ZMP
osbpl7
Ensembl ID:
ZFIN ID:
Description:
oxysterol binding protein-like 7 [Source:RefSeq peptide;Acc:NP_001005927]
Human Orthologue:
OSBPL7
Human Description:
oxysterol binding protein-like 7 [Source:HGNC Symbol;Acc:16387]
Mouse Orthologue:
Osbpl7
Mouse Description:
oxysterol binding protein-like 7 Gene [Source:MGI Symbol;Acc:MGI:1918490]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27969 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42049 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22120 | Nonsense | Available for shipment | Available now |
sa22119 | Nonsense | Available for shipment | Available now |
sa6256 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27969
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020667 | Nonsense | 176 | 888 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 30339198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28676135 |
GRCz11 | 12 | 28791037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCACAGGATGTATAAAAAGAACGAGGCTGCGCACGTTCACAATGGCTA[T/A]CTCCAGGTCCTGTCCCATACCAGTAATTTATCTCACAAAACCAGTCCCAT
Long Flanking Sequence:
GCTTCCTTAGTATTTGTACCTAGTCAAAGTATAAAATATAAAAAAATATACTAAAAACTTTGGCTTCGCCAAAAAATATAATATACTCATAATTTACTCAATCTCAAATTTATCTAAACCTTGATTCATTTCTGAACACTAAAAAAAGTATTTTGAACAATGTTGTAAATTAGTAGCCATTGACGTCCATAGTACAAAATAAAGGGTAATGGCTGCTAGTTTTTAGCATACTTCAAAACATAATTGTTTTTTGTGTTCAACAATAGAAAGTACCTTAAGCAGGTTTGGAAGAAGTGATGGGTTAGTAAAATGACAGAATTAAAATTTTTAGGTGAATTACCTTTTTAAACAAATGTTTATGCAGATAAAAAATGTTAACTAAACACATTTGACTTTTCATTATAGGCCAAGAGTCAGGATTTATATTTCATATGGGTCACCAAACTGAGCGCCCACAGGATGTATAAAAAGAACGAGGCTGCGCACGTTCACAATGGCTA[T/A]CTCCAGGTCCTGTCCCATACCAGTAATTTATCTCACAAAACCAGTCCCATGCAGGACATGGTGAGTAAATACGTCTTCTACAGTGACTTCCTGTTGCACTCTAAATCACCAGGGATTAGGACAAAGTGTCCTCACAATTTAAGAACAAGCGGTATTAGCGATTAGACCTTATGTCCTTGATCTGTAAATGCACTCTAATAGATATTTTGAGTTAATTTGGCTAATGAAAGTTACAAATAAATGTCTTGTGAACAACTCTAGGGCACATCTGGGTCTTCTATGGGTGAAAATCTTCAATATGTAAGTCCTGCTGTTAATGGGAAGGTGTCAGCTTGGCTTCAGACCCAAGAACCAGATTTTTGTGGACAAGGTATTGTGGTGTTATATTGAACACTAGAAAATGTCAATAGTAATATGCATGAGAACAAAGAAAGGATTTTAAAATGCCACTTTGGGCTGTTTTCCAGAGCTGACACGTTGTCAGATGGAGCTGAATGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42049
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 |
---|---|---|---|---|---|
ENSDART00000020667 | Nonsense | 280 | 888 | 9 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 30336687)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28673624 |
GRCz11 | 12 | 28788526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAGTCATACATCTGTTTGATCCACAGAATCTTTCTCTTGACAAACCC[A/T]AAAAGAAATCCGCCAAGATTTTTGGTCACTCACGCACACTCTCCCGAGTT
Long Flanking Sequence:
ACCCTGATTTAAACTATATCAATTTTCTGGCTAGTATTGTGCAAATTGACAACATTTTACAATTACAATTGTGTGGATGCTTAGCTGAAAAACAAAATATAACTATTAGGCAAGAGACGATAACTAGTTTTAAGTTTTAAAACTTAAACTAGTAATAGTATAACTAGTTTTAAGTTTTTTTTCTATACCAAGGTATGGAAAGTCAAGGATTTTTTTCCCATGTTTTTATGACTATCAAATTTTTTTAAAATTGGACACAGGCAGGCAGGGATTTTTTATTGGGGTGGCCAAGCATGGGCCGGCAGTTACTTCGGGGTGAATATCGAAACTGGTGGGGGGTCACGGATGAAACCGAGGAGAGGGTAGGGGTTATGAGTGGGTTGCACCCCAAGCTACACTCTAACTCCGCCCCTGATTATATACATATAAGATTGGTCTAGAGCATATATAAAACAGTCATACATCTGTTTGATCCACAGAATCTTTCTCTTGACAAACCC[A/T]AAAAGAAATCCGCCAAGATTTTTGGTCACTCACGCACACTCTCCCGAGTTGAGGGTCTTGGAATGGTGAGACTGCTCATTTTTTCTTTACTTGTATTAGGACATCTTAGATAAAGTCTTGGAAGCAATTTTAATCTTTGTCCACAGGGATTGCCCTCTCATTGGGATTATTCCATGTTTTCCACAAAGGTTTGGAAAGTGTTATGGAATTTTATTCCATGTTACATAATGTGCAGTGTCATCCCTAAAAATCTCTGTATTTTATTTGAAATACAGTAGACAGGCATTTGTGTTGTGTTGATGTGTAGTAAGCAATAGAGCTTCAAAACCCCCAGTAATTTAGTCAACTGCTTTTTTACATGAAGCCTTTTCGTGGGATTACTAAATCGGTAAGTCAGCACAACACACATTTCCTGTAATTTAAAATATATTATATATCAGGTTGCTAATGCATTCAACCATTTGACGCTATTGCATTTTGCATATTGTGCACTATCATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22120
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 |
---|---|---|---|---|---|
ENSDART00000020667 | Nonsense | 386 | 888 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 30334809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28671746 |
GRCz11 | 12 | 28786648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTGCGGGACACCTGGTCCGGCAGAGACCTTCACCAGAACACCTCTGCC[C/T]AGCTCAACAACCTCTGCAGTCTAGCTGAGGTGAGAAGGACTTCTGTTGCT
Long Flanking Sequence:
GTAATTCTGTGTGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCATGCAATCAAAAAACAAGATGAGAAAAAGGAATAGTTGTCGTCACCCTGAAGTGGTTCCTAACCATTTGAGTTCAAATATTTTGAAGAATGTTGGAAATTTGTTGCCATTGACTTCAATAGTTGGAAATATTTTATAGGGAAGTCAATGGGTTTCAATAAAACATTTTCATATGTGTTCAACAAAAGAAAGAAACTCAAACAGGTTTTAAGCAAATGACAGAGCTGTAAACGCTGACATAGTTTTCATTTTTGGGTGATCTATCACTTTAAAACTGGTCTGTCCTGCTTGGTGCGTTAGACTGAATGAAGACTGAGGGTCAGATGGTTGTCTTTTCTTTTCAGTTCATGCCTCTCTGCGAACTGCACATGAGGCTCTCGCTCAGGAGCGCCAGCGACTGCGGGACACCTGGTCCGGCAGAGACCTTCACCAGAACACCTCTGCC[C/T]AGCTCAACAACCTCTGCAGTCTAGCTGAGGTGAGAAGGACTTCTGTTGCTTAGGGAAATGCCCATAGAAATCCCCTGAATGCATGCAAAGAGTAAATTTACTACAGCTTTTCTTGTTTAATCTGCTGTAAAGAATCAAACTAGCTCCTGTTTTAGTTTAAATGATTTAATTGATTGTAATGACACACACTGGATTGTCATCTAATCAACTTTAATCCAATAATGTGTAATAATAGTCATACACTGCAAAGATTGTTTTCTTACTTTAGAGTGTTTTTTTTTTTCATGTTTGAAATCCAAATGTATAAAAAGGCTTTTTTTAGATGAGTAAGCAAATAATCTTTTGTTTTCAGAAATAATTTGTCAAATTGGGTGTCTTGTTTTCATTTTGAAATAAGTATTGTTTTACTTAACCAATTAGCAGATTATTTAGCTTTTTTACCAGAAAAAAATGTATTCTTTTTGACTCGCACAATTATTTACATTTTTCCAGACTAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22119
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 |
---|---|---|---|---|---|
ENSDART00000020667 | Nonsense | 493 | 888 | 14 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 30328427)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28665364 |
GRCz11 | 12 | 28780266 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTATCAATTGAACAGCAATGGCATCTCGCAAATATCGAGCCAGCCTTT[C/A]GAAAGCAGCAGCAAAACCGAACACCATCAAGAGCACTGGACGGCGCACGA
Long Flanking Sequence:
ATGGTCTAAAGATTGGACCAACAGTCTAGAAGTTAAAAAAAATTACTTGAACAAAATCAAAATGGTAGACAGGAAGTTTAGCAGATGATGGCATAATTGATATCAGTGTTGTCGGCATGACCCAAGGAATTATTTGATCTTTAATATTTCTTCAAAATAAGCATATGCAGTCAAAAGTTATTCCCAAATTTTTAAGTTTCAATAATGATGGCTAATAAATGTCTTAAAACTTTTGAACTATAGATGGCTCTGTCACCAAATGTTTATGGCGTGGTCAGTGTGAGGAGACAGTGACAGACCAAAAATTTGGTGTCATTACCTTAAAATTTTTTTTTTAGGGAAATATTAAACAATATTTAAAATGAAAAATACAAACACAAATGACAAGATCTAAATTCTGTACCAACCTCAAAGTTTTGCATTAAATTCTTGGTTACACCATTAACTTTTTCTTATCAATTGAACAGCAATGGCATCTCGCAAATATCGAGCCAGCCTTT[C/A]GAAAGCAGCAGCAAAACCGAACACCATCAAGAGCACTGGACGGCGCACGACTCTGCCTGCGGTTTGTCCTGACAACAGCCATGTGGGTCTGATGACGATTCTTTACAACAACATCGGGAAGGATCTGTCCCGGGTCTCCATGCCAGCAGCTCTGAATGAGCCTGTGTGTTTGCTGCAGAGACTCTGTGAGGAGCTGGAATATTCAGACCTGCTGGACACTGCCAATCACACTGATGACCCCTTCCAGAGGATGGTGAGCATAATAGAAGATCACTTGCAAAGAGACGACACCCACATCAGATTACATGTACAAAAGTGATTTTATAAAAGGGTCTAATGTAATAAGACAAAATTAAATTATTATATTCTTAAATGTGTATTCTAAACCCCTGCTCTTTAAAAAAGCATTGAATATACTTGCGCTTGTTTTTGAAGACACCAAAATTTGTTTATTTAACAGTTTTTTAATAAAATAGAGGCTACATAAATATTTGTAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6256
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020667 | Nonsense | 549 | 888 | 14 | 22 |
Genomic Location (Zv9):
Chromosome 12 (position 30328258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28665195 |
GRCz11 | 12 | 28780097 |
KASP Assay ID:
554-5333.1 (used for ordering genotyping assays)
KASP Sequence:
AAGGATCTGTCCCGGGTCTCCATGCCAGCAGCTCTGAATGAGCCTGTGTG[T/A]TTGCTGCAGAGACYCTGTGAGGAGCTGGAATATTCAGACCTGCTGGACAC
Long Flanking Sequence:
GTCAAAAGTTATTCCCAAATTTTTAAGTTTCAATAATGATGGCTAATAAATGTCTTAAAACTTTTGAACTATAGATGGCTCTGTCACCAAATGTTTATGGCGTGGTCAGTGTGAGGAGACAGTGACAGACCAAAAATTTGGTGTCATTACCTTAAAATTTTTTTTTTAGGGAAATATTAAACAATATTTAAAATGAAAAATACAAACACAAATGACAAGATCTAAATTCTGTACCAACCTCAAAGTTTTGCATTAAATTCTTGGTTACACCATTAACTTTTTCTTATCAATTGAACAGCAATGGCATCTCGCAAATATCGAGCCAGCCTTTCGAAAGCAGCAGCAAAACCGAACACCATCAAGAGCACTGGACGGCGCACGACTCTGCCTGCGGTTTGTCCTGACAACAGCCATGTGGGTCTGATGACGATTCTTTACAACAACATCGGGAAGGATCTGTCCCGGGTCTCCATGCCAGCAGCTCTGAATGAGCCTGTGTG[T/A]TTGCTGCAGAGACTCTGTGAGGAGCTGGAATATTCAGACCTGCTGGACACTGCCAATCACACTGATGACCCCTTCCAGAGGATGGTGAGCATAATAGAAGATCACTTGCAAAGAGACGACACCCACATCAGATTACATGTACAAAAGTGATTTTATAAAAGGGTCTAATGTAATAAGACAAAATTAAATTATTATATTCTTAAATGTGTATTCTAAACCCCTGCTCTTTAAAAAAGCATTGAATATACTTGCGCTTGTTTTTGAAGACACCAAAATTTGTTTATTTAACAGTTTTTTAATAAAATAGAGGCTACATAAATATTTGTAAGCAACATAAATATTTTACACTTTTGATTAATTTAATGCATGTTTTCTGAATGAAAATGTAATTTAAAAATCATTCTAACTGACCTCAAACATTTTCTAAAGTAAATTTATACGGATCTAATAATAATTCTATTATTTCTTCAAACAAAGTATGTTTAAACTTATGCTTGCAT
Associated Phenotype:
Not determined