ZMP
si:rp71-68g1.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLC23A3
Human Description:
solute carrier family 23 (nucleobase transporters), member 3 [Source:HGNC Symbol;Acc:20601]
Mouse Orthologue:
Slc23a3
Mouse Description:
solute carrier family 23 (nucleobase transporters), member 3 Gene [Source:MGI Symbol;Acc:MGI:104516]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21432 | Nonsense | Available for shipment | Available now |
| sa27338 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41354 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21432
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 |
|---|---|---|---|---|---|
| ENSDART00000125054 | Nonsense | 88 | 582 | 3 | 12 |
| ENSDART00000132392 | None | None | 61 | None | 1 |
| ENSDART00000144003 | None | None | 292 | None | 5 |
| ENSDART00000145456 | None | 19 | 32 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 7435785)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 7415878 |
| GRCz11 | 9 | 7394269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCAGTTGTGGCGTTAAATGAAATGTTTCTTGTGCTCTCAGTTTGCCAT[T/A]GATTCAGGCTCCATCTTTGGACTTTCTGATCCCGGCCATGGCCTTACTTT
Long Flanking Sequence:
GCTCTGTTAAACATCATTTGGGAAACATAAGGAGGGCTAATCATTTTGACTTCAACTGTATAATTATTCATAATTTTTTTCAAGTTCTAATTATGATTTCGATGACCTTTGCAAGCTGATAAACTTGTGTGCAACATTAGTGCATAACAATAAGCCTGGTGTGGATTTTCAATGTTCACTTTTTTATCAGCCTAATTTTTACTAATGAATGAACAACATGAATGTAAGTTGAGCAGTTTTGAAGTCTGCTTTGTGTGTTTCTCTCCAGCATGTGTTGGTGTTGTCTTCTCTCTGCGCTCTGGTTGTCTGTACATTAATTCAGGAAGTAGAAAGGGACACAATAGTGGCCTATGTGCTCTTTCACTCTGGTATATCTACACTGCTGCAGAGCTGGATTGGATCACGGTAAGATTACGTCTACCCTTTTGCTTCTGTAGGTAAGCTGATATATTGCAGTTGTGGCGTTAAATGAAATGTTTCTTGTGCTCTCAGTTTGCCAT[T/A]GATTCAGGCTCCATCTTTGGACTTTCTGATCCCGGCCATGGCCTTACTTTCTGATCAGTCAGGTAAGAATGACAAGCAATTAAAAGGGGTCAGGAATGATTTTTGTATTCTCTGAAAGTGAGTCTTATAACTTATAATGTGAAAGTTCCTTTTTCATTGTTTGCCTCTCACTATTAAACTTCTGGCAAGTACAAATAACATGCTCCACCGATTCTTCCACTCCTCAACAATATCATAATCCTGTTGCGTATTTATTTATCAATCTTAAGGTGGTGTTTAACATGGTATGGTCAACTTTTAACCTTTTTAAAAAGTTTCTCCTTCAGTATTTCTAGTTATCTTCACTACCCCCACTTCTAATCCTATTTTGCATAGATGTCCTAATTTGTGGCTTTCACATTTTCTTTGCCATTCAATGGACATACATGCTTAAATGATTGCTTTTGCTTCCGATATTTAAAGATGCTCATAACATTTTACACCTATATCACCCTCTATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27338
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 |
|---|---|---|---|---|---|
| ENSDART00000125054 | Essential Splice Site | 463 | 582 | 10 | 12 |
| ENSDART00000132392 | None | None | 61 | None | 1 |
| ENSDART00000144003 | Essential Splice Site | 173 | 292 | 3 | 5 |
| ENSDART00000145456 | None | None | 32 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 7416336)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 7396429 |
| GRCz11 | 9 | 7374820 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAGCACTGCCGCACTGGTTCAGACTTCACTCTGGATTTATACAAACAG[G/A]TACCATTTCATGTGTGACGTGTTTTGTTACACTTAATTTAGATTTGGAAA
Long Flanking Sequence:
ATTATCGTACCGTGAAATTCTGATACCGTTACATCCCTAGTATGAATGCTAAGCAATTGAACCCACACACAAAAAATACTTTAGTAATTTGTACTAAATGAATATCGAATCTAATAAATATAGTACCTTTACATTTGTAACCACAGCAGTGAGATTTATAAAGAAAAGAAGAACAAAACATATTTTGAGTGGCAATGTTTGTAGTTTTTGGTGTAAATAATTATATAAAATTCATGCGCACATTGAGGTTTCCTTAGGTTAAGCTATAGTTTTATTCAGTCTAATTACCTTGTTAAGACAATAGTATTAACACCTGTTTCATGTTCTCTAAGGTGCTGTGCTTAGTGTAACCTACGCACTTGCTGTAGCAACAGGCATAACGTACTTCCAACATGCTGATGTGGACTCAGGACGCAACATCTTTAACATCGGCTTTACAATGTTCATGTCATTAGCACTGCCGCACTGGTTCAGACTTCACTCTGGATTTATACAAACAG[G/A]TACCATTTCATGTGTGACGTGTTTTGTTACACTTAATTTAGATTTGGAAATTAAATTAGGAAATTTAAATGAATTAATTGTTATCTCTGTGTCTTCAGGTGTTGGCAGTGTTGACGTTTTTCTTCAGTCTCTTTTAACCTTACCTGTTTTTCTTGTGGGAGTCTTGGCTTTTCTTCTAGAGCACACGGTTTCAGGTAGAACAACAATTTAATTACTTTTTTAAGTTAGTCTGTTAAAGGAACACTTCATTTTTTTTTGGATATAGACTGATTTTACAATCACCACAGCCTGTTTTATGTCGCCACATTCATATCACCCTGCAGCCCAAGATCGGTTACTCACTGAAGCTAAGCAGGGCTGAGCCTTGTCAGTACCTGGATCGGAGACCACTAGGGAACACCAGGTTGCTGTTGGAAGTGGTGTTGGTGAGGCCAGCAGGGGGCGCTCAACCTTTGGTCTGTGTGAGTCCATATGCCCCAGTAAAAGTGAAGGGGACACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41354
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125054 | Nonsense | 476 | 582 | 11 | 12 |
| ENSDART00000132392 | None | None | 61 | None | 1 |
| ENSDART00000144003 | Nonsense | 186 | 292 | 4 | 5 |
| ENSDART00000145456 | None | None | 32 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 7416201)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 7396294 |
| GRCz11 | 9 | 7374685 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGTGTCTTCAGGTGTTGGCAGTGTTGACGTTTTTCTTCAGTCTCTTT[T/G]AACCTTACCTGTTTTTCTTGTGGGAGTCTTGGCTTTTCTTCTAGAGCACA
Long Flanking Sequence:
TGTAACCACAGCAGTGAGATTTATAAAGAAAAGAAGAACAAAACATATTTTGAGTGGCAATGTTTGTAGTTTTTGGTGTAAATAATTATATAAAATTCATGCGCACATTGAGGTTTCCTTAGGTTAAGCTATAGTTTTATTCAGTCTAATTACCTTGTTAAGACAATAGTATTAACACCTGTTTCATGTTCTCTAAGGTGCTGTGCTTAGTGTAACCTACGCACTTGCTGTAGCAACAGGCATAACGTACTTCCAACATGCTGATGTGGACTCAGGACGCAACATCTTTAACATCGGCTTTACAATGTTCATGTCATTAGCACTGCCGCACTGGTTCAGACTTCACTCTGGATTTATACAAACAGGTACCATTTCATGTGTGACGTGTTTTGTTACACTTAATTTAGATTTGGAAATTAAATTAGGAAATTTAAATGAATTAATTGTTATCTCTGTGTCTTCAGGTGTTGGCAGTGTTGACGTTTTTCTTCAGTCTCTTT[T/G]AACCTTACCTGTTTTTCTTGTGGGAGTCTTGGCTTTTCTTCTAGAGCACACGGTTTCAGGTAGAACAACAATTTAATTACTTTTTTAAGTTAGTCTGTTAAAGGAACACTTCATTTTTTTTTGGATATAGACTGATTTTACAATCACCACAGCCTGTTTTATGTCGCCACATTCATATCACCCTGCAGCCCAAGATCGGTTACTCACTGAAGCTAAGCAGGGCTGAGCCTTGTCAGTACCTGGATCGGAGACCACTAGGGAACACCAGGTTGCTGTTGGAAGTGGTGTTGGTGAGGCCAGCAGGGGGCGCTCAACCTTTGGTCTGTGTGAGTCCATATGCCCCAGTAAAAGTGAAGGGGACACTACACTGTCAGTGGGTGCCGTCTTTCGGATGAGACGTTAAATCGAGGTCCTGACTCTCTGTGATCATTAAAAATCCCATGGCACTTCTCGTGAAAGAGCAGGGGTGTAACCCCGGTGTCCTGGCCAAAGTCCCTCTA
Associated Phenotype:
Not determined