ZMP
slc20a1a
Ensembl ID:
ZFIN ID:
Description:
Sodium-dependent phosphate transporter 1-A [Source:UniProtKB/Swiss-Prot;Acc:Q6NV12]
Human Orthologue:
SLC20A1
Human Description:
solute carrier family 20 (phosphate transporter), member 1 [Source:HGNC Symbol;Acc:10946]
Mouse Orthologue:
Slc20a1
Mouse Description:
solute carrier family 20, member 1 Gene [Source:MGI Symbol;Acc:MGI:108392]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16896 | Nonsense | Available for shipment | Available now |
| sa13777 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16896
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010993 | Nonsense | 192 | 652 | 4 | 11 |
| ENSDART00000142528 | None | None | 179 | None | 3 |
The following transcripts of ENSDARG00000020114 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 31916740)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31059466 |
| GRCz11 | 8 | 31068698 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCWTCATGTCTGCTRTTCTCTTCTACTTTGTCCGCAAGTTTATCTTGAAC[A/T]AGGTAAAAAAGCAARTCTGAGCTCACTTGTTGCATAATGTACCAATGTCT
Long Flanking Sequence:
TCGGCTTTTCCATGGTTGCCAGAGGTCATCAGGGGGTCAAATGGCTGGAACTGCTCCGCATTGGTATGTGAAATTGAGTGTTTTTGAGAATTTGCACAAGCACGCTTAGTCAGATTACATATTTTATCCCTGAGTCAGTAAATGGAAAGAGAATATTTTCTCATGTGACCCCAGAAATAGCAAGTGGTAATGCCTCCCGAACATGCAGATCTCCTCGTATTATTATTCTTTCACATGACCTAAATGAGATCTATTTATGGAGCGGAACATTTTGGACTCTTCAGACAGGAAACATGATTAACCATGGTGACTTAAGGGGTCTTTGTTGATACTTGTCGTGCAGTCCTGAGAAAATTTGAGGAGTTTAATGATACATTGACCATATTTATGTGGCTCATTGATTTATGTGTTTTCCAGTGGCCTCTTGGTTTCTCTCACCTCTCCTCTCGGGCATCATGTCTGCTGTTCTCTTCTACTTTGTCCGCAAGTTTATCTTGAAC[A/T]AGGTAAAAAAGCAAATCTGAGCTCACTTGTTGCATAATGTACCAATGTCTGTTTTGGTGCTTCATAATCTCTTGTTGTAGTCAATAATGAAAGAACATGCGCTTTTTCTTTAATCACGTGCTAAACAACAGCATTTCCATGTGCTCTAGGATGATCCAGTGCCCAATGGTTTAAGAGCATTACCGGTTTTCTATGCTGTTACAATGGGAATCAACCTGTTCTCCATCATGTTTACTGGAGCACCAAGTAAGCTTTTTTCTTTTATTTTTAGATATTTTTTCTTGAACAAGTAGGAAAAAGAGAAAAGAGACAGCTTTGGTTGTATTATTTTATGTTATTCACCATAAATAGGTATGTGTTGTAAGTAAAAATGTAATTTATATTTTATAAACTATAGATAAGGTTTTTGCAAAGTTTTGAAAGCTATCATATAGAGCATTTATTAGCAGAAAATGACAATAGAGTTAAATGATGCAATATAAATCACTAAAATACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13777
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 |
|---|---|---|---|---|---|
| ENSDART00000010993 | Nonsense | 436 | 652 | 8 | 11 |
| ENSDART00000142528 | Nonsense | 16 | 179 | 1 | 3 |
The following transcripts of ENSDARG00000020114 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 31910808)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31053534 |
| GRCz11 | 8 | 31062766 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCGSACGGGACTGGATGGAGAAAAGAGGCGCTCGCGGTACGACAGCTA[T/A]AACAGTTACTGTACGGCGGWAGCTGATGGTGAAGCTGCATTGGAGGATGC
Long Flanking Sequence:
TATCAATACATAAATAAATATTTAAAAATATCGCTAATAAAAATAGCATCATAAAAAATATTGTTATCGCAATACTTAACAATAGTACTGAATATTTTCCCAGGATTATTCACCCCTAATGAAAACAATGTGTTTGCCTACAGTGTCTTGCCTTAAACTTCAGCTTCTTTTTTAACTGACGGTAAAACATTAAAAAAAAATTTGCTACTTCTTGCAGCTTTAAACGGCGGTGGCGGTATTGTTATTCCCGACTTGAGCGGAAACCAGTTTCACACCGTTCACAAAGACTCAGGAATCTACAAGGATCTTCTTCACAAACTTCACCTGGCCAAAGTAGGTGAATGCATAGGAGAGCCCGTAGAAAAGCCCATCCGCCGCAACAACAGCTACACCTCCTACACCATGGCCATTTACGGCATCCACGGCTCACTAAAGGACGGAGAGGGAGGAAGCCGGACGGGACTGGATGGAGAAAAGAGGCGCTCGCGGTACGACAGCTA[T/A]AACAGTTACTGTACGGCGGTAGCTGATGGTGAAGCTGCATTGGAGGATGCGGCTCTGGCGGTGGGGATGGAGGATGAGGCACTCAGAGGAGATGTGCTGGAGGAGGATATTGATGAGCTGGAGATCGACAAGCCTGAGGTGTCCACACTCTTCCAGTTCCTTCAGATCCTCACCGCCTGCTTCGGCTCATTCGCACATGGGGGGAATGATGTTAGGTATGTAAGATGGGATTTTTCAGACTTCTTTAAAAAAAAAAAAAAAAAAGTGAATTTAGGTGTATTTATTTTGAGATTTAATTAATTGGCAATTAATTATTAGTGATTTTTCTAACTATAATTATGTTTATTGGATTTTTTACAATAATACAAACAAAACAATACATCTTCAAAAGACACGCAAAGAAAAATATCAACACAAAACTATGAAGAAAAAAAAAGGAAAAAGAAACGAAAGAAAAAAAACTTAGATTATATATAAAACAGCACTACCCCAAATAAAAC
Associated Phenotype:
Not determined