ZMP
si:ch211-89p1.1
Ensembl ID:
ZFIN ID:
Description:
F11 receptor [Source:RefSeq peptide;Acc:NP_001076451]
Human Orthologue:
F11R
Human Description:
F11 receptor [Source:HGNC Symbol;Acc:14685]
Mouse Orthologue:
F11r
Mouse Description:
F11 receptor Gene [Source:MGI Symbol;Acc:MGI:1321398]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa26496 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa26497 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26496
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098315 | Essential Splice Site | 15 | 294 | 1 | 7 |
| ENSDART00000146331 | Essential Splice Site | 15 | 222 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 31458981)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29220338 |
| GRCz11 | 5 | 29820491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAAATGTTGACTTTAGTCTTTGTGTGTCTCTCTTTTTCACTCACAGG[T/G]AAGAGTCCATTTCTTCAGTGGTTGTTTGTTTTTTTTCTTTGTGGATCATA
Long Flanking Sequence:
TCTTTTTTAAAGCAAATAAAAAATTTCAGGCTTCACCAATTCAAACTTGTTTCAACAAATTGTACTCCTGATATTAAACAATATCCTTTCTTCTTTTGTTTTGGCAAAACCAGTATGAATTATAATCTGTAATTAGTTTCCTTCCTGACAGGTCTGTTCCTGTGTCTTATCTTGTGGGCTACTAACCAAGTATGCACATAAAGGCAATGTTTGGACTCCCAAGGTTCATTCTGAGAATGATTTCCAATTATTTGTCTAACCTCAAAACTGTGCTTGCTTTCCTAATGTGCAGTTGGAGCTTCTAACCAGTTTCAGATAAGTTTCTGCTTATCTTCACTCAGTTTTGTGCGGACCTAGCAAATAAACAGCTGCAACACGGTTCTGCTAAAATAATATACTTTCGGGTAACATTTGAAACGCATACCGTAGAAAACCTTCTATCATTTCAGACTGGAAATGTTGACTTTAGTCTTTGTGTGTCTCTCTTTTTCACTCACAGG[T/G]AAGAGTCCATTTCTTCAGTGGTTGTTTGTTTTTTTTCTTTGTGGATCATATTATTTCGTTCAGACAGTTTTCTCATTTTCTTAAATTTTTTTTCTCTTGTAAATTCATGAAAAAATATTGTCTAAAGTTCATACACTGTGAAAAAAAAGCCTTATTTTTGTTTAAACAAATAATACTAACTTAAGACATCAATGCAAAATTTGTGTAAATTAACTTATGTTAAAACCTGATTAACATAATTAAAAAGCTGAAGTAACATAACTCATTGTCAACTTTTTAAATCTTATTTGTAACAGTTCTGTATGGGTGTTGTGTTGTTTTTTGGTATTTATAAAGGGAGCAGAAAGCATCTCTTTGCCCTTGTCATGATTTTTACTTTTAAAAAGTATTAAAATAGCTTATTTAACTCATTTTTTCATATTTTCAGGACATTTTTATTTACAACTATTAATGCAGTTGAATCATTTTTAAAAGTGATTTAAAGAACCTGTATATGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26497
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098315 | Nonsense | 101 | 294 | 4 | 7 |
| ENSDART00000146331 | Nonsense | 101 | 222 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 31460102)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29221459 |
| GRCz11 | 5 | 29821612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGAGGACTGAGATTTCAAAAAGTAACGCGAGCAGACGCTGGAGATTA[T/G]AACTGTGAGGTTTCTGGAAACGGTGGATATGGAGAGAATACCATCAAACT
Long Flanking Sequence:
TATTCATCGTCTTTTCTGTATAGAATAGTAATTTTGTTTGTGTGGTGGTGTTAATATGAGTTTATTGAAGAGCACCTCTGTATTGATCCTCACTCAAGACTTCGGTCATGAGAAACAGTATACTCATTTAACCAAGTGTTTTATTTATCTTATGTTTATCTTGTCAGGAGTTGACTTGCAATGTTCCTACACCGCTGACTTTGGAGCAACACCCAGAGTAGAATGGAAGTTCAGAAATCTGAAGGGCTTTCAGTATTTCATCTACTTTAATAACAAACCAACTGGTATAGATAAAAACTTCCCTGATGTCTTCAAGTATATTTTTTTGTCCGTGCAGTTTCATTCCTTAATTGTGATTTTGTTGATTGGTCTCAAAATTGGAATTGAGAAAAGATGTTTTTTGTTTTTTTTCTCTCCTCAGTTGAATATGAACAGCGCATCACTGTGTACGCTGGAGGACTGAGATTTCAAAAAGTAACGCGAGCAGACGCTGGAGATTA[T/G]AACTGTGAGGTTTCTGGAAACGGTGGATATGGAGAGAATACCATCAAACTTGTAGTCTCTGGTAAATTTGAATTATGTGTGTACATATAAATACAATAGCATTTGAAGTGGATCAAAATCTTCCATCTGATTCTTGTCCTGGGACAACTTTGATGAACTTCAAATGTTGGCAACTCTATAAATACCAGTGTTGGGAAGTTAAGCTATAAGTAGCTCAGCTACTGTCTTAGCTACATTTTCAGTAGCCTGACAGTAGCTCACCTACTTGATGATACAATGTAGCTTTTCCAGTAGCTACTTTTCCAGCAGTTTCCAATTTCCAGCAGCTCTACTTTACAGTGAAGTCTTAAAGATCACATACTACAATAGTAAATAACAGCCATCTATTAGTAAATCACACATCTCATGGTCTCACGTTTATATATCAGTGTTATTTTGCAAAAAATCATATTCAATTTTATAAAGTATTCTAACAGTTGCCATTCAATGTAAAGTTAGAA
Associated Phenotype:
Not determined