Busch Lab

ZMP

LPL (1 of 2)

Ensembl ID:
ENSDARG00000091659
Description:
lipoprotein lipase [Source:HGNC Symbol;Acc:6677]
Human Orthologue:
LPL
Human Description:
lipoprotein lipase [Source:HGNC Symbol;Acc:6677]
Mouse Orthologue:
Lpl
Mouse Description:
lipoprotein lipase Gene [Source:MGI Symbol;Acc:MGI:96820]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa39502 Nonsense Mutation detected in F1 DNA Not yet available
sa30345 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39502
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000124328 Nonsense 123 530 3 10
Genomic Location (Zv9):
Chromosome Zv9_scaffold3497 (position 33047)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 17537013
GRCz11 2 55369565
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGCTAATGTCATTGTTGTGGACTGGCTGGATCGGGCCAACAAACACTA[C/A]CCCAAATCAGCAGAAAACACCAGGCTAGTGGGGGCCGACGTTGCCAAGTT
Long Flanking Sequence:
TGCACATTATTCAGACACTAGATGGTGCCAAACAGCCAAAAACGCAAAGCAGACAGAAACAAAAATAGCAGAATAAAGCGACTGACCAAGTATTATTACAAAAACAGTCGCATGTCAGACAAGCAGATGCATATGAATGTAAAGGTACTTAAAGTATATAGATATGAACGTGTTTACTGACGGACAAGGTGATTCGAAGTTCCCAGATGAGGTGTTATTTAGCAGTTGTTATCTCAGAATAACAAACCTTGGAATGTTGCAAATCTGACCAATCAGATTTGAGCATTCCAGACAATCATATATTTTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTAATCCCTCTTATACTGTCTCTAGGTTGCGGGTCTGTTTGAGAGCTGGGTTTATAAGCTGGTGACGGCTCTGTATGATCGTGAACCCAGCGCTAATGTCATTGTTGTGGACTGGCTGGATCGGGCCAACAAACACTA[C/A]CCCAAATCAGCAGAAAACACCAGGCTAGTGGGGGCCGACGTTGCCAAGTTTGTCAACTGGCTGGAGGTAGGCAGAGATTTGCATTGCTAGCATTGTACGTTTTATCGCTGTTGTATTTTTGTAATAACGTCATGACAGCCAAATATTACCTCAACCTTAGTACACTAAGGTTGAGCAAAAACACATAAATTAGAGATAATCCTTCCAGGTAAAAATATATAAATAATAATATAATAATAATAATAATGATAATATAATTTAATAATATAAAATATAAATTAAATAATATTTTAAAAAATTATATATACATATATAAATTTAAATAAATAAGTTTTCTATTCTGATTTCATGGTAACTTCTAATTTTTACCTATGTATATATACTTTTAAAATAATAATAAAAATAAAAACAAAACAGTTTTAAATTAAATAAAAAAGTTAAGTTAAATTAAATTACTCACTCACTGTTCTTTAGCTTCAGGGCTCACCACAGTCTAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30345
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
ENSDART00000124328 Nonsense 332 530 6 10
Genomic Location (Zv9):
Chromosome Zv9_scaffold3497 (position 45510)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 17549476
GRCz11 2 55382028
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATACAACGTCAAGAAGATCCGCAGCACCAGAAGCACCAAGATGTACCTC[A/T]AAACCCGCGAGATGATGCCCTTTAAAGGTAAGGGGGGATATTTTGACTGT
Long Flanking Sequence:
GTCTTTTTAAAGAAGCATAATCGATTTAAAAGTTGATGAGTGTGCTGTAACTGATGTGTTTTATGTCGTAGAACAAAACGTGAAAGTATATTGAGTTGGTGTTAGCCACGGACCTTATTTGAGCGATTTTACTGAAACCCCATTCAAAAAACCCATTGACTTTGGGACGAGGGAACCGGAAGTGCTAAAATGCTAACTCGCTTCCGGGTTTTTGCATACAAATTGACGTCATAGTTCCTCCACTCTATATCTGACTGTGATCTCCTCTGTTTTGGTTTGTGTCAGATATGGACCAGATCGTGAAATGTTCTCACGAGCGCTCCATCCACCTGTTCATCGACTCTCTTGTGAATCAGGCGTATCAGAGCTGGGCGTTTCGCTGCGCCTCCAGAGACTCCTTTAATAAAGGCCTGTGTCTGAGCTGCAGGAAAAACCGCTGCAACACACTGGGATACAACGTCAAGAAGATCCGCAGCACCAGAAGCACCAAGATGTACCTC[A/T]AAACCCGCGAGATGATGCCCTTTAAAGGTAAGGGGGGATATTTTGACTGTGAAACATACTGGGCTCCATTTTAAGGATCTAAGCGCAAAGTCTAATGCTGTGTTCACACCAGACGCAGAGTGCTGGATAAATCACGCTATTCGCGTGTAAATAGCCGCGTGAACATTTGAGTTTACTCGCTTCATTCGCGTGTCAAATTCACTTCAGAACAGACGCGGATTCGCGTGATGGGCAGGGCTTCTGTCTGCCCGGTGACTGTAGCTTCGTTGCTAAATGGCTAACATGGATTTTATGAAGAAAATAACAGTGTTTATGTACTTTATAAAGGCTGAAAAACAGTGTCGATACGTTTAGGGTCGTGTCTGAGTCCACTGCATGCTTTCAGAGGTGCATCCAGCTGTGTGAGCTCATAAACTCCTCCAGAAACTGAACCTGGATCACGGAGGCTTTCAACGGTGCTTCTGACTGAGCCAAGCCGAGTTTGATGAACTGTTGTCGGT
Associated Phenotype:
Not determined