ZMP

pla2g4a

Ensembl ID:

ENSDARG00000017141

ZFIN ID:

ZDB-GENE-041014-325

Description:

Novel protein similar to cytosolic phospholipase a2 (Cpla2) [Source:UniProtKB/TrEMBL;Acc:Q5RIP7]

Human Orthologue:

PLA2G4A

Human Description:

phospholipase A2, group IVA (cytosolic, calcium-dependent) [Source:HGNC Symbol;Acc:9035]

Mouse Orthologue:

Pla2g4a

Mouse Description:

phospholipase A2, group IVA (cytosolic, calcium-dependent) Gene [Source:MGI Symbol;Acc:MGI:1195256]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43487	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37091	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43487

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000023211	Nonsense	105	729	4	18
ENSDART00000135915	Nonsense	80	697	3	16

Genomic Location (Zv9):

Chromosome 20 (position 34157329)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	34229842
GRCz11	20	34132721

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTAATGGATGCTAACTATGTTGTGGATGAAACGTTGGGTACAGCCTCATA[T/G]GACATCTCTAAACTCAAAGTTGGACAAACAATGCTGGTGTCATTCCTAAT

Long Flanking Sequence:

CTTTTATTCTAGCTAAAATAAATCAAATATGACTTTCTTCAGAAGAATAAAAATATTGGAAATGCTGTGAAATATTCCTTGCTCTGTTAAACATCATTTGAGAAATATTAGTTTTTAATTTTTGTAATTTGATTTTGTACTTTTGACACAGTATTTAACTGTAAAATGAACAGTATTTTACTGTAGGAAAGTTACGATATGTTACTGTATTTTAAATTTGCACTTTAAAAAAATTACTGTATACATACAATTCAGTAAATACAACAAGATTATGATACGATTGTAAATGATTAACAGCACGTTACTTGTTAACTGCTGCCAGTATGATACTGTAGATTCTACAGGAAACTGTTAACAGTGTTCAAGTGTATGTTGATCAGGCTTTAAGCACACACTCTTCATGTGCGCATCAAGTTGTATTGTGTTTGTCCTCTTGTTTCCAAGCTGACATTAATGGATGCTAACTATGTTGTGGATGAAACGTTGGGTACAGCCTCATA[T/G]GACATCTCTAAACTCAAAGTTGGACAAACAATGCTGGTGTCATTCCTAATAGGCAAAGTAAGTTCAATCAAACTAAGGATTTGAAGTTAAATATTTGAGGAGCGCTTTCATTTAAAAAACACATGGGTTGCTTATAGTTGCACCAATAATAAAGCTGTACATTTATGTTACATTTACTTTTTTCCTTACTTGATCTGTATTGTGGTATTAATGCCTGTGGTTGTTGTTTCACAGATGACCAATGTGTTTTTAGAACTTTCCTTGGAGGAGTGGTATGTATCATCATGAACAAAACTATACAATATTATGAAAAGTTTAGAGTTAAAACTACCCAAATTGGACTTTTTCACCGTTCTCAGCTTAGCGATGGACCTGCGATTCAATCTGGATCTGTGTCCTAAAGAAAAGCTCTACAGACAACACAGACGAGACAAAGTCATGCTGGCCATCAAGAAACTGCTGAACATCGAGAAACCTTCTTCCCTCCCTTGCTCTCCTCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37091

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000023211	None	729	729	18	18
ENSDART00000135915	Nonsense	692	697	16	16

Genomic Location (Zv9):

Chromosome 20 (position 34168959)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	34241472
GRCz11	20	34144351

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGATTCCATCTCGCTGCTCTGCATCTCTTTCTCTCAGTGAAGCACAAAAG[A/T]AAAAACGCCTAAAGAAATAGTCTAAAGGACAAGCCTGTTAATAAGGAGGT

Long Flanking Sequence:

ACAAAGAGAGAGAATTTGCAGACTTTGACATCTTTGATGACCCACAGACGCCCTACTCCACCTTCAACTTTTATTATTCCCATCAAGCCTTTACCCAGCTGCATGATCTGATGGAGTTCAACACACTTAACAACATAGAGGTCAGTTCAGCTCAGAGGAATCATGCTGCTTCATGTGTTTTAAAAATATGAACATTCCATGGAAATTATAGTTGATAGTACAATTTTTTTTCCCCCAGTTTCAATGGGAAAGATAAAGTTTACTTGATAATATGAAACACTTGAATACAATGAGGTGTAGCTGCTATCGTGTTCTTTTGTCTAATCCTTGAATCGTTTATGAAATATTTTGTGTGTTAGCTTGTTTATGCAGGTCTTGTTTTGAATGTTCTATCACACTTTATCTAGGTCATCAAAGAAGGCATAAAAGATAGCATATTGTACAGGAAGGAGATTCCATCTCGCTGCTCTGCATCTCTTTCTCTCAGTGAAGCACAAAAG[A/T]AAAAACGCCTAAAGAAATAGTCTAAAGGACAAGCCTGTTAATAAGGAGGTGGCGTAAGATGGCATTCTACGCACAAGAAGTTTACACATGTCACATCTCTTCATGGAAACCTTTTTTTTAAACTGAAAACAGCTCAAGAAACTGTGAAACCTGATAATCTGGTTTGGGCCACATGAACATTTTCCATCTAGTTGTTTTCAATGTTATCTTTTAAAGTTAAAGGAAGAACTGACTGACTCAATGAAAACAGCGTTTACAGTCTCGTTGTTGAATTGAGCCAGACAATATGGTATGTAATGCCAGAGTAAACAAACTATATTCTTAAACATTTGTCTGTTTAAAGTGCTGAAAGATGTACTTCAAAGATGTGAAGCAGACAATTGTCTTAAAAATTGATTGTCTTCAGCAAAACAGACTTTGCAAAGACTGTTGGTGTCCAAGCAACATTTTAATTTTCTGACTGCACAGAAATGTTTTTAGAGATCTTCTTTTGTTTTCTA

Associated Phenotype:

Not determined