ZMP
si:dkey-1a7.2
Ensembl ID:
ZFIN ID:
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13948 | Nonsense | Available for shipment | Available now |
sa15649 | Essential Splice Site | Available for shipment | Available now |
sa24317 | Nonsense | Available for shipment | Available now |
sa18232 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13948
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 |
---|---|---|---|---|---|
ENSDART00000087110 | Nonsense | 274 | 1700 | 8 | 34 |
ENSDART00000145172 | Nonsense | 198 | 1624 | 6 | 32 |
The following transcripts of ENSDARG00000074331 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 22316355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22095662 |
GRCz11 | 23 | 22022213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATAYGGAATTTKTCTTGTATGTTTTATSAGCAGCAGGACCTCCCTACTA[T/A]CCTGGGCAGCCCGTGTACACACCATCTCCACCCATYATAGTGCCTACACC
Long Flanking Sequence:
AGTTGATGCTCAATTGTCGCTAATTAGAAAGTAAAAGAAGTGAAATAGCACACTGAACTTGTAAGTTATTTAAAAGCACCCTTTCCCTAGTGATCCTGGTATAAGCGGTGTTATCACTCGTCAGTTAAGCAGTGGGAAAATTACATTGCTGTCACAACCCTAAAACTAATCACATGCCAATGTTCATTTAAGACCCTGTTCATTTAAGCATGTAGATGTGGTTAAGATAATCTGTCAACGTTCAAGCAGAGCATCAGAATGAGAAAGATGATTTAAGAGAAATTGTCAGGGGTTTTAGTGCCAGGCAGGCTGCAGAAACTGTAGGTCTACAGGGTTTTCATGCACAGGTCAGGTGTGAGTGATTGGTTCAAGCTTATAGAAAAAAAAGTTATTTTTATATACTTGGAGGAATAGTTCACTCAAAGAGCAAGAATTGTCATCATTTACTTTAATACGGAATTTTTCTTGTATGTTTTATGAGCAGCAGGACCTCCCTACTA[T/A]CCTGGGCAGCCCGTGTACACACCATCTCCACCCATTATAGTGCCTACACCACAACAACCTCCACCTGCTAAGAGGGAAAAGAAAACAGTGAGTCTACATTAACTTATTGTTCTGCATCGTCTTTTGCCACAGAGTTTACATTTTGATTTGTTTTCAGTTTTTACACATTGAAATACAGCCTTTTACATTTCTGGCTTTAACAAACACTGAGAATGTTTTATTTAAGCTTTTGGTTTATCCTTTGTCTGCTTTTTCGATTAATTTATTTTTATTTTCAAAGATCCGCATCCGAGACCCTAACCAGGGTGGCAAGGATGTCACAGACGAAATATTATCAGGAGTGGGTTTGAGTCGAAACCCAACCCCGCCTGTGGGACGGCCCTCTTCCACTCCTACACCTCCACAGGTAAGATGGCAAATCAAAGATCGAATCACACACTAAAACCAAAGTTAAGTCATTGTTAAAAGATTTTGGTTCAAACACCATTGTAATCTTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15649
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 |
---|---|---|---|---|---|
ENSDART00000087110 | Essential Splice Site | 303 | 1700 | None | 34 |
ENSDART00000145172 | Essential Splice Site | 227 | 1624 | None | 32 |
The following transcripts of ENSDARG00000074331 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 22316444)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22095751 |
GRCz11 | 23 | 22022302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGCCTACACCACAACAACCTCCACCYGCTAAGAGGGAAAAGAAAACAG[T/C]GAGTCTACATTAACTTATTGTTCTGCATCGTCTTTTGCCACAGAGTTTAM
Long Flanking Sequence:
GTGATCCTGGTATAAGCGGTGTTATCACTCGTCAGTTAAGCAGTGGGAAAATTACATTGCTGTCACAACCCTAAAACTAATCACATGCCAATGTTCATTTAAGACCCTGTTCATTTAAGCATGTAGATGTGGTTAAGATAATCTGTCAACGTTCAAGCAGAGCATCAGAATGAGAAAGATGATTTAAGAGAAATTGTCAGGGGTTTTAGTGCCAGGCAGGCTGCAGAAACTGTAGGTCTACAGGGTTTTCATGCACAGGTCAGGTGTGAGTGATTGGTTCAAGCTTATAGAAAAAAAAGTTATTTTTATATACTTGGAGGAATAGTTCACTCAAAGAGCAAGAATTGTCATCATTTACTTTAATACGGAATTTTTCTTGTATGTTTTATGAGCAGCAGGACCTCCCTACTATCCTGGGCAGCCCGTGTACACACCATCTCCACCCATTATAGTGCCTACACCACAACAACCTCCACCTGCTAAGAGGGAAAAGAAAACAG[T/C]GAGTCTACATTAACTTATTGTTCTGCATCGTCTTTTGCCACAGAGTTTACATTTTGATTTGTTTTCAGTTTTTACACATTGAAATACAGCCTTTTACATTTCTGGCTTTAACAAACACTGAGAATGTTTTATTTAAGCTTTTGGTTTATCCTTTGTCTGCTTTTTCGATTAATTTATTTTTATTTTCAAAGATCCGCATCCGAGACCCTAACCAGGGTGGCAAGGATGTCACAGACGAAATATTATCAGGAGTGGGTTTGAGTCGAAACCCAACCCCGCCTGTGGGACGGCCCTCTTCCACTCCTACACCTCCACAGGTAAGATGGCAAATCAAAGATCGAATCACACACTAAAACCAAAGTTAAGTCATTGTTAAAAGATTTTGGTTCAAACACCATTGTAATCTTAATTCTAAATGATCACAATTAGCATGTTTATTCAAGAGAGCCGGCCTCTTGTATGGTTAAACATCTTTAACTAGCATTTCTTTTTTCTGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24317
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 |
---|---|---|---|---|---|
ENSDART00000087110 | Nonsense | 1491 | 1700 | 30 | 34 |
ENSDART00000145172 | Nonsense | 1415 | 1624 | 28 | 32 |
The following transcripts of ENSDARG00000074331 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 22348811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22128118 |
GRCz11 | 23 | 22054669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATTGTATGTTTTCTGTATGCAGAGCCATAAGAAAGTGGGATCATTATG[G/A]AGGGATTCTGGGTTGAGCTGGGCAGATTTTATACCTGAAACAGAGGATGT
Long Flanking Sequence:
GTGTAAAAGGGGCTATTATCTGTTTACACTTAATATTTGCATGTACATTTTTTTTATATGATATCAAGAAGTTTTGATGCTAACAGTGTGTTTGTTTTGTCCCTAAAGGTTTTCTGAAACTCTTGAATTAGCAGATGATATGGCCATTGATATTCCCCATATATGGCTGTACCTTGCGGAGCTGGTAACCCCTGTGCTTCGAGAGGGGGGAATCTCTATGAGAGAATTATTTAGGTGAGTTTTTACCCAGCAGTGTTGTTGGATTCGGACTGAACTCATTGAGCAATTGATTTAATTTGCTTCTTTCCACAGTGAATTTAGCAAACCATTACTCCCTGTGGGAAGAGCTGGGATATTATTTTCTGAAATATTGCACCTTCTATGCAAACAAATGGTAAGCGGAAACACTGAAATCAATCATTTTTTTGCCATTTGTAAATATGGTAGAATCGATTGTATGTTTTCTGTATGCAGAGCCATAAGAAAGTGGGATCATTATG[G/A]AGGGATTCTGGGTTGAGCTGGGCAGATTTTATACCTGAAACAGAGGATGTGCACAGCTTCATCACAGAACATGTGAGTTTTCAAGGCCTTTATGCACTTTCATACTGCGCTTAACCCTTGATACTGCTTTTTACCCTGGCTAAAAAAATGTTTCAAACCTTTTGTTTCATAGTTTTGTTAACTCCACATTGTGGTGTTAAGTTTTATTCAATGTAAAATGGATCAGTGCTTGCTTTTGACCATTGGATGCTTGGCAATAGACAGCCAATCAGACATTGAGCAGAGAGGCTCATGTCAATTACAGTACATAAGCATCCTGGAAGTGGTAGAGCTGTAATGGATCACGGTTGATCTATGATTCGTACGGATCACAAACCACTGTTCGGCACACACTTGACCCGCGGATTAATACTTTTTTTTTCTTAATCCTAAATTTGTAACGATCACAAAGAGATCCTCTTGCGTCATTCAAATCACATGTATAAAAGCATTAAGGCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18232
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 |
---|---|---|---|---|---|
ENSDART00000087110 | Nonsense | 1642 | 1700 | 34 | 34 |
ENSDART00000145172 | Nonsense | 1566 | 1624 | 32 | 32 |
The following transcripts of ENSDARG00000074331 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 22353811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 22133118 |
GRCz11 | 23 | 22059669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATAATGGGTTAAAAATKAATGATWWATCTTTGTATCTTTATTGCAGATT[T/A]GCTCCGGATGTTTTTTGACTGTTTGTATGATGAGGACGTGATCTCTGAAG
Long Flanking Sequence:
ATCACACATTAAAGTGTATTTTATATAGTCATGATGTACACAACAGTCTCTGGACTTTCTGCAACACAGACACCAATATTTTAACAATTTTTAAAAAGTTAATCACTTTCTGGCCATCTGATATTAGTCATGGAAATATTTAAAGTATTACATTGCTTTGTAAACATTTATTATTACCATTTGTTGAGTCTCCCCATACAGTTTAATAGCGCAATTGGACCCAGCAACTGCTTCGCATGACGTTACATTTAACAAATGGTTAATAAAACACATATTATTATTATTATTGTATTTATCTATTTTGTTTTTAATGCTTATAATAGTCAAGGGCTAAAAATCAATGGTTTATTTTATAAAAACTAAATAAATATAGTAATTTAAAAAACTAAAGTATATTTAAAAAACATACTTCAATTAATACAATTATTATTTTATTAATTTTTTAATGTTTATAATGGGTTAAAAATGAATGATTAATCTTTGTATCTTTATTGCAGATT[T/A]GCTCCGGATGTTTTTTGACTGTTTGTATGATGAGGACGTGATCTCTGAAGACGCTTTCTATAAATGGGAGGTCAGTAAAGACCCCGCTGAACAGCAAGGCAAAGGTGTTGCCCTGAAGTCCGTCACAGCCTTCTTCACGTGGCTGCGCGAGGCCGAGGAAGAGTCCGAGGACAATTGACGACAGGACAAACAGGGACACATTGGTCAACTAGTGCTGAAAAGACAATAGTCGCTGAAACAATAACTGCATCAAATTAAAATGTAACATAACAAGCAACACATTATGCATCAGGATGGATTTCCAATGGTACGGTTCACTGACACGCAGCGACCCGACAACAACTTACAAATTGCTGGAGCACTAAACAAAAATGTATTATTTATAGAAATGTTGCATTTAAGTTTTTTTTTTATTATTTTTTTTTTGTTTTGTTACTTTTTAAGAGGACTTTAATAATACAAACATGCAACAGTGAAACAAAACGTACGTTCAGACTCGT
Associated Phenotype:
Not determined