ZMP
slc16a9b
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 16 (monocarboxylic acid transporters), member 9 [Source:RefSeq peptide;Acc:NP
Human Orthologue:
SLC16A9
Human Description:
solute carrier family 16, member 9 (monocarboxylic acid transporter 9) [Source:HGNC Symbol;Acc:23520
Mouse Orthologue:
Slc16a9
Mouse Description:
solute carrier family 16 (monocarboxylic acid transporters), member 9 Gene [Source:MGI Symbol;Acc:MG
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9331 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19027 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9331
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 |
|---|---|---|---|---|---|
| ENSDART00000025669 | Nonsense | 204 | 486 | 5 | 6 |
| ENSDART00000146685 | None | None | 61 | None | 1 |
| ENSDART00000025669 | Nonsense | 204 | 486 | 5 | 6 |
| ENSDART00000146685 | None | None | 61 | None | 1 |
Genomic Location (Zv9):
Chromosome 12 (position 8255347)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 7561522 |
| GRCz11 | 12 | 7595644 |
KASP Assay ID:
2260-4962.1 (used for ordering genotyping assays)
KASP Sequence:
GCGCCGGACTCATGCGCCCKYTGCACCTGCCGGCCTACTACCTRAAACAA[C/T]GAGCRGCGATGGYCGAGAAAGCCGAGGAGAACGTTCTGGAAAAAWCTYCT
Long Flanking Sequence:
CCCGTGGTGAACGAATGACTCAGACCCGATAGAGGACTCGAGAGATGAACGGATCAATTCTTTTTTCGGCTCTAAAGCATATGACTGGCCTCTGCCTTTCCGAGAAGAATGGCTCAAAAGACTTATAATGATTGATACCACCTGCACAAATGTGCGCACGCGTGGATGAACGAGTCACTTCCTGAGAGGACTCGTAGTTCCCGAGTCATATTGAAGATTCGTTTAAAATGAACAAATCGTTCAAGAGTGACCCATCACTAATAAAAACCAATAAAAGTTCAATAAAACAGTTCAATCCCATTATAACACTCGTTCCCCTTTATCTCATGTTTTCAGGTACAAGCGTGGGAGGTTTTCTTTACGCTGCTGCGCAGAACGAATTCATTGCACTCTTCGGACTCGACGGCTGCCTTTTACTGATTGGCTGTTTTGCACTAAACATCATCGCCTGCGCCGGACTCATGCGCCCGCTGCACCTGCCGGCCTACTACCTAAAACAA[C/T]GAGCGGCGATGGCCGAGAAAGCCGAGGAGAACGTTCTGGAAAAATCTCCTGTGGTGGAAGACCCCGTCAAAAAAACCCAATCCATCGTCCTCATCACAGGAGACACCAAAGACACGCACGAAAAGAGAAAACTCCTCAATTACGTGACGCTGGTGCGGCTCATGAAGAAGAAGCAGAAGCAATACTCTGAATACTTGCACTCCATTGGCCAAGTGCTTCAGAACCGAGTCTTCTTGGCCACTTGCGTGTCTTTATTCGCGTATTGTTTGGGAGCGTACACTCCGCTCCTGTTTCTAGAGGATTTGGCTCAAAGCGAGGGTCTCATCACTGGGATCAGCACCATCCCTCTGGTCTCCATCATGTCCATCGCTGCTGGAGTTGGAAAGCTGCTGCTGGGCGTCATGATGGACGTTCGCTGGATGAACAGTATTTATTTGTACGCGGTCACCCTGCTGGGTACAGGGGTGGCTCTGCTCATCATCCCTGTCACCAAGAACTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19027
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 |
|---|---|---|---|---|---|
| ENSDART00000025669 | Nonsense | 204 | 486 | 5 | 6 |
| ENSDART00000146685 | None | None | 61 | None | 1 |
| ENSDART00000025669 | Nonsense | 204 | 486 | 5 | 6 |
| ENSDART00000146685 | None | None | 61 | None | 1 |
Genomic Location (Zv9):
Chromosome 12 (position 8255347)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 7561522 |
| GRCz11 | 12 | 7595644 |
KASP Assay ID:
2260-4962.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCCGGACTCATGCGCCCGCTGCACCTGCCGGCCTACTACCTAAAACAA[C/T]GAGCGGCGATGGCCGAGAAAGCCGAGGAGAACGTTCTGGAAAAATCTCCT
Long Flanking Sequence:
CCCGTGGTGAACGAATGACTCAGACCCGATAGAGGACTCGAGAGATGAACGGATCAATTCTTTTTTCGGCTCTAAAGCATATGACTGGCCTCTGCCTTTCCGAGAAGAATGGCTCAAAAGACTTATAATGATTGATACCACCTGCACAAATGTGCGCACGCGTGGATGAACGAGTCACTTCCTGAGAGGACTCGTAGTTCCCGAGTCATATTGAAGATTCGTTTAAAATGAACAAATCGTTCAAGAGTGACCCATCACTAATAAAAACCAATAAAAGTTCAATAAAACAGTTCAATCCCATTATAACACTCGTTCCCCTTTATCTCATGTTTTCAGGTACAAGCGTGGGAGGTTTTCTTTACGCTGCTGCGCAGAACGAATTCATTGCACTCTTCGGACTCGACGGCTGCCTTTTACTGATTGGCTGTTTTGCACTAAACATCATCGCCTGCGCCGGACTCATGCGCCCGCTGCACCTGCCGGCCTACTACCTAAAACAA[C/T]GAGCGGCGATGGCCGAGAAAGCCGAGGAGAACGTTCTGGAAAAATCTCCTGTGGTGGAAGACCCCGTCAAAAAAACCCAATCCATCGTCCTCATCACAGGAGACACCAAAGACACGCACGAAAAGAGAAAACTCCTCAATTACGTGACGCTGGTGCGGCTCATGAAGAAGAAGCAGAAGCAATACTCTGAATACTTGCACTCCATTGGCCAAGTGCTTCAGAACCGAGTCTTCTTGGCCACTTGCGTGTCTTTATTCGCGTATTGTTTGGGAGCGTACACTCCGCTCCTGTTTCTAGAGGATTTGGCTCAAAGCGAGGGTCTCATCACTGGGATCAGCACCATCCCTCTGGTCTCCATCATGTCCATCGCTGCTGGAGTTGGAAAGCTGCTGCTGGGCGTCATGATGGACGTTCGCTGGATGAACAGTATTTATTTGTACGCGGTCACCCTGCTGGGTACAGGGGTGGCTCTGCTCATCATCCCTGTCACCAAGAACTAC
Associated Phenotype:
Not determined