ZMP

mylka

Ensembl ID:

ENSDARG00000090738

ZFIN ID:

ZDB-GENE-030131-8207

Human Orthologues:

STK17A, STK17B

Human Descriptions:

serine/threonine kinase 17a [Source:HGNC Symbol;Acc:11395]
serine/threonine kinase 17b [Source:HGNC Symbol;Acc:11396]

Mouse Orthologue:

Stk17b

Mouse Description:

serine/threonine kinase 17b (apoptosis-inducing) Gene [Source:MGI Symbol;Acc:MGI:2138162]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10145	Nonsense	Available for shipment	Available now
sa41343	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10145

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
Order Allele From EZRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124885	None	None	243	None	5
ENSDART00000146782	Nonsense	473	674	8	9

Genomic Location (Zv9):

Chromosome 9 (position 4110961)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	4106714
GRCz11	9	4075371

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCACCACTAAGAGCGTCTCMGAGGAAGAYCTGAAGGAGATCACGGCTGAG[C/T]AGATGGACTTCAGAGGGAACCTCCAACGGCAGATCAAGCCCAAGACTCAG

Long Flanking Sequence:

AGTCAGCTGTGCAGTAGTCTACATTAGAGTGTGGGTTAGTCTTGGGGCCCCGTTTCGTTCTCATTTCCCTATAAGGCCTCTGAAGTCATCTCTGATGCAACTCTGTCATGTTGAACTTGCTCTCCTCTTGATTAAGCAGCTCTCAAGTGTGGGCTGAGCTTGCTGGGGCTTTAAACATCTCTGTATGTTTTTTTCTCCTCCACTCTTCCTGTTGCAGCCGAGGGGTGGAGAAGACTGCGCTAGGCAGGGGAGGACAGCCAAAGACTCCCAGCCCTGCAGCATCGTTGCACTCTGAGGAACATAGCAGTGGGACAGATCAGCAAGAAGAGGAGGGGGGCTCCACGCGTGGGCTTCTCAAACGGCGTGTAGAAACGAAGGAGCATCGGGAAGATCAGATCCGACAGCAGGAGGCCGAACAGATCGACTTCAGAACCGTGCTCGGCCGCAAGGTCACCACTAAGAGCGTCTCAGAGGAAGATCTGAAGGAGATCACGGCTGAG[C/T]AGATGGACTTCAGAGGGAACCTCCAACGGCAGATCAAGCCCAAGACTCAGACAGAAGAGCAACGCAAAGTCAACACTCCGCAGCAGGTGGACTTCAGAGCGGTGCTAGGGAAAAAAGCAAGCCAAGGCCCAAAACCTGCTCCTGGATCCTTGAAAACGCAACCTAGCAAAAACGAAGCCGTTGACTTCAGATCTGTTTTAGGCAATAAGAAAAAGCCACCAACCCAGGATAGGAATGGAGAAAGCCAAGGCGACCCCAGAGGAAAGGAAAATGACGTGAATTGTGTGGATGGAGAGATAAAGGAGACCACGAAGGCAGCTGGGAAGAAGGAGCCTGTTTTTGTAGAGAAACTGAGTGATGTGACTGTGCTGGACGGAGAGCGTTTGCATCTACAGTGCCAGCTGTCATCTGAGTCTCCTGCTAAAGTGACATGGATGCTTGATGGAAAAGTCATCAGACCCTCCAAATTCATCATTATCACTAATGAGGGTTAGTGTTAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41343

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124885	Essential Splice Site	121	243	3	5
ENSDART00000146782	None	None	674	None	9

Genomic Location (Zv9):

Chromosome 9 (position 4208537)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	4142502
GRCz11	9	4111059

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTAACGATGCTGGGAGCTGCCAGGTTACTGTGGAGATCATTGTGGAAGG[T/C]AAAGCACACCTTGATTGGCTTAAGTTTAATATTATTAATCTACACAGATC

Long Flanking Sequence:

ATTCTGTTCACTGGGTTTTAAGCATTTCCAGAACGCTGTTCATATTTGTCTCACTGAACCTTTTAATTATGGAGCACACTCTTGGCTTGTTTCACACAACAAACAGCTTCCTTTTGGCTCACACAAGAATGCTGGTCAATGGCAGAATTCTTGCGATACATCTGTCCCACACTTGTTCACTTGGACTATCTTGTTTACTGATTACTGCTGAGTTGCTGTGTTTATGTGATTGACCGTCTGTTTTATGTACAAGACTTTTAACACCTACTGTTTATATGTGATCTCTGTCAGGTACGTGGTTTCCCAGAGCCTCAGGTATGCTGGTTTAGGAATGGCAAGCTACTGATAGCAGGAGATCATTATTCTATGGAACAGAGTGTCCGTGGAACATTTAGTCTGGTGGTCCAGGAGGTAGAGGATGCCGATGGAGGACGTTACACCTGTGAAGCTGTTAACGATGCTGGGAGCTGCCAGGTTACTGTGGAGATCATTGTGGAAGG[T/C]AAAGCACACCTTGATTGGCTTAAGTTTAATATTATTAATCTACACAGATCACAGTAAAATAATGATTTTACAGATTTAAGGCTGGCTCATACTGTGGAATAGTCTGGATGATTGTAGCATGTCAGACTGCATGAATGCAATCCCCATGTCTGTTGTAATAACGTCAGACTGATAGACAGTCACAATGTTTACATGGACATCAGTAATCAAATTATTTGACTTAATCTGAAAAAAACAATAATATGATTTGCTTTTGAATGTTTCTTTCATGATTTTGTTTTATATGTTATAGCAAATAATTTGAATAACGTCATCAAGTGCATCCCATACTGAAAAAAAAAGCTTAAACCAGCCTAGACTGGTTGGCTGGTTTTAGCTGGTCAACCAGCCTGGTTTTAGAGGGGTTTTGGCCATTTTCAGGCTGGTTTCCAGCCATTTCCAGCCTGGTCTTAGCTGGTCAGGCTGGAAAATGACCAGCTAAATCCAGCTAAAACCAGCTT

Associated Phenotype:

Not determined