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 |
---|---|---|---|
sa37650 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39401 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa3224 | Nonsense | F2 line generated | Not yet available |
sa13094 | Nonsense | Available for shipment | Available now |
sa12662 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37650
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010119 | Nonsense | 196 | 463 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 16064682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16105219 |
GRCz11 | 23 | 15861296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATTGGTTATAGTCCAGCTTCCGTACCCTTTGTCCCTATTTCAGGCTG[G/A]CATGGCGACAACATGCTGGAACCGTCTTCCAATGTGAGTCTCCTTGGGGT
Long Flanking Sequence:
AAAGTGCACTTGGTAATTAATGACAGGTGTGTTTGATCAAGGTTGCAACTAAACTCTGCTGCAAGGTAGATCTCCACGAACACGGATGGACATCGTGGTATAGAGCAACCATAACAGCCTTATATATTTGTCAAATATTTTTTTAAATTCCAAACAAAAAACAATGATGGCACTTGACTTAAAAACAACATTTTCATTTGTAGGTATACAATATTACTTTCCTCCTTTATCTCCCAGGCGGATTGTGCTGTCTTAATTGTAGCGGCTGGAGTGGGTGAATTTGAGGCAGGCATTTCCAAAAATGGCCAAACAAGGGAACACGCCCTGCTGGCCTACACACTTGGTGTCAAGCAACTGATCGTAGCCGTCAACAAGATGGACTCCACCGAGCCTTCCTACAGTGAGAAACGCTATGATGAGATCGTCAAAGAAGTGAGCGCCTACATCAAAAAGATTGGTTATAGTCCAGCTTCCGTACCCTTTGTCCCTATTTCAGGCTG[G/A]CATGGCGACAACATGCTGGAACCGTCTTCCAATGTGAGTCTCCTTGGGGTTTGTCTGGTTGTTTATTTTTTGCAATGACCTCATACCATTTACCAGTTTCTAATTAAAGAGTTGGCAGTTTTGATTAATACTATGGTCTCACTTGCGCTTGGTAGATGCCATGGTTTAAAGGCTGGAAGCTGGACAGGAAGGAGCACCATGCCGGTGGTGTTACTCTATTGGAAGCTCTTGATACCATCATGCCTCCAACACGGCCCACTGATAAACCCTTACGTCTTCCACTACAAGATGTCTACAAGATTGGAGGTGAGATCTAATGTTATTTAAAGAATTAGTTCACCCAAAATTTGTTAATAATTACTCACCCTCATATTGTTATTACCTTTTGTTCATCTTCCGAACACAAATATATTTTAGATAAAATTCAAGTGGTCTCAACCAAAACAAACTAAGAGAGCTCTCAAATTTCATTTAAAACATGTTAATTTATTTTTCTGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39401
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010119 | Essential Splice Site | 257 | 463 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 16064375)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16104912 |
GRCz11 | 23 | 15860989 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGATAAACCCTTACGTCTTCCACTACAAGATGTCTACAAGATTGGAG[G/A]TGAGATCTAATGTTATTTAAAGAATTAGTTCACCCAAAATTTGTTAATAA
Long Flanking Sequence:
AAACAAGGGAACACGCCCTGCTGGCCTACACACTTGGTGTCAAGCAACTGATCGTAGCCGTCAACAAGATGGACTCCACCGAGCCTTCCTACAGTGAGAAACGCTATGATGAGATCGTCAAAGAAGTGAGCGCCTACATCAAAAAGATTGGTTATAGTCCAGCTTCCGTACCCTTTGTCCCTATTTCAGGCTGGCATGGCGACAACATGCTGGAACCGTCTTCCAATGTGAGTCTCCTTGGGGTTTGTCTGGTTGTTTATTTTTTGCAATGACCTCATACCATTTACCAGTTTCTAATTAAAGAGTTGGCAGTTTTGATTAATACTATGGTCTCACTTGCGCTTGGTAGATGCCATGGTTTAAAGGCTGGAAGCTGGACAGGAAGGAGCACCATGCCGGTGGTGTTACTCTATTGGAAGCTCTTGATACCATCATGCCTCCAACACGGCCCACTGATAAACCCTTACGTCTTCCACTACAAGATGTCTACAAGATTGGAG[G/A]TGAGATCTAATGTTATTTAAAGAATTAGTTCACCCAAAATTTGTTAATAATTACTCACCCTCATATTGTTATTACCTTTTGTTCATCTTCCGAACACAAATATATTTTAGATAAAATTCAAGTGGTCTCAACCAAAACAAACTAAGAGAGCTCTCAAATTTCATTTAAAACATGTTAATTTATTTTTCTGACCAAATTTGAAGAGAAAATTTCTCCTTACAACCAAATCAATTCTCCTTTATTCAGCTGCAATGATTTCTGAGACTTTTTGAGCGAGTTTTGAGCTAAAGTCCGCATCCACACATCTTTGATATTAAGAACACATCAGACAACTTTACCGCTTCCTCTGTTCTTACGGTCTTGAGTTTTAGAACTGAACTTTTACAGTTGATGATTTTACACGAGAACACAAGGACGCAAAAATGCTGAAGAACATATATTAAAACAGCCATGGAAAAATGTTCAGAGCTGGAGGTCGTCCGGTAACGCGGATGAGAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3224
Status:
F2 line generated
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 |
---|---|---|---|---|---|
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:
554-2956.1 (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
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