ZMP
si:dkey-253e7.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate solute carrier family 12, (Potassium-chloride transporter) membe
Human Orthologue:
SLC12A5
Human Description:
solute carrier family 12 (potassium/chloride transporter), member 5 [Source:HGNC Symbol;Acc:13818]
Mouse Orthologue:
Slc12a5
Mouse Description:
solute carrier family 12, member 5 Gene [Source:MGI Symbol;Acc:MGI:1862037]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17824 | Nonsense | Available for shipment | Available now |
sa9823 | Nonsense | Available for shipment | Available now |
sa41263 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17824
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009569 | Nonsense | 218 | 1117 | 7 | 26 |
ENSDART00000140365 | Nonsense | 200 | 1119 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 38429560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37284975 |
GRCz11 | 8 | 37317409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTCTTCTTTATTTGTAGATCTACATTGTTCCATCAGCTGCCATATTY[A/T]AAATGGAGRGTCTTGAGGGRKCAGAAGCCGAGGCAGCGCTGTTGAATAAC
Long Flanking Sequence:
CTTGCATAATATCTTAACTAATGACTAAACATGATTTTGCAGACAATTTAAGATTATAAGGCTGAACTGAAATGCCATCAGTCTACAGAGATTTCCCAGTATTTCTTTGTTGCAATCGGGAGATCACAATAATTAACACCGAAAAAGCCAAAGCAGTGCAAATACTACCAGATTACTGTTTGTGAAAAGGTAAAATGCTAAACACATCCAAGCATGTCTCTTTTTTTTTTTCTTTTTACTGAACTAGTCTGCAGTAACGAAAACAGGAGACTCGTCAAAAACAAACAGATGGCTAACCAAATAGTAACTCACATCAACCGTCAGCTCAATGACGCGCTGTCTCTCAGAAATGATAAATATTTAAAATAGGCACTATCCTTGTAGATAAACTGCATAGTTGCAATCTAAACAACTACATTCTCAACTGAAAAAGTGGTTTCATTTTACTTTTTTCTCTTCTTTATTTGTAGATCTACATTGTTCCATCAGCTGCCATATTT[A/T]AAATGGAGGGTCTTGAGGGGTCAGAAGCCGAGGCAGCGCTGTTGAATAACATGCGCGTGTACGGTACCATCGTTCTCACCTTCATGGCTATAGTCGTCTTTGTTGGTGTGAAGTATGTCAACAAGTTGGCTCTTGTGTTCCTCGCCTGCGTCATTCTCTCCATCCTGGCTATCTACGCGGGGGTCATCAAGACTTCTTTTGATCCACCTGACTTTCCGTAAGTAGACTTATACAATCTATATAAATTTAATATAATATATACATAATAGTTTTAATAACTCATTTCTAATTACTGATTTATTTTATCTTTACCATGATGACAGTAAATAATATTTTAAGGCTTAATTTGGTAAGTTCCTTGCTTTTGGTAAATATTTTAAAAAGAAAAAATTCAAAGGGGGTTTATATATATATAATTTTTCTTTTTTTTAAACCACTTATTTAAAAAACAGCTGAAACCACACCATTCTTATGATTTTTGGGTGTAACATATTTATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9823
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 |
---|---|---|---|---|---|
ENSDART00000009569 | Nonsense | 395 | 1117 | 9 | 26 |
ENSDART00000140365 | Nonsense | 377 | 1119 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 38425614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37281029 |
GRCz11 | 8 | 37313463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACAGGCAGTACAGGACCCTGAACTCCCAGTAACCAACAGTAACCGATA[T/A]GTGYTRGCTGATATCACCAGTTTCTTCACCCTGCTGGWWGGAATCTACTT
Long Flanking Sequence:
CAATAAGAATATGTCAATAACTCAATTTTGAGAAAAATGTCAGATAGAACCTTATAATTCTAAGGTGACAACATTATAGTAAATAGGGGTAATATAGATGCTCTTAAGCTTTTAAAACTTATTTAAAAAGTATTTTAAACTGTAACAATATTTCACAATATCACTGAATTAATACTTTTTAACAATATTTTTGATCTTTTATACATACGTTTTGTACAATAAAAAATCTACAAATTGACAACAATATTTTTCAGTCTGAATTTTATTTTACCAGTATTTTTTATATTAAATACACTCTGAACTTAACCATCATTAAAATTAAATTAACTTGATGACCAGCTCTAATGTAAAAAAAAAAAAAAAACTTATTGTATTTTCTAAATCATTTTGTCTTCAGAAAACCTTTTCAGTGGCTATATGGAGAAAAATTCTGTCTTAGAAAAGAGAGGTCTACAGGCAGTACAGGACCCTGAACTCCCAGTAACCAACAGTAACCGATA[T/A]GTGTTGGCTGATATCACCAGTTTCTTCACCCTGCTGGTTGGAATCTACTTCCCCTCTGTCACAGGTCAGTATAATGATAATTAATAATATTTCAACGAAATTGGTGGTTCAATGTTATGGCGACCCTTGATAAGAAGAGAATAGGCCAAAGAAAAGTGAGTTAGTGAATGAAAAAATTTAATGAAATTTGTTATGATAAGTTATTAAATTACAGAAACTGTTTGGTTACAGTAAAAGTTTGGTTTGGTTAGATCTAAACATTTTATGGATTATTTAAAACACTATTGAAAAAACAATTATCCATAAAAAGTTTAGATCTAACCAAATTTTTTTTTTGTAGTATACATTAAAAAGATACAGTATTTACTCATATAAATGTGTTTCTTAACTGTTTTATTCACTTAATTATTTACTGCCTTAAAACAGGATGTAACCCAAAATATTTAATGTGTGCCATAGGTATCATGGCAGGTTCCAACCGTTCTGGTGACCTGCAGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41263
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009569 | Nonsense | 688 | 1117 | 17 | 26 |
ENSDART00000140365 | Nonsense | 670 | 1119 | 16 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 38415820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37271235 |
GRCz11 | 8 | 37303669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTATCTTGCAGGCCCCAGATTTTGGTGCTCACAACTTTGGATGGAGAG[C/T]AGAACGTGGAGCAGCCTCGACTGCTGTCCCTGACCAGTCAGCTGAAAGCA
Long Flanking Sequence:
AATACATGCGCTATAGATGAATTATAGGTAAGCGAAATTGTCCGTAGGGTATGTGTGTATGTCCTGGTCCTCCAGGTTGAAGTTTGAGCATTAGACTTATGAGCGATCTCGCAAAAATTTGATGTCACAAAACACTAACATGGTGCAGCTAAATATCAACTTCAATATAAATGGCCCTGGGAGTAAGAACTGTAAGTTTTAAAAAACTGAAAAAGACTTCAATTGGATGCTTGTGTGTTCTCACCTTGTAGAGCAGAGAAAGAATGGGGTGATGGAATCCGTGGTATCTCTTTGAGCGCTGCTCGTTTTGCTCTGATGAGGTTGGAGGAAGGTCCTCCTCACACTAAAAACTGGAGGTCAGTGGCATATCAGTAATGCACTGTTCTCATAAAATCATCCAAATATTGTCATCCAAAATACTGAGTATGTATTTTACATGTTTGAAATATTTCTTATCTTGCAGGCCCCAGATTTTGGTGCTCACAACTTTGGATGGAGAG[C/T]AGAACGTGGAGCAGCCTCGACTGCTGTCCCTGACCAGTCAGCTGAAAGCAGGCAAAGGTTTGACCATTGTAGGAGCGTGTATAGAAGGCACCTACTTAAACAACCAGCCAAAGACTCAGAAAGCAGATCAGGTACGCACGCAGAATTTAATCTGTGCACCCAAACTTTAACATGAGGCAATAGTCCATCATTAAAATTAAACTAATAACCTCTTTGACCTCCATATTTTTCAGTCCCTAAGGAAGCTGATGGAGGTTGAGAAGGTGAAGGGATTCAGTCAAGTGGTGATCTCTTCTAACCTGCGGGATGCCACCTCACACCTAATTCAAGCTGGTGGTCTGGGTGGGCTACGCCACAATACTGTTCTGGTCAGCTTTCCCAAGAACTGGAAACAGGCTGAGGAGCACCACCGTTGCAGGAACTTCATTGGTAAGACAACAATTTACACTGCACTACATATGGTGACATAGACTTTGGTATCTGCTTTATGACTTTTTACA
Associated Phenotype:
Not determined