Busch Lab

ZMP

vldlr

Ensembl ID:
ENSDARG00000006257
ZFIN ID:
ZDB-GENE-040426-803
Description:
very low-density lipoprotein receptor [Source:RefSeq peptide;Acc:NP_957217]
Human Orthologue:
VLDLR
Human Description:
very low density lipoprotein receptor [Source:HGNC Symbol;Acc:12698]
Mouse Orthologue:
Vldlr
Mouse Description:
very low density lipoprotein receptor Gene [Source:MGI Symbol;Acc:MGI:98935]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa14068 Nonsense Available for shipment Available now
sa38785 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17714 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa14068
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023766 Nonsense 280 866 6 19
ENSDART00000139047 Nonsense 280 842 6 18

The following transcripts of ENSDARG00000006257 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 15315993)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 15329300
GRCz11 10 15287419
KASP Assay ID:
2260-3014.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTGTCCATGCCCTTTCCAGCTGCCCGTAACTGCAGACCTGACCAATTC[A/T]AGTGTGATGACGGCAGCTGTATCCATGGCAGCCGACAGTGCAAYGGATTC
Long Flanking Sequence:
ATTTACAGCACTGGCATACATTAAGAAAAATTTGAACAAAGAATAGTCTTGGGTCAATTACTCACCTCAGAGGATATTGGGGGATATTCACAAGTCACTGGCATTGCTATTTTGGGGGTCATGGGCTGAGAAGTTAGAGATCCACTGACATAAAAACCAAGATTAGTGCAAACTAACTGGCTAACCAGCTAATCCAGCTTCATGGTACAGGCCCTTGGTCTGGTGTTTTGATTTTGTCTTTGGTTTAGTTTTATTTCTTTTACTTTTTGCTTTGGTCTACAATTTAGTTTTTGTTTGCTATTGGGTTGATTTGATTGGTGTTATTTTGGTTTCCTGGTTTTATTTTCTTATTAATTGAGGTGTGTGTTGCTGATTTGGATTTACCTATTTTGACTTGGCCTTTTTTTGGTGGTTTTTGTAGTGTGGTCTATGGTTTTTACTTCAATAAGTGTTTGTCCATGCCCTTTCCAGCTGCCCGTAACTGCAGACCTGACCAATTC[A/T]AGTGTGATGACGGCAGCTGTATCCATGGCAGCCGACAGTGCAATGGATTCAGAGATTGTGTGGATGGAACAGATGAAGTCAACTGCAAAAACTGTGAGTCCACTGAACTGAAAACAATTCTCTCTAAGTGCTTTTACTTGGAAAAGACATCCTCAATTCAAGAGATTATGTTGACTGGCCAGTAATCTGCAAGATTCAGAAACTTTTTTTAACACCTGAACCAAATATTGAATGTTAACCGATTAAAGTACTGCAGGTATGTGGTATGTCAACCAAAATTTGGGGAGTATTTTTATTAATGTTTATTTGCAATCCTAACAGTGTTAACAACAGATTTGATGACTGCTTCACAATTATTATTTTTTATTCCTTGACTAGTTTCATGGACTAATTGGATGTTTTTGTTGTTGTTTTTTTTTTCCCTCCAGTAACTCAATGTAACAGTTCTGACCAGTTCAAGTGTCGAAGTGGAGAGTGCATTGAGATGAGTAAAGTGTGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38785
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023766 Essential Splice Site 352 866 8 19
ENSDART00000139047 Essential Splice Site 352 842 8 18

The following transcripts of ENSDARG00000006257 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 15319692)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 15332999
GRCz11 10 15291118
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAACATTGATATTCCAGATGTGTAAAAAGCCGCCATTCACTTTGTTCT[A/T]GATATGAATGAATGCTTGATCAATAACGGAGGCTGTTCGCACATCTGTCG
Long Flanking Sequence:
ATGCCGTGCTACATCAGCAGTCTGGTGACCAGCTGGAGGGTAGAACCGAGCAACTGCTGAGATTAAGTATAAAATGACGTCTCAGCTTTGTTTTTTGACACCATTCACAACAATACTGTGTGTTTTAGCCTTTGGGCCTGAAAAACAACACTTCAACATTTACATTTGGCTGTCACAAAAGTCACACACACAAATACCATAGTTTGTGGACCATAGACCTAAATTGTTCTTGTTTTTTTTTTTCACAAACGGGATAAAGTAAAACCCAAAACACTGGGTTTTATGGCAAATTTGTCCAGCTTGGAGTCAGTTCAATCACACACAGTGTTTTTAACCCCCTATTCAAGGACACTGCCATGCATCACCCTGTGGGATGTTCCTCATGTGGACCCCATCTGGATTTATTGATCCCTGTAAATCTCAGCATGTCGACAGTTTGTGTGTAAAATGTACAACATTGATATTCCAGATGTGTAAAAAGCCGCCATTCACTTTGTTCT[A/T]GATATGAATGAATGCTTGATCAATAACGGAGGCTGTTCGCACATCTGTCGAGACTTGACGATTGGCTTCGAATGCGACTGCACACCGGGACTCCAGCTCATCGATCGCAAGACCTGCGGTGGTATGAATAACCACACATGCTGTTGTAATGTAGTCAAATAATGAATATATTATTGATTATCTGATGATGGATCTTTTGTGAGCGTACTCTCCAATAGGAACTCGGACTATGATTGTTTCTCTGCAGATGTCAACGAGTGCCTCAACCCAGGGATATGTAGCCAGATATGTATAAATCTTAAAGGAGGATACAAATGCGAGTGTCACAATGGTTACCAGATGGACCCCACCACTGGAGTGTGCAAAGCTGTTGGTAAGTTCACTTTGAATTTAAGCCTTTCATTTTTTTTTCTTCTTTTTAATTTAATTTTTTTTATTTAATATTATTATTTAGTTATTTTGCTTGGTGATTTCAAGAAATATACAGTTCATCTGAAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17714
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023766 Nonsense 563 866 11 19
ENSDART00000139047 Nonsense 563 842 11 18

The following transcripts of ENSDARG00000006257 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 15324594)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 15337901
GRCz11 10 15296020
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTAACAGYGGCCTGAAGGAACCAGCCTCTATTGMTGTAGACCCTCTAW[C/A]AGGGTAATTTGATTTGGAATGAATATCATTAAAACATTCACACTGCTTTT
Long Flanking Sequence:
ATTATTAACATTCAAGCCCATGCTTGTTAACATTAGTTAATGCACCATGAGTTAACATGAACTAACAATGAACAACTATATTGTCATTAACTAACGTTTAATAGCATGAATAAATACTGTAGTAAATGTATTGTTCATGTTAGTAAATGAATTACTTAACATTAACTAATGAACCTTATTGTGAAGTGTGACCGTATGTTTGTTTGTCTTTTTACAGATTGTGTATAAATGTTAGAAATTTCTTTGTTCATCCAACCACTTTGACTTCTTTTTTTTCACCCACAGCACAGTGTTGGATAAGCAGGATGAAAGTCATAAGAAAGTGATTGACGATGTTCAGATGCCTGTTGGGATTGCAGTAGACTGGATTTACAAAAACATCTATTGGTCAGATCTGGGAAGTAAGAGCATAACTGTGGCCAACTTCAATGGGACCAAGAAGAAGGTGCTTTTTAACAGCGGCCTGAAGGAACCAGCCTCTATTGCTGTAGACCCTCTAT[C/A]AGGGTAATTTGATTTGGAATGAATATCATTAAAACATTCACACTGCTTTTAATGCTTCTGGATTGAGCCTATAAATAAATCTAAATTGGATGGTGTCCTTTTTAAATACAGGTTCCTCTATTGGTCAGACTGGGGTGAGCCAGCTAAGATTGAGAAGTCTGGTATGAACGGGAATGACAGACAGGTCCTTGTTGAGACGGACATTCAATGGCCCAATGGAATCACTCTTGGTATGTGATGTTTTCTTGATTTGAGTTAAACCAGGGGTGTCCAAACTCGGTCCTGGAGGGCCGATGTCCTACATATTTTAGTTCCAACCCCAATTAAACACACTTAACCAGCTAATAAAGCTCTTTCTAGGTATACTAGAAGCTTTCAGGCAGGTGTGCTGAAGCAAGTTGGAGCTAAACTCAGCAGGACCCCGGCCCTCCAGGACTGAGTTTGGACATCCCTGCATTAAACTCTGCGAGACTGGCTACATTATATTTTTAATAAGAATA
Associated Phenotype:
Not determined