ZMP

prkd1

Ensembl ID:

ENSDARG00000075949

Human Orthologue:

PRKD1

Human Description:

protein kinase D1 [Source:HGNC Symbol;Acc:9407]

Mouse Orthologue:

Prkd1

Mouse Description:

protein kinase D1 Gene [Source:MGI Symbol;Acc:MGI:99879]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6481	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa23102	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa6481

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
ENSDART00000110322	Essential Splice Site	268	878	5	18

Genomic Location (Zv9):

Chromosome 17 (position 28998596)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	28922523
GRCz11	17	28939486

KASP Assay ID:

554-5194.1 (used for ordering genotyping assays)

KASP Sequence:

TTGCAAGAAGCTCCTCAAGGGCCTGTTCCGTCAGGGACTGCAGTGCAAAG[G/A]TAGGATCCGCAATATCTCAAGCTTTAGTTAGAAAACAATCATCTTGAAAC

Long Flanking Sequence:

CAGATTAATTTAATTTATTAATTAATCTAAATTTAAAAAATATGACACTTTTAGGACTTGATTTGTTGTCCAGGGTCATATATGAAACCTAAAACAAAACAATAACAATCATAAAACAGAACAAAATGTAGGAGGTTGTGCATGAATTCATGAATGAAAATGTGATCGTTTATCAGGTTAAACACAGTTAAACATGTGACGTATACATAAAGGTCTTTGTGTTGTGGGGATAATTAAAAAAAGTCTATCTCAGATGATGCACATCACAATGTTCTACATTATTCATCCACAGCAAAAAACCCCATCAGACATCTTTCCAGGAAGAGGCCGTTCCAATTCCCAGTCCTATATAGGTCGACCGATAGAGCTGGACAAGATCCTGCTGTCTAAAGTGAAGGTGCCACACACGTTTGTCATCCATTCCTACACGCGACCCACTGTTTGCCAGCATTGCAAGAAGCTCCTCAAGGGCCTGTTCCGTCAGGGACTGCAGTGCAAAG[G/A]TAGGATCCGCAATATCTCAAGCTTTAGTTAGAAAACAATCATCTTGAAACTTTTACGCCTCATTGTCACTCAGTAATTCTTGTAATGTCTTATTGCTTCGCATAATAATGCGCCTCATCTAAATCCCTTCTGATTCCAATGTTCCTGTGTAATTCGAATTCTCTGTAGTAAAAACGATATTAACTGATCTAAGCCTCCATTGGAGAATAATCATACATTTTCGTGACTCATTACTTTATACAGAATATCCATGAAACTAATTATACAAAGTACACAAATGTGTTTTATGTAATATTCACTGCAATATCTCCAGAAGATTATTTTCCAATTATATGAGTGATGTATGGTTTTAAAATGAAGCTCAGTGGGGCTGTTTTCCCACATATAAAACTAAAATGCTGAACATTGAATGTGCTGAATATGACTGAATACAGCCTATCATTAATGAATAGATAATCAAACAATAATATGAAACTGACTATATAAATATTGGGTGATTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23102

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

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110322	Essential Splice Site	361	878	7	18

Genomic Location (Zv9):

Chromosome 17 (position 29004357)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	28928284
GRCz11	17	28945247

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTGGAGATTTTCAAGACCTAGACCCGGATGAGTCCAACAGGATCATCAG[G/A]TAGATCCTCTGCACTTCTAGAAGCCCTGTAAACATAACCAACATCACAAA

Long Flanking Sequence:

TAATATCAGAGCGACACAAAAGTGTTTTTGTACATTTACAGTAAGCATAAAATCTTTTGCAAAGGCTAAAGAACAAAATGATATACAGTAACTGCAGTGAGTCCTCTATTATGCTATTGCCTATTTATATTAGAATATTTTAGAATAAAACATTATTGATGTACTTTTCTGAATGGGAATTTGAAACTGCTCATTTTCAAGTTCCAGGATTAATGGTGTTAAACTGACAGCTTTTTTTCATCAAATATATAACATCACATGACTCACTTTATCTTCCTGTTCTCTTCTTATGGCGGCTCAGATTTGTTGAGTCCCGGTGCTGAATCAGATGTGGTCATGGAGGAGGGCTGTGATGACCACGATGGGGACAGACACAGTCCGCTTATCGATGACATGGAAGAGTCTCTGGTGGGGGATTCTGCTGCTTATTTGGAAGCTGGACATGGTGAGCTTGGAGATTTTCAAGACCTAGACCCGGATGAGTCCAACAGGATCATCAG[G/A]TAGATCCTCTGCACTTCTAGAAGCCCTGTAAACATAACCAACATCACAAATGTTCAGTTTTTTGACAATATCACTCACTTGTCTTAAGTCAATGACTGTGTATTGTAGATAAAAGTACTGGATGCAAAATAAAGAAATACTGACTTTAAATGACTAAATATAATCAAAGTCAAAATGATTAGCCTTCCTGTAAAAATGATCAAGACTCTTTTCAGCAACACATTTTTAAGCAAATTAATTTTTAAAACTAATTTCTTTAGTTTTTGCCGCAATTACAAGATATTAGTACTTGGCTTAATTTGCAATTTAAAGGCTGAACTAGGGTATTAGTCTAGACAAGTTGATTAGACCAGTGTTTCTAAACCACGTTCCAGGAGCACCACCAGCTCTGCAACCGAGCATACAATATAGCTTGCTAAAATCAGTATGCAAGCAGAATTGTATGTTCGAATTAACATAATTAAAATAAAATTAGGTAATCATGTAATCAAGTACACGGA

Associated Phenotype:

Not determined