ZMP
osbpl9
Ensembl ID:
ZFIN ID:
Description:
oxysterol-binding protein-related protein 9 [Source:RefSeq peptide;Acc:NP_001071273]
Human Orthologue:
OSBPL9
Human Description:
oxysterol binding protein-like 9 [Source:HGNC Symbol;Acc:16386]
Mouse Orthologue:
Osbpl9
Mouse Description:
oxysterol binding protein-like 9 Gene [Source:MGI Symbol;Acc:MGI:1923784]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21238 | Nonsense | Available for shipment | Available now |
sa21237 | Nonsense | Available for shipment | Available now |
sa21236 | Nonsense | Available for shipment | Available now |
sa31638 | Essential Splice Site | Available for shipment | Available now |
sa6094 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21238
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 |
---|---|---|---|---|---|
ENSDART00000100727 | Nonsense | 172 | 733 | 8 | 24 |
ENSDART00000135319 | Nonsense | 75 | 239 | 5 | 10 |
ENSDART00000146774 | None | None | 52 | None | 4 |
The following transcripts of ENSDARG00000069298 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 17162857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16607745 |
GRCz11 | 8 | 16643457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTGTTTTGCTTTTTTTTTTAGAATATGGTAGAGTCCATCAAACACTG[T/A]ATCGTACTGCTACAGATTGCCAAGGTAAAACACTTGTAATTTAGACTCAT
Long Flanking Sequence:
ATATAGGAAGTACTATGAAAGATTCTTTGCTCTTTTAAGCATAATTTTGAAAAAAATCAAAGGAGAGCTTGTCATTTTTGACTTTAACTGTATTGTAGTTTGTATATTTATATTATAAATAGTTCACAAGCAGAACTCAGGATGTGTTAGATACTAAATTTGAAACGAGGCATTTACTGAGAGTCACATTTTAAGCCTATTTATGGGGATTAAACTCATGAGACTGTCAGGCTTTCATTTCTGCTTTTTTTAGGGTTGGTAAAGGTGCATCTTAGTTTGTAAGTTAAGGGAATTTCACAATTCTTACTGAAACTGTTTATTTTCTTCTATTTGTATGTCCTGTTGACAGAAAATCGAGAACCTGAAGGACACCACTTGTGTAAGAGCGTCTGCACCTTCACCCTCTTAATGCATTTTGGATCAGGTTTTGTTGTTGGAATGCATTCTCATTTCTTGTTTTGCTTTTTTTTTTAGAATATGGTAGAGTCCATCAAACACTG[T/A]ATCGTACTGCTACAGATTGCCAAGGTAAAACACTTGTAATTTAGACTCATAATGTGTATGCTCCTGTGTTTTGTCTGCCCACTGTGTTCATATTGTGTCTTGTGCAACCCAGCCTGTAATTTTCCATAACCCAGTTAATGTTTATAAACATTCCAGCAGGTTCCATATTAATGGTTTGGAGAGGTGATTTTTCCTACACTAAGGTCATGTTCACACAGCAGGAGAAATTAAATGTTAGTTGTTTTTTTACTGTGCTAAATATGATCTTTTCACATTAACCAGCACATTTGACAGAGGAACTCGCACCTCGATTGGAATCAGATGGTCTCGATTTTGTCAGATAGTGCCGTCTTTCTTTCTTTTTTCTTTTTTTTTTTTTTTAGTATGTGCCTTTGGTAATTCATTCAGTGTTTGACTCACTCCTGTAAGCTGTACTATGAAGGCATGTGTTAGTAAATATGGTTGACAATCCCAAACCCTACTGTGTGAACATAGCCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21237
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100727 | Nonsense | 204 | 733 | 10 | 24 |
ENSDART00000135319 | Nonsense | 107 | 239 | 7 | 10 |
ENSDART00000146774 | None | None | 52 | None | 4 |
The following transcripts of ENSDARG00000069298 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 17158807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16603695 |
GRCz11 | 8 | 16639407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTCTGTGGTTCTCCGCAGAGCACCATAAACCCAGTGGATGGGGTATTC[C/T]AGCCTACCCCTCTCAACGCCGCTGTAGTCAGTGCTAGTGCCATGCCAACG
Long Flanking Sequence:
ATTTTCTTTACAAAAAACATACTGACCTCAGACTTTTAAAATTCTGTTTAAAAATTAAAATTAATAATTAATTTAAAATTAATAGTTTTTTTATCTTTATCATTAGAAATACGTGATTTATTTCAAAAAGTCTGCTTAAAGAACAAAACTCGAATACATATTTAGTCTTAAACAATAGGTACTTGACCAATTTACTTCATTTTCTTGCCCTCATGCTGTTCCAAAATCTTCATCTTTATACCTTCAAAGAATGTCCATCTTTTATTTTTCATATAAGAAAAGGTCATATAAAGCAAAACTCAGGGTGAATTGTCTCTTTAAGAAACAGTTCTAGTAACTTAATTTCAGTCCTTGAGGATTTCTCTGATAGTTGGGTTGGGCATTGAGACTGAAGGCTACTGTGAGAGTGTATTTATAACATGTTTTCCTATGAGAGCTGTGTTTTGTATCATGTCTGTGGTTCTCCGCAGAGCACCATAAACCCAGTGGATGGGGTATTC[C/T]AGCCTACCCCTCTCAACGCCGCTGTAGTCAGTGCTAGTGCCATGCCAACGCAGACCACTCTACCCACAGGTGAGCTCTCTGCCTGTGTCTTTTTCTGCATTATATTTCTTAATAATGCTTTATGCGCTTTTGTTGTCAGTTTCTTGGCTATGTTATCTATTAATTTGAAACCTCTAATATTACATTTGACTTGCAAATTGTGTGTATTTTTGCGTGCCAAGGGTATTTGAAGGGTGTGTGTTCATCCGTAGATGGAGCTCAGGTGTGTAAAGCGGAGCAGAGGCCTTCTTCTTTACCCGTGGGCCCTGTTGTCACGGTGATGGGCAGCCTTCAGACCCCCACTCCCAACAGCACAGGTACAAACCAACAGACAGAAAGTAAACAAACAAAACTAGGTGGAGGCTTACAGATAAAGTATACTTTTTTATCTAATGTGCATTTAATTTAAGCATACACTACCAGTCAAAAGTCTGAAGACATTAATGTTGTTAAAAGAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21236
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100727 | Nonsense | 298 | 733 | 12 | 24 |
ENSDART00000135319 | Nonsense | 201 | 239 | 9 | 10 |
ENSDART00000146774 | None | None | 52 | None | 4 |
The following transcripts of ENSDARG00000069298 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 17152185)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16597073 |
GRCz11 | 8 | 16632785 |
KASP Assay ID:
2260-0345.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCACACTGTTCCCGACTTCTCCTATTCCAGCAGCGAAGACGAGTTTTA[C/A]GACGCAGATGAGTTTTATCAGAACAGCACGTCACCAAAACACTGCATAGA
Long Flanking Sequence:
ATGGTTATAAAAATATTAAAAACGGCTTTTATTGTTGCCGAAATCAAACAAATTAGACTTTTTCCAGAAGAAATAATATTATCGGAAATATTTGAAAACAGTCCTTGCTCTGTTAAACATCATTTTGGAAGTATTAAAAAAAGAATAGAAAATTTACTGGAGGGCAAATAATTTTGACTTCAACTGAATGTACTTTTTGTTGGCAATGTAGATTTGTGTAGATTAACTCATTGGTCATGCTACTTATTTTGAGGCAAGAAGTCAGCCACATATACAAAAGCATTAAACCTCAACCCACACTGAGCCTCATCTGTGGTGCTGTTTAAATGAGTGTGGTTAGTCATAGTTCCTCAACACATTTATTGCTATCATTTTCTTCCTGTGGTTTTAGGGAGCGGTCCTTCAGGTCCCAGCAGCAGCGTGACTTCACCCAGTCACATGAACGTACCGGCTCACACTGTTCCCGACTTCTCCTATTCCAGCAGCGAAGACGAGTTTTA[C/A]GACGCAGATGAGTTTTATCAGAACAGCACGTCACCAAAACACTGCATAGAGTGAGTTAAACAAACACACACACACAAAAACACACACACACTCTAAAAAACAGCATAGAAACTAAGGTGGACAATTATAAAAACAGACTTCTATACTGTGGAGATCAAAACTGAGCATCTGTCTGGTAAATGATTAGCTAATCTGGGCATTTCCAGTAAATCGAAATCCTTGGTGACAAAGTAATGGCTAATAAACTCACTACAGTGAGAAAAACTGAAGAATACAAATCAAGATCAGCAGACTAGTGATGTCCTGTGAGAGACTAGTGATGTCCTGTGAGAGACTAGTGATGTCCTGTGTTTGGAGATGTGTTAAAGTCATTTAAACAAATGCCTGCACACTTCCTACTCATTATTGACTGCTGTAACCTTGAGAAATATTAGTCTTCCTTTTTGCAACAAAGGACAGCACAAACTAAAGCAATTCTCAAATACACTTGATTAAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31638
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 |
---|---|---|---|---|---|
ENSDART00000100727 | Essential Splice Site | 419 | 733 | 15 | 24 |
ENSDART00000135319 | None | None | 239 | None | 10 |
ENSDART00000146774 | None | None | 52 | None | 4 |
The following transcripts of ENSDARG00000069298 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 17147775)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16592663 |
GRCz11 | 8 | 16628375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGGAAATGTATGCAGATTTCTTTGCACACCCGGATTTGTTTGTAAGG[T/C]AATGCTTGTCTTCAGATCTCACAGCTGCTCTGCCATATGGACTTGATTCT
Long Flanking Sequence:
TTAGAAAAAAATCCTTAGTGTTTAGCCTTGTGTAAATCTGAAAGTTAATGTATAGTGGTCTTAAAAAGTCTTAAATTTGACTTAATAAAAGCTATAGAAACCCTGGTTAAATGTTTTTTATTCCCTTTTAATTATGTGTTCACGCTTCATGTTCACTGTTCGCTGAGTTCATTTTTGGCCATGTGTTTTTCTCAGATCAGTTTGACAGTCATGATGAGAAAGATGATGACGGTGAGGGTGAATCTGTGGAAGAGCATAAAAGTGTCATCATGCATCTGCTGTCTCAAGTGCGCCTGGGCATGGATCTCACCAAGGTAAACACAAACCACCTTCTCTCTTTTTTTTCATCTATCTCCACTTTTCTTTTTTTTCCCTAAAATTTCTTCTTTGCAATCCATCTCTGTCACCCTTAGGTAGTCTTGCCAACATTTATCTTGGAGCGGAGGTCGTTGCTGGAAATGTATGCAGATTTCTTTGCACACCCGGATTTGTTTGTAAGG[T/C]AATGCTTGTCTTCAGATCTCACAGCTGCTCTGCCATATGGACTTGATTCTTATGTCTGATTACGGCAGTGCTGTTATCACTGATGAATGTAGCAGTGCTACTAAGCTGAACACATTCTTGAGTAGCTTGAAAAGTAGCTGTTCATCTAATGGAGTGCTTTTTTCTAACAAGTAGCAGTGAAGCGTGACAGAATATTGCATTGATTTTTATTAAGCTGTCCGGCCAGATTTACTAGCAAAGAATATAATCAAACATGCTCTGCTCAAAGCAAACTGGAACCCAATTCTAAGAATTATGCATAAAGTAACTAACTTTAAACATAGAATGTAGATTTAGTAAACAGCCACATTATATACAAAAGTATATGAAACATCCCCCAAGTTCATTTGCTCAGATAGTCATGTCTTTTTTTTAAATGGGGGGGTCCAGAGTGTATTTTTAAGGCTTGGTTGTGCTTATAAGATGCTAAGCAATTTATAAGCGATTTATAAGAAATTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6094
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 |
---|---|---|---|---|---|
ENSDART00000100727 | Nonsense | 553 | 733 | 19 | 24 |
ENSDART00000135319 | None | None | 239 | None | 10 |
ENSDART00000146774 | None | None | 52 | None | 4 |
The following transcripts of ENSDARG00000069298 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 17142571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 16587459 |
GRCz11 | 8 | 16623171 |
KASP Assay ID:
554-3901.1 (used for ordering genotyping assays)
KASP Sequence:
ATCATCCACTCTTGTCTACCATAGGTTGCGTGTCTTGTCTTGAATATGAT[G/T]AGCATTATATTCTTAATTTTCCCAATGGCTACGGGAGGTAAGGGTCGCTT
Long Flanking Sequence:
AAAAACAACAATTTAGTCATGGCAGAAAATATATTATTTAGCAAAAAATGTGCAGCATTTAAGAAAAAAATTTAAGGGCTCTTGTTCACCTTAAATTTGTTTTAAATTATTTTGTTAAAAAGAAATTGTGACTAAATCATGTGATTCGTATCGTGAGTCGTATCGAATTGTGAGTTAGGTGAATCTTTACATCCCCAGGTGCCTTTCATTGGATTTTATCATTTGCTATACTTTTTTTATTTGCAGCATTTTCTAATATATTTGTGCTTCTGCAGTATCTGCGTTTTACGCCGAATGTTTCAGCAAAAAAATCCAGTTCAACGCCCACATCTGGACGAAATCGAAGTTCCTGGGAATGTCTATTGGAGTCCATAATATTGGTCAAGGTAGTCAAACAAATTATTTACAGTACAAATGGTCATTAATACACAATAGTGCTACTAGTGCTTAATCATCCACTCTTGTCTACCATAGGTTGCGTGTCTTGTCTTGAATATGAT[G/T]AGCATTATATTCTTAATTTTCCCAATGGCTACGGGAGGTAAGGGTCGCTTTATCACAATAATATTCTGTATTTGAGATTTTGTGTCACTCATCTCGCTGTCCTTCCAAAGGTCAATCCTCACCGTCCCGTGGGTTGAGTTGGGTGGAGAGTGCAATATTTCCTGTTCCAAATCTGGCTACAGTGCCAATATAGTTTTCCACACCAAACCCTTCTATGGAGGAAAGAAGCACAGGATAACAGCTGAAATATTGTAAGTCAGAATGATACTTATTAAAAATACTCATAACATTAACAGATCATTAATCAATTTCCACACATGGGATGAATATAATAATTTAATAACACTTCAAAACAATGGCCTATTATTTAATGTTAGTTAATGTATTCACTAACTTGAACAAACAGTTAGTAATACATTAATTATGCTATTTATTTGTCTTTGTTAACGTTAGTTAGTGTTATTTAAGTTAAATAGTGTTAGTTCAGATTAACTCATGGT
Associated Phenotype:
Not determined