ZMP
tbx3
Ensembl ID:
ZFIN ID:
Description:
T-box transcription factor TBX3 [Source:RefSeq peptide;Acc:NP_001095140]
Human Orthologue:
TBX3
Human Description:
T-box 3 [Source:HGNC Symbol;Acc:11602]
Mouse Orthologue:
Tbx3
Mouse Description:
T-box 3 Gene [Source:MGI Symbol;Acc:MGI:98495]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1334 | Essential Splice Site | Available for shipment | Available now |
sa16346 | Nonsense | Available for shipment | Available now |
sa26643 | Missense, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18035 | Missense, Nonsense | Available for shipment | Available now |
sa40617 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1334
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006380 | Essential Splice Site | 215 | 689 | 3 | 7 |
ENSDART00000122340 | Essential Splice Site | 215 | 279 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 75418872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 71537708 |
GRCz11 | 5 | 72322214 |
KASP Assay ID:
554-1248.1 (used for ordering genotyping assays)
KASP Sequence:
TATTTAAAAATCACGAATATTTAATATAACGTCAGGCTAATTTGTGTTTT[A/G]GACGATACTAAACTCCATGCACAAATACCAGCCAAGATTTCACATCGTGA
Long Flanking Sequence:
CCCCGAAATGCCAAAACGGATGTACATTCACCCCGACAGTCCGGCCACTGGCGAGCAATGGATGTCTAAAGTCGTCAATTTTCACAAACTTAAACTGACAAATAACATCTCCGACAAGCATGGATTCGTAAGTTACAGTCATCAACTCCTATTAATGCATTATGATTAGCATTATTATTGCTGTAAGTATTAGAAGTATTGTGGTTGATATTGATATAGGTGTAATCTTTATACAGTTTATTTGTATTAATCGAAAACACTCGATGCTGTCTGGCAAGCTTCAGTAATAAGAATTTAAACTATTGGATAATTGTTTTTCTTTATTAATACTTTGTATTATATTTCAAATAAATACACGGATGTGTTTGAGCTGGAAAAGATTGTTTAGAGGAGAAAATAAATAAAATGTATTTGATTTGCACCATTCGTAAGTGCAGGATTACTAAATGTTATTTAAAAATCACGAATATTTAATATAACGTCAGGCTAATTTGTGTTTT[A/G]GACGATACTAAACTCCATGCACAAATACCAGCCAAGATTTCACATCGTGAGAGCCAACGACATACTGAAGCTCCCCTACAGCACGTTCAGGACCTACGTGTTCCCCGAGACAGACTTCATTGCTGTCACTGCCTACCAGAACGACAAGGTTGGTCAAAACGAACTTCTGTGTGTTTAAAATGACTGCGATGCATATCGCTGAATGCTTGTTGTAAATGTTTGGAAACCAGAAGAGCAGTCGTTGTTGCATTTCGGTCAAATATAAGCGAGTGTGTTGTTAAATGCTCCAGTGAGGCCTACATCATCACAAAAACTCGCACAGACAGAAAAACACAGAATCGCAGCCGCAGAAATTCAAGTTTGTTAGTGGAAGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTAAAAGAATGAGAAGAGGGAGGAAGGAAGGGAGGACTGCTCAC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa16346
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006380 | Nonsense | 341 | 689 | 5 | 7 |
ENSDART00000122340 | None | None | 279 | None | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 75420211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 71536369 |
GRCz11 | 5 | 72320875 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCGYCAGGCTTCATCTCCTGCGGTCTCGACTGCTGGACACAATCATTTA[A/T]AAGGTACGACAGTCAGACAGACATGAGCCGTATGCATTTTCTCCTAGATC
Long Flanking Sequence:
TTAAGCTTATTGTATTTGCACAGAATGACGTAAATAAAAGCTCATGTTCTGTTTAAATGTGATTGCATTTTAGATCACACAACTGAAAATTGACCACAATCCTTTTGCAAAAGGATTTCGGGACACTGGAAATGGGAGACGCGAAAAAAGGTAAAGCTGGGCTCATTTAAAGACTGGACTCTGTTGGTTTTAATAATTGAATCGTGCATTTTCGTCGTAAAACGCGAGGAGAGCGGTGAACTCAAGAACACGCTCTTGTTTGAATCGTCTGTAATACAATTCTGAGTTTGCTTACAGAGGCAATTTCTCTTCTCAATGGCCTGTCTTGGAAATGTGTGTGATACAGGAAGCAGCTGGCTCTGCAATCGATGCGTTCATATGAGGAGCAGCAGAAAAAAGAAAACGGGACGTCAGACGATTCCTCAGGCGAGCAGGCGTCCTTCAAGTGTTTTCGCCAGGCTTCATCTCCTGCGGTCTCGACTGCTGGACACAATCATTTA[A/T]AAGGTACGACAGTCAGACAGACATGAGCCGTATGCATTTTCTCCTAGATCAAAATCGACATTTCTTTTTCTAGAGAATGTCCTTGGAAATGCGACAACAAAAGTAGCCTGCGATTAATTCTGTCCGGGAGACTAAAACAAGTCATTGCTAATTTAAGAGCACGATGATTAGTTTTGTACATGCAGTTATTTAGATGCTGGATGAAAGTGTGCTGCAGGAAGTCTGAGTCTGCTGTCCGCAGTGCACCATATTAGTATTAATGCGTGCGCGTTCTGAGTTGTGCTTTCGCCGTTTAAAACGATATGCATCTCGCTGCTGGTGTTTATAAAAAGTGACACATGTGTGTGTGGTGTAACCTTTCGGTTAGATTCGCATGATTAAACAATGAATGGTCTTACAACTTTCCCGATCTGTGTTGACAGATTTCTGTGACAGCGATGAAGACAGCGATGAAGAAGACAAAGACGCGAACGCAAAAGAAGGGCCAGACTCCAGCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26643
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:
A > T
Consequence:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006380 | Missense | 353 | 689 | 6 | 7 |
ENSDART00000122340 | Nonsense | 275 | 279 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 75420667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 71535913 |
GRCz11 | 5 | 72320419 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGATCTGTGTTGACAGATTTCTGTGACAGCGATGAAGACAGCGATGAAG[A/T]AGACAAAGACGCGAACGCAAAAGAAGGGCCAGACTCCAGCAAAATCTCCA
Long Flanking Sequence:
AGGCTTCATCTCCTGCGGTCTCGACTGCTGGACACAATCATTTAAAAGGTACGACAGTCAGACAGACATGAGCCGTATGCATTTTCTCCTAGATCAAAATCGACATTTCTTTTTCTAGAGAATGTCCTTGGAAATGCGACAACAAAAGTAGCCTGCGATTAATTCTGTCCGGGAGACTAAAACAAGTCATTGCTAATTTAAGAGCACGATGATTAGTTTTGTACATGCAGTTATTTAGATGCTGGATGAAAGTGTGCTGCAGGAAGTCTGAGTCTGCTGTCCGCAGTGCACCATATTAGTATTAATGCGTGCGCGTTCTGAGTTGTGCTTTCGCCGTTTAAAACGATATGCATCTCGCTGCTGGTGTTTATAAAAAGTGACACATGTGTGTGTGGTGTAACCTTTCGGTTAGATTCGCATGATTAAACAATGAATGGTCTTACAACTTTCCCGATCTGTGTTGACAGATTTCTGTGACAGCGATGAAGACAGCGATGAAG[A/T]AGACAAAGACGCGAACGCAAAAGAAGGGCCAGACTCCAGCAAAATCTCCACCACCACCGAGGACTCCAAGGACCAGGACGCGGGTTTGGGCAAGAGTGTGTTCGGCGAGAGCGACTCCTCCTCGGGTCGCAGAAGCGAGAAGACCCGCGCGGACTCTCGGAGCCCCATCACCCTCATCTCCAGCACCACCCGCTCCGGAGAGGAGCTCAAGAGTCCGGTAAGAGAACCGGCCAAGACTACAGACGACTGCCGGACAGTGAGCAAGGAAAATTACATGCCATTGACTGTGCAAACAGACGGCGCAGCGCACTTAAATCAAAACCACTTGCACAATTTCGGATTTCCGCCGGGTTTGGCCGGGCAGCAGTTTTTCAATCATTTGGGTGGTGCCCATCCTTTCCTCCTTCACCCCAGCCAGTTCAACATGGGAGGCGCTTTCTCCAACATGGCCGCAGGGATGGGCCCCATACTGGCCGCGGTGTCCTCTGGTGGAGTAGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18035
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006380 | Missense | 357 | 689 | 6 | 7 |
ENSDART00000122340 | Nonsense | 279 | 279 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 75420679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 71535901 |
GRCz11 | 5 | 72320407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAGATTTCTGTGACAGCGATGAAGACAGYGATGAAGWAGACAAAGACG[C/T]GAACGCRAAAGAAGGGCCAGACTCCAGCAAAATCTCCACCACCACCGAGG
Long Flanking Sequence:
CTGCGGTCTCGACTGCTGGACACAATCATTTAAAAGGTACGACAGTCAGACAGACATGAGCCGTATGCATTTTCTCCTAGATCAAAATCGACATTTCTTTTTCTAGAGAATGTCCTTGGAAATGCGACAACAAAAGTAGCCTGCGATTAATTCTGTCCGGGAGACTAAAACAAGTCATTGCTAATTTAAGAGCACGATGATTAGTTTTGTACATGCAGTTATTTAGATGCTGGATGAAAGTGTGCTGCAGGAAGTCTGAGTCTGCTGTCCGCAGTGCACCATATTAGTATTAATGCGTGCGCGTTCTGAGTTGTGCTTTCGCCGTTTAAAACGATATGCATCTCGCTGCTGGTGTTTATAAAAAGTGACACATGTGTGTGTGGTGTAACCTTTCGGTTAGATTCGCATGATTAAACAATGAATGGTCTTACAACTTTCCCGATCTGTGTTGACAGATTTCTGTGACAGCGATGAAGACAGCGATGAAGAAGACAAAGACG[C/T]GAACGCAAAAGAAGGGCCAGACTCCAGCAAAATCTCCACCACCACCGAGGACTCCAAGGACCAGGACGCGGGTTTGGGCAAGAGTGTGTTCGGCGAGAGCGACTCCTCCTCGGGTCGCAGAAGCGAGAAGACCCGCGCGGACTCTCGGAGCCCCATCACCCTCATCTCCAGCACCACCCGCTCCGGAGAGGAGCTCAAGAGTCCGGTAAGAGAACCGGCCAAGACTACAGACGACTGCCGGACAGTGAGCAAGGAAAATTACATGCCATTGACTGTGCAAACAGACGGCGCAGCGCACTTAAATCAAAACCACTTGCACAATTTCGGATTTCCGCCGGGTTTGGCCGGGCAGCAGTTTTTCAATCATTTGGGTGGTGCCCATCCTTTCCTCCTTCACCCCAGCCAGTTCAACATGGGAGGCGCTTTCTCCAACATGGCCGCAGGGATGGGCCCCATACTGGCCGCGGTGTCCTCTGGTGGAGTAGGCTCATTGGACGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40617
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006380 | Nonsense | 397 | 689 | 6 | 7 |
ENSDART00000122340 | None | None | 279 | None | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 75420798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 71535782 |
GRCz11 | 5 | 72320288 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGGTTTGGGCAAGAGTGTGTTCGGCGAGAGCGACTCCTCCTCGGGTCGC[A/T]GAAGCGAGAAGACCCGCGCGGACTCTCGGAGCCCCATCACCCTCATCTCC
Long Flanking Sequence:
AAATGCGACAACAAAAGTAGCCTGCGATTAATTCTGTCCGGGAGACTAAAACAAGTCATTGCTAATTTAAGAGCACGATGATTAGTTTTGTACATGCAGTTATTTAGATGCTGGATGAAAGTGTGCTGCAGGAAGTCTGAGTCTGCTGTCCGCAGTGCACCATATTAGTATTAATGCGTGCGCGTTCTGAGTTGTGCTTTCGCCGTTTAAAACGATATGCATCTCGCTGCTGGTGTTTATAAAAAGTGACACATGTGTGTGTGGTGTAACCTTTCGGTTAGATTCGCATGATTAAACAATGAATGGTCTTACAACTTTCCCGATCTGTGTTGACAGATTTCTGTGACAGCGATGAAGACAGCGATGAAGAAGACAAAGACGCGAACGCAAAAGAAGGGCCAGACTCCAGCAAAATCTCCACCACCACCGAGGACTCCAAGGACCAGGACGCGGGTTTGGGCAAGAGTGTGTTCGGCGAGAGCGACTCCTCCTCGGGTCGC[A/T]GAAGCGAGAAGACCCGCGCGGACTCTCGGAGCCCCATCACCCTCATCTCCAGCACCACCCGCTCCGGAGAGGAGCTCAAGAGTCCGGTAAGAGAACCGGCCAAGACTACAGACGACTGCCGGACAGTGAGCAAGGAAAATTACATGCCATTGACTGTGCAAACAGACGGCGCAGCGCACTTAAATCAAAACCACTTGCACAATTTCGGATTTCCGCCGGGTTTGGCCGGGCAGCAGTTTTTCAATCATTTGGGTGGTGCCCATCCTTTCCTCCTTCACCCCAGCCAGTTCAACATGGGAGGCGCTTTCTCCAACATGGCCGCAGGGATGGGCCCCATACTGGCCGCGGTGTCCTCTGGTGGAGTAGGCTCATTGGACGGGTCCAGCCTGCCCTCGCCCTCACAGAGCCTCACCGGAGCCCCGATGCCGTTTCATCTGCAGCAGCACGTGCTGGCGTCTCAGGTAAGTCCATTAATATTAATGCACAGCAGTGAAAGTCAT
Associated Phenotype:
Not determined