ZMP
lrrfip2
Ensembl ID:
ZFIN ID:
Description:
leucine-rich repeat flightless-interacting protein 2 isoform 2 [Source:RefSeq peptide;Acc:NP_955773
Human Orthologue:
LRRFIP2
Human Description:
leucine rich repeat (in FLII) interacting protein 2 [Source:HGNC Symbol;Acc:6703]
Mouse Orthologue:
Lrrfip2
Mouse Description:
leucine rich repeat (in FLII) interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:1918518]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10914 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10914
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022154 | Essential Splice Site | 209 | 739 | 9 | 26 |
ENSDART00000099729 | None | None | 161 | None | 7 |
ENSDART00000099738 | None | None | 405 | None | 13 |
ENSDART00000133848 | None | None | 131 | None | 6 |
The following transcripts of ENSDARG00000010400 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 43297579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 42518538 |
GRCz11 | 13 | 42644598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTCCATCCAGCAGCAGTTCTGCAGGTCTGACGCGAAGCTATAGTGTGG[T/C]TAGTCTGATTTTCATCACATGTGATTAAACCACACTGATCACATGTAAAG
Long Flanking Sequence:
TCTGGTCAGTGCTGATCAATATTGTGCACTCAAGTGCTGCTTCCTTCTTGATACATCGACTTGATCACATTTATCCTGATTTAGAACATAGTATTTTAGATTTTTGACATTTCTGTCAAATATCTGTGCTCATTTCCATTGCTTTGCACCATTTCCTTAGACTGGACTGTATCACGACCAAAGAAACTACACAAGCTTAAAGAACTCCAAACCTCCTCCTTCTACCGCCTCTACTTATACACCACGGGTTTGTCAGCTTCCTTTCTGAATTATTAATACTAGCTAATTTGAACTTGCTAATTACGATTTGAAATGTGAGAAGTTGATTTGTCTTGGCAAGGTTTTGATTCCAGTGTAGGCTCTTTCCTCGGTTTTAAAATTGGTCATCAGTTTGATTCAGTGGTTTAGTGGCGTTATCTGACAGAAATTGCTTATTGTTTGACCTTCTCAGGCTCCATCCAGCAGCAGTTCTGCAGGTCTGACGCGAAGCTATAGTGTGG[T/C]TAGTCTGATTTTCATCACATGTGATTAAACCACACTGATCACATGTAAAGAACTGTTGTTTAAGCCCCTTTGTCATCTGTTCATTTAAAAATGGCAAGATCTGTATTCGCAGGCTTCCATATGTGACGATGGTCTGTATGGCTCATATAGTTCCAAAGCTGTAAGTAACGCATCAGTATATGCTAAAATAATCAGGGATGCACGATTTTGAATTTGTTGCCTATATCCGATTCGCCATTATTTTATTTTATTAAACTCCTTTTAAATAAAAAAAAAAATTGTTTTATTTGTTTGTTTTATTTTTGAGCAAATATTACAAGTGTCTAGAGCAGGGGTGTGCAAACTTTTTCAAATGAGGGGCAAAAAGCCAAATATTATTAAAAGCTGTGGGCAAATATAAATATACCAAACTATTTTACATTAAAGTTGCCATGGGTAATTTCCTAATTTATTTCATATTAATATTATTTGTAAAAATTAAAAACATTTTTTCATAGTAA
Associated Phenotype:
Not determined