ZMP

si:dkeyp-81f3.3

Ensembl ID:

ENSDARG00000078745

ZFIN ID:

ZDB-GENE-070705-553

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:A5WVZ4]

Human Orthologue:

PNPLA8

Human Description:

patatin-like phospholipase domain containing 8 [Source:HGNC Symbol;Acc:28900]

Mouse Orthologue:

Pnpla8

Mouse Description:

patatin-like phospholipase domain containing 8 Gene [Source:MGI Symbol;Acc:MGI:1914702]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15305	Nonsense	Available for shipment	Available now
sa33425	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15305

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
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Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108928	Nonsense	141	688	1	10
ENSDART00000134709	None	None	429	None	8
ENSDART00000145953	None	None	109	None	2

The following transcripts of ENSDARG00000078745 do not overlap with this mutation:

ENSDART00000135165

Genomic Location (Zv9):

Chromosome 4 (position 12692907)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	13629534
GRCz11	4	13628383

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACAGAGGAGAATCAAYACCATCTCAAATCAAACCTCTTCCCAAAGTGAAT[A/T]AAGATCATATTATAGCAGCGCCTGTGTGCCATAAATCTAMACCTGAAGCT

Long Flanking Sequence:

CTTTCATCTGCAGGGCTCAGCTGCTCTAATGCCAGATCCACACTTCAGGAGTATCCCAGAATTCCCTGTAATAACCCCACCGCATGTCGCGCATCAGGAGCACACTGGACACCGTTACCAAAGCCGTGAGCGGGACGGTGAACACAGACCTCCTCTCTAAAATCACACGCCTCAAACCAGGAAAAGCTTTAGAGGTCAAGGTGGAATGTCCTGCCGTGGAAGCCGAGGCCGGAGCGGTCATGACTGTGGCTGCAGCTGAGCCACAAATGGAGAAAGAGGGGAAAAAAGACATGGAAGACTCCCCCAAATCTGGAAACGCATCCAGCACGGGTGCAAAGCAAACACTACAGCGCTTCCAACCCTCTGCGTTCACAACCAACATGGACGAAACATACAATCACCTGGCTGAACATGTCAATACCTACTTTGGAAGTGATGACAAGCGGTTGGACAGAGGAGAATCAACACCATCTCAAATCAAACCTCTTCCCAAAGTGAAT[A/T]AAGATCATATTATAGCAGCGCCTGTGTGCCATAAATCTACACCTGAAGCTAATCCTGCTATTGATAAAAACAGCTCTGTCCCACAAGCACCGTCCATTCCAGTTCAGGATGAGGGGGTTTCGTCTGTTCCCATTTCACCGAGAAAAGGCATCAGTCATTATCTGTCATACCCTAGGCCCAGCGTTCAGGCTTTTGTTGGGAACTATATTGCGCCTCTGGTACCGAAGTTCAGGGCGGATGCAAAAAGTGGTGCAGGGGAGAAGGACAAAGCCTCTGGATCTGAACCGGATGTGTCTCAGGATGTAAAGAAAGCAGAGAGCAAGGAGCAGAAAGAGGCTGAGGAGAAAGCACAGAGACTGCTGTCTCAGAGGGAGAAGGTAAAACACTAGGCCAGTAAATATAATAGAACATGTCAGTTAATTTAACTGCACAATCAAAATAAATCGAAAATATTGAAATCATTAAAGCAAGATTAAAGTAAAGCTTAAGAAGATAGTAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33425

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108928	Nonsense	673	688	10	10
ENSDART00000134709	Nonsense	414	429	8	8
ENSDART00000145953	None	None	109	None	2

The following transcripts of ENSDARG00000078745 do not overlap with this mutation:

ENSDART00000135165

Genomic Location (Zv9):

Chromosome 4 (position 12707161)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	13643788
GRCz11	4	13642637

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGTCCTCACGCAGGAAAAAGGTATCGTTCAGAAGCTCGCAGAATGGGTA[C/T]AACTCAAAGCTGACATGTACGACGGCCTTCCCTTTCGCTCTAAACTCTAA

Long Flanking Sequence:

TCTATATAAATTAATTAAAAAATATAATGCGAGTGTATATTTATATATTAATAAAATATAGTTAGTAAAAAATATTATTAATAATATAAGATGAAGTAAATACATATAAAAAATAATTTTAATAGATTTTGTTTCATTCATTTACATGAAATTTGTTACTTAAAAAAAACTAAATAACGAAAACTGTGATATGACCCTTTTAAATCATTAAACACAGTTATTATTTTGCTGTTTGTGACTATATAATCCTATATTTCTCTCTTATTTTAATTATAGAGGTCCACACAATGCTGGACGCCCTCCTCCCCCCGAACACCTACTTCCGTTTCAACCCTTACATGAGTGAGGACGTCCCGTTAGACGAGAACAGACAAGAGAGGCTGGACTACCTGCAGGCTGAGGGGCGTCGTTACCTGGAGCGCAATGAGAATAAGCTAAAGAAAGTGGCTAGTGTCCTCACGCAGGAAAAAGGTATCGTTCAGAAGCTCGCAGAATGGGTA[C/T]AACTCAAAGCTGACATGTACGACGGCCTTCCCTTTCGCTCTAAACTCTAAAACCCACACTCTAAACCAAACTAGCACAACCCCTGACGTTTTCCGTGTAGTGTTAAAAACAATGCAAACTGTGTACTGCAGTGGAAAGGAGTGTTACCGTGCCATTTGATAACTGAAAATAGGGAATCAAGTCTATTGCCTCATATTGACGAGCACATTAGAAGGTAAATTGGTTCATCTGGTTTGATTTATACATTATATATATATATATATACATAAATATTTACCTTGTGGATCTTATTTGAAATGAAGAGCCTCGCAAGCATGAAATGTTAGTGGCAATGCTAACTAGCTAACATTTGAGTTTGCTGTTTGTTTGTTCCTACTAATGTCATTTTGAGTCTGAAATAGTATAAAATTGCTGTTGTGTAGTGTTTTCACTTAAAAAAAAAAAAGTTTCAAGACAATACTGCGAGTAGTTGACTAAACTAACACTACTGTAGTTAGCAT

Associated Phenotype:

Not determined