Busch Lab

ZMP

NP_001154179.1

Ensembl ID:
ENSDARG00000089572
Description:
TCF3 fusion partner homolog [Source:RefSeq peptide;Acc:NP_001154179]
Human Orthologue:
TFPT
Human Description:
TCF3 (E2A) fusion partner (in childhood Leukemia) [Source:HGNC Symbol;Acc:13630]
Mouse Orthologue:
Tfpt
Mouse Description:
TCF3 (E2A) fusion partner Gene [Source:MGI Symbol;Acc:MGI:1916964]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa17486 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa17486
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
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Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122861 Essential Splice Site 162 186 4 5
ENSDART00000126425 Essential Splice Site 170 194 5 6
Genomic Location (Zv9):
Chromosome 16 (position 5482599)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 4709152
GRCz11 16 4538441
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGAGYAAAGAGAAAGAGACACCGGCTCCARAARGACAGAGACACGCAG[G/A]TACATAAATAAAGACTATTAAAGATTTTACWGCTCCTGAACTCTCCAGGG
Long Flanking Sequence:
ATCATCACTGCACCAAAACAGAGAATTATAACATTATTTTTAGACCATTTTTTGTCAGCCAAATGTAAAAAACGTGAGATGTTTAAAAGTTCTGGCATTGTATTGATGATGATGCATATATATATATATATATATGCATATATGCATCATCATCACAAACTCTATCTAGAAGTGAAGTTATGGTATAAACCTTTCATGTACACACAGACATCACCTATATGTTGTAAATTTGCAGGTTGACTGTGTCTGTATATAATAACTTATATTTAATTGCAATCATGTAATGTGAGTCTTTTGTAAAGCTGCTTTAAAACAGTAATTATTGTAAAGAGCGCTACACAAATAAACCCGAGTTGAATGTGTGTGTCCAGGATGAAGGGAAGGCTGTAGAGTCAGCTCTCGGTGGAGATGAAGACGTCTCTTCTCCAACATTTCCACCTCAGTCCACTGGAGGAGCAAAGAGAAAGAGACACCGGCTCCAAAAGGACAGAGACACGCAG[G/A]TACATAAATAAAGACTATTAAAGATTTTACTGCTCCTGAACTCTCCAGGGCTGCATTGATTTGGTTAAAAACACAGTGCGGTTGGTAAATATTAAAGGGACAGTTCACCCAAAAATACCATTTACTCATTTATTAAAGGGCACCTAGGTTACCCCTGTTTCCAGATTTAATGTAAGTCTTTTGTGTCTACAGTATGTGTCTGTAAAGTTTCAGCTCAAAACACCAATCAGATTATTTATTATAGCTGTCTGAAGTTTCTGTTTTATAGCTCGAAACAGCCTGTTGCTCTTTTTGTACTGCGCCTTTAAGGCTAGTCCTCCCCGCCCACTATTCCCGCGTGCCTGTCATGCATTAATCTCCACCCTCGGCTGCCTCAGACAACAGACAGACATGAAGGAAGCAGATCTCACGTAATGTTTGTGAGACATACTACAGTAAGAGCTTGATCAATTAGTATTTGTTGTGGAGTTGCATCGATGAGTCACACACAATGTAGTTAT
Associated Phenotype:
Not determined