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 |
---|---|---|---|
sa103 | Nonsense | Available for shipment | Available now |
sa22132 | Nonsense | Available for shipment | Available now |
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