ZMP

si:ch211-39e15.2

Ensembl ID:

ENSDARG00000029501

ZFIN ID:

ZDB-GENE-060503-796

Description:

glycogen synthase kinase 3 alpha [Source:RefSeq peptide;Acc:NP_001038386]

Human Orthologue:

GSK3A

Human Description:

glycogen synthase kinase 3 alpha [Source:HGNC Symbol;Acc:4616]

Mouse Orthologue:

Gsk3a

Mouse Description:

glycogen synthase kinase 3 alpha Gene [Source:MGI Symbol;Acc:MGI:2152453]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa29147	Nonsense	Mutation detected in F1 DNA	Not yet available
sa36771	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa29147

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000049707	Nonsense	211	462	4	10
ENSDART00000082012	Nonsense	211	359	4	11
ENSDART00000122065	Nonsense	211	359	4	8
ENSDART00000143941	Nonsense	211	462	4	10

Genomic Location (Zv9):

Chromosome 19 (position 6699047)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	6157722
GRCz11	19	6076753

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGGTGGCTCGACACTTTAGCAAGGCTAAAACCATTATTCCCATCTTTTA[T/A]GTGAAGGTAAAGTTGACCAAACAAATGATCTCAACATCTTACAACAACAA

Long Flanking Sequence:

CAGTTTGTTTCCATTAGATGACTCCGCAGCTAACCGTTTACATGACCCACTTTTGCTGTCCACCACTACTAAAGTAAACACTGTGCCCTTGAACGAGGCACTTAAACCCAGGCTGAGAGGGATGGAACTGTCATGACTGTTTGCTTGTAAATATGGTGACGTGTTTTATCCCTGAGAGACGCTGACAGTGTTTTCCTCCATGCTTCTCAAGAACCGAGAACTTCAGATCATGAGAAAACTGGACCACTGCAATATAGTGAGGCTGCGCTATTTCTTCTATTGCAGCGGAGAGAAGGTAAACACCTATGATAGTTGTTGCATAATTCTAATTAAAATGATATGAGCATGTACATTACACAACCACACATTTTGTTTTGGTCTGTTTGTATTCCACAGAAGGATGAGGTTTACCTCAATCTAGTGCTGGACTACGTGCCTGAGACTGTCTACAGGGTGGCTCGACACTTTAGCAAGGCTAAAACCATTATTCCCATCTTTTA[T/A]GTGAAGGTAAAGTTGACCAAACAAATGATCTCAACATCTTACAACAACAACAACACAAAATTTCTTTCATCTTAAGGAGATAGTTCACCTAAAAATAAAAATTCTGTCATCATTTATTCACTATTTGCTTGTTATAAACCTGTTTATTTACTTTATTCTGTTCATATATTGAGGAATGCTGGAAACCTATGCCTAGATTTCCGCAGATTTTTAGCACATTATGGATTCTGTTTATTTACTTGTGTAAATGTGTGCAAATTTTTATTTATTCAGTTTTTAAATTAATTTCAATAATATTCTTGAATAATATGAAAATATTCATAAGATCTATTTACAATACAGTTTGTAAAAGTAACATTTTCTGTCTTTTAGTAGAGATATTTGTTGTAAACTTCTAAGAGCCCAAAAAACCAGGGAGAATCTTTCGGTTGTCTTCAAAGCAGAATCCTTTTTAATAAGAAGAACTCTGCGTGGCTGTGGCGTCATCGAAAGCAAACTCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36771

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:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000049707	Nonsense	377	462	8	10
ENSDART00000082012	None	None	359	8	11
ENSDART00000122065	None	None	359	None	8
ENSDART00000143941	Nonsense	377	462	8	10

Genomic Location (Zv9):

Chromosome 19 (position 6692023)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	6150698
GRCz11	19	6069729

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCCAGAACTCCTCCTGAGGCGATCGCGCTGTGCTCTCGGCTGTTGGAGTA[T/G]ACGCCAGTGACTCGGCTGTCTCCGCTTCAGGCTTGTGCTCATGCCTTCTT

Long Flanking Sequence:

TTTGCTATAATGACAGTTTATAATATTTTGCAAGATACTAGTATTCAACTTAAAGTGACATTTAAAGGCTTAATTAAGTTATGTTAACTAGGAAAGTTTGGATAATTGGGTAAGTTATTGAACAACAGTTTTTTTTTCTGTAGACAATTGAAAAAATAATAATATTGACCTCAAAATTGATTAAAACAAATTTTAAACAGATTTTTTTCTATTTAAACTTCAAAAGAAATCAGACTTTCTCCAGAAGATGAAATAAAATAGGAAATACTGTGAAATTTGTTAAGTGTTACTTGGAAATTTTTTCAAAAGAATAAAAATTTCTCAGGAGGGCAAATAAATTTGACTTTATAATTTCCACTGTATATATAATCGAGTTCATTTTCAGAGAATTCAGTCTTTTTTTAATCTTTCATTGTTTTCTCTCATATCTCTTTCTTGCAGGTGTTTAAACCCAGAACTCCTCCTGAGGCGATCGCGCTGTGCTCTCGGCTGTTGGAGTA[T/G]ACGCCAGTGACTCGGCTGTCTCCGCTTCAGGCTTGTGCTCATGCCTTCTTTGACGAGTTGCGCCAACCTGGCACCCGTTTGCCCAGCGGCCGAGAGCTGCCTCCGCTTTTCAACTTCACCACAACAGGTGAGTTTCCCTTCATGCGCATCCTCAAAAAAAAACATCTCACTGATTGAATGCAGATATCATCTATCTCAACAAAACAGGGTTTCACATGATACGTAAAAGTTTTAGCTTAATCTTGCTCAGAAGTTGATCTTTCACTGTATTTAGAAATCTTTGGAAACTTTAGAAATCTCTCCCCAGTGGACTCATTTATTAAAACTAACCTACAGTTTTTACTTTAAACTGCCTTTTGTTTACTGCCGAACAATTTTTTTTGCTCTGATAAAATATTGGGTGGCACGATGGCCCCGGCTGGGCCAGTTTGCATTTCTGTGTGGAGTTTGCAGGTTCTTCCTGTGTTGGCGTGGGTTTCCTACAGGTGCCTCGGTTTTCC

Associated Phenotype:

Not determined