ZMP
tcf12
Ensembl ID:
ZFIN ID:
Description:
transcription factor 12 [Source:RefSeq peptide;Acc:NP_999981]
Human Orthologue:
TCF12
Human Description:
transcription factor 12 [Source:HGNC Symbol;Acc:11623]
Mouse Orthologue:
Tcf12
Mouse Description:
transcription factor 12 Gene [Source:MGI Symbol;Acc:MGI:101877]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa27060 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa45298 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14175 | Nonsense | Available for shipment | Available now |
| sa31600 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27060
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000009938 | None | None | 533 | None | 13 |
| ENSDART00000073766 | Essential Splice Site | None | 336 | 1 | 13 |
| ENSDART00000127387 | None | None | 591 | None | 14 |
| ENSDART00000131282 | Essential Splice Site | None | 702 | 1 | 19 |
| ENSDART00000136745 | Essential Splice Site | None | 54 | 1 | 4 |
| ENSDART00000138263 | None | None | 177 | None | 6 |
The following transcripts of ENSDARG00000004714 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 54164770)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 52434620 |
| GRCz11 | 7 | 52709690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGACTGGCACACCCGATCGCCCTAGTTGGATTTTTGACAGGATAAAAG[G/T]TAAAATAATGCACAGCGAGTTTCTGAGTGGTTTCGGACTGGGTGAAAGAA
Long Flanking Sequence:
AGTTCTGAAAGAGTGTGGATAAGTTCAGAAGGCTCCTGTGTATTTCAGCTGCTGCACTTGTTCCCCTGCTGCTACGATGTTCATGTTTCAGATATTTTCAGTTCCTAAAAATACGCATAGATCTAAACGAAGCCCACATTTATGTGAAGGGAGTTTGTAGGTAAACCAAACTGATTTTAGGAGGTGCTCCAGTGGTCCCCTAGCAAGGTTGTGTGTCAGGCTTTATGATTCGCCACACATGATATCCATCCGCTCCGCTGAAGAACAGCCGAGTCTACGGCGCTGGCGGAAGAACACGATTTCAAACGTCATCGCTGCGCTTCGGTTATCGCCAAGCAAAAATGTCTGCCTAAGGGAAACTCGCAAGTTACATAGTGGATATTTGCAAAACACAATCGCAAACGATATCGATTTCATTAATTTTCCGACGCGAGACAAGGAAATCTACGCCGTGACTGGCACACCCGATCGCCCTAGTTGGATTTTTGACAGGATAAAAG[G/T]TAAAATAATGCACAGCGAGTTTCTGAGTGGTTTCGGACTGGGTGAAAGAAGTTGGGATAGAAGAAAAGACGGGAGCCGATATTTGAGCGAAAGGGGTCGGCTTTCGCAGCTTGACATCGCACTGTTCATTCTCCGCGTTAAAACGTGTTGTGACAGTGTTAACGGAGCGTTTTGCTTAGTCGTCTGCTGGTCGCGGCACTATTATGAATAGGTTAACTGGCAATTAGCGAACAACAACAACAGCGGCGGCGGCGTTGTTTGTAAAGTAACCATTCTCATGCAAAATAACAACAAAAGTGTAGCTTCGGATGTTTTGACAGCCCGCGTGCGTTCATCGAGAGCTCGCGACTTTTGATACATTGAGGAATCAAACACATACAGTTGAAAAATGATGCTGCGGGTCCATGTGTGAGTGAGTGTGTGTGTGTGTGTGTGACACCGTCGAGCTCAGCGTATTTCTCAACATGTCCACGTTTGGTCATCCCAAAAAAAAAACGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45298
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 |
|---|---|---|---|---|---|
| ENSDART00000009938 | None | None | 533 | None | 13 |
| ENSDART00000073766 | Nonsense | 84 | 336 | 5 | 13 |
| ENSDART00000127387 | None | None | 591 | None | 14 |
| ENSDART00000131282 | Nonsense | 84 | 702 | 5 | 19 |
| ENSDART00000136745 | None | None | 54 | None | 4 |
| ENSDART00000138263 | None | None | 177 | None | 6 |
The following transcripts of ENSDARG00000004714 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 54092449)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 52362299 |
| GRCz11 | 7 | 52637369 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGATCTCTTTCCCCCAGGGGTTTGCAGACTCTCATTATGCTGATCACT[T/A]GAGTGACAGTCGATTAGTGTCCCATGAAGGATTGTCCCCAACACCTTTCA
Long Flanking Sequence:
TAATAATAAGCAAAACACAATGTAAGCTATACACCAATCGTTAGTATTGCTTAGAGATCTTAGGAAAGTAATGTCTGTATTACTATCGTTATATCAGATCCCAGTGTGCTAACATTAAAGGGAATGAGGCGGAAAAAAAAACATGTTAATGTGACGTGAATTTTGTTGATAAATGCAAATCGCTCATTTTCTGTTGTTGTTTGTGCCTCATTAACTTTATTACAATTACACAATCCCAGCACAAGCGCTGTCATCTCTTCGGGGCTTTTGTTTGCCCTTTTAATGAAATTCATCAAAGACTTTGAAGAAAGTGTTTTTTAATGAGGAGAGTAGAGAAGTATTGATCGTTTCGGGGGACAGTTGACCAGTCGTGCTCCCCTCTTTCCCCCAGTAATTAGAAGAGTGTCATAGCACTCAATTAGCAGGTCCGGCTAATAATGTGTTTAATGCTGTGATCTCTTTCCCCCAGGGGTTTGCAGACTCTCATTATGCTGATCACT[T/A]GAGTGACAGTCGATTAGTGTCCCATGAAGGATTGTCCCCAACACCTTTCATGAGCTCCAGCATAATGGGTGAGTATCCAAGGTGATTCTGACCCCGTCTCTCTTTCGCACCCGTCTTTCTGTCATCAATCCATTTAGCAAAGTGTGGACCGATCAGCCACTTCTTCTCTTAGAAAGCAGTCACCCCAGGAAGTGATAGAAATGGGTGAGGGTGTTTGTGCACTGTATATACGCTGCATTTATTTATACTGCATGCATGTGGACAGTAAAAGCAATATTAAAATAGTGTACTCAAAAATTAATTTTAGGATTGTTTGTTGAAAGACGTCAAGAACTATTGATCAGTAATATTGTGAGATATTAAAAATTATTATTTTATTAATTTTAATCCTTTTTTCCTAGTAAATACAGTGCATCCGTAAATTATTCATAGAGCATCACTTTTTCCACATTTGTTTATGTTACAGCCTTGTTCTAAAATGGATTCAATTAATTTATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14175
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000009938 | Nonsense | 22 | 533 | 2 | 13 |
| ENSDART00000073766 | Nonsense | 191 | 336 | 9 | 13 |
| ENSDART00000127387 | Nonsense | 86 | 591 | 4 | 14 |
| ENSDART00000131282 | Nonsense | 191 | 702 | 9 | 19 |
| ENSDART00000136745 | None | None | 54 | None | 4 |
| ENSDART00000138263 | Nonsense | 22 | 177 | 2 | 6 |
The following transcripts of ENSDARG00000004714 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 54006676)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 52276526 |
| GRCz11 | 7 | 52551596 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTCTCAGTAGTAATRCTTTTTTTTNATTTATGTGTGTCTGCAGGTGTA[T/A]GCACCATCTCCCAGCTCAGAGGACTWCAACAGAGACTCTCCGTCTTATCC
Long Flanking Sequence:
GGCCGTAGCCTCATGCCTTTGATCCTCCTCTACTGGAATGGGCATTTCTGCAGCTGTAACCACTGCTCTGCTGGCCCGACCCCATCCAACCCCAAAGCTCCTAAAATACACATGCAGAAACACAAACACATGCACCCCCAACGCTCTTGCTTATTAATCCATTTGTTTCGATGCTTTGTTCCTGCATGTCGTCATCATTATACTACAATTAAGCACCGAAGCACACACACTCTATGTCGCAGATAATCCTCCGCTTTCTTATTATACGACTTCTAAATTAGCCATCTGCTTCATCAAAGACTTTGTAATTTGCCATGTGTGTTGCGTTGTGTTGTTTGTGCTCTATTATGCAGTCAGGTTTCATGGTATGTGTGTGTTAGACCGAGGGGTATGAGGATAGCTTAATGACGATGGTCGCTGTGGTTTATATTTGGTACAGAAACACCTGTCGGTTCTCAGTAGTAATGCTTTTTTTTTATTTATGTGTGTCTGCAGGTGTA[T/A]GCACCATCTCCCAGCTCAGAGGACTTCAACAGAGACTCTCCGTCTTATCCGTCTCCAAAACCCCCCGGCAGTATGTTCGCAAGCACTTTCTTTGGTCAGTCATCAGCATTTTATTCATTTATATTTAATTCTTTGTTTGATTGTCATATTTTTTTGGAGGGTGGGGGGTGTTGACTTTCTTTGAAAGGTTGTGTTTTTTGTAAACAGCAAAAGTCAGTCCAAGGCACTCAAAAATGTGGAAAAAATATTAAAAAGCCTTTATTGACATGGCTATTACTTAAAACTGCATTTCGGCAAACAACTGCCATCGTCAGGGTAGTGAAGACAATGTGCATCTGGAGTTTCTTTTGAACACTATGATCTCATGACTCATTAGAATATCTAAACAATACTAAAATAATATATTGAACACAATGTCAACTTAATTGTTATTAATTCAGCATTTCAGAATGGAAAAAACTCTTAATGGAAAAAAAAGATCATGCGTTATGCAACATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31600
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 |
|---|---|---|---|---|---|
| ENSDART00000009938 | Essential Splice Site | 54 | 533 | 2 | 13 |
| ENSDART00000073766 | Essential Splice Site | 223 | 336 | 9 | 13 |
| ENSDART00000127387 | Essential Splice Site | 118 | 591 | 4 | 14 |
| ENSDART00000131282 | Essential Splice Site | 223 | 702 | 9 | 19 |
| ENSDART00000136745 | None | None | 54 | None | 4 |
| ENSDART00000138263 | Essential Splice Site | 54 | 177 | 2 | 6 |
The following transcripts of ENSDARG00000004714 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 54006580)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 52276430 |
| GRCz11 | 7 | 52551500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCGTCTCCAAAACCCCCCGGCAGTATGTTCGCAAGCACTTTCTTTGG[T/G]CAGTCATCAGCATTTTATTCATTTATATTTAATTCTTTGTTTGATTGTCA
Long Flanking Sequence:
GCTCCTAAAATACACATGCAGAAACACAAACACATGCACCCCCAACGCTCTTGCTTATTAATCCATTTGTTTCGATGCTTTGTTCCTGCATGTCGTCATCATTATACTACAATTAAGCACCGAAGCACACACACTCTATGTCGCAGATAATCCTCCGCTTTCTTATTATACGACTTCTAAATTAGCCATCTGCTTCATCAAAGACTTTGTAATTTGCCATGTGTGTTGCGTTGTGTTGTTTGTGCTCTATTATGCAGTCAGGTTTCATGGTATGTGTGTGTTAGACCGAGGGGTATGAGGATAGCTTAATGACGATGGTCGCTGTGGTTTATATTTGGTACAGAAACACCTGTCGGTTCTCAGTAGTAATGCTTTTTTTTTATTTATGTGTGTCTGCAGGTGTATGCACCATCTCCCAGCTCAGAGGACTTCAACAGAGACTCTCCGTCTTATCCGTCTCCAAAACCCCCCGGCAGTATGTTCGCAAGCACTTTCTTTGG[T/G]CAGTCATCAGCATTTTATTCATTTATATTTAATTCTTTGTTTGATTGTCATATTTTTTTGGAGGGTGGGGGGTGTTGACTTTCTTTGAAAGGTTGTGTTTTTTGTAAACAGCAAAAGTCAGTCCAAGGCACTCAAAAATGTGGAAAAAATATTAAAAAGCCTTTATTGACATGGCTATTACTTAAAACTGCATTTCGGCAAACAACTGCCATCGTCAGGGTAGTGAAGACAATGTGCATCTGGAGTTTCTTTTGAACACTATGATCTCATGACTCATTAGAATATCTAAACAATACTAAAATAATATATTGAACACAATGTCAACTTAATTGTTATTAATTCAGCATTTCAGAATGGAAAAAACTCTTAATGGAAAAAAAAGATCATGCGTTATGCAACATTTCTTAAATAACATTATCTTTTTTATTCTTAATTTTAAAATTTTAATATTGTTTAGATATTTTATCATAGATCATAGTGTTGAAAAGAAACTCCAGACA
Associated Phenotype:
Not determined