ZMP
fxr2
Ensembl ID:
ZFIN ID:
Description:
fragile X mental retardation syndrome-related protein 2 [Source:RefSeq peptide;Acc:NP_956505]
Human Orthologue:
FXR2
Human Description:
fragile X mental retardation, autosomal homolog 2 [Source:HGNC Symbol;Acc:4024]
Mouse Orthologue:
Fxr2
Mouse Description:
fragile X mental retardation, autosomal homolog 2 Gene [Source:MGI Symbol;Acc:MGI:1346074]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11430 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11430
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027718 | Splice Site, Nonsense | 448 | 676 | 12 | 17 |
| ENSDART00000143341 | Splice Site, Nonsense | 448 | 583 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 23906210)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 22467962 |
| GRCz11 | 7 | 22739119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGGAGGAAGAGGACGCGGACGCAAACCGAACAATACATACTCCGGCTA[T/A]GGTGAGACTGGAACTTACACAATGCATATCTGTCTGTGTGTGTTTARTAG
Long Flanking Sequence:
TCTATTATTATCCTTTGTACAATATTGTTAAAGATATTAATAAGATATATAATTTTCCTCTTTATAGCAACTTATATATTTTTTTTAAATAAAGTCAGAATTTAGTGTTTTTTTTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATACAATAACTAAACACAGAATTATATCAGTAATGTTAATGTAATCTTTTGTAAAGGATCTCTATTGCTCTGCATATGCACCTGACAGTAGTTTGTTTCTGTGTGCTGGACAGGAGGTGGAGCAGCTGCGTCTGGAGCGTCTGCAGATCGATGAGCAGCTTCGTCAGATCGGCGTGGGATATCGAGCTCCCCCAAGTCGCTCTGGTTCAGGTGTTGCGGGTGAGCGGGAGCGAGGTTACCTCACAGACGAGAGCACCAACTCCCTGCAGACCACACGCACATATGGAGGAAGAGGACGCGGACGCAAACCGAACAATACATACTCCGGCTA[T/A]GGTGAGACTGGAACTTACACAATGCATATCTGTCTGTGTGTGTTTAATAGAAAGATGCACAACAGACTTAAAGGGATAGTAAGGATAATAATTTAGTCTTAAGTCGTTCAAAATCATTGAGTTCCTTTTTCTGTTGATCAGAGAAGATATTTTTAAGAATGCTGAAAGTAGTTGACATCCATCGTAGAAAATGAATATTAGGGCCATTCTACCAGAAACATACATTATCTGTCCCTGAAATAAAAACATAAATACAGAGTATAAACAGTATTTTCTCCAAAAATGTCTAAAATTAACTGATGGTTGATTTCTGTGAGTTTACATTTACATTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACCACTAAGAGCAACAATGAATAAGTACTAAAGGCAAGTTTCAGGTCTGTAAAGTCTAAGAAGGGAAGTGTTAGTAATTTTTTTTTTTTTTTTT
Associated Phenotype:
Not determined