ZMP
LOC100007221
Ensembl ID:
Human Orthologue:
SLC46A2
Human Description:
solute carrier family 46, member 2 [Source:HGNC Symbol;Acc:16055]
Mouse Orthologue:
Slc46a2
Mouse Description:
solute carrier family 46, member 2 Gene [Source:MGI Symbol;Acc:MGI:1353616]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18145 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18145
Status:
Available for shipment
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For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060226 | Essential Splice Site | 277 | 356 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 14537012)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 14238308 |
GRCz11 | 11 | 14295967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGATGGCAATCATGGCATTCRCAATGGAAAGCTGGATYTATTTCCTGG[G/A]TGAGTTGATCTTAAGWTAATTRAAAGTCTYTTTTAKGTGTTCTGGGTGAT
Long Flanking Sequence:
CTGTTTTGGGATCGCAGGGGTTGTGGGAGGTCTGCTTTCTGGATATCTGTACCAAGTAGGACCATCAGTTCTCCTCCTGACAGCCATTTTGATCACCGCTGTTGCACTATTGTACTCTGTGTTCGCCCTCTCTGATTCAAGATTGTCTTTGCCTTATTCTGAGGGTGAGCCGCTTCTGCCAGAATCTGAAAGTGGGAAGACAATGGATCGAGTTTCTTTAGGGTTGCTAATGACATCCATGATGTTGTTCATGCTAGGAATGGTCGGAGCAGAAAATGTGCTCCAGCTGTTTGTGCTGAAGCCTCCTCTGAGCTGGGACTCAGTGTGGGCAGGATATGGCAGGGCCGCCACCAGCGCCATGTACCTCAGTAGTTTTTTAGCAGTCCTAAGTTTGTTCAATGTGATGGGGGACACAGCCCTTACACTTCTTGGTATTGTGTCCAACTGCACTGGGATGGCAATCATGGCATTCGCAATGGAAAGCTGGATCTATTTCCTGG[G/A]TGAGTTGATCTTAAGATAATTAAAAGTCTTTTTTATGTGTTCTGGGTGATATACATTGGAACATCACAGCTTGCAATACATGGATAAGTGTCCTAGAACAGGGGGTTTCAACAGAGGTGTTTGAAACCTTGGTAAACTCCTGAAGAACTTAACTTAAGTTTAAATAAATAAGAAAAAAAAAGCTAAATATAAGGTTTGTGTACTATTTAAGTTATCATTGTCTTAAAAATTTGGATATAGACTATTTCAATGTGGCAATATCATTGGCCCATGAACATTTCCTACTTGCTGTCAAACTATTTCGTAACTGTAACAAGATGTAATTGAATCATATCTTAACATTAAAACAGCTGTCATAACATTATCTAGCAATATGTGGACCTTTTTGGATTCTTGGAAGCTATGTAAATTAAAAATGTAATACAGGAAAGACGTTAGGACCATTTTATTGTTTACATCCCTCAAAATGGTCTATATGACACATGAGGACTTTTCAATTA
Associated Phenotype:
Not determined