Busch Lab

ZMP

APOL2

Ensembl ID:
ENSDARG00000073718
Description:
apolipoprotein L, 2 [Source:HGNC Symbol;Acc:619]
Human Orthologues:
APOL1, APOL2, APOL3, APOL5, APOL6
Human Descriptions:
apolipoprotein L, 1 [Source:HGNC Symbol;Acc:618]
apolipoprotein L, 2 [Source:HGNC Symbol;Acc:619]
apolipoprotein L, 3 [Source:HGNC Symbol;Acc:14868]
apolipoprotein L, 5 [Source:HGNC Symbol;Acc:14869]
apolipoprotein L, 6 [Source:HGNC Symbol;Acc:14870]
Mouse Orthologues:
AL591864.1, AL592187.1, AL592187.2, Apol10a, Apol10b, Apol6, Apol7a, Apol7b, Apol7c, Apol7e, Apol8, Apol9a, Apol9b
Mouse Descriptions:
apolipoprotein L 10a Gene [Source:MGI Symbol;Acc:MGI:3036238]
apolipoprotein L 10b Gene [Source:MGI Symbol;Acc:MGI:3043522]
apolipoprotein L 11a [Source:RefSeq peptide;Acc:NP_001171004]
apolipoprotein L 11b [Source:RefSeq peptide;Acc:NP_001137158]
apolipoprotein L 6 Gene [Source:MGI Symbol;Acc:MGI:1919189]
apolipoprotein L 7a Gene [Source:MGI Symbol;Acc:MGI:1923011]
apolipoprotein L 7b Gene [Source:MGI Symbol;Acc:MGI:3583950]
apolipoprotein L 7c Gene [Source:MGI Symbol;Acc:MGI:1920912]
apolipoprotein L 7e Gene [Source:MGI Symbol;Acc:MGI:3704456]
apolipoprotein L 8 Gene [Source:MGI Symbol;Acc:MGI:2444921]
apolipoprotein L 9a Gene [Source:MGI Symbol;Acc:MGI:3606001]
apolipoprotein L 9b Gene [Source:MGI Symbol;Acc:MGI:1919148]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa17264 Nonsense Available for shipment Available now
sa33186 Nonsense Mutation detected in F1 DNA Not yet available
sa6898 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17264
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112891 None None 275 None 3
ENSDART00000130102 Nonsense 4 557 1 4
Genomic Location (Zv9):
Chromosome 3 (position 29830579)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 29548618
GRCz11 3 29679460
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTTGATTCTTGAMACAGAGAAGAACTACAGCATCTCCTCTCMGAGTA[T/A]GTCGAAAACACTCTAAACTACATCCAGACAGTGAGAGACTTCTGCGACAA
Long Flanking Sequence:
TGATGATTAGCTGATACTATGCTAAATGCATAAAATCTATTTGACAAAAATGATCACCATAGACATTTAGGTCAATATACTTTCAAAATCCGAGTTTTCAATATCAGCTTCATGATTGTTTACATTTGAAACATTTGGTGACACAGTTGGCATGAATTTATGTGATTGCAAAATATTGCGAAAGTTAGAGCAAAACCCAACAGTGTATTGCAGTAAACGCGATGCAACAAACTGTTGTCACGAACCTAACCTAGATATTATCACAAAAGGGAACTTCAGCTCTCTTGTTTTGCATGACTGTAGGGCAACCTAAAATCTGCCCTGCCCATTCAGAATGAGCTGCTAGTTATGTTAAGATATAATATCATATATTATACATATTTTGAAATGCTTTAATCACATAATTATGTGCTCTGATTAAATATATTATTGATTTCTAACAAATTTTGCTGTTTTGATTCTTGAAACAGAGAAGAACTACAGCATCTCCTCTCCGAGTA[T/A]GTCGAAAACACTCTAAACTACATCCAGACAGTGAGAGACTTCTGCGACAAGCAACCAAAATGGACCCTTCAGAGAGAGACAGAGCTGGAGAACATGAGAGACATCAAGGACCAAGCAGACCAAGTCAGTCTGAAGTTTGACCACGTTCAGCGCTCCGAGAACAAGTTCAAGGCTTTCGGGGAATTCCTGTGGAGTGGTTTAACTCAGGTCACAGCTGAGTCCAGATATCAGGAGCTGGAGAAGAATCTGGGTGCCGTCCTGAAGGACACCCTCGAGGGGCTAGAGAAACTTGACCACTTTCTGGATGCAGTGGAGAAGCTTAGAGTCACATCGCTGTTTGTGTTCACCGGACGAAGCTTCTTGCCAAAAGGAGTGAGTCCAGAGAGTGTGCGATCGGTCATCACAGCTGCCAGGATGGCTTCTCCTCTTCTAATTCACTTCAAACGAAATGCAGAAACCTTTTTCCTTCCTTCACTCAGTAATCTGGATGTCCTGACCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33186
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
ENSDART00000112891 None None 275 None 3
ENSDART00000130102 Nonsense 153 557 1 4
Genomic Location (Zv9):
Chromosome 3 (position 29830134)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 29548173
GRCz11 3 29679015
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTCATCACAGCTGCCAGGATGGCTTCTCCTCTTCTAATTCACTTCAAA[C/T]GAAATGCAGAAACCTTTTTCCTTCCTTCACTCAGTAATCTGGATGTCCTG
Long Flanking Sequence:
TTTGCTGTTTTGATTCTTGAAACAGAGAAGAACTACAGCATCTCCTCTCCGAGTATGTCGAAAACACTCTAAACTACATCCAGACAGTGAGAGACTTCTGCGACAAGCAACCAAAATGGACCCTTCAGAGAGAGACAGAGCTGGAGAACATGAGAGACATCAAGGACCAAGCAGACCAAGTCAGTCTGAAGTTTGACCACGTTCAGCGCTCCGAGAACAAGTTCAAGGCTTTCGGGGAATTCCTGTGGAGTGGTTTAACTCAGGTCACAGCTGAGTCCAGATATCAGGAGCTGGAGAAGAATCTGGGTGCCGTCCTGAAGGACACCCTCGAGGGGCTAGAGAAACTTGACCACTTTCTGGATGCAGTGGAGAAGCTTAGAGTCACATCGCTGTTTGTGTTCACCGGACGAAGCTTCTTGCCAAAAGGAGTGAGTCCAGAGAGTGTGCGATCGGTCATCACAGCTGCCAGGATGGCTTCTCCTCTTCTAATTCACTTCAAA[C/T]GAAATGCAGAAACCTTTTTCCTTCCTTCACTCAGTAATCTGGATGTCCTGACCTTTCAGCTGGACAAATACATACGAATCACAGAACAGATTTGTGAGAGGATTGAGAAAAAGTTAGTACTTGAATTCATTTGTTTTACTTATTTGATTGACACAGGGTAGCAAATCATCTTAGTGGCAATTTCAAAGTAAACTGGTAAATTTCATTATTATTGCATTATTTTTTTTTCCTGTCTTACAGATCCAAGAGTTTTTTGTGGTTTGAAGATGTCTATAGGTAAGTGTTCTAAATCATACAATTAAGAAAAAAAAAAACAATAAGAGAAGATGAGGAAAGATTCAAACATCATAATTCACAGAGGTGTATGAACATATTAATACAAGTGAGTATTGTGACGCTACACTACCTGACAAAAGTCTTGCTGCCTTTTAGGAACAACAAATAATAAATTTGACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTATATGAGAGGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6898
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
ENSDART00000112891 None None 275 None 3
ENSDART00000130102 Essential Splice Site 190 557 1 4
Genomic Location (Zv9):
Chromosome 3 (position 29830020)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 29548059
GRCz11 3 29678901
KASP Assay ID:
554-4565.1 (used for ordering genotyping assays)
KASP Sequence:
ACAAATACATACGAATCACWGAACAGATTTGTGAGAGGATTGAGAAAAAG[T/C]TAGTACTTGAATTCATTTGTTKTACTTATTTGATTGACACAGGGTAGCAA
Long Flanking Sequence:
AATGGACCCTTCAGAGAGAGACAGAGCTGGAGAACATGAGAGACATCAAGGACCAAGCAGACCAAGTCAGTCTGAAGTTTGACCACGTTCAGCGCTCCGAGAACAAGTTCAAGGCTTTCGGGGAATTCCTGTGGAGTGGTTTAACTCAGGTCACAGCTGAGTCCAGATATCAGGAGCTGGAGAAGAATCTGGGTGCCGTCCTGAAGGACACCCTCGAGGGGCTAGAGAAACTTGACCACTTTCTGGATGCAGTGGAGAAGCTTAGAGTCACATCGCTGTTTGTGTTCACCGGACGAAGCTTCTTGCCAAAAGGAGTGAGTCCAGAGAGTGTGCGATCGGTCATCACAGCTGCCAGGATGGCTTCTCCTCTTCTAATTCACTTCAAACGAAATGCAGAAACCTTTTTCCTTCCTTCACTCAGTAATCTGGATGTCCTGACCTTTCAGCTGGACAAATACATACGAATCACAGAACAGATTTGTGAGAGGATTGAGAAAAAG[T/C]TAGTACTTGAATTCATTTGTTTTACTTATTTGATTGACACAGGGTAGCAAATCATCTTAGTGGCAATTTCAAAGTAAACTGGTAAATTTCATTATTATTGCATTATTTTTTTTTCCTGTCTTACAGATCCAAGAGTTTTTTGTGGTTTGAAGATGTCTATAGGTAAGTGTTCTAAATCATACAATTAAGAAAAAAAAAAACAATAAGAGAAGATGAGGAAAGATTCAAACATCATAATTCACAGAGGTGTATGAACATATTAATACAAGTGAGTATTGTGACGCTACACTACCTGACAAAAGTCTTGCTGCCTTTTAGGAACAACAAATAATAAATTTGACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTATATGAGAGGCAAATGCCTCTTGATTACGCTTATTTACCAAAATAAAATATGATAATGCCTTGATTTTTAATTATTTAATTAGGTCAGAAAGGTCTAACTTTGCTTAGACAAAAGTCTTGTCACTA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa2137
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112891 Nonsense 18 275 1 3
ENSDART00000130102 Nonsense 242 557 3 4
Genomic Location (Zv9):
Chromosome 3 (position 29826785)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 29544824
GRCz11 3 29675666
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAGTGAGGACTCCATGCAAAACATGCKCGMTCATTTGAAGCAGTTGTGC[A/T]AAATAAGGTGAGACCTCTAGCTTTTTTNATTTGATCAGCTGCTTCTTTTT
Long Flanking Sequence:
TTGGAATACAGTCTGTCACAACCCCATATTGTGTTGCAATGCAAGATCTTTGACAGTACACAGACCAAAATAATCTATCATGACCTTTAGGCCAAATTAAGTGAATTGAGAAAGATATACGAGTATGGGTGGAAGGGGGATTCTTAAAGACGAAGATGACTGGAGTAGAAAGCTCTGGTAATTTATAGTGTGTCGGTAATCATCTGATTGGTACAAATATATGGAGCTAATGCAGTACCAGCTGTGTTTAATCAATAAATAAATAAACTATAAAATAAACCACACTTATTACAGTTTAACAGTAAATGTTTGGCATCTTTCCTCATCTTACCCTACAATGCAAGCACTTTCATTCCTTATGGTGTTTGAGATACAATAAGATTGTTAAACTTGTTAAAACTCTTTACAGTTGTAAAACGGGTGAACCTCTAGTGAAGTTCAGTTTGAACTTAAGTGAGGACTCCATGCAAAACATGCTCGATCATTTGAAGCAGTTGTGC[A/T]AAATAAGGTGAGACCTCTAGCTTTTTTTATTTGATCAGCTGCTTCTTTTTTGTCTTGAATGCCTGCTGTAAACAATATACACTTTTATTGTTTAGGATGGATCAGAACATCAGGCTGACCTTCATTTTTCAGGAACATGCTCAGCGCTTCATTGGTATATTCAGTCAGCGTTGCTCTAGAATGGAGCAGTTCCTGACAGATCTGGAGGAGAGCGCAGTTCAGCTGGACAGGATGAAGATGGGCGCCAGTATCTCCACTGTGGCTGGCAGTTCAGTAGGGGTGGCTGGAGGTGTTTTGTCCATCGTTGGTCTTGCTCTTGCCCCTGTAACAGCAGGGGTGTCATTGGCTCTTACACTGACAGGTGTTGGTCTTGGCGTGACCAGTGGTGTCAATGGTATAGTAACAGGCATCACTGAAGCAGCAGTCAACAACCATCATGGGAAAAATGCACAGAACATTTTTCAGAGATACATGGAGGATGTTGGGAAGATACTAGACTG
Associated Phenotype:
Not determined