Busch Lab

ZMP

LOC562421

Ensembl ID:
ENSDARG00000035961
Human Orthologue:
KCNG2
Human Description:
potassium voltage-gated channel, subfamily G, member 2 [Source:HGNC Symbol;Acc:6249]
Mouse Orthologue:
Kcng2
Mouse Description:
potassium voltage-gated channel, subfamily G, member 2 Gene [Source:MGI Symbol;Acc:MGI:3694646]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa23472 Nonsense Available for shipment Available now
sa23471 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa23472
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
ENSDART00000103646 Nonsense 172 546 1 2
Genomic Location (Zv9):
Chromosome 19 (position 12169435)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 11627934
GRCz11 19 11546001
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGCTGTCGTATTGGGGTGTGGAGGAGGCCAGTTTGGAGTGGTGTTG[T/A]TTGAGAAAGCTCCGTCTGCGGCAGGAGGAGCAGCGGGAGAGACTACGGCT
Long Flanking Sequence:
GCTTTCCTAGCAGGCAGCACCGATCATCAGTTTACCTCCTTCCACTTTAACCCTTTGGAAAACAAGCATGAAATCAGCAGTAAAAAGGGAGTGTTTTACAAGCGCGCACAAGTGCAACGCAAGGCCACAGCACAGGAGGACGAAGTTCACAGAAATCGAGGAGCTGGAGCAGACGAGGGTTCTTTATTTGACCGTACTGCCATCATCAACGTAGGTGGCATTCGTTATCGCATACCGTGGTCCACTCTTGAGGAGTTCCCATTGACACGTCTTGGGAGGTTGCATAACTGCAACAATGCCGAGGAAATCCTGGACTTGTGCGATGACTATGATGCTCGCTGCAACGAGTTCTTCTTCGACCGAAGCCCCAGCGCCTTCCGGTCCATTGTCACGTTCCTGGCAGCCGGGAAGCTTCGGCTCCTGCGGGAGATGTGCGCACTGTCCTTTCAGGAGGAGCTGTCGTATTGGGGTGTGGAGGAGGCCAGTTTGGAGTGGTGTTG[T/A]TTGAGAAAGCTCCGTCTGCGGCAGGAGGAGCAGCGGGAGAGACTACGGCTAGAGGAGGAGGAGGCCGAGTTGACTTCTCCCCATTCTTGTGAGGAGGCGCCAGCAGTTGGGAGCCCAGAGGAGGGTCGTTTGTCGGGCTGCATGCACAGCCTAAGAGATATGGTGGAGAATCCTCACTCTGGTATTCCTGGGAAGATATTCGCATGCCTCTCTGTGGTGTTTGTGGCCATTACTGCGGTTACACTGTGTGTCAGCACCATGCCTGACCTAAGGGAGGAGGAGGAGAGGGTGAGTGTACACTTCAATGTTCTACAAACTATGGCTTGTGTCACTACATGTGTTTGTTCAGAAAATAGACAGTCTAGTAGATTATGAGATGCCTTGTCTCTCATTCTCGTGCTGTAGATGCTCTGTTTCACTGTTTCCTTGCTATTGAAATGCTAAGTTTTTACACTTACACTTATACTTTACATCATGTAAATAGCAAATGCACCATGGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23471
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103646 Nonsense 539 546 2 2
Genomic Location (Zv9):
Chromosome 19 (position 12132380)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 11590879
GRCz11 19 11508986
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTGCACTCCACCGCAGATCTGTGGCTGTGGCAAGTCAAGGAGCGCCA[C/T]AGCTGCGGAGATCACTGAAGTCATAACGCAAACAGCTGACTGTAAGACTG
Long Flanking Sequence:
GACTGCAGACACTTGGGTTGACGGTTCGCCGCTGCACTCGAGAGTTCGGACTCCTCCTGCTGTTCTTGTGTGTGGCCATGGCCCTGTTTTCTCCATTGGTCTTTCTGGCCGAGAGTGAGCTGGGTGCCAAACAGGAGTTTACCAGCATCCCTGGGAGCTACTGGTGGGCTGTCATCTCAATGACGACGGTGGGATACGGTGATATGGTTCCGCGCAGTATTCCTGGCCAGGTGGTGGCGCTCAGCAGTATTTTGAGTGGAATCCTGCTCATGGCGTTCCCAGTCACATCCATATTTCACACATTTTCACGCTCCTACCTGGAGCTTAAAGAGGAACAAAATCGGGCCACAAGACACAAGCCTGATTCGCAGGACAGCACAAAGTCCCAAAACAGTGAGGATTCACAGGACACTGACAGTTCTATACATGGGATCACGGAGACCACCGCAGTCAGTGCACTCCACCGCAGATCTGTGGCTGTGGCAAGTCAAGGAGCGCCA[C/T]AGCTGCGGAGATCACTGAAGTCATAACGCAAACAGCTGACTGTAAGACTGAAGGAAAAAATGTGAGGCCATATTTAGTACCTGTATGATCAGGTGACTTGACAATTATTGATAACAGGACCAGGAGAATTACAAGGAAATGTTTGTATGTCCAAAGCACAATCATTTAAGGTGTTGGTTTTTACCTGAAAGGAATATTCTGTCATTTACTCACCCTCATGTTGTTCTTGATGACTAGGGCCAGACAGAATCTGCTCACTTTTTTTGCTATTTCTGCACAGAATTTTTGTAAAAAGAAAAAAAAAAGTGCTAAAGGTTTTGTTTTGTTTTTTTTTTTTTTTGGTAAAAAAAAATAAAAAATCTGTGAATTTATCCAGAATGATTTTGGAAGTATCATAACTAAAAACTTTATATGACAAATACATGAAAAATAATGCGGTTTTTACCTTTATTTAATGTTTACAAAGCAAATCCAATTAGAAAAACAAATCTACTAAATGA
Associated Phenotype:
Not determined