ZMP
si:dkey-101k6.7
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 12 member 8 [Source:RefSeq peptide;Acc:NP_001121749]
Human Orthologue:
SLC12A8
Human Description:
solute carrier family 12 (potassium/chloride transporters), member 8 [Source:HGNC Symbol;Acc:15595]
Mouse Orthologue:
Slc12a8
Mouse Description:
solute carrier family 12 (potassium/chloride transporters), member 8 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25433 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2505 | Nonsense | Available for shipment | Available now |
sa41489 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25433
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 |
---|---|---|---|---|---|
ENSDART00000110651 | Nonsense | 123 | 708 | 3 | 13 |
ENSDART00000133849 | Nonsense | 123 | 253 | 3 | 6 |
ENSDART00000135505 | Nonsense | 77 | 158 | 2 | 3 |
ENSDART00000135774 | Nonsense | 112 | 697 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 9 (position 39699594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38837490 |
GRCz11 | 9 | 38647285 |
KASP Assay ID:
554-7521.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTCCACTGTGCTGGGAGGCAGGATTGGAGGAACTGTGGGACTCCTGTA[T/A]GTTTTTGGACAGGTGAGCAGCTCGTGCCTGCATTATGTTGCATGTTCACA
Long Flanking Sequence:
ATTGTTCAACCAAAAGTGAAAATGTACTTAGTATTTACTCACCCTCAAGTGCTTCCAAAACTACAGTATATACACGTTTCTTGATTATTCTAAACACCAAAGAAGATATTTTGAAGAAAGCTGAAACCAGGTAAGCGTTGACGTCCATAGTAGTAAAAACAAATACTATGAAAGTCAATGGTTTGAAAGAAAGAAACTTAAACAGGTTTGGAACAAGTGAAGTTTGCTTACATGATGACAGTATTTTCAGATTTGGGTGAATCTCTTTAAATGAACATCCATTGAACTGTTATTTTATTTTTCCCATTCGATAATCTTCAGGGTAACACGGGTGTGTTTTTGGGCATGCTGCTGGTATCATTGGTGGTGCTGGTGGCCTTGGTCACAGTGATGTCTGGTGTTGGCGTGAGTGAATGTTGCAGCGTGGGAAACGGGGGAGTTTACTCCATGATCTCCACTGTGCTGGGAGGCAGGATTGGAGGAACTGTGGGACTCCTGTA[T/A]GTTTTTGGACAGGTGAGCAGCTCGTGCCTGCATTATGTTGCATGTTCACAGGATTATATGCTCAGGGTTGTGCTGATACCGATAATAGTATAGAAAATACTCATCAATAATGCAAAAATTGTGTCATTGGTATTGGTGGGAATTTTCTAATCTAGTATCGGTATCAAAACAACACTCGGGTATCGGTTCAGTACTCTTTATAAGCCGATATCCTTAGCTCAGGTATTGAAATCGGTACTGGGAAAGAAAAAATGGTATCGGAACATCCCTAATAAGGAGTTTGATGACAATTATGTGTGTCTCTCTCTCTCTCTCTTTTGGCAGTGTGTGGCTGGAGCGATGTACATTACAGGTTTTGCTGAGTCCATTGCTCAGGTGTTGAGTTTGCAGAGCACATGGGTTGTGAGGGGCATATCTGTGGCCGTTCTGCTCGGTCTGCTTGGAATTAATCTGGCCGGGGTCAAATGGATTGTACGACTTCAATTGGTTCTGCTTGGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2505
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 |
---|---|---|---|---|---|
ENSDART00000110651 | Nonsense | 178 | 708 | 4 | 13 |
ENSDART00000133849 | Nonsense | 178 | 253 | 4 | 6 |
ENSDART00000135505 | Nonsense | 132 | 158 | 3 | 3 |
ENSDART00000135774 | Nonsense | 167 | 697 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 9 (position 39700069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38837965 |
GRCz11 | 9 | 38647760 |
KASP Assay ID:
554-3032.1 (used for ordering genotyping assays)
KASP Sequence:
TTCTGCTCGGTCTGCTTGGAATTAATCTGGCCGGGGTCAAATGGATTGTA[C/T]GACTTCAATTGGTTCTGCTTGGGATTTTAGCAATGTCAACTTTGGATTTC
Long Flanking Sequence:
TTGGAGGAACTGTGGGACTCCTGTATGTTTTTGGACAGGTGAGCAGCTCGTGCCTGCATTATGTTGCATGTTCACAGGATTATATGCTCAGGGTTGTGCTGATACCGATAATAGTATAGAAAATACTCATCAATAATGCAAAAATTGTGTCATTGGTATTGGTGGGAATTTTCTAATCTAGTATCGGTATCAAAACAACACTCGGGTATCGGTTCAGTACTCTTTATAAGCCGATATCCTTAGCTCAGGTATTGAAATCGGTACTGGGAAAGAAAAAATGGTATCGGAACATCCCTAATAAGGAGTTTGATGACAATTATGTGTGTCTCTCTCTCTCTCTCTTTTGGCAGTGTGTGGCTGGAGCGATGTACATTACAGGTTTTGCTGAGTCCATTGCTCAGGTGTTGAGTTTGCAGAGCACATGGGTTGTGAGGGGCATATCTGTGGCCGTTCTGCTCGGTCTGCTTGGAATTAATCTGGCCGGGGTCAAATGGATTGTA[C/T]GACTTCAATTGGTTCTGCTTGGGATTTTAGCAATGTCAACTTTGGATTTCGTCATCGGAACTTTTAGTCATCTAGATCCAGGTAAGATCTCTTCAAGGTTGTTGTTTTTGATGCACTAGTATAAGGGTTCTAGTAAGGGTAACACTAGCTTTACATTTTATTGCATAACAAGGTTAAATTGAAGACTAAATTATCACAATAGATCCTCTTTTGAGAAGATCAGTCAGCAAGACAAGAAAAGTATGTGTAATAATTAGCTTCTGGAACAGGTGTAAATGTGTTTATGTTTTTGTTAAAATTCAAAATACATGGGAAAAATGCAGGGTTCTACACAATTGCTTTCGTTGTCCCAACACAAGTCAGTTAAGTTAACTTAAGTGGATTGAACATAAAACTATTAAGTTGTTCTTTAAAAGCTCTCAAGAATTGTGTAGTTTCAACTCTTTTTACAGAAGTTGTTTGAACTTTTTGGAGTGTAATACTATTATATTAAAGAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41489
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 |
---|---|---|---|---|---|
ENSDART00000110651 | Nonsense | 310 | 708 | 8 | 13 |
ENSDART00000133849 | None | None | 253 | None | 6 |
ENSDART00000135505 | None | None | 158 | None | 3 |
ENSDART00000135774 | Nonsense | 299 | 697 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 9 (position 39724268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38862164 |
GRCz11 | 9 | 38671959 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCTGTGTTTGTTTTTTTCCCAGGTCTCCTTGGTTGGTTTCCTGTTTT[T/A]GCTGGGCCTCTACATCTCCTCCCTGGCCTCCTGCATGGGCGGCCTGTACG
Long Flanking Sequence:
TATTCCAGTTTAGTTTTACGCAGCGTATGCTTATATATATATATATATATATATATATATATATTTTTTTTTTTTTGATGGTGTAACTAAAAGATTTTTATGAAGGGCCATTTAAAAAAAAAACCTAGTGCTTTTTCTTAAAGTCCTAAATTTGACTTTCAAAACTCACAATATGTGTAATGCAATACCAATGACCAGAACTATGGTCAGTGCATACAATACAATTAATCTGAACCTTATTAAAATCACAAAAGGTGCATTGTTGTGTTGCAAGATTTACACATAATCACCATCAACATCATCATCATACTGTATTCTTTGCCATTGAGCACTCATTATGGGCTCTGACGGATTACGCATTGTTTCTTTGATTTACTTTCAGCACATTATAAGCTCTTTTCAGTCTGGCCAAGCGGAACAGAGCTGGGTGGGGCCCTCTACACTCTCTTCCCCTCTGTGTTTGTTTTTTTCCCAGGTCTCCTTGGTTGGTTTCCTGTTTT[T/A]GCTGGGCCTCTACATCTCCTCCCTGGCCTCCTGCATGGGCGGCCTGTACGGTGCACCCAGGATCCTCCAGTGCATCGCCCAGGAGAGAGTCATTCCAGTTCTTGCGTTTCTTGGAAAAGGGGTGGGTGATTTTATGGATATGATAACCATATTAATGTGGTTATTTCAATGTTTTATACTAAATAATGGTTCATTGTGTAAATTGCTCATGTTTTGATTCTAATCAAGGCTAAATCTGTTCCCCTAAAGCTCTGTTTCAGTGATCTGATCACAAGTGGCTTTGATTTTAATCTGTATGTTTTGGTACAACACAAAGAAATACAGTGTGAACACCTTGTTTTGGTGCACTTTTGGTTTCACAAGATGTCCCATATGAATAATAATATTAATTTAATTTTGTCTAGTGCCTTTTAAAATTAATTCTCAAAGCACTTTACACTCAATGAAATGGAAGGATAGCAAGAAAAAAGTTATGCAGAAGATAAAAATTATATATATAT
Associated Phenotype:
Not determined