Busch Lab

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