ZMP
zgc:162495
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 13 member 4 [Source:RefSeq peptide;Acc:NP_001083020]
Human Orthologue:
SLC13A4
Human Description:
solute carrier family 13 (sodium/sulfate symporters), member 4 [Source:HGNC Symbol;Acc:15827]
Mouse Orthologue:
Slc13a4
Mouse Description:
solute carrier family 13 (sodium/sulfate symporters), member 4 Gene [Source:MGI Symbol;Acc:MGI:24423
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12751 | Nonsense | Available for shipment | Available now |
| sa12487 | Essential Splice Site | Available for shipment | Available now |
| sa40211 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa16821 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12751
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089566 | None | None | 206 | None | 6 |
| ENSDART00000101419 | None | 268 | 603 | 7 | 15 |
| ENSDART00000129252 | Nonsense | 275 | 610 | 7 | 15 |
| ENSDART00000136962 | None | 112 | 200 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 4691904)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4810085 |
| GRCz11 | 4 | 4818655 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGGCCTCATCACCATCACCGGCACCTCCACCAATCTCATTTTCGCTGAA[C/T]AGTTCAACAAGTACGNNNGTAGCATCCTGGACATCATTTTTCTAATGTTCRCA
Long Flanking Sequence:
GAGATCTGCCTTCAGAAAGCTGACAATAATCACAGTGTGCTTTTTCTACTTCTAAAAATCATTCATTTGTACACTGCAAAAAAAAAAACGACAAAAATCAACACAACAACAATATTCTTCATGTTGATTTAACTTAAATAACGCAATCAATAAATTGATTTAAATTCATCAGGTCTTACAACTTAATTTGTTTAAGTTATACAAAGTTTAACTCATATTTTAGTCAGTTTGAATGATGTAAGTTGAGATGATTAGAAAGGTTTGATTCAACTAAAAGAAATTGGGTCAGCAAGAATTTTTTTTGACAGTGTATTGTTTCCAAACAGGCTCCAATTAGCATTCCAGTGCCAAAGAAGCCCAAAATCCGCAGGGATTCTCTGTACCCCACCAAACGGGATCACATGATCTGCAAGTGTCTCACTCTGAGCATCACTTACGCCGCCACCATTGGCGGCCTCATCACCATCACCGGCACCTCCACCAATCTCATTTTCGCTGAA[C/T]AGTTCAACAAGTACGGTAGCATCCTGGACATCATTTTTCTAATGTTCGCATAATTTTATGTCTGATAAATTTTCCTGTGTACATAATCGATTGCACTTTTTAAAGTGCAATATAGGGAGTCAACAATACGGTATATGCTAAAGCAGGGTTTTTCAAAGTCTAAGACAGTGGGCCTCCCTTTTGACACAACTTATTCATTGGCGCCTCCCTCCTCCCAAACACGAACGCACACACGCACGCACACGCACAAAATTCTGGACGTTTTCCTGCTACCTCATCATGCTTGGTTTCAAGGTGTCGCCGAAGTTTAGCAGGTCTCATGCTGTCATTAGCCAAAATATCTTGACAATTCACACATAAAGGTCGTGGTTCATCAGCTGGTCCTGTCCACGTAAATCCTAAACTCAAATACTGATCATCATATTGTCGTCTTTTGGGTTTAAGCCCTGAACTTGAAGGCTTTGAATCGGGGGGTCTCAGAAACCGATCCATTGTATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12487
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089566 | None | None | 206 | None | 6 |
| ENSDART00000101419 | Essential Splice Site | 271 | 603 | 8 | 15 |
| ENSDART00000129252 | Essential Splice Site | 278 | 610 | 8 | 15 |
| ENSDART00000136962 | Essential Splice Site | 115 | 200 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 4695971)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4814152 |
| GRCz11 | 4 | 4822722 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTTATANNNNNNNNNNNNNNNNNNNNTTTGCTATGAAATGTGTTTTTC[A/T]GTCGTTACCCAGAAGCAAAAGTCATCAACTTCGGYACGTGGTTCATCTTC
Long Flanking Sequence:
TTTATTCTTTTACATTTTTTCTTATTATTTATTTATTTATTTATTTATTTATTGATTCATTCATTTATTTATTTACATTGTTTATTTCTATTTTTTTTGTTATTTATTCATTCATTTATTCATTTATTTACATTATTTATTTATTCTTATTATTTATTCATTTATTTATAAATGTATTTATTTATATTTTTATTTTATTTTATTTTATTACAAATAAATTTCAGCAAGACTATGAATAAATTACTGGGGCAATTAACTATCACAGCTTAAATATTATTATTTTTTGTTTAAGTTTTCTTGTTTCTTGACAAAACAATCTATAGTATATTTCCATATTTAGATGAAACAAACATTTGCCATTATCAAAACCTACAAATTTGAAAAATTAGCAATTAAATAGCTTGAGATAACCAAGCTGCCTCTTGATTCAACTCAACTTAACTCCAGCTTAAGTTATATTGTGCTTGCAAAACTAAGTTTTGCTATGAAATGTGTTTTTC[A/T]GTCGTTACCCAGAAGCAAAAGTCATCAACTTCGGTACGTGGTTCATCTTCAGTCTGCCGATCGCTCTCATCATGCTGATTCTCACCTGGATCTGGCTGCACTTTTTATTCCTGGGATGCAAGTAAGAATAAAAGAGAGTGTTTTTGATCTTGAGTTTGTGAAAGGATATTTGCTGACTCTGTTCTCTTTCCACAGTTTCAGAGAAACCTGCTCACTCAGCAAGAAACGCAAAACTAGAAGAGAAATCCTCTCCGAGAAGCGCATTCATGAGGAGTACCAGAAACTCGGCCCCATCAGGTACACTTTTTTTTTATAAAATCACTTTTATAAGGGTTTTAAAAATCTGTGAATATAAGCAGCTTCTAATGGTAAATATGTATTATATTTTATTTTTTCTAATCCCACTTGATTATCTCACCCTCATTAACATATGACGTTAGTCTTGTTTTTAAATCTGCCACTATGCTGACACACAGGCATCTGTAGCTCCGCCTTCTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40211
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 |
|---|---|---|---|---|---|
| ENSDART00000089566 | None | None | 206 | None | 6 |
| ENSDART00000101419 | Essential Splice Site | 311 | 603 | 8 | 15 |
| ENSDART00000129252 | Essential Splice Site | 318 | 610 | 8 | 15 |
| ENSDART00000136962 | Essential Splice Site | 155 | 200 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 4696093)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4814274 |
| GRCz11 | 4 | 4822844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTGATTCTCACCTGGATCTGGCTGCACTTTTTATTCCTGGGATGCAA[G/A]TAAGAATAAAAGAGAGTGTTTTTGATCTTGAGTTTGTGAAAGGATATTTG
Long Flanking Sequence:
TTTATTTACATTATTTATTTATTCTTATTATTTATTCATTTATTTATAAATGTATTTATTTATATTTTTATTTTATTTTATTTTATTACAAATAAATTTCAGCAAGACTATGAATAAATTACTGGGGCAATTAACTATCACAGCTTAAATATTATTATTTTTTGTTTAAGTTTTCTTGTTTCTTGACAAAACAATCTATAGTATATTTCCATATTTAGATGAAACAAACATTTGCCATTATCAAAACCTACAAATTTGAAAAATTAGCAATTAAATAGCTTGAGATAACCAAGCTGCCTCTTGATTCAACTCAACTTAACTCCAGCTTAAGTTATATTGTGCTTGCAAAACTAAGTTTTGCTATGAAATGTGTTTTTCAGTCGTTACCCAGAAGCAAAAGTCATCAACTTCGGTACGTGGTTCATCTTCAGTCTGCCGATCGCTCTCATCATGCTGATTCTCACCTGGATCTGGCTGCACTTTTTATTCCTGGGATGCAA[G/A]TAAGAATAAAAGAGAGTGTTTTTGATCTTGAGTTTGTGAAAGGATATTTGCTGACTCTGTTCTCTTTCCACAGTTTCAGAGAAACCTGCTCACTCAGCAAGAAACGCAAAACTAGAAGAGAAATCCTCTCCGAGAAGCGCATTCATGAGGAGTACCAGAAACTCGGCCCCATCAGGTACACTTTTTTTTTATAAAATCACTTTTATAAGGGTTTTAAAAATCTGTGAATATAAGCAGCTTCTAATGGTAAATATGTATTATATTTTATTTTTTCTAATCCCACTTGATTATCTCACCCTCATTAACATATGACGTTAGTCTTGTTTTTAAATCTGCCACTATGCTGACACACAGGCATCTGTAGCTCCGCCTTCTTTTGAAAAGAGCACAACCTCATATAAATTTAACGTGACAGTCACCAGAACCGCACAGTTAGAGATATAAAGAGACATAAAACATTTTTTGTGTGGTATTTTGAGCTGAAAACTCTTTTGAGCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16821
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089566 | None | None | 206 | None | 6 |
| ENSDART00000101419 | Essential Splice Site | 415 | 603 | 12 | 15 |
| ENSDART00000129252 | Essential Splice Site | 422 | 610 | 12 | 15 |
| ENSDART00000136962 | None | None | 200 | None | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 4699590)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 4817771 |
| GRCz11 | 4 | 4826341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GRTGAACGTTCTGCTGGTCCTAATCTGTAACTGTGTCATTGTGTCTGTGC[A/G]GATGATGAGGATGAGGATGARGAACAGGATCCGCTGGCTCCAATGATCAC
Long Flanking Sequence:
ATTTTAGACAGCATTTTTGCATCTGAAGTCTTTAATATATAACATTGACAATTTTCTGTTCATAACCTTACTACAACGTGCTAACAACATTCCTTGGTTGTTATCTGTATGCACAGTACTGACTAACACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTTCCAGAAAGGGCTACAGAACTGATGCCACAGTGTCGGTGCTGCTGGGATTCCTCCTGTTCCTCATCCCCGCTCGAAAGCCATGGCCATCTGCATTCTCCAGCCAGAGCAAAGGTCAGATCCCAGCCGCGAGTGTGTTCGCTCAGCAGGCCGTAATGCTGTACAGGCTGTTCAGTGGAGTTCCAGGACATGAGAGTAAAGGTGAACGTTCTGCTGGTCCTAATCTGTAACTGTGTCATTGTGTCTGTGC[A/G]GATGATGAGGATGAGGATGAGGAACAGGATCCGCTGGCTCCAATGATCACCTGGAAGGACTTTCAGAGACTGATGCCCTGGGAGATCGTCATTCTGGTGGGTGGAGGATACGCACTGGCTGCCGGGTGCAAGGTGAGATCAAACAATCAATCAACCTGTATTTATATAGCATCTTACTTCAACCAAGGTTGCTTTACACCAGTAAAAACTAATTATACAACACAACTAGAAAGCAAGAAATGCAAAATCAATACAAGAAATGTCACAAAAAAAGGGCAATGCATTAAAACAGAGCAAAGTGTCAGAGTTACTATGCATTAAAAGCCATTTTGAGCAAGTGAGTCTTAAGCTTGGCTTTAAACAGCAGCAGGTCAGTGATTGTACGAAGCTCAATAGGAAGGGAACTCTTTAGATTAACCTGCCACTGCAAAAAAAGGTTGTACCTTAACCCTGGGACTTTTAGCTAGTTGGGTTTTAGCTCTGCTTGGTTGGTGAATGTG
Associated Phenotype:
Not determined