ZMP
im:7147988
Ensembl ID:
ZFIN ID:
Human Orthologue:
STARD13
Human Description:
StAR-related lipid transfer (START) domain containing 13 [Source:HGNC Symbol;Acc:19164]
Mouse Orthologue:
Stard13
Mouse Description:
StAR-related lipid transfer (START) domain containing 13 Gene [Source:MGI Symbol;Acc:MGI:2385331]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35944 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa35945 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35946 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa10794 | Essential Splice Site | Available for shipment | Available now |
| sa17556 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35944
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 |
|---|---|---|---|---|---|
| ENSDART00000114382 | Nonsense | 114 | 1487 | 1 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 32247834)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 33768713 |
| GRCz11 | 15 | 33626692 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATGCATCAAAAGTGCTTCAGATTCAATTTCAAGTCCAAACCCCAAGT[T/A]GAACGGAATTAATCATGAATCTCACATGAAAAGCCATTTTTTGACTCCCT
Long Flanking Sequence:
CTGTTCTTTCTTTTCAGCATGATTAACACAAAGCCCTGACTTTCACAAAGAAACCCGTTCAGTCCAAATGGTGGAACATGACAAACATGGCAGTTTCTGGAATAATACAAAGACTTTTCTGGATATTCCATATGCCTAGCTCCAAACAGTAGACTGAAACATGGACAATCCACCCATGATGGCTTTAGAGGAGCGACGATCTTCAGCGCTCAAAATGACTTTCTCCGGAGAGCTTTCAATGGCGGACTCAACCAAGGCTTGTAACCAGACCTCAAAAAACACTCCTAATTCCCTCTCAATCACAGATGATCCTTTGGAAGACCAAACCAAACTGGAACTGAAAAATAAAAGTTCACTGGAAAGAGAGATCAGTCAAACTGTATCCTCACAAATCAGCAAAGACGGCCCTTGTATTCAAATCTCAAATCATCTCACAAAGGAAAAGACTAAAACATGCATCAAAAGTGCTTCAGATTCAATTTCAAGTCCAAACCCCAAGT[T/A]GAACGGAATTAATCATGAATCTCACATGAAAAGCCATTTTTTGACTCCCTCGGGTAGTCCTCTGACCAACAACGCTGATGTTGATCCCTCAAACGTATCATTGACCTCCTACCCTTTCTCTAGTTCAAAAATCAGATCCATTTCAAACCCCGCTTACTCTTTTACATCCTCTCCAGTGGGATCGTCCCACCTCAAGCACCCCTACTCTGCTCCTTTGCCAGTTTCCAAAGGGTCCGATCTACCCCGAATCATCAAACACAAACCCAGCTCCATTACCTTTGCAGATTACAATGACTTTTTGGGTTTGATCCAGAACTCCAGAGCCACCGAGAGTTCAGATGCGTTTGAGACCTCTTCTGAAGATGAAGGCCAGGATGTGGTTTTCCATGATGGCAATGAGGTTTTGCCCAAATGCAAAGAGCTTCAGGCCTGCTCCAGGAGAAACAGGGCTGGATTGGAGAAGCTGAGAAGGAAAGGAACCTGTGGACAAGGAGTTGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35945
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114382 | Essential Splice Site | 408 | 1487 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 32266462)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 33750085 |
| GRCz11 | 15 | 33608064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCAGGAGCCACTTCCTCTATGGGGAGATCACATGCTAGAAAGACAGAG[G/T]TGAGCATTTCCGCTTTGAAGAATTTGAAGGAATTGTTCTCTCTATAGTGT
Long Flanking Sequence:
GTGTCGTTTAAAAAAAAAAAAAATGCATGCAAGCTCACGACAGAACCACCCTGTAGCAAGAGTTCACAGCAAGACAAAAGTGCCTTTTGGTTCCTCGAGACAACGATGTCTTGTGCTGGGGGTCTGTTGATCTGTTTGAATCACTATATCCTTTAGGGATGGTAAGTGAAATGACATGATGGATTTCAGAGCTCTTGTTTTTAGTGAAAGACAAGATCTACATATTGCATTGGACAAGGTCATCATTTTCCTTCAGGTTCTTCCGATATCAATAGTTTAACTGTCTGAGGTGTTGCATTGATGTTGTCTTATCTGGATCAAACACATCCCATTTGATTGTAATGGTTGTGTTGTTGTTTCAGAGCGGGGCTGTGGAAGGAAATCAGTCCATCAACTGGATCAACATGGCTAGAAGAAGCGACACGAGGGAACGCCAAAGCCAAGAGAGACACGCAGGAGCCACTTCCTCTATGGGGAGATCACATGCTAGAAAGACAGAG[G/T]TGAGCATTTCCGCTTTGAAGAATTTGAAGGAATTGTTCTCTCTATAGTGTTACCACCTGGAAGCATTTAGAAATTTTAGTTTAAAAAAAAAATTAGATAGTTAAAGTGAAAATTATGGGCCTGTTATTAGTCCTCTTGTGATTTATGTCTCTTTTTGTTTTTAAATATTTCCCAAAAGATGTTTAACAGAGCAAGGAATTTATTACAGTATTTCCTGTAATATTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCGGCTAATATAAAAGCAGCTTTGTAAAAGCAGTGATTATTCTGACAATATTTTTTATTACTTTTTCTTAAGGTATTTTTTTCTTGGATATAAATAACTATATAGTTTGAACCGAAGTTAAATTATACTTTGAGAAAAAAAAAAATTTCATTTGAAGTAGCTTCGTTTGCAGGTGTGTGGTTAATTTGATTAATAATTCTATTTACCACAATATGTTTTATTAAATAAAAAATTTATATAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35946
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 |
|---|---|---|---|---|---|
| ENSDART00000114382 | Nonsense | 460 | 1487 | 6 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 32392459)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 33624088 |
| GRCz11 | 15 | 33482067 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCAATTTCCCATTGACATCTCTCCTGTGAAGAAAGACCATGACTTCT[T/A]GGACAAAGACCTTGTGGAACCTCTATGCCGGTAAGAACTGTGTTGTATCT
Long Flanking Sequence:
TGATTTTACTTATTTCATTCAGCAGAGGCAAAAAAATATGATGAAACATTTAATTGTACTAGTGGAATGTCAACTCTGGCGGGGTCTGGATCCAGTCACCCCATTACATAAGTTGGACACTATACTCAGTTGAAGACGTAATGGCTTCTCAAAGCCAAGCTCAGAATTTGGGGGGCAAACCCTGTCTCACTTTATTAGCATCTGGAAGTTTAAAACAAGTTAGCTACTCTCTGTGTCTTGGCTATCGCTCTGGAAAGAATGTGTTGTCAGGGTTTTTTTAAAGAGTGTGGGCGCCTGGATTCCTCTGTGTTCACTGTGAACATGCAAGATTGGCCTATTAACGAATCAGAAGGAAATCGTTATGGTGCTTAAAAGACATCTGTTTTTTCCTGAATTGGACTGTAATGGACTTGATTGTTGAAATGGGATACGCCTGTGTTTCTTTGCAGATTCTCAATTTCCCATTGACATCTCTCCTGTGAAGAAAGACCATGACTTCT[T/A]GGACAAAGACCTTGTGGAACCTCTATGCCGGTAAGAACTGTGTTGTATCTACAGTCTTCTCGACACCCTGAAGAAATCAAGCCATATCTTTGGAGAAACATTGAAACTACCTAAGCTTAATAATAAATAATAAATACAACAGATAACAGCAGCAATAAAACAGAGGAAAAAATACTTTTAGAACCATGTTGTTGTAATGGCGGCCATCAAGAGGAGTTGTACAAACCTCACTCCCTGGAGATGCACCAGCAACTGACACTATAGATTTGTGTCTTTAATGTCCTTGTTATCATGACTTGCTGGAAACCCTGGATCAGATCCCACTCAGGTGGGGTTGCATTAGTGCCATGACCCGGTTGAAAGTGAAGCCAATGGAGACCAGCAAACAGGAACTGCTAGGGGTCATTGTGTTTAGCTTCCTCGTTAGAGCAACCGACTTCCATTTGGAGAGTCAACAGTTCAATTCCAGCTCGGAGCGGGTTGGGTGGTGCAGGACTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10794
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 |
|---|---|---|---|---|---|
| ENSDART00000114382 | Essential Splice Site | 1198 | 1487 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 32401212)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 33615335 |
| GRCz11 | 15 | 33473314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTTCACTTTTTCATCTCAACATCCTGAAGAARGACAATCTTACGCCAAG[G/A]TAGAAAACACTTCTTTTGATWGTCTGTGATGTSTAAAGTTATGTTCAWCC
Long Flanking Sequence:
CCTAGGTGGGTCTTTTTCGCAAATCAGGAGTGAAGTCTCGTATCCAAGCACTCCGACAGATGAACGAGAGTTCTCCAGATGATGTTAACTATGAAGATCAGTCTGCATATGATGTTGCTGACATGGTCAAACAGTTCTTCAGGGATCTGCCTGAGCCACTTCTGACCAGCAAACTGGGTGAAACCTTCCTCCACATTTACCAATGTAAGAAACACTCTCACTTTAACACCCACCCTTCTCCTGCTCTCAGAAAAATAAATGCAAGCAATTTTCCTTTCCATTTCAGATGTGCCCAAAGAGCAGCGCTTACAGGCTGTGCAGGCGGCCATCATGCTGATGTCAGATGAAAACAGGGAGGTATTGCAAACACTGCTTTGCTTCCTGAGTGATGTCACTTCCTCCGTTCAAGAGAATCAGATGACGCCCATGAACCTGGCAGTGTGTCTGGCACCTTCACTTTTTCATCTCAACATCCTGAAGAAGGACAATCTTACGCCAAG[G/A]TAGAAAACACTTCTTTTGATTGTCTGTGATGTGTAAAGTTATGTTCAACCATGGACTTTCACCAATATTATGGCCAAAAATAAAATAAATAATATATTAATTAAATTACATAATAAATAATAAAAAATTGCTAATGTGGCAGTGTGGCATATTATGTACTGTATATTCGTAATTCTTTTAGTATCAAATATCATATTATAGTCAATATAGTTATATCATGATAACCCAAATAACATGATAATGATAATAATTCAAAATCATTGTGAATACTAGTATATTTCAACAGCTCTAGTTCATCCATAACATCCATCTATCAATACGATAACTGTATTTGGACATTTGGAAATGTCATACAACTTTGTCATATGTTAATAATACATTTAATTTGTGTATTTTCTGCCTTTTAAAATGATTATTTTAACGTTGTAGTTAATAATAATAAGAAGAAAATAAATACATTTTAAAAACAACTGATTGTTTTAATATTTAAATGATATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17556
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 |
|---|---|---|---|---|---|
| ENSDART00000114382 | Nonsense | 1257 | 1487 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 32402059)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 33614488 |
| GRCz11 | 15 | 33472467 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAYGAAATGGTGACACAGTCGCGTAATTCGTACGYGGAGGCCGARCTT[C/T]AGRCTCCCACCATTGAGGAGCTSTGCAAGCGGCAGCATCCRGAAGATGAT
Long Flanking Sequence:
TGTCATACAACTTTGTCATATGTTAATAATACATTTAATTTGTGTATTTTCTGCCTTTTAAAATGATTATTTTAACGTTGTAGTTAATAATAATAAGAAGAAAATAAATACATTTTAAAAACAACTGATTGTTTTAATATTTAAATGATATAATCTTAAAGGATTTCCAAATCTGTCTGCAGAGCTATGCACATGCAGAAAAAGTATGCCACAGGGAGGCCAGACCAAAAGGACCTGAATGAAAACCTGGCTGCCACGCAGGGCCTGGCACACATGATCACAGAGTGTAATCGCTTGTTTGAGGTGAGACACATATCTGTTTCACATGAGGCATATTTGAATGCAATTCGAAAGTGTCCAAGAAAACCATCATGGACCCCTAATCTGAGTGGAAATGTGTTTTTCATTTGCCTATTCATTTAACTTGTGTTCCTTTTTTCCCCTAGATTCCTCACGAAATGGTGACACAGTCGCGTAATTCGTACGTGGAGGCCGAGCTT[C/T]AGGCTCCCACCATTGAGGAGCTGTGCAAGCGGCAGCATCCGGAAGATGATGGGGAAGATGAAGGCTCCTGGCCTGCATTCATGGAGGCTAGACTACAGGGTCTCCTCAAAGACTCACGGGAGAAGGCCAAAGGCTGGGTGTCCTGCCAGAGCACCGGCAACACCGAGCTGTCCTATAAGAAAGTAAGAATAAAGAAAACCAGGCTTTTTCATTCGTTTAGACTCAAAATCCACAATATTTATGTTGCCAGCTCACATTGTTATTCTTAAAGTCAATAATTAATCTGTGCAAAATAATCCAATAAAAAATGTTTTTGTTAAGCTTCAATCAAAGTCTGACCATTTGTTTCTGCCTTTGGAGTGGCAATCCTTCTGTTGATGTTAAGTTGAGGGCTTCCATAGCAACTGCTTATCGTTATTCCTAACCCAGCCCCTTTTTCTGTTAGCTTCCTATGAGGGAATGATACACAAAACAAAGCCCCACCCACTACTCAATATTCA
Associated Phenotype:
Not determined