ZMP
eif3jb
Ensembl ID:
ZFIN ID:
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]
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.
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
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.
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