ZMP
slc26a11
Ensembl ID:
ZFIN ID:
Description:
sodium-independent sulfate anion transporter [Source:RefSeq peptide;Acc:NP_956061]
Human Orthologue:
SLC26A11
Human Description:
solute carrier family 26, member 11 [Source:HGNC Symbol;Acc:14471]
Mouse Orthologue:
Slc26a11
Mouse Description:
solute carrier family 26, member 11 Gene [Source:MGI Symbol;Acc:MGI:2444589]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24093 | Essential Splice Site | Available for shipment | Available now |
sa43785 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15196 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa29736
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063157 | Nonsense | 211 | 572 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 11620327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 11480495 |
GRCz11 | 22 | 11510177 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATTGACATTTATGAAGAATTCTCTGAGTTCGGCTGAAGACGAGGCTT[C/A]GTTTCTCGTGCGATCTGCACGACAGCTGCTGTGGAGTTTAGCTACTAGTA
Long Flanking Sequence:
ATTTTTAACTAATCAGATGAGTGATTCAATGATCCATTCATAAATACAGTCACTTGCTTTGATTCTCAGTGAACCAGTTGTTTTGAACAAATCATTTAAATGATTCATTTAGTGAATCGTTGATTTAGTCAGAGATTTGTTGCCTCTTACTAGTTTTAATGTCATATTTATCTATGTAAAACACACTGTTGTCTGATTTGTTAGTTTTGCTGGTGAAAATCACCAAAAACAATTCCCTACATTGTTTAATGGATTGTTGCCTACTGGCAGTATTATTATCACATTTATTTATCCTATAACAAGTCTAAAGCAACCAATGAAATGAAATGTCTAAGTATCATTAGCAAAAATATATACATTGATATATAATTTATTGAGAATTTTCTCTAATCTGTGTTTTCTTAGAGTAGGAGATGTGATTCTGGGCCTGTCCTGTTTGTTTTTCCTGCTTATATTGACATTTATGAAGAATTCTCTGAGTTCGGCTGAAGACGAGGCTT[C/A]GTTTCTCGTGCGATCTGCACGACAGCTGCTGTGGAGTTTAGCTACTAGTAAGTGCTCTGAAAGCCTTGTGTATATTAATGATAAACAATATATATTGTTATTAATGTCTATTTTCTGCTGGTGTCTTCAGTTCGTAATGCACTGGTGGTCATAGCAGCGGCGGGTGTCGCATATTCGGCTGAAGTCACAGGAAACCATTTCTTCAGTCTCACGGGGAAAACAGCAAAAGGACTGCCTCCTTTCAGAGCACCGCCCCTTTCAGAGACAATAGCCAATGGCACGGTTATTACGTTCAGTGACATCGCGAAGGTGTGCATAAAGATTTTAGCTTTCATATTGCATTTTTCATTGTTATATTATGAATACATAAATTAGAATATGAATTTTAATTATATATATTATTTATAATATGATTTCTAGCAAATTGAAAAAATATTGTTTGTTTTTCTTATATAAAATGTATTTTAATATGAAATATAATGCAGTTGTATTAAAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24093
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063157 | Essential Splice Site | 227 | 572 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 11620197)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 11480365 |
GRCz11 | 22 | 11510047 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATAAACAATATATATTGTTATTAATGTCTATTTTCTGCTGGTGTCTTCA[G/A]TTCGTAATGCACTGGTGGTCATAGCAGCGGCGGGTGTCGCATATTCGGCT
Long Flanking Sequence:
AGAGATTTGTTGCCTCTTACTAGTTTTAATGTCATATTTATCTATGTAAAACACACTGTTGTCTGATTTGTTAGTTTTGCTGGTGAAAATCACCAAAAACAATTCCCTACATTGTTTAATGGATTGTTGCCTACTGGCAGTATTATTATCACATTTATTTATCCTATAACAAGTCTAAAGCAACCAATGAAATGAAATGTCTAAGTATCATTAGCAAAAATATATACATTGATATATAATTTATTGAGAATTTTCTCTAATCTGTGTTTTCTTAGAGTAGGAGATGTGATTCTGGGCCTGTCCTGTTTGTTTTTCCTGCTTATATTGACATTTATGAAGAATTCTCTGAGTTCGGCTGAAGACGAGGCTTCGTTTCTCGTGCGATCTGCACGACAGCTGCTGTGGAGTTTAGCTACTAGTAAGTGCTCTGAAAGCCTTGTGTATATTAATGATAAACAATATATATTGTTATTAATGTCTATTTTCTGCTGGTGTCTTCA[G/A]TTCGTAATGCACTGGTGGTCATAGCAGCGGCGGGTGTCGCATATTCGGCTGAAGTCACAGGAAACCATTTCTTCAGTCTCACGGGGAAAACAGCAAAAGGACTGCCTCCTTTCAGAGCACCGCCCCTTTCAGAGACAATAGCCAATGGCACGGTTATTACGTTCAGTGACATCGCGAAGGTGTGCATAAAGATTTTAGCTTTCATATTGCATTTTTCATTGTTATATTATGAATACATAAATTAGAATATGAATTTTAATTATATATATTATTTATAATATGATTTCTAGCAAATTGAAAAAATATTGTTTGTTTTTCTTATATAAAATGTATTTTAATATGAAATATAATGCAGTTGTATTAAAATTCATTTATAAATAAGAATATAAATGATCTGAGGTATTAGGATATTTTATTGATATAATATGTTCGATTTATACAATGTAAAACATTTAAATATTAAAAGTATCTAAAAGCAAACTATTTTGTAAATATTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43785
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063157 | Nonsense | 297 | 572 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 11619120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 11479288 |
GRCz11 | 22 | 11508970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGGTGTGAATTTGTCAGGATTTAGGTGGTGGTCTTGCTGTCATTCCTT[T/A]AATGGGTGTTTTAGAGAGCATCGCCATTGCGAAGGCATTTGGTAAGGACC
Long Flanking Sequence:
AGCATTTACAAATAACAAAACTATTTAAGGTATTTAAAAGGCTTAAATATTTTTGCATATCAATAGTATATTTATTTATTTGAAATATTTAAATTTCAATCAAATATAAATCTTTCTTTAATATTTCTTAAAACACTATTAAAATACAATTGCTTTGTGTGTAAATTAATATTAAATGCATTAAAAGAGCTAATATGTTTGATTATACAGTATAAACACTGATTATTACAATAAAATATAATATTGAATAAAAATGGGAAGCTAATAATTAAATGCGTAATATTAATTACTTTATTGCACTACTATTGTCAGCTTAGGCTGTCTATAAAATAATACAATTATTTATTATGATACATTTTAAAAACAATAAATATTTTAAAGCAATCTAGTGCCCCCTTGTGGCTGAATAAGTATGACATTACAACACATTTTAGAGATTTAATTAATCGCTGAGGTGTGAATTTGTCAGGATTTAGGTGGTGGTCTTGCTGTCATTCCTT[T/A]AATGGGTGTTTTAGAGAGCATCGCCATTGCGAAGGCATTTGGTAAGGACCTTATTCTCTTTAAAATACACTTAAAAGTGTACTTCCATGCATCTGGCTATACTTTACAGTCTTTTCTCAATGCAGGCAGCAAGAACAACTACAGAATTGATGCAAACCAAGAGCTCTTCGCCATAGGTGAGAGTTTCCCTTTCTGTTTCTACTATTTAGCTTTTTTGCTTTTGCGCTTGTTATTTATGAGACTACCTAAACAACATCAAACTTTTAAAATGACTCAAGATGTTCTGTTTAAATATGCAAATGAGTCCTTGTTAATTATGTGCTGATTTGCATACATTTCTAGCGCATTAAGTCAGGTTTATTTTTTATTTATTTATTTTTTTGGAGACATTAGAGTTAAGGAGGTTTTTTGGAAATCTTTTTAATAACCTATATATTTATTTATTGATAATTTTTTATTTGTAGAATAAATATTGGACATATTTATTATCAGCCAAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15196
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063157 | Essential Splice Site | 366 | 572 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 11615689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 11475857 |
GRCz11 | 22 | 11505539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTAATTCTCAGACTGGAGTGTGTTCTCCTGCTGGAGGMATCATCACAA[G/A]TAAAACTCACACTTTATRATGGYGTTGATGTTGATRAGGATGCAGAWGTT
Long Flanking Sequence:
AAATCTTAAAAATTAAACCCGATCTGAATATTTTTATGGTGGACGAAGTTGTGACTGACATAACGTGAAGTCATATTTATTTTTTTTAACATGTGCAAATTTCAGACTCTGTGTGCAATGAACTTAAATTCCTTGTGAAATCTAAAAGTACAAAGTTTATTTTGTTAGCAATTCATTTGTGCAAGCTAATCAAGTAAAAAAAGTTTGTTTTGGTAATTTTCAATACAAATTTGAGCATTTGCTTCTGCGTTTGGAGTGGTTAGGCTTTTCTTGATGACTTCAGTTTACCGGCTTCAGCCAGAATATTCTTAGCCACGGTCCTTGTACCGATAGTTTGCTATAAGGGAATGCAATAAGAAAGCCCCACCCCTACTAGATATTCCATGTCCGTTGGAAGTGCATCAACAAATGCAGATTTTAGCTGTTGTTTATTTTTCCTTCCAGAACGGCTGTTAATTCTCAGACTGGAGTGTGTTCTCCTGCTGGAGGAATCATCACAA[G/A]TAAAACTCACACTTTATGATGGCGTTGATGTTGATAAGGATGCAGATGTTATAATGTCAGTACGTGTGTGTGTGTGTGCAGGTGTTATAGTGCTGCTATCACTGGCCTTCCTCATGCCGCTGTTCTTCTACATCCCCAAAGCGTCTCTCGCTGCCGTCATCATCTGTGCTGTGAGCCCAATGGTGGATTTCAGAGTGCCGCTGCACATCTGGAGAGTCAAGAGTGAGAATTTAACATCATGTTCACATGAAATTGCATATACAAATATTCGAAACATATTATTAAATGTAATAAGGATTCATTGATTTTTTTATTTTAATAAATATATGTATTTTTTTTAAATATACATACACCATTAATCTATTTTAATATTTATAAAAAAATTTTTTTTTTATAAATTTGTAAATAAATATAAAAATTGTTTAAAAAAATTTACAAAATCATTAAAATAATTTATTATTTACATTACAATAGTTATATATTTCATGCACTATTATTGT
Associated Phenotype:
Not determined