ZMP
stard10
Ensembl ID:
ZFIN ID:
Description:
START domain containing 10 [Source:RefSeq peptide;Acc:NP_956514]
Human Orthologue:
STARD10
Human Description:
StAR-related lipid transfer (START) domain containing 10 [Source:HGNC Symbol;Acc:10666]
Mouse Orthologue:
Stard10
Mouse Description:
START domain containing 10 Gene [Source:MGI Symbol;Acc:MGI:1860093]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24962 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35717 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24962
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048130 | Essential Splice Site | 62 | 271 | None | 6 |
| ENSDART00000132850 | Essential Splice Site | 62 | 271 | None | 7 |
Genomic Location (Zv9):
Chromosome 14 (position 34252401)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 32937101 |
| GRCz11 | 14 | 33277415 |
KASP Assay ID:
554-7504.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTCGATTAACAACAAAGGAAACTACAGCAAAGTGCACAAAATCAGGG[T/A]AAGATGTTTGCCTACGTCTAATCAAACTGTTTATAGTGTGTGTGTGTGTG
Long Flanking Sequence:
CAACGTAATGTCATTGTGTAAAATCACTGTCGTTCAGTACTGCTGGCTGCGCTCTGCTGGTTTTGTAACACGAATACACCTGTCCTACTTCCGGAAGCAGTGACGAGATTTTTCCACGCGCTTACGTCGACGCCAGGTAAGGAATTTGCGAAAAAATCTTGTCGAGCTTGAAATGTTAATCTGACTGCGACTACAATAAGCGCTGCTCATACTGAACAGAGACCAGAGATATCGAGTCTTGACACAAGCGACATCCCTCAGACGAATCTTGTACTTTCGCTGTGATTTTCATTGGTGAAATTGTCTTTTTAGAATGTCTCGCGGTTCAGGAATCCTTCCAGATGAATCCATGTTCGCTGAGTTCAAGAGACAATGCTTGTCTACGGAGAATTGGGTCAACAAGTATGATAAAAATGACATGGAGGTTTGGGTCGAGCAGGCCCCTTTATCTGCTTCGATTAACAACAAAGGAAACTACAGCAAAGTGCACAAAATCAGGG[T/A]AAGATGTTTGCCTACGTCTAATCAAACTGTTTATAGTGTGTGTGTGTGTGTGTGTAGGATTTTATATTGTTAAAGAGTACCTTAAACAGATTTTCAGCCTTTATACATATCAATATAATTGTTATTGATGAAGAAAATAATAAACTTTAGTAGTAGAAGTGACATAGCTACAGTACACCATAGTCTTATAGTGAGTTAGACATATATTATAAACAATTAAGTAGATTTTACTCAAAATATTTTATTTTCTGCATCGCATATATTAAATTTCAGTTTATTTACATGTCATGTGTAGCTACTGCTGCCATAACAACACACATGCAAATGCCTTTGTTTCCAATACAGTGTCAAATAAACATAAAGGATGTATCTGCTGCCACCATGTATGATGTTCTTCATGACGGCCAATACCGGAAAACATGGGACCCTACCATGCTGGAGAGTTTTGACATCGCCCGTCTGGCTCACAATGCTGATGTGGGCTACTATTCATGTGAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35717
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 |
|---|---|---|---|---|---|
| ENSDART00000048130 | Nonsense | 63 | 271 | 2 | 6 |
| ENSDART00000132850 | Nonsense | 63 | 271 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 14 (position 34252053)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 32936753 |
| GRCz11 | 14 | 33277067 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCTGCCATAACAACACACATGCAAATGCCTTTGTTTCCAATACAGTG[T/A]CAAATAAACATAAAGGATGTATCTGCTGCCACCATGTATGATGTTCTTCA
Long Flanking Sequence:
CATGTTCGCTGAGTTCAAGAGACAATGCTTGTCTACGGAGAATTGGGTCAACAAGTATGATAAAAATGACATGGAGGTTTGGGTCGAGCAGGCCCCTTTATCTGCTTCGATTAACAACAAAGGAAACTACAGCAAAGTGCACAAAATCAGGGTAAGATGTTTGCCTACGTCTAATCAAACTGTTTATAGTGTGTGTGTGTGTGTGTGTAGGATTTTATATTGTTAAAGAGTACCTTAAACAGATTTTCAGCCTTTATACATATCAATATAATTGTTATTGATGAAGAAAATAATAAACTTTAGTAGTAGAAGTGACATAGCTACAGTACACCATAGTCTTATAGTGAGTTAGACATATATTATAAACAATTAAGTAGATTTTACTCAAAATATTTTATTTTCTGCATCGCATATATTAAATTTCAGTTTATTTACATGTCATGTGTAGCTACTGCTGCCATAACAACACACATGCAAATGCCTTTGTTTCCAATACAGTG[T/A]CAAATAAACATAAAGGATGTATCTGCTGCCACCATGTATGATGTTCTTCATGACGGCCAATACCGGAAAACATGGGACCCTACCATGCTGGAGAGTTTTGACATCGCCCGTCTGGCTCACAATGCTGATGTGGGCTACTATTCATGTGAGTCACGTGTTCAGTGTTGAAACTGTAGCAGTTTGAAACCTTATGTTGAGAGTTATTCTATAATGTTTGATGATAGTTATTTGAATAGTCCTCAAGCTCTTGTTCTTCTAATGTGACTGCAGTAACGGCTGAAGATAAGGCTCCTGGGAGCATGTTTTTGTGTGTATTTATAGTCAACACCAAGATAGCTTTGTTCCTCTTTTTTTCTTTCCCAGTCAGTAAAAGCTATTTATAGACCTACGGGCTGTAAAAAGACTTTTTTTTTCTCCTTAATTCACAGGGATTTGTCCGAAACCATTGAAAAACAGAGATGTGGTGACCCTGCGCTCATGGCAGGCGTCTGAAAATGAGT
Associated Phenotype:
Not determined