Busch Lab

ZMP

eef2a.1

Ensembl ID:
ENSDARG00000042094
ZFIN ID:
ZDB-GENE-050522-500
Description:
eukaryotic translation elongation factor 2a, tandem duplicate 1 [Source:RefSeq peptide;Acc:NP_00103
Human Orthologue:
EEF2
Human Description:
eukaryotic translation elongation factor 2 [Source:HGNC Symbol;Acc:3214]
Mouse Orthologue:
Eef2
Mouse Description:
eukaryotic translation elongation factor 2 Gene [Source:MGI Symbol;Acc:MGI:95288]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa29761 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa29762 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa29761
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024751 Essential Splice Site 204 854 None 13
ENSDART00000110200 Essential Splice Site None 160 None 15
ENSDART00000143641 Essential Splice Site 204 854 None 13
Genomic Location (Zv9):
Chromosome 22 (position 20457353)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 20114046
GRCz11 22 20139024
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTCCACCTATGCTGAGGATGAGAAAGGCCCTATGGGCAATGTCATGG[T/C]GAGTGCCTCAAGGCTCCGTCATGGGTCCATTAATGCTTTCTGTTTTATCT
Long Flanking Sequence:
GAGTGCAAAGATGGCTCCGGCTTCCTCCTCAACCTGATTGACTCCCCTGGGCATGTTGACTTTTCTTCAGAAGTTACAGCTGCACTGCGTATCACAGATGGAGCATTGCTGGTGGTGGATTGTGTGTCTGGTATGTGCAGAAATAGTTTTTTTGTTTGTTTTTCCCAAATGACCGTTTTATTAATCAAAGACTTCCTTGGTATAATTTGATTTGCATGCTTTACTTTGATTCTGTAACTAAATCTATAGTTTTTTGGGCCGCTTATAAAAATGTCATTGTTTGGCAGGTGTGTGCTTACAGACAGAGACTGTGCTCAGACAGGCCATTGGTGAGAGGATTAAACCAGTTTTGATGATTAACAAAATGGATCGAGCTTTGCTCGAGCTACAGTTGGTCCCTGAAGAGCTGTACCAGATCTTTCAGCGCATTGTTGAGAAAGTCAACGTGACCATCTCCACCTATGCTGAGGATGAGAAAGGCCCTATGGGCAATGTCATGG[T/C]GAGTGCCTCAAGGCTCCGTCATGGGTCCATTAATGCTTTCTGTTTTATCTCTGGGCTTATTTCTAATATTCATTGTGAATGTTTTTAACATCCTGATCTTAGATTGATCCTGTCATTGGTAATCTTGCCTTTGGATCTGGACTGCATGGATGGGCCTTCACTTTGAAGCAGTTTGCTGAGCTCTATGTGAAAAAGTTCGCTGGTAAAGCTCAGCTGGGACCGGAAGAGTACATCAAGAAGGTGGAGGACATGATAAAGAGACTTTGGGGCGACAGGTGAGAGGATGTTCCAACACAACTGAATGAATGTAATGTTGCATTTCTGTACGTGACATTTTATGTCCATTTGTTTGCAGCTACTTTGACTCTACTACTGGCAAGTTCAGCGAGTCTGCGACATCGCCAGATGGCAAGAAGCTTCCCAGGACTTTTGTTCACTTAGTCCTGGACCCCATCTTCAAAGTGAGGAAACTAGCAACAATTCTGTTTTTAATGCAAGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29762
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000024751 Nonsense 637 854 10 13
ENSDART00000110200 None None 160 12 15
ENSDART00000143641 Nonsense 637 854 10 13
Genomic Location (Zv9):
Chromosome 22 (position 20459413)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 20116106
GRCz11 22 20141084
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCCAGCCAGGAGATGAATGCCCGTGCCCAATACCTTGCTGAAAACTA[T/A]AAGTGGGAAGTGACTGAAGCTCGTAAGATCTGGTGCTTTGGCCCTGAGGG
Long Flanking Sequence:
TGAAGTTTAGTGTCAGTCCTGTGGTGAGAGTGTCCGTGGAGGTCATGGACCCTGCTGACCTTCCTAAACTGGTGGAGGGATTGAAGCATCTGGCCAAGTCAGATCCCATGTTGCAATGCATCATTGAGGATACTGGTGAACATATCATTGCTGGAGCTGGTGAGCTTCACTTGGAGATTTGCCTTAAGGATCTTGAAGAGGACCATGCCTGCATTCCCCTCAAGGTACCAATAGCTAGTCCAATCGGCAACACATTATACCAACTATGATTGTTCTCTAACATGCTGTTCTTTACAGAAATCAGATCCATTTGCTTCCTACAGAGAGACGGTCAGTGATGGCTCCAAACAATTGTGCCTTGCCAAGACGCCAAACAAGCACAGTCGTCTCTTCATGAAGGCCTGTCCTCTGGCTGATGGTCTTGCAGAAGATATTGATAAGGGTCGGGTCACTGCCAGCCAGGAGATGAATGCCCGTGCCCAATACCTTGCTGAAAACTA[T/A]AAGTGGGAAGTGACTGAAGCTCGTAAGATCTGGTGCTTTGGCCCTGAGGGAACTGGACCCAACATCTTGGTAGATTTGACCAAGAGAGTGCAATACTTGAATGAGATTAAGGACAGTGTGATTGCTGGATTTCAGTGGGCCACTAGAGAGGTATGATAAAAGCACAACATTTATTCATTGTATTATAACTCTAATGTAAGACAGTTTTACCTTTCTTTATAATCTAGAGTGTCCTTTGGATTCTCTAAGGTGAACGCCACCTTGATAAATTTTGCATCTTTACACCTTTCTGGGATTTTCTAAATTGCAAAGACTAATTTGGTTATGTTCAATTGGATTAAGATGTCCCTCTATAATCAACTAGACACCTTTTGCTTTAGTTTGAGTCACTGCTCTGTTTTATTTAATCGTTTTGTGCTTTCTAGGGAGTCTTGTGCGCAGAGAACATGCGTGGCATTCGCTTTGACATTCATGATGCAACTTTGACTTCTACTGCCATT
Associated Phenotype:
Not determined