ZMP
slc27a2
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 27 (fatty acid transporter), member 2 [Source:RefSeq peptide;Acc:NP_001020470
Human Orthologues:
SLC27A2, SLC27A5
Human Descriptions:
solute carrier family 27 (fatty acid transporter), member 2 [Source:HGNC Symbol;Acc:10996]
solute carrier family 27 (fatty acid transporter), member 5 [Source:HGNC Symbol;Acc:10999]
solute carrier family 27 (fatty acid transporter), member 5 [Source:HGNC Symbol;Acc:10999]
Mouse Orthologues:
Slc27a2, Slc27a5
Mouse Descriptions:
solute carrier family 27 (fatty acid transporter), member 2 Gene [Source:MGI Symbol;Acc:MGI:1347099]
solute carrier family 27 (fatty acid transporter), member 5 Gene [Source:MGI Symbol;Acc:MGI:1347100]
solute carrier family 27 (fatty acid transporter), member 5 Gene [Source:MGI Symbol;Acc:MGI:1347100]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23199 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23199
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052638 | Nonsense | 537 | 614 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 18 (position 233566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 72346 |
GRCz11 | 18 | 72346 |
KASP Assay ID:
2261-1672.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGCGCTGCAGCTGACAGACGGGATGGAGTTTGACGGTTCTGCTGCTTA[T/A]GAACACATGAAGAACCTCCTGCCGGCGTACGCCAGACCGCGCTTCATCAG
Long Flanking Sequence:
CTGTAAATGTACTTCAAGCTTTCAGACTGGACTCTCTCACGCCACCATGAGGTCCGTCTGTGAACTGCACTGCTCTAGTTCTAGTTCCAGATCTTCATCTATCAGCTGATCAGTATTCTCCATGGTGTGATCAATAGTCTCCAGGATCGTGCTGATCTGTGATGCTCTTGTGAGTGAGGGCTGCTCTTCATCCGTGGCGTCTGGAGCTCTGATGTTCTCTGGATTCTGATTGGCCGTCAGTGTTCTCTGGGAAACTCCTCTGTGTGTGTGTGTATGGCTGTAGTTGTGCTGTTCTCGAACACCGACACACATCTACAGCTAGATCTTTATCACGGGGATCCTGCTCTGTGTGAACGGCCTTTAGGGTCAGCGTGATCTGGCTCAGGGGTCAGAGGTCAGGCTCAGGTGTTTCTGCTCTTCTTCTCAGGTCATGAGGGTCGTGTGGGGATGGCGGCGCTGCAGCTGACAGACGGGATGGAGTTTGACGGTTCTGCTGCTTA[T/A]GAACACATGAAGAACCTCCTGCCGGCGTACGCCAGACCGCGCTTCATCAGGATACAGGTACAGCTCTGACCCACACGTGCCCAGCGGCTGACCATGACCAGTGTTGGGGGCCGCATTACAGGTGACGCGAGGCGCTGGACACTCTCATACATCTGTACATACGCCATGTAGAGCTCTGCATCACCATCCATTCTCCTTCAGCTCAGCCCCTTTATTCATCAGGGACCGCCACAGCGCCATGAACCACCAACTATTCTAGCATATGATTTACACAGTGGATGCTCTTCCAGCTGAAGACCAGTACTGGGAAACACCCATACACACTCATTCACACACACACACACACACACACACACACACACACACACACACACACTCATACACTACGGCCAGTGTAGTTGATCAGTTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCCAACACGGGGAGAACATGCAAACTCCACACA
Associated Phenotype:
Not determined