Busch Lab

ZMP

eif4enif1

Ensembl ID:
ENSDARG00000016177
ZFIN ID:
ZDB-GENE-050320-113
Description:
eukaryotic translation initiation factor 4E transporter [Source:RefSeq peptide;Acc:NP_001013556]
Human Orthologue:
EIF4ENIF1
Human Description:
eukaryotic translation initiation factor 4E nuclear import factor 1 [Source:HGNC Symbol;Acc:16687]
Mouse Orthologue:
Eif4enif1
Mouse Description:
eukaryotic translation initiation factor 4E nuclear import factor 1 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa40766 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9362 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12435 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa40766
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002728 None None 747 None 16
ENSDART00000123022 Essential Splice Site 351 944 7 18
ENSDART00000133599 Essential Splice Site 351 944 8 19
ENSDART00000145153 None None 747 None 16
Genomic Location (Zv9):
Chromosome 6 (position 40862021)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 40933621
GRCz11 6 40931157
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGCAGTCTACGGTCCACACCACATGAGGAGTTGGAGAGATTGGCAG[G/A]TAAATCTTTTCTACTCCAGTCTCTTCACCTAGCTCTGGTTGTAGGTTTTG
Long Flanking Sequence:
CTGTTAGAAATGTGAAATTGTTGGTTTTATGGTTGTATGGCATCAAGCTATTTGTTAAGTTTTGTTCTACTGAAAGCTCAATGAAATGCAAATTTATGCCCATCTGACTCTATAAGGATTGTAATAACTCTGTTGAAACTTTGGGGATGCACATCTTGACTGTACAAAATTAGACTTGCTATTTGGAATTTAAGTGGGATTCTTGTAATTGAACCAATTCTCCACAATGCCCATTTTCACCCCATTGTGCTAAGCAGTCTGCAGACACTCTTCACGTAAGTGTCACTCACTCCCCAAGGCCGTTTCCTGCTTCTATGCTGTAACCGTTTAAACAATTGGTTTCTTTTTTTTCCTCCTCCAGATGATTGAAGATGTTCTTGCTGATGGTCCAGTCATGGCCAGCCGTTTTAGCCGCTGGTTCTCCAGTAACAGAAGTCCCTCTGGCAGCCGCTCCAGCAGTCTACGGTCCACACCACATGAGGAGTTGGAGAGATTGGCAG[G/A]TAAATCTTTTCTACTCCAGTCTCTTCACCTAGCTCTGGTTGTAGGTTTTGACTGATATTGAGCTTAGAACTGTTACTGATACCCTCTGTTTTCCTATTTAAACTCCCCATTTAGCATTTTAACTAAATATTTTTGTTAAATGTTAATAATTCCTTTAGGCTTTTTAACCAACTGTTCTACCTAGTCATCTAAATGCCCATTTTTCTGCTAGAGATGCAATAACCGGTTTCACTATTAACCGCGCTTTAATTCGTCATGGTTATTTAATCGTAAAGGCTTCTCAACACCGCGTTTCTGCACAGAACAAAACTGCAGCAACTAAACAAAGTTATGCAAACTGTGTGCTAGTTTGTACACTGAGACTAATAACCATGCACACTGAATTAATTATGACTGAGGCTATTAACTAAGGCAAGCTCGTGAAAGTTCATTATTTTCAATGGAGGGAACGGCTGAAGTTTAAGGACGAAGCAATGAAAAGTATACAGGTTTGCAAACCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9362
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002728 Essential Splice Site 444 747 11 16
ENSDART00000123022 Essential Splice Site 641 944 13 18
ENSDART00000133599 Essential Splice Site 641 944 14 19
ENSDART00000145153 Essential Splice Site 444 747 11 16
Genomic Location (Zv9):
Chromosome 6 (position 40871751)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 40943351
GRCz11 6 40940887
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAACAAGCCTACAACAAACAGGCTCATGAWAAGATGTTTCGTAACAGG[T/G]AATTTTGATTATCCAAGATTAAAGCAGGTCACTGGTGTTATAATAGTTCA
Long Flanking Sequence:
CCATTCTTAGGGTTCCATGGTGGTCCGCAAACAGTGTTGGATCAAATTCCAGACTTGCACCGGGCCAGGAATACACAACCGGTAAGATTCAAAGAATATAGATTTAAACTTTTTTTTTTTTTTTTTTTTTTGGTAAGGTTCATTGAAATAAATGGCTGTTAAGTGACTTGCAGCCTAGTAATTTTGTGCATACTCAGAAGTTTTTTTTTATTAGTAGAAGCAGTATAGTGTTTGCTGAACATCCACATTCCCAATGATGTGCTTTTTTCCCTCTAAAAAACAAACATTAAACCGAAATGACAGCATTAAGAGGTTATTGGTTTTAGATTAACTTGAATATTTTTTTTTATTTATTTTTTTTTTAGATGAGAGCTTTGCCAATGGGAGTGGACCAGACCAATCTTGAAGCTTTGTTTCAGCAGGATTTGGCAGTTCTTAATCGCCCACAGTACCAACAAGCCTACAACAAACAGGCTCATGATAAGATGTTTCGTAACAGG[T/G]AATTTTGATTATCCAAGATTAAAGCAGGTCACTGGTGTTATAATAGTTCAACTTGTGAACAGAGATGCATTTCAGTACATTTATACGCCTATATTGTAAGATGTTCTATGTAAGTAATGTGCGTGCGTGCTCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATACTCTTAACTATGCTGTTCATTTTGATGGGGTAAATAATGGCTGTATCCCAAACTGTGTATTGGAAAATCTAAATTTCTTTGCAAGGAATGGATAAAGAATGTTGTTTTTAAGTTAAGGGGATCCTTTTGAAAATGACAATTTAAAATCATTTAACCAGTTAAACCAATATTTTTGCCTCGACAAAAATCAGTTTTAGAGATACTTACAGATTAGACATCTATTAAATAGTACTTATAAGACTGGTAGTCGAGCTCCAGAAGATGACTAGAGTTTATCGGTAATTTTTAGAGCATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12435
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002728 Nonsense 484 747 13 16
ENSDART00000123022 Nonsense 681 944 15 18
ENSDART00000133599 Nonsense 681 944 16 19
ENSDART00000145153 Nonsense 484 747 13 16
Genomic Location (Zv9):
Chromosome 6 (position 40873516)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 40945116
GRCz11 6 40942652
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCAGTTGTCTCCATCCTTCACTCCCACCTCTGTRATCAAAAAAATGTA[T/A]GAGTCAAAAGAGAAAAGTCGGGATGATCTTGGGAGTAGACCAGGAAGCAA
Long Flanking Sequence:
AACATCTAATTACTGTAACTGCCGCTTTTGGGGAGTGGAGGGGAAAAGGATGGTGTTGAATGGATGTAAAAATGTGTAAACTGATGGTACTGTTAAATTACTGAAGAAAATAAAAAATTTGAATCATAAAAGATGGAGTAAATAAAGGGCCAGATTAACCGTATATACAGTGTAAAATCAGTTTTGAGCTCTGTATCTCCTATTTTGTAGGCCAACTCGGATGAACCGTTCACCTGTTCCTCACTTACCTGGCCGGACATCACCTGGCAGTACAGTTACAAGTGTCGTAAGTCGAATCTAAAAGATTGTAATTAATAGAGTCTTTTGAACCCATGTCATTCCATAATTATATTTTACAGTGTCTGTTAATCATTAGGTAACCTGTTAGTAATCTGTTGACTAAACATGAAAAATGTAACTTTTTTTTTTTTTTTTTTTTTTTTCCTCCATCTCCAGTTGTCTCCATCCTTCACTCCCACCTCTGTGATCAAAAAAATGTA[T/A]GAGTCAAAAGAGAAAAGTCGGGATGATCTTGGGAGTAGACCAGGAAGCAAAGAGGAGACTGTGAACTCTCATAACTCACAGGACGGTATGAAACCATGCTCAAGTCTTTCCCTCTCCCATTTTTTTTTTCTTCTTTAACTTGTCTAAACTCTCTTACATGTTTTATAGATGGACCTCCATCTCCCAGTTCCTTCCTGGAAGACGTAGACACCAGTGGTCCTCAGACTGGTGGGGTAAAAGCCTGCTCCACCCCTGTTCCCACTCAAAACCGCCATATCAAAGACCCAGAGCGGCCCAGGCCACCATCGGTAACAGGCCCCCACACTCCCACCATGCTGTCCCCAGGGCCTTCGTCTCCTTTCCCCAGACCCCAGATGTATCCGGTCCCTCTGCTTCCTCACGTCCCCTTGGTCAGACCTCCACCCCAGCTTCACCCCGGTGTGATGCAAAGGATGCTGGCTCAGGGCATCCAGGCTCAACAGCTCGGACCCACATTATTA
Associated Phenotype:
Not determined