ZMP
eif4g2a
Ensembl ID:
ZFIN ID:
Description:
eukaryotic translation initiation factor 4, gamma 2a [Source:RefSeq peptide;Acc:NP_001014311]
Human Orthologue:
EIF4G2
Human Description:
eukaryotic translation initiation factor 4 gamma, 2 [Source:HGNC Symbol;Acc:3297]
Mouse Orthologue:
Eif4g2
Mouse Description:
eukaryotic translation initiation factor 4, gamma 2 Gene [Source:MGI Symbol;Acc:MGI:109207]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31614 | Nonsense | Available for shipment | Available now |
| sa34229 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31614
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 |
|---|---|---|---|---|---|
| ENSDART00000027616 | Nonsense | 450 | 891 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 7 (position 67339792)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 66418654 |
| GRCz11 | 7 | 66642302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGCAAGCTCAGTCTAAGGATATGCCACCACGTTTCACTAAGAAAGGA[C/T]AGCTGAATGCTGATGAGGTAGGAGCACATTTTATTTCACCAACTCAACAG
Long Flanking Sequence:
TTTCAAGAGAATTCGTTCATGCCGACAAGAATAAAACCTGATCGAGAAACTCTTGGGGGATTAGCGGATATGTTTGGGCAGATGCCAGGTATGTCCTGAAGTGTATTGACATTTCTGGGGCAGGTGGTGCATGACTGGATTTGCACTATGGTTCATTGCAAGCTTAATAACGGTGTTGTCTGGTCTTAGGCAGTGGGATTGGAACTGGCCCTGGGGTCATTCAGGACAGGTATTCGCCAACCATGGGCCGCCGCACAAACCCTCTTTTCAATGGGCACAGTGGCCACATGGCTCCTGCACCCCAGCCTTTCATTAAATCCAACCAGGTAAATGCCAAGCTACCAAATAATTGATTATTCGGGGTATCGAAATGTTAGCGGAACTAACAAGTATGTTTCTTTTTGCCAAAGGGGCAGAACCTGCTTTTCCAAAACCAGACTCATTCATCTCAACAGCAAGCTCAGTCTAAGGATATGCCACCACGTTTCACTAAGAAAGGA[C/T]AGCTGAATGCTGATGAGGTAGGAGCACATTTTATTTCACCAACTCAACAGCCTTTCAGTCGTTATCAATGTAAGTGTGTTGGGTGCAAAAATAAAATTGAAGGTTACAGTACAGCAAAAGAATCAATTTTAAGTCAGTTTGTTTTCGTTTTTCCTCATTTTTTACTAATGTTTTTGTAATATATTTCTATTTTCTTGTGGTCGTTATTGTTGTTATTATTCATCTTTATTAAGATTTATTGGGTGATGAAACCTAATGCAAAATAATACGATGACTCATACGGATGGCTTTCTCTTCATAATTCAGATTAGCTTGAGACCAGCTCAGTCATTCATCTTGAACAAAAACCAAATGCCAAAGTTGCAGCCTCAGATCCCAACCATGATTCCTCCTAGTGCTCAACCTCCACGTACATCCACACCACCGCTGGGACAGGTAATAAAGACAAATATTTTGCAAAGGAACGAAGTCTGTTTCTTTTTTAAAATGTGCTTAACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34229
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027616 | Nonsense | 816 | 891 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 7 (position 67332385)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 66426061 |
| GRCz11 | 7 | 66649709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAAAAATTCCTGCATGATCATGTGGAGCTGCAAGTCAGTGCTCTCTA[T/A]GCACTGCAAGTCCACTGCAATGCACATGCTTTTCCTAAAGGTATGTAAAC
Long Flanking Sequence:
TCTTTTCGGACTTCATGGTTTTCCCATATTCCTGTCACTTCCTCCAGAAATTGATCAAAACAAAGATCGCATGTTGGAGATTCTGGAGGGGAAGGGCCTGAGCTTCTTATTCCCTCTCATGAAGCTGGAGAAGGAGCTGCTGAAGCAGATTAAAGCAGATCCTGCCCCGCAGACCATCTACAAGTGGATAAAGGACAACATTTCTCCCAAACTGCACACCGATAGGGGTTTCGTTAACATTCTGATGACCAGGTATGGCTGACTGTTTCTATTGAAGGCGTTTGTTAAAGTTTAGTTGGTGTACAGTTGGTTTAACCTCTCAATTCTCCCAGCTTTTTGCAGTATATTTTCCATGAGATGTATGCCACTGATGATGAAGAGCAGTTATCTGCGCCTACGAAAGAGCAGCTTGACCAGGAGAAGCAGCTGCTCCTTGCCTTCAAACCGGTGATGCAAAAATTCCTGCATGATCATGTGGAGCTGCAAGTCAGTGCTCTCTA[T/A]GCACTGCAAGTCCACTGCAATGCACATGCTTTTCCTAAAGGTATGTAAACGCTTTTAGATAAGAAATTGTGAATTATTATTATTATTATTATTATTTTTAATATACATTAGTTTTGTGATGTAGATGAAAAAAAAATGATTTTGAAGTTATTCTTATATTATTTCAATATAAATGTATATATTTTCAATTTGTTACTATCAATCTGTAGTACAAGTAGTGGTTAGATTTAATTACTAAAGTGTTCCTTATACATTTTATGGTACTAAAGTGAATAAAATCGATTGGTCTGAATGTGAAAACAGTCAAATTTGTTTAGAGTATTTTAAATATGGATTTTTATTTTTTTTTTTATCCCACGTCATTTCTGTAGGAATGTTACTGCGCTACTTTGTCAACTTTTATGATATGGAGATAATTGAAGAAGAGGCCTTCCTAGCATGGAAAGAAGACATTACCCAGGAGTTTCCCGGGAAAGGGAAAGCATTGTTCCAGGTAAAGA
Associated Phenotype:
Not determined