ZMP

prkag3

Ensembl ID:

ENSDARG00000017537

ZFIN ID:

ZDB-GENE-091204-419

Description:

PRKAG3 protein [Source:UniProtKB/TrEMBL;Acc:Q5BLG8]

Human Orthologue:

PRKAG3

Human Description:

protein kinase, AMP-activated, gamma 3 non-catalytic subunit [Source:HGNC Symbol;Acc:9387]

Mouse Orthologue:

Prkag3

Mouse Description:

protein kinase, AMP-activated, gamma 3 non-catatlytic subunit Gene [Source:MGI Symbol;Acc:MGI:189134

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa8490	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa39537	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa8490

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024358	Essential Splice Site	66	252	3	10
ENSDART00000126468	Essential Splice Site	66	344	3	13

The following transcripts of ENSDARG00000017537 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 1 (position 5037395)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	5475957
GRCz11	1	6173735

KASP Assay ID:

2259-0110.1 (used for ordering genotyping assays)

KASP Sequence:

ATGCAATTCCTACCAGCTGCAAACTGGTCATTTTTGACACAACACTGCAG[G/A]TTGGGACTTAACATAATTTTAATATTTWAAATARTTTAAATGTGATTTTT

Long Flanking Sequence:

ACTTCACATTATAATGTATATGGTTGTATATACAATATACAACCCTTTTTTTCGTAACTTGTCAATTTCAGTAAATTTCATCATAAAATATTCAGTGACTATTGCAACACACACACACACACACACAGGTAACACAATAAATAATGTGATAATAAAATAATGTGACACAATAATGTGACATCAAAATTGATTTGATTTGACACACACACACATACACACACGTCCATTATTAATCTGTTTTGTTTCTGACAGGACGATTGCCATGAGGACTGTTTAGTGAACATCACAGGTATGTCAATTCACATTTCCTAAATCATTATTATTTAGATACCCTAGGTTGATATCCTAAAAAAACAATCTTCAATCTAATTTGGTGTGTTTTATGTCCTCCAGACCTGGATCCAAATGCCGAAACTTATATGAACTTTATGAAGAAGCACTGCTGTTATGATGCAATTCCTACCAGCTGCAAACTGGTCATTTTTGACACAACACTGCAG[G/A]TTGGGACTTAACATAATTTTAATATTTAAAATAATTTAAATGTGATTTTTATAGAGTTTTATTTTTTTATTTTTTTCTAAAATAGTTTTACATTTATCCAAGTTCTGAAACACTTAAAATGTCTCTGTAATTCCGGTTGCAGCGTCAGCCCCTATTGCATTGCATCTGAAATGGTTGGTTAAGGAGTCTAGTCTCTTAAATCCTGCCTTTCCTTGAGTCTTTACTCTGATCTGATTGATCAGATGGCCCAGTCTGTGGTGATTGGTTGAAAATAAAACGTTCATTAGCATGTAGACTATTTCAATGTGGTCATGTCATTGGCCCATGCACATTTCCTGCTTGTTATCAAACTATTTCATAACCGTAAAAAGAGGCAATTCAATCACAACCTAATGTTAAAACAGCTACAATACCATTATTTATCAATATGTGGCTCTTTTTTGGATTCTCAAAAGCTATAGAAAGTAAAAAATATAAAACGTTGGGACTATTGTTTTTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39537

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:

A > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024358	Essential Splice Site	147	252	None	10
ENSDART00000126468	Essential Splice Site	147	344	None	13

The following transcripts of ENSDARG00000017537 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 1 (position 5042342)

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTATAAAC[A/C]GCCTCTTTGACGCCGTCTACTCTTTACTGAAGCACAAAATCCACAGGCTG

Long Flanking Sequence:

GTCTTTTTTTTTAAATGTGTTTATAGATTTTATTTTAAGTTATTTTAGTACATTAAGTTATAATATTTCAGTGGAAATATTTCATTGGTAAATAGATTAAATAAGACAAGTTTACATTTTTTATATATATTATTTGAGTCAATATGAATTTTATTTATTGTATATTTAATTTAAAGGAGCAAATTGTTTAAATTTGTCAACTATAATAACAATGATTAAACGTAAAAGCTCATCTTTCTCATGTCTGTACTTTAGCTACAATTATTATATATAATAATTAGTAAATTATTATTGCTTTGTTTTTAAATTAGTACATTTATTTATTTGTTTTGTTGGTCTTGTTTTGAGTGGTGGTGTATGTATTTATAATATACTGTATATTAAAATATATTCATAATTCTTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTATAAAC[A/C]GCCTCTTTGACGCCGTCTACTCTTTACTGAAGCACAAAATCCACAGGCTGCCGGTCATTGACCCAGAGTCTGGAAATGTCCTTCACATACTGACCCATAAGAGGATCCTCAAGTTCCTTCATATATTCGTAAGACTGATAAACTCATTGAAATACACAATTTCACAGTTCATTTTTTTTTTTTTTTTTTAGCACATTCGTTAGTTATTGTCTCCATCACATTACAATTACAAAAGTGATTTTATTTATGGGGAAGCTCAGTGGCTAGCACTGTCGCCTCACAGCAAGAAGGTCGCTGTTTGAGTTCTGGTGGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTCAGCATAGGTTTCTTCCTGGTGCTCCGGTTTCCCCCTTAGTCCAAAGACATGCGCTATAGGTGAATTGAATAAACTAAATTGGCCGTAGTGCATGAGTGCATGTAATTGTGTATGGGTGTTTCCCAATACTGGGTTGCAGCTG

Associated Phenotype:

Not determined