ZMP
zgc:171734
Ensembl ID:
ZFIN ID:
Description:
forkhead box protein R1 [Source:RefSeq peptide;Acc:NP_001096594]
Human Orthologues:
FOXR1, FOXR2
Human Descriptions:
forkhead box R1 [Source:HGNC Symbol;Acc:29980]
forkhead box R2 [Source:HGNC Symbol;Acc:30469]
forkhead box R2 [Source:HGNC Symbol;Acc:30469]
Mouse Orthologues:
Foxr1, Foxr2
Mouse Descriptions:
forkhead box R1 Gene [Source:MGI Symbol;Acc:MGI:2685961]
forkhead box R2 Gene [Source:MGI Symbol;Acc:MGI:3511682]
forkhead box R2 Gene [Source:MGI Symbol;Acc:MGI:3511682]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40575 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30620 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40575
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019561 | Essential Splice Site | 146 | 321 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 60151212)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 58012830 |
GRCz11 | 5 | 58682539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGAATGACAGTGTAGCTAGTCTATAATGCATCCCCACTATGTCACCTC[A/G]GCTGACAGATGAAGATGACGCTTCGTCTGTGGATGTGCCAATCTGCCGGA
Long Flanking Sequence:
ATTATTATTATTAATAATATTATTATTATTATGTGGGGACGTAGTGTCGCAGTGGGTAGCGCTGTCACCTCACAAGGAGGTCGCTGGTTCGAGTTCCGGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCTATGTTCACATGCGTTTCCTCCAGGTTTCCCCCACAAGACCAAAGACATGTTGTATAGGTGAATTGGGTAAGCTAAATTGGCTGTATAGTATATGGGTATTTCCCATTGATGGGTTGCAGCTAGAAGGGCATCCGCTGCGTAAAACATTTGCTGGATAAGTTGGCGGTTCATTCCTCTGTGGCGACCACCGATTAATAAAGGGACTAAGCCGAAAAGAAGAGGGACAACTTAATTGTTTTATGTTCCATTCATTTAAAAGCAGTCAAGCTAACTTAATAGGTTGGTTAAGACAACATAAAGGAATTATGTGGAATGACAGTGTAGCTAGTCTATAATGCATCCCCACTATGTCACCTC[A/G]GCTGACAGATGAAGATGACGCTTCGTCTGTGGATGTGCCAATCTGCCGGAAGGTGAAGGGCACTCGTAAGGGAAGGACCCCGAAGGCAAACACTCGTAGGCTGGGTTTGACTCAGAGCCGACGTCTCCAGAGAGCCCTGCAGGACAGCATGAGCCTGAAGAGCGGCGTCTGGCCTCGACCTCCTGTCAACTACTGCATCCTCATCGCCATGGCCCTCAGCAGCAGCCGCAGCGGCAGTCTCAACGTTCAGCAGATCTACAACTTCACCAGGTCTCCGAGCGCTCCATACACAAACACACACATATGCTTACACATAAACACTAAGCTAAGGGGATTCAACAGAGATTCAGGGTACAGTAGAGTGTGTGTGTGTGTGTGTGAATAATAATTGTAGAAAACCTTTCACGTTTTTTATATTTAAATCATTTATTATATTTGTATTTGAATCAAACAATAATCAAAGTTAAGTTAAATCAATTTATTATTATTTCTAATTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30620
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019561 | Essential Splice Site | 235 | 321 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 60151483)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 58013101 |
GRCz11 | 5 | 58682810 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCCGCAGCGGCAGTCTCAACGTTCAGCAGATCTACAACTTCACCAG[G/A]TCTCCGAGCGCTCCATACACAAACACACACATATGCTTACACATAAACAC
Long Flanking Sequence:
CATCCGCTGCGTAAAACATTTGCTGGATAAGTTGGCGGTTCATTCCTCTGTGGCGACCACCGATTAATAAAGGGACTAAGCCGAAAAGAAGAGGGACAACTTAATTGTTTTATGTTCCATTCATTTAAAAGCAGTCAAGCTAACTTAATAGGTTGGTTAAGACAACATAAAGGAATTATGTGGAATGACAGTGTAGCTAGTCTATAATGCATCCCCACTATGTCACCTCAGCTGACAGATGAAGATGACGCTTCGTCTGTGGATGTGCCAATCTGCCGGAAGGTGAAGGGCACTCGTAAGGGAAGGACCCCGAAGGCAAACACTCGTAGGCTGGGTTTGACTCAGAGCCGACGTCTCCAGAGAGCCCTGCAGGACAGCATGAGCCTGAAGAGCGGCGTCTGGCCTCGACCTCCTGTCAACTACTGCATCCTCATCGCCATGGCCCTCAGCAGCAGCCGCAGCGGCAGTCTCAACGTTCAGCAGATCTACAACTTCACCAG[G/A]TCTCCGAGCGCTCCATACACAAACACACACATATGCTTACACATAAACACTAAGCTAAGGGGATTCAACAGAGATTCAGGGTACAGTAGAGTGTGTGTGTGTGTGTGTGAATAATAATTGTAGAAAACCTTTCACGTTTTTTATATTTAAATCATTTATTATATTTGTATTTGAATCAAACAATAATCAAAGTTAAGTTAAATCAATTTATTATTATTTCTAATTTGTAAAATATGTTGTTGTTGTAGTTTATTCAATTGTTTGTACTTTTATGTATTTTTAAATAATTTGCCATTTAAGCATTTTAATTGGTCCCCCAATTAATATAATATAATATTACAATATTTAATATTTATTATAATGTTTCATATTATAATAAAATAAAAAATAAAAACTCAATCTTTTGAAAAGAATGAAATGTGTACATTATAATTAATAAATTTACTTTAGATTTTACTTTATTAATGTTCTTTTTTATATTTATGTTAATATATTTAATA
Associated Phenotype:
Not determined