ZMP

kcnj8

Ensembl ID:

ENSDARG00000045589

ZFIN ID:

ZDB-GENE-060308-1

Description:

ATP-sensitive inward rectifier potassium channel 8 [Source:RefSeq peptide;Acc:NP_001025324]

Human Orthologue:

KCNJ8

Human Description:

potassium inwardly-rectifying channel, subfamily J, member 8 [Source:HGNC Symbol;Acc:6269]

Mouse Orthologue:

Kcnj8

Mouse Description:

potassium inwardly-rectifying channel, subfamily J, member 8 Gene [Source:MGI Symbol;Acc:MGI:1100508

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38432	Nonsense	Mutation detected in F1 DNA	Not yet available
sa33428	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38432

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
ENSDART00000067031	Nonsense	187	416	2	2

Genomic Location (Zv9):

Chromosome 4 (position 13784554)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	14720407
GRCz11	4	14719162

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTATGAAGACCGCTCAATCCCACCGGCGTGCCGAAACCCTTATCTTTAGC[C/T]GACACGCAGTCATCGCTGTGCGCAACAACCGCCTCTGCTTTATGATCCGA

Long Flanking Sequence:

CTAATATATATATATATATATGATCTTATAATATAATTATGAAGCCATTATATTAAATGTAGATTTTATACAAAAATAATTCAACTAAAATTGCTAAATAAAATCCAAATTAACAAAACCAAATAAAAAAAAGACAAATCTAAATGTATAATAAAGTAATAACAGTAATTAAGGCAATTGTGTATTTTTTTTTACATATGGGCCATATAATTTAGGTCAAATTATTAGGTTGTTTTATTCCATGTGGATGTTATTTCTGCCGCCTAAAACTGATGTTTTTTTTTCCTTCCAGCTCTTTCACCTCTGCCTTCCTGTTCTCCATCGAGGTGCAGGTGACTATAGGTTTCGGAGGGCGTATGATAACAGAGCGGTGTCCCATCGCCATCGCCTTTCTCATATTGCAGAACATCATTGGCTTGATAATAAATGCCGTCATGCTTGGCTGCATCTTTATGAAGACCGCTCAATCCCACCGGCGTGCCGAAACCCTTATCTTTAGC[C/T]GACACGCAGTCATCGCTGTGCGCAACAACCGCCTCTGCTTTATGATCCGAGTGGGCGACCTGCGCAAAAGCATGATCATCAATGCAGTTGTGCGCCTCCAAGTGGTCCGGAAGACCATGACCCCAGAGGGCGAGGTCATCCCCATCCAGCAGATCGATGTCCAGACTGAGAGTGCAGTGGCTGGTAACAGCATCTTTCTTCTGGCACCCTTGATCATATGTCATGTCATTGATAAAGACAGTCCTCTGTACGATCTGTCGGCGATGGAGCTGCAGTGCAGTGATCTGGAGGTCATCGTGATCCTGGAAGGAGTGGTGGAGACCACAGGCATCACCACTCAGGCTCGCACCTCCTACGTGACCGAGGAGATCCAGTGGGGACACAGATTCGTGCCTATAGTGACAGAGGAAGAGGGTGTCTACTCAGTGGACTACTCCAAGTTCGGGAATACAGTCAAAGTGGCCACCCCTCGCTGCAGCGCTCGTGAGCTGGACGAGAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33428

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
ENSDART00000067031	Nonsense	278	416	2	2

Genomic Location (Zv9):

Chromosome 4 (position 13784827)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	14720680
GRCz11	4	14719435

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGTCATTGATAAAGACAGTCCTCTGTACGATCTGTCGGCGATGGAGCTG[C/T]AGTGCAGTGATCTGGAGGTCATCGTGATCCTGGAAGGAGTGGTGGAGACC

Long Flanking Sequence:

TGTTTTTTTTTCCTTCCAGCTCTTTCACCTCTGCCTTCCTGTTCTCCATCGAGGTGCAGGTGACTATAGGTTTCGGAGGGCGTATGATAACAGAGCGGTGTCCCATCGCCATCGCCTTTCTCATATTGCAGAACATCATTGGCTTGATAATAAATGCCGTCATGCTTGGCTGCATCTTTATGAAGACCGCTCAATCCCACCGGCGTGCCGAAACCCTTATCTTTAGCCGACACGCAGTCATCGCTGTGCGCAACAACCGCCTCTGCTTTATGATCCGAGTGGGCGACCTGCGCAAAAGCATGATCATCAATGCAGTTGTGCGCCTCCAAGTGGTCCGGAAGACCATGACCCCAGAGGGCGAGGTCATCCCCATCCAGCAGATCGATGTCCAGACTGAGAGTGCAGTGGCTGGTAACAGCATCTTTCTTCTGGCACCCTTGATCATATGTCATGTCATTGATAAAGACAGTCCTCTGTACGATCTGTCGGCGATGGAGCTG[C/T]AGTGCAGTGATCTGGAGGTCATCGTGATCCTGGAAGGAGTGGTGGAGACCACAGGCATCACCACTCAGGCTCGCACCTCCTACGTGACCGAGGAGATCCAGTGGGGACACAGATTCGTGCCTATAGTGACAGAGGAAGAGGGTGTCTACTCAGTGGACTACTCCAAGTTCGGGAATACAGTCAAAGTGGCCACCCCTCGCTGCAGCGCTCGTGAGCTGGACGAGAAACCCTCCATCCTGATCCAGACGCTGCAGAAGAGCGAGCTTTCACACCAGAACTCTCTGCGCAAGAGGAACTCTATGCGCAGGAACAACTCCATGCGCAAGGGCAACTCCATGCGGCGCAATAATTCAGCTCTCGCTGTGCCCAAAGTGCAGTTCCTCACCCCTGAGGGCGGAGCCAATCTAGCGGTCACATGACAAACCGCCTGTAAAGCACTTATCACCTGTCTGTCTTTAAAGCCCGGCTCACACTGTGCAATTTTGGCCATGATTTGGCCT

Associated Phenotype:

Not determined