ZMP
eef2a.2
Ensembl ID:
ZFIN ID:
Description:
eukaryotic translation elongation factor 2a, tandem duplicate 2 [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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24152 | Essential Splice Site | Available for shipment | Available now |
sa32399 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24152
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036757 | Essential Splice Site | 203 | 853 | 3 | 12 |
ENSDART00000137624 | Essential Splice Site | 204 | 853 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 20469753)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20126446 |
GRCz11 | 22 | 20151424 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTCCACCTATGCTGAGGATGAGAAAGGCCCTATGGGCAACGTCATGG[T/G]GAGTGCCTCAAGGCTCCGTCATGGGTCCTTTAATGCTTTCTGTTTTATCT
Long Flanking Sequence:
GTGCAAAGATGGCTCCGGCTTCCTCCTCAACCTGATTGACTCCCCTGGGCATGTTGACTTCTCTTCAGAAGTTACAGCTGCACTGCGTATCACAGATGGAGCATTGCTGGTGGTGGATTGTGTGTCTGGTATGTGCAGAAATAGCAGTTTTGATTTTTAAATCACTGTTTTATTAATCAAAGACTTCCTTGGTATAATTTTGATAGTCATGCCTAATATATGAATTCTGTAACTTGAACTTGAGCTCTCTTGGAGGCTTATTAAAATGTCAAATTGCTGTTTAGCAGGTGTGTGCTTACAGACAGAGACTGTGCTCAGACAGGCCATTGGTGAGAGGATTAAACCAGTTTTGATGATTAACAAAATGGATCGAGCTTTGCTCGAGCTACAGTTGGTCCCTGAAGAGCTGTACCAGATCTTTCAGCGCATTGTTGAGAAAGTCAACGTGACCATCTCCACCTATGCTGAGGATGAGAAAGGCCCTATGGGCAACGTCATGG[T/G]GAGTGCCTCAAGGCTCCGTCATGGGTCCTTTAATGCTTTCTGTTTTATCTGTGGGCTTATTTCTAATATTCATTGTGAATGTTTTTAACATCCTGATCTTAGATTGATCCTGTCGTTGGTAATCTTGCCTTTGGATCTGGACTGCATGGATGGGCCTTCACTTTGAAGCAGTTTGCAGAGCTCTATGTGAAAAAGTTCGCTGGTAAAGCTCAGCTGAGACCTGAAGAGTACATCAAGAAGGTGGAGGACATGATGAAGAAACTTTGGGGCAACAGGTGAGAGGATGTTCCAACACAACTGAATGAATGTAATCTTGCATTTCTGTACGTGACATTTTATGTCCATTTGTTTGCAGCTACTTTGACTCTACTACTGGCAAGTTCAGTGAGTCTGCGACATCCCCAAATGGCAAGAAGCTTCCCAGGACTTTTGTTCAACTAGTCCTGGACCCCATCTTCAAAGTGAGAAAACTAGCAACAATTCTGTTTTTAATGCAAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32399
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036757 | Essential Splice Site | 747 | 853 | 10 | 12 |
ENSDART00000137624 | Essential Splice Site | 745 | 853 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 20472325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20129018 |
GRCz11 | 22 | 20153996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACAGCTGAACCAAGGCTTAGTGAGCCGGTATACCTGGTGGAGATGCAG[G/T]TATAAAAGTAGCATTAAAACTCCTGCTCATTGATCTTTTGGTATTTGATG
Long Flanking Sequence:
CCATTCAGCTAATTTCTGGATCTGGCAGAAGAAAACCTTGGCATAAATCAATGAATCAAATTAAACCTTTAACACTATGGGAGTTGTAAAATAAACTTCCAAAGGTGGAGTGTTCTTTAAGCTAGAGTGTCCTCTGGATTCTCTTGGGTAAAGGCCACCTTGATAGATTTGATAGACCTTTCTGGAATTTTCTAAATTGCAAAGATTGATTTGGCTTATGTTCAATTCTGATTGGATTAAGATGTCCCTCTATTATCAACTAGACACATTTGCTTTAGTTTGAGTCACAGCTCTCTAAAGTGTTTTGTGCATTCCAGGGAATCTTGTGCGCAGAGAACATGCGTGGCATTCGCTTCGACATTCATGATGCAACTTTGACTTCTACTGCCATTCACCGTGGTCCAGGTCAAGTGATTACTGCAACCCGCCGAGTGCTTTATGGCTGTCAGCTCACAGCTGAACCAAGGCTTAGTGAGCCGGTATACCTGGTGGAGATGCAG[G/T]TATAAAAGTAGCATTAAAACTCCTGCTCATTGATCTTTTGGTATTTGATGCCAATCTCTAATTGTACCACACTTTTGATCTGCCTACAGTGCCCAGAGTCAGTTATTGGTATTATTCATGCTGTACTGGTCAAGAGGCGTGGAGTAGTGTTTTTAGAGTCCCAGGTTACGGGAACTCCTATTTATTTGCTCAAGGCTTACTTGCCTGTCAGTGAGTCATTTGGTGAGTGAAGCTGAAAAAAATCTTGGCTTGTCTTCTCCGGTTAATGATTCAAGTTACATAGTGTAAATGGTATCTCCTTTTCTTTGCAGGTTTTACAGCTGACCTTTGTGCCAACACATCTGGCCAAGCCTTCTCACAGTGTGTGTTTGATCATTGGCAGATCATGCCTGGAGACCCATTGAATACTACCTCCAAAACTGCTCATATTATGGCTGACATACGAAAGCGCAAGGGCTTGCCAGAAGCCAATCTAGCTTTACATCGCTTCTTGGACAAAT
Associated Phenotype:
Not determined