ZMP
LOC557734
Ensembl ID:
Human Orthologue:
LRP8
Human Description:
low density lipoprotein receptor-related protein 8, apolipoprotein e receptor [Source:HGNC Symbol;Ac
Mouse Orthologue:
Lrp8
Mouse Description:
low density lipoprotein receptor-related protein 8, apolipoprotein e receptor Gene [Source:MGI Symbo
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33898 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30873 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20743 | Nonsense | Available for shipment | Available now |
sa20742 | Essential Splice Site | Available for shipment | Available now |
sa33897 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33898
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000102554 | Essential Splice Site | 147 | 984 | 4 | 19 |
Genomic Location (Zv9):
Chromosome 6 (position 35143296)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34698235 |
GRCz11 | 6 | 34681618 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAAAGAGACTGTGAAAATGGAGCAGACGAGGAGCAGTGTGCCGCAGG[T/C]AAGACCACAGAGAGAAAAAGAAATGGCTAAAAATAGAGCCTGTCTGGATA
Long Flanking Sequence:
CACAGGACACTAAAGAAACAGCCAAAGAAAAGCAAATCTTTGCCATCACAGGAATAAATTATATTTTAAAATATTTTGGATTGGAAAGCAGTTGCATTTTTATAATATATCTTATATTACAGTTTTGCTGTATTTTTAATCAAATAGCCAATTCCTCTTTGACGCATAGGCTATAGACTTCAAATATTTTAATGTGAATATATGCCCATATAAATATATAATTTATTTTAATGAAAATATGTCACTGTATTGTATATTGTATATGCAATTTGTACATAATGTGTTGTACATAGCATCTGGAAACTACACATTTTTAATGTTAGTTGATACAGTATGTCATCCTTTAAAATGTCTCTGCTGTTGCTCACAGGTCGCCAGACGTGTCCGCCAGAGAAGTTTGACTGTGGCGGCTCAACCAGCAAGTGTGTGTCTTTGTCATGGCGCTGCGATGGAGAAAGAGACTGTGAAAATGGAGCAGACGAGGAGCAGTGTGCCGCAGG[T/C]AAGACCACAGAGAGAAAAAGAAATGGCTAAAAATAGAGCCTGTCTGGATAATGCATAGTCAGACTTCAGTGCGGTATGTGGGTGAACTTAATGGAGCGAGGTGTAGGTTGGGTGTGCATGTGTGTTCGTGTGTGCATTTTTGAGTGTGCCAGTGCGTGTGTGTGTGTGGGGGGGGGGGGGGAGGCCTGCTTGTGTGTGCGCGAGTGCATGGAACACATGAAACACTGATGTTGGAAGTTATCGTCGATCGATGTTCAGGAAAGATATTACAGATTGCCCTGTTTTAAAAATTGGATGAAATTTTTGTAACACTTCCTATGACGCTCATGCTTGTAATGAATTATAACTCTGTTTATGATTATTTATAATCAAGCATAATAATTCTAAAAATGCATTTATGTAATGCATTTATAATAGTGGTATTAATACTTATTGGTAATTCATTTTATTGTTCAATATACAGTTGAAACCCGAGGTTTACAAACACTCTAAAAAAAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30873
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000102554 | Nonsense | 297 | 984 | 6 | 19 |
Genomic Location (Zv9):
Chromosome 6 (position 35105825)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34735703 |
GRCz11 | 6 | 34719086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCTGATCAGTTCCAGTGTGGCGACGGCTCCTGCATTCACGGCACTAAA[C/T]AGTGTAACAAAGTGCACGACTGTCCAGATTTCAGCGACGAGGCCGGCTGC
Long Flanking Sequence:
TTCCAAAACTGTCAACTTTTTTTCACAAAAACTTTAAACTTTCACAAAGTCATAAATTCTTCAATAAACCACTGTTGAATAATAATAAAAACATTTATGTCCAGTCATTCCACCCAGGTTTTTAGAATACCAATGGTTAGTGAGATGAAAAAAATATATACATTTTACAAGATTTTAGTGTGTTTTCACAAAACACAATAATTGAAGCAAATAAATCTATAGATTTGGTGAAAAGCTATCACTAAATCAGTCATTTTATGCTGCATATATATATATATATATATATTAGCTCCAACTTAAACTGGGATTAAGCCAGATTCTGCTCCGCAATTTCCTGCTGCCATGATAATCTCCAAAAGATTGCTTGCTTAATTGGCCAGGCTGATAAATAAGAAAACAATAGTCTCACATGCGAATTTGTTTTGTGTCCTGCAGCTGTGTTGACCTGCCGTCCTGATCAGTTCCAGTGTGGCGACGGCTCCTGCATTCACGGCACTAAA[C/T]AGTGTAACAAAGTGCACGACTGTCCAGATTTCAGCGACGAGGCCGGCTGCGTCAACAGAAGTGAGTAGCTTCAACAGTCTCCCATTTGATTAGCCTCTTCATCTCGCCTCTATTCCAGCAGCGTTTTTCACTGAAGATGAAAGGCTAGAGTGAGCCCAATCATGCGGCCCCAATCAACTTAACATTCACACAAAGCACTTCGAGACCAAGCAGATGTACTCCTACATGATGCCAGGGTTCTGTGGCACACTTCCCATATGGCACCTTCAATCAAAATCACCTTGAAAGATTCATTATTCCATGGTTATATCTGGTGATTGATGCATAACACGATTTATTTTGAGTACATTGGATCATAATTCATGTCGACCAATTAGTGCCCTGTGTTTGTATTTGGTTAGGTTTATGGATACTATCAGGGCTTTACATTAACTTTTTTAGTCACTGGCCACTTTGGCTTCTAGTTTTCCAATGTTACTAGCCACTCTGCATTTTTGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20743
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102554 | Nonsense | 388 | 984 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 6 (position 35090709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34750819 |
GRCz11 | 6 | 34734202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATGTAAAGACCGGCAGATCGGCTTCGAGTGTCAATGCCCCTCGGGCTA[C/A]AAGCTCCTGGACAAGAAGACTTGTGGAGGTAACATCAATACTGCTTCACA
Long Flanking Sequence:
TTAAACAGAATTATTTGCAGTTTTGTCCTATTATTATTATTATTATTATTTATTTATTTATTTATTTATTTTTTATTATTATTATTTAGGTTGCATCAATGTCAACTCTAATGTGAAATTTTCTGTCTGGTGGTTTATAGTGGTTCATGTCACTAGAAAAAGAGAATCATTATTGTAGCCCTAAAGTGTGTGCGTGCGTGCGTGTTTGTGTGTCTGAGAGCATTTTTTTCCCCAGTCTGTCATGATTGATTTTTTCATAAAGTGTTCAAGCTCAGCCTAGAGAATGAGAACCAAGCAGTCTAGCCGTCAGATGTGTCAGTTTGCCATGAGCTTTTACAGTTAAGTTTCTGCCAGTCATTGTGACCTTTGACACCACCTTTCTTGTTTTTGTTATTTTTTTCCATTACAGGACTGAATGAATGTGCCATAAACAATGGCGGCTGCTCTCACATATGTAAAGACCGGCAGATCGGCTTCGAGTGTCAATGCCCCTCGGGCTA[C/A]AAGCTCCTGGACAAGAAGACTTGTGGAGGTAACATCAATACTGCTTCACATACTGACCTTTTGATGCTACACAGCCCTACATTGTACCCACTTTCCCAAGAGCCAACATTGCAAGCATCTATGATTTGTTTACTCTTAGCGTCATCACTTTGATAGTCGTGAAATCCCCAGATGGCGTTTGCAAGCATCATTTATCTTGTCTGAGGACACTGCACTACAAAAGCCTCTGTTCTCTCTGTCTCTCTGCTCTGTTACTAATGCTTTTCTGATGGTCCTCGCCAGACATAGACGAATGCGAGAACCCAGAGGCCTGCAGTCAAATATGTATCAACCTCAAAGGCGACTACAAATGCGAGTGTTACGAAGGCTACGAGATGGACCCAGTTACCAAGACGTGTAAAGCAGTGGGTAAGACAGTATACATTAACATCTCCATCAATCACTTTTCTGAACAGTGTGGCCTGATATAGCTGACTTTTTCCAGCCCAAAAGCACAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20742
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102554 | Essential Splice Site | 440 | 984 | 9 | 19 |
Genomic Location (Zv9):
Chromosome 6 (position 35090299)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34751229 |
GRCz11 | 6 | 34734612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACGAAGGCTACGAGATGGACCCAGTTACCAAGACGTGTAAAGCAGTGGG[T/G]AAGACAGTATACATTAACATCTCCATCAATCACTTTTCTGAACAGTGTGG
Long Flanking Sequence:
ACTGAATGAATGTGCCATAAACAATGGCGGCTGCTCTCACATATGTAAAGACCGGCAGATCGGCTTCGAGTGTCAATGCCCCTCGGGCTACAAGCTCCTGGACAAGAAGACTTGTGGAGGTAACATCAATACTGCTTCACATACTGACCTTTTGATGCTACACAGCCCTACATTGTACCCACTTTCCCAAGAGCCAACATTGCAAGCATCTATGATTTGTTTACTCTTAGCGTCATCACTTTGATAGTCGTGAAATCCCCAGATGGCGTTTGCAAGCATCATTTATCTTGTCTGAGGACACTGCACTACAAAAGCCTCTGTTCTCTCTGTCTCTCTGCTCTGTTACTAATGCTTTTCTGATGGTCCTCGCCAGACATAGACGAATGCGAGAACCCAGAGGCCTGCAGTCAAATATGTATCAACCTCAAAGGCGACTACAAATGCGAGTGTTACGAAGGCTACGAGATGGACCCAGTTACCAAGACGTGTAAAGCAGTGGG[T/G]AAGACAGTATACATTAACATCTCCATCAATCACTTTTCTGAACAGTGTGGCCTGATATAGCTGACTTTTTCCAGCCCAAAAGCACAAAAATAAAACACCCAAAATATTAAAATAACTATTTAAATCAGAAATTAGCCTAGTTATTGTAATGTGAAGTGGGACGCTGTCAAAGGAGTGTGGATCCAAATGCAGGGTTTTTTATGCAGAGAATAGTCAGGCAAGCAACAGTCAACACAGAAGCAAACAGATGTTTACGGGCAGTCAAGAGTCATGGTCAATAAACAGGCAAATGGTCAAAGTCAGGCAGCAGACAGGAATAAACATACAAACAAACAAACAAAGCAAGGGTCTAACACGGAAAGCAAGGCTTTCACTCACAGATAAAACAAGACTCAGCACTGATGTGTGTGTCTGTGCTGTTTTTAAAGTCCATCTAATCAGTCTTTGAACAGCTCCCAGCTGTGTGAGTGTAATCAGTCGTGGTCTGGAATGGGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33897
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000102554 | Nonsense | 484 | 984 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 6 (position 35071933)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 34769595 |
GRCz11 | 6 | 34752978 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCGACCCTGAAGAATGCTGTGGCCCTGGATGTGGATGTTACCACCAAC[A/T]AGATGTACTGGTGTGACCTTTATCATCGCAAGATCTTCAGGTACACACAC
Long Flanking Sequence:
TCATTATTTACTTACCATTCACTTGTCGTAAACATGTTTGTGTTTCTTTTTTCTGTTGAACTCAAAACAAGATATTTTGAAAAATGCTGAAAACCTGTAACCTTTGACTTCTATAGTATGTGTTTTGCTACTATGGAAGTCAATTGTTACAGATTTTTTACATTTTCAAAACATTTTCTTGTTTTGTGTTCAACAGATTAAAGAACTCATAGATTTTGAAACCACTTGAGGGAGAGTAAATACTGAATTTAAATTTTTGGGTGAACTATCCCTTAAAATATACTATTAAACTGTTTATCAGCTCAGTCACCTATTCCTGATCCCATGTTGACAAATGGCCTGATGAACAATTTTCTGGTCCCTTCACAGGTAAGAGCCCATACCTCATGTTTACTAACCGCCATGAAATCCGCCGCATTGATCTGTTGAAGAAGGACTACACACAAGTGGTGCCGACCCTGAAGAATGCTGTGGCCCTGGATGTGGATGTTACCACCAAC[A/T]AGATGTACTGGTGTGACCTTTATCATCGCAAGATCTTCAGGTACACACACAGCATTACAGCACAGGGCATATTGCGTTCCTCCCTCTAACTTGACAGCTGTTTAATCTTTGTTTGAAAAGGATAATTTGCAATTAGTGTAGAGCGCTGAGGTAGGAGAAGATGTTGCGGTTCTGAGAAGCTCTTCCCGCCTCCTCTCAGCTGTCTGATATTTAAATGCATGAGAACAGCTGCTGCAGAATAACTGGAGATTTCCTGACGGCAGCATCATCATGCAGTGATCAATTGAAAGCTGTGCAGGAAATTGCTTGTGTGCACATTTCCATATAGACTTTATTCTCTGGTTTCCTAGGAGTTGGGATGAAAATGTAAAAAATTACACAAACAAAACAGCTGTACGTGAGGAATTATTTTAGGTTTTTGGGTACAAAATTTATTTTTATTATTTGGTTCTTGTTTTTGATTGTTTGTATTTATTTATTATCAGATCTCAATTCCTCTG
Associated Phenotype:
Not determined