ZMP
EIF4G3 (2 of 2)
Ensembl ID:
Description:
eukaryotic translation initiation factor 4 gamma, 3 [Source:HGNC Symbol;Acc:3298]
Human Orthologue:
EIF4G3
Human Description:
eukaryotic translation initiation factor 4 gamma, 3 [Source:HGNC Symbol;Acc:3298]
Mouse Orthologue:
Eif4g3
Mouse Description:
eukaryotic translation initiation factor 4 gamma, 3 Gene [Source:MGI Symbol;Acc:MGI:1923935]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38848 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2588 | Nonsense | F2 line generated | Not yet available |
sa35102 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27796 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38848
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111576 | Nonsense | 530 | 1561 | 10 | 31 |
Genomic Location (Zv9):
Chromosome 11 (position 28741715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27617701 |
GRCz11 | 11 | 27864875 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTGCTCTGCTGGAGATGAGATGGTCTTGCAGTCAAGCTTAGGGACCTA[C/A]AGCAGCCCCTTTACAGTGCCTGAGCACCAGGAGAAGCACTCTGAAGAAAA
Long Flanking Sequence:
ATGTAATATAATATAATATAATGTAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATGTAATATAGTATAATAATATAATATAGTATAATAATAAAATATAATTATTTCTTAACATTTCATTATACTTTTTTAATTTGCTTGATTATTTTTCAGATTGAGCATTAAATGATACTAGTCCATCCACTTAATCGCCCTTAAATAATAGAAATGATTTACTTTTGTTTTGTCTTTTACCTTTAGTTTATAGATAGTTTAAATGTGATTGTTAATTATATTGGAAAGTAGGCGAACTCCCTCTGCATAGCGTAACAGCAACTAATGACATTGTTATCATGACACAAGTCATTATGCAGTAATTCATCTCGCATAACCCCTTGTGTAATGCTGCTTTTTTTGCGCTTCACATCAGGAGGAGACCTCAAAGGACTGCTCTGCTGGAGATGAGATGGTCTTGCAGTCAAGCTTAGGGACCTA[C/A]AGCAGCCCCTTTACAGTGCCTGAGCACCAGGAGAAGCACTCTGAAGAAAACGGTGAGACCGAGACAGAGCCTTTCAGGAACGGGGTTGAGACGGAGAGCACGGACAGTGGTGTGACGCTCGGGGACAGTAGGGGCTCCATGTGTTCCCCAACTCCACTCATTCAGGAAGGTAAGATTTCCCTCAGGAATTGGTTGGGGTTTCGTATAGCATGCTGAAAGTGTTTATTAAATGGTGAAAAAATCGAAATTAAAATCAAATCGAAAAGGTAGTTCACCCAAAAGTTTAAACACAAATAAAGATATTTTGAAGAATGTTGCAAACTGGTAGCCATTGACATTTATGAAATGAAAAAAAATACTGTAGCATTCCTCAATATCCTATTTAGTAAAATAAATTCATTATGAATTAATTGGAAACACTTGAGTGTGAGATTTATTTTTTATTTTTTTGGGTGAGCTATGCCATTAAGTCATTGTTTATTCAGACATTTTACTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2588
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111576 | Nonsense | 702 | 1561 | 13 | 31 |
Genomic Location (Zv9):
Chromosome 11 (position 28736270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27612256 |
GRCz11 | 11 | 27859430 |
KASP Assay ID:
554-2607.1 (used for ordering genotyping assays)
KASP Sequence:
ACCTGTCTGTCAGTGATGATGTTCAGCTCAAGAAGGCAGAAAATGCTTGG[A/T]AACCTGGGATGAAGAGAGAGGGTGTCGCAGAGGACCCAGAAACCATCAGA
Long Flanking Sequence:
TTCATGCCAAACTCTAATAATAAATTTAAAGAATAGAAAATATCTTATTCGTGCAGTAGTTAGTTGCTAAGCTTTTGTGAATTTTATATTTATTAGTGCTTTTAATTAATTTGACATTTAAAATGTTACTTAATCTTACACATCTTCTATTTTCTAATGTTTAATATATTTAATTATTTCAATATTTAAATTATTTATATGATTATTTTTCATATATAATATTCATAACATTATAATTATAAATGAAGTAATAAAAATAAAATCTATGTGAAGCTAATTACCTCTGAGCGCTCAAAACATTTATTCCATATCATGATGCAGCTAAATGTCATTTTATATTTATACATTATAAAACATGCAATTATTTTTAAAGTCATTACTTTTTTTGTACAACAATCTGTTAACAGCTTTTAAATGTGCGACGACTCCCACCACGCAAGATCATCGTAAACCTGTCTGTCAGTGATGATGTTCAGCTCAAGAAGGCAGAAAATGCTTGG[A/T]AACCTGGGATGAAGAGAGAGGGTGTCGCAGAGGACCCAGAAACCATCAGAACCCAGGTTTGGCCTCTAGAGCTTATATATCCATCATGAAACATCCACAGTAAAAGTAGCACTCAAGACAAGGTGCTTGTCAATTGTTTTGATCAGGATTTTTATTCATTTGTTTCAGCTACACAATTTAAGTCCTGATTTGTTAATGATGAAAATGTGTTTACTTTATTTGATGAACGTTTAGTTGATTTTACTACAATGTGTTGGCTATCTTTTGGCACTTCAGGAGTTGTTCCGGAAAGTTCGTAGCATTTTAAACAAGCTCACGCCGCAGATGTTTCATCAGCTGATGAAGCAAGTGACGGATCTTACTATCAACACAGAGGAGAGGCTTAAAGGAGTCATCGATCTTGTGTTTGAGAAGGCCATCGATGAGCCCAGCTTCTCTGTGGCCTACGCCAACATGTGTCGCTGCCTGGCCACGGTACGTTCCAAACACACTGCTTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35102
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111576 | Nonsense | 1194 | 1561 | 23 | 31 |
Genomic Location (Zv9):
Chromosome 11 (position 28717056)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27593042 |
GRCz11 | 11 | 27840216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCAGAGACGCTGCTGGTCAGCGGTGTTTCAGAGAAGCCTGTCCTGTCT[G/T]AAGAGGAGATCGAGCGGAAGTCCAAAGCTATCATTGATGAATTTCTGCAC
Long Flanking Sequence:
CTGAAAACTACCACGTCATTTATTCCTTTAAGCTTTGTTTTTTCCGAGCGTATCTGAGTTCTGTTGCATGGTTGTGCTACATTGATTTATTTAACCACAACTGTTTATTAGGTGAAAGGTTTGATACTGATTGGAACTTGTAGTAGCGATGAGGTCTTAATTACCTTTAGGATTCAGGCGTATATCCTGTGAAGAATGTTGGGAAAAAAGCAGCCATTTAATTCCATAGTATATTTTGTACCTACTATGGATGTAGGTTGCACCTCCCCAACATTCTTCTGCAGATCTTTTTTTTTTTGTTGTTCAAAAAAAATTCATAAAAGTTTAGATCACTTGAGTTTGAGTAAATGTTGAGGGAATGTTTGGGTAAATGATGCTGACTTTTCCAAGTGTGCATTAACGTTTGTAAATATATATTGTAAATACTGAGCTTCTGCTTTATTGCAGTGAAATCAGAGACGCTGCTGGTCAGCGGTGTTTCAGAGAAGCCTGTCCTGTCT[G/T]AAGAGGAGATCGAGCGGAAGTCCAAAGCTATCATTGATGAATTTCTGCACATTAATGACTACAAGGTACAATGACCTGTATAAACAAGAACAAAAGCCACTCAACATTGACAATTAAAAACAAATGATTGTATATAATATTGTTCAAATGCTTCTGTTTAAAATCAGTACATTTTATATTGCAAGGATGTATTAAATTGATCAGAAAAATACATTAAATACATAAACTTTATAAAAAATATATTTAAAAAAATGTTTGATGGAACTTACTCTTCATCAATTAATCTTAGAGGAAAAACAAATTCCACAAAAATGTAAAGTTGAGCAATTGTTTTAATACTAATAATAAAGATAAATGCTTCTTGAGCACAAACGAATCATATTAGATGGATTTCTAAAGTATTGTGTGATTTAAAAAATTTAAGTTAGAAACTAAAAGAATGATTATTAAATTCATTCATTAAAAAGAAAAGAGATGAGCCATAATAATCTTGTTTTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27796
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 |
---|---|---|---|---|---|
ENSDART00000111576 | Nonsense | 1534 | 1561 | 31 | 31 |
Genomic Location (Zv9):
Chromosome 11 (position 28706536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27582522 |
GRCz11 | 11 | 27829696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAGAGGACGCTTTCTATCAATGGGAGACGAGTAAAGACCCGACAGAG[C/T]AGCTGGGAAAAGGCGTAGCGCTGAAGTCTGTGAACGCTTTCTTCACCTGG
Long Flanking Sequence:
TTTGGACGAATCTCAGATGAGTTCTTCTCCTTTTTTGAGAGCTTTAATGACTGCTATATGTAAAGCAGCAGTTAAAGGTGAGCAAGCTACTCGCTTTTGAGCCTTTTATTAAACAAAACCCAACTCCTCTTCCTCACACCAGTCACTTTCATCTGTTTTTATTCTCTCTTCTCTAGATGAAAGCACGTCCTGTCGAGTGGACACTGCTATCATCCAGAAACGCCTGCCTATATTACATAAGTACTTCGACTCGGACACCGAGCGGCAGCTGCAAGCACTTTATGCTCTTCAGTCTCTGATTGTCGCCCTGGATCAACCACCCAGTACGTAGCCAATGAAAAAAATTAAGCCAGGTGACAGGAGGATTTGTTTGGATGGTCATTTTTGATTTGTTTTTTTCCGCAGACCTACTCCGGATGTTTTTCGATTGTCTCTACGATGAGGACGTCATTTCAGAGGACGCTTTCTATCAATGGGAGACGAGTAAAGACCCGACAGAG[C/T]AGCTGGGAAAAGGCGTAGCGCTGAAGTCTGTGAACGCTTTCTTCACCTGGTTACGTGAAGCCGAGGAAGAATCTGAGGATAATTGACATGAACTGCTGGCCGATGCTCGGAGGCCTCGTGCTGAAACACATAATAAAATCCATTCAGACTCTGCAAGTCTAGCCACATGGGAACTTTGAACCACTGGCCTATTTGAGCTGGAACTCTCTACGACATGGAGGGAACACTAAATACTTGTATTATATATATAGAAAATATTTTTGTTTTAAAGTTTGACTTTTTTTCTTTTCTTTTTTTTGTTACTTTTAAAAGAAGAGACTTAAAATAGGTTCTGAACTCTTTAATTTATTATTTTTTTAAGAGACTGCAAATATGGAGTTCTATTTAACATTTGCAGGCAAAAAGAACATTGATAGAAATAACAGAATAAACAGTGTATCATAACAGTAATATTAATTTTGTTTTAATGTGTCGGCAGCCTCCCTGGATTCACCTTAAAA
Associated Phenotype:
Not determined