ZMP
si:ch211-124k10.2
Ensembl ID:
ZFIN ID:
Description:
StAR-related lipid transfer domain containing 8 [Source:RefSeq peptide;Acc:NP_001119949]
Human Orthologue:
STARD8
Human Description:
StAR-related lipid transfer (START) domain containing 8 [Source:HGNC Symbol;Acc:19161]
Mouse Orthologue:
Stard8
Mouse Description:
START domain containing 8 Gene [Source:MGI Symbol;Acc:MGI:2448556]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1039 | Essential Splice Site | F2 line generated | Not yet available |
| sa45212 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa940 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa1039
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022043 | Essential Splice Site | 39 | 614 | 1 | 9 |
| ENSDART00000051333 | Essential Splice Site | 39 | 1076 | 1 | 14 |
| ENSDART00000127383 | Essential Splice Site | 39 | 1076 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 37404493)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35186442 |
| GRCz11 | 5 | 35786595 |
KASP Assay ID:
554-0942.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGCCCTGACTTTACTGCGGAGGAAGGCGAAACAGCGGCAGTTTGCGGG[T/A]AAGTWATGCCACTGTTTGGAGGAGGCTGTGAGATTTTCTTAAGAAACTAG
Long Flanking Sequence:
AGTATAAAACTGCAAAGAACCACAAGGAATGAATGACCCACAGTAAAGCATGACCAGCTCAGCACTGTTTTAAAAAAGACCACTAGGCGTCATAACGGAAACTACTACCCTTAAAAGACGCACAAGTTCAGAGACTGCATGTCCCGTGATGCTTCGCGGTTTGAATGGTTGCAAGGCAGCGTTCACGGAAAGTCCTTTTAATTAGAGTCTCCTTTTAAAGAAATGAAACGACAGTGTTAACAGCCACCGAAAAAAGCAGCATGAATAAACACTACTCCGTGTCAGCATTAAGACTGTACCCGCATCTGGAGTCTCCGAAAGAAAAAGTCCAGGGTTAAAGGCTGGGTTCAGAAGTCAGGAGAGAGTTGGCGAAGGAGTTTGGAAATGGATAAAAACTGTAATGGCCAACAGTCGCGATCTCTAACCTCACAACTCAGGGAATCTACATTCAGAGCCCTGACTTTACTGCGGAGGAAGGCGAAACAGCGGCAGTTTGCGGG[T/A]AAGTTATGCCACTGTTTGGAGGAGGCTGTGAGATTTTCTTAAGAAACTAGTCCGTTTGGCGTTATAACCTTCCAAACGAACTCGACAGTCTGTTCAAATGTCTGAATGCTTTCTTTACTGTAGCGTTTCGTTTATCAACAAATGAGTTTTTGTCACTTTATGAAAAAAGCCATCAGGAAACTTTTATAAAACAGATATCTGAGAGTTTCAGGAGCTGGTTTGCAATAATGAAACGGACTCCCGAAGTTTCCTTCGTGCATTAATGAACCAAACAACCCTCGGACATTTACCATGGTAACCATGGTTTCGCTGATGGCATGGTTACAGTTATTCAATAACTTCTGCATAAGGAAGTTTACCATTATTCAGTAGAACACTTTACTGTTTTATTACCCTTCATTAGAATTATTTAATAATTAATTCCCAACATTATTTAAGAGACTAATGAGAGTTTTTAGTAGAAACGAAACGTGTAGAGCTTTAACGTTAATGGAAACTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45212
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022043 | Nonsense | 48 | 614 | 2 | 9 |
| ENSDART00000051333 | Nonsense | 48 | 1076 | 2 | 14 |
| ENSDART00000127383 | Nonsense | 48 | 1076 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 37439224)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35221173 |
| GRCz11 | 5 | 35821326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTCATGTTTCTCTCTTCCAGAGCTGGAGGCAAAAGACGCCTGTGAGTG[G/A]CTCCGAGCGGCGGGGTTTCCTCAGTATGCTCAGCTTTATGAAGGTAATCC
Long Flanking Sequence:
CATTTTCCTTAAAAAAAAAAAAAAGGTATAATGGATATCAGCCTAAATGGGTATTGTACATCCATACTAATGAATATTTATTATTCAAATAATATTATGAATATCATAAATTATCTCCTAGCACATGGCAAAGATTATTGGGTTTCAGTAATGGCATGTTTCAGTCTCATGTAAAATGAGCTTAATATTCCAAATCCGCTCTCATTGTCGAGCTGAATGTGTTTCTTTTTTTCCATAGACAGAACTAATAATGTAGCCACAGATTATCTAAACAAATTTAAACAGCTCTTATTCATGGTGGAATGAGCATCGGGCCAGATATATTCTCCTTGTCTCATTTTAATCAAGTGATGCCAGTTTATAGCATGAAGACCACAGCATTCATTCTCTTCCTATCATTTTCATAAATCAGCCCTAATGAATCGGCATATTATCTTATTGATTTTTCTCCCTTCATGTTTCTCTCTTCCAGAGCTGGAGGCAAAAGACGCCTGTGAGTG[G/A]CTCCGAGCGGCGGGGTTTCCTCAGTATGCTCAGCTTTATGAAGGTAATCCAGAACTCATCTCACAGAAGTCCACTCATCCTTCCATTTCCATACCATTATCTGTCTCTTTCACTTGCCCCTTACCTCTGCTCCTTTCTGTAACTCAGTGTTGTCTTCCTTTTTTTCTCTTTTCCTCTGGTTTCCTTTCATATCATCTCTTCGGAAAGGTGTAGAATTGTTTCTTCTTCCCTTATCTTTGCTGAACGGATTGAAATGACCCCCCGCGGAGAGCTTCAGTGTTATTATATTTCAGGTTTACTGATTGGGGAAACGCATGTGGCTTTTGGTTCATATGCCTTTTAGGTTGTGTTCAGTAAATATTCCACTTTTCTGCTTCACATCTGCCATCTCAGGTGTTGCAGATTTTCAGACCTTCTTCTTTTGGTCTCTTTGCCTACTCAAACCTCACCCCCCCACCCCAAAATAATTGCCAGGTTCAGCCAAAAGAGACATTTGTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa940
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000022043 | Nonsense | 375 | 614 | 5 | 9 |
| ENSDART00000051333 | Nonsense | 375 | 1076 | 5 | 14 |
| ENSDART00000127383 | Nonsense | 375 | 1076 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 37461844)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35243793 |
| GRCz11 | 5 | 35843946 |
KASP Assay ID:
554-0845.1 (used for ordering genotyping assays)
KASP Sequence:
GACCACAAGCCTGGAACTTTCCCCAAATCTCTGTCAATTGAAAGTCTCTG[T/A]CCTGTCTCTGTTTCTGAAAGTCCTGACCATATTGACTGGGCAGRAGTAGA
Long Flanking Sequence:
GGTGCATCGTCAGTTTTTGTCTCAGCCAGCAAAGATGAGAACGACGACACAGGATCTTCATCTTCTCTTCCATCAGTTAGAGAAAAGCCAAAGCGTCCTTCTAGATCATTTTTACGAAGGAAAGAGTCAGTAAAGAAGCGGGACAGTGAGAATGAGAAAGTCTTGAAAAGTGTTTCGACTGTAACTCGGCATCAGCCACTTTCAGGTCTGCACTGCACGTCTGATGCAAGCTTGCCTGGCCAAACCACAAATAAGTGCCGAAACACCAAAGATCCATCATGGAGGGCACATACCATATGTCGGAGTAATGTTAGCCAGAAAGTAACTCTGCACAAGCCTCACAGAGCATGTCTTTACCTGGAAGACTACCAGTTGACTTGGGAGATTCCCAAGTCAACCAGTCACAACAACCGTCAGAGGAAAGAGGATCGTGTGGTCCACCTCCCCTTTGACCACAAGCCTGGAACTTTCCCCAAATCTCTGTCAATTGAAAGTCTCTG[T/A]CCTGTCTCTGTTTCTGAAAGTCCTGACCATATTGACTGGGCAGGAGTAGACGGAGACCTTTCATTGGATGGAAGTGTTAGTCGGAGTGGGTCACAAGACTTTCTGTCAGGTTTCGGGCAGAGGAGGAACTCCATTAGTTCACTTGGAAGCATTTATGATAATGTTCCAGAAACGCCAGGCAGCCCAGGTGACATTTTTGACCCTGGAAAAAAGAAAGTCTTCCAGCATCTTGATGACATTTTACAGCACGTACACGGGCTACAGCACAACATTGAGGAATGGTCACGCTCCCTTGGTATTCAGCCACAGGATCAATCGAATGCAGAGACTGTGTCTACAGCAGACACAACATTACCCAGCAGTCTGAACTATGATGAGCAATCCATGTCAGATGTTGGGACCACAGTAAGCGATTACGATAGTGCGGGAAACTCTGTGAATGAGGGAGAAGGAGAAGGAGAAATGAGAGAGAGGAGAGACTCTGGTGTGGGGGCATCACT
Associated Phenotype:
Not determined