ZMP
im:7162646
Ensembl ID:
ZFIN ID:
Description:
LOC562826 protein [Source:UniProtKB/TrEMBL;Acc:Q4VBH0]
Human Orthologue:
SLC12A4
Human Description:
solute carrier family 12 (potassium/chloride transporters), member 4 [Source:HGNC Symbol;Acc:10913]
Mouse Orthologue:
Slc12a4
Mouse Description:
solute carrier family 12, member 4 Gene [Source:MGI Symbol;Acc:MGI:1309465]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11950 | Nonsense | Available for shipment | Available now |
| sa18878 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11950
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 |
|---|---|---|---|---|---|
| ENSDART00000005053 | Nonsense | 646 | 1095 | 15 | 24 |
| ENSDART00000005053 | Nonsense | 646 | 1095 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 36749538)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 35023381 |
| GRCz11 | 7 | 35294858 |
KASP Assay ID:
554-6141.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGGCATGAGTAYGTGTTTAGCCCTTATGTTCATCTCCTCTTGGTACTA[T/A]GCCATTGTAGCGATGGGCATTGCCGGAATGATCTACAAGTACATTGAGWA
Long Flanking Sequence:
TTCATTTATTTGATCTTATTTGTGGAAACTCTTCACTTGTAGTCACATTTGAATTTAGGCCAAACTGTCTCAAACTCAAAACTCTCAGCCCTTGATTTCCACTATTCACTTCCAGCCATTGTTTACAAATGAACTTTATTAAAGGGACAGTTCACACAATAATGAAAACCTTGCTGAACAACAAAGAAGATCATTTGAAAAAGTTGGAAACTGCTAACCATTGACATCTATAGTAGAATAAACAAATGCTATAGATTTGAATAGTTACAGGTATCCAACATACTTCTAGATATCTCCTTTTGAGTTCAATTAAACAAAAGTAAATGTCAATGAATAAATAAATGTTCATTTTTAATTGTATTATCCCTTTAAATCAATTTCTGCTATTGTAACAATCATGCAGAGTCTTTTATGATATGTTGTATGTTGTCTCTTAGGGCTCTGTCTTTTCTGGGCATGAGTATGTGTTTAGCCCTTATGTTCATCTCCTCTTGGTACTA[T/A]GCCATTGTAGCGATGGGCATTGCCGGAATGATCTACAAGTACATTGAGTATCAGGGGTGAGTGCTTCTTAATTGCACCCATTAAACTGATATGAATCGCTGGAAAGCACTTAAAGAGGAATTGTAGCTCCCCACATTTGGTCCAAATCTCCGCTTGGTGTTTTCTTGTGTTTTAGAGCAGAGAAGGAATGGGGTGATGGGATCCGTGGTTTGTCTCTGAGCGCCGCCCGCTACTCTCTGCTTCGCCTGGAGGCTGGACCACCCCACACCAAAAACTGGAGGTTGTGTCTTAGTTTGACAACTGTGTTTGTTTTCCACAGTAAAATAATTCTTAAAAATTAAAAAAAAAAAAAAAAAAAGAAATATACATTGTCAGTGCAGTAAAATTTTACTTAAATATCATGATTGGCCATTTTTCAAAACTTTTGAAAATGAATTTGATAATGACTGGGGAACACCTTCAATATTGTTTGATAAGCTGGAGGATGTTGTTTGATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18878
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 |
|---|---|---|---|---|---|
| ENSDART00000005053 | Nonsense | 646 | 1095 | 15 | 24 |
| ENSDART00000005053 | Nonsense | 646 | 1095 | 15 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 36749538)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 35023381 |
| GRCz11 | 7 | 35294858 |
KASP Assay ID:
554-6141.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGGCATGAGTATGTGTTTAGCCCTTATGTTCATCTCCTCTTGGTACTA[T/A]GCCATTGTAGCGATGGGCATTGCCGGAATGATCTACAAGTACATTGAGTA
Long Flanking Sequence:
TTCATTTATTTGATCTTATTTGTGGAAACTCTTCACTTGTAGTCACATTTGAATTTAGGCCAAACTGTCTCAAACTCAAAACTCTCAGCCCTTGATTTCCACTATTCACTTCCAGCCATTGTTTACAAATGAACTTTATTAAAGGGACAGTTCACACAATAATGAAAACCTTGCTGAACAACAAAGAAGATCATTTGAAAAAGTTGGAAACTGCTAACCATTGACATCTATAGTAGAATAAACAAATGCTATAGATTTGAATAGTTACAGGTATCCAACATACTTCTAGATATCTCCTTTTGAGTTCAATTAAACAAAAGTAAATGTCAATGAATAAATAAATGTTCATTTTTAATTGTATTATCCCTTTAAATCAATTTCTGCTATTGTAACAATCATGCAGAGTCTTTTATGATATGTTGTATGTTGTCTCTTAGGGCTCTGTCTTTTCTGGGCATGAGTATGTGTTTAGCCCTTATGTTCATCTCCTCTTGGTACTA[T/A]GCCATTGTAGCGATGGGCATTGCCGGAATGATCTACAAGTACATTGAGTATCAGGGGTGAGTGCTTCTTAATTGCACCCATTAAACTGATATGAATCGCTGGAAAGCACTTAAAGAGGAATTGTAGCTCCCCACATTTGGTCCAAATCTCCGCTTGGTGTTTTCTTGTGTTTTAGAGCAGAGAAGGAATGGGGTGATGGGATCCGTGGTTTGTCTCTGAGCGCCGCCCGCTACTCTCTGCTTCGCCTGGAGGCTGGACCACCCCACACCAAAAACTGGAGGTTGTGTCTTAGTTTGACAACTGTGTTTGTTTTCCACAGTAAAATAATTCTTAAAAATTAAAAAAAAAAAAAAAAAAAGAAATATACATTGTCAGTGCAGTAAAATTTTACTTAAATATCATGATTGGCCATTTTTCAAAACTTTTGAAAATGAATTTGATAATGACTGGGGAACACCTTCAATATTGTTTGATAAGCTGGAGGATGTTGTTTGATTAAT
Associated Phenotype:
Not determined