ZMP
tcf7l2
Ensembl ID:
ZFIN ID:
Description:
transcription factor 7-like 2 [Source:RefSeq peptide;Acc:NP_571334]
Human Orthologue:
TCF7L2
Human Description:
transcription factor 7-like 2 (T-cell specific, HMG-box) [Source:HGNC Symbol;Acc:11641]
Mouse Orthologue:
Tcf7l2
Mouse Description:
transcription factor 7-like 2, T-cell specific, HMG-box Gene [Source:MGI Symbol;Acc:MGI:1202879]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35328 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35327 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa103 | Nonsense | Available for shipment | Available now |
sa22132 | Nonsense | Available for shipment | Available now |
sa2624 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa35328
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 |
---|---|---|---|---|---|
ENSDART00000005562 | Essential Splice Site | 161 | 477 | 4 | 15 |
ENSDART00000009237 | None | None | 438 | None | 14 |
ENSDART00000031408 | Essential Splice Site | 161 | 610 | 4 | 14 |
ENSDART00000121527 | Essential Splice Site | 161 | 597 | 4 | 15 |
ENSDART00000122972 | None | None | 235 | None | 6 |
ENSDART00000123318 | None | None | 426 | None | 13 |
ENSDART00000125046 | Essential Splice Site | 161 | 268 | 4 | 7 |
ENSDART00000128703 | Essential Splice Site | 145 | 181 | 4 | 5 |
ENSDART00000133854 | None | None | 118 | None | 4 |
The following transcripts of ENSDARG00000004415 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 32758000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30955997 |
GRCz11 | 12 | 31070899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAGACAAGCACTTAAAGATGCCAGGTCACCTTCTCCAGCACACATCGTT[G/T]TAAGTAACACTCATGAGTCATTGCATTTACAAAGCTCTTTGTTCTACAGC
Long Flanking Sequence:
ACAAAAAAACTCGACACAGAATTGTTAAAAACCTACTGCCAGCTAGCGTTTTGGAAGGGTTACTGCAGAGCAACACCAAAGTATAAATGCAGAAGTATAAATGCACGACTATGTACAAGGCTGGCGCCGTGGATCACGTTGATCACTCGATGCAGAAGTATAAACAGCCTTAAGATGTCAATTAATCATTAGTTTCAACTGTCAAGGATTTCCACCTCATGCATCATTCGACCTCAGATCTTTTTGACATAATTTATTTTTGTTTACTTTTTTTTTTCATGTCACAGTCACTTTTTATTTGGGATATTTTAGCTCTTATGTTGTGTTTCCCTTTGTTTTCTGCATTATTAACATGTTTTTCTTTTGTTTTTCTCCATTCTTTTCTTTCTGCCATCCAGTATCTACAGATGAAATGGCCCCTGCTAGATGTTCAAGCAGGAAGTCTTCAGAGTAGACAAGCACTTAAAGATGCCAGGTCACCTTCTCCAGCACACATCGTT[G/T]TAAGTAACACTCATGAGTCATTGCATTTACAAAGCTCTTTGTTCTACAGCACAGTCCATGAAAATTTCCTGTATCCTGTGTATTTGGTGCTTTGGGACCTTACGCTCCTCTCCTAACTCACAGCTGTCAATGGGATGACCTATAAGTAACTGTAAATCCGATTGCGTTGGAAAATTATATGTCATATGGGCGCTTTTGTTTTTTAATATGGCTTTTTTATGGAAACAAGAGGGTGAGATATCCACATGTGTAGCTCAGAAGAGTTTTCTCCCCAATTCTTATGCTGTAAAGTGGCAGAGGACAAACCATCCTTACAGTGGAGACGGATAATTAACACCCATGCTAAGCTTGGTTCAGGGAATGAGTGTGTGGAGTAGGGATGCTATGTTTATTTTGTTTTATGTGCTGGATCCGCTGGTGCTGTTATACATGTGTTTAACGCTAAATTTATCACTCTTCAAGGTTAGCCATGCTTCTGGGCAGAAATAATGTTACAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35327
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005562 | Essential Splice Site | 162 | 477 | 5 | 15 |
ENSDART00000009237 | Essential Splice Site | 128 | 438 | 4 | 14 |
ENSDART00000031408 | Essential Splice Site | 162 | 610 | 5 | 14 |
ENSDART00000121527 | Essential Splice Site | 162 | 597 | 5 | 15 |
ENSDART00000122972 | Essential Splice Site | 128 | 235 | 4 | 6 |
ENSDART00000123318 | Essential Splice Site | 128 | 426 | 4 | 13 |
ENSDART00000125046 | Essential Splice Site | 162 | 268 | 5 | 7 |
ENSDART00000128703 | None | None | 181 | None | 5 |
ENSDART00000133854 | Essential Splice Site | 11 | 118 | 2 | 4 |
The following transcripts of ENSDARG00000004415 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 32691226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30889223 |
GRCz11 | 12 | 31004125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTGTTCTTCTTCCCACCCCCTTCCCTCTCTTTTTCTGTTTCTTGCTA[G/A]TCTAATAAGGTCCCCGTGGTACAGCACCCTCACCATGTGCACCCGCTCAC
Long Flanking Sequence:
TAGGTAATTGAAAATGGGGCCTGTGCCACTTAAGAACACAAAGAGCAGATTACATAGCTAAAACCAATTTGACCAAAATGCAGAAATGGATTTTCTCTCTTCCCTCCCACCCCTCCTCTCTTATCTTTTATAATGCAAACCCTTTCCAAAAGCAGACCCTGAAGGAAGAGGAAGGGGTGCGAGAACGAGACATGGGTAACCCAGAGAAAAAGGAGGGAGTGTGCTTAGATTGACTGTCATTTGGTTCATTAGGTGGTTTCTGTGGTTGCAAACGTGAAACACAATGAAATCAAGCACTGTGCGGATCCAATGACTGTTTGAATCAATGTAAACTGTTTTTAATTACAAACCACATTGTTCTGAGAATCGGCCTGTGGTTTGTGATGAATGCATAGTTGAAATAGAGGCGCCGGTGTTGCCCCAACCCAAACATATATTAACAGCCTCTTCTTCTTGTTCTTCTTCCCACCCCCTTCCCTCTCTTTTTCTGTTTCTTGCTA[G/A]TCTAATAAGGTCCCCGTGGTACAGCACCCTCACCATGTGCACCCGCTCACACCTCTGATCACCTACAGCAATGAGCACTTCACGCCTGGGAACCCCCCTCCACATCTACAGGCAGACGTGGACCCCAAAACAGGTACATATGCATGCACGTCTTCCTTTACATTCATGAATTTCAAAACAGGCAGGACGAAACCCAAGGCTAACCTTCAGGCCTGGCTAACTAACGGCTACAGTGTGTGATCTCGCTTGTAGCACTGCATTCATAGCTACCTGGCAAGATGCACTGAAGCGTTTCAGAGTCGTCTTGGCTCAGGGCCAAGGTTGCGCCCCTCCTTTTGTGTGCATGTTGAGATGGAGCTGTTGACCTGGGTCGGTTAAGCCTGTGGAGCCACTTGACTCATGGGAGATGTAGACAGGGACTTCTGTTATTTAACTGCCAGATACCAAAACCGCTGTTTGTTTTTATTCTAAAGCGTGATAACATTAGCAATTTCAGCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa103
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005562 | Nonsense | 376 | 477 | 10 | 15 |
ENSDART00000009237 | Nonsense | 337 | 438 | 9 | 14 |
ENSDART00000031408 | Nonsense | 376 | 610 | 10 | 14 |
ENSDART00000121527 | Nonsense | 376 | 597 | 10 | 15 |
ENSDART00000122972 | None | None | 235 | None | 6 |
ENSDART00000123318 | Nonsense | 337 | 426 | 9 | 13 |
ENSDART00000125046 | None | None | 268 | None | 7 |
ENSDART00000128703 | None | None | 181 | None | 5 |
ENSDART00000133854 | None | None | 118 | None | 4 |
The following transcripts of ENSDARG00000004415 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 32676376)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30874373 |
GRCz11 | 12 | 30989275 |
KASP Assay ID:
554-0075.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTGATGGATGTCTGTGTGTTTCTCTGTGTACAGTGGCACGCTCTGTCA[C/T]GAGAGGAGCAGGCCAAATACTACGAATTAGCCAGGAAAGAACGACAGCTT
Long Flanking Sequence:
CCTCCTTCTCATTTGCAGGAAACATCAGGATGCGAAAAAGGAGGAGGAAAAGAAGAAGCAGCCGCACATAAAGAAACCTCTGAACGCGTTCATGCTTTATATGAAGGAAATGAGAGCCAAAGTGGTGGCGGAGTGCACACTGAAAGAGAGCGCAGCTATCAACCAGATCCTAGGCCGAAGGGTGAGTGTCACACACTACTGGGCCAAACTACTGTAGCAGAAGGCCATCTCATACTTCTAAGACCACAGATTGCTGTATACCCCAGATCAAGAGGACATTTTTTAACTCATGGTGGTTGGAAACCCCAAGTTCACTCAACAATTAAAATTTACTCACTATTTACTCTCCCTCAAGTGGTTCCAAACATTTATATATTTCTTTTTCTCTCAGACTTTTCATTTTTGAGTGAACTATCCCTTTAAATATCAATATCTCTGTAATGGCTGTGGATTTGATGGATGTCTGTGTGTTTCTCTGTGTACAGTGGCACGCTCTGTCA[C/T]GAGAGGAGCAGGCCAAATACTACGAATTAGCCAGGAAAGAACGACAGCTTCACATGCAGCTGTACCCCGGCTGGTCGGCACGAGACAACTATGTAAGTTTTTAAGTTTTCAACATGTAACAATCTGGATTCCTTCCCTAGGGGGTCACATTTAAGCCCATGCAGATGCGTATACAAATCATGACAAACAGCCTTAGGAGGAAGCTAAAGCACATGTGGCTGGCTGTTCTTGACCGGTTTAGCTGCTGGAAGACAAAATTTTCCGTCAGTTGACTGTACATGCGCTTTCCCTCAGATCTGTGCTGTGCGATTTTCCTCTGCTTTCATTAGTATTCCACTGGTTCACCTAAAAAGAGAAAGGCGAGCTGAGATCAGAGTAATTAAATAACCACAGGGCCTAAACGCCTCGTAGCTTTGATGAAAGAGGACATCGCTCTCCGCCGGCAGAAATGTGGAATGAGCGCACCGTTTACTGTTTCGCTGGAGTTTTGCGCCTGACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22132
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005562 | Nonsense | 400 | 477 | 10 | 15 |
ENSDART00000009237 | Nonsense | 361 | 438 | 9 | 14 |
ENSDART00000031408 | Nonsense | 400 | 610 | 10 | 14 |
ENSDART00000121527 | Nonsense | 400 | 597 | 10 | 15 |
ENSDART00000122972 | None | None | 235 | None | 6 |
ENSDART00000123318 | Nonsense | 361 | 426 | 9 | 13 |
ENSDART00000125046 | None | None | 268 | None | 7 |
ENSDART00000128703 | None | None | 181 | None | 5 |
ENSDART00000133854 | None | None | 118 | None | 4 |
The following transcripts of ENSDARG00000004415 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 32676302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30874299 |
GRCz11 | 12 | 30989201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATTAGCCAGGAAAGAACGACAGCTTCACATGCAGCTGTACCCCGGCTG[G/A]TCGGCACGAGACAACTATGTAAGTTTTTAAGTTTTCAACATGTAACAATC
Long Flanking Sequence:
AACCTCTGAACGCGTTCATGCTTTATATGAAGGAAATGAGAGCCAAAGTGGTGGCGGAGTGCACACTGAAAGAGAGCGCAGCTATCAACCAGATCCTAGGCCGAAGGGTGAGTGTCACACACTACTGGGCCAAACTACTGTAGCAGAAGGCCATCTCATACTTCTAAGACCACAGATTGCTGTATACCCCAGATCAAGAGGACATTTTTTAACTCATGGTGGTTGGAAACCCCAAGTTCACTCAACAATTAAAATTTACTCACTATTTACTCTCCCTCAAGTGGTTCCAAACATTTATATATTTCTTTTTCTCTCAGACTTTTCATTTTTGAGTGAACTATCCCTTTAAATATCAATATCTCTGTAATGGCTGTGGATTTGATGGATGTCTGTGTGTTTCTCTGTGTACAGTGGCACGCTCTGTCACGAGAGGAGCAGGCCAAATACTACGAATTAGCCAGGAAAGAACGACAGCTTCACATGCAGCTGTACCCCGGCTG[G/A]TCGGCACGAGACAACTATGTAAGTTTTTAAGTTTTCAACATGTAACAATCTGGATTCCTTCCCTAGGGGGTCACATTTAAGCCCATGCAGATGCGTATACAAATCATGACAAACAGCCTTAGGAGGAAGCTAAAGCACATGTGGCTGGCTGTTCTTGACCGGTTTAGCTGCTGGAAGACAAAATTTTCCGTCAGTTGACTGTACATGCGCTTTCCCTCAGATCTGTGCTGTGCGATTTTCCTCTGCTTTCATTAGTATTCCACTGGTTCACCTAAAAAGAGAAAGGCGAGCTGAGATCAGAGTAATTAAATAACCACAGGGCCTAAACGCCTCGTAGCTTTGATGAAAGAGGACATCGCTCTCCGCCGGCAGAAATGTGGAATGAGCGCACCGTTTACTGTTTCGCTGGAGTTTTGCGCCTGACAAACGGCCCCACCGCCCAGCCTGTCAACTCTCCTTGGAGTCTGACCACGTGTCTTGACTCTCCTAGTCAAAGTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2624
Status:
F2 line generated
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005562 | Essential Splice Site | 422 | 477 | 11 | 15 |
ENSDART00000009237 | Essential Splice Site | 383 | 438 | 10 | 14 |
ENSDART00000031408 | Essential Splice Site | 422 | 610 | 11 | 14 |
ENSDART00000121527 | Essential Splice Site | 422 | 597 | 11 | 15 |
ENSDART00000122972 | None | None | 235 | None | 6 |
ENSDART00000123318 | Essential Splice Site | 383 | 426 | 10 | 13 |
ENSDART00000125046 | None | None | 268 | None | 7 |
ENSDART00000128703 | None | None | 181 | None | 5 |
ENSDART00000133854 | None | None | 118 | None | 4 |
The following transcripts of ENSDARG00000004415 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 32675341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30873338 |
GRCz11 | 12 | 30988240 |
KASP Assay ID:
554-2443.1 (used for ordering genotyping assays)
KASP Sequence:
GGGGAAAAAGAAGAAGAGAAAAAGGGAAAAGCAGGCAGGAGAGGGCAATG[G/A]TAAGTGTGCTGCAATTATCTCTCATATTAAAGCAGACCCATCATCTGTCA
Long Flanking Sequence:
GAGTCTGACCACGTGTCTTGACTCTCCTAGTCAAAGTTCCTCAAACGGAGCAAGCTGATCGCTCTGCTCGGACTTGACCTCGGCCTCGGCGCAATCAGCATCGTTTTCGAGAAAGGACTAACGCAACAGAAGTTCTCCTTCTCCGCTCTCCCCCCTCCAGTAAACCGAGCTGTTCAAAGAAACCTCAAGAGCTTCCAATCGTTTCACAAAGAAAGGAAAACTAAGCAGCGAGACAACAAGGAATAAACAAAAGAAGAGAAATAGGACGAAGGGAAAGATAGGGAAAGTTCTGTTCTGTCCTGCAGTGGCAGCTCGAACCTTCAGGCTGTTGCATGAATAAATAAATCAGTAAAAACATTGGGCTCTCTTGTTCATTTCATGTCTTGGTCTTTTTTGCAGTATAATAACTAATGTTCCTGTCTATTTCTCTTTTCTGGCGGGTAACTATCAGGGGAAAAAGAAGAAGAGAAAAAGGGAAAAGCAGGCAGGAGAGGGCAATG[G/A]TAAGTGTGCTGCAATTATCTCTCATATTAAAGCAGACCCATCATCTGTCACAAGTGTGACATCTCAAAGATGAAAGTCCAGCCTTTTTTTTTTAATCTCTTTTTTGTGCCTGCCTCATTTTGTATATAGCTATGCTACCCAATGCAATATTTACACGATAGACTGCTTGTTATCCCCTTCCCCTCCCCTTGCCCCATGTCGAGCATTAATAACATTGAATATGCATGACCCCCCACCTCCTCCCCTCCCACCAGCTGGCCCCCCCACCCCTTTGCCCTGCCCCCCTCCAGCATTTATTGTACTGTGATATGTATGTTTTGAGAGTGTGAGCGTTAATCACACTTGTGACTGATTGCCAGCCTCTGAATGTGCCGCCCATGCTTGTGTCACTGTGCTTATGTGGTCGTAACTTTGGGCCGTGCCTGCTGCATGCTCTGATACATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTATATAGTGATAATATGTATAA
Associated Phenotype:
Not determined