ZMP
si:dkey-37o8.1
Ensembl ID:
ZFIN ID:
Description:
eukaryotic translation elongation factor 1 alpha [Source:RefSeq peptide;Acc:NP_001157466]
Human Orthologues:
EEF1A1, EEF1A2
Human Descriptions:
eukaryotic translation elongation factor 1 alpha 1 [Source:HGNC Symbol;Acc:3189]
eukaryotic translation elongation factor 1 alpha 2 [Source:HGNC Symbol;Acc:3192]
eukaryotic translation elongation factor 1 alpha 2 [Source:HGNC Symbol;Acc:3192]
Mouse Orthologues:
Eef1a1, Eef1a2
Mouse Descriptions:
eukaryotic translation elongation factor 1 alpha 1 Gene [Source:MGI Symbol;Acc:MGI:1096881]
eukaryotic translation elongation factor 1 alpha 2 Gene [Source:MGI Symbol;Acc:MGI:1096317]
eukaryotic translation elongation factor 1 alpha 2 Gene [Source:MGI Symbol;Acc:MGI:1096317]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12176 | Nonsense | Available for shipment | Available now |
sa37833 | Nonsense | Available for shipment | Available now |
sa24453 | Nonsense | Available for shipment | Available now |
sa8935 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37834 | Nonsense | Available for shipment | Available now |
sa14507 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12176
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106272 | Nonsense | 16 | 483 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 10670947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 10758350 |
GRCz11 | 24 | 10898717 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTCTGAAGTCACAAGAASAACAAAGAGTGTATCTRAAATTTGGTAGYT[T/A]GGAGGGTGTAAAACGWGTAATTTACCAAATGGCAAAAGAAAGGATTCATA
Long Flanking Sequence:
AGAACAATAAAAAAATAATCATAATACAAATTATAATAATAAATTATAACATTAAACAGACAACAGTCATGTAAAGCAGCTAGTTGTTGGAATTCCCGGTCTGCCTTTAAAATATCAATGATTATAAGTTTAGAATCTGGATAGATCTCAGCTTTTAAATGCAACCATAGCTTCCGCTCATTTGCATTATTTATCACTAGCTATTGTTAGAAAACAATTGGTAGGCTATCTGGTTCCACTGACGTCGAGAGAAAAAAAAAATAACACACATAAAGGATTAGGCTACGGTTTTCAGTAGAAGTTATTATGGATGACTGATATTTGTTTGTTGTACTTATAAGCCTATACGATTACGTATTTTAGTTAATAGCTTAATAGATTAAGGTGTTATTGATCACACCAGAACTTAATTAGCAGTTTCCATACTTAAGCGTTCAATTTGCTTGATACCGGTCTGAAGTCACAAGAAGAACAAAGAGTGTATCTGAAATTTGGTAGTT[T/A]GGAGGGTGTAAAACGTGTAATTTACCAAATGGCAAAAGAAAGGATTCATATCAACTTGGTTATCATTGGCCATGTAGATGGTGGCAAATCCACAACCACTGGTCATTTGGTTTATAAATGTGGAGGAATTGACCATCGAACAATTGAGAAGTATGAGAAGGCTGCAACCCAAGTAAGTATTCACCTTTAATTCCTTTTAGTTATTTCTTAAACTGCTTTGGCTATTTATGCTTTTTTTTTCTTTCCCTCTCTTTAAGATGGGAAAGAGTTCCTTCAAGTATGCCTGGGTTCTGGACAAACTGAAAGCGGAGAGGGAACGTGGGATCACGATTGACATTTCCCTGCTGAAATTCAACACTCAGAAGTACACCTTTACCATAATCGATGCACCTGGTCATCGTGATTTCATTAAAAACATGATCACTGGAACCTCACAGGTATTTATTTCAGGTGTTGACCTAGATTTTAATTTATATTTAAATAATAAAATCTCTCGGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37833
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106272 | Nonsense | 87 | 483 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 10671244)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 10758647 |
GRCz11 | 24 | 10899014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTTTAAGATGGGAAAGAGTTCCTTCAAGTATGCCTGGGTTCTGGAC[A/T]AACTGAAAGCGGAGAGGGAACGTGGGATCACGATTGACATTTCCCTGCTG
Long Flanking Sequence:
GAAGTTATTATGGATGACTGATATTTGTTTGTTGTACTTATAAGCCTATACGATTACGTATTTTAGTTAATAGCTTAATAGATTAAGGTGTTATTGATCACACCAGAACTTAATTAGCAGTTTCCATACTTAAGCGTTCAATTTGCTTGATACCGGTCTGAAGTCACAAGAAGAACAAAGAGTGTATCTGAAATTTGGTAGTTTGGAGGGTGTAAAACGTGTAATTTACCAAATGGCAAAAGAAAGGATTCATATCAACTTGGTTATCATTGGCCATGTAGATGGTGGCAAATCCACAACCACTGGTCATTTGGTTTATAAATGTGGAGGAATTGACCATCGAACAATTGAGAAGTATGAGAAGGCTGCAACCCAAGTAAGTATTCACCTTTAATTCCTTTTAGTTATTTCTTAAACTGCTTTGGCTATTTATGCTTTTTTTTTCTTTCCCTCTCTTTAAGATGGGAAAGAGTTCCTTCAAGTATGCCTGGGTTCTGGAC[A/T]AACTGAAAGCGGAGAGGGAACGTGGGATCACGATTGACATTTCCCTGCTGAAATTCAACACTCAGAAGTACACCTTTACCATAATCGATGCACCTGGTCATCGTGATTTCATTAAAAACATGATCACTGGAACCTCACAGGTATTTATTTCAGGTGTTGACCTAGATTTTAATTTATATTTAAATAATAAAATCTCTCGGGGGTAAACATTTAAAACAATTCTTAGACCCATTTCTTTCTTTTTCCTCTGAGACATCAAACCATGTGATTTTGGTAGACTGAATTTGGGTGTGTATGACCAGAACTTGTTGAGAGAAAAGGAAACTGAGCAATGTGGGGGGGCTCCAGGTTTTTAACTACTCTGTGCCACCTAATTGTAGTTGACCTAAACCCGTTTTGTTTGTTGATTTTTCTTAGGCTGATGCTGCTCTGCTGATCGTCTCTGCAGCAAAGGGTGAATTTGAGGCTGGAATTTCTCGGAACGGTCAGACAAGAGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24453
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106272 | Nonsense | 110 | 483 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 10671315)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 10758718 |
GRCz11 | 24 | 10899085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGGGATCACGATTGACATTTCCCTGCTGAAATTCAACACTCAGAAGTA[C/A]ACCTTTACCATAATCGATGCACCTGGTCATCGTGATTTCATTAAAAACAT
Long Flanking Sequence:
AGCTTAATAGATTAAGGTGTTATTGATCACACCAGAACTTAATTAGCAGTTTCCATACTTAAGCGTTCAATTTGCTTGATACCGGTCTGAAGTCACAAGAAGAACAAAGAGTGTATCTGAAATTTGGTAGTTTGGAGGGTGTAAAACGTGTAATTTACCAAATGGCAAAAGAAAGGATTCATATCAACTTGGTTATCATTGGCCATGTAGATGGTGGCAAATCCACAACCACTGGTCATTTGGTTTATAAATGTGGAGGAATTGACCATCGAACAATTGAGAAGTATGAGAAGGCTGCAACCCAAGTAAGTATTCACCTTTAATTCCTTTTAGTTATTTCTTAAACTGCTTTGGCTATTTATGCTTTTTTTTTCTTTCCCTCTCTTTAAGATGGGAAAGAGTTCCTTCAAGTATGCCTGGGTTCTGGACAAACTGAAAGCGGAGAGGGAACGTGGGATCACGATTGACATTTCCCTGCTGAAATTCAACACTCAGAAGTA[C/A]ACCTTTACCATAATCGATGCACCTGGTCATCGTGATTTCATTAAAAACATGATCACTGGAACCTCACAGGTATTTATTTCAGGTGTTGACCTAGATTTTAATTTATATTTAAATAATAAAATCTCTCGGGGGTAAACATTTAAAACAATTCTTAGACCCATTTCTTTCTTTTTCCTCTGAGACATCAAACCATGTGATTTTGGTAGACTGAATTTGGGTGTGTATGACCAGAACTTGTTGAGAGAAAAGGAAACTGAGCAATGTGGGGGGGCTCCAGGTTTTTAACTACTCTGTGCCACCTAATTGTAGTTGACCTAAACCCGTTTTGTTTGTTGATTTTTCTTAGGCTGATGCTGCTCTGCTGATCGTCTCTGCAGCAAAGGGTGAATTTGAGGCTGGAATTTCTCGGAACGGTCAGACAAGAGAACATGCTCTACTGGCGTACACTCTTGGGGTCAAACAGCTTGTAGTTTGTGTGAACAAAATGGACCTGACAGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8935
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106272 | Essential Splice Site | 134 | 483 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 10671660)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 10759063 |
GRCz11 | 24 | 10899430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCASCTAATTGTAGTTGACCTAAACCCGTTTTRTTTGTNTGNNTTTTCTT[A/T]GGCTGATGCTGCTCTGCTGATCGTCTCTGCAGCAAAGGGTGAATTTGAGG
Long Flanking Sequence:
CTGCTTTGGCTATTTATGCTTTTTTTTTCTTTCCCTCTCTTTAAGATGGGAAAGAGTTCCTTCAAGTATGCCTGGGTTCTGGACAAACTGAAAGCGGAGAGGGAACGTGGGATCACGATTGACATTTCCCTGCTGAAATTCAACACTCAGAAGTACACCTTTACCATAATCGATGCACCTGGTCATCGTGATTTCATTAAAAACATGATCACTGGAACCTCACAGGTATTTATTTCAGGTGTTGACCTAGATTTTAATTTATATTTAAATAATAAAATCTCTCGGGGGTAAACATTTAAAACAATTCTTAGACCCATTTCTTTCTTTTTCCTCTGAGACATCAAACCATGTGATTTTGGTAGACTGAATTTGGGTGTGTATGACCAGAACTTGTTGAGAGAAAAGGAAACTGAGCAATGTGGGGGGGCTCCAGGTTTTTAACTACTCTGTGCCACCTAATTGTAGTTGACCTAAACCCGTTTTGTTTGTTGATTTTTCTT[A/T]GGCTGATGCTGCTCTGCTGATCGTCTCTGCAGCAAAGGGTGAATTTGAGGCTGGAATTTCTCGGAACGGTCAGACAAGAGAACATGCTCTACTGGCGTACACTCTTGGGGTCAAACAGCTTGTAGTTTGTGTGAACAAAATGGACCTGACAGAGCCACCATTCAGCCAGAAACGTTATGATGAAGTGGTTAGGAATGTTTCCGTGTTCGTCAAGAAGATCGGCTTTGAGATAGGTGCTGTACCTTTCATACCCATTTCTGGTTGGAGTGGTGAGAACATGATTGTCCCATCCCAAAAGGTATGTAGAATTTTCAACCTTTCTATACAAAAATGCTTTCAGTTGCCTTGTTCTGTTTCTGGAGAGCTACTGAGTTTAAGAGTTCTTGAAGGCTTTAACTAGCTGGACCTTGTGCGTTTAAGACTGGGGTGCCCAAACTCTGTCCTAGAGGGCATGTGTCCTGGATATTTTCGTTCCAACCCCAATTAAGTGCACCTGAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37834
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106272 | Nonsense | 171 | 483 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 10671773)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 10759176 |
GRCz11 | 24 | 10899543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAACGGTCAGACAAGAGAACATGCTCTACTGGCGTACACTCTTGGGGTC[A/T]AACAGCTTGTAGTTTGTGTGAACAAAATGGACCTGACAGAGCCACCATTC
Long Flanking Sequence:
CACGATTGACATTTCCCTGCTGAAATTCAACACTCAGAAGTACACCTTTACCATAATCGATGCACCTGGTCATCGTGATTTCATTAAAAACATGATCACTGGAACCTCACAGGTATTTATTTCAGGTGTTGACCTAGATTTTAATTTATATTTAAATAATAAAATCTCTCGGGGGTAAACATTTAAAACAATTCTTAGACCCATTTCTTTCTTTTTCCTCTGAGACATCAAACCATGTGATTTTGGTAGACTGAATTTGGGTGTGTATGACCAGAACTTGTTGAGAGAAAAGGAAACTGAGCAATGTGGGGGGGCTCCAGGTTTTTAACTACTCTGTGCCACCTAATTGTAGTTGACCTAAACCCGTTTTGTTTGTTGATTTTTCTTAGGCTGATGCTGCTCTGCTGATCGTCTCTGCAGCAAAGGGTGAATTTGAGGCTGGAATTTCTCGGAACGGTCAGACAAGAGAACATGCTCTACTGGCGTACACTCTTGGGGTC[A/T]AACAGCTTGTAGTTTGTGTGAACAAAATGGACCTGACAGAGCCACCATTCAGCCAGAAACGTTATGATGAAGTGGTTAGGAATGTTTCCGTGTTCGTCAAGAAGATCGGCTTTGAGATAGGTGCTGTACCTTTCATACCCATTTCTGGTTGGAGTGGTGAGAACATGATTGTCCCATCCCAAAAGGTATGTAGAATTTTCAACCTTTCTATACAAAAATGCTTTCAGTTGCCTTGTTCTGTTTCTGGAGAGCTACTGAGTTTAAGAGTTCTTGAAGGCTTTAACTAGCTGGACCTTGTGCGTTTAAGACTGGGGTGCCCAAACTCTGTCCTAGAGGGCATGTGTCCTGGATATTTTCGTTCCAACCCCAATTAAGTGCACCTGAACCAGCCAATCAAGCTCTTTTTCTAGGTATACTGAAACTTCTAGTCTTTAAGTAGGAGCTGAAGTATGTAGGACTCTGGCCCTCCAGGACACTGTTTAGACACCCTTTCCAGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14507
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106272 | Nonsense | 239 | 483 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 24 (position 10672349)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 10759752 |
GRCz11 | 24 | 10900119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATTCTAATTGTTTGTACTCTTCTCTCAGATGCAATGGTTTAAAGGGT[G/A]GAAGCTCAAGAGAAAAGAAGGCCACTGTCATGGCCGAACCTTGTTGGAAG
Long Flanking Sequence:
TTAGGAATGTTTCCGTGTTCGTCAAGAAGATCGGCTTTGAGATAGGTGCTGTACCTTTCATACCCATTTCTGGTTGGAGTGGTGAGAACATGATTGTCCCATCCCAAAAGGTATGTAGAATTTTCAACCTTTCTATACAAAAATGCTTTCAGTTGCCTTGTTCTGTTTCTGGAGAGCTACTGAGTTTAAGAGTTCTTGAAGGCTTTAACTAGCTGGACCTTGTGCGTTTAAGACTGGGGTGCCCAAACTCTGTCCTAGAGGGCATGTGTCCTGGATATTTTCGTTCCAACCCCAATTAAGTGCACCTGAACCAGCCAATCAAGCTCTTTTTCTAGGTATACTGAAACTTCTAGTCTTTAAGTAGGAGCTGAAGTATGTAGGACTCTGGCCCTCCAGGACACTGTTTAGACACCCTTTCCAGGAAGATTTGGCACCCTTGTAAAGTAGATGATGATTCTAATTGTTTGTACTCTTCTCTCAGATGCAATGGTTTAAAGGGT[G/A]GAAGCTCAAGAGAAAAGAAGGCCACTGTCATGGCCGAACCTTGTTGGAAGTGCTTGATTCCCTACATCCTCCAGTGCGCAATGCAGGCAAGCCCCTGCGCCTTCCCCTACAAGATGTCTATAAGATTGGCGGTGGGTAATGTTGATTGTTGAAAACCACTTTTAGTCAACTAAGTCTTTGACCAAATCCTCCACTTATTCACAGGTGTTGGAACTGTCCCTGTGGGTAAGATTGAAACTGGGGTCTTAAAACCAGGCATGGTTCTCACCTTCTCACCAGCAAAACTGACTGCTGAGGTCAAGTCCATAGAGATGCATCACCAGGGTCTTCAGACTGCTCTTCCTGGGCATAATGTGGGCTTCAACATTAAAAATGTATCTGTGAAGAACCTTCGAAGAGGTGATGTAGCTGGGAATGCACAGCAGGACCCACCATCAGATGTCAGCAGTTTTATTGCTCAGGTTTCTATGCTCTTTACTTTCTAATGCTAATTATGGTTG
Associated Phenotype:
Not determined