ZMP
hdlbp
Ensembl ID:
ZFIN ID:
Description:
vigilin [Source:RefSeq peptide;Acc:NP_958882]
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 |
---|---|---|---|
sa18003 | Nonsense | Available for shipment | Available now |
sa14220 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18003
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 |
---|---|---|---|---|---|
ENSDART00000011863 | Nonsense | 790 | 1272 | 18 | 28 |
ENSDART00000055771 | Nonsense | 793 | 1285 | 16 | 27 |
ENSDART00000121511 | None | None | 690 | None | 18 |
ENSDART00000134259 | None | None | 433 | None | 10 |
The following transcripts of ENSDARG00000009830 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 26591570)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 26892781 |
GRCz11 | 6 | 26883342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCATGAGCTGATCACAGTCATCGGTACAGAGGAAGCTGTCGCAGAAGCA[C/T]AAAAGGAGCTGGAGGCACTTATTAAGAGCTTGGTTAGTGGTTTTGWTGAA
Long Flanking Sequence:
TCCATTTCCCAACAGAGGGCTCTGGCATCGATGCAGTGACAATCAGAGGCCCAGCGGAGGAGGTGGAGAAAGCCAAGAAACAGCTGCTGTCCCTGGCAGAAGAGAAGGTATGTTTGAAGAGATGGGTTTCCTGTAGAACTTGAAGCTTAATGCCGGTAAGGCTGATGTTATGCTTGGAATGTTGTCTGGGCTCAGTGTTTAATACAAGTATTCAAACTGCTTTTAAAACAAGTTCACTAAAAGTTAGTACACTAAAAAGTTTAATCTGTTTTTGAACTGTACGTTGACTTTTTGTATTTCGTTGGTACTAGCAAACGAAAAGCCACACTGTTGAGCTTCGTGCCAAACCTGAATACCATAAGTTCCTTATTGGAAAAGGAGGTGGAAATATCCGGAAGGTGCGGGACAGCACAGGTGCTAGGATCATCTTTCCCACTGCTGAAGATAAGGATCATGAGCTGATCACAGTCATCGGTACAGAGGAAGCTGTCGCAGAAGCA[C/T]AAAAGGAGCTGGAGGCACTTATTAAGAGCTTGGTTAGTGGTTTTGATGAAGGAATATCTGAATATCTTCTAAATGGGATATGTTTGGTCTAATTATTCTTAAATGCTATTTCTATCATCAGGATAACATTGTAGAGGATTTCATGATTGTGGATCCCAAGCATCATCGGTTTTTCGTGGCACGTCGTGGGCAAGTCCTGAGGGACATTGCTGATGAGTACGGTGGTGTTATTGTCAGTTTTCCTCGAACTGCTGCACAGAGCGACAAGGTAACCCTAAAGGGAGCCAAAGACTGTGTGGAGGCTGCAAAGAAACGCATGCTGGAGATGATCGAGGATTTGGTAAATACATGTGTAACAATATGCAGTTATAACTCTGAAAACTGCACATTTTGTGCTGATGTAAGAAGCGTGTGTTGACTATTTTTCTCAATCTGCAGGATGCTCAAGTGACCATGGAGTGTGTGATCCCTCAGAAGTTCCACCGCTCCATAATGGGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14220
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011863 | Essential Splice Site | 1241 | 1272 | 27 | 28 |
ENSDART00000055771 | Essential Splice Site | 1254 | 1285 | 26 | 27 |
ENSDART00000121511 | None | None | 690 | None | 18 |
ENSDART00000134259 | None | None | 433 | None | 10 |
The following transcripts of ENSDARG00000009830 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 26585345)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 26886556 |
GRCz11 | 6 | 26877117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGGGCTTTGTTGTGCGGGAGGCTCCTTGGRCTACTGGCAACGAAAAGG[T/A]AAACTAATGTTTTGAGTGTSAAYTATTTATTGTGAAATTAAAAAGCAGGT
Long Flanking Sequence:
CCATAATACAAGAGTTATTCAAACTTTAAACTGTATTTATGAAGTGAGTTTGGAGTAAACGTGTTATGTTGTATTTTTCTATATAGATAATGTAATGTTAGCAGCCATAGCTGTGGTTTGAGAAGCTACACAAAAAGCTGACATTATCTTTTATTTCATTATTGCACAATTTGTCTTTGATTTTTTTGAATGTAACATTTTATAGTTTGGTAACTATAGCTCCACGTAGTAAAGGCTGCTACATTTAAAAGCATGTGCTGAGAAGATACTATAGTTACTGGCTGAACTGACAAAAAAAATTCAAACCGGTCTTATTTCCCAGCCCTAGAAAATGCTAAACGAATGTCTATCTTTATAGATGGCAGACGTCGTTGAAAATGAAGCCAAAATGGCCTATATGAAGCCTTCTGGTTCCAGTGCCTCAAGCATGGAAGAACCCCGTGGTCCATCCAAGGGCTTTGTTGTGCGGGAGGCTCCTTGGGCTACTGGCAACGAAAAGG[T/A]AAACTAATGTTTTGAGTGTCAATTATTTATTGTGAAATTAAAAAGCAGGTTAGTGACTTTTAAATGGGTTTCCCATGGGTCATGGGGTTTCTGGGATATCAATGAGTTTTAAATGATCTATACCAGACATTGATGGTCAATGGTTATTTTTTTTGTCCAACTCATGGAAAAACAGGGACTTTTGTTTGTCATCTTTAAATTTTATGTTATCAAAATGTGTTTTTCCTCTACCAAACATGTTTCATTCTTGTTTTCATGGTTAGACTGTGTTTCAGCTCCATTTGATTGCTTTTAAACTCATCAGCTGGCACTCACTTAGGTCAAATGCAGATAATGAATATTATCTGATGTAAATTTATCTTAGTAAATTTTTACATTAACAAATGAATAATATATTAATAGACAAACAACCAAATGATAAGTTTGTAAAACTATGGAGCAATCAGATATGGGAGAGGGAGTACAAACAAGAACAATTCTTACATGTTATTTTAAAAATC
Associated Phenotype:
Not determined