Busch Lab

ZMP

eif3jb

Ensembl ID:
ENSDARG00000053370
ZFIN ID:
ZDB-GENE-040426-2900
Description:
Eukaryotic translation initiation factor 3 subunit J-B [Source:UniProtKB/Swiss-Prot;Acc:Q803P1]
Human Orthologue:
EIF3J
Human Description:
eukaryotic translation initiation factor 3, subunit J [Source:HGNC Symbol;Acc:3270]
Mouse Orthologues:
Eif3j, Gm9781
Mouse Descriptions:
eukaryotic translation initiation factor 3, subunit J Gene [Source:MGI Symbol;Acc:MGI:1925905]
predicted gene 9781 Gene [Source:MGI Symbol;Acc:MGI:3704486]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa40927 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38619 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40927
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075400 Essential Splice Site 130 264 None 8

The following transcripts of ENSDARG00000053370 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 32763256)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 31157596
GRCz11 7 31428746
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATATATATATATGTATAAAGTTAATCGATGAATTTCTTCCCGTCTTT[A/G]GGTGTGGATCCTGCTGCTGCAAATGCCTCAACTACTGTTAACACAACAAA
Long Flanking Sequence:
TCGATACAGACGAACACAACATAACCTACTGCCAGCTAGCGTTCCGGACATGTTATTGCAGAGCAACACAAACACGCAGAAGTATAAATGCACGACTGCGCACAAGATATGTGCCGTGGTTCACAGCGATCACTCAACGCAGAAGTATAAACCAGCCTGTAGTTTTTAAGCATTAATTCTTAATCTTCTAATTTTACAACCATGTATTATTTATGAAATGAATAGAATCAGGAAACAGCAGCTAGTGAGAGTCTGACGTTAGAGGAGCAGCTAGCAGAAAAAGCTAGACTGAAAAAGCTGCAGGAGGAGGCAGACATGGAATTGGCCCGTGAGGCTTTTGGTAAGAAACAGCACTTTGGTGAAGTCTTCCAATTTCTTCATATGTATATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATAAAGTTAATCGATGAATTTCTTCCCGTCTTT[A/G]GGTGTGGATCCTGCTGCTGCAAATGCCTCAACTACTGTTAACACAACAAACGCCTCTGGAATTGAAGCCATGTGCCCGTCATCCAAAGATGACTTTGTTACATTTGAAAAATTACTGAAAGAAAAGATAACACAGTTTGAAAAATCTGTGCATTATTCAAGCTTTTTGGAATCATTGTTTCGAGAACTTTGTATTTCATGTAAGTGCAGAAGGTTTTATGAATATGTAGTTATTTTGTTAGCACTCAGTTTTTTCAATTCTTATTAACATTTTTTTAAAGGGACCTATTATGCCTGTTTTTACAAGATGTAAAGTAAGTGTATGATGTCCCTAAAGTGTGCATGTGAAGTTTTCACTCGAAATTCCCCACAAATATTTTCTATAACTCTTTGAAACTGCACCTTTTAGGCTTTGAACCAAAATTATGCTATTGTGGCGACTAAATTCAAATGAGATTGTGCCCGTTTCAAAATAGGGCAGAGCTACAAACATCTGTTCAA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa8271
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075400 Nonsense 139 264 6 8

The following transcripts of ENSDARG00000053370 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 32763285)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 31157625
GRCz11 7 31428775
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGAATTTCTTCCYGTCTTTAGGTGTGGATCCTGCTGCTGCAAATGCCT[C/A]AACTACTGTTAACACAACAAAYGCCTCTGGAATTGAAGCCATGTGCCCKT
Long Flanking Sequence:
TGCCAGCTAGCGTTCCGGACATGTTATTGCAGAGCAACACAAACACGCAGAAGTATAAATGCACGACTGCGCACAAGATATGTGCCGTGGTTCACAGCGATCACTCAACGCAGAAGTATAAACCAGCCTGTAGTTTTTAAGCATTAATTCTTAATCTTCTAATTTTACAACCATGTATTATTTATGAAATGAATAGAATCAGGAAACAGCAGCTAGTGAGAGTCTGACGTTAGAGGAGCAGCTAGCAGAAAAAGCTAGACTGAAAAAGCTGCAGGAGGAGGCAGACATGGAATTGGCCCGTGAGGCTTTTGGTAAGAAACAGCACTTTGGTGAAGTCTTCCAATTTCTTCATATGTATATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATAAAGTTAATCGATGAATTTCTTCCCGTCTTTAGGTGTGGATCCTGCTGCTGCAAATGCCT[C/A]AACTACTGTTAACACAACAAACGCCTCTGGAATTGAAGCCATGTGCCCGTCATCCAAAGATGACTTTGTTACATTTGAAAAATTACTGAAAGAAAAGATAACACAGTTTGAAAAATCTGTGCATTATTCAAGCTTTTTGGAATCATTGTTTCGAGAACTTTGTATTTCATGTAAGTGCAGAAGGTTTTATGAATATGTAGTTATTTTGTTAGCACTCAGTTTTTTCAATTCTTATTAACATTTTTTTAAAGGGACCTATTATGCCTGTTTTTACAAGATGTAAAGTAAGTGTATGATGTCCCTAAAGTGTGCATGTGAAGTTTTCACTCGAAATTCCCCACAAATATTTTCTATAACTCTTTGAAACTGCACCTTTTAGGCTTTGAACCAAAATTATGCTATTGTGGCGACTAAATTCAAATGAGATTGTGCCCGTTTCAAAATAGGGCAGAGCTACAAACATCTGTTCAAAAACAGGATGGACGTTATTTCTATAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38619
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075400 Nonsense 260 264 8 8

The following transcripts of ENSDARG00000053370 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 32765684)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 31160024
GRCz11 7 31431174
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGACTTTGCTGACTATGGTGGTTTTGACGGTGGTTACGGCAATGAATA[T/A]GATGACTTCATGTGACAAAGGATCATCGTTCCCCTTCCCATTCCCTCTGT
Long Flanking Sequence:
AATAGGTCCCCTTTAATGAATTACCGATTTGTTTCTCCCAGCTGTTAGATTATGTATTGGATTGCTTAAACACAAATACGCACACATGTATGAAGGCTTGTAATTCTGTTCTCTATTTTTGTTGTTTTTTGTATAGTGGAAGTAGACGACCTGAAGAAAATATCTACTTCTTTATCAGTTCTGCTCACTGAAAAACAGAAGCAAGAAAAGGTGAGATAATTGTAGTCTTTTAAGTGGAAATGCCTTTGTTATTATTCAGTCAATGACCATATATGCATTTACCACTACTTAACTCATTGTTTTATTACAGTTTTGATGTTTATTATTATCAAAATGTGAACAGATTTTTTTTTTGATTTGTTGCTGTTGTGTAATTCATAGGAAAAGAAGGCAAATAAGAAAAAGAAAAAAGGTGTTGTACCTGGTGGTGGATTGAAAGCAAACATGAAAGATGACTTTGCTGACTATGGTGGTTTTGACGGTGGTTACGGCAATGAATA[T/A]GATGACTTCATGTGACAAAGGATCATCGTTCCCCTTCCCATTCCCTCTGTGCTCAGACAGCTCTGCAGACATGCAACATTACCCTTTTCATGCTACTTGTTGCCATCTTGAAAACTGAACAATGTGTCAACCCTTTTCAGTGGTGACAGACTCCTCATAAAGCTGCTATCAGCCCTTTGCACCCCAGTGACAAATGGGGAGAAGCAAATTTATTCAGATGGCCTTGAATTTAAAATGGACTGTATGATGTGGGACATTTTTGATGGAGGAATTTGCTGATTGGCCTAAATACGAATTTCAATGCCTTATAGAGAACTTTGTAGATTTTTTTTTCCTCCCTTTACTTTGTTTTTAAAGCTGTGCAATTCCAGTTTCACAAAAGTAAATATGATTCTCTATGCAAATTAATTTCTTCCAAGAAAGATTGGTTGTATTTTCTTGCATATTTTAGCACAATTCGATAAAAGTTGAAAATAAAGAATCTAAATTTAATGATAAGA
Associated Phenotype:
Not determined