ZMP

LOC562001

Ensembl ID:

Human Orthologues:

KCNJ3, KCNJ5, KCNJ6, KCNJ9

Human Descriptions:

potassium inwardly-rectifying channel, subfamily J, member 3 [Source:HGNC Symbol;Acc:6264]
potassium inwardly-rectifying channel, subfamily J, member 5 [Source:HGNC Symbol;Acc:6266]
potassium inwardly-rectifying channel, subfamily J, member 6 [Source:HGNC Symbol;Acc:6267]
potassium inwardly-rectifying channel, subfamily J, member 9 [Source:HGNC Symbol;Acc:6270]

Mouse Orthologues:

Kcnj3, Kcnj5, Kcnj6, Kcnj9

Mouse Descriptions:

potassium inwardly-rectifying channel, subfamily J, member 3 Gene [Source:MGI Symbol;Acc:MGI:104742]
potassium inwardly-rectifying channel, subfamily J, member 5 Gene [Source:MGI Symbol;Acc:MGI:104755]
potassium inwardly-rectifying channel, subfamily J, member 6 Gene [Source:MGI Symbol;Acc:MGI:104781]
potassium inwardly-rectifying channel, subfamily J, member 9 Gene [Source:MGI Symbol;Acc:MGI:108007]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa16099	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa16099

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
ENSDART00000059630	Nonsense	32	335	1	2

Genomic Location (Zv9):

Chromosome 15 (position 36123709)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	37523385
GRCz11	15	37424970

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAAAAGATGGGAAATGCCGAGTAGACTTGGCACACATGGCAGAAAAGGAG[C/T]GMTTTCTGGCRGACATCTTCACTTCGTTTGTGGACCTCCAGTATAGATGG

Long Flanking Sequence:

AGATTCTCCCTCAAAGTGGCAATCAATCAAATTCAACAGGTGACTACTCCCTTCCTCTGCCGGACATCATGCAGAGTGAGGCCTCCAACCCCTATGTGTCCATACGCCGCCACAAGAGCACCACAGATCTGCCATACAGCCCACAGCGTGGGTACTTGCGTGGACAGAGAACTAGTATCTGCGCCCCCACCGAGGCCGAGCTGGCAATGATGAGGCGTTGCTCTTTACGTGATCCGAACGTTCGTCCATGTTGCCGACATGCTCTTAGCGTTCCCAATATGACCAGTCCAAGCGCTAGCCCTCTGTACAGCACCCCATCCCGCAGTGCTCACTGCACTCCTGTACGGGAAGTGGAGTGCAATGCTAAAGCCCGCAATAAGCTAATTGAAAACGAGAGCGTGCAAACTCCCACATGCCCACCAGAGATTCGCCAGCAGCGTCGCTACGTCTCAAAAGATGGGAAATGCCGAGTAGACTTGGCACACATGGCAGAAAAGGAG[C/T]GATTTCTGGCAGACATCTTCACTTCGTTTGTGGACCTCCAGTATAGATGGTTTCTGTTTGTATTCATGATGTGCTACACGGTCACTTGGTTTATATTCGCAGGGCTTTATTCGCTAAATGCTTTTCTGCGTGGAGATCTTGAACATCCTGCGGACACTGATGTTTGCTTCCAAAATATAGATGGATTTGTTTCAGCGTTGCTCTTTTCAGTGGAAACACAGAGGACTATTGGTTATGGCGCTCGTACAGTCTCACCACGCTGCTATGAAGGTGTGTTTTTAGTCATGGCACAATGTATTGTGGGATCCATGATTGACGCTCTAATGGTGGGCTGCATGTTTGTTAAAATCTCACGTCCTAAGAAGCGAGCCGAAACACTTCTTTTTAGTCGGACTTGTGTTGTGGCCAATCGGGATGACCGTCTCTGCCTTATGTTTCGTCTTGGAGACTTGCGTGAGAGTCACATGGTTGACGCCAAAGTACGTGCTAAACTCATCAAG

Associated Phenotype:

Not determined