ZMP
zgc:158450
Ensembl ID:
ZFIN ID:
Description:
eukaryotic translation initiation factor 4 gamma, 1 [Source:RefSeq peptide;Acc:NP_001073669]
Human Orthologue:
EIF4G1
Human Description:
eukaryotic translation initiation factor 4 gamma, 1 [Source:HGNC Symbol;Acc:3296]
Mouse Orthologue:
Eif4g1
Mouse Description:
eukaryotic translation initiation factor 4, gamma 1 Gene [Source:MGI Symbol;Acc:MGI:2384784]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19719 | Essential Splice Site | Available for shipment | Available now |
sa19718 | Nonsense | Available for shipment | Available now |
sa31270 | Nonsense | Available for shipment | Available now |
sa15272 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19719
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087107 | Essential Splice Site | 156 | 1592 | None | 30 |
ENSDART00000087120 | None | 145 | 1585 | 7 | 32 |
ENSDART00000145778 | None | 156 | 155 | None | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 16558781)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17146202 |
GRCz11 | 2 | 16814792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGTGGAACTGCAGGCTTTTATGGTGGAAGCAGTCCAGCTGAATACGG[T/C]ACATATGGTAAGAGGCTCTTCTCTGGGCCTCCCCTGCTTGTTTGACCACC
Long Flanking Sequence:
GCATAACTACATTCGGCCCTGTTTGTATGTAGTGTATAAAACAACTTCAAATGTAGTGTAAAAGTCAGTAATGTTTGAAGTAACAGAAACCGTTTGCCCATGTACAGCTTGTTTTCTGACTTTGCCTTTTTCTTTTCTCTTCTCAAAAGCCATACTACACCAACCGACCCAACATGCAAGGCAGTGCCCCTCGGGTCCCAACCAGCAACACCACCCGGCCTGTTGCACCTACTCATGTCTACCAACCTACCTCACAGGTTATGATGATTCCCCAGCAACAGTTGCAGTTCGCCGCTAACTCTCAGGGCCATCCCATATATTTACATGGACAGGTAACTCCCAATCCGTCTCTGTGCTGTTTTTATAAAGCGGTTCATGCGTCTAATACCGATTTGTTTTCTATCGCAGTTCCGCTCCCCCTACATGCCCCCAACCCAACAGTTCCCTGTGTCCAGTGGAACTGCAGGCTTTTATGGTGGAAGCAGTCCAGCTGAATACGG[T/C]ACATATGGTAAGAGGCTCTTCTCTGGGCCTCCCCTGCTTGTTTGACCACCCAACCCTCTTTTGTTTTTACTGTGCCATGTGTTTTGTCTTGCTTATCTTGCTCCTTTTGGTCAAATGCCACTTTTTTCCAGTCTGTAGAACATGTGCATTAGTTTAGCCTTTTGGAGGTTTTCTGAAACATTTGTTGCATAAACCTCAAAAACTGACCTGTTATATATACTAATGTAAACACCATGCATTCAAAATAAGGAAATGCATTTATATACCATGTAATTATATGTGTTAAACTACATTAATTTCAATTAGATAGTTGGATAGTCCACCTAAAATTGTCTGTCATCTAAAAACTTTGACTTTCTTCAACTACATAAAACATGTTAAAGACAATAAGATTCTGGTGTTTTTATCCATACAGTGGAAGTTCATAACTTTTTTTTTGTTTGTTTTTTTTAACCACACTTTGACTCATTGACCAGTTTTAATGTGTATTTTCCCCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19718
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 |
---|---|---|---|---|---|
ENSDART00000087107 | Nonsense | 182 | 1592 | 6 | 30 |
ENSDART00000087120 | Nonsense | 175 | 1585 | 8 | 32 |
ENSDART00000145778 | None | None | 155 | None | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 16554603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17150380 |
GRCz11 | 2 | 16818970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAAACGCCAGTGCCTCCTACACCTGTGATGATGAACCCTGCTCAGCAG[C/T]AACAGGCTCCACTTCCACAGCAAGCTGCTCCACAGCCGACAGGGCCAGTC
Long Flanking Sequence:
ATCGTTGCATCCCTACCTGTACCTCAGCTCCAGTGTGAACAAAGCACGAATGCGTGGTGGTGCTGTCTTGTATCGAGGAAGTAGTACAAGAAATGCTCTTGTGAGCCTGCATTTTTTAACGCAATTTTTACTACCTTTCTGGACCCTTCAATGGAGTGGCATTAAGGATGAATTAGAGTTTTGAGTGTATAAAACAACCTGAGGATGATTATTACAGTTTTTGGGTGAATTAGCCTTTTATTATGAATAGAAAGAAGCTATGTTAATGAAATATTGATTTTTCTTTGTTTTCCTCAGGGAGTCTGGAAGTGATTTTACAGGGTAGGGGGGTACTTTGCATGTGGGTCCCCCTCCCATTACAGCAAAAAGTCTTATCTTGGTGTCTGATCTTGTCTTTTTTTTGCCTTATTTGTGGTCTAGCAGCTGCCTACTACCCTGCAACACAGCAGTACCAAACGCCAGTGCCTCCTACACCTGTGATGATGAACCCTGCTCAGCAG[C/T]AACAGGCTCCACTTCCACAGCAAGCTGCTCCACAGCCGACAGGGCCAGTCAAACCCAGAGAACGCAAACAGGTGGGTGGAAACGACTTTTGCTGTGTTTTTCGATTTAGTACTTTTTTTTTTTTGTCACTTACCTGATGCCGCTTAACAGATAAGGATACGTGACCCCAACCAGGGTGGACGTGATATCACAGAGGAGATAATGTCTGGTGGAAGAACGACTTCCACACCAACTCCTCCACAGGTTTGACACTTTCATGCTTTTGTTCATTATGCCATGCTCATTTATATTACAATGAGTTCATTGTTTTGTTTTGTTTTTCCAGACTGCTGGTACAGAAGTGGGAAGTCCAGTTCAGACCAATGGTGAAAGCGTTCCAACTTTTCCTGCTGAGATCAGCACTGGTGAGTATACATTCTTAATAATAATAATAATAATAATAACAAGCAAAAAAAGTACATTATTGCCAAAACTGTTTTTCCATCCTGAAAAAAGTGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31270
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087107 | Nonsense | 422 | 1592 | 9 | 30 |
ENSDART00000087120 | Nonsense | 415 | 1585 | 11 | 32 |
ENSDART00000145778 | None | None | 155 | None | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 16551892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17153091 |
GRCz11 | 2 | 16821681 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTGCCCCTGTAATCACAGAGATGCCCGTTCCAGAACTGGCTGCCGAT[G/T]AGCCAAAGGAACAGCCTTTGTTAAACGGTTTGCCCCAGGACTCTGCAGAG
Long Flanking Sequence:
ATGTTTACTCTGCTTGATCTTCAGATGATGAAGTGAAGGCCATGGTAAGTCCTGCATCTGCGTCCACCCCTCCTCCATGTAAGACACCAGAGCCCCCAGCACCTTCATCCATCGACTCTAAACCCGAGTCAGAAGTCAGACCTGCTTCACCAGAGAGCAAGATTCCCAGTCCTCCAGAAGAGGATCTTGTGGTACCCTCTCCTTCTCCTCCTCCTGCAAACAATCCCCAAACTTCAGAGCCTCAAATTGCAGACAGTGTGGATGCTCCAGTGCTCCCTGAAGCCTCTGCTCAGAAGGAGCCCAAGGAGCCCTGTGCTCCTGTGGAGCCAGAGGAAGCCGAGGAGAAAGAGTATGAACCTGTGGCTGAAACAGAAGTTACAGCAGCCTCAAGTCCAGCTGTTGTCGCCTCCAGTGCGGTGGAGTCTTCTCCTAATGTAGCTGAAGATCGTGATGGTGCCCCTGTAATCACAGAGATGCCCGTTCCAGAACTGGCTGCCGAT[G/T]AGCCAAAGGAACAGCCTTTGTTAAACGGTTTGCCCCAGGACTCTGCAGAGGTTCCAGATGTAAAGCCAGAGAGCTCCGCTAATCCAGTTGCTGAACAAGTGGTTCCACAGGACCAGCAGAGCTGCCTTACAGCTGTTAAAGCATCTGTGGAGGAAACCGAAAAGGAGAAAGCGGAAGAGGCCCCCACCCCTGCACCAGTCTGCCTTGTTGAAGAAACAACTATGCAAGGTTGGTAAATTATTAAATTAGGATTGTAAAGAATATTATTTGTTTATCTCCTTTCCAAGTTTGACTCTAGTTACTGTCTCCCTAGCTGCCTCCCCAATAGTGCTAAAGAAGAAAAAGAAGATCAAGGATCTGAATAAGAAGGATGTTGGAGATGTTCTAGATGCCTTCAAGGAGGTTTGTGCTGTCATTATACATTTGTTTTTACAGTAGCACCTTTTGTGATTTTTTTTTTTATTTATTTTTTTATTACGTTTTTATTTTCTTTCTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15272
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 |
---|---|---|---|---|---|
ENSDART00000087107 | Nonsense | 757 | 1592 | 14 | 30 |
ENSDART00000087120 | Nonsense | 750 | 1585 | 16 | 32 |
ENSDART00000145778 | None | None | 155 | None | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 16548982)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17156001 |
GRCz11 | 2 | 16824591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGTGTCCTGAACAAGCTCACACCACAGATGTTCCAGYAGCTGATGAAG[C/T]AGGTGACCGAGCTCGCCATAGACACTGAAGAGAGGCTCAAGGGTGTCATT
Long Flanking Sequence:
TCACTTGTTGTTTGTATAACAGGCAAATAAAACCCCCTTGCGGCCCTTGGACCCCAGGAGTCTGATGAACTGTGGGCCTGATTTCACACCTTCATATGCTAACTTGGGTCGGCAGTCATCCGGAGGAGGAGGGCGAGGACCGGTCAGTTCAGTTTCTTTAGTCATAGGATTTTAATAGTTAAAATATTTACTCTGTGTTGAGGTCAGTCATTTATTTTTAAATGTTGAACTCCTTTCAGTCTGCACGGCGCCCTCAGCCGGGTCGAGGCAAAGACCAGATCAGTCGCAACCCCAAGATCATCACCAGCGTTTCTCTCAAAGACAACATTGAGCTCAACCAGGCTGAGAACGCTTGGACACCCTCGGTCAAGAAGCAAGTACGAAGTCGTGGAGAAGAGGAGGAGGATGATGCGGAAGCCGCTAAAACACAGGAGCTGTTCCGCCGTGTGCGCAGTGTCCTGAACAAGCTCACACCACAGATGTTCCAGCAGCTGATGAAG[C/T]AGGTGACCGAGCTCGCCATAGACACTGAAGAGAGGCTCAAGGGTGTCATTGACCTCATCTTCGAGAAAGCCATCTCTGAACCCAACTTCTCTGTAGCTTATGCCAACATGTGCCGGTGCCTTATGGGGGTAAGTAACTTTTTTCTGCAGGGTTGCTCGTGTCTGTTGCTTCATTGATGACCTGTTTTGTGCCACTGATGTATTGTAATGGTAATGAGGATCTGAAGAGCTTTCTTTTGGTTGGCACTCAAAAAAAACATGAAGCCATATTGTTGTTGTTCATTTTAAAATCACACAAATTGCAATTCTATTAATAATTACTGGGAGTGTTTCGGTTTCTCCAAATCACCAAACCGTACACTTCAAGAAGTTTTTAAAAGAAACGTAAATAGATCAAGCATTTTTTTCAGGAAACTTTGTTTATTGAATAAATAAAACATCTTATTTCTGTAAGAATCGATGCACCTACACAGCTCAAAGTTAATCAATTGAAGTGTAGTC
Associated Phenotype:
Not determined