Busch Lab

ZMP

zgc:195027

Ensembl ID:
ENSDARG00000008485
ZFIN ID:
ZDB-GENE-080723-53
Description:
hypothetical protein LOC100170796 [Source:RefSeq peptide;Acc:NP_001124106]
Human Orthologue:
LRP3
Human Description:
low density lipoprotein receptor-related protein 3 [Source:HGNC Symbol;Acc:6695]
Mouse Orthologue:
Lrp3
Mouse Description:
low density lipoprotein receptor-related protein 3 Gene [Source:MGI Symbol;Acc:MGI:3584516]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa7077 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa40956 Nonsense Mutation detected in F1 DNA Not yet available
sa7078 Nonsense Mutation detected in F1 DNA Not yet available
sa38628 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa7077
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016265 Essential Splice Site None 820 1 9
Genomic Location (Zv9):
Chromosome 7 (position 39671101)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 38007741
GRCz11 7 38278999
KASP Assay ID:
554-4996.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCCGTCCACAAGAGWGCAGGCTTTCACTTCCACAGTCCCGACAGCTGG[T/G]AAGTCTCCATCAGACAAATGATGAAAACAAACCCAAGCAAAATTCATATA
Long Flanking Sequence:
ATTCTGAGTATAATAACGAATAATTTCTTTCAAGTGTGTAACTAAACGTGTGTCGGACTGTTGTATGACGTACGTATAGGAAAACCGATGACCAATCACGCAGCGGCGCCGTGGCTTAGTTGGTTAAAGCGCCTGTCTAGTAAACAGGAGATCCTGGGTTCGAATCCCAGCGGTGCCTTTTATGCCCTGAAGATCCAAAGCCACGTTTAGGTACATAAGATTAGATTGATTTAAGCAGTAAAAAATTAATTCAAAAGTACTAATGCAACCGGAAATATGTCGTGAAGAACAGTCTAGTCGTAGGTAGTTTACATTGTTGAAATTAGGCAGTATATTTTGAAACCACGCAGAATTTTTTGTTTGCTTCAAAAGGCTCGGTAGGAGGTATTGTTTAGCATGTAAATAAAGGAATGTGGCCCACACGTCATGGCTTCCTTCCACCGATGCAACCCTCCGTCCACAAGAGTGCAGGCTTTCACTTCCACAGTCCCGACAGCTGG[T/G]AAGTCTCCATCAGACAAATGATGAAAACAAACCCAAGCAAAATTCATATATAAATGTCTATTTATGATACTGTCAAATACACACGCATCAAATGAGAGCCCTCAGTCTTGTGTGTTATACTGGCTATTCAGGGGAGCAGTCAGTCATTTACATGAGCAGTATATTGTATATGTAGCTGTGTTGAAAATTGATCCGAGTGTTATTTTGTGTGAGATGCGCTCCAGCAGATGGACAGCACTTCACTGATCTGCAGTGCCCAGATTAGTAAACCACAGATTATTACATAACTGACACATACTGTCAAGTAGTGGACGATATCATTAGGCTACTCGATGGGATGTATTGAAAAGAAACAAAAACGTAATAAGCAAGTAACCAAGAAAGTCAATTCCTGGATGAAGGATGTGTCCTGTTGTTCCCACTGAACCTCCAATCCCGTCTCTCTCTCCTGCCTGAAGGTCTTTCTGCTTTTCCCTCCAGACAGACAGCGCGATGAGCCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40956
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016265 Nonsense 344 820 6 9
Genomic Location (Zv9):
Chromosome 7 (position 39692612)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 38029252
GRCz11 7 38300510
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTACCACGCTAAACCACACAGCCCCGGACATGGATTCAATGCCACCTA[T/A]CAGGTATCTCATTCTCATATGCTTTCTGGGGTTAAGAAAATGAAAAGTTA
Long Flanking Sequence:
ATGATAAAATAATAAAATGACAGCTACAAAGAAAGGCACAAGCACACAAAGCAACTGTCATGCTATGGGTGGAATCACAGAACATAAACAAATACAATGAGCGTTTACTTGCACATGGCTAATTTTGGTCTCTTTAGAATTAAAAAAGAAATTGCACCATTGTAACAGTTTTAATTCACTTTAAAATACACTTAGTTCTGTTTTAATTTAAACAGATTCTGGCCTGAAGTTTAATAATTAAAGTATGTCTGAATTAATTAAAGAGTGTTCTGCTTGCTTCAGGACCCAAAGCCGCTGGTGCTGCAGGTGGATCTACAGCTGGGTGTTGGAGACTCTGTACGAGTTTATGATGGTTTGGGAGAGCAGGCAGAACGGCTGCTGCAGAGTCTTTCTCACCATAATAACCACAGACGAGCCCTGCTGGAGTCTTCCCAGGGCCAGATGAGCATCTTCTACCACGCTAAACCACACAGCCCCGGACATGGATTCAATGCCACCTA[T/A]CAGGTATCTCATTCTCATATGCTTTCTGGGGTTAAGAAAATGAAAAGTTAACTCGCACTAAAGTGGTTCCAAAACTGGATGAGATTTAAAAGAGAAAAGTTTGGAGAACATCTGTAACCAGCCAGTTGACAGTAGGCTTTGACTTTCACAGTTCTACTTCAGACTTCTACTGAAACTCATACAGGATTGGATGATGGCAGAACTTTGATTTGGTGTGAACTATACCTTACTTGCTCCAGTTTTAAAATCTGCATTGTATTTTCCTCCAGTACTATACAAGCTTATTTTTTTTAGGCCCAGTTTGAAGATATTATGAAGGTCTTTCTGTATGTATATGCTTGCATGAACTTTACAATAAACTAGAAAACACTTTCACTTTCATTTCTAATATCATTGGTTGACTGTGTGCAATGTGATTATAGGGGAATAGAGGTTTCCACCTAAAAACTTTTTTTAACTGCATTGTAAAATGATTCCAAGTACTTTATTGTCATTCACAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7078
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016265 Nonsense 376 820 7 9
Genomic Location (Zv9):
Chromosome 7 (position 39695194)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 38031834
GRCz11 7 38303092
KASP Assay ID:
554-4983.1 (used for ordering genotyping assays)
KASP Sequence:
GATGAGGGCTGCTACTCTGATCTGCAGCKCTGTGACGGATACTGGCATTG[T/A]CCTGGTGGTCGAGATGAGGAGGCCTGCCCRCTGTGCCAGCCGGGTGAGTA
Long Flanking Sequence:
ACAGCAACTGGCAGCTGACATACAAAAGAATTAACGTTAAATGATTTAACACATAAAATGGTAAACAACTCAGAAAAAAGTTGTTTCCGATTCTTCAAGATTCCAGGTCCACTTAAGAGGTCTCTATATGACCTCTAACCTGGCTGCGTAGATCCTGATTAAACAAATCATTTGGCATACAGAAAAAGCAATGACAAATATTATTCCAGCTTTACTCTGAAGTGGGAAGACACTGAATTGATCATATTATCTAGTCTCTTAAACATTCAACTTTATTAATAATCATAAAGATATAGGTATTTATATGTGTTACTCCTTCCTGGAGCGGACATCCATCAGAAAACCCACGCCATCAAAAGTCAGCTAACACACACTGTGCCACTGATCAAGTTGATGCTCTGTCTGCAGGTGAAGGGCTACTGTTTTCCCGGTGAGCATCCGTGTGGCACAGATGAGGGCTGCTACTCTGATCTGCAGCGCTGTGACGGATACTGGCATTG[T/A]CCTGGTGGTCGAGATGAGGAGGCCTGCCCGCTGTGCCAGCCGGGTGAGTACCCATGCGAGGGTGGCAGCGGGGCATGTTACTCCGCTTCTGAGAGGTGTAACAATCAGAAGAAGTGTCCCGACGGCTCCGATGAGAAGAACTGCTTTGACTGCCAGCCTGGAAACTTCCACTGCGGAACCAACCTGTGCATCTTTGAGACGTGGCGCTGCGACGGGCAGGAGGACTGTATGGACGGCAGTGACGAAAGAGATTGTCTGGCTTCTGTGCCCAGGAAGGTCATCACAGCGGCTCTGATTGGCAGTTTGGTCTGTGGGCTGCTGCTGGTCATTGCACTGGGTTGTGCCTTTAAACTCTACTCGCTCAGGACAAGAGAGTACAGGTGAGGACTTTTCCATCATTCCATCAACCAGCCAGATCAAATCAGGAACTGTGGAATAATCACTTTTTTACTTCATAAGATGCTTTATACCAATTATTTGTCATTATTTTCATTGTTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38628
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
ENSDART00000016265 Nonsense 389 820 7 9
Genomic Location (Zv9):
Chromosome 7 (position 39695231)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 38031871
GRCz11 7 38303129
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATACTGGCATTGTCCTGGTGGTCGAGATGAGGAGGCCTGCCCGCTGTGC[C/T]AGCCGGGTGAGTACCCATGCGAGGGTGGCAGCGGGGCATGTTACTCCGCT
Long Flanking Sequence:
TAAATGATTTAACACATAAAATGGTAAACAACTCAGAAAAAAGTTGTTTCCGATTCTTCAAGATTCCAGGTCCACTTAAGAGGTCTCTATATGACCTCTAACCTGGCTGCGTAGATCCTGATTAAACAAATCATTTGGCATACAGAAAAAGCAATGACAAATATTATTCCAGCTTTACTCTGAAGTGGGAAGACACTGAATTGATCATATTATCTAGTCTCTTAAACATTCAACTTTATTAATAATCATAAAGATATAGGTATTTATATGTGTTACTCCTTCCTGGAGCGGACATCCATCAGAAAACCCACGCCATCAAAAGTCAGCTAACACACACTGTGCCACTGATCAAGTTGATGCTCTGTCTGCAGGTGAAGGGCTACTGTTTTCCCGGTGAGCATCCGTGTGGCACAGATGAGGGCTGCTACTCTGATCTGCAGCGCTGTGACGGATACTGGCATTGTCCTGGTGGTCGAGATGAGGAGGCCTGCCCGCTGTGC[C/T]AGCCGGGTGAGTACCCATGCGAGGGTGGCAGCGGGGCATGTTACTCCGCTTCTGAGAGGTGTAACAATCAGAAGAAGTGTCCCGACGGCTCCGATGAGAAGAACTGCTTTGACTGCCAGCCTGGAAACTTCCACTGCGGAACCAACCTGTGCATCTTTGAGACGTGGCGCTGCGACGGGCAGGAGGACTGTATGGACGGCAGTGACGAAAGAGATTGTCTGGCTTCTGTGCCCAGGAAGGTCATCACAGCGGCTCTGATTGGCAGTTTGGTCTGTGGGCTGCTGCTGGTCATTGCACTGGGTTGTGCCTTTAAACTCTACTCGCTCAGGACAAGAGAGTACAGGTGAGGACTTTTCCATCATTCCATCAACCAGCCAGATCAAATCAGGAACTGTGGAATAATCACTTTTTTACTTCATAAGATGCTTTATACCAATTATTTGTCATTATTTTCATTGTTTTACTCATTCATTCATTTTCCTCCGGTTTAGACCCTTTAT
Associated Phenotype:
Not determined