ZMP
tlx1
Ensembl ID:
ZFIN ID:
Description:
T-cell leukemia homeobox protein 1 [Source:RefSeq peptide;Acc:NP_739571]
Human Orthologues:
TLX1, TLX2, TLX3
Human Descriptions:
T-cell leukemia homeobox 1 [Source:HGNC Symbol;Acc:5056]
T-cell leukemia homeobox 2 [Source:HGNC Symbol;Acc:5057]
T-cell leukemia homeobox 3 [Source:HGNC Symbol;Acc:13532]
T-cell leukemia homeobox 2 [Source:HGNC Symbol;Acc:5057]
T-cell leukemia homeobox 3 [Source:HGNC Symbol;Acc:13532]
Mouse Orthologues:
Tlx1, Tlx2, Tlx3
Mouse Descriptions:
T-cell leukemia, homeobox 1 Gene [Source:MGI Symbol;Acc:MGI:98769]
T-cell leukemia, homeobox 2 Gene [Source:MGI Symbol;Acc:MGI:1350935]
T-cell leukemia, homeobox 3 Gene [Source:MGI Symbol;Acc:MGI:1351209]
T-cell leukemia, homeobox 2 Gene [Source:MGI Symbol;Acc:MGI:1350935]
T-cell leukemia, homeobox 3 Gene [Source:MGI Symbol;Acc:MGI:1351209]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11549 | Nonsense | Available for shipment | Available now |
sa22315 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11549
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 |
---|---|---|---|---|---|
ENSDART00000006393 | Nonsense | 200 | 301 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 28494207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 28140155 |
GRCz11 | 13 | 28270605 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCGCCTTCAGATATGTGAGCTGGAGAAACGCTTTCACCGTCAGAAGTA[T/A]CTGGCGTCAGCCGAGAGAGCAGCCTTAGCGAAAGCACTTAAAATGACTGA
Long Flanking Sequence:
ACAGTTGTTACTTTAATGTGTCATTGATTTGACAGCAAAAATAACTTTCATTTATGTGATCTAGTTGATTCAAGGCTGAATATGAAGTGTTTAATGTCTAACATTTATTTAAATATTTTATTTCATTCATTATTTTAACATTTAACACGTTACTAGGAAATATTTTGAAATGAGATAGCCTACTCATGTCTATTTGCTTGCTTGGCTGAACTAATTTAATATATTTTGTGATTGTTGCATGTTTTAAAAGGACCAATGTCAACCTTCTTTTCTAAAAGCCGCATTTGCCTTCCACTGCTTGGCTTTTGTCGTTTTGCTGATTTCTTCCGCTTGCTTTTCACTCTGTCTCTCAATCCAGTGGCCCTCTCACCGTTCACTGTAACACGCCGTATAGGTCACCCGTACCAGAACCGAACACCTCCGAAGAAGAAGAAGCCCCGGACGTCGTTCACGCGCCTTCAGATATGTGAGCTGGAGAAACGCTTTCACCGTCAGAAGTA[T/A]CTGGCGTCAGCCGAGAGAGCAGCCTTAGCGAAAGCACTTAAAATGACTGATGCGCAGGTCAAAACATGGTTCCAGAACAGAAGAACGAAATGGAGGTGAGCTTTTGCGATCTAATCAAGGCTTTACACTCACACGTAATGCATTCTTTTTCGTCTCAGCACTAAACCCAGCAGAGTATTTTGTTTTTAAATAAACCGTGAGGTCAGCTGGGTCAGTTTCATAATGCATTCCATAGGTTTGAAAGGTCTGTTCACTCAATATAGATGCAATCAATAGCTATGTCAGTGGCTAAATGTACTATTTTTATTAAACATATTCCAGGTTATAGTGAAACCAATATATAACCTAAAAATTTTAGTCTTAGTTGCGAAGGTTAATTAACTGATGTTCAATATAGTGATTTAAAAAAGGTTTATGATTAGATCATTTTTATGCAAATTAGTAGAGATATTTAGTACAAATTAATAATTGACATGTGAAATATAAATTATGATGATTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22315
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006393 | Essential Splice Site | 232 | 301 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 28494111)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 28140059 |
GRCz11 | 13 | 28270509 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGATGCGCAGGTCAAAACATGGTTCCAGAACAGAAGAACGAAATGGAG[G/A]TGAGCTTTTGCGATCTAATCAAGGCTTTACACTCACACGTAATGCATTCT
Long Flanking Sequence:
TCTAACATTTATTTAAATATTTTATTTCATTCATTATTTTAACATTTAACACGTTACTAGGAAATATTTTGAAATGAGATAGCCTACTCATGTCTATTTGCTTGCTTGGCTGAACTAATTTAATATATTTTGTGATTGTTGCATGTTTTAAAAGGACCAATGTCAACCTTCTTTTCTAAAAGCCGCATTTGCCTTCCACTGCTTGGCTTTTGTCGTTTTGCTGATTTCTTCCGCTTGCTTTTCACTCTGTCTCTCAATCCAGTGGCCCTCTCACCGTTCACTGTAACACGCCGTATAGGTCACCCGTACCAGAACCGAACACCTCCGAAGAAGAAGAAGCCCCGGACGTCGTTCACGCGCCTTCAGATATGTGAGCTGGAGAAACGCTTTCACCGTCAGAAGTATCTGGCGTCAGCCGAGAGAGCAGCCTTAGCGAAAGCACTTAAAATGACTGATGCGCAGGTCAAAACATGGTTCCAGAACAGAAGAACGAAATGGAG[G/A]TGAGCTTTTGCGATCTAATCAAGGCTTTACACTCACACGTAATGCATTCTTTTTCGTCTCAGCACTAAACCCAGCAGAGTATTTTGTTTTTAAATAAACCGTGAGGTCAGCTGGGTCAGTTTCATAATGCATTCCATAGGTTTGAAAGGTCTGTTCACTCAATATAGATGCAATCAATAGCTATGTCAGTGGCTAAATGTACTATTTTTATTAAACATATTCCAGGTTATAGTGAAACCAATATATAACCTAAAAATTTTAGTCTTAGTTGCGAAGGTTAATTAACTGATGTTCAATATAGTGATTTAAAAAAGGTTTATGATTAGATCATTTTTATGCAAATTAGTAGAGATATTTAGTACAAATTAATAATTGACATGTGAAATATAAATTATGATGATTCGACTAAATGCGATATTTTCTATGAGAACTTCCAAATTATAGGATATTTACACACACACACACACACACACACACACACACACACACACACACACACA
Associated Phenotype:
Not determined