ZMP
apobl
Ensembl ID:
ZFIN ID:
Description:
apolipoprotein B, like [Source:RefSeq peptide;Acc:NP_001025233]
Human Orthologue:
APOB
Human Description:
apolipoprotein B (including Ag(x) antigen) [Source:HGNC Symbol;Acc:603]
Mouse Orthologue:
Apob
Mouse Description:
apolipoprotein B Gene [Source:MGI Symbol;Acc:MGI:88052]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18137 | Nonsense | Available for shipment | Available now |
sa12118 | Nonsense | Available for shipment | Available now |
sa16833 | Nonsense | Available for shipment | Available now |
sa10039 | Nonsense | Available for shipment | Available now |
sa32301 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18137
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028709 | Nonsense | 1336 | 3730 | 23 | 27 |
ENSDART00000133353 | Nonsense | 1336 | 3730 | 23 | 27 |
Genomic Location (Zv9):
Chromosome 20 (position 31302873)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31374086 |
GRCz11 | 20 | 31276965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCCATGATTGAAGTCACRGGAACAAGTCCAGTGGATCTACTCTCCTTC[A/T]AAATAGAAGGTACTTGTATGYTTTCATATTTTCTGTTAATCACNTTTTTG
Long Flanking Sequence:
TCCTGAATGCGTGAGTGATTCAGAAACAGCTAAACTAATTTTAAATGCAGAACCATTATGAATTATAAATGTTTTGTTACACATTGTACTAATTTATGACATTACATTAATTAAAAAATATTCTGTATTTTAACAGTGAGGGTGCTGCTAAATACAAGTTTGGCCAGAATTATTACACCATAACCATACCTGTTCCTCTTGGTGGAAAAACTTCAAGAGATTTCAACCTCCCTGCTGCTCTGGAAACACCAGTACTGAACGTACCACAGCTTGACCTTCAGGTTAAATCCATTAATATCCCACTTCCAGTGTTCTTTATACCAGAGAGTCTGTCTCTGTCACTACCTCTTGTGGCAAAGGCGGAGGTGTCCAGCAAGCTGAGCAGCAACTTCTATGACATGGAAGCAAAAGCTTCTGCAGGGAGTGAACTTGTAGATAAACCAACCTATTCTGCCATGATTGAAGTCACAGGAACAAGTCCAGTGGATCTACTCTCCTTC[A/T]AAATAGAAGGTACTTGTATGCTTTCATATTTTCTGTTAATCACTTTTTTGTAATCTGTAAAAAATAAATATTGAATGTTGTTCTGTTTATGTTTAGGATCAACCTTCCTGGTAGGTAGACTTGGAGAATCTTTGAAGACTGAGATGAAATCCTCCCTTAATCACAAGCTCCTTGAAGCCAGTGTCAATTATTTTGAGGAAATAACAACTGGAGAAAAAATCACAATGAAATCAAGCAGCAAGATGGAGGCGAAAAGTCCCTTTGGTCTGAAGATTTCTCTGGAACACACGGGCCAGGTTGGACTCGATGAAGATGAGATCTCTGGAGATGGAAATCTGTTGGGCTCTATCAAGGCTGGTCCTTTGAATGGTGAAGTTGCTCTCAGACAATCACTTATCCTTCTTCCATTCAAGCCAGAGCTGAAAATCGACTCTTCTCTGAAAGTAGACTTAGAACAAATCCAAGCAGAGAACATAATTGAAGCAGCTTTTGCCAATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12118
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028709 | Nonsense | 1967 | 3730 | 24 | 27 |
ENSDART00000133353 | Nonsense | 1967 | 3730 | 24 | 27 |
Genomic Location (Zv9):
Chromosome 20 (position 31304855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31376068 |
GRCz11 | 20 | 31278947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATATCAACAGAGAAGAAATCATTGTAGAAATTCAGAAACTGGCCACATA[T/A]GTTAGTGACTTTGTGAATGAACTGAATCTGGAAGAGAAAATCATAAAATT
Long Flanking Sequence:
AGCGCACAAGTCTACTCTAAATTCCTTATGAAGGCAGAACCACTTGCTTTTGCACACTCACATGAATGCAGAGTCTCAACAACTTACAACCTGTATGATGATCTGGTATTCGAAACCAACCTTGATAATAAAATTGATACTGTGCTGACACCGTCTGAGCAAAAGGCCACAGTGAGAGTAAAATCTAAGTTCAACAACCATGAGTTTAACAAAGACTTGAGTGCTTACAATACCCCTGAAAGACTTGGAGTTGAAATGTCTGGATCCATCATCACCAACATCTTCAATACAGTTGACTCTGACAATCAAGACCACTTTTTCTCTGCCTTCCTAAAATATGATAAAAACAGCAACAGCCGTGCCTTAAGTCTGCCATTTATTGATGAGTTTCCATTTGACCTGCAACACATGAAACTTGCAGTTTTGAGGATTGTTGAGGCCATGCAGAGTTATATCAACAGAGAAGAAATCATTGTAGAAATTCAGAAACTGGCCACATA[T/A]GTTAGTGACTTTGTGAATGAACTGAATCTGGAAGAGAAAATCATAAAATTCAGCAAGGACCTGACTGCGCTGTATGAGGACTATGGAATTACTCTCGACGACCTGGAGGCTTCTCTGATGAATCTAAAGCCTGTTTTGTTGAAGCTAGTCACTGAACTTGACACTTATGTAGTAGAGATAGAAAAGATTGTGAGGGAAATAATTACAAGTGGCACACCATCTGATGCTGCAATACAGAGGTTTACAGATATCCTGAATTCATTCAATGAGAAATATGACGTCAAAGCCATTGTTCTCACTGTTATTGAGGCTATTGAAAAATTTCTTAGGGAAATCGATGTAATGAGTATAAAGGGCAGCAGGGAAGTCTTCAAGCAATATGTTGATGAATATTTTGCTATTAAATCCAAAGTGGAGGAAATTTTGAGTGAACTGAAGCAGTTTGTTGCAAACTTTGACCAAGAAAAGTTCACTGAGGATGTGAAGAACTTTGTTACCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16833
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028709 | Nonsense | 2304 | 3730 | 24 | 27 |
ENSDART00000133353 | Nonsense | 2304 | 3730 | 24 | 27 |
Genomic Location (Zv9):
Chromosome 20 (position 31305866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31377079 |
GRCz11 | 20 | 31279958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACTTGAAATCCGTCAAAAGCTTGAGGCAATCAGAGAGTTTGTTAACTA[T/A]GCTTTGTCATCTATGWGCGCTTGCATCGAAAAGCTGGAAAAAGTCAAART
Long Flanking Sequence:
AGAGACTATGCAGACAATCTGGTGGCTAAAATCCCAACAGAGCAAATCAGCAAGATTCTTGAAAAAGCAAAACAACTGCTTAATCTACTGGGTAACAGAATGAATGCCATCTATACAAATGTGAGAGAAATTCTGGTGAAATCTGGGGTTGACAAGAAGATCGAAACTCTCCTCAAAAAAGTTGTTGAGCTTATCAAGAAGTTCAACATTGAAGAAACTGTTAAGACTCTTGCGGACACTTTGAAATCTATTCTGACCCCTGTCACTGAGCTGGTGGATAAGGCCATCAACTACTTGAAAACAACAGAGGCAAAGGAAATCATTGAAGATCTGAACAACTGCCTAAACCACTGCATTAAATATATTAGATCATTTGACTACAACGCATTTGTGGATGAGGCCAATCAGAAAATCAAGAAGTTAACAAATGATCTTTACACCATGAGTTTGTCACTTGAAATCCGTCAAAAGCTTGAGGCAATCAGAGAGTTTGTTAACTA[T/A]GCTTTGTCATCTATGAGCGCTTGCATCGAAAAGCTGGAAAAAGTCAAAGTTGTGGATGTCGTCAAAAAATTCAGTGACATTGTCGATAGTGTAGTCTTCATTGACACCGAGGCACTCATTGAGGACCTTAGGAAAATACTTGCAGACATTGATATCAGAGAAGAAATCCAGAAGTTTCTGAAGCACGCAAGTAGCATCTCCACCAAGGTTGTGACCACTGCAACAGATGCATGCAGTGCTGTTATGCAAGTGATCCAAAACATCCTTAAAGATCAAGCAGTTGTCAACGAGCTGAAGCAAATCTGTGACAGAGTCAAAACAGTACTGAGAACAGCTGAATTTAAGATTCCATCTTTCATTTTTCCACTGACTGACCTTGTTGTGCCATCCATAAAAATAAGCTTAAAGAATCTTCAGGAAATCAACCTCCCATCTTCACTGATTGACCTTCCAGGGTTTACAATTCTGCAATATTACACTGTGCCACCAATCAGAGTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10039
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028709 | Nonsense | 3214 | 3730 | 24 | 27 |
ENSDART00000133353 | Nonsense | 3214 | 3730 | 24 | 27 |
Genomic Location (Zv9):
Chromosome 20 (position 31308596)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31379809 |
GRCz11 | 20 | 31282688 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTYGATGTGGATGAAAACCTGTCTGTAGAGACAGCCAATGAGCAYGTATA[T/A]GCTACAATGAAGTTTACTTCCAATAATGAAGCAARTGTTGGATCTTTCAA
Long Flanking Sequence:
CTTCTAGAAAATCGCCACATTGAAGGAACCCATGAAAGCACTGCAACTATGAACCTGAATAACTTTGAAGTTACACTGTCTATGGCCACAGATGCAAAAATGAATCTACCAATTCTTACAGCTAATGCCAACCACCAACTTACTGCTGACAACAAGGCCAACCCAAAAGCAGACTCAACATTTAAGATGGATTACAACTTTGACGTTCCCATTATTAAGCTTGTTGGAAAGGGAAATGCTGAAACCATCTTAAAAGGCGAAGGAACTCGTACGTTTATCTCTGCTGAGACACTTATAAAGAGCAATATTGATGGAACATTCCTAGATCGTGGTATTTTGAAAGGAACTCTGAATTACGATGAATCCCTGTATGTGAATGGTAATAGTTTGCGATATGCCCTTAAGACTGGTGGTAATGGAGACCTGAACTATGGTGATTTCAAGGTGGCTTTTGATGTGGATGAAAACCTGTCTGTAGAGACAGCCAATGAGCACGTATA[T/A]GCTACAATGAAGTTTACTTCCAATAATGAAGCAAATGTTGGATCTTTCAACACTAAAGGAGTTCATTCCAGCCAGGCTACTCTCGATATGGCTCTTCTGAAGTCACTGGTGGCTGATATGAAAATAGACTTGTCTCAACCGAGCACCTTTGGTGAACTTAGCATCTTCGAGACAATGAAAGTAGATCTCAGTGCTCCCAAGCAGAAAATTGATATCCTTTCAACAATCAAGTCTCCGGTATACACCACAGATGTTCGTGCTAAACTAGACGGTAATGCCCCAGATTACAAAACGGTTCTGAAGGCTTCAGCCACTTCACCAGTTGTGCGCCTGCAGTATGATCTTGACAGTAAGTTTCAACATATACTATATGTACAATGATACTCAATGTTAATAAAAGGAAATTAAATCTTGGATTTGTGTGCTTTTACACAAAACAGGCTCCATGAGTTCTACTATGGAGAATGGTGCCCTTGTTGTCGGAGCTAACGCTGTACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32301
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028709 | Essential Splice Site | 3331 | 3730 | 24 | 27 |
ENSDART00000133353 | Essential Splice Site | 3331 | 3730 | 24 | 27 |
Genomic Location (Zv9):
Chromosome 20 (position 31308947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31380160 |
GRCz11 | 20 | 31283039 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGCTTCAGCCACTTCACCAGTTGTGCGCCTGCAGTATGATCTTGACAG[T/C]AAGTTTCAACATATACTATATGTACAATGATACTCAATGTTAATAAAAGG
Long Flanking Sequence:
AATTACGATGAATCCCTGTATGTGAATGGTAATAGTTTGCGATATGCCCTTAAGACTGGTGGTAATGGAGACCTGAACTATGGTGATTTCAAGGTGGCTTTTGATGTGGATGAAAACCTGTCTGTAGAGACAGCCAATGAGCACGTATATGCTACAATGAAGTTTACTTCCAATAATGAAGCAAATGTTGGATCTTTCAACACTAAAGGAGTTCATTCCAGCCAGGCTACTCTCGATATGGCTCTTCTGAAGTCACTGGTGGCTGATATGAAAATAGACTTGTCTCAACCGAGCACCTTTGGTGAACTTAGCATCTTCGAGACAATGAAAGTAGATCTCAGTGCTCCCAAGCAGAAAATTGATATCCTTTCAACAATCAAGTCTCCGGTATACACCACAGATGTTCGTGCTAAACTAGACGGTAATGCCCCAGATTACAAAACGGTTCTGAAGGCTTCAGCCACTTCACCAGTTGTGCGCCTGCAGTATGATCTTGACAG[T/C]AAGTTTCAACATATACTATATGTACAATGATACTCAATGTTAATAAAAGGAAATTAAATCTTGGATTTGTGTGCTTTTACACAAAACAGGCTCCATGAGTTCTACTATGGAGAATGGTGCCCTTGTTGTCGGAGCTAACGCTGTACTTACACATCAGGACTTCACTATGGATATCAGCAATGCTATTCGCATGAGGTAAATAAAAAATCTTTCTGATTTTTTGTTTGAATATTAGTACTATGTTTGCAATTATAATTTATTTTATAAAGCAATTCTGAGTGTAAATCTAAATTCTACTTATCATTAGCGAAAGGAGCCATATTCTGAATGTGGACATCACCAGCCAAACATTTACCGATGTTAACCTTCGCTATGCTGCTCGGAGTGATGGGATAAGTGGCTCTGTTTCCACACCGGGGTCTGGCCTCCTTGGCTTTCAGCTCCAAGGAAATATTCCATCCCAAATGAATGCAAGGCTCTACTGTCGTTATGCTGTAAGT
Associated Phenotype:
Not determined