ZMP
tbc1d15
Ensembl ID:
ZFIN ID:
Description:
TBC1 domain family member 15 [Source:RefSeq peptide;Acc:NP_001166096]
Human Orthologue:
TBC1D15
Human Description:
TBC1 domain family, member 15 [Source:HGNC Symbol;Acc:25694]
Mouse Orthologue:
Tbc1d15
Mouse Description:
TBC1 domain family, member 15 Gene [Source:MGI Symbol;Acc:MGI:1913937]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13834 | Essential Splice Site | Available for shipment | Available now |
sa14248 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13834
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079820 | Essential Splice Site | 64 | 367 | 3 | 16 |
ENSDART00000079824 | Essential Splice Site | 64 | 664 | 3 | 17 |
ENSDART00000129146 | Essential Splice Site | 64 | 664 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 16676042)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17027808 |
GRCz11 | 18 | 17016874 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAACCCCTAGAGGATGCAGATCCCTCAAACATGYTGTGTGCCTGCAAGG[T/C]TTGTTAGTTYACTCATCTGTGAGAGTTWGCATATTTAAATTGACTGAGAG
Long Flanking Sequence:
AATATTTTTTGGATACTGCTTTACAGAGGGAAGGGCATCCGCTGTGTAAAATATATGCTAGAATAGTTGGCGGTTCGTTCCACTGTGGCGACTCCTGATTGATAATGGTCTAAGCTAAAGCAAAATGAATTAATTAATTAATTTTTGTGGATTCCCACATAGATTTCTGTATGATCATTTGTTTAATAGTCGTTTTAGAACTTTAGTTGTTTAATGTTTAAAAAAATTGAATTTATTGACGTATTAATAGTTTGTAACATTATATCTTTTAAAATAAATACACCTTTAATGATTAAAAGTATGAATTTCTCTCCAATAAGACCCATTTTGTAAATATTAGTCTAAATATCGTAAATGGAAACCTCATAGCCATCTAACAACACTCCTCCAATATCTTTTTGTTTGATTGTTTCTTCTGTATCTGTAGGAAGGTGAAACCCTTGTGGAATATAAACCCCTAGAGGATGCAGATCCCTCAAACATGCTGTGTGCCTGCAAGG[T/C]TTGTTAGTTCACTCATCTGTGAGAGTTTGCATATTTAAATTGACTGAGAGTTCAAATATCTCCGACAGTTTCTCTGTGCTTTATGGTATGATTGAGAATGGCTCTTTATTGAGATCACCTGATTTCTGTTTATATGATTGTGTGAAGGACTCCAGCTCAGTGGTGGAATGGACACAAAGTTCAGAAGAAAACCCTCATCGTCCTGTTGACCATCAGCTAAGCTATGAAACAGAGTGGGACATGATCAATGCGGTCTCATTCCGGAGAAAAGTCCATGCAAATGGAGATGGTAAAGCAATTGCACATCTCTATATAAACCCTCTTTTTTTTATCAAATCGCTGTCACTGTGCATTTTCTCTCACACATATAATGCTAATTCAGCCTGTAAATTGTGTCTTTTCCTTTTTTTTTCTTAACCTGAAGATAAAAATCTAAAACGGTAACTAAGTGTATTATTTATTTTGACAGGTGGATCAAATCACGTGAATGAACAGAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14248
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079820 | Nonsense | 114 | 367 | 5 | 16 |
ENSDART00000079824 | Nonsense | 114 | 664 | 5 | 17 |
ENSDART00000129146 | Nonsense | 114 | 664 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 16675566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17027332 |
GRCz11 | 18 | 17016398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNAATCTAAAACGGTAACTAAGTGYATTATTTATTTTGACAGGTGGAT[C/A]AAATCACGTGAATGAACAGAACAAGCGAGCTTTCTCTTTTAATSTGTGTG
Long Flanking Sequence:
CAAACATGCTGTGTGCCTGCAAGGTTTGTTAGTTCACTCATCTGTGAGAGTTTGCATATTTAAATTGACTGAGAGTTCAAATATCTCCGACAGTTTCTCTGTGCTTTATGGTATGATTGAGAATGGCTCTTTATTGAGATCACCTGATTTCTGTTTATATGATTGTGTGAAGGACTCCAGCTCAGTGGTGGAATGGACACAAAGTTCAGAAGAAAACCCTCATCGTCCTGTTGACCATCAGCTAAGCTATGAAACAGAGTGGGACATGATCAATGCGGTCTCATTCCGGAGAAAAGTCCATGCAAATGGAGATGGTAAAGCAATTGCACATCTCTATATAAACCCTCTTTTTTTTATCAAATCGCTGTCACTGTGCATTTTCTCTCACACATATAATGCTAATTCAGCCTGTAAATTGTGTCTTTTCCTTTTTTTTTCTTAACCTGAAGATAAAAATCTAAAACGGTAACTAAGTGTATTATTTATTTTGACAGGTGGAT[C/A]AAATCACGTGAATGAACAGAACAAGCGAGCTTTCTCTTTTAATGTGTGTGACCTCAGGTCCGTCACAGTCAAATGTGAGGGCTGGTCATACCTCACTTTCCGCTTGAAGGATGGCACAGCATTGCCAGCCATTCATTTCCACCAGGGAGGAAGCAAAGCGTTCCTGGATAGTCTGAGGAAATCAGTTCAGATCAACGAGTGAGTTGACTTTGTCTAAATGGGTAATCTTTGGCTCCATTGTAGGCAAATATTGTGCAATATCTATTTGATGGCATAGTTCAAGAGATAGTAAAGGGAAATGAAAATTAGCTCATTGTTTACTCACCCTAAGTGGTTCCAAACCTTTGAATTTCTTTTAAACACAAAAGAAGATAATACTAAATTAAATACTATGGGAGCCAGTGGTTACTGGTTTTTAATATTTTTTATAAAATAACAGAAGAAAGAAACTCAAACCGGTTTTTGAGAAGTGAAGGGTGAGTATATAATAACAGAATATT
Associated Phenotype:
Not determined