ZMP
si:dkey-120m5.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
TBC1D14
Human Description:
TBC1 domain family, member 14 [Source:HGNC Symbol;Acc:29246]
Mouse Orthologue:
Tbc1d14
Mouse Description:
TBC1 domain family, member 14 Gene [Source:MGI Symbol;Acc:MGI:1098708]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12027 | Essential Splice Site | Available for shipment | Available now |
sa10659 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12027
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040946 | Essential Splice Site | 368 | 711 | None | 14 |
ENSDART00000133420 | Essential Splice Site | 368 | 711 | None | 15 |
The following transcripts of ENSDARG00000003520 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 41086400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 39422657 |
GRCz11 | 7 | 39693674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATTTCACTGCTATTCTGCCTCTCACTCTGTGCACTTGTGATTCTGTCC[A/T]GAGCTGAAAGAYGCCCAGAAACGAAAGAAACAGCTGGAGGACCGGTGTAA
Long Flanking Sequence:
TTTCTTACAAACAGTAACGTGTACATGTGTTGACTGTTGTTGTGTATTAATCTTCAGGAATCTTCCTGCAAAACCTGAGGAAGAAGCCCAAAAACACAGACAACAATATGAGGAAATGGTGGCTCAAGCCAAGAAAAGAGGTAACTTGCTTGATGTGCTTTTGCTATTCTGCGCGTGTTTGAGCTGAAGATCTACAGTTTAAGCAGCATCACAGTAACATTTGGGCTCAGTCTATATATATATAAATATATATATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTAATGCCATTCATTTAAATAGATTTGACTGATCCTTTTTTCATTGTGTGCCTAAAATTTGTGCTCTAGAGGGCGCTGTTGTAAAAGCTTCAATGTAATCCTTTTAACAGAGATTTCCATTTCACTGCTATTCTGCCTCTCACTCTGTGCACTTGTGATTCTGTCC[A/T]GAGCTGAAAGATGCCCAGAAACGAAAGAAACAGCTGGAGGACCGGTGTAAACTAGAGGAAAGCATTGGCAATGCTGCTCTCACCTGGAGTCAGGAGATATTACCCAACTGGCAAAGCATGTGAGTTAAAGTGGAGACTGTGTCAGAGATATTATCACATTTATAGTTAAAACGTTTGTCATTTATTGATGTTCCATGTAAAGAATAACCTCAATAGATTAGAGTAGCTGAAAAACTTTGTAAACAGAATAGTTGACAAGTGATGGACGGATTGATGTAAACTTAGTGAGAGCCACGAATGTCTCTGTTGTGTGCTGAATTGAGTTTAAATCTGGCTTGCAACATTTTAAGGTCCAGTTTAACAATGTACCATTTTTCTGCTTTGTTATATCCTATAATCTCTCTTTTGTCCCAATTATACAAAATATAAAAGTAGATATAAAAAAGAATGTAAAAATATGGTTTGAGAAATAGACAGTATATTCATGCATACTGAAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10659
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040946 | Essential Splice Site | 472 | 711 | None | 14 |
ENSDART00000133420 | Essential Splice Site | 472 | 711 | None | 15 |
The following transcripts of ENSDARG00000003520 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 41088280)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 39424537 |
GRCz11 | 7 | 39695554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAATGCCTTTGTAGCCCCAACRGCTGCTGYGGAAACTGAAAGTGAAGG[T/G]GATTTAATMAAWTCTATTTTTMAGCTTTCTAAYATTTTAAAACTTAAGYA
Long Flanking Sequence:
TGATGCATTCTGTTCATGCATTTTATGTTTAGTAAATATATGGGTGCAATCCTTGGAGATGAGTTAACACTTTACTTTAGCAGATCTCCAATGAAACTTTTGGGTGACACCACATCAATTTTTTAGTTGGATTGTTACACGTTCCATATAGAAATAACAATAAATTATTTATGATTGCATTTAACTAACCCTAAATTTAACCCTTATCTTAATGTAAACCAGACAGTAACGATAAGTATAGTTCATTAATATCGTTCATTGCTTGGTTAGACTGTAACAAGGATATCCTAAAATAGCATGACCCAAATTTTGATTCATAAAACCAGTTACATGTAATAACCATACTGTACCACAAGAGGGTGTCATTGGAAAGGAAATGAGAATCTGATATTTACATTTACGTTTATAACAGAGCTGTATGACATCTGCCTGGCAAGAGCGAAGGAGAAGTGGAATGCCTTTGTAGCCCCAACAGCTGCTGTGGAAACTGAAAGTGAAGG[T/G]GATTTAATCAATTCTATTTTTCAGCTTTCTAACATTTTAAAACTTAAGCACAACTTGCATGGTTTCATTATTTTTTAAATCCAATATAGTACATTCTATTTTTTTAAGCTTGTTTATTTATTAACTTTTTTTTTTTCTGTTGAACTCATTACTCATTTAACTACTGCTCATTTTTTAGATGCAGGCTTGTCTCATGCTGATCGAGAGGCCAGTCTAGAACTAATCAAGTTAGACATTTCCAGAACATTTCCCAATCTCTGTATATTCCAAAAGGTAGGACGTATTTCTCTTTCTGGTCTTTGATATCATCTACTGACAATTGGGGTCATTATCTCTTTATTTAATAAATTTTTTTTTATTGATTTCAAGGGGGGCCCATACCATGATGTATTGCACAGCATTCTGGGAGCTTACACTTGCTATCGTCCCGATGTGGGTTATGTAAGTACTACTTTGTTTAAGTGATGATTATTTTAAACATGCTGTGCACCACAGTACTG
Associated Phenotype:
Not determined