Busch Lab

ZMP

chrnb2a

Ensembl ID:
ENSDARG00000008674
ZFIN ID:
ZDB-GENE-090312-169
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa12396 Nonsense Available for shipment Available now
sa39606 Nonsense Mutation detected in F1 DNA Not yet available
sa32662 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12396
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002532 Nonsense 66 490 2 6
ENSDART00000142524 Nonsense 45 469 1 5
Genomic Location (Zv9):
Chromosome 1 (position 21341103)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21876270
GRCz11 1 22567009
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTCAATAAGAGTCAACAGGTCACAATTGGCATCAAAGTCTCTCTCGCA[C/T]ARCTCATTAGTGTGGTAAGTCTCTSTTTCTTTCTTTGTTTCTCTCACTCT
Long Flanking Sequence:
CTTTTCCTGGTGACATGGAGCCAATCATCGAATCACAGCACATTATGTTAGCTGACTAATCAGAGCCTCTTGAGATTGGGCCTTTCAAAGGGACTAGGAAATATGACAGTCATTTTCATGTTAGCTGAGTAGCAGTATATAATTAAAGTAAGATATATGAAAAATAATTAGATTATTAGAATATTAGAATCCCAAGGATTTGAGAATGAGGTTTTTGGTTTCAAGTTATCTATGATCAAGAAAAGTTTGATTTGTCATGATATGAGCTATTTGTCATTTATTGATCATCCTTTTTAATCTCCATGCGGGACTGTTTGTGTATGTGTGTGTCTGTGTGTATCTGTGTGTGTATGTATGTGTGTGTGTTAGGGTCTCTTGCTGCTGATGCTGAGGAAAGGCTAGTAGATTTTCTGCTTGGTCCTGAGCGTTATAATAAGCTTATCCGGCCTGCAGTCAATAAGAGTCAACAGGTCACAATTGGCATCAAAGTCTCTCTCGCA[C/T]AACTCATTAGTGTGGTAAGTCTCTGTTTCTTTCTTTGTTTCTCTCACTCTCTCTCTCTCTCTCTCTCTCCCACACACACACACACGCACGCCCGCACGCACGCATACACACACACACACACACAAACACACACACACACACACACACACACACACACACACACACACACACACTTTATAATGTTCCTTCTGCAGAGGTTTATTCCAACATTAGTCAAACAACACTCTTAATTTCTCTAAAATAAAATAAAATAAAAGCTATTTTCTTTTCCAACCAATTGAATGACAGTATATATATATATATATATATATATATATACACATATATAACAGTATAGATAGTATTTAAAGGGCCATGTCCACCCCCCACCCGTCACAGAAGGTTGCTTTCACACGAATAACACCTGTAGTTTGAAAAAAAAGAAAGTGGGTGAGTCCAGCTTAGGTGGGTGTGGCGAAAGAGGGAAGAGTTTGCATAAAAAGGGGAGTTTCAGCATGTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39606
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
ENSDART00000002532 Nonsense 75 490 3 6
ENSDART00000142524 Nonsense 54 469 2 5
Genomic Location (Zv9):
Chromosome 1 (position 21337330)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21872497
GRCz11 1 22563236
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTATAAACACACCCAATGTTCTATGCTTTTTTACAGAATGAGAGAGAG[C/T]AAATCATGACAACAAATGTCTGGCTGACTCAGGTAAACTCACCTGCTGTA
Long Flanking Sequence:
TTACAGAAAGGTCATATATAGTCTTTATCTAGTTCATATTTATGGGTTGGCAAATTTAAAAATAGGTTTAACCCTTGTGCACTGTTCAAGTTTACTACCCTTTTGTTATGTTAGAGATAAAAACATCTATTAAATTGAACTGCTGTGAAAATGCAGCATTCATTTTCTTAATTTTTTTGCATAAATCTGTTAAACCCCAGTCCTGATTAAAACTCCTAAATTGCTTGGATCTTAACGCTTTAATTGCCAAATTCACAAATGTTGTCACTTATTTGGTGAAAAAATTATTATAATTATAAAAATTATGTATTTTCATTGTAAAAATGAATTGTGGACTGGATTTTTTTTCTTTTATCAAAGTCTTGGACATGTGAAGCAACATTGCCTTTGATGCGTTGTTTTTTTATTTGCATTATCCCTAATTTACTGTTGGTGGTTTATAAATTGTTTGTTTATAAACACACCCAATGTTCTATGCTTTTTTACAGAATGAGAGAGAG[C/T]AAATCATGACAACAAATGTCTGGCTGACTCAGGTAAACTCACCTGCTGTACCTGTGCACTCATCTGGATACTGTTATAAAACACAGTGAAATGAACTGTCCCACACATGAGTGCACATACAGCACAGGGCAGATTTCAGTTTTGATTAACCCACTGTTCACTTTGAACTTTTTTTCCCATGGAAATCATGTTTAATGATTTTGTACAAATACAGGCCTGGAAAAATATTTATAATGTAGTGATAATGTGTCTTAAAAATTTCAAGTAGGAATATTATCATTTTGGCAGAAAGTGACAAAAGAACTATAAAATATGTGTTCAAATTTTAAATACATGATGTTATTTATGAATATTAATAAAAAAACATTTAAGGTCCAAAAAGATGCAGTAATTTCTAATGCTGTCAAATGCTCTACACAATATACTTTTTATTTTAAATATTGAAGACATGTTATCAGTAGGCAAATAAACATTTTACCTAATACACACATATTAATTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32662
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
ENSDART00000002532 Nonsense 130 490 5 6
ENSDART00000142524 Nonsense 109 469 4 5
Genomic Location (Zv9):
Chromosome 1 (position 21329861)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 21865028
GRCz11 1 22555767
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAGTGTGTATTTTCTTCCCTTACAGTGCAGATGGTGTGTATGAAGTAT[C/A]ATTTTACTGCAATGCAGTCGTCTCCAACACTGGTGACATTTTCTGGCTCC
Long Flanking Sequence:
TTTTTTAACTAATACTCGATACAGAAGCTACGATACAGATTATTGAGCTGAAGCTTGACTACAAAATTAAATCGCAATTAGATATTTTCTCCAAATCGCACATCCCTTCTTAGCATAATAATTTTGACACAGTTTTATTTTACTATTACAGGTTCATTTTCATGCATTATATTCAATTTAATATAAGACTTTTAATGTATTATAAAATACACTTCAACTAATACCAAGATACCATTTTAATAATTTGCTTTGCCTTTAGTAAACTTTTAAAGAAAGATATTTGATTTTGAAATTAAACACCGTTTATTTAACATTACATCAGAAACCAAATTTTAAGCTAATTAATTTAAAACAAAAATATATAACATTCATTATTTAATATTTGTCAAAAAAACTGTATTAAAGTGCTAACTTCATTTTGTCATGAACAAATAAACATTATATGGATATTAGAGTGTGTATTTTCTTCCCTTACAGTGCAGATGGTGTGTATGAAGTAT[C/A]ATTTTACTGCAATGCAGTCGTCTCCAACACTGGTGACATTTTCTGGCTCCCTCCTGCCATCTACAAGAGCGCCTGTGCCATTGAAGTCCGCAACTTCCCTTTTGATCAACAGAACTGCACACTTAAATTCCGCTCTTGGACCTACGACCGCACAGAACTAGACCTCTACTTGACATCTGATTTTGCCAGTCGTGATGACTACACCCCTAGCGGAGAATGGGATATTGTGTCTCTCCCTGGCCGAAGAAATGAAGACCTCAGCGATCCCACTTACCTGGACGTCACGTACGACTTTGTCATCAAACGCAAGCCTCTCTTTTACACTATCAACCTCATCATTCCTTGCGTCCTCATCACGTCTCTTGCCATCCTGGTTTTCTACCTTCCTTCAGACTGCGGGGAGAAGATGACGCTGTGTATTTCGGTTCTTCTGGCTCTTACTGTGTTTCTGCTCCTGATCTCGAAGATCGTTCCTCCAACATCACTGGCCGTTCCATTAA
Associated Phenotype:
Not determined