ZMP
efr3bb
Ensembl ID:
ZFIN ID:
Description:
Protein EFR3 homolog B [Source:UniProtKB/Swiss-Prot;Acc:Q5SPP5]
Human Orthologue:
EFR3B
Human Description:
EFR3 homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:29155]
Mouse Orthologue:
Efr3b
Mouse Description:
EFR3 homolog B (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2444851]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43518 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37134 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43518
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 |
---|---|---|---|---|---|
ENSDART00000100761 | Nonsense | 42 | 816 | 3 | 23 |
ENSDART00000134855 | Nonsense | 42 | 816 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 20 (position 42951348)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43022507 |
GRCz11 | 20 | 42919585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTACAGGATGGCTTGGTCAAGGCCAACATGGAGAAACTGACTTTCTA[T/A]GCCCTGTCAGCTCCAGAGAAGCTGGATCGGATCGGGGCATACCTGTCTGA
Long Flanking Sequence:
CAGGTGTCTGAGGAAGCAAGCCAGAAACCCATCGACTCCCAGTCTTTGCTGAGTTTAACACCATTTTATGTTATTTTCTTAAAAAGCGCCCAGTGGAAAAGCTGAGATTTCTGAAATGTCTCCATTAACTCTCGTTGGTCAGCATTTGAGCTGCGGTAGCTCAGTTCATTAGTCATGTTCAGTGTGGTTTAAAGCCAGCAGGGTTTTGCATTGCAATAATCATCTTCCACATTACAGATTTCCATCAAAATCATCCAGAAATCTTGATGATGCCAGACTTTTGACCAATAATGTACTTCTGCAGTTTCTCAAACATTTTTTATATAGCAAATAGGACTTGCGATACAAGTCATGTCATATTCTAATAACAATATATCCACTCAACAATATATGTAATTCCTAGTCTGCTCTGGTCATGATATTGATACTTGTGTGTGGTGTTGTTTTCTGTGTGTACAGGATGGCTTGGTCAAGGCCAACATGGAGAAACTGACTTTCTA[T/A]GCCCTGTCAGCTCCAGAGAAGCTGGATCGGATCGGGGCATACCTGTCTGAAAGACTGTCCCGTGACGTAGCTAGACATCGATATGGGTACCAAAATTCATAACATGACCGATCTGAATTTTTTTCTTTTCACTCTTGGTATTGAGTTCACTCTTGATACTTCCTGTATTGAGTGTGTGTTTGTCTTTTCAGGTATGTGTGTATTGCGATGGAAGCTCTTGACCAGCTTCTAATGGCCTGCCACTGTCAGAGTATCAACCTGTTTGTAGAGAGTTTTTTAAAGATGGTGCGAAAACTCCTGGAAGCTGACAAACCCAACCTGCAAATCCTAGGAACAAATTCAGTACGTACACACTGTTGTATGTCTACACTAAACTGCATCAATTGTTGCTTTAATTTCCGTAAAATGTAAAAAAAAAAAAAAATTTAAATGTACTTTCTCTCAGTATTCAGTGGTTCCATAACTTTGATTTTCCTTAGAAGTTATTTTGAAGAATGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37134
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 |
---|---|---|---|---|---|
ENSDART00000100761 | Nonsense | 72 | 816 | 4 | 23 |
ENSDART00000134855 | Nonsense | 72 | 816 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 20 (position 42951543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 43022702 |
GRCz11 | 20 | 42919780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCACTCTTGATACTTCCTGTATTGAGTGTGTGTTTGTCTTTTCAGGTA[T/A]GTGTGTATTGCGATGGAAGCTCTTGACCAGCTTCTAATGGCCTGCCACTG
Long Flanking Sequence:
CAGCAGGGTTTTGCATTGCAATAATCATCTTCCACATTACAGATTTCCATCAAAATCATCCAGAAATCTTGATGATGCCAGACTTTTGACCAATAATGTACTTCTGCAGTTTCTCAAACATTTTTTATATAGCAAATAGGACTTGCGATACAAGTCATGTCATATTCTAATAACAATATATCCACTCAACAATATATGTAATTCCTAGTCTGCTCTGGTCATGATATTGATACTTGTGTGTGGTGTTGTTTTCTGTGTGTACAGGATGGCTTGGTCAAGGCCAACATGGAGAAACTGACTTTCTATGCCCTGTCAGCTCCAGAGAAGCTGGATCGGATCGGGGCATACCTGTCTGAAAGACTGTCCCGTGACGTAGCTAGACATCGATATGGGTACCAAAATTCATAACATGACCGATCTGAATTTTTTTCTTTTCACTCTTGGTATTGAGTTCACTCTTGATACTTCCTGTATTGAGTGTGTGTTTGTCTTTTCAGGTA[T/A]GTGTGTATTGCGATGGAAGCTCTTGACCAGCTTCTAATGGCCTGCCACTGTCAGAGTATCAACCTGTTTGTAGAGAGTTTTTTAAAGATGGTGCGAAAACTCCTGGAAGCTGACAAACCCAACCTGCAAATCCTAGGAACAAATTCAGTACGTACACACTGTTGTATGTCTACACTAAACTGCATCAATTGTTGCTTTAATTTCCGTAAAATGTAAAAAAAAAAAAAAATTTAAATGTACTTTCTCTCAGTATTCAGTGGTTCCATAACTTTGATTTTCCTTAGAAGTTATTTTGAAGAATGATACAAACCTGTAACCATTGACATCTATAGTATTTGTGTTTCCTACTACACTTCCTGACAAAATTCTTGTCAGTGATCTCAGTTATAGTAACAACTAATAATAACTTGACTTCTAGTTAATCATTAGAAGAAGTGGCACAAGATAATTGGGACTGCATGCCAATCAACACACATACTGCAGAAAACCTACTGGAACCC
Associated Phenotype:
Not determined