Busch Lab

ZMP

tbc1d15

Ensembl ID:
ENSDARG00000057218
ZFIN ID:
ZDB-GENE-041111-251
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
sa43074 Essential Splice Site Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
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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
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa29010
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079820 Nonsense 210 367 6 16
ENSDART00000079824 Nonsense 210 664 6 17
ENSDART00000129146 Nonsense 210 664 6 17
Genomic Location (Zv9):
Chromosome 18 (position 16672038)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17023804
GRCz11 18 17012870
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAAAGCCTTTTCGCAGTCTTTTGAGAATCTTCTGGATGATACAAACTA[T/A]GGCTTTGTACAGGTATGTGATGTATAGTCTACAGTAAAAATGTCTACATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43074
Status:
Mutation detected in F1 DNA
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
ENSDART00000079820 Essential Splice Site 358 367 9 16
ENSDART00000079824 Essential Splice Site 358 664 9 17
ENSDART00000129146 Essential Splice Site 358 664 9 17
Genomic Location (Zv9):
Chromosome 18 (position 16667041)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17018807
GRCz11 18 17007873
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGGAGCAGCACTCATGAAGAAAGAAAGCTCCTGCAAAAGAGAAAAACG[T/A]ATGCTTGTTTTTCCTCAGAGAACAGAAAGCATTTGACTTTGACTTTTTTG
Associated Phenotype:
Not determined