGTGCTCGTCTGCGTCTGCGCTGCTGGCTGCGTCTTCGGCGTCCGCTCTTTCCTCTCCGGGACTCTTGTATAATAAAGGGCATTTCGGCTCTCGGAGAGCTGAAGGTCTGAATAATGGACACGGCTCCGCACAGGACCTGAAGGGGAACAGGCTGTATTGTGAATGGGGATCTGAGATTCAGGAGGCTGTGGACGGAGTTCGATATGTTGCTGATCACATGATGGGGAATGACGACGATCAAAGCGTGAGTTTCTACGTTTTATTTATTACACTGGTAATCCTTGATCCTGATTGGTTAATTGGCAGATTCTAAGGCGTGTTACTGTATGTTAGGGGTAAAGTGCATACAGGTGGCTGCTATCGCAGAATAAAGCATGACAGGTTTATCAGCAGCTGTACTTTATCTTATTACATCACTACTGGACACAAACACAGAGCATTGTTCTGAGCTGACTGCTTGCAGCCGGTC

Associated Phenotype:

Not determined