ZMP
wu:fa07b03
Ensembl ID:
ZFIN IDs:
Description:
Wu:fa07b03 protein [Source:UniProtKB/TrEMBL;Acc:Q0P3X3]
Human Orthologue:
HDLBP
Human Description:
high density lipoprotein binding protein [Source:HGNC Symbol;Acc:4857]
Mouse Orthologues:
4921511C20Rik, Gm382, Hdlbp
Mouse Descriptions:
RIKEN cDNA 4921511C20 gene Gene [Source:MGI Symbol;Acc:MGI:2685229]
high density lipoprotein (HDL) binding protein Gene [Source:MGI Symbol;Acc:MGI:99256]
predicted gene 382 Gene [Source:MGI Symbol;Acc:MGI:2685228]
high density lipoprotein (HDL) binding protein Gene [Source:MGI Symbol;Acc:MGI:99256]
predicted gene 382 Gene [Source:MGI Symbol;Acc:MGI:2685228]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22089 | Nonsense | Available for shipment | Available now |
sa35286 | Nonsense | Available for shipment | Available now |
sa35287 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22089
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 |
---|---|---|---|---|---|
ENSDART00000039725 | None | None | 290 | None | 8 |
ENSDART00000128279 | Nonsense | 374 | 1259 | 7 | 26 |
ENSDART00000128454 | None | None | 292 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 23771736)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22294898 |
GRCz11 | 12 | 22416117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTAAAAGTGTTATAGTGGCAGAAGTGATTGCTCCGGCTTGGCTTCAT[C/T]GATTCATCATTGGCAAGAAAGGACAAAACATCAGTCGCATTACACAGCAG
Long Flanking Sequence:
GTAGTTTTTTTTCCATAACCTTTATTGCATGTCATGGCACCATGTTGCATTTAGTTAGGACACTATGTCAGAGGCGTATTTCCAAAAACATTGTATATTTTTTTTGCATGAATTAGTGTGTACAAAAATGCATCTGGTGGCAATTTTACTGATTTCTTTATTTTGACGAGCAGAAACGAAAAACTACCACAATCTCGGTGGAGGTGAAAAAGTCCCAACACAAGTACATTGTTGGCCCAAAAGGAAACACCCTGCAGGAGATCTTGGAGAACACAGGGGTGTCTGTGGAAATGCCTCCTTTGGACTCCGCATCCGAGACCATCATCCTCCGAGGAGAGCCAGATAAACTAGGTCCTGCTCTTACACAGGTCTACGCCAAGGTCAGATGTTTTAAATATAGTAGATATTTTTCACTTTCGCTTCCTTTCCTTGACATTTGGTATTTTTTGCAGGCTAAAAGTGTTATAGTGGCAGAAGTGATTGCTCCGGCTTGGCTTCAT[C/T]GATTCATCATTGGCAAGAAAGGACAAAACATCAGTCGCATTACACAGCAGCTGCCTAAGGTATAGAAAAGTGAAATCAAAGCACAATGTTATGAGATGTCAGATTTGGAATTTAGCAAGTAGAGCTGAGCTGTATGATGGCAGATAATACCCCCTTTTACACAGTGATACCAGTAAATACCCAGAAAATAATTTCCAGAACAACTTAAAAAATGAACAATTTCTTTTAAAAAAATGCTGTTCACGGAGACAATAAAGTTCTGGAATTTTCTTGGAAAAGACCATTACACATATTCCAAAATATCTGTAAATTCTGACATCTTTAACCAGAAATGACCTCTAAACAGCTGTGCTTGTATTGGTATATATATGAGGGGCAGTATTTTGTTGATGGTTTCACTTTTATTTAAAGCTTTAGCATTTATGCAGCTGTTTTTGTCCCCGAGACATCCAAAGGCTGAAGTGCGAACCGCGGCTAAATGTTCACACATTTGATTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35286
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 |
---|---|---|---|---|---|
ENSDART00000039725 | None | None | 290 | None | 8 |
ENSDART00000128279 | Nonsense | 951 | 1259 | 19 | 26 |
ENSDART00000128454 | None | None | 292 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 23790838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22314000 |
GRCz11 | 12 | 22435219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCACTGTGACGGGACGAGCTGAAAAGTGTGAATTGGCACGGGCTGCTT[T/A]ACTTGTAAGACAATATCTCAATTCTAGCTCTCGCTTTTGTGTTGTTGTTG
Long Flanking Sequence:
TTTATTAACTAATAATATTTAAATATCTTTTTACAGTAAGCTGCTTTTTACAGTAAGCTGCTACAGAAAGCTGCTTATAGGTGAAATCTCAAAGAAGAAACACTAACACACATTCGCTTCACTGACTGCAATTACCTGCTGCTGTTTTCACCAGGAGTCGCAGGTGAGCATGGAGGTGTTGATTCCTCAGCGGTACCACAGAGCCATCATGGGCCCCAAAGGCTGCCGAATACAACAGATCACACGTGAACATGAAGTCCAGATCAAGTTTCCAGACAGAGACGAGTCTGCAGGTCTCTTCCTCTCACAGCACTCCACATACTATGTCTTCACATTTATTGAAAACAACAATATTTACAAGTGCCATTGTTTGTTATTTTCATCTGCAGCTCAGGAGCCTACATCTCAAGAGAATGGGGACACCGATCTCACCCCTCGAAAATGCGATATCATCACTGTGACGGGACGAGCTGAAAAGTGTGAATTGGCACGGGCTGCTT[T/A]ACTTGTAAGACAATATCTCAATTCTAGCTCTCGCTTTTGTGTTGTTGTTGGTTTTATTCTCCTCATCCTGCTTTTTTTCACTCAAGGCTTTAGTTCCTGTGACCATCGATGTTGAGGTTTCCTACGACCTTCATCGTTATATCATAGGACAAAAAGGAAGTGGAATAAGGAAGATGATGGAGGATTATGAGGTAGAGATAGAACTTTTCAAAATATTGGAGTTAGTAATATTTTTAAATGCCATTGAAAAAATCCCCTAGTGGTATTATTTGAATTTACAAATAAATAAATAATAAAATAATAATAATAATAATAATAATAATAATTATAATAATTATTATTATTATTATTGTTATAACAATTATTATTATTATTATTATTATGGGTGAAGCATGGGTGCAGTAGGTAGTGCTGTTGCCTCACAGCAAGAAGGTCACTGGGTTGCTGGTTCGATCCTCAGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35287
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039725 | None | None | 290 | None | 8 |
ENSDART00000128279 | Essential Splice Site | 1080 | 1259 | 22 | 26 |
ENSDART00000128454 | None | None | 292 | None | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 23794594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22317756 |
GRCz11 | 12 | 22438975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGTACGATGTAAACGTTCAGTTCCCGGACAAGGGTGATGAGCAGCAG[G/A]TATGTATTAACCACAGAGCACATTTCCTCGTGCTTGAGCACAGACCAGCT
Long Flanking Sequence:
TCATTCCCAAGATTAACTGATGCTGTATTGGCCAAAAAAGTAGGCGCGACACCATACAAATGATTCAGCTATGCCTATGTATCTCCAGACTTTTATTCTTTGACACTTTGTACAAAAAAAACTAGCCTAGTTTTATACAGTTGTAGATCACAACAACCACAAGTATAACAACCTCATTGTAGCACATCACTAATCACACCAGTGTGACGTCTAACAAAATTCGATTGTACCAAGACCAAAAAATGCAGCCATTTACTCACTATCCAGAGCCATTGTGCTACATGCTACCAAAACATAGTTCACGTGTATATCCTGAGATTACTCTGAGAATAAATTATTTTACTGTTCTTTTACAGGCCTTGCGGAGCTATAAAGTAACGCTCTCGGTGGACCCCAAATATCACCCCAAAATCATCGGTCGCAAAGGAGCCGTCATCTCCCAAATCCGCAAAGAGTACGATGTAAACGTTCAGTTCCCGGACAAGGGTGATGAGCAGCAG[G/A]TATGTATTAACCACAGAGCACATTTCCTCGTGCTTGAGCACAGACCAGCTCTGCCCTCATTCTTCAGCTCATGCCATTCATGTTTCTCTGGCTGTAGGATGTGATCGTGATCTCGGGGTATGAGAGGAATGCTAACGATGCTAAGTCGGCCATCGAGCAGCTGGTGGCCGCGCTGCAGGAGATGGTGAGCGAGGACGTCCGGCTGGACCGGCGGGTTCACGCACGCATCATCGGGGCACGTGGAAAAGCCATCCGCAAAATCATGGAGGAGTTCAAAGTAAGAACATTTACCGAAACAACTTAAATGTGTAGATATTTTTACAGTTGAAGTCAAAATTATTTTAGACCATCTGTGAGTTTTTTTTTTTATTTGCCAAATGATGTTTAACAGAGCAAGGATTTTTTCACAGTATTTCCTATGACATGTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGTTAAAATCAAAGCTGTTTTTATTTTTTATTTAAACAT
Associated Phenotype:
Not determined