ZMP
slc25a12
Ensembl ID:
ZFIN ID:
Description:
calcium-binding mitochondrial carrier protein Aralar1 [Source:RefSeq peptide;Acc:NP_997947]
Human Orthologue:
SLC25A12
Human Description:
solute carrier family 25 (mitochondrial carrier, Aralar), member 12 [Source:HGNC Symbol;Acc:10982]
Mouse Orthologue:
Slc25a12
Mouse Description:
solute carrier family 25 (mitochondrial carrier, Aralar), member 12 Gene [Source:MGI Symbol;Acc:MGI:
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa8444 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8618 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8444
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049827 | None | None | 292 | None | 7 |
| ENSDART00000113771 | None | None | 682 | 1 | 18 |
| ENSDART00000122718 | Nonsense | 24 | 714 | 1 | 18 |
| ENSDART00000049827 | None | None | 292 | None | 7 |
| ENSDART00000113771 | None | None | 682 | 1 | 18 |
| ENSDART00000122718 | Nonsense | 24 | 714 | 1 | 18 |
The following transcripts of ENSDARG00000029218 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3852899)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3821944 |
| GRCz11 | 6 | 3982764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTTTTCACACGCTTCCTCAGTCSTCGGCCACGCGCCTGCGCAACCCCA[C/T]GACYACACGTGACGTCAGACAGCAGCATGGCGGCCAAGGTGACTCCAGCG
Long Flanking Sequence:
TTTCATTCAGTTGTCTTTCAGGTTTGACTAGTAAATTGATTTAAGATACAATAGTAGCCTCATGATTATTAATGTATTACATATATATATATATATATATATATATATTATTGAATACAAGAGTGATAACATCACTGCATTAAAGAAAAAATACAATAACGAAATATAAGAAAGAGGAGAGAAAAAACTTTACAAAGCCTCAATCATTAAGAAAAAAAGATTATCATAAGCTTTAAGAAAGTTTTTATTTTTAGTATCATTAATAAGCTTAAGAGATTCAATATTGTACGATATTTCAACGAGGAAAGTATTAAATATAGGCATTGTTTTTAGGAACTTATTTTTGTGAGAGCATGAGAAAGCGATAACAATAAGATCGAGAGCATGAGAGACAGCGATAACCTATGATAAAAACAGGTGTGACATCACAAATGCGCGCGCACCTCTTGGCTCTTTTCACACGCTTCCTCAGTCCTCGGCCACGCGCCTGCGCAACCCCA[C/T]GACCACACGTGACGTCAGACAGCAGCATGGCGGCCAAGGTGACTCCAGCGACACCGCTTTTGACTGAAAATTTGTATTTTATATTTCTTAACTGTCGACTATTAGCTGCAAGTTGGTGTTTATCAGAAGGAGAAACCATAATAGACGTGTAAACGAAGTAATTAGAGGAACTGATAAGCGTTTTAAACGGACCGGCGGCAGCATCACTGAGCTTATCACTGGACTCGCGCTCAGACTTGACTGAATTCAGTGTCTCTAAGCTTCATAAAACCATAAAAAATATCAGAAATCTGTCTTAGACAGAGTTAATCAGCTTTTTAACAGCTTTTTAGTGTTGTCAGAGATTAGTTTTTGTTAATAAAGTGTAGTCAAGCGTGAGGATCATGCTGTGTTGGCGAAATTGGGCTCATATTAACGTATTCTTCAGGGACTTTGTGTGTTTGTGTTTGTCAATTATATTTTTAGGTATTTTGTGCTTATTTTAAAAAAACTGGTTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8618
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049827 | None | None | 292 | None | 7 |
| ENSDART00000113771 | None | None | 682 | 1 | 18 |
| ENSDART00000122718 | Nonsense | 24 | 714 | 1 | 18 |
| ENSDART00000049827 | None | None | 292 | None | 7 |
| ENSDART00000113771 | None | None | 682 | 1 | 18 |
| ENSDART00000122718 | Nonsense | 24 | 714 | 1 | 18 |
The following transcripts of ENSDARG00000029218 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3852899)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3821944 |
| GRCz11 | 6 | 3982764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTTTTCACACGCTTCCTCAGTCSTCGGCCACGCGCCTGCGCAACCCCA[C/T]GACYACACGTGACGTCAGACAGCAGCATGGCGGCCAAGGTGACTCCAGCG
Long Flanking Sequence:
TTTCATTCAGTTGTCTTTCAGGTTTGACTAGTAAATTGATTTAAGATACAATAGTAGCCTCATGATTATTAATGTATTACATATATATATATATATATATATATATATTATTGAATACAAGAGTGATAACATCACTGCATTAAAGAAAAAATACAATAACGAAATATAAGAAAGAGGAGAGAAAAAACTTTACAAAGCCTCAATCATTAAGAAAAAAAGATTATCATAAGCTTTAAGAAAGTTTTTATTTTTAGTATCATTAATAAGCTTAAGAGATTCAATATTGTACGATATTTCAACGAGGAAAGTATTAAATATAGGCATTGTTTTTAGGAACTTATTTTTGTGAGAGCATGAGAAAGCGATAACAATAAGATCGAGAGCATGAGAGACAGCGATAACCTATGATAAAAACAGGTGTGACATCACAAATGCGCGCGCACCTCTTGGCTCTTTTCACACGCTTCCTCAGTCCTCGGCCACGCGCCTGCGCAACCCCA[C/T]GACCACACGTGACGTCAGACAGCAGCATGGCGGCCAAGGTGACTCCAGCGACACCGCTTTTGACTGAAAATTTGTATTTTATATTTCTTAACTGTCGACTATTAGCTGCAAGTTGGTGTTTATCAGAAGGAGAAACCATAATAGACGTGTAAACGAAGTAATTAGAGGAACTGATAAGCGTTTTAAACGGACCGGCGGCAGCATCACTGAGCTTATCACTGGACTCGCGCTCAGACTTGACTGAATTCAGTGTCTCTAAGCTTCATAAAACCATAAAAAATATCAGAAATCTGTCTTAGACAGAGTTAATCAGCTTTTTAACAGCTTTTTAGTGTTGTCAGAGATTAGTTTTTGTTAATAAAGTGTAGTCAAGCGTGAGGATCATGCTGTGTTGGCGAAATTGGGCTCATATTAACGTATTCTTCAGGGACTTTGTGTGTTTGTGTTTGTCAATTATATTTTTAGGTATTTTGTGCTTATTTTAAAAAAACTGGTTTGCA
Associated Phenotype:
Not determined