ZMP
lrp5
Ensembl ID:
ZFIN ID:
Description:
low-density lipoprotein receptor-related protein 5 [Source:RefSeq peptide;Acc:NP_001170929]
Human Orthologues:
LRP5, LRP5L
Human Descriptions:
low density lipoprotein receptor-related protein 5 [Source:HGNC Symbol;Acc:6697]
low density lipoprotein receptor-related protein 5-like [Source:HGNC Symbol;Acc:25323]
low density lipoprotein receptor-related protein 5-like [Source:HGNC Symbol;Acc:25323]
Mouse Orthologue:
Lrp5
Mouse Description:
low density lipoprotein receptor-related protein 5 Gene [Source:MGI Symbol;Acc:MGI:1278315]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11097 | Nonsense | Available for shipment | Available now |
sa13599 | Nonsense | Available for shipment | Available now |
sa14611 | Nonsense | Available for shipment | Available now |
sa32520 | Nonsense | Available for shipment | Available now |
sa45019 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24618 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11097
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 |
---|---|---|---|---|---|
ENSDART00000121724 | Nonsense | 284 | 1615 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 25 (position 10931525)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10622150 |
GRCz11 | 25 | 10718946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAACAAACACAGCGGAGAGAAGCACAGGGAAATTCTCAACGGCATTTA[C/A]TCGCCGATGGACATCCAGGTGCTTGGCCAAGAGCGCCAGCCCAACAGTGA
Long Flanking Sequence:
ATAATGAATTCATTTTGATATAATTCGTGTATATATATTTATAATTTCATTCAAGTATTTAAATGTACTGATTTCATTTTTGTTGTCGTTTTTGTTCGCCATTACTTCTGTTTTGAATAATTCTTCAGAAATCTGTATAGCATGCTAATTTAGTACTTGTATTTTTAGTACATTGTGCTACATTTTTTGAAATGGACATTCTTTATGGACATGGACATATCTTTTGGAATATTATTAACATTTGCTGTCACTTTTAAATGCTCATTTATCATTTTAGGATCCACAAATGCTACAGATGTTGTTTTATTTGAGGGGTGTTTGTTTTTACATCTATGTGTTGACGTTTACAGGGAGGCTGTGGTGGAGGGTTCCCTCACCCACCCGTTCGCCCTCACCCTTTACGACGAAACGCTCTACTGGACCGACTGGCAGACCCGATCCATCCACGCCTGCAACAAACACAGCGGAGAGAAGCACAGGGAAATTCTCAACGGCATTTA[C/A]TCGCCGATGGACATCCAGGTGCTTGGCCAAGAGCGCCAGCCCAACAGTGAGTCTATACATCTCAAGAATTCCCAGACCTTTTTTTTCTTGCATATTTTTATCAAACGATTCAAAGGTTTAGGTGTTGGCTTACATCTAAATTTGTGAACGCAGAGAAATGATCTGTTTTGCACTCAGGTCAGGTTTTCTTATGAGACCCCTCAACTTCTGTCAACACATATATTTAATTTTTTACTCAATCTTGTTCTTTCACCACTTTCTCTACTGCATCTTTGTAAAAGTGTCAGCCTTTTGGCCTGTGAGGCAATCTGAATAGTTCTCAGGGAATGAGATTTTTCAAGTGTCCTGCATTCCACTCTGAACAAATAAACACAGCTCCTCAGTGGAGATGGGGAACAGTCCCAGCACGATCCCACCCCCACCTTGGTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13599
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121724 | Nonsense | 347 | 1615 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 25 (position 10922018)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10612643 |
GRCz11 | 25 | 10709439 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCACTATTGTTCTCTGAGCAAATCTCTATTTTTTTCCTAGGAGCAGAA[C/T]AGGTGCTTTTACTTGCTCGTCGCAYYGATCTTCGGCGGATATCCTTGGAC
Long Flanking Sequence:
TTCTTATTGGTGTCAGCACTGATGGATGTCACTACTTATTGGGTGCCGTGGACCGCAGCTGGTGTTGTGGGTACTGGAGCGTGCTCGGTTACAAAGAGAGATTAAATAAGGACAAGGTTGGACCTAATTGCTTCCACAGATTGGGTCTAGACAGATTCTACTGTTGGTATTTCAAACCTGGCGTGCGGTTTTTGTAATGGAGCAATGCGATCTTGCAGTGCACCGTCTGCAGGGACAACTCTGCAATTCATGTTGCTAATTGCTACTGTCAGACTCTGTTTTCTTTGACGAGTTGAGTCTGTGCCCTAGGCATGGTAGTTGTCTTAATACACCACATCTTTGTAGACTGTGTTACATGGGTTTAACTTGAATGAAGTAGACAGTTCAGGTCAAAGTGCAAGGCATTTCTAATACTTGATGAATATTTTGCAGGATGTACATAAAGACAGATGTCACTATTGTTCTCTGAGCAAATCTCTATTTTTTTCCTAGGAGCAGAA[C/T]AGGTGCTTTTACTTGCTCGTCGCACTGATCTTCGGCGGATATCCTTGGACTTGCCTGACTTTACAGATATCGTCCTTCAAGTCAATGATATTCGTCATGCAATTGCCATCGATTATGACCCGGTGGAGGGATATGTCTACTGGACGGACGATGAGTTGAGGGCTATACGGCGTGCTCGAATTGATGGAAGCGATGCCCAGACTTTAATCACCAATGAGATCAATCATCCTGATGGAATTGCTGTGGATTGGGTGGCACGAAACCTCTACTGGACGGACACTGGCACAGATCGCATTGAGGTGACCAGACTCAATGGCACTTCTCGACGGGTCCTCATATCTGAGAACCTGGACGAACCACGAGCCATTGTATTGGATCCCATAAATGGGTACGAACTTCACATTAAGATCATTTCTGAGATTTCTTTCCTAAGAATTTTCATGTGATTTTTGCAGATTTTCATTTTTTTATGTATATATGTACAGATACATGTATTGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14611
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121724 | Nonsense | 406 | 1615 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 25 (position 10921841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10612466 |
GRCz11 | 25 | 10709262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGATATGTCTACTGGACGGACGATGAGTTGAGGGCTATACGGCGTGCT[C/T]GAATTGATGGAAGCGATGCCCAGACTTTAATCACCAATGAGATCAATCAT
Long Flanking Sequence:
CTGGCGTGCGGTTTTTGTAATGGAGCAATGCGATCTTGCAGTGCACCGTCTGCAGGGACAACTCTGCAATTCATGTTGCTAATTGCTACTGTCAGACTCTGTTTTCTTTGACGAGTTGAGTCTGTGCCCTAGGCATGGTAGTTGTCTTAATACACCACATCTTTGTAGACTGTGTTACATGGGTTTAACTTGAATGAAGTAGACAGTTCAGGTCAAAGTGCAAGGCATTTCTAATACTTGATGAATATTTTGCAGGATGTACATAAAGACAGATGTCACTATTGTTCTCTGAGCAAATCTCTATTTTTTTCCTAGGAGCAGAACAGGTGCTTTTACTTGCTCGTCGCACTGATCTTCGGCGGATATCCTTGGACTTGCCTGACTTTACAGATATCGTCCTTCAAGTCAATGATATTCGTCATGCAATTGCCATCGATTATGACCCGGTGGAGGGATATGTCTACTGGACGGACGATGAGTTGAGGGCTATACGGCGTGCT[C/T]GAATTGATGGAAGCGATGCCCAGACTTTAATCACCAATGAGATCAATCATCCTGATGGAATTGCTGTGGATTGGGTGGCACGAAACCTCTACTGGACGGACACTGGCACAGATCGCATTGAGGTGACCAGACTCAATGGCACTTCTCGACGGGTCCTCATATCTGAGAACCTGGACGAACCACGAGCCATTGTATTGGATCCCATAAATGGGTACGAACTTCACATTAAGATCATTTCTGAGATTTCTTTCCTAAGAATTTTCATGTGATTTTTGCAGATTTTCATTTTTTTATGTATATATGTACAGATACATGTATTGGACTGACTGGGGGGAATTGCCCAAAATTGAACGAGCAAACCTGGATGGCACGGACCGGGTCGTGCTTCTCAACACTTCTCTTGGCTGGCCGAACGGTTTGGCTATAGACTATATAGCCGGAAAGCTTTACTGGGGTGATGCCAAAACAGACAAAATTGAGGTAAGGCAGCTGAGGTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32520
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121724 | Nonsense | 932 | 1615 | 13 | 24 |
Genomic Location (Zv9):
Chromosome 25 (position 10881300)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10573260 |
GRCz11 | 25 | 10670056 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGCCAGTGTGCCCACCTGTGTCTGGCATCCCCCTCTGGAGCCCAGTGT[C/T]GATGCGCGTCTCACTACACCCTGGAGGCCAACGGACGCAACTGCAGCTGT
Long Flanking Sequence:
TTTTTAGACCAGAACGCCTATGGGCGCACATATTAGGCAAATGCATTTGCTATTTAAACAGCGTGGCGCAAACCGTCAAAATGACTCCGAGCGAAACTAGCAAACAACAGTTGCGTCGCACCGCATTGCACCGGGTGAATGATAGGGCCCACTTAGTTGATTAGTAAAACAAGCTTTCACACCATCCAAGCTCTATTAAACTAAAAACATTGTTATCATCTGCAGGTCTACAGCGAGAGATCGTGGCTGATGATCTTCCTCATCCGTTCGGGTTGACCCAGTATCGGGACTACATTTACTGGACGGACTGGAACCTGCGCAGCATCGAACGGGCTGACAAGCGCAGCGGCTTGAACCGAACCGTGGTGCAGGGACACCTGGAATACGTCATGGACATCCTGGTTTTCCACTCCTCCAGACAGGACGGTGCCAATGATTGTTCACAAAACAACGGCCAGTGTGCCCACCTGTGTCTGGCATCCCCCTCTGGAGCCCAGTGT[C/T]GATGCGCGTCTCACTACACCCTGGAGGCCAACGGACGCAACTGCAGCTGTGAGTTTTGCATTTTATTTATTGAATTATTTTAGGGCTCAACAATTAAACAGGTATTTGAGGTGTTTTTTGCACTGATAAAAGTTTGATGCTGTGTTTACAACAGGCACGGCACGTGCAGATAAATTGCGCTATTTGTGCGTAAATAGACACGTTTGAGTTTACTCGCTTCATTAGCACGTCAAATTCACATTACAATAGACACGGATTGGCCTCATGGGCAGGGCTTCTGTCTGCCCGGTGAATCTAGCTTTGTTGCTAAATGGCTAACATGGATATTATTGAGAGAACAGCTGTGTTTATGTGCATTTATGAAAGCTGAAAAACATAGCCGATTCGTTTGAAGCCGAGCCCAGTTTGATTAACTGTTGTCTGGTGTCGGCAGAAGGATTTTCCCCCGGGACCTCAACTGTACGTCATAGTCATGGCCCTAAAAAACAAAGCTCATGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45019
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121724 | Essential Splice Site | 1335 | 1615 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 25 (position 10861219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10553170 |
GRCz11 | 25 | 10649976 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATGGAGAGCCTGACTGCGCAGACGGCTCCGATGAACAGGACTGTGAAA[G/A]TAGGTCTCGTTTCGCAGAAGCTAGTTGCACTAATGGAAGCCATCTAAACT
Long Flanking Sequence:
AAATTGAAAAATTGAAGTTCCTGTTTCGAAACTTACAGATAGATGGCTAATTTGTATGTCATTGATATGTTCACTGCTAAGGTAAATAAACACTTTTGACACTTTTTTTCAAGTATTTTCATTAGTTTTGTTTTTCCTGTAAATTATTCAATAAATACCGTACCGTACCATTCATACCGAGGTATTATCGTACCGTGAAATTCTGATACCGTTACATCCCTAGTATATACGCTAACCACAAAAATACCCACAATTCTCTTCAGAGCCTCCCACCTGTTCGAGCGAACAGTTTACCTGTGCTACCGGTGAGATTGACTGTATCCCCATGGCGTGGCGCTGTGACGGCATCGCTGAATGTGCAGACAACAGTGACGAGATGAACTGTCCCATCTGCTCCAAACTGCAGTTTCAGTGTGACAAAGGCCAGTGTGTGGACATTCAGGTGCGCTGCAATGGAGAGCCTGACTGCGCAGACGGCTCCGATGAACAGGACTGTGAAA[G/A]TAGGTCTCGTTTCGCAGAAGCTAGTTGCACTAATGGAAGCCATCTAAACTAACAGCCTCTCTTTTTGCAGCCATTTGCCTGTCTAATCAGTTCCGTTGCGGCAACAGCCAGTGTATTCTGAAGAAGCAGCAGTGCGACTCCTTCCCAGACTGCACTGATGAATCTGACGAGCGTTTCTGCGGTACGTTAACCAATACCTTAGCATCTGACCACACATCGATATAACAGTGCCAGCAAGACACACTTATCCCTATTTGGCTTGTTCACAGACTTCCCACCACCACCCAACGATCTTCCACGTCACACCAGCACCATCGGCCCAGTCATCGGCATCATCCTCTCTGTCTTCGTAATGGGAGGCATGTGTTTCGTGTGCCAGAGAGTCGTGTGTCGTCATTACAAAGGCCCCAATGGAGGATTTCCACACGAGTACATCAGTGGGACGCCCCACGTGCCACTCAACTTCATCGCACCCACAAACTCGCAGCATGGTAAAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24618
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121724 | Essential Splice Site | 1529 | 1615 | 24 | 24 |
Genomic Location (Zv9):
Chromosome 25 (position 10858417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 10550368 |
GRCz11 | 25 | 10647174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACAGCTAAGTATTTTTTCAGCTTTTACTGACCCAATATTCCCCTCTTT[A/C]GACCATATCTGATGCGAGGGGTCGCGCCCCCCACCACCCCCTGCAGCACA
Long Flanking Sequence:
TGGATAGTCAGTTGGATGGACGGATAGTGGGATGGATAGATAGTTGGACGGACTGACGGATGGATGGAAGGATGGATAGCCAGATGAATAGACAGATGGATGGATAGTCAGATAGATGGACGGGCAGTGGGATGAATAGATAGTTGGACAGATAGTCAGATGGATGGATAGTCAGATGGGCGGATGGAAAGACAGACAGTAAGACAGATAGACAGATAAATAGACAGACAGATGGACGGACGGACGGACGGACAGACGGACGGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGATAGATAGATAGGGGAATGGAAATGTTGATTGTCTGGTCAGTAGGTGAGTAGTAGGTGACAGTATACAGGTAAGTGGTTTGAGAGGTTGCTAGATATATATAAACTCTTATAAATGCACAGCTAAGTATTTTTTCAGCTTTTACTGACCCAATATTCCCCTCTTT[A/C]GACCATATCTGATGCGAGGGGTCGCGCCCCCCACCACCCCCTGCAGCACAGACGTGTGCGACAGCGACTACACCACCAGCCGCTGGAAAAGCAACAAGTACTACATGGACCTCAATTCAGACTCTGACCCCTACCCTCCACCCCCGACCCCCCGCAGCCAGTACATGTCAGCAGAGGAGAGCTGTCCACCTTCACCCTCCACCGAGCGCAGCTACTTCCACCTGTGCCCGCCGCCCCCCTCGCCCTGCACAGACTCCTCATGACACCCGGCCACCTGCCGCCCTCTGTAAATACTTTTAAATAGCTCCAAAAAGAAGACACTAAAGATTTTATTTTATTCTCCCATACACACACACACACACACACACTCACACACGCTTTTGTTCAAGAATCATTTCAGCTTTTTGAGAAGAGGAGCAGGACATTTTCGGCCTCAGTTTTAGATGTACAGTGGACGTGATTGGACGAGTGAATTATATTATGACATTATTTTTTAGATA
Associated Phenotype:
Not determined