ZMP
slc25a15a
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15a [Source:RefSeq p
Human Orthologues:
SLC25A15, SLC25A2
Human Descriptions:
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 [Source:HGNC Symbo
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 2 [Source:HGNC Symbol
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 2 [Source:HGNC Symbol
Mouse Orthologues:
Slc25a15, Slc25a2
Mouse Descriptions:
solute carrier family 25 (mitochondrial carrier ornithine transporter), member 15 Gene [Source:MGI S
solute carrier family 25 (mitochondrial carrier, ornithine transporter) member 2 Gene [Source:MGI Sy
solute carrier family 25 (mitochondrial carrier, ornithine transporter) member 2 Gene [Source:MGI Sy
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9698 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9698
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092942 | Essential Splice Site | 152 | 303 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 3373771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3277029 |
GRCz11 | 15 | 3264545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCATGCATGAAATGGAGGCATCCGGCAAGATCGCCAGCGGACAAAAAAG[G/T]TCAGTTTGGACTGAGGACAGTTTGGTAGTCAATAAAAAACATGAGCCTGT
Long Flanking Sequence:
CGTGTCTGAGTCCACTAGATCCTTTCAGAGGTGCACCCTGCTCTGTGACTTCATAAACTCCTTAAGAAACTATACCTGGATGATGGAAGCATTCAGCGGTGCTTCCGACTGAGCCGAGCGCAATTTGATCAACTGTTGTTTGGTGTCGACACCAACAACATGGGCTATGTCATAAGCACTCCCCTACAAGAGAAAGCTCCTGATTGGTTAGCGTGGTGTGAATGTCTGCTAAAGTTCAGATTCTCAAACTTGAGCGATTCTTGCGTTAAGGATGTCAATCACTTGAATCGCTCAACTCGCGCCGCTTCGTTCATGGGTATGTGTGTGTGTGTGGTGCTGATCTGTATGTTGTGTTTCAGTGATGTCCAGAAGGCCTGCTCCGGCTCTGTGGCCTCTGTCTTCTCCTCTCTGGCTTTGTGTCCCACTGAACTGGTCAAATGTCGACTGCAGGCCATGCATGAAATGGAGGCATCCGGCAAGATCGCCAGCGGACAAAAAAG[G/T]TCAGTTTGGACTGAGGACAGTTTGGTAGTCAATAAAAAACATGAGCCTGTTGTAAATTTATGTTCAGTTTTGAAGATATGTACAAGGAACACTCAACTATTTTCATTATTTTTTTTTTTTTGAAAGTAGGATCATTTTACATCTCCCCTTGAGTTTACAGCCGATTCTAATGTTATCACTCGATTGGATTAGCGCTATCAGTAGGGGCCTTCTGCACCTACTGGTAGGTTTAGAAAGCTATTATAATCCATCCACATACAGTTAGGTCCATAAATATTGGGACATCGAGACAATTCTAATATTTGTGGCTCTATATACCAACACAATGCATTTGAAATTAAATAATTAATTTAATTTGAGGGTATTTACATCCAAATCAGGTGAACAGTGTAGGAGTTAAGCTGTGGTCACACTGGACTTTTCTCCCCATAGACTTCCATTCATATGCAGGCAAATGTGGAAATGTGAGCTCGTGCAACAAGTTGCTCAGTTCGCTGCGT
Associated Phenotype:
Not determined