ZMP
slc25a47a
Ensembl ID:
ZFIN ID:
Description:
Solute carrier family 25 member 47-A [Source:UniProtKB/Swiss-Prot;Acc:Q1ECW7]
Human Orthologue:
SLC25A47
Human Description:
solute carrier family 25, member 47 [Source:HGNC Symbol;Acc:20115]
Mouse Orthologue:
Slc25a47
Mouse Description:
solute carrier family 25, member 47 Gene [Source:MGI Symbol;Acc:MGI:2144766]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9955 | Essential Splice Site | Available for shipment | Available now |
| sa19250 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9955
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083876 | Essential Splice Site | 108 | 294 | 4 | 6 |
| ENSDART00000083876 | Essential Splice Site | 108 | 294 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 53989746)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 53845689 |
| GRCz11 | 20 | 53635145 |
KASP Assay ID:
2261-5034.1 (used for ordering genotyping assays)
KASP Sequence:
ACACTAAGCTGGATGTCTTTATGTCCGGTCTGGCCGGTGGTGTGGCACAG[G/A]TCAGATTTACTTTWTAGGGGTCGKTCACACAGAATGYGTTATTCCATTCA
Long Flanking Sequence:
AATTAGATTTAATAATATATTTTAATTTTTGTTAACTTCTCTCTGAACCCCTAGAAATGAGGTAAATGTAACAGAAATAAACCGGGAAATAAATAAATAAATAAAACAGGAATCACAAAGCATGAAATCTGATAACTTACTGATATTTTTACAGTGTGTATTTGTTGTAATAATGCCTGTAATATTTCCAACTGCAGCTCTGTTGAACACGCTTGGGAAATATTTGAAAAAGAATACAAATATCAGTATTTTTGTTTACATAATGTTAGTCTGTAATTACAGCTTGTTCTCTCTAACTGACACTGACCTCATTGTGTGTTTTCCTGCAGGTTCATGGCTTCTTCAAGGGCATGTTTTTACCCATCACCACTATATCCATGACCTCCTCTGTGGTATTTGGCACTTACCGTAACTGTCTGCAGGCTCTCTCTTACATCCGCAAGGCAGAAAACACTAAGCTGGATGTCTTTATGTCCGGTCTGGCCGGTGGTGTGGCACAG[G/A]TCAGATTTACTTTATAGGGGTCGTTCACACAGAATGCGTTATTCCATTCAAATGCTCTACTTTTCGATTGTTTTTCATTGTAAACATGCGCTTGTAATACGTATGGAATAACTGAGCCCATTGAATTATTAAAAAATAATGCACAACAGAGGTGCTGTTCAATACTATAGAACATAATTTCCTCTAACAAAATCACCACAACAGATCAATTACTATAGTCCTGTTACTATAGTAACTGTAGAATCACCACAAAATAACATGTCCTGTAGTTGAGTTACCGTAGCAATTGTAATCACCACAACAGATCAATTACTATAGTCAAGTTACCATAGCAACAGTAGAATTCCTACAAAACATCAATTACGATAGTTGTGTTACCAGAGCAACTGTAGAATTGCCACAAAAGATTAATTACAGCAGTTATGTTACTATTGTGTTACCATAGCAACTGTAGAATCGCCATAACAGATCAATTACTATAGTTGAGTTACCATAGCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19250
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083876 | Essential Splice Site | 108 | 294 | 4 | 6 |
| ENSDART00000083876 | Essential Splice Site | 108 | 294 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 53989746)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 53845689 |
| GRCz11 | 20 | 53635145 |
KASP Assay ID:
2261-5034.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTAAGCTGGATGTCTTTATGTCCGGTCTGGCCGGTGGTGTGGCACAG[G/A]TCAGATTTACTTTATAGGGGTCGTTCACACAGAATGCGTTATTCCATTCA
Long Flanking Sequence:
AATTAGATTTAATAATATATTTTAATTTTTGTTAACTTCTCTCTGAACCCCTAGAAATGAGGTAAATGTAACAGAAATAAACCGGGAAATAAATAAATAAATAAAACAGGAATCACAAAGCATGAAATCTGATAACTTACTGATATTTTTACAGTGTGTATTTGTTGTAATAATGCCTGTAATATTTCCAACTGCAGCTCTGTTGAACACGCTTGGGAAATATTTGAAAAAGAATACAAATATCAGTATTTTTGTTTACATAATGTTAGTCTGTAATTACAGCTTGTTCTCTCTAACTGACACTGACCTCATTGTGTGTTTTCCTGCAGGTTCATGGCTTCTTCAAGGGCATGTTTTTACCCATCACCACTATATCCATGACCTCCTCTGTGGTATTTGGCACTTACCGTAACTGTCTGCAGGCTCTCTCTTACATCCGCAAGGCAGAAAACACTAAGCTGGATGTCTTTATGTCCGGTCTGGCCGGTGGTGTGGCACAG[G/A]TCAGATTTACTTTATAGGGGTCGTTCACACAGAATGCGTTATTCCATTCAAATGCTCTACTTTTCGATTGTTTTTCATTGTAAACATGCGCTTGTAATACGTATGGAATAACTGAGCCCATTGAATTATTAAAAAATAATGCACAACAGAGGTGCTGTTCAATACTATAGAACATAATTTCCTCTAACAAAATCACCACAACAGATCAATTACTATAGTCCTGTTACTATAGTAACTGTAGAATCACCACAAAATAACATGTCCTGTAGTTGAGTTACCGTAGCAATTGTAATCACCACAACAGATCAATTACTATAGTCAAGTTACCATAGCAACAGTAGAATTCCTACAAAACATCAATTACGATAGTTGTGTTACCAGAGCAACTGTAGAATTGCCACAAAAGATTAATTACAGCAGTTATGTTACTATTGTGTTACCATAGCAACTGTAGAATCGCCATAACAGATCAATTACTATAGTTGAGTTACCATAGCAAC
Associated Phenotype:
Not determined