Busch Lab

ZMP

tle2

Ensembl ID:
ENSDARG00000042484
ZFIN ID:
ZDB-GENE-030131-2826
Description:
si:ch211-81i17.1 [Source:RefSeq peptide;Acc:NP_001124076]
Human Orthologues:
AC010547.1, AES, TLE2, TLE6
Human Descriptions:
amino-terminal enhancer of split [Source:HGNC Symbol;Acc:307]
transducin-like enhancer of split 2 (E(sp1) homolog, Drosophila) [Source:HGNC Symbol;Acc:11838]
transducin-like enhancer of split 6 (E(sp1) homolog, Drosophila) [Source:HGNC Symbol;Acc:30788]
Mouse Orthologues:
Aes, Tle2, Tle6
Mouse Descriptions:
amino-terminal enhancer of split Gene [Source:MGI Symbol;Acc:MGI:95806]
transducin-like enhancer of split 2, homolog of Drosophila E(spl) Gene [Source:MGI Symbol;Acc:MGI:10
transducin-like enhancer of split 6, homolog of Drosophila E(spl) Gene [Source:MGI Symbol;Acc:MGI:21

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa9041 Nonsense Mutation detected in F1 DNA Not yet available
sa12775 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa9041
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105553 Nonsense 366 811 12 20
ENSDART00000133939 Nonsense 366 810 12 20
Genomic Location (Zv9):
Chromosome 22 (position 21981755)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 21635003
GRCz11 22 21659981
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGWCCAGCACTCCAGGGATGAAGCCTGGAACGCCCATGTCCCAGGAGT[C/A]GTCCACTCCAGGCCCCAGCGTTCCTCCACAGTTTCGTCCTGTTCCTGGGA
Long Flanking Sequence:
AAACAAACTCTCTTTTATATCAAAGCTTGTTCCTCGAATAAAATTGTTAGAATTGTAAAACTGGCACGCCAGAAATTTGAACAGTCCTAAATGGCAAAGATATGCAGCAATTTTACAAAAATTAGCTTGAGTTCGCCTACAATTCTTTGTGAAATTTCAAAATCCTGGATGGTCTATAACATCAAACAAGTTTTCCCTCCCCCAAACTGTAGATTCTTGCAATGTCTTTCATTTACCAAAGTGTCTTTCTCCAGCAAAAAACAAACTCTCTTCTATATCAAAGCTTGTTCCTCGTCTTGCTTTTGCTGTCAGTTTTCTAAAACTGCAAAGACTGACAGTTCTCACTTGAGTTTCACTACCTCTGCTCTTTTTTTTTTTGAGCCCCATTGGCTATGTATGTTTCTTGAATAATTAATGTGTGCAAATGCGTTCCCTAACCTTGCAGAGAGAGAAGTCCAGCACTCCAGGGATGAAGCCTGGAACGCCCATGTCCCAGGAGT[C/A]GTCCACTCCAGGCCCCAGCGTTCCTCCACAGTTTCGTCCTGTTCCTGGGAAACCAGGGGTTGACCCTCTTGGTAAGATCTTGTTAAGCTGATAGTCTTTGAGTGAACGTAGAGAGGGTTTAGTTCAACCTGGTTTGAAAGTCTTTATTCAGGGTTGACAGCTAGTCAGCCAGCAGAGGGCAGTAGTGGTCTTCCTCTTTCAGACAGGATGTCTTGTTTTATTTTAAATGTATCATGGTTCTGAGCCCGTGTCCTTGGAGGCTGTGTAATTGTTTTAGCATTCTTGGGAATGATATTAATGGGTCAATGACATGACACTCATCTCTTTCTGACAGTATCTATTCATTTATTCCAAAGTGCAATTCATGCATACAATGACTTGATTACGCCTCTTCTGTTATGGGCATGTTTTTAATATCTGAATTCTTTAGAAAGACTTGGTTCTTTAATATAAATCTAAATCAATATAAATCTAAATTAATATAAATTTTTAATCTAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12775
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
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105553 Essential Splice Site 390 811 12 20
ENSDART00000133939 Essential Splice Site 390 810 12 20
Genomic Location (Zv9):
Chromosome 22 (position 21981828)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 21635076
GRCz11 22 21660054
KASP Assay ID:
2261-6805.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCCACAGTTTCGTCCTGTTCCTGGGAAACCAGGGGTTGACCCTCTTGG[T/C]AAGMTCTTGTTAAGCTGATAGTCTTTGAGTGAAYGTAGAGAGGGTTTAKT
Long Flanking Sequence:
AATTTGAACAGTCCTAAATGGCAAAGATATGCAGCAATTTTACAAAAATTAGCTTGAGTTCGCCTACAATTCTTTGTGAAATTTCAAAATCCTGGATGGTCTATAACATCAAACAAGTTTTCCCTCCCCCAAACTGTAGATTCTTGCAATGTCTTTCATTTACCAAAGTGTCTTTCTCCAGCAAAAAACAAACTCTCTTCTATATCAAAGCTTGTTCCTCGTCTTGCTTTTGCTGTCAGTTTTCTAAAACTGCAAAGACTGACAGTTCTCACTTGAGTTTCACTACCTCTGCTCTTTTTTTTTTTGAGCCCCATTGGCTATGTATGTTTCTTGAATAATTAATGTGTGCAAATGCGTTCCCTAACCTTGCAGAGAGAGAAGTCCAGCACTCCAGGGATGAAGCCTGGAACGCCCATGTCCCAGGAGTCGTCCACTCCAGGCCCCAGCGTTCCTCCACAGTTTCGTCCTGTTCCTGGGAAACCAGGGGTTGACCCTCTTGG[T/C]AAGATCTTGTTAAGCTGATAGTCTTTGAGTGAACGTAGAGAGGGTTTAGTTCAACCTGGTTTGAAAGTCTTTATTCAGGGTTGACAGCTAGTCAGCCAGCAGAGGGCAGTAGTGGTCTTCCTCTTTCAGACAGGATGTCTTGTTTTATTTTAAATGTATCATGGTTCTGAGCCCGTGTCCTTGGAGGCTGTGTAATTGTTTTAGCATTCTTGGGAATGATATTAATGGGTCAATGACATGACACTCATCTCTTTCTGACAGTATCTATTCATTTATTCCAAAGTGCAATTCATGCATACAATGACTTGATTACGCCTCTTCTGTTATGGGCATGTTTTTAATATCTGAATTCTTTAGAAAGACTTGGTTCTTTAATATAAATCTAAATCAATATAAATCTAAATTAATATAAATTTTTAATCTAAAAATCTGTTGTCATTTATGTACCCTTCACTTGTTCAAAACCTGTTTGAGTTTCTTTCTTCTGTTTATCACAAAAC
Associated Phenotype:
Not determined