ZMP

LOC100329854

Ensembl ID:

ENSDARG00000087203

Human Orthologue:

STK39

Human Description:

serine threonine kinase 39 [Source:HGNC Symbol;Acc:17717]

Mouse Orthologue:

Stk39

Mouse Description:

serine/threonine kinase 39, STE20/SPS1 homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:1858416]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa17537	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa17537

Status:

Available for shipment
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Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000125090	Nonsense	231	343	8	12

Genomic Location (Zv9):

Chromosome 9 (position 50067792)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	49322620
GRCz11	9	48975844

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GATATATACGTTCTGCATTYCCCCCCCCTCCTGCCTCTGTGTTGTAGAAT[C/T]GAGAGTACTTGATGGAAAAGCTGCTTACTAAAGGACCAAATATAAGCCAA

Long Flanking Sequence:

AGTAGTGTATAATTATTATAAAATGCTCTACAGTTTAGTAGTGTATATAGTTTATATTTCTGTAATGATTAGTTGCATTGTAATGCATGTTATTGATTTTTATGATACATAATCTTAGTGTATAAATATAACATTATAAACCAGCCTTGAGAATGTTCAAAAAATGTTGCCTTAGGGACAGTTAAATTGTTGACTGGCCAAAATGAAAACCTGAACTTCTCTCTCAACTTCGCCAAAGCAAAAAATAAACCCTTACTGTGAGTCTCGAAACATGCACTCTATCGGAAAATGTCAGCTTGGACTGCTTTAACCGGGGCTCTTCTCATCTCCACAGGCCCACTGCAGCCGAGCTTTTGAAATGTAAATTTTTCCAAAAGGCTAAGGTACGTCAGTATACTCTCCCTCCATACTTCAAATGCTTTAACCAGTGCCTCGCAGCGGTCTGTCACTGATATATACGTTCTGCATTTCCCCCCCCTCCTGCCTCTGTGTTGTAGAAT[C/T]GAGAGTACTTGATGGAAAAGCTGCTTACTAAAGGACCAAATATAAGCCAAAGAGCCAAAAAGGTAACGCAGTCTCATTCTCCCAGTGTATTTTTGTTTCCACGCAGGCCACATGGGTCTCTCTGCTCTTATGTTCGGTGAAGTGCTCTCCTGTATTGATTAAAGAGTGTAGCTTCTTTTGATTGAGGGATGGGAAGCTGTAATGTTTCTCATCTGCCCTGAACACTCGCTCAGAGTCTCACTCGTCCGCTTATATACACTAGAGATGCACTCCAACTTATTACTGTAAGAGCCTTGCATTGGAGTCAGTGATGAACTCCTGCCCAGAGTGTTTGCTGCTTTATTTCTCATAGATGTTGTGTTTGTCTATGTATTGTTTTGTTTTTTTCCCCCCAAATGATCTCCTCTGTGCTATTGTATTTTGCTCTGTTACATTGTCTCTTCCTGTATGTTTTAGCACTCTATCTTCCAATCGAATGCTGCATATACACGAGGCCCGAC

Associated Phenotype:

Not determined