ZMP
slc20a1b
Ensembl ID:
ZFIN ID:
Description:
Sodium-dependent phosphate transporter 1-B [Source:UniProtKB/Swiss-Prot;Acc:Q6PFM1]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17030 | Nonsense | Available for shipment | Available now |
sa11277 | Essential Splice Site | Available for shipment | Available now |
sa31775 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17030
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 |
---|---|---|---|---|---|
ENSDART00000039969 | Nonsense | 18 | 665 | 1 | 10 |
The following transcripts of ENSDARG00000010641 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 17745164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17757510 |
GRCz11 | 10 | 17714944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GWGTCAACAACTCTTGCCACGATAACAATTATGAGCAYCCTCGTCGGGKA[T/A]ACTACAGGGCMTCTGACAGMCTATATGTGGCTCCTGATCGTAGGCTTCAT
Long Flanking Sequence:
ATAATGCGGGAACCTTACCAATTTCTCTTCTCTTTTTTTTTCAGGAATGAGCTACCATTCACCCATCGTGTCTGTTGCACAATGGATGTCCGCTGTATCTGCTTAATTGTCCAAGCCAAAACAAACCGTAACAGATCTAGCCTATTTAGGGGATAGCAATAGGCCCTCACTCCACCCTCTCCCTTTACGATACACATCAGTTTAGAGCAGGGCAGTGCAGATTCTCTCTCTAGTGTCTGGATTGCTTTGATTTTGCTGGTTTAGCAAAGGGCGAAGGTAGGTCTGAGGCAGAAAACGGATTTAGAAACAATAGTACCTCAATTAGCTGGGGATAAAATATCCAGTGTGCTGCTGCTTGAATTATTTATACATTTTTGGTTCTCTTCCCTGTAAGATTGTGAAGTAATTATTTTTTTTGCTTGAAACTTGAAAAACCATCTGCGCACAATGGTGTCAACAACTCTTGCCACGATAACAATTATGAGCACCCTCGTCGGGTA[T/A]ACTACAGGGCATCTGACAGCCTATATGTGGCTCCTGATCGTAGGCTTCATCATAGCATTTGTCTTGGCCTTTTCAGTGGGCGCTAATGACGTTGCCAACTCATTCGGTACGGCAGTAGGCTCAGGTGTAGTTACCCTTAGGCAGGCCTGTATTCTTGCTTCTATCTTTGAGACTCTGGGCTCTGTGCTGCTTGGAGCCAAGGTCAGCGAGACCATCCGCAAAGGCATTATCGACGTGACCATGTACAACGATTATGAACATGTGTTGATGGCTGGCTCGGTCAGCGCTATGTTTGGTAAGTAACTTATGAAGCTTAGTTCTTGTGTGTTATGTAGTAGGGTTGTCGCGATACCATTCCCATTACGATACTGTACCAGCTGAAGTATCGGGATACCAAGTAGTATTGCAATACTATAACTCAAACCAATGAAATAAAGAGAATTGTCAGAAATACTGTTTTATAAGTCCTTATAGGCCTACTTCAATTGAATTCATAGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11277
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039969 | Essential Splice Site | 192 | 665 | None | 10 |
The following transcripts of ENSDARG00000010641 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 17746448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17758794 |
GRCz11 | 10 | 17716228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
MATGTCTGCCGTCCTTTTCTACTTTGTTCGCATGTTCATCTTGCAAAAGG[T/C]AAACAGGATSTAATTTTCAGCTTATTATAAAGCATTGTAGAATTCAAGAT
Long Flanking Sequence:
ACATTTGCGCTGCCAGTATATTGGAGCCATAGTATCACAATTCTACCATAGTACCGGTATACCGTGCAACCCTATTATGTAGTAATACTTGTTTTTTATTTGGAATACTTGTGGTTTCTTCTTTTAAACTCTCAATTTTTCTACTGCATATCAGGCTCTGCTGTATGGCAGTTGGCTGCTTCTTTTCTGAAACTACCTATTTCTGGGACCCACTGCATCGTTGGAGCTACTATAGGCTTCTCGCTGGTTGCTAAAGGTCAGCAGGGAGTCAAATGGCTGGAGCTTCTCAGAATTAGTGAGTCAGCAGCATTCACAAGCACTATCCATTTGTTGTTGTGCTCGTATGATTAATATTGTTGTCAAGAAACATTTGTTTGATTACTTCTATTTCATTGTTCTTTCTTTCCTTACAGTTGCTTCATGGTTCCTCTCGCCTTTGCTGTCCGGCGTCATGTCTGCCGTCCTTTTCTACTTTGTTCGCATGTTCATCTTGCAAAAGG[T/C]AAACAGGATCTAATTTTCAGCTTATTATAAAGCATTGTAGAATTCAAGATTCAGCTGTTTATATTGACTTTTCTCTTCCATATGCAGGGTATGGAATAAGATGTAGTGTCTTTGAAAACACTTGCACAGTCTATCTTAGAAAATGTGAAATTACAAATCATTCATAAGCAATTATACATTAAGCTGACTACAACCTGTCTTTGTATGTGATGTTAATATATTTATGAACTAGCTAAGTGTGAATAGGATTGTCTATTTGTTCAAAGTGCACATCTGCCGGTCTTTCAGTATGATTGTAATTTGAGAGATCACAAATTTGGAAATCGTTTTAATTCTCTTGCACATGCAAACATCACATGGCATCTTTTTTGTTTTGTTTTTATTTTCAGTACGTTGTTATTGATATGTATCCAACCTTTGCACCTGTGAGACGATGTTCTGTTTCAGTGTTGATATTTATGGATAAACAAAGTAGTGTGAAAACAATTGAAAGTTAATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31775
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039969 | Essential Splice Site | 586 | 665 | 9 | 10 |
The following transcripts of ENSDARG00000010641 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 17756265)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17768611 |
GRCz11 | 10 | 17726045 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAACCTCCCGCATGGCAGACTTCCCTAAACAACACTTGTTTAATTTCA[G/T]CGGTTTCAGCATCGAGCTCGCCTCCGCTGTCACTGTTGTGGTGGCTTCCA
Long Flanking Sequence:
TTATTTGACAATTAAGTCGAAGCGGTGCACTAAAGGAAAACTAATATGATGTACTTTTTGTTCATACTGTTGAAAGTACTAATGTTATGAGATCAAAGTCCTTACTGTAAAAACTTCTTGACTTTTTAATTAACCTTACTAATTTGTAAACTCAATCAACCCACTCTTGCCATAAGCTTTTGAAGTAATTTAACATAATCTTTTACTTTCAGTAATGCAATTGGTCCCCTGGTTGCTCTCTGGCTGGTCTATGAGAGTGGGTCTGTTATATCGAGTGCACCGACTCCAATCTGGCTGCTGCTGTATGGAGGAGTGGGCATCTGTGTGGGCCTGTGGGTCTGGGGCCGTAGAGTCATCCAGACCATGGGCAGGGACCTGACCCCCATCACCCCATCAAGGTATAAACACACACCCATGTTGCCACATCAAAAAGCACCTGCTGTACAGAACACAAACCTCCCGCATGGCAGACTTCCCTAAACAACACTTGTTTAATTTCA[G/T]CGGTTTCAGCATCGAGCTCGCCTCCGCTGTCACTGTTGTGGTGGCTTCCAACATCGGTCTTCCAGTTTCCACTACTCACTGCAAGGTAAAAAAAAGACTTGTATGCAAAACAAACTGATGCAAAGCAAGTCCTAGATGGCGTGTATTTGAATGAGATTGATATCTGCAGGATTTTGATGAGGGCATTTGGTGTTTTCATTTTCAGGTCGGGTCTGTGGTGGCTGTGGGGTGGCTGCGCTCCAGGAAAGCTGTGGACTGGCGGCTGTTCAGAAACATCTTCATGGCCTGGTTTGTCACGGTGCCCATTTCTGGCCTTATCAGCGCCGCCATCATGGCCCTTTTCACCTACGTCATTCTTTGAGGCCTCGAAGGTTCGCTCTGCCTCCCTCTCCGCTCGCACAGAGCCTCCACCTGCAACCAGGATCCCAAGAGAGTTGGAGGGCACGTCTCCATCTTCCCCTCCCGTCTCTCTTCATCTTCCCCCTCCTGTCATCCTCGTG
Associated Phenotype:
Not determined