ZMP
slc12a9
Ensembl ID:
ZFIN ID:
Description:
Solute carrier family 12 member 9 [Source:UniProtKB/Swiss-Prot;Acc:A2BFP5]
Human Orthologue:
SLC12A9
Human Description:
solute carrier family 12 (potassium/chloride transporters), member 9 [Source:HGNC Symbol;Acc:17435]
Mouse Orthologue:
Slc12a9
Mouse Description:
solute carrier family 12 (potassium/chloride transporters), member 9 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33660 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38493 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9521 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33660
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084917 | None | None | 515 | None | 6 |
ENSDART00000139479 | Essential Splice Site | None | 899 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 39848895)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37648285 |
GRCz11 | 5 | 38248438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTTTTTTTAACAAACAGAGGCAGGAGGTGGTACAGGCTCTGAGAGGG[T/G]ACGTTGCAGGTTACAACCATCATCACATCTCAATAAACCGTTATATAAGA
Long Flanking Sequence:
TACAAAATGCCTCATCAGGAGTCCAACATGACTGTATGAGTTGTTTCCACTTAACATAATTTAAGCGTTTTAAAAATTTGCTTCAAACATGAATAAAAGTTCACAATTGTGCATTTTCTGGTTATAGACCAGTTACTTTTATTGATACAACCATGTGCATCCTTTATAAATAAGAACTGAAACTACATTTTTTTAAAGTTTGGATGAATGCAGCACTTTCAATACATATAAATAATTAGGCTATTTTGTACCACTAAAGCATTTAAGTGCATTGTTTGTATTGTAAGTGCTTGCTGTAACCTGAGGTTTACATTTTATTTCTGATTAAATGTTCCACTAGTGAGATTTACGGGTGTATTATAACAAACCAAATGGTAAACAACACGGTTCCCACATGTTCCTCTGACTCTCTTTCCTCCGTAGAGTCACATGGGCGCTTCCTCTGTCCCGTGACTTTTTTTAACAAACAGAGGCAGGAGGTGGTACAGGCTCTGAGAGGG[T/G]ACGTTGCAGGTTACAACCATCATCACATCTCAATAAACCGTTATATAAGAGATGAATGTTTTGAAGAGGTCTGCTGTCTGTCGTTCACAGCCTGACACAGGAGCGCGTTTCACCATCCGTCATCATGATGATGATGTCCCGGAGGTTTGACGGTCACGAGATCTGAGGCTGCGGAAGAAACTTTCTACACGCGAGTCTTTGGACAAACGAAAGCTGCTCGGCGTGATGCTCTTATCGAACAGATAGGAGTCAGGACATCCCGGGTCCACATTATCAAAACGAGTATTTTGGTTTCCGTTGTTTTGTGCAGCTTCTTGAAAGCGGAAGTAAAACACCGCTTTTTTGGATTTGTCTTGGCGCTGTTATACGGACAGGTAGGTCGCGGTTGTTTCTCTTCACTTTAATTACTTCACCGCTATTTCTGTCTTGATAACCTCATCCACCCAACATCTGCTGGAGATCATGATGATGATGATGACGGTGGTCAGGAAATGTCAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38493
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 |
---|---|---|---|---|---|
ENSDART00000084917 | Nonsense | 142 | 515 | 4 | 6 |
ENSDART00000139479 | Nonsense | 526 | 899 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 39825669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37625059 |
GRCz11 | 5 | 38225212 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGATGGTCTTTCTGTGCTTCTTTAGGTGAGGAAGTACCTTCTGATGT[T/A]GGACTCTCGGAAGGATCATGTGAAGTTCTGGCGGCCGCAGGTGTTACTGA
Long Flanking Sequence:
TTATATCATCATATAATGCTGGGGGATTGGCTCTTTTGTCAACTTATATACAGTATATACTGTTCAGCCTGTACAGTCTCTGATCTTTTAAACCAATACCACAAAATAAGGTTGTGTATCTTTCATACTGTACAAAAATCTTTAATAATAGTTCATTCATTGCAAATTTTAGATTTCTGAATTAGAAATGTAATTTCTGTTTTATAAATGTATCAATGTGATCTGAGGTCTAACTACTAACCCTAAACTAAAACAGACAGTACTGATACTTGTGAAATACATGTTTGAAGCCATACTTTACTTTTACTTGAGTAAAAATGAGTACTTCACTTCATACAAGAATCATTTTAAACTCGAGTGTCTGTATTTCTACTCTAGTAAAGGATGTATGCCATCTCTTCTCTCTCTCACACATACACAACACATATGAATGTACTAAACTTCAAATTGATGAGATGGTCTTTCTGTGCTTCTTTAGGTGAGGAAGTACCTTCTGATGT[T/A]GGACTCTCGGAAGGATCATGTGAAGTTCTGGCGGCCGCAGGTGTTACTGATGGTGTCCAACCCACGCTCCTCCTGTCAGCTCATCTGCTTTGTCAACCAGCTGAAGAAAGGGGGCCTGTTTGTCCTTGGACACGTGCAGATTGGAGATCTGGGTAGGTTCAGACAAGGGTCAGGGGACAAATGTGTAATAGTTGGAGGAAGTTGCACAAAATTCATTGACCAAGATTTTGATCCTTAGCCAATTGCTGTTTTTGACCTACAGCTGAATACCAGATGTTTTAACCCCTTCCTCTTAAAGCCCAATGTACACTTCCTCACATGCATGCACACACACACACACAAACATGCATACATAAATGCACAGCTATTCTTATTATCCTAAGGGGTCCTCAAGGGAGTCAAATCTGGACTGGCCAGAACAGGCAGCTAGTATGGACCCTTTTCACATTTCCGAGGTCCCAGTAGTGTAAGTCATCACCGCTGGGTAAATTTAGAGCGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9521
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 |
---|---|---|---|---|---|
ENSDART00000084917 | Nonsense | 201 | 515 | 5 | 6 |
ENSDART00000139479 | Nonsense | 585 | 899 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 39821585)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37620975 |
GRCz11 | 5 | 38221128 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTCTCTCTGGACWCTGTCTCCCAGATGTGCTGCCAGCAGACCCGGTG[C/T]AGCCGCAGTATAATTTCTGGTTGAGTCTGGTGGATAAGCTGGGTGTGAAG
Long Flanking Sequence:
CCAATGAATTAGTTTTGCAGACCTTTTGGCAGCTAATGTTTTGTTTTTGTGTTATTCCACAGTAAACTATTCATTTAAATCAGATTAGCTGTTAACTCAGGCTCATTCACCCTTATAGAGGACTTGCTCTTTCATTAAAATTCATGATACAGACCTGTATGACCAGTTTTCCTCTCTGAAACCTAAAAGAAGATATTTAGAAGAATTTTCTCAGCTGTCTCTTTGAGATCTGACAGAAAACCTTCATGCTCTTTAAAGTCTGTTTGCATTGCCATTTTTGAATGACTGTACAGCGAAGCGCATCAGAAATGCAGCATGTTGTCAATGGAAATGCCATGTTTTTTAAATGCTGGCAGTGTAGCCGGGCACTGACTTGTTTTATGGTCGGAGTTTTTTTTATTCATACCTGTAGAAATACCTGGAAATGGAAACAAGCAAACAAATAAGCATATATTCTCTCTGGACTCTGTCTCCCAGATGTGCTGCCAGCAGACCCGGTG[C/T]AGCCGCAGTATAATTTCTGGTTGAGTCTGGTGGATAAGCTGGGTGTGAAGGCCTTTGTGGATCTGACTCTTTCTCCCTCGGTCAGGCAGGGCACTCAACATCTGCTCCGCATCACTGGACTTGGTGAGACGTTCCTTATCACATTATCTTTACAGCGTGGAGCCAGAAAGCTGCTTTCAGATTAGATTTATCTGCATTGTTATTGTACAAAGTGCAAATGCATAGCAAGTGAATTAGTACAGTAAGTACAGTAATGTTATCTTTTCCACAGCTAGTTCAGAAACTGCAGCTGCTTCACAATATTAAACATCACTCATGTTGTTTTGACCCTTCCGACTCATCTTACATGAATACTATTTTTTGTATGTGTGCATAATTGAGAAGACACCAAAGAAATGTTTAATGTGAACTGATTTACATGGAAAACACAGAAATTTCATAATTTAAAAAAGAAAATGAATAAAGAGAACTTTGTAAGATAATTTTTAAGGTATTTGTGA
Associated Phenotype:
Not determined