ZMP

LOC571888

Ensembl ID:

ENSDARG00000061014

Human Orthologue:

KCNJ5

Human Description:

potassium inwardly-rectifying channel, subfamily J, member 5 [Source:HGNC Symbol;Acc:6266]

Mouse Orthologue:

Kcnj5

Mouse Description:

potassium inwardly-rectifying channel, subfamily J, member 5 Gene [Source:MGI Symbol;Acc:MGI:104755]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9146	Nonsense	Mutation detected in F1 DNA	Not yet available
sa44899	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9146

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086547	Nonsense	127	425	2	3

Genomic Location (Zv9):

Chromosome 18 (position 47183764)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	48625455
GRCz11	18	48620152

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCTAATTGCACTGATACGAGGAGATCTTCTACACAGCGAYGAGGAGGGCT[G/A]GACCCCCTGCGTTGAAAACCTCAACAGCTTTGTATCCGCTTTCCTGTTTT

Long Flanking Sequence:

CGAGTCGGACGTAATTTGTAGCTATTTTCATACAGGTGCAGGATTTGGACACACCCTTAATGCTTTTGCGCCACTCACAAAATGTTCAAATAGAGCCCTAAAAATAGAGTCAAGTGTAAAAATACCACCACTACACACTACTGCGTGTCAAACTAAAGCTGTTACTTTCTCTACCTCCAAACAGCAGGTGAAGAAACTCCCCAAACACCTGAGGGAATCCCAGATCCCCACAGACCGTACCCACCTCATCTCTGATCCGGTTAAGAAACCCCGTCAGCGCTACGTCCAGAAAGACGGCAAGTGCAACGTTCATCACGGAAACGTTAAAGAGACCTACCGTTATCTCAGCGACCTCTTCACGACACTAGTGGACTTACGATGGCGTCTCAGTTTCTTCATCTTCACCTTGGTCTACGTGGTCAACTGGCTGTTTTTTGGGTTTTTATGGTGGCTAATTGCACTGATACGAGGAGATCTTCTACACAGCGACGAGGAGGGCT[G/A]GACCCCCTGCGTTGAAAACCTCAACAGCTTTGTATCCGCTTTCCTGTTTTCCATCGAAACCGAGACCACTATTGGGTATGGCTATCGGGTGATCACGGAGAAGTGTCCGGAAGGGATAATACTTCTAATGGTGCAAGCCATATTGGGGTCGATTGTCAACGCCATGATGGTAGGGTGTATGTTTGTAAAGATTTCACAACCCAAGAACCGAGCAGAGACGTTGATGTTCTCCCACAATGCTGTGATCTCGGTGCGGGACAACAAGATGTGCCTGATGTTCAGGGTGGGCGACTTGAGGAATTCCCACATTGTGGAAGCGTCAATTCGGGCCAAACTCATCCGCTCGCAGCAGACCAAGGAGGGCGAGTTTATTCCGCTCAATCAGACAGACATCAACATTGGCTTCGACACAGGAGACGATCGCTTATTCTTGGTATCTCCTCTTATCATCTCACATGAGATCAACGAGAAGAGTCCTTTCTGGGAGATGTCGCGGGCAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44899

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086547	Nonsense	127	425	2	3

Genomic Location (Zv9):

Chromosome 18 (position 47183765)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	48625456
GRCz11	18	48620153

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTAATTGCACTGATACGAGGAGATCTTCTACACAGCGACGAGGAGGGCTG[G/A]ACCCCCTGCGTTGAAAACCTCAACAGCTTTGTATCCGCTTTCCTGTTTTC

Long Flanking Sequence:

GAGTCGGACGTAATTTGTAGCTATTTTCATACAGGTGCAGGATTTGGACACACCCTTAATGCTTTTGCGCCACTCACAAAATGTTCAAATAGAGCCCTAAAAATAGAGTCAAGTGTAAAAATACCACCACTACACACTACTGCGTGTCAAACTAAAGCTGTTACTTTCTCTACCTCCAAACAGCAGGTGAAGAAACTCCCCAAACACCTGAGGGAATCCCAGATCCCCACAGACCGTACCCACCTCATCTCTGATCCGGTTAAGAAACCCCGTCAGCGCTACGTCCAGAAAGACGGCAAGTGCAACGTTCATCACGGAAACGTTAAAGAGACCTACCGTTATCTCAGCGACCTCTTCACGACACTAGTGGACTTACGATGGCGTCTCAGTTTCTTCATCTTCACCTTGGTCTACGTGGTCAACTGGCTGTTTTTTGGGTTTTTATGGTGGCTAATTGCACTGATACGAGGAGATCTTCTACACAGCGACGAGGAGGGCTG[G/A]ACCCCCTGCGTTGAAAACCTCAACAGCTTTGTATCCGCTTTCCTGTTTTCCATCGAAACCGAGACCACTATTGGGTATGGCTATCGGGTGATCACGGAGAAGTGTCCGGAAGGGATAATACTTCTAATGGTGCAAGCCATATTGGGGTCGATTGTCAACGCCATGATGGTAGGGTGTATGTTTGTAAAGATTTCACAACCCAAGAACCGAGCAGAGACGTTGATGTTCTCCCACAATGCTGTGATCTCGGTGCGGGACAACAAGATGTGCCTGATGTTCAGGGTGGGCGACTTGAGGAATTCCCACATTGTGGAAGCGTCAATTCGGGCCAAACTCATCCGCTCGCAGCAGACCAAGGAGGGCGAGTTTATTCCGCTCAATCAGACAGACATCAACATTGGCTTCGACACAGGAGACGATCGCTTATTCTTGGTATCTCCTCTTATCATCTCACATGAGATCAACGAGAAGAGTCCTTTCTGGGAGATGTCGCGGGCACA

Associated Phenotype:

Not determined