ZMP
si:dkeyp-88f5.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate apolipoprotein B (Including Ag(X) antigen) (APOB) [Source:UniPro
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37185 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23825 | Nonsense | Available for shipment | Available now |
sa17651 | Nonsense | Available for shipment | Available now |
sa43552 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6658 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37185
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113074 | Nonsense | 550 | 2476 | 10 | 19 |
ENSDART00000113553 | Nonsense | 689 | 962 | 13 | 17 |
ENSDART00000138336 | None | None | 1531 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 53800231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53645010 |
GRCz11 | 20 | 53450427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATTCCACTCTCAGTCTTCTGTGTGCTTTAGGCGACTCAGAACATAGTC[A/T]AAGAAATCAGTGACAGTGTCAACAAGCTTTCTGAAGACTTAAAGGCCCAA
Long Flanking Sequence:
AGTAAAGCAAAGACCATGTGGGTCAGGTAGTGAAAACGGTAGGCTACAATTAATTAATTCGTTATGAATTAATTGATATTCAACAACCAGAACCCCCACCTACGACGACAATGCCATCGTCCATCGCGATGTTTCACATTAGACATCGTATGATGCCAAATCGGTCAACATCGCCCAACCCTAGTGTGAAGCACACTTGGCAATAAAACTGCTTCTGATTCTAATGCTTTGTAGATTGGCATGGAGGGTAAGGGCTTTGAGCCCATTCTAGAGGCTCTCTTTGGTGAAGATGGTTTCTTCCCAGACATTGTCATGAAGAGCATTTTATACGCTACTGACAAGATGCCTGCTGAACTGAATGAGGTCTGGGACAACATGCTGCCAAATTTGAACAATTACAGGAAGAAGAGACAGGTATTACATTATATTAGCAAATACATTTGTATAGAAGGATTCCACTCTCAGTCTTCTGTGTGCTTTAGGCGACTCAGAACATAGTC[A/T]AAGAAATCAGTGACAGTGTCAACAAGCTTTCTGAAGACTTAAAGGCCCAAGATGCCCCTGAAGCTATGGTTTACCTCAAGCTATTGGGTGCTGAACTTGGGTATCTCGATGCAAAAGATGGCAAGATGATTGGCAGTCTTCTTAAGATGATCCCCACTGACGTGAGTACAGCTCTACCAAATGCACATATGCAACTTTCATGAATTTCAAATGGATTAAATCATCAGAATTATATTTTTTATATAGTTCACCAAAAGACTGTTCTCGAGTGTCGACAATGAGCTTTTCCTTCACTACATCTTTATGGATAATGAGTTCTATCTGCCCACCGCTGCTGGATTTCCACTGAGAGTTGCTCTGTCTGGCACCTTTACTCCTGGAATCAAAGGAGGATTGAGCTTTAATCCAGGCATGGTAAATCCAACACACTTCAATCATCCATGTGTTATTGTCCACTGATTTTTATTTTTTAAAGGGGCCATGAACCGACAAACAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23825
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113074 | Nonsense | 671 | 2476 | 12 | 19 |
ENSDART00000113553 | Nonsense | 810 | 962 | 15 | 17 |
ENSDART00000138336 | None | None | 1531 | None | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 53801444)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53646223 |
GRCz11 | 20 | 53451640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTACATGATTACAGGGGGACTTTGCGTTCATGCTGTCTGCTGGGGTT[G/T]AGTTGGTGACTGAGATTGGGACTCATTTACCCGACTATGTTCATTCTGGA
Long Flanking Sequence:
GTTTTGCCCTGTCACTATCCAAAACTGTCAACAATCACATCAGTGGCTATTTACTTCAGAGTCTACAATTGACCACGCCCACTCCCAAATTTTGATGGGAGTGAAAACAACACAGCACATCTTTTTTACTAAATTAAATAAATTGAGGTTAATGTGTCAGTCAGACTTGCATTGAAATTCAGTTGATTTCAATTGTTAACAATTTTAATACTGCCACTTACTATAGTGAACTTTGACAAGTTTACACTTCTTACATCTATATGTGCAAGCAAGACTTATGTAAATGTAACTTGTCATGTGACACTGACACACATCTATTTTCTAATTTAATAGTTGAATTCCTCGCCCAAACCACACTTTCAGAACTTCCAGAAATAATAAGAAAGACTCGTTGTGACCAGTGGGATTAAATATGATTCATTTCTACAATTATGCTATCCTGAATAAACATGACTACATGATTACAGGGGGACTTTGCGTTCATGCTGTCTGCTGGGGTT[G/T]AGTTGGTGACTGAGATTGGGACTCATTTACCCGACTATGTTCATTCTGGACTGGAGATGCACACTAACATCTATCATGAGAGCGGCCTCAGAGCCAAAATCTCTGGGACCCAAAAAAGGCTCAAACTCTCCATTCCAGCTCCTCGTGAGCCAACTGAGCTCATCAGTGTCACGTAAGATATAACTCAGTTTTCTGACCGCACTTCGCTATTATTGCTCATTGATTCCTTTGCTGGATATTAGAGCTGAATTTAGAAATAGTTTTGACACAAATTTTTGTGCTTAACAAACTAAATTAAATATGTAGGCTGATGGATGTCTTCAGTGGGGTGAGTTTTCACAGTTTCCTTACTCCACCAAAGTAAATGAGTAAAGAGTAAAAGCAAAGATAAAGAGGCTGAATGAGCAGGCTCGTTCTTTATCCTCGTGCTGCAGATGCTCTGTTTTTCTCGTTAGTGAAGCGTTCAGTTTTTACACATACAAAGTCCACCATGTAAATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17651
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 |
---|---|---|---|---|---|
ENSDART00000113074 | Nonsense | 1170 | 2476 | 19 | 19 |
ENSDART00000113553 | None | None | 962 | None | 17 |
ENSDART00000138336 | Nonsense | 225 | 1531 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 53815931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53660710 |
GRCz11 | 20 | 53466127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGTGMTGCTGGGCAAATTTCTGGAGATGGGARCCTGGAAGGATCCTTC[A/T]AGGCTGGTTCAATCTATGGATCAGGAAATCTAAAACAATCAGTTTTGCTT
Long Flanking Sequence:
AACGATGGACTATAAATGTATCCCCCTGACCTCTTCCCCCCAAAGACCAATCAGGTCCCTTTACCTCTATCTTTTGTAAGTTTAACATGTGTATATTGAAATTCATTGTGCACTTTTGTGTAATGATCATCAGAACCGAATAATGTTCTTTTTAGAAACATCATATGCTCCTTTTAAAGTACCACATGATAATTAATGTATTGAACTCATTTGATTTGGTTGATTGATTCCTGACTTATTCCACAGGATCTGCTCTAGCTGAGGCCACATCTGGCGATTCTCTAAAAGCTAGCATGAAAACAGTGATTGAACACAAGTTTTTCAATGCCACCATCAGTGTTGAAGAAGAAGTGCAATCTGCAGCAAAACTCAGTGTGAAATCTAAAAGCAAGCTTGAAGTTACTAGTCTTGTTGCAGAGCAAATGTCCGTGGAGCATAATGCAATATTTGAAGGTGATGCTGGGCAAATTTCTGGAGATGGGAACCTGGAAGGATCCTTC[A/T]AGGCTGGTTCAATCTATGGATCAGGAAATCTAAAACAATCAGTTTTGCTTATCCCATCCAAACAAGAAGCAAAGATTGACTCCTTACTGAAAGTAGATTCAAAGCTTCTTCAGGCTCAAAACTCCTTTTCTGTGGCTTTTGCTAATCGAGAATTGACAGTTTTGTCCACCACCACAGCATTTGATGACATTCTAACAAACACTGCTAAAGTTGCCATCAATGAATCACAGATTGGTTTAAGTTATTATACAAAAGCACAAGGATTTGGACTGAAGATCGAAAACACAGCTGAGACGAGAGCTGATGCTAAAGCTATCAGTGTTAAGATCGAGACCTCTGGTGATTTATCTCAAGAACGTATTTACTCGATAGTCACTGGAGAACTGGACATTAACGGACTGGCTATTAAAAGTGATGCCTCGGCTAAACTAATGGGACACAGAGCTGCACACAATGCCATCCTGAACTTCAATAAAGATGGCTTGACATCCAGTGGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43552
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113074 | Nonsense | 1864 | 2476 | 19 | 19 |
ENSDART00000113553 | None | None | 962 | None | 17 |
ENSDART00000138336 | Nonsense | 919 | 1531 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 53818013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53662792 |
GRCz11 | 20 | 53468209 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCAGTGATTTTAAAAGTTCTGAATACAGGAATTGGCAAATTTACCCTT[G/T]AAGACTTCTCTGATGAAGGCACCCATGACAGTGATCTACTTTTTACCATG
Long Flanking Sequence:
AGATTCCTGCAAGTACTAAATCCTATCAACTACCCTGTTTTGAAAAAATGCATGGCGAGATCAGATTCACCAGCCCTGTTTACAGCCTAAACACATCTGCAGAGTTCAAGAACGTTTCAGCAACACATCCTCAATTCGCAGGTGTCATCAAATCTAAAGGAATCTCTGCAAGTCTTGAGGTTTTGAATTATAATATAGACTACACCATGCAGATCTCCATTCCTGAGATGACCCCTGTATCGGTGTCTGAAACTCTTAAGATAACACACTCTTATTTGACTTTAGACCAAAGTGCGTCTTTGACTCTGAATGCGTCGATCACTAAAGGTCCTGATTTTTCATCCCTTTCTCTGGACACATCTTATAAGAACCAGGTTAACATCCCTTTGCACTCTCTGTCAAGTGAAGTTACACTTGCTTCGAAGGCTGTAGCAGTGTATCAGAATAACGCTGCAGTGATTTTAAAAGTTCTGAATACAGGAATTGGCAAATTTACCCTT[G/T]AAGACTTCTCTGATGAAGGCACCCATGACAGTGATCTACTTTTTACCATGGGTCTTAGCGCTGCCAAGCTGAGACTTAAAGGCCACACTGACAGTTCTGCGTTGCAGATGGAAATGAATGTCGATGTTGACGCTGATGCCGTAGCTCTAAGCTACCTTAAATTCAATGTCTTTGCTGAAACAAAGTCACCATTTATCAAGAAGAACTTGCTGGTTGCTTCTGGGAATGTCTCCATCAATGACATGGATGTAAAAATCAGTGGAAACCATGAGACCGAGTTTGATGGAGTGGTCAGTGTAGTTCTGTCTAATACTGCTAGCGTGATCATCTGTCCACGTGAGATCGCAGTTGAGTTTCAGAACAAGGGAAATGCCAAGACTGACCTTTATGAGTTTTTAATAACCAGTGTTGATCTCCAGAATGACTACACTGTTATTGTCAACTCCGACTTACAAGAAGTCAGCACTATTGCAGTCGCCCAGATAAATCATTATAAGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6658
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113074 | Nonsense | 2363 | 2476 | 19 | 19 |
ENSDART00000113553 | None | None | 962 | None | 17 |
ENSDART00000138336 | Nonsense | 1418 | 1531 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 53819510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 53664289 |
GRCz11 | 20 | 53469706 |
KASP Assay ID:
554-5058.1 (used for ordering genotyping assays)
KASP Sequence:
TTYATTATTTGCTGGACATTGATTCAAACTACACACAYAAATATAGAAGA[G/T]AAGAAGTTGCAGTGAAACACACTGCTCWCGGTAAAACTACAATTATTCCC
Long Flanking Sequence:
GCTCAGTGACCCTGCAGGACAACTATGAGGTGGTTTTGGTGTCAGACACAATTGCGAAGATTAATCTGACGATATTCTCAATCGAAGCCGATCATCAGCTTTCTGCTGACACGAAAACTCATCTGAAGGCTTTGTCAAACTTGAAGATCAAGTACAGCTTTGATCATCCAGACTCACGTGGAGGTGGAGATGCTGAGAATACCTTAAAGATGAATGCATATTTGTCTTCCATCACTGTTGAGTCTACATCCCAAGTAACCACCAATTCTACACTGCCTGATGGTGGCGCTCTTAAGGGAACTCTGGATAGTGATGCAAACATCAGTGTGAATGTTGCGGGTCTGAAATCGAATGTGAAAGCCTCTGCAAATGGATACTATGATTATAGAAACAACAAGCTGAGCTTCGATATGAATGACCAAGTGATCTTAGAGGGAAATTTTAACCGTATTCATTATTTGCTGGACATTGATTCAAACTACACACACAAATATAGAAGA[G/T]AAGAAGTTGCAGTGAAACACACTGCTCACGGTAAAACTACAATTATTCCCATGAGCACCTTCATGGCAGCTGTCGACTTCTTCTTGACTCAGCCAGATCATGATGATTTTGAACATAGAGGTGAAGGATTTGGCTATATTAATAAAACATCTTTATATAATGGCCAGATTTACTCCCGTTGGTTCAATTCAAGTACAGCGATATCAGTCGAGTCTGATAATGATTCACCAGACAGAAAGTTTTTGCTCGAGTGTTCTTTCAATTTCACAGCTCCATCAGTGCTTGTGGAGTATGAGAGTGAATTAAGATCAATTCCCATTAAAATAATCGACGATTATTATTGATATTTTAAGAATTCATCAAAGTAATGATGTCAGCTAATCGTTGAAGTTTAACATGTGCTCAGCTCAGCTCACAGATCCACTTCGTTTTTAAAAATGTATGTAGCTTTTCTGTTGTGTATGAAAGTATTATTAAAATTCCCTGAAATATTTCTTGTC
Associated Phenotype:
Not determined