ZMP
slc25a15b
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC565335 [Source:RefSeq peptide;Acc:NP_001121816]
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 are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45199 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa18799 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45199
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089851 | Nonsense | 236 | 302 | 5 | 6 |
| ENSDART00000136570 | Nonsense | 241 | 307 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 25830881)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23658146 |
| GRCz11 | 5 | 24161946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTGGTGGAGCTTGTCTCTGGCTGGTGGTTTACCCAATGGACTGTGTT[A/T]AATCCAGGATACAGGTCATGTCGATGACAGGCAGACAATCAGGCTTCTTC
Long Flanking Sequence:
GACGAAATCTTAGAATTTAACGAAAAACTAACAGGAAGTGCAATTTAAGATTTAAATTTTAGACAATGAGGGCAAACTATTTATTTTAAACTTTTATTTAAACTTTTATGTTATTAAACTTTTTTATGTCATACACAGATGAATTGATCACCACAAAATGAGCAATGTGAGCTTACAAAATTATATGGTTTGATTTGATTTGATTTAATTTACACTTTAAACTGAATAAATGTTCATGATTTCTGCTAAATAAATGTGGGCTTGGAGAGCAGAGAGAATATTTTAAAAAGTGTTTTTAGTTGTTTTGAAATACTTCAGTTTCTCTGTTTTGCATCATTTTGCTCATGATTGCGGTCGGTGTATATACTCTTAGATCTAAGATGTCCTGTGTTATCGGCTGTGACGTGTGTTTGTGTTTTGTAGGTGTCGCACCCATCGTGTTCAGTGGAGGTTTTGGTGGAGCTTGTCTCTGGCTGGTGGTTTACCCAATGGACTGTGTT[A/T]AATCCAGGATACAGGTCATGTCGATGACAGGCAGACAATCAGGCTTCTTCAAGACTTTCATGCATATCTTCAGAACCGAAGGTAAGACAAAGATCTGAGCATTGATATTATGATTTACCCAATAACAATTGCTGAAACCAGATTTAAATATGTCTTGTTTATTTTCAGGTGTAAGAGCTCTATATTCTGGTCTGACTCCCACTATGATTCGGACATTTCCAGCAAACGGTGCACTGTTCTTAGGTTATGAAGCCAGTCGGAAAGTCATGATGGCACAGTTTGACAGCTGACCTTCCAGTCTCGTTTATTAGCATTAAACAGTTTTGTATTTACTGTGCCATGGTTTGTGCGCACACTAACAGTCAGTTTTATAACAAGGCTTTATTTATTTTAACGCTTTAAAATAAGATTCAATTGAATTAACACATCAAATATATCATGACCTATCAGTGAACAATACTTTTTGAGGCAGTACATACTCCAGGTTACTGTTACTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18799
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089851 | Essential Splice Site | 263 | 302 | 5 | 6 |
| ENSDART00000136570 | Essential Splice Site | 268 | 307 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 25830964)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23658229 |
| GRCz11 | 5 | 24162029 |
KASP Assay ID:
2259-5766.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACAATCAGGCTTCTTCAAGACTTTCATGCATATCTTCAGAACCGAAGG[T/A]AAGACAAAGATCTGAGCATTGATATTATGATTTACCCAATAACAATTGCT
Long Flanking Sequence:
TTTTAAACTTTTATTTAAACTTTTATGTTATTAAACTTTTTTATGTCATACACAGATGAATTGATCACCACAAAATGAGCAATGTGAGCTTACAAAATTATATGGTTTGATTTGATTTGATTTAATTTACACTTTAAACTGAATAAATGTTCATGATTTCTGCTAAATAAATGTGGGCTTGGAGAGCAGAGAGAATATTTTAAAAAGTGTTTTTAGTTGTTTTGAAATACTTCAGTTTCTCTGTTTTGCATCATTTTGCTCATGATTGCGGTCGGTGTATATACTCTTAGATCTAAGATGTCCTGTGTTATCGGCTGTGACGTGTGTTTGTGTTTTGTAGGTGTCGCACCCATCGTGTTCAGTGGAGGTTTTGGTGGAGCTTGTCTCTGGCTGGTGGTTTACCCAATGGACTGTGTTAAATCCAGGATACAGGTCATGTCGATGACAGGCAGACAATCAGGCTTCTTCAAGACTTTCATGCATATCTTCAGAACCGAAGG[T/A]AAGACAAAGATCTGAGCATTGATATTATGATTTACCCAATAACAATTGCTGAAACCAGATTTAAATATGTCTTGTTTATTTTCAGGTGTAAGAGCTCTATATTCTGGTCTGACTCCCACTATGATTCGGACATTTCCAGCAAACGGTGCACTGTTCTTAGGTTATGAAGCCAGTCGGAAAGTCATGATGGCACAGTTTGACAGCTGACCTTCCAGTCTCGTTTATTAGCATTAAACAGTTTTGTATTTACTGTGCCATGGTTTGTGCGCACACTAACAGTCAGTTTTATAACAAGGCTTTATTTATTTTAACGCTTTAAAATAAGATTCAATTGAATTAACACATCAAATATATCATGACCTATCAGTGAACAATACTTTTTGAGGCAGTACATACTCCAGGTTACTGTTACTTTATAAATATTCTGTTTTTAGCCATTGCTAATTTGTGTTTGTTCATAATCCACACAACACAAAATATAAAAAAAAATTCTAAATTAG
Associated Phenotype:
Not determined