ZMP
si:dkeyp-106g6.1
Ensembl ID:
ZFIN IDs:
Human Orthologue:
SLC12A7
Human Description:
solute carrier family 12 (potassium/chloride transporters), member 7 [Source:HGNC Symbol;Acc:10915]
Mouse Orthologue:
Slc12a7
Mouse Description:
solute carrier family 12, member 7 Gene [Source:MGI Symbol;Acc:MGI:1342283]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17478 | Nonsense | Available for shipment | Available now |
sa37961 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24565 | Nonsense | Available for shipment | Available now |
sa24564 | Nonsense | Available for shipment | Available now |
sa24563 | Nonsense | Available for shipment | Available now |
sa24562 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17478
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 |
---|---|---|---|---|---|
ENSDART00000089232 | Nonsense | 163 | 1119 | 5 | 26 |
ENSDART00000134251 | Nonsense | 141 | 1055 | 5 | 24 |
The following transcripts of ENSDARG00000062058 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 41384282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39923476 |
GRCz11 | 24 | 39811323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTAGTAATTGTGTTTTATTGTGTTTTTGTTTTTTGTTCACAGACAATGT[T/A]GACCGCCATWTCAAKGAGTGCCATTGCCACAAACGGTGTTGTCCYAGGTA
Long Flanking Sequence:
TATAAATAAATGTGAAATAATAGTAACTATATAAATATAAACAAAGAAAAATAAACGAAAGTCATTTTTTTTATATATATATAATATTGTGTGCGCATGCGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTATGCGTGTGCGTGCGTGTGCGTGTGCGCGTGTGCGTGTGTGCGCGCGCGTGTATGACTAAAATTTAAATGTAATTTTTTTATTTTATATTTAATTTACTTTTTTAAGCTAAATTTAATGTTTAATTTTAATTGTTAATTTAATTTAAAATGTGTTTTTTTGTATTTAGATTTATGTAACATTCATTTACATATTGTATATTCTCGTTTTAAACTCTAAATAATGTTAATTATTTGATTTTAATTTACATTGAAAAAATGTCATCAATATGTTTAATGTTTAGTTTTATTTTATAGCATTTTATTTCATTTTAGTTAGTAATTGTGTTTTATTGTGTTTTTGTTTTTTGTTCACAGACAATGT[T/A]GACCGCCATATCAATGAGTGCCATTGCCACAAACGGTGTTGTCCCAGGTAAGACACTTTCATATTAATTTACAACGTAAACGTGTGTGCATGTCAGAAATCTTTTCTAAACCAGTGTTTTCCACAGTGTTGTCATTGACGTTGAGTGTTTTGTTTTGCTGTGTTGACTGATGATGTGCTGGTGTTTTTGTGCAGCCGGTGGCTCGTACTACATGATCTCTCGCTCTTTGGGCCCTGAGTTTGGTGGCGCTGTGGGTTTGTGTTTCTATCTGGGCACCACATTCGCCGGTGCCATGTACATCCTCGGCACCATCGAGATCCTGCTGGTGAGAGTTCATTAATACAGCTTCATTAAGACACTGTGAAGCAGGAATATCTGTAAACGAGTGTATAATATATTAAATATTCATGACATATTCTTATTTGACTCCTAAGAATGTTCTCTTTCCTCTGTTCAGTATAAAGTTAAACACTTGACCTGACAGTAAACTGAAGTGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37961
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 |
---|---|---|---|---|---|
ENSDART00000089232 | Essential Splice Site | 178 | 1119 | 5 | 26 |
ENSDART00000134251 | Essential Splice Site | 156 | 1055 | 5 | 24 |
The following transcripts of ENSDARG00000062058 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 41384234)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39923428 |
GRCz11 | 24 | 39811275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGACCGCCATATCAATGAGTGCCATTGCCACAAACGGTGTTGTCCCAG[G/A]TAAGACACTTTCATATTAATTTACAACGTAAACGTGTGTGCATGTCAGAA
Long Flanking Sequence:
AAATAAACGAAAGTCATTTTTTTTATATATATATAATATTGTGTGCGCATGCGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTATGCGTGTGCGTGCGTGTGCGTGTGCGCGTGTGCGTGTGTGCGCGCGCGTGTATGACTAAAATTTAAATGTAATTTTTTTATTTTATATTTAATTTACTTTTTTAAGCTAAATTTAATGTTTAATTTTAATTGTTAATTTAATTTAAAATGTGTTTTTTTGTATTTAGATTTATGTAACATTCATTTACATATTGTATATTCTCGTTTTAAACTCTAAATAATGTTAATTATTTGATTTTAATTTACATTGAAAAAATGTCATCAATATGTTTAATGTTTAGTTTTATTTTATAGCATTTTATTTCATTTTAGTTAGTAATTGTGTTTTATTGTGTTTTTGTTTTTTGTTCACAGACAATGTTGACCGCCATATCAATGAGTGCCATTGCCACAAACGGTGTTGTCCCAG[G/A]TAAGACACTTTCATATTAATTTACAACGTAAACGTGTGTGCATGTCAGAAATCTTTTCTAAACCAGTGTTTTCCACAGTGTTGTCATTGACGTTGAGTGTTTTGTTTTGCTGTGTTGACTGATGATGTGCTGGTGTTTTTGTGCAGCCGGTGGCTCGTACTACATGATCTCTCGCTCTTTGGGCCCTGAGTTTGGTGGCGCTGTGGGTTTGTGTTTCTATCTGGGCACCACATTCGCCGGTGCCATGTACATCCTCGGCACCATCGAGATCCTGCTGGTGAGAGTTCATTAATACAGCTTCATTAAGACACTGTGAAGCAGGAATATCTGTAAACGAGTGTATAATATATTAAATATTCATGACATATTCTTATTTGACTCCTAAGAATGTTCTCTTTCCTCTGTTCAGTATAAAGTTAAACACTTGACCTGACAGTAAACTGAAGTGTGGATGTTTATTGTGTGTTGTGTGTCAGACGTACATCGTGCCGAGCGCCGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24565
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089232 | Nonsense | 336 | 1119 | 8 | 26 |
ENSDART00000134251 | Nonsense | 314 | 1055 | 8 | 24 |
The following transcripts of ENSDARG00000062058 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 41381946)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39921140 |
GRCz11 | 24 | 39808987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCATGAAGACAGAAATAATCGACAACGTGACGGTGACCACCAAACTCTG[G/A]TCCCTGTTCTGCTCGGGGCCGGAGCTCAATGCCAGCTGTAATGAATATTT
Long Flanking Sequence:
CCGGTTTCCCCCACAGTCCAAACACATGCAGTACAGGTGAATTGGATGGGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGTGAATGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGAAAGGGCATCCGCTGCGTAAAAACGTGCTGGATTAGTTGGTGGTTCATTCCGCTGTGGCGACCCCAGATTAATAAAGGGACTAAGCCGAAAAGATAATGATTGAATGAATGGATATTTTAATCAGTTAAATTTCATGTTAAGTGCGCATTAATTATAATAATATTTATATGCTAATCATTTTTTTTTAGCTTTTTTGTGCTTTGGTGAATAAAAAAATCCAAACAAATGTACATAGCCTTCTCATAAATGTGAATGGTGTGTTGTGTGTCCTGCAGGGTGTGTGTGTTGGGCAACAGGACACTGCAGAACCACGACTTTGACAAGTGCATGAAGACAGAAATAATCGACAACGTGACGGTGACCACCAAACTCTG[G/A]TCCCTGTTCTGCTCGGGGCCGGAGCTCAATGCCAGCTGTAATGAATATTTCACCCTCAACAGCGTCACCGAGATCCAGGGCATCCCCGGCCTCACCAGCGGAGTCATCTCAGGTCAGAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAACAGCTCAGATCAGTTTTATATAGGGTATAGGAAAATATTAATGGGGTGGGAAAAAATAATAAGCTAATCCGCTTCATTTCCAACTAGTTTTAATATTGAGTTCACACAGATATGAAGATATTTGGCTGAGTATGATGAAATGTGTTTGTCTTTGAATCATTGTAAATAAATTAATCAAATCCAAAAACTAAATCAAATAAAAAAATACAAACTATTTTATAAATAAACTGTGTCCATGGATCTGTGTGTGTGTGTTTGTGTGTGTGTCTACACGTGTGTTTGTGTGTGTTTGTTTGAATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24564
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089232 | Nonsense | 377 | 1119 | 9 | 26 |
ENSDART00000134251 | Nonsense | 355 | 1055 | 9 | 24 |
The following transcripts of ENSDARG00000062058 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 41379761)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39918955 |
GRCz11 | 24 | 39806802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACACATCACTAATATTGAGCTGTTGTATGGTTTGCACAGAGAACATGT[G/A]GGGAAAGTACGGTCCGGCCGGGATGCTGGTGGAGAAAGATATACCGTCTG
Long Flanking Sequence:
GCAAAACAAATGCACTGTGGACACTTTTATTTTAGCGCAGGCTTGTTTTACTGCTATAAATGCTGTCAACACATTGATCATTGCATGTTCTTGTAAGAATGTAACAGTAACAGATATTTCAGTGCAGAAATAATGCATGCGTCATCAGCACACAGATATATAAAAGCAGTATCACAATTTCTATGATGCACACATGCTGATATCGTCATCCTTTCCTGTATAATAATACTGAACCATATCATCTCTTATGAATATTAAAACACAAAACCATACAGGGTTTTTTTTGTTGTTGTTGTTGCGTGTTTTGAAGAATTCAATCTGTATTCTTCATCATGCAGTCAATTCTTGTATACTCTGAAGTTAATTTGTTTTAGTTTGTTTTATAAAGTGAACAACATGTTATCAAAGACTAATAACCATTAGATTCATTAGATTAAAGATTAATAACCATCACACATCACTAATATTGAGCTGTTGTATGGTTTGCACAGAGAACATGT[G/A]GGGAAAGTACGGTCCGGCCGGGATGCTGGTGGAGAAAGATATACCGTCTGTGTCTGCCAGTGATTCCTCGCAGGATAAATACATGCCGTATGTGGTCAATGACATCACTGCCTTCTTCACGCTGCTGGTGGGAATCTACTTCCCCTCAGTCACAGGTATGAACATCTTTACGCATCATAGGGAGGAAATAATCAACTGTGCAGCATCCCAATTCACACACTTCTACATCCTAATATTAGTGAAGCAAAGGTTCATACTTTTGAGTGTGTAACAGAAGAGCATGCAAGCTTTTGAACATACTACTTCCTCATTAATAGTATGTTGCTGAGTTGCATACCTTGTCAATAATCTCGACACATTATCCACATTTCTTTTATATTTAATTACCATATTGAAGATTCAGCAGCAACAGCAGCAGCAGGTTAATCTGCCATTCACGAGTCCTTCATGCAGAGAAATCTCCTCAGGTGTTTGGGTAAATCTGCATTCAGAGAAGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24563
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 |
---|---|---|---|---|---|
ENSDART00000089232 | Nonsense | 407 | 1119 | 9 | 26 |
ENSDART00000134251 | Nonsense | 385 | 1055 | 9 | 24 |
The following transcripts of ENSDARG00000062058 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 41379670)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39918864 |
GRCz11 | 24 | 39806711 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACCGTCTGTGTCTGCCAGTGATTCCTCGCAGGATAAATACATGCCGTA[T/A]GTGGTCAATGACATCACTGCCTTCTTCACGCTGCTGGTGGGAATCTACTT
Long Flanking Sequence:
TGTAAGAATGTAACAGTAACAGATATTTCAGTGCAGAAATAATGCATGCGTCATCAGCACACAGATATATAAAAGCAGTATCACAATTTCTATGATGCACACATGCTGATATCGTCATCCTTTCCTGTATAATAATACTGAACCATATCATCTCTTATGAATATTAAAACACAAAACCATACAGGGTTTTTTTTGTTGTTGTTGTTGCGTGTTTTGAAGAATTCAATCTGTATTCTTCATCATGCAGTCAATTCTTGTATACTCTGAAGTTAATTTGTTTTAGTTTGTTTTATAAAGTGAACAACATGTTATCAAAGACTAATAACCATTAGATTCATTAGATTAAAGATTAATAACCATCACACATCACTAATATTGAGCTGTTGTATGGTTTGCACAGAGAACATGTGGGGAAAGTACGGTCCGGCCGGGATGCTGGTGGAGAAAGATATACCGTCTGTGTCTGCCAGTGATTCCTCGCAGGATAAATACATGCCGTA[T/A]GTGGTCAATGACATCACTGCCTTCTTCACGCTGCTGGTGGGAATCTACTTCCCCTCAGTCACAGGTATGAACATCTTTACGCATCATAGGGAGGAAATAATCAACTGTGCAGCATCCCAATTCACACACTTCTACATCCTAATATTAGTGAAGCAAAGGTTCATACTTTTGAGTGTGTAACAGAAGAGCATGCAAGCTTTTGAACATACTACTTCCTCATTAATAGTATGTTGCTGAGTTGCATACCTTGTCAATAATCTCGACACATTATCCACATTTCTTTTATATTTAATTACCATATTGAAGATTCAGCAGCAACAGCAGCAGCAGGTTAATCTGCCATTCACGAGTCCTTCATGCAGAGAAATCTCCTCAGGTGTTTGGGTAAATCTGCATTCAGAGAAGTTCACATTGTTGTTGCAGATGAAATATAGCATGAATAGTGTGATTGAAATATTTTCCACTTGGCTAGATATTAACAGTCAAACAAACAAATAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24562
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089232 | Essential Splice Site | 864 | 1119 | 19 | 26 |
ENSDART00000134251 | Essential Splice Site | 842 | 1055 | 19 | 24 |
The following transcripts of ENSDARG00000062058 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 41363233)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 39902427 |
GRCz11 | 24 | 39790274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGGAGGAATGCTGATGCTGCTGCCCTTCCTGCTGCGCCAGCACAAGG[T/G]CAGAAAACAACACAGCAATTTAATTTAATTTAATTTTATTTTATTTTATT
Long Flanking Sequence:
ATTATATAAATATTTATGTTTTATACCCTTATTTTTTGTTTTTATTACTGTTATTAAATAATGATAAGATATAATTATGAATATATATTCATAAACTTTATTGCAGTCGATAAAATGAGTTTTTTGTGCTCTTTAATGCATCTGAAAAACTATTTTATTATATTATTAATGCATTCAAAAAATCTTAGATATTTAGATATTTTCAAGAAACAAACCTATTTCTAGGATTTTTTCCTGATCACATGCATGTATGGTGTTTACAGCTGATTTGTCTGCTCTGAAGGCATCAGGTATGTTGTTGAATGTTGTTTTGTGTGTTTTCCTTTCCTCAGAGACGGTCAGAGAGACGACAGCGGCTCATCTGGCTCTGCTGGTGGCCAAGAACGTGGACAGTTTCCCTCATCAGGAGCGTCTGACTGAAGGAACTATCGACGTGTGGTGGATCGTCCATGATGGAGGAATGCTGATGCTGCTGCCCTTCCTGCTGCGCCAGCACAAGG[T/G]CAGAAAACAACACAGCAATTTAATTTAATTTAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTAGTTTAAATAAATTTAAGAAACTTTAGGAACTTTAAGAAGTAAACAATAACTTATTAATAAATAATAATATGAATTAATTGTTAATATAAATATTTTGTATTAATGAATATTAATTACCATTTTAATTACATTTAAATTAAATTAATAAATTAATAACAATAACTATTATAATAATTGACAATTAATTATTAATAAAAATAATAAATAAATGTCTAAAAAGTAAACAAAAGCTTACTAATAAAAATTTATATTTATTAATTAATTAATTTAATTGATTTATTTATTAATAAAAAATATCTTGCCATAAATAAATTTAACTGGCATTTACAAATACACATGTTTTTTTTATCTTCACCTTTAAGTCCCTTTAGATAAAAGTATCTGCTTAATGTTAAATGTAGAGAAACCCTGTCAGAGAAACAA
Associated Phenotype:
Not determined