ZMP
fam92a1
Ensembl ID:
ZFIN ID:
Description:
Protein FAM92A1 [Source:UniProtKB/Swiss-Prot;Acc:Q1LU86]
Human Orthologue:
FAM92A1
Human Description:
family with sequence similarity 92, member A1 [Source:HGNC Symbol;Acc:30452]
Mouse Orthologue:
Fam92a
Mouse Description:
family with sequence similarity 92, member A Gene [Source:MGI Symbol;Acc:MGI:1915349]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32249 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32249
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 |
---|---|---|---|---|---|
ENSDART00000020301 | Essential Splice Site | 262 | 296 | 7 | 8 |
ENSDART00000114714 | Essential Splice Site | 261 | 295 | 8 | 9 |
ENSDART00000134045 | None | None | 162 | None | 4 |
ENSDART00000146559 | Essential Splice Site | 134 | 168 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 34627624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 33675830 |
GRCz11 | 19 | 33262950 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCCTGAATCGAACTGGTACATCAATGAGTAAATCAGGAACAATGCAGG[T/C]AAGTACTTTCTACCAATAACTATTGCAGTGAAAAAGGTGGAAAAAACAAT
Long Flanking Sequence:
CCTCGTTCTTGTCTGAACTTTGCCTGTAACTGGATGTCATAGTCATTTAGTATATTGGCACATGATGACGGGTTTATGAAGACACAGCTAATGCATATAGAGATAGGTTGTAAATTTCCTTCCTGTAATATTTAACTGGAGTTAATAAAGTTGAGGTGACAGTGTTTGTTGGCACACCCTCACCAGGACAGTGTGTGTAAATGTTTTTCCCCCAATCTAAATGACATCTTGCTCTGTTGCTACAACACAGAATGTGCTTAGTTGTGTTGACTCGTTTCTCTTTTTAATGGATTTTGTTTGAGTTTGGCTACTCGTTGTTTATTTAATAGGTTCTTGGTGGTCCGTATGAAGAGCAGTCCTTTTTGTTTTGTCTTGACAGGTATTCAGGAATTCACTGCATCCTCCTGATTACCAGTCACGTTTAGAAATCGTTCGTGCAAATTCTAAACTGTCCCTGAATCGAACTGGTACATCAATGAGTAAATCAGGAACAATGCAGG[T/C]AAGTACTTTCTACCAATAACTATTGCAGTGAAAAAGGTGGAAAAAACAATATAAATAGAGGTTTAATATTAACTAAGGGTGCTTTCACACCTGTGAATCGATTCAGTTGTTCCGAAACAAAGATTACAATTGTTACATTGTTGCTCTTTGCTCTTGGAGCGGTGCGCTTTCACATTGCAAAGTTTCTAATCGGACCAAAAGAGCTAAAACAAGTCACGTGCGAGTAAACTCTACTCACATTGGTCAGAGTGTAAGGGTTTATTTTGCAGCGTCCCGCTAAGCTGTCAGGAGAGGTGGTAGTTTGATTGTGATTGACAGGTTGCGCGCACGATGTGTCTGAGGAGAGATGCGGTGGGGAGGGTTGAGAAGGGTGCGCGACGTAGCCTATTAGAGGACCGGGAGGGAGACGCGAGATTACCGGGAGATCATCACTCGTTTCAGAAGACGAATGCATCAGAAGACTCGCGAAACTTCCCGACATGCTCATAATTCTCTCTTCA
Associated Phenotype:
Not determined