ZMP

si:dkey-14o18.6

Ensembl ID:

ENSDARG00000070950

ZFIN ID:

ZDB-GENE-060503-428

Description:

Novel protein similar to vertebrate serine/threonine/tyrosine kinase 1 (STYK1) [Source:UniProtKB/TrE

Human Orthologue:

STYK1

Human Description:

serine/threonine/tyrosine kinase 1 [Source:HGNC Symbol;Acc:18889]

Mouse Orthologue:

Styk1

Mouse Description:

serine/threonine/tyrosine kinase 1 Gene [Source:MGI Symbol;Acc:MGI:2141396]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39233	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa6546	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa11436	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa39233

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104596	Essential Splice Site	18	435	2	9
ENSDART00000132124	None	None	255	None	6

Genomic Location (Zv9):

Chromosome 19 (position 10294680)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	9753219
GRCz11	19	9672144

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACACTAGATCTGTTTATTATTATTGAAATTGTGTTTCTATTTCTCCTTGC[A/T]GAGGTGCTTTTTTATCAAGTCGAACTGATCGTCGTTCCAGTTCTGTTCCT

Long Flanking Sequence:

CAGTACCTACTGAGTAGTAGGCAGTTTCGGACGCAGCCATTGTCTTGTTTTTAGAAATGATAAGTCAAAATTGAGTTTTTCTTTAAATCAAGCTAAATAATCAACCAACGAGGTGAGCAAAATAATCAATTTTTGCTTTGAAATTAGTTTAGTTTGCTTACTCCATTGGCAGATTATATTTACCTCATCATTTAAACCAGCGATTCGCAACCCTGTTCCTAAAGGCAAACCAACAGTACATAGTCAATCTCTTCCTAATTAAACCAACATAAATCAAATCAGTGGAACATTAGAAGATTCCAAAACCTGATTCAGATAAAGGAAACATCCACAATATGTACTGTTGGTGTGCCTTCAGCAACAGGGTTGGGAAACACTGAGCTAAACCAATGCAACTGCATACAATCAGAACTCCAAATTGCATTGGTGTAGACTCGAATAAGAGAAGGGACACTAGATCTGTTTATTATTATTGAAATTGTGTTTCTATTTCTCCTTGC[A/T]GAGGTGCTTTTTTATCAAGTCGAACTGATCGTCGTTCCAGTTCTGTTCCTCTTGCTTTTTCTTGCCATAATGATCATCTTGCTGGTGCTCAAATGCTCCCATAAGAAATCGTATCGTCACAAACACCACAGAAAGGAAAACGACCACACGCAACACCATCATAACACACAGGGATCGCATAGAAGCAACAGACGACACCTGCAAGGCATTGACGGTAGCTATGGCATCCCAGTTTAATATGCACTAAATACTCAAGTCACTGTGTTCTTTATTTAAAGGGTCTTCCAGATCATGCCCCCTTGACTTCCATTATAACAATATTTTTTATTGCAAAGCCATGACACTAAATCATCATGCATGATCATGCAATAATCATGTAAAAAAGTCAATGGGGCAAAAACAGCCACAAACATAATGAAAGGGTGGTCAATTTGCCCAGAGTGTATTGTTGAATTTTTTTTTAAATTTCAAAGCATTTTGCCAAAATATATGTCAAAATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6546

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
ENSDART00000104596	Essential Splice Site	339	435	7	9
ENSDART00000132124	Essential Splice Site	169	255	4	6

Genomic Location (Zv9):

Chromosome 19 (position 10299476)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	9758015
GRCz11	19	9676940

KASP Assay ID:

554-4581.1 (used for ordering genotyping assays)

KASP Sequence:

CTTCATAGATGGTCCTTTGGYATTTTGCTCTATGAGATGGTGACATTAGG[T/C]GAGTGTGTCCGTTGACAAGTTTTGTGGTTTTCAGTTACAGAGAGCATGAG

Long Flanking Sequence:

TCAATCAATCAATTCAGACCTTTTACTTTGGCATGCATTAATCATGGCCATTCTTTTATGAGCACTTAAACAGAAAATTCTTGATTTATACAGTAGAGCAAAGCCTTTATTGTCACACCCAGTGTTATTGCACTGACAAAACCTGTACTGATTGCAGGAGTATCTGCATAGTAAGAACTGCATTCATGGGAACGTCAAAGCTCGAAGTGTCCTGGTTGGTCAGGATCTCTCAGTCAAGCTGTGGGGTTTGGGTCCAGCATATCACAGAAAATCAAATGCGAGCTCTATAGAGGATCTAGAAGAAATAGAAACGAGAAAATGGCAAGCTCCGGAATTGCTGGCACGACAGCCTCTGCAGCAAAGCAGCGACGTGTATGTTTCTTGTGATGTTTTATTTTTGGTTATTTATTAGTGTTATTGTGATGTTTAAACTTAAAATTGTTTTCGTTTCTTCATAGATGGTCCTTTGGCATTTTGCTCTATGAGATGGTGACATTAGG[T/C]GAGTGTGTCCGTTGACAAGTTTTGTGGTTTTCAGTTACAGAGAGCATGAGGAATAAAAAAACATCTATAAAATTGCAGTTCAGACTAGGGCTGGGCAATATAACAGAAATCTTATACCATGATATCGAGATATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATCATGATATAGTACCATTTCGGTACATTCAATCAAATAATAGTTTATATTACATCTATATATACACTCATAAATGAACTACCCATGTGATACTATTTCTCATTTAACTTTAAACTTCAGGAGAGATGTTTGATTAAAAATATATGTAGAGTTGCTGAAGTTTGCCCTGCGCGCTTACGGTTTTTAAGAAACTTCTTTGGTGCGTCAATCTGGTCAATGCTATTATTCAAAAAGGTAATGATTCGCACTCATCAAGTAATTGCTTTGTGTTGTTTTTATTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11436

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
ENSDART00000104596	Nonsense	410	435	9	9
ENSDART00000132124	Nonsense	240	255	6	6

Genomic Location (Zv9):

Chromosome 19 (position 10303640)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	9762179
GRCz11	19	9681104

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCCGAAAGCTCCAATCAGGAGAGRGAAGYGCAAATGATCAGGCAGTGCTG[C/T]GAGTGTCGGAGCCGCTGGACATAGAGAAATACATGCAAGAGGCGGGATWT

Long Flanking Sequence:

TGATATAATTTGTGTATTTGATAATTTCTGTTTTTGTTTTTTAAAATAATAGAAGGTCTATCTTGGAGAAAAAGAATGTACGTGTAAAAAATCTCAAGACAACAAATTTTTTTTTTGTTGCTTTAACTTATTTTAATAAATTAATCAGGTTTTAACTACATTTTTAAACTTATTGAAAGTTTAACTTAATGTATTAGTCAGTTTGATAAATGTAAGTTGAAACGACTAGAAAAAGTTCATTTGATTTAACTAAAAATAGCAACAAGATTTATAGAGTGTATAGAATCACCTATATTTCTAACATTTTATTTGGATGTTATTTTTATAGTATGATTTTTTTAAATGCAATTTTTATTATAGTTCTGTATGCCTTTATATTTTCTAGATATTCTATCATGAAGTCCTGCTGCAAGTGGAGAGCAAAGGACCGTGTCTCATTGGCAGAGCTGATCCGAAAGCTCCAATCAGGAGAGAGAAGCGCAAATGATCAGGCAGTGCTG[C/T]GAGTGTCGGAGCCGCTGGACATAGAGAAATACATGCAAGAGGCGGGATATGGAGAATCACTCAATTATGCTGTGCTCTAATGATGACTTAAAGGTGTAGCTTACTCAAAAATGAAAATTCTGTCATCATTTACTCACCATTGACTTGTTCCAAGCCAGTATGTGGAATACAAAATAAGATTTTTAAATATGTTGAATTCCATATTATTTGTTTTTCCTACATGAATGTCAGGGATTGCAGCCCACCAAGCATTTTTTTTTGTTTTTAAACGATATCTAATAGATGTCTTATAGACGTCTAAACATAGTCATCCTGGCTTAAGTAAGGCTAAATTTGGGCTGTCAGTGAAAATCTAATAGATGTCTAATAGGCTAAAACTAGACTAGTCATCAAATAAACGACTACACATATAAAGTCTGTTTGTCTATTTGACGACTAGTCTACTTTTGGGCTATTCTTAGATGTCTATTAGATTTTCACTGACAGCCCAAGTTTAGCCT

Associated Phenotype:

Not determined