ZMP
zgc:110335
Ensembl ID:
ZFIN ID:
Description:
eukaryotic translation elongation factor 1 alpha 1 [Source:RefSeq peptide;Acc:NP_001017795]
Human Orthologue:
EEF1A1
Human Description:
eukaryotic translation elongation factor 1 alpha 1 [Source:HGNC Symbol;Acc:3189]
Mouse Orthologue:
Eef1a1
Mouse Description:
eukaryotic translation elongation factor 1 alpha 1 Gene [Source:MGI Symbol;Acc:MGI:1096881]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11028 | Nonsense | Available for shipment | Available now |
| sa18700 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11028
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075340 | Nonsense | 69 | 462 | 3 | 8 |
| ENSDART00000137863 | Nonsense | 69 | 462 | 4 | 9 |
| ENSDART00000075340 | Nonsense | 69 | 462 | 3 | 8 |
| ENSDART00000137863 | Nonsense | 69 | 462 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 30173588)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 30313400 |
| GRCz11 | 1 | 31117331 |
KASP Assay ID:
2259-0711.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCCTTTAAGTATGCTTGGGTCCTTGACAAACTGAAAGCTGAGAGAGAG[C/T]GAGGCATCACCATCGATATCTCCCTGTGGAAGTTTGAGACAAGCAAATAC
Long Flanking Sequence:
CTCGGTTAAACATCTCATCTAAAAAATTTTGTTCACTGCGCAGTATAGAGTTTCCATCAATATACTGGGACGTTAGGAACCAGACAGACCACAGGTTGAACACCCTTTGCTAGTTTTACTAACATAATTTCTGGCAGCAATCTAGCTTCCCATTCAGGTACTGATCGGGCCCAGCCCTGCTTTGCTTCAGTAGGTGACCATGTGAGAGCTCTATGCTTGCTGTTGGCTATTGTTGTTTACGTTTTGCAGCAAATAAATCTCAAATATTTCACATTTGGCGGATACTATTTAATAATGCTAGAATGCTCTTTCGCTAATTAAATTAGTAAACTGAAAATTACTTCTGCAAAATGCAATATAAAGTGTGACAGGTCAGCCTTTTAAGAAATGTGTTTATAGAGTTTTTTCTTTAACAAATATATTTTCTTCTCATTTTATAGATGGGAAAAGGCTCCTTTAAGTATGCTTGGGTCCTTGACAAACTGAAAGCTGAGAGAGAG[C/T]GAGGCATCACCATCGATATCTCCCTGTGGAAGTTTGAGACAAGCAAATACTACGTCACCATCATTGATGCACCAGGACACAGAGACTTCATTAAGAACATGATCACTGGCACCTCACAGGTTTTTATACTACCACAAACCAATGTCTTTCCCCTTACACTATTTTAATAATCTTATACATTTCATTCCTCTTGTTGATACAGGCAGACTGTGCTGTGTTGATTGTAGCGGCTGGTGTTGGTGAATTTGAGGCTGGTATCTCAAAGAACGGGCAAACACGTGAACATGCCTTGCTGGCGTACACTCTCGGTGTTAAACAATTGATCGTGGGCGTTAACAAGATGGACTCTACGGAGCCCAATTATAGCCAGAAGCGCTATGAGGAGATTGTGAAGGAAGTCAGCACTTATATCAAGAAAATTGGCTACAACCCTGATACTGTGGCATTTGTTCCCATCTCTGGATGGAATGGGGATAACATGCTGGAGGCCAGCCCAAACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18700
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075340 | Nonsense | 69 | 462 | 3 | 8 |
| ENSDART00000137863 | Nonsense | 69 | 462 | 4 | 9 |
| ENSDART00000075340 | Nonsense | 69 | 462 | 3 | 8 |
| ENSDART00000137863 | Nonsense | 69 | 462 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 30173588)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 30313400 |
| GRCz11 | 1 | 31117331 |
KASP Assay ID:
2259-0711.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCTTTAAGTATGCTTGGGTCCTTGACAAACTGAAAGCTGAGAGAGAG[C/T]GAGGCATCACCATCGATATCTCCCTGTGGAAGTTTGAGACAAGCAAATAC
Long Flanking Sequence:
CTCGGTTAAACATCTCATCTAAAAAATTTTGTTCACTGCGCAGTATAGAGTTTCCATCAATATACTGGGACGTTAGGAACCAGACAGACCACAGGTTGAACACCCTTTGCTAGTTTTACTAACATAATTTCTGGCAGCAATCTAGCTTCCCATTCAGGTACTGATCGGGCCCAGCCCTGCTTTGCTTCAGTAGGTGACCATGTGAGAGCTCTATGCTTGCTGTTGGCTATTGTTGTTTACGTTTTGCAGCAAATAAATCTCAAATATTTCACATTTGGCGGATACTATTTAATAATGCTAGAATGCTCTTTCGCTAATTAAATTAGTAAACTGAAAATTACTTCTGCAAAATGCAATATAAAGTGTGACAGGTCAGCCTTTTAAGAAATGTGTTTATAGAGTTTTTTCTTTAACAAATATATTTTCTTCTCATTTTATAGATGGGAAAAGGCTCCTTTAAGTATGCTTGGGTCCTTGACAAACTGAAAGCTGAGAGAGAG[C/T]GAGGCATCACCATCGATATCTCCCTGTGGAAGTTTGAGACAAGCAAATACTACGTCACCATCATTGATGCACCAGGACACAGAGACTTCATTAAGAACATGATCACTGGCACCTCACAGGTTTTTATACTACCACAAACCAATGTCTTTCCCCTTACACTATTTTAATAATCTTATACATTTCATTCCTCTTGTTGATACAGGCAGACTGTGCTGTGTTGATTGTAGCGGCTGGTGTTGGTGAATTTGAGGCTGGTATCTCAAAGAACGGGCAAACACGTGAACATGCCTTGCTGGCGTACACTCTCGGTGTTAAACAATTGATCGTGGGCGTTAACAAGATGGACTCTACGGAGCCCAATTATAGCCAGAAGCGCTATGAGGAGATTGTGAAGGAAGTCAGCACTTATATCAAGAAAATTGGCTACAACCCTGATACTGTGGCATTTGTTCCCATCTCTGGATGGAATGGGGATAACATGCTGGAGGCCAGCCCAAACG
Associated Phenotype:
Not determined