Busch Lab

ZMP

tcf7l2

Ensembl ID:
ENSDARG00000004415
ZFIN ID:
ZDB-GENE-991110-8
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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