ZMP
fosb
Ensembl ID:
ZFIN ID:
Description:
protein fosB [Source:RefSeq peptide;Acc:NP_001007313]
Human Orthologue:
FOSB
Human Description:
FBJ murine osteosarcoma viral oncogene homolog B [Source:HGNC Symbol;Acc:3797]
Mouse Orthologue:
Fosb
Mouse Description:
FBJ osteosarcoma oncogene B Gene [Source:MGI Symbol;Acc:MGI:95575]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9219 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43149 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9219
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 |
---|---|---|---|---|---|
ENSDART00000078151 | Nonsense | 162 | 234 | 2 | 3 |
ENSDART00000130206 | Nonsense | 183 | 352 | 3 | 6 |
ENSDART00000133487 | Nonsense | 183 | 411 | 3 | 5 |
ENSDART00000136463 | Nonsense | 183 | 198 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 35112281)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 36791437 |
GRCz11 | 18 | 36772445 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGTTTCACCCCACCGAGCTCTGAYACTCCTGGCYCAGTGCGTCAGTCT[C/T]GAAGCCGCCGCCGTGCACGAGATGAAACGGTGAGTGGGACCCATTCATGA
Long Flanking Sequence:
TAACAGTATATTAAAAATGTTATGTTAGAAAAATTATATTGTCCAGTTTAGTTCACAATATGTTAACTTACGTTTATTACTGTTTATTTAATTTCTGGTAAAATAACTGTAAAATATTTTGGTGTTTTATTTGAATTATAATCACTCTGAATACAGTGTGATTTTGAAGGCCATGGCTTCATACGGTGTATGTTTTTGGTTCCTAGGAGTGTGTAACAGCCACTGGCGGGGTAGGGGTGGGTGGAGGGTCAACCGGGGCAGGGGTGGACATGCCCAGCTCATTTGTGCCAACAGTGACGGCCATCACCACAAGCCAGGATCTGCAGTGGATGGTGCAGCCCACTCTAATATCCTCTGTGGCACCAGGTCAAAGTGGCACGGGCTCCAGCACCATGACGCAGCCTGTTGCATTGGATCCTTACGACTTGCCGGGCCCAAGCTTTTCGTCCGGTGGTTTCACCCCACCGAGCTCTGATACTCCTGGCCCAGTGCGTCAGTCT[C/T]GAAGCCGCCGCCGTGCACGAGATGAAACGGTGAGTGGGACCCATTCATGATTTGGTTAAAAAATTTCTATACAAACTGCAAGAAATAAGGCTTAATGTGATACTAAATTTGTTGTGTTCCCAGCTGACCCCCGAGGAAGAGGAGAAAAGACGTGTTAGAAGAGAGAGAAATAAACTGGCTGCCGCTAAGTGTAGGAACCGACGGCGTGAGCTCACAGACAGGTTACAGTCGGTGAGCGATGCTGTACTCATATTTAAAAACACAAAAATCCAATACAGTATTTTATATATGGTATCAGACAAATACAGGGCCTAAAATGAACATTTTGCTGCACCTGCCAATGGACGGTGACATAAGGAAAATTTATTAGCTAGAATTTAATCTGCATTAAAATTGTTTTTTGCACTTGGAAATTTAATAATAATAAAAAAAAACAAATACAAATTAGGGGCGGTAGTATTCATACATTATATTCATTTAAAAAAATAATAATTAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43149
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078151 | None | None | 234 | None | 3 |
ENSDART00000130206 | Nonsense | 252 | 352 | 5 | 6 |
ENSDART00000133487 | Nonsense | 252 | 411 | 5 | 5 |
ENSDART00000136463 | None | None | 198 | None | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 35114085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 36793241 |
GRCz11 | 18 | 36774249 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGAAGGCCGAGCTAGAGGCTGAAATATCCGAGCTGCAGAAGGAGAAA[G/T]AGCGCCTGGAGTTTGTCCTGGTCGCCCACCAACCTGGTTGCAAACTTCCC
Long Flanking Sequence:
CCAGCTGGTGGGTAACATTGTTTCATCAACTCACCAGCATCGATTTTTACTCACATTTGGGGGGATTTACTCAAAATGGCGAATGCTATTTTTAGGCCCTGGATGAATGCAAAAGCATCATAATTACAGGATTCGTAACATGCCAATCCGCTCATAACAATCATTTTTTACAATTACAGTTTGTAAATGATACCAACACACATACACATCAGGCTCCATTGTAATTAGAAAGGGCTAGTTTGAACAAAGAGTCAATAAACCCACCGTAATTATCTAGTGGCAACAGACTCAAGCAAGTTTATTTGGTTGTTGCTATCTAAAACTAGCAGCATGTAGTGAATGCTAAACGGAAACCCTTGCTTTTGTCCTAATTTTATGTGATCATAAAATCTCTGTCCCCTTGTGTCCTCCTCTTGTCTCTCCAACCCAAGGAGACAGACATTTTGGAGGAGGAGAAGGCCGAGCTAGAGGCTGAAATATCCGAGCTGCAGAAGGAGAAA[G/T]AGCGCCTGGAGTTTGTCCTGGTCGCCCACCAACCTGGTTGCAAACTTCCCTACCAGGACCAGCCCCCTGCTCCGCTGCCGCAGACGTCCCCACAGGCGCCTTCTGTCTCCGTGGTGGGTTTAACTGTGAAGGAGGACTCTTTCTACCTGCCGCCGGCCTACTCATCCCACCACCACCACCACGTCCCGGTTTCACAGCCCACGCAGACACAGCCGGCACCAGCGCAACAGCAGCAAGGGATGATGCAGGAGGTAGCCTTTTCTAGTTCTTTCTATGGGCCGGGCCAGCCGGCGCCGGACGGCCCGTGCCTTGTTGCCGACGGTGGCGGTAACCCTGACGCCGGCAGCTACATCCCCTCATACACATCTTCATTTGTGTTCACCTACCCAGAGGGAGCCTGCGGGGCCAGCGCTAACCAGCGAACCAGCAGCAGCGATCAGTCCTCTGATTCCCTGAACTCACCCTCGCTTCTTGCACTTTGAGAGCTCTGCTGATCTCTC
Associated Phenotype:
Not determined