ZMP
si:dkey-26i13.2
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa32612 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6576 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32612
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111041 | Nonsense | 192 | 594 | 5 | 16 |
ENSDART00000134531 | Nonsense | 149 | 648 | 4 | 17 |
The following transcripts of ENSDARG00000074213 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 10874352)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 11006429 |
GRCz11 | 1 | 11693229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATCCAGACTGTCGTGATCAATACAGTGTAATCTATGAGTCGGGAGAG[C/T]GAACCGCCATATTCTCGAATGACCCAAAGGAGCCGATACTGGTGGAAGAG
Long Flanking Sequence:
ACAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTAGTAGTTAAGGCTATTTGATTTAAAGTGAGGCCAACTCTTTTGTCAGCTTTAAAAAATAAGAATGATTTCCTATACAGATATTCATGAATCATGTATCTGTGTGTTTCAGGTACATGAACATCAGTGATCTGTGGGAAACCCCTGAAAAACAGCCATTTAAAGACTTTGTATGTAGTTTTGCATCTGTATTTCTTTATTTTGATAACAATTTATGAATACTTAAAAAACCTAGTTAAAACACATCAGGATATTTTAAACTATTGAAATATGGGTTTATGGCTTGGTATCTGTTTGTTTCAAATGAGAAGCTATTTATGTCTTGGCATTACATCATTTCATTTCCCTTCTCTGTTAACTGCAGGGCAACATGAGGCACTGGCTTGAGGATCCAGACTGTCGTGATCAATACAGTGTAATCTATGAGTCGGGAGAG[C/T]GAACCGCCATATTCTCGAATGACCCAAAGGAGCCGATACTGGTGGAAGAGAGAGCTGTGAGCACATTTACTTGTAAACGGATTTGCTTCAGTGTTATTTTAGTGTTAGAGTTTTGCTTCAGTATTATATAAGCATTTATTTTATGCTATTTCAGTATTTATTCATATTTTAAATTTACTATTAATTTTGTTTTAGCTTATGTTTTTTCGTTTTTGGTTTTCATAGTTCTATTTGGATTGAGCAAAATATAGGGAAATTTAGTTTTCTTTCAATCAAAAAGTATTTACTATCTGCTCCTAAGACATTTCTTAAAGTGTTAAAAATTATTCATAATTTACATTTTACAAATGTGGTAACCTTCTTTTTTCTCATGCCAAAAAAAATGTGTGTGCATGTGTCCATATAATGGCAGTGAATGCACTGATTTGGAAATTTTGTAAAATATCAAAAAGTCTTTACATTTGGAAGCAGACAAATGACATATAGTCTGATAAAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6576
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111041 | Nonsense | 572 | 594 | 16 | 16 |
ENSDART00000134531 | Nonsense | 530 | 648 | 14 | 17 |
The following transcripts of ENSDARG00000074213 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 10881735)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 11013812 |
GRCz11 | 1 | 11700612 |
KASP Assay ID:
554-4742.1 (used for ordering genotyping assays)
KASP Sequence:
ACGCATACTGGCTTTGGACRTTCCAGGGTCGTCTTCTGCAAAAGAACAAC[A/T]AAGATAGATTCTGCCAATTGCTWYGGAGACCACGCCCTCCTACTTTACTC
Long Flanking Sequence:
TTCCGTTTATTTGAAATAGATATGTTTAGTTACATGTTTCTACTGCCACCTTTTATCAATTTAACTGCAACCAATTTTTGCAGTGCCAGTTTAGAAGATTTGGGGACAAAAGTTTTTATTGAATTTTAATAGCGTGGCTCGTATGGATGCTGTTTTTCTTCTTCTGTGCAGTATGAATGGTGCTCTTGCATTTGTGGACACGTCAGATTGTACCATTATGTACATCGCAGAGCATTACATGGCCTCTGATGTAGAATGGGACCCTACAGGCAGATATGTGGTGACTTCTGTTTCCTGGTGGAGCCACAAGGTAATCTGACATTTAATGTCATGTCGGTAAGAAAGTAAACATTTTTTTTTTTTACTTTAAGTAATTTGATAATCTAACACTCCTAATGTTTCATGTTAACTACTATATATGTGCTTTCATTCTACACACACAGGTGGACAACGCATACTGGCTTTGGACATTCCAGGGTCGTCTTCTGCAAAAGAACAAC[A/T]AAGATAGATTCTGCCAATTGCTATGGAGACCACGCCCTCCTACTTTACTCAGTCAAGAGCAAATAAAGGTGACAGCGTTTAATACTGTTCGCATTAGTAATATCATGGTTTTGTATGGTTTTATTCCTTTATTCTACAATGTGTTCATTTTCCAATTTATTTAGCGATTTTTTTTTCTTTGCTTGTAATCATTAGTTTTTGTATAGTGTTTTATATTTTATTAATATTTATTTTATATATTTTCTATATTCTTAATTAAACATTTGCCCTGAAGATCTAAATAAAGTGACAAATATGATGCTACAGTTCAAGTCAGATTTATTAGACCCTCTTTGATTTTTTAAATATATATTTTTTTAATATTTCCCAAATGATGTTTAACAGAGCAAGGAAATCTTCAATGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCGGCTAGAATAAAAGCTGGTTTTAATTTTTTTTAAAACAATTTTAAG
Associated Phenotype:
Not determined