Busch Lab

ZMP

eif4e1b

Ensembl ID:
ENSDARG00000014565
ZFIN ID:
ZDB-GENE-980526-127
Description:
Eukaryotic translation initiation factor 4E-1B [Source:UniProtKB/Swiss-Prot;Acc:Q9PW28]
Human Orthologue:
EIF4E1B
Human Description:
eukaryotic translation initiation factor 4E family member 1B [Source:HGNC Symbol;Acc:33179]
Mouse Orthologues:
AC138218.1, Eif4e1b
Mouse Description:
eukaryotic translation initiation factor 4E family member 1B Gene [Source:MGI Symbol;Acc:MGI:2685119

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa20588 Essential Splice Site Available for shipment Available now
sa40603 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa20588
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017881 Essential Splice Site 71 214 3 7
Genomic Location (Zv9):
Chromosome 5 (position 71170881)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 67121354
GRCz11 5 67799065
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAATCTAAGGCTCATCACCAAATTCGACACGGTCGAGGACTTCTGGGGG[T/A]AAGTTATGCTCAAGACCTCTTAAAGGTTGAATGCCTTTAAAATCCAAAAT
Long Flanking Sequence:
GGTGAGCAATAGTGTCCAAAACGTTACAAAGCTCTCATTTAACCACATACACACGTCAGTCTTTTAATATATGCGCTGTTTTACCTGAGGTAACTCTTAAATACGTTTATGTTCATTTCCTGAAGCGTTTTACGCCATAACAGAGGCGTCAACGCACGATTAGCATTTAAATGATTTGATTTTGTCCTCAAATTCATGTTTTTACGTTTCACCAGATTGATAAAGTACCGAAGAAGAAGGTTGAGAAAAAGAAATTCGAACCAAACATCTTGAAGGAGCCTTGTATGAAGCACCCTTTACAAAACAGGTGAGTTCACGTTTGTTTGAGCATGTCTTCATTCTCAATATCTGCTCTTTTTAATTTTAGTTCCTCCCCTTAATTTTGTATGTGTACTGTCTGCAGATGGGGACTTTGGTTCTACAAGAATGATAAGAGCAAAATGTGGCAGGACAATCTAAGGCTCATCACCAAATTCGACACGGTCGAGGACTTCTGGGGG[T/A]AAGTTATGCTCAAGACCTCTTAAAGGTTGAATGCCTTTAAAATCCAAAATATTCAACGTGATCATTGTATTTGAATGAATACTGAACAGTCTATTGTTTTGTGAAAGGTGGAGTAGAGCATTGAGGTGAAGTTGGCTTTATATTCGCACATTTATTCAAAGACTACTTGTGGCTATATTTTTTTACCATGGTATTTTCAATATATTGAGGTAAATTTAGTTTTATATTCACACATTCAGACTTTCCCCTTAATAATATCATTTCAGAAATGTATTCTTTGCTAATTCTAAATAGGGAAATCCTATTAGCAGCCAATCACTGTCAAAGTACAACAGTTTTCACTGTGAATTAGAGTTAATGCTGTTTAGAAGTCACTTGCATGCTAATTCCGATCAAAAATCCAAAGTAACATTGTAAACACTTTAGGGACTTCTAAATGAACGAATGTGCGAATAAAAAAAACCAACTTTACCTCTATTTTCAATATCCGGGTTAATGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40603
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
ENSDART00000017881 Essential Splice Site 177 214 6 7
Genomic Location (Zv9):
Chromosome 5 (position 71179846)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 67113684
GRCz11 5 67791404
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTCTGGACATCCAATGCTGAGAACTGTGAGACGGTCACATATATAGG[G/A]TAAGCATGCTTTTAAATCCATGCTTTTTATGGCCAATATTTTAACTTTTG
Long Flanking Sequence:
TTTTGAATGGTTTACAGAACAAACTCGTTATACAATGACTTGCCTAATTACCCTAACTTGCCCAGTTAACCTAGTTAAGCCTTTAAATGTCACTTCAAGCTGAATACCAGTATCTTGGAAAATATCTAGTGAAATATTATGTACTGTCATCATGACTAAGATAAAAGAAATGAGTCATTAAAACTGTAATGTTTAGAAATGTGTTAAAAAAATCTTCTCCGTTAAACAGAAATTGTGGGAAAAAAAAAACACCAGAGGACTCATTATTCAGGAGGTCTAATAATTCAGAATTTAACTTTATATTTAAACATTTAAACTAAATCAATTAAATGTGTTGCTGAACATTTATTCCTATGGCAGTTGCTGTGTCTTATTGGTGAGGGCTTCAGCTCCTTTAGTCGGGATATCTGTGGAAGTGTAATCAACATCCGTGCCAAAGGGGACAAAATTGCTCTCTGGACATCCAATGCTGAGAACTGTGAGACGGTCACATATATAGG[G/A]TAAGCATGCTTTTAAATCCATGCTTTTTATGGCCAATATTTTAACTTTTGCCTTTTTTTTTCACCTTTTTTGGGATAGGATAGTGGAGGACAGACAGAAAAGTAAAGTAAACAACCCGAGGAATTGATCTCGGGTTGCCGTGAGCATGTCGGCACACTTAACCACTAGGCTATTGGTGCCAACATTTTTGCACAGTTAAAGAGAGAGTTCATCCAAAAATGAAAATTAAGTCATTATTTGCTCACTCTTTACTTGTTTTAAACCTTCTTGTTAACACTAAAGAAGATATTTTGAAAAACATCAAACCATTGACTTTCCAAAGTATTTTTCCTACTATGGATGTAAGTGGATGCAGGTTTTTGGCTTTCTTCAAAAAAAAAATCATCATGTTCAGTTTGCGTTAACTATCCTTTAAGTTAAACTAAACGCTGATTATATATTTTTTATAAATGCTTTGCTGAACTTCACATTCTGTATGTTTTATTTATTAACAATACAGT
Associated Phenotype:
Not determined