ZMP
zgc:110154
Ensembl ID:
ZFIN ID:
Description:
eukaryotic translation initiation factor 4E-like [Source:RefSeq peptide;Acc:NP_001017851]
Human Orthologues:
EIF4E, EIF4E1B
Human Descriptions:
eukaryotic translation initiation factor 4E [Source:HGNC Symbol;Acc:3287]
eukaryotic translation initiation factor 4E family member 1B [Source:HGNC Symbol;Acc:33179]
eukaryotic translation initiation factor 4E family member 1B [Source:HGNC Symbol;Acc:33179]
Mouse Orthologues:
AC138218.1, Eif4e, Eif4e1b
Mouse Descriptions:
eukaryotic translation initiation factor 4E Gene [Source:MGI Symbol;Acc:MGI:95305]
eukaryotic translation initiation factor 4E family member 1B Gene [Source:MGI Symbol;Acc:MGI:2685119
eukaryotic translation initiation factor 4E family member 1B Gene [Source:MGI Symbol;Acc:MGI:2685119
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35452 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35452
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 |
---|---|---|---|---|---|
ENSDART00000036718 | Nonsense | 132 | 213 | 6 | 7 |
ENSDART00000132073 | Nonsense | 149 | 230 | 6 | 7 |
The following transcripts of ENSDARG00000012274 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 18370331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18190366 |
GRCz11 | 13 | 18321358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCATTTCTGACTGTCCATGTGTCTGTCATCTTCTTTTGCAGCTGTTGTG[T/A]TTAATCGGAGAGTCCTTTGACGAGGCCAGTGAAGATGTGTGTGGTGCTGT
Long Flanking Sequence:
TAATTATTCATAATCGAAAATCGAATCATGCCTTTAGAATCGAAAATGTAATCGAATCAGGGATTTGGAGGATCGTGACACCCTTAATTGCTATATTTTGGCAGTATTACTCACCCATTTTGATGGAGCTAAACTAAAATGTGTGGCATTATTGCAGAGCATTCAACAGACATTTAACGGACTATAAATAACTAATTTTATGCTAATAAATGCATGAATGTTAGGCCTTAGCAACAATTACTAAACTAATATTGTGTGTTGTGTCTCAGGATGGTATTAAACCCATGTGGGAGGATGATAGGAATAAACTGGGTGGACGGTGGTTAATGACCCTCAGCAAACAGCAACGGCACAACGACCTTGACCGCTACTGGATGGAGACCGTAATAGTCTTTTTTTTTTTTTTTTTTTTTTTTGCTTGGGTCATATATTTTGATAGACAGCTGGATGTGCATTTCTGACTGTCCATGTGTCTGTCATCTTCTTTTGCAGCTGTTGTG[T/A]TTAATCGGAGAGTCCTTTGACGAGGCCAGTGAAGATGTGTGTGGTGCTGTTGTCAATGTCAGGCCAAAAGGGGATAAAATAGCCATTTGGACAGGCAACTGCCAAAACAGGGACGCAATCATGACGATAGGGTATGTAACCATCCACACTTGAAGACATTGTTGAAATAGTGTACATCAGAACAGATGTAAATGTTCTGCTTAGTGTAGCCATGGAAAAATACACCATAATTCAAACATTTTAGGTTATTACTGTATACAAGTTGGCACCTGCACTTTACTACATTATAGATTATTCTAATATTACATTTTGTGGCTTAGAAATGCACAATTGACAGCTTGAACTGACAGTGGCAGTATGTAAAGTGTGGGTTAGAGGCTGAAAATAAAAATTATTTGCTCAGATTGAACTAATCGTACATTAACAAAGCAGTAAATATTGTCTACAGTTGGTAAACCACAATGACCTCAAGCAACTCAAAAGAGTGATAAAAATAGCCT
Associated Phenotype:
Not determined