ZMP
si:ch211-153j24.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate FOS-like antigen 2 protein (FOSL2) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
FOS
Human Description:
FBJ murine osteosarcoma viral oncogene homolog [Source:HGNC Symbol;Acc:3796]
Mouse Orthologue:
Fos
Mouse Description:
FBJ osteosarcoma oncogene Gene [Source:MGI Symbol;Acc:MGI:95574]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37154 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43527 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37154
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 |
---|---|---|---|---|---|
ENSDART00000098968 | Nonsense | 33 | 135 | 1 | 6 |
ENSDART00000122115 | Nonsense | 75 | 312 | 2 | 4 |
ENSDART00000134163 | Nonsense | 42 | 101 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 46811798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 46657081 |
GRCz11 | 20 | 46560801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAGTGGATGGTCCTGTCGACTGACATCTCTTCAGTGTCACCCTGCAGA[C/T]AGCAGAAAACACAGAGCTCATCTCACTCCACAGATGCCAAAGCTGCTCGA
Long Flanking Sequence:
CCTCAGTCTAGAGATTTATTTTTTCCTGCCTTCCTCCAAAAGCCTGCATTTGTTGACATTGCTCATATATTAATTCGGTTTCCAGCATTTTCCTGGCGCGACCTACAGTAGCATTAGTGATGCCAAAAAACGCGAGTGTTTCTGCAGAACAGCTGCTGCACACATCAGCTGCTGGGATGAAGGATACGCAGGTACCACCAGACTGCACATTTACCTGGAATGGGGATTATTTCATTGAGCTGTGGGATTAGTGATGCATGTTGTCTAATATTTCTGTACAGTCAGACACATGTCAGTTGTGTTCATATGTAGTTTTGTTCTGAATGCTCATATGTGGTGGTGGTGGTGGTGGTGAACACATCTCTTCTCTTTCTCAGAAGGCAGGTGTTTTGAAGGATGCTGATGCTGCCTTTGTTCCTACGGTCACTGCTGTTGCTTCAGCTCCAGATCTCAAGTGGATGGTCCTGTCGACTGACATCTCTTCAGTGTCACCCTGCAGA[C/T]AGCAGAAAACACAGAGCTCATCTCACTCCACAGATGCCAAAGCTGCTCGAAAGACCTTCACTGGCAGGAGAAAGGGGGCAAAGGATCAGGTAAACACTTACTTCATCGGATGATTTATGTATATATATATACAAGGCAGAATTATTAGCCCCCCCTGAATTATTAGACCGCTTGTTTATTTTTTTCCCCAATTTCTGTTTAATAGAAAGCAGATTTTTTTTTTAAACACATTTCTAAGCATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGTCATGATGACAGTAAAAAATATTTGACAAGATATTTTTCACGACACTTCTATACAGCTTGAAGAGACATTTAAAGGTTTAACTAGGTTAATTAGGTTAACTAGGTAGGTTAGGGTAATTGGGTAAGTTATTGTATAACAATGGTTTGTTCTGTAGACTATCGAGGAAAAAAATAGCTTAAAGGAGCTAAAATTTTATTCCTAAAATGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43527
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 |
---|---|---|---|---|---|
ENSDART00000098968 | Nonsense | 34 | 135 | 1 | 6 |
ENSDART00000122115 | Nonsense | 76 | 312 | 2 | 4 |
ENSDART00000134163 | Nonsense | 43 | 101 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 46811801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 46657084 |
GRCz11 | 20 | 46560804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGATGGTCCTGTCGACTGACATCTCTTCAGTGTCACCCTGCAGACAG[C/T]AGAAAACACAGAGCTCATCTCACTCCACAGATGCCAAAGCTGCTCGAAAG
Long Flanking Sequence:
CAGTCTAGAGATTTATTTTTTCCTGCCTTCCTCCAAAAGCCTGCATTTGTTGACATTGCTCATATATTAATTCGGTTTCCAGCATTTTCCTGGCGCGACCTACAGTAGCATTAGTGATGCCAAAAAACGCGAGTGTTTCTGCAGAACAGCTGCTGCACACATCAGCTGCTGGGATGAAGGATACGCAGGTACCACCAGACTGCACATTTACCTGGAATGGGGATTATTTCATTGAGCTGTGGGATTAGTGATGCATGTTGTCTAATATTTCTGTACAGTCAGACACATGTCAGTTGTGTTCATATGTAGTTTTGTTCTGAATGCTCATATGTGGTGGTGGTGGTGGTGGTGAACACATCTCTTCTCTTTCTCAGAAGGCAGGTGTTTTGAAGGATGCTGATGCTGCCTTTGTTCCTACGGTCACTGCTGTTGCTTCAGCTCCAGATCTCAAGTGGATGGTCCTGTCGACTGACATCTCTTCAGTGTCACCCTGCAGACAG[C/T]AGAAAACACAGAGCTCATCTCACTCCACAGATGCCAAAGCTGCTCGAAAGACCTTCACTGGCAGGAGAAAGGGGGCAAAGGATCAGGTAAACACTTACTTCATCGGATGATTTATGTATATATATATACAAGGCAGAATTATTAGCCCCCCCTGAATTATTAGACCGCTTGTTTATTTTTTTCCCCAATTTCTGTTTAATAGAAAGCAGATTTTTTTTTTAAACACATTTCTAAGCATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGTCATGATGACAGTAAAAAATATTTGACAAGATATTTTTCACGACACTTCTATACAGCTTGAAGAGACATTTAAAGGTTTAACTAGGTTAATTAGGTTAACTAGGTAGGTTAGGGTAATTGGGTAAGTTATTGTATAACAATGGTTTGTTCTGTAGACTATCGAGGAAAAAAATAGCTTAAAGGAGCTAAAATTTTATTCCTAAAATGTTTTTTTT
Associated Phenotype:
Not determined