ZMP

si:ch211-214c7.6

Ensembl ID:

ENSDARG00000060184

ZFIN ID:

ZDB-GENE-061207-17

Description:

Novel protein similar to H.sapiens PKN1, protein kinase N1 (PKN1) [Source:UniProtKB/TrEMBL;Acc:A2BGV

Human Orthologues:

PKN1, PKN3

Human Descriptions:

protein kinase N1 [Source:HGNC Symbol;Acc:9405]
protein kinase N3 [Source:HGNC Symbol;Acc:17999]

Mouse Orthologues:

Pkn1, Pkn3

Mouse Descriptions:

protein kinase N1 Gene [Source:MGI Symbol;Acc:MGI:108022]
protein kinase N3 Gene [Source:MGI Symbol;Acc:MGI:2388285]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25649	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa38288	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa25649

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
ENSDART00000084512	Essential Splice Site	383	929	7	22
ENSDART00000132555	Essential Splice Site	358	904	6	21

Genomic Location (Zv9):

Chromosome 1 (position 46289257)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	45126769
GRCz11	1	45818564

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTGGCAGCGTTAGTGGAAAAACACCCCTCAAAACCGACGAACTCTCCTG[T/C]GAGTGTGTGAGGATGTCACGCTTCTAGTGCGTTTTGGCTGTAGTGATGTG

Long Flanking Sequence:

TTGGCCATAGTGTTTGAGTGCGGGTGTGAATGTTAGGTGTTTCCCAGTACTTGGTTGCGTCTGGATGGGCATCCGCTGCGTAAAACATATACCGTTTCCGGTTCATTCCTCTGTGGCGAACCATGATATAGTGTAGAGGACTAAGCCTAAGGAAAATGAATGAATGAAGGAATATTATAATTTTAATGCTGTGCCAACATTTGCCCACGGCGTTAAAATTGGTATCAATAGTATTCAAGTTAGAAAGTCAACATTAGTCGTAATGTACAATCTTCTAATAATGTTTTTTCCCCTGTTTTTGCAGGTCGGCTCCAGGTGACATTATTGGGCTGTATGGGTCTTCTGGAGGTGGTTCCCGGACGCTCTCGTGGTAGCCAGGTGGTTTTACCGTGTTACAGTCCAGGAGAGGGACGATCATTCATGCGCAGTGGAAAAGGCCTGTATAGTCGCAGTGGCAGCGTTAGTGGAAAAACACCCCTCAAAACCGACGAACTCTCCTG[T/C]GAGTGTGTGAGGATGTCACGCTTCTAGTGCGTTTTGGCTGTAGTGATGTGCGAGTTCTGATATAACTCAGTAATCTGTTGTGTCTGTCATGTGTGATGACAGCCCTGCCTTGAGCAGAACAGGATGTCGTGCATCTGAGCTTTTAACACATGGGGTGTTGCATTGCCAGTCTGGCAAGTCGTTTGCTGACGTTTGCAACATTTGCAGCTTGTGTTTACTCGCATAGTATATTTTTTGAAAAACAAGTTGTGTTTAGCATCTCAAATGTGCTGCGATTTGTGTTACAAAATGACGTGTATAGTGCAGTAATTACTAGTAAGGCGTACTTTTATTTCTTTTTCTGTCCGTATTGGGGTTTGTTTTGGAGAGGAAGTAAAATACATTTTTATGATATTAGTAGACTATGCAGACGATGCATATATACATTATCTGACAAAAGTTTTGTCATCGATCCCATTATAACCTGACTTCTAGTTCAATCAATTGGAAAATTGGCCGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38288

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000084512	Splice Site, Nonsense	494	929	11	22
ENSDART00000132555	Splice Site, Nonsense	469	904	10	21

Genomic Location (Zv9):

Chromosome 1 (position 46296501)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	45134013
GRCz11	1	45825808

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGTAACTTTTCTCTTTTGTGTATGTGTTTGTTTGTGATCATACACAGGT[A/T]AAGCATTTTTGCGAGCTCGACAGATGAACGTTGATATTGGCACATTCGTG

Long Flanking Sequence:

ATCACAAGTCTCAGCTGTGCCTCATCAGCCTTGATGAGCAGCTGGTGTTTGGCATGGCCTGATAGGACTTGTAGTTCCTAAACATGACATTTGTAGTTCTCCAGCGATCTGTCAGGAAGGATCACTAGTGAACATAACTGAGAAAATAATAATAATTAACAATAATAACAATAATGATCATTTACCCACCTTTTTCTCTCACTCGTGTTTCTAAACTTTGCTCAAATTCTTTTTTCCGTTGATCACTAAGCAAGATATTCAGATAAATGTTGTGCCATTTACATCCATAGTAGGAATTAAAAATACTATGAAAGTCATTGGCTGTTTTTTCACCATTCTTCAGTATATCATCCTTTGTGTTCAATAGAAGAAAGAAAATCAAACAGATTTGGAACAAGAGGATGGGTAAATGATGGCATGAGGTCAGTGAGCTCCATCTAGTGGTCAGTGTTGTAACTTTTCTCTTTTGTGTATGTGTTTGTTTGTGATCATACACAGGT[A/T]AAGCATTTTTGCGAGCTCGACAGATGAACGTTGATATTGGCACATTCGTGAGGTTACTGAGGAACGCCATACCAACCGTCAACAACACAGGAACCTACAGCCCTAACGCGCACACTCTACAGACTGGGTAAATCACACACACCATCAGATGTGCCTGTACCATCTTCCGCAATTTGTAATAACAGTGTCAACAAAACAAAAACGGTTGCTTGTGTATCTTTTTGTTAAGGTTATAATGTTACACAAATAGTACATATTTAGATAAAATGGTAGATTTACATCTTTGTCATCCTGTTTATTATTTATAAAAGTCTAAAATGTCCATACTTAACTGAAATTACATTTGTTCTTAGATATTTTTTTGCAGTTACTAACATATGTGTTTGTTACAGGGAGATATCAGTGGAGAAGTTGAGTTTAGATTTTGATTCACCAATGAAGGTGGACATCCGGCGGGAGGTGACAGATATAAGCACTCCGGTTAGAGACTTTCTCTCTCT

Associated Phenotype:

Not determined