Busch Lab

ZMP

eif3b

Ensembl ID:
ENSDARG00000059654
ZFIN ID:
ZDB-GENE-030131-2748
Human Orthologue:
EIF3B
Human Description:
eukaryotic translation initiation factor 3, subunit B [Source:HGNC Symbol;Acc:3280]
Mouse Orthologue:
Eif3b
Mouse Description:
eukaryotic translation initiation factor 3, subunit B Gene [Source:MGI Symbol;Acc:MGI:106478]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa40138 Nonsense Mutation detected in F1 DNA Not yet available
sa16634 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa40138
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083129 Nonsense 122 683 3 18
Genomic Location (Zv9):
Chromosome 3 (position 41711689)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 41575049
GRCz11 3 41716907
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTCTGCACCAAGTCACGCTCATGAAGCGGTCAAAAACGCTGATGGCTA[C/A]AAGCTGGACAAGCAGCACACCTTCCGTGTCAATCTGTTCACTGACTTTGA
Long Flanking Sequence:
TTTGACATTACAAGTACTACTGTGTGTGACTAAAAGGCTTAAATGTATTGGTGGTTTAACCATTACAGAAAAAAAGAGGGCAGCTGTGGCACAAACCTTACATTTTTTTTTATGGTCTAATAAAATGAGTTTAGCACAAACTATCTGTATTAGTTTTTAGGTTTCTGTTAAGGTTTTAAAGTGTATATGTGTACTAGTTATTAATGGCATGTTTGCAATGTTGTATATGTTTTCTATGGATTATAGGACGTATTGACAGATCGCACTATTATGTCTTCTTTTTCATTCTTTTAAAACCTATTTATTCTTTGTTGATTTTATTTTCTTATACTTTTATTCCTGTTTATGTAAAACACTTTGAATAACCACTGAGTATAAAATGTGCTATAGATATAAACTTGTCTATAATAATTTTCCATGCTTTATCATTACAGGTACATTTTCCTAGAGTATTCTGCACCAAGTCACGCTCATGAAGCGGTCAAAAACGCTGATGGCTA[C/A]AAGCTGGACAAGCAGCACACCTTCCGTGTCAATCTGTTCACTGACTTTGACAAGTAAGTTATCTTTTAGGGTCTGCAGTAGTGTACTGCAATAGGTTGCTTTAATGAAAGAACCTTTACAGTGTTGTATAATTTATACTCAGTATTGTCTATCATTTCCAGAATGCATTTTGGCAAGCTGTTTCTAATGCCTCAAACTTCATTTAGGGCAGATCAGTTCGTCTCTCAATTTAGCTTGAAATATATCAGGGCTGTGCAGATGCTGATATCAGTATTAAAAAAATCTATTAATATTTAATAGATTAATATTAAAATGTAATTTTTTGATAACTTTTGGGATATTTTACCCCAATTGTCGCCTTTCTTTTGCTTTAAGCAAATATTTCAGCTTCTTTCTTCTGATGAACAAAAATGAAGATATATTGCAAAAAGCTGAAAACTGGTAGTCATTGACTTGTATTTTTGTTTCACTATGGTAGGCATTGGCTACCATTATCCAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16634
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083129 Nonsense 179 683 5 18
Genomic Location (Zv9):
Chromosome 3 (position 41713779)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 41577139
GRCz11 3 41718997
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCCACTGGATGGAGGATCCTGAYTGTCGTGATCAGTACAGYGTWATCTA[T/G]GACTCTGGTGAAAGAAYGGGCATATTCGCCAATGATGTCAAGGAGCCTAT
Long Flanking Sequence:
CATCGTTCTTTTCCCAAAGGATGCATCGTACTATGATAGTTCAGCTGCGAGTTACGTCGTTGTTTGGGAAACGCACCCCTGACCGATGGTGCATTGTCATTTGGGATTCCTGCCTGATATCTTGTGATGTGACTTGCAGATGCACACATTGTGATGCTGCAGCCCTACATACTTTGCTATACATGCAAAAATGTGGCACATACAATAACATGGAAGAGAAAAATCAGGTGATGCATTAGTAATCAACTGATCACTAATCTAAAGTCTTTTGTCCACATAGGTACATGTCAATCTGTGATGAGTGGGAAGCTCCTGAAAAGCAGCCATTTAAAGATTTTGTGAGTTTAATAATATTTTTGATTGTCATTGTTGTCATAACCTACTGAAAATCTTTTATTACAAAAAATAAATGAATGTTAACATTTGGTGTTTCTCTTTCAGGGTAATCTGCGCCACTGGATGGAGGATCCTGACTGTCGTGATCAGTACAGCGTTATCTA[T/G]GACTCTGGTGAAAGAACGGGCATATTCGCCAATGATGTCAAGGAGCCTATTGAAGTGGAGGAGAGAGCGGTGAGTTAAGTGTAATGTTATAGAAGACTATCATTCATCTGTAAGAATATATAGATATTGTGGACGTGCATGCTCTGACAATCAGTATTTTTCGTTGTATCTTACTTGTAGCGCTGGACTGAGACATACGTGCGCTGGTCTCCGAAAGGCACATATCTGGCTACATTCCATCAGAGAGGCATCGCTCTGTGGGGTGGGGAGAAGTTCAAGCAGATCCAGAGGTTCAGTCATCAGGGGGTTCAGCTCATTGACTTCTCTCCCTGTGAGAGGTATGTCATGTTCTCCTGTTTAGAAATGGCCTCATGTTTGTATTTTAACACATTTTGCTCCTTGATTTAGACTCAAATAAACATTCCATATGTTTTTGTTTCTATACTGTACGTACTATCACCCTATCCTCAACCCAAACCTCACAGGAAACAATTTTACTT
Associated Phenotype:
Not determined