ZMP
tcf7l1a
Ensembl ID:
ZFIN ID:
Description:
Transcription factor 7-like 1-A [Source:UniProtKB/Swiss-Prot;Acc:Q9YHE8]
Human Orthologue:
TCF7L1
Human Description:
transcription factor 7-like 1 (T-cell specific, HMG-box) [Source:HGNC Symbol;Acc:11640]
Mouse Orthologue:
Tcf7l1
Mouse Description:
transcription factor 7-like 1 (T-cell specific, HMG box) Gene [Source:MGI Symbol;Acc:MGI:1202876]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44731 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa384 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44731
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 |
---|---|---|---|---|---|
ENSDART00000099262 | Essential Splice Site | 237 | 560 | 6 | 12 |
ENSDART00000140341 | Essential Splice Site | 108 | 431 | 3 | 9 |
The following transcripts of ENSDARG00000038159 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 43576951)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 42383446 |
GRCz11 | 10 | 42211826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGGGGCAGTCGGACAGATCCCTCACCCTCTTGGATGGTTGGTTCCTCA[G/A]TAAGTCTGAACTACCTTGAAAAACACCTCATTTTACACCCCAGTAGATGA
Long Flanking Sequence:
AACAAAATAATAACTTAGGATACAATCATCAACTACAGCGGGGGATCAGAACCAGAGAAAAATTCCCTCGTGAAATCTAACATTATATCACTCTTTTTGTTTTTAATTAGCATTAGAGGATTTTTCAAACTTTCCATTTGAGATGATCACTAGTGGGCGGGGCTTTCACCTTTTGATGACACGTACAAAGAGAGAATGTCAATCAAAGTGTTTCCGAAGACTCTTCAAGAGTGATCATAAAAATTAGACTGAATTAATTTTCACCATTATAGGCTGGCTATATTCACACATTGCTCCACACAACTCCCTTAAAAAGTGATTTTTGCTTAACAGGTCCTCTTTAAGAGGAAGCAATGTGGTTTTATAATCTAAATAAATAAATCGATTGTTTCTACAGGCATACCAAGGACCCCTCACCCCTCAGAGCTGTCCCCATATTACCCTCTCTCTCCTGGGGCAGTCGGACAGATCCCTCACCCTCTTGGATGGTTGGTTCCTCA[G/A]TAAGTCTGAACTACCTTGAAAAACACCTCATTTTACACCCCAGTAGATGACGGAATCAAATGTGGAGCTATTTTTAAAAGTTCTCGTAGCTAAAAGAGCATCTGCGTGTCCTTGATTTTTGCCTCAGCTGGTTTATTTGAGTGCTGTTCCTCCATCTTTATAGGCAAGGCCAGCATATGTACTCCATCCCTCCCGGAGGCTTCAGACACCCCTACCCTGCACTCGCCATGAACGCCTCCATGTCTAGGTATGTAACGGAGAGCTGGCTTCTCGTTTTTCTGCACGAATGTGATGATTTAAAGTTGAACTCGCATCTATAATTAGAGCTGAGATGCAGACAGTGCTAATCCTCCCTGAAGGGGAAGAGAAGAGGAAGCTGCTGATGTGTTTTCGCTCCATATTGGCGCCTTGGTACATTTCTCTTTCCACCCCGCGCAATGTTCCAGAGAGGAAACCTGCTTTTTCGGGTGCAGTACAATTTAGTTTATCTTGCTCCGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa384
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 |
---|---|---|---|---|---|
ENSDART00000099262 | Nonsense | 321 | 560 | 9 | 12 |
ENSDART00000140341 | Nonsense | 192 | 431 | 6 | 9 |
The following transcripts of ENSDARG00000038159 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 43567542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 42374037 |
GRCz11 | 10 | 42202417 |
KASP Assay ID:
554-0186.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTCCCTCTTTCTCTCTCTCCATGCAGAAAGCCCTCGGTGCCCGTGAAG[A/T]AAGAGGAAGAGAAAAAGCCTCACATCAAGAAGCCTCTTAATGCCTTCATG
Long Flanking Sequence:
ATGGATCCATGCTTTCATGGTGTAGATGCCAAATTCTGACCCGACTATCCAAAGAAATTGATTACCTGATTAGAAATTTGCGATAATTAACAGTTGGACAGGTGTACCTAATAAAGTGGCCGGTGAGTGTATACCGCAATATTTATTGCAGGGAAAAAAACATTGCAATGTCAGATTTTTCCAATATCGTGCAGCCTTATTATTAGTGTATTATTTATAATTGTTGATGTATTTTTATTGTTATAAACCTTTTTTGTTATTTATATGATTTATTTGTAAAGTGTATTATTATTGTACACCTGTTTTACCAGGTTTAATTGTTTAAATGGTTTATTCTTATTTATGTATAGTACGTTGAGTTACAGTTGTGTATGAAATGTGCGTTGGAAATAGTTTTGCCATGAAATATCCAGGGAAGCTGAAACCTAAAATCTCCAAACTTCTCTGAAAATCTCCCTCTTTCTCTCTCTCCATGCAGAAAGCCCTCGGTGCCCGTGAAG[A/T]AAGAGGAAGAGAAAAAGCCTCACATCAAGAAGCCTCTTAATGCCTTCATGCTCTACATGAAGGAAATGAGGGCCAAAGTAGTGGCTGAGTGTACCCTGAAAGAGAGCGCCGCCATCAACCAGATCCTGGGCAGAAGGGTGAGCGCTTACAGCTCCATTATCAAGGATGCATTAGTGTGTTTCTCTTCATCTGCTCTTAAAGGAACAGTTCGCGCCTTGTGGGTGAAAAAAGGCCATCATTTACTCTCTTTCTCAATCTTGTCATTGCAAACCTGTGTGAGGCACAAAAGGAGAAGGTGTTTTGAAGAGTTTTGCTGTGAAAAGTAACTATGCATTAGTGAATCTGTGTGTGCTGCTGATAATCCAGGGTTTTAGGTTATCAAAGGATAGGTTTACATGAGAATGATGTCGTCAAAAACAACGCTTTTGTTGTTATGCAATTTTCTACATTAGTACAAAAGTTCTGATGCAGTCATATGCATGCATTTATTTAATGTTTTA
Associated Phenotype:
Not determined