ZMP
slc26a6
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to solute carrier family 26, member 5 (Slc26a5) [Source:UniProtKB/TrEMBL;Acc:A
Human Orthologue:
SLC26A6
Human Description:
solute carrier family 26, member 6 [Source:HGNC Symbol;Acc:14472]
Mouse Orthologue:
Slc26a6
Mouse Description:
solute carrier family 26, member 6 Gene [Source:MGI Symbol;Acc:MGI:2159728]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10168 | Nonsense | Available for shipment | Available now |
| sa18277 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10168
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045602 | Nonsense | 130 | 733 | 4 | 21 |
| ENSDART00000078228 | None | None | 360 | None | 8 |
| ENSDART00000113763 | None | None | 292 | None | 10 |
| ENSDART00000138882 | Nonsense | 127 | 598 | 4 | 15 |
| ENSDART00000140112 | None | None | 141 | None | 3 |
| ENSDART00000142031 | None | None | 313 | None | 10 |
| ENSDART00000147411 | None | None | 224 | None | 7 |
The following transcripts of ENSDARG00000055835 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 27124337)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 26252255 |
| GRCz11 | 8 | 26271394 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NAAACTGAGCAGCATTTKCTCATATTCTCATATCTGTCTCCAGGTACATA[T/A]GCAGTTATGAGTGTTATGATTGGCAGTGTGACAGAGCGTTTGGCTCCAGA
Long Flanking Sequence:
AAACGCACCCCAGATTGGAATATTGCTGATTACGGATGAGAGGCTAGCCACGATCAATCATATTACATGCTCTCTTGAAACTAGTTTGAAAAACTTCTCGTAATATTGTCAATGTTTTTACAAAATTAAAATATGTTTAAAAGTATATAAAGAATATTGTTTTTTAAAGAATATCAGGTCGCCATAATGAAGTTAAGCAGCTAAAATGCATCCAAAACGTTTTGGTTGAAAAAGGTCATGTGTAAATATAAGCCTCACTGATAAAACTTATCTCCATTTCAACAATTAAAGAGAAAACTGTGCCATTTGAAATTTCTCATGTCATACCTAAATGACTTTCTCTGGCAGGAGATATGACTGCAAACAATTCTATATTTCTTTAATTTTTGAGTGAATTATTCCTTCAAATTTCACTGTGGAGTTCATTCCCACAAACATAATGTAGTAAAACAAACTGAGCAGCATTTTCTCATATTCTCATATCTGTCTCCAGGTACATA[T/A]GCAGTTATGAGTGTTATGATTGGCAGTGTGACAGAGCGTTTGGCTCCAGACTCAGACTTCACGTTCCCAGGCAACGAAACCAACAGCACCTATATAGACTTTAGCAGCCGTGATGCAGAGCGGGTCAAAATCGCTGCCACTGTCACTTTCTTATCTGGCATTTTCCAGGTAGGCTGTCTGTCTTTGAAGTGTGCTCAGCTCTGAAGGTGTGTTTGTGACTGAAGTATTTCTGTGGCATCTGTGTGTTTGTAGTTGCTCCTCGGTGTGGTGCGCTTTGGTTTTGTGGTGACGTATCTCTCAGAGCCATTGGTGAGGTCTTACACGACAGCGGCTGCTATACATGTCATCGTGTCCCAGCTCAAATATTCCTTTGGCATCAATCCACATCGATACAGTGGACCTTTGTCTCTCATATATGTGAGTATGAACATACAGCAGTTTATTCCATGTGAATAATGGTTCTAGAATACCCTTTATTTAGCGGGGAAAACTAAACAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18277
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045602 | Nonsense | 245 | 733 | 6 | 21 |
| ENSDART00000078228 | None | None | 360 | None | 8 |
| ENSDART00000113763 | None | None | 292 | None | 10 |
| ENSDART00000138882 | Nonsense | 242 | 598 | 6 | 15 |
| ENSDART00000140112 | None | None | 141 | None | 3 |
| ENSDART00000142031 | None | None | 313 | None | 10 |
| ENSDART00000147411 | None | None | 224 | None | 7 |
The following transcripts of ENSDARG00000055835 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 27126067)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 26253985 |
| GRCz11 | 8 | 26273124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WTGAAGTATAAAGCTTTTCTTTATTTTCTTTCTCTCTTCAGACAGTCATC[G/T]AGATTWGTGCATTGCTYGGAAAGACCAACATYGGTACACTGGTTGTCAGC
Long Flanking Sequence:
ATTGTCTTTCACAGGGTTTCTCTAATCTCTCACACTGATCTGCTGTGATGTTGATCAGCTTTTCTTCAATTTCTTGCACAGTTCTGTGTCTAATGGGTATTGTTGTCATAACTTTAATGCCAAGGATTTTCCACAGATTTTCAATCAGGTTTAGATCAGGACTTTGGGCTGCCATTTCATTTTTAGTGTTTTCAGCTTCAAATAACTGCTTTGCCCATTTTGCTGTGAAACAGGGTTCATTGTGCTTTTATTAAAATGCAGACAGAGCTTCTGATACAAATTTGCATTCACTCTTTAATGTAGCTGTAAAACAAGCCAAATTTTAGCAGAAAACATCCCCAAACCTTGGCACTTTTAACTGACTTCTTTACATACCTTTGTATTTAAATGTGTAAATAGTGTTTACTACCTCCTAGTAGAGGGGTTATTAAAAGCACTTGTAAACTATAGATGAAGTATAAAGCTTTTCTTTATTTTCTTTCTCTCTTCAGACAGTCATC[G/T]AGATTTGTGCATTGCTTGGAAAGACCAACATCGGTACACTGGTTGTCAGCATTGTTACTATTGTTGGCTTAATCATTGCAAAGGAACTCAGCGCATTGGCAGCAAAAAAAATCCCTATTCCGATTCCAGTTGAGCTAATTACTGTGAGTAACATCATTCAGTTAAACCAACCCAGTCAAACCAATCCACTTAAACTTTTGATTACATTTTTACCTGGTGGTTGAGTTTGTCTATATTTTACCCAAATTTGCATTTATAAGTGTCAGTTTTGGTTGCATTTTTGATCTCACTTTGTTCTGTTGCTGAGAGAGCAACTCAAAGCGTTCATTTTGCTGTGTGTATAGATTATTATAGCCACTGTGGTATCATGGTATATGGATTTGAAGACCATTTACAAAGTCGAAGTTGTTGGCGAAATCCCATCAGGGTGAGTCTAATACACAGTTTTGAAACCTAAATATAACACATTTGCATTTGGTTCGTCAAGTTTTGGTGTCTGC
Associated Phenotype:
Not determined