ZMP
zgc:92085
Ensembl ID:
ZFIN ID:
Description:
elongation factor 1-alpha 2 [Source:RefSeq peptide;Acc:NP_001002371]
Human Orthologue:
EEF1A2
Human Description:
eukaryotic translation elongation factor 1 alpha 2 [Source:HGNC Symbol;Acc:3192]
Mouse Orthologue:
Eef1a2
Mouse Description:
eukaryotic translation elongation factor 1 alpha 2 Gene [Source:MGI Symbol;Acc:MGI:1096317]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12662 | Nonsense | Available for shipment | Available now |
sa13094 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12662
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 |
---|---|---|---|---|---|
ENSDART00000010119 | Nonsense | 352 | 463 | 7 | 8 |
ENSDART00000010119 | Nonsense | 352 | 463 | 7 | 8 |
ENSDART00000010119 | Nonsense | 352 | 463 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 16057497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16098034 |
GRCz11 | 23 | 15854111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTATGTTTTTTTTTTTGTTATCAGGTCATCATTTTGAATCACCCAGGA[C/T]AGATCAGTTCAGGTTACTCTCCTGTCATAGACTGTCACACTGCTCATATC
Long Flanking Sequence:
ACAACTATTTAAGCCATATGATGTATTGTTGTGATGACGTTGTTGATACTGAAGTATAGCTGCAATATAACTGAAAATGTTGTATATTTTCTATGTTGAACTGACTGTTCATTAATAAAATTATTTGTTCACAAAAAAGGAATCGGGACTGTGCCAGTGGGCAGGGTAGAGACGGGTGTTCTCCGGCCCAGTATGGTGGTGACCTTTGCCCCAGTCAACATCACTACAGAAGTGAAGTCCGTGGAGATGCATCACGAGTCTCTAAGTGAAGCTCTTCCAGGAGACAATGTGGGCTTTAATGTGAAGAACGTGTCCGTAAAAGACATTCGAAGAGGTAACGTTTGTGGAGACAGTAAGTCCGACCCGCCTCAGGAAGCATCAGGGTTTACAGCACAGGTGGGACAGCTAGCTTATTGCATTATCTTACATCAACCCCTATCAGGATTTTTGTTTTATGTTTTTTTTTTTGTTATCAGGTCATCATTTTGAATCACCCAGGA[C/T]AGATCAGTTCAGGTTACTCTCCTGTCATAGACTGTCACACTGCTCATATCGCCTGCAAGTTTGCTGAACTCAAGGAGAAGATTGATCGCCGCTCAGGCAAGAAGCTAGAAGACAATCCCAAAAGCCTGAAGTCTGGAGATGCCGCCATAGTGGACATGATCCCAGGAAAACCAATGTGTGTGGAGAGCTTCTCTCAGTATCCTCCACTGGGTATGTGTCCATCTTCCATGAATAATTCTTTTTTTTTTTTTGGTATTTTCACATAGATTTTCTTTTGTGTTTTTTTTTTTTTTGCTTTCTTTTCTTTTTAGCTTTGCGTTAAATTTTTGTTGGCTTTTTTTTTTTTTTGCTTACCTACTCTCACCGGCCACTTTATTAAGTACACCTTACAAGTACTGGGTTTTATTCCCTTTTGCTTTCAGAACTGCCTTAATACTTCGTCATAGATTTATCAAGGTACTAAAAATATTTCGGTTCACATTGACATGATAGAATCATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13094
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 |
---|---|---|---|---|---|
ENSDART00000010119 | Nonsense | 352 | 463 | 7 | 8 |
ENSDART00000010119 | Nonsense | 352 | 463 | 7 | 8 |
ENSDART00000010119 | Nonsense | 352 | 463 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 16057497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16098034 |
GRCz11 | 23 | 15854111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTATGTTTTTTTTTTTGTTATCAGGTCATCATTTTGAATCACCCAGGA[C/T]AGATCAGTTCAGGTTACTCTCCTGTCATAGACTGTCACACTGCTCATATC
Long Flanking Sequence:
ACAACTATTTAAGCCATATGATGTATTGTTGTGATGACGTTGTTGATACTGAAGTATAGCTGCAATATAACTGAAAATGTTGTATATTTTCTATGTTGAACTGACTGTTCATTAATAAAATTATTTGTTCACAAAAAAGGAATCGGGACTGTGCCAGTGGGCAGGGTAGAGACGGGTGTTCTCCGGCCCAGTATGGTGGTGACCTTTGCCCCAGTCAACATCACTACAGAAGTGAAGTCCGTGGAGATGCATCACGAGTCTCTAAGTGAAGCTCTTCCAGGAGACAATGTGGGCTTTAATGTGAAGAACGTGTCCGTAAAAGACATTCGAAGAGGTAACGTTTGTGGAGACAGTAAGTCCGACCCGCCTCAGGAAGCATCAGGGTTTACAGCACAGGTGGGACAGCTAGCTTATTGCATTATCTTACATCAACCCCTATCAGGATTTTTGTTTTATGTTTTTTTTTTTGTTATCAGGTCATCATTTTGAATCACCCAGGA[C/T]AGATCAGTTCAGGTTACTCTCCTGTCATAGACTGTCACACTGCTCATATCGCCTGCAAGTTTGCTGAACTCAAGGAGAAGATTGATCGCCGCTCAGGCAAGAAGCTAGAAGACAATCCCAAAAGCCTGAAGTCTGGAGATGCCGCCATAGTGGACATGATCCCAGGAAAACCAATGTGTGTGGAGAGCTTCTCTCAGTATCCTCCACTGGGTATGTGTCCATCTTCCATGAATAATTCTTTTTTTTTTTTTGGTATTTTCACATAGATTTTCTTTTGTGTTTTTTTTTTTTTTGCTTTCTTTTCTTTTTAGCTTTGCGTTAAATTTTTGTTGGCTTTTTTTTTTTTTTGCTTACCTACTCTCACCGGCCACTTTATTAAGTACACCTTACAAGTACTGGGTTTTATTCCCTTTTGCTTTCAGAACTGCCTTAATACTTCGTCATAGATTTATCAAGGTACTAAAAATATTTCGGTTCACATTGACATGATAGAATCATGG
Associated Phenotype:
Not determined