ZMP
zgc:112426
Ensembl ID:
ZFIN ID:
Description:
protein FRG1 [Source:RefSeq peptide;Acc:NP_001017793]
Human Orthologues:
AL592183.1, CU459211.2, FRG1, FRG1B
Human Descriptions:
FSHD region gene 1 [Source:HGNC Symbol;Acc:3954]
FSHD region gene 1 family, member B [Source:HGNC Symbol;Acc:15792]
FSHD region gene 1 family, member B [Source:HGNC Symbol;Acc:15792]
Mouse Orthologue:
Frg1
Mouse Description:
FSHD region gene 1 Gene [Source:MGI Symbol;Acc:MGI:893597]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39578 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39578
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 |
---|---|---|---|---|---|
ENSDART00000079001 | Nonsense | 206 | 255 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 15418007)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 15983175 |
GRCz11 | 1 | 16676112 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATATTGCAGATGAAGACCGAGGCGATGTCAAGAACTGCGAGCTCAATTA[T/A]GTGTGAGTGTCTACATTTATTACATTCAGAAGCGCTGCTGTTCATTCAGC
Long Flanking Sequence:
CATTTTGGAAACAAGAGATGGGCCCCTGGTCTAATTCGCCACCTGGCTTGAGAAACCCATTCTCCAAGACTTATTATTTGGGTAGCACACATATTCTGAATGCCTTCTGCAAAATTCAAATGAGCCATTTTAATCTAGATTAATTCCGAGATTAATCTAGATTTTTTTTTTATCTAAAAATATATATACACATATATATAGTTTTAATAATTTTTAATAACTTAATAAGTTTTATATAACTTTAATAAGTTTAATAACTTGACTCTGCTGTAGTGACAAGCAAGTTGAAATTTCCACCACTACAATGTACAGTCTACTTTGTTATGGACGCAAAGCTATAACTGTCAAATGAGAATGTATTATTTTCCTTGGCTATAAACATTGTTTTTCCTGCTTACCTGTCCTGCACAGATCCGTTCATGCACAGAAAGGGAGGTGAAGAGGAAAGATGATATTGCAGATGAAGACCGAGGCGATGTCAAGAACTGCGAGCTCAATTA[T/A]GTGTGAGTGTCTACATTTATTACATTCAGAAGCGCTGCTGTTCATTCAGCATTCAGTCAAGTTCTAATGCTTGCGTCAATGTTTGCATGCAGAAAGAAGTTCCAGAGTTTTCAGGACCGGAAGCTGAGGCTGAATGAGGAAGACAGCGGTTCACTCAAAAAAGCCAGAACAGATGGAAAGTTCCATGAGGCACTGCTGGACAGGTAAAAAACACTTCTGAATTCATACCCTGGTCATACTGAAGAATGAATGACTGTAGCCTGTGTATAATTCAGCTTATTCTCAGATGGATGAAAATACAGAACATTATATTTTATACACCACCTACGTTGTACTGGATGACTTATTTTAGAAGATGTGAGATATGCAAACCCTTATAAATCTTTTGTCATGGCTAGTGATGTATTGATCACGTGCATGTATTGATTGTTGTTGTTTTATTAGGAGGTCAAAGATGAAGGCTGACAGATACTGCAAGTGAAACCAGAAGAAGCACATCA
Associated Phenotype:
Not determined