ZMP

LOC100000044

Ensembl ID:

ENSDARG00000062672

Human Orthologue:

KCNJ3

Human Description:

potassium inwardly-rectifying channel, subfamily J, member 3 [Source:HGNC Symbol;Acc:6264]

Mouse Orthologue:

Kcnj3

Mouse Description:

potassium inwardly-rectifying channel, subfamily J, member 3 Gene [Source:MGI Symbol;Acc:MGI:104742]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11886	Nonsense	Available for shipment	Available now
sa41993	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11886

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
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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000090881	Nonsense	79	505	1	3

Genomic Location (Zv9):

Chromosome 12 (position 17155741)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	16035451
GRCz11	12	16084261

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTCGTCGACCTTAAGTGGYGCTGGAACCTGCTAATTTTCCTTTTAACGTA[C/A]ACGGTCGCGTGGCTCATCATGGCATCGATGTGGTGGATCATCGCGTACAT

Long Flanking Sequence:

TCAGTTCAGATACAGTGCCGCAGTTTATCTACACCGGACATCTCGCTAAGAGAAGTTGCGGGAAAGACACGGGATTCACTTGCTTTGTTTTAACTGGTCAACTACTTTTGCGCATCCATACATGTCAATAACTAGAGGACGGCAGGTAGATATTCTTTAAATAATCAACTTAAAGGCTGACCGCTCGTCGATGGAGTGCCACGGGGATCGTGAAACTTGAGACACTTCTAGCGTGTTTATTCACACCATTGTGGCTCGAGCATCATGTCCGCGATCCGCAGAAAATTTGGCGAAGACTATCAGGTGGTGAACACCAACCGGGCCATGTCCTTTTCTGCCCCTGCTAAAAGGAAGCGTCAGCGGTTTGTGGAGAAAAACGGGCGCTGCAATGTCCAGCACGGTAACCTTGGTGGGGAGACCAGCAGGTACATCTCTGACCTTTTCACCACGCTCGTCGACCTTAAGTGGCGCTGGAACCTGCTAATTTTCCTTTTAACGTA[C/A]ACGGTCGCGTGGCTCATCATGGCATCGATGTGGTGGATCATCGCGTACATCCGCGGAGACCTCGGCCACGGCCACGACGACTCGTACACGCCGTGCGTCGCCAACGTTTACAACTTTCCATCAGCTTTTCTCTTCTTCATTGAGACTGAGGCGACTATAGGCTACGGGTACCGATATATAACAGAGAAGTGCCCGGAGGGCATCATACTTTTCCTTTTTCAGTCGCTGTTGGGCTCCATCGTGGACGCGTTTCTCATCGGCTGTATGTTTATTAAGATGTCTCAGCCCAAGAAACGCGCAGAGACCCTCATGTTCAGCCAGGACGCAGTCATCTCACAACGGGACGGGAAGCTCTGCCTCATGTTTAGAGTCGGAAATCTCAGGAATAGCCACATGGTGTCGGCGCAAATCAGGTGCAAGCTCATCAAGGTATAGTGTTGTTTGTAGAAAATGAATATTGAAATGTTAATACTGAACCCTTGTGAATGGTGATGTGTGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41993

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000090881	Nonsense	373	505	3	3

Genomic Location (Zv9):

Chromosome 12 (position 17135004)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	16014714
GRCz11	12	16063524

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTCCCCTGGTCCTGTTCTCTCCCCTACATTGATTGAAGGTCGTCGCAGA[G/T]AGCGCATCTTTTCTTTAGATGGGGTTCCTCATTCTGATGAGCCTGGAAGT

Long Flanking Sequence:

ACAAGCAGTTTGGTGACTTATCCTTTATTATTCGATTATATGTCCCTGTAATTATCATTAGTGTAAAAAAATAACAAAAGTTTTTACATTTACATTTGTTTTTGGCATTATACCTCCTCATAGCATTCATTTTACGTATGTATACTAAAACAGGGCTTTTCAATGAGCCTGTGTTGAATGTATTAACTTATTTAAATGAGGTCATTTTTGGCAAAATAAACTGAATCAAGTCTCTATTGTAACATGAATCCTTGGCTTCCCTTTCAGGCATGACGTGTCAAGCTCGAACCTCTTATACAGAGGATGAAGTGCTGTGGGGTCACCGCTTTCTACCAGTCATGTCGCTAGAGGAAGGATTCTTCAGAGTCGACTACTCACAGTTCCACAACACATTTGAGGTGCCCACTCCTCCATACAGTGTGAAGGAACAAGATGAAAAGTCCTCCCTGCCCTCCCCTGGTCCTGTTCTCTCCCCTACATTGATTGAAGGTCGTCGCAGA[G/T]AGCGCATCTTTTCTTTAGATGGGGTTCCTCATTCTGATGAGCCTGGAAGTAAATTACCCAGCAAACTCCAGCGTATGTGCTCTAAGAATGGAAAAGAGGTCCTCAAAACTGGAAGTCCTCAGCCAACAGAAAAGGCCAGCAGCACAGGTGATCTGCCTCTCAGGGTACAGCGGCTTGGTTCCCTGGTGGGTCACGGAGAGACAGAAAATCACCTGCGTCTCAAACCTCTTAAGATGGGTTCAGAGACTCACACCCAGTCAGCAGGAGAACTGGAGCATCGCAGAAAGCTCTCAGCGCCTGCTCCAGTACCTGGCCCAAGTCTCAACCTATTGCCTGGTTCTAGTAGCCGACCAGAGGACAATCTCCCTGCTAAATTGCGCAGAATGAACGCAGACCACTGAATTGGTCTTAATGTTTGCCTTTATTTCTGAACATTGCGGCCTAGGAGGTAGAGATAATTCTTGAAATCATTTACTATTGAATAATATTTATTTAAAAAG

Associated Phenotype:

Not determined