Busch Lab

ZMP

LDLRAD2

Ensembl ID:
ENSDARG00000090297
Description:
low density lipoprotein receptor class A domain containing 2 [Source:HGNC Symbol;Acc:32071]
Human Orthologue:
LDLRAD2
Human Description:
low density lipoprotein receptor class A domain containing 2 [Source:HGNC Symbol;Acc:32071]
Mouse Orthologue:
Ldlrad2
Mouse Description:
low density lipoprotein receptor A domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:3588210]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa14056 Nonsense Available for shipment Available now
sa6218 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35139 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14056
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128245 Nonsense 124 378 2 5
Genomic Location (Zv9):
Chromosome 11 (position 37323152)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36220380
GRCz11 11 36482363
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGGTCGTCTGCATCTGGCCTGACCCGGCCTGACCTGGAGCCCACCACT[G/T]AAGARGGGCCCGAAGACCCCTGCCATGCTGGATCTTATATCCAGTTTTAT
Long Flanking Sequence:
TTTACTAGGACTTAAGCTGCTTAAGAATAAACTTAATTTGAACTTAAGAATGTTAAGCTGCTTTGACAAAATCTACATTGTAAAAGTGCTATAGAAATAAACATATATTGAATTGAATACATAAATTATGTGTACTTTGTATGTATTCTTTTCTTTTTGTTTTGATCTGTATTTCTACTTTTTTATTAAAATCTATCTGATTCTCAATTCTCCCAACAGTGAATGTGGTGGACTTTTGTGGACAGACAATACAGGGGGACGGCATGATCGTAAAGTCCCACCAGGAGTCCCGCAAATACTACTTTGTCTCAATGGGAACAGATTGCCACCTCACCATGCAGTCCGCGACCCCCCGAGACAAGGTGCAGTTCTACTTCCGCTTCTTCCTGGTCTACAGCCTGCTGAGAGTGTCTCCACACAGCCCCGCTCCACTCTTCCCAGAATCACCCAAGGGGTCGTCTGCATCTGGCCTGACCCGGCCTGACCTGGAGCCCACCACT[G/T]AAGAGGGGCCCGAAGACCCCTGCCATGCTGGATCTTATATCCAGTTTTATGATGGGAGGGATAGGTCTGCGCCCCTGATCGGACCGCCGCTCTGTGGGAAGAGTCCTCCTCGACCGGTCTTGTCCACAGGCAAATTTCTCACTCTCCGACTGGTGACGCGAGGAACTCAGCCAAGGGTGGACTTTGTTGGAGACTTCACTTCATTCAGGCTGGGTTAGAATGTGTTTACATCCACTTCTCACTCGATTTCTCCTCAAACTTAGTGCACGCAAATTAGAAAATTCCATTTATTGATATCATTTTAATGATGTGTAAGCTAGTACAGTGGCTTAGTGGTTAGCACTACAGCAAGAAGTTTGCTGGTTTGAGTCCCAGCTATGCCAGTAGGCCCCATGTTCGCGTGGGTTTCCTCCGGGTGCTTCGGTTTCCCCCACAGACCAAAGACATGCACTATAGGTGAATTGGAAGAACTAAATTGGCCGTAGTATGTAAATTCTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6218
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128245 Essential Splice Site 244 378 3 5
Genomic Location (Zv9):
Chromosome 11 (position 37325706)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36222934
GRCz11 11 36484917
KASP Assay ID:
554-5293.1 (used for ordering genotyping assays)
KASP Sequence:
GACAACTGTGGGGACGGCAGTGACTTAATAGATTACCCTGGTTGCAATGG[T/A]ACAGTATTGMTTTTAAACRGRCATTTTCACCTGGAGTTAGTTTYGGAATC
Long Flanking Sequence:
AATATACATCCATAGTAGGAAAAACAAATACTATGGTAGTCTATTGTTACAAGCTTATTCAAAAAAATCTTCTTTTGTGCTGAACAGAAGAAGTAAACTAAAGGGACAAGTGAAGGGTGAATAAATAATGACACAATAATCAATTTAGGGTGAACTATTCCTTTAAAGTTAAATAGCATATAAAAAATACAAACTTGTACATTTTGAAAGAGTATTGCCTCAGTGCAGCTTTTGCACCTTTATTTCTGAGATTGTAATGAAGTAATCACAATGTAGTACTACCGTATACTTCTTAAAACAATTACAGTTAAAAAATAGATGATTGCTAATACACTCAAATATTTGTCTTCAGGTTTTAACCAATCAGAGTGCAGCGGTGAGCCCTACTTCAACTGCCGCAACGGGAAGTGTATCCCCAAGAGTCTGGTTTGTGCAGACGATAAAGGCATCGACAACTGTGGGGACGGCAGTGACTTAATAGATTACCCTGGTTGCAATGG[T/A]ACAGTATTGCTTTTAAACGGGCATTTTCACCTGGAGTTAGTTTCGGAATCATCTTGTTTTTGTGTATTTCAGCTCCTCAGTCTACACCCAATCCTCCACAGCGCCATGCTACCCAACCGGCACCAATGCTGAATGGTCCCACTCTGACAGTGTCCACTTTAAAGAACTGCGCCACTCCAAAAGCCATTCCTGACCCAGACTCTGTGACCGGTAAGCTCTCCAATGATGCTGGAAAAATATATAATGGTTATTTTTATTTTGATGAATATGCCTAACTTGATGAATATGCCTAAACAACTCAAATGACGCCATTTCGAACAAAATCCAGTTAAAATAAAGTTTTTTTTAGTTAGGTTTGGGAGTTTGTCATGGACAAAGAGCAGTTCAAAGGTGTTTAGGACCAAAACGAACTCCCCCAGAAAGATTTGTGAAGACTATGCAATCGATGGGTGTGTCATGGAGCTCCGCCTTCTTCAACATGCTTCATACACTGCAAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35139
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128245 Nonsense 322 378 5 5
Genomic Location (Zv9):
Chromosome 11 (position 37330029)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36227257
GRCz11 11 36489240
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGACGGCGGCTGGTGTTCTGCTCTGCTGGTGCTGCTGGGCTCCTGGAT[G/A]GTTCCTGTGGCGCGTCAGTGTGTTCCGCTTTATGCCTTGCTGTAACTCCT
Long Flanking Sequence:
AACTAATATATGTAAAGAGATGGTTTGAGTGTATAATTTCACTCAGCTGGGAAATAGAGGCAACTTGAATGGCTTGTGAGCTCAATTAAGTGCACACAGCAAGCCATATCATCTGATAATAGTAAGAAATAATTCCAAAGAGCAACTGACAGTGTAAAACCACATAAAACAAAATAAAAATATAATATATATGCCGAGTTCAGCAGCTAATCAGCCGGAATCAGCTGAGGTGACATGACAGCGATCAGTGAGATCTAGCTGTCACTCAATAAAAATTCAGTGGGTTGTTCATGACCCTTCAAATCAAATCCATTCATGGCTTACTGTTTGTAAAACATGCATCATTAATGTTTGATGAGTACGTGACTAGGTCCTGTAATTGTTGGAATTGTTTTCTGCTGCAGACTCTCAGTCGTCCATGTCTCTGCTGGCGCTGTATGTGGTTCTGGGGGTGACGGCGGCTGGTGTTCTGCTCTGCTGGTGCTGCTGGGCTCCTGGAT[G/A]GTTCCTGTGGCGCGTCAGTGTGTTCCGCTTTATGCCTTGCTGTAACTCCTGCTGTGCCTCCTGCCAGTTCTGTGGGCGGAGCTGCTCGCAGAACAAAGACCACCGATTGGCTAAAGTCACACCTGAAGGAGCCGCAACACCTGTGTCTTCTACCACCACCGTGGCTGTGTAAAAACAGCACAGATGCAGAAAAAGATTCAGAACTTGAGGACTATTTTTGAAAGTGGTGTTATAGCAGAAATATAGCATAATTATTTTTACATGTATTATTATTTTTTTTTGCTTGTATTCTATGAGCAATTGGTGGATAGATTTTCACCGATGTTGTTTTGTTTTTCCAAATTTTTGAAGGTAATATAAATTGTCTGTATTTGTTGTGTGTATTTCATACAGGATTTATAAAAACTCATTAGCTGGCATTGCTAGTTTTTAATCAGTTTGGCGAAGTGAGTAATATTTTCCACTTTGTAATACCTCAGTGGGATACTGCTAACAATATA
Associated Phenotype:
Not determined