ZMP
zgc:153764
Ensembl ID:
ZFIN ID:
Description:
H(+)/Cl(-) exchange transporter 4 [Source:RefSeq peptide;Acc:NP_001070786]
Human Orthologue:
CLCN4
Human Description:
chloride channel 4 [Source:HGNC Symbol;Acc:2022]
Mouse Orthologue:
Clcn4-2
Mouse Description:
chloride channel 4-2 Gene [Source:MGI Symbol;Acc:MGI:104571]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41920 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41919 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41920
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 |
|---|---|---|---|---|---|
| ENSDART00000047126 | Nonsense | 36 | 768 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 11 (position 45256839)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 43859106 |
| GRCz11 | 11 | 44161498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAACCTGATGGACTTCTTAGATGAACCATTTCCAGATGTTGGCACTTA[T/A]GAGGACTTTCACACCATCGACTGGCTCCGAGAGAAGTCCAAAGACACAGA
Long Flanking Sequence:
TTGTATTTTATTTACATTTTTTTTTGTTATGATTCCTTTTTTAGATTACTACCTGACAAAAGTCTTGTCGCCTATCCAAGTTTTAGGGACAACAAATAATAACTTGACTTCTAGTTGAGCATTTGGCATCAGAAGTGTCTTATATGAAAGGCAAAGGCCTCTAGATGACGCTTATTTGACCACAATAAAATATGATCATGCCTTGATTTTTAATTATTTAATTAGTACAGTAAGGTATGAGGTAAGTCCAGTATATATATAGTTTACAAATGATCAACTAGAAGTCAAGTTAGTATTTGTTGCTCTTACAACTGGGATCGACAACCCCAGATCGAAGGCTTTTTTCAGGCAGTGTAGTATAATTTTAGTAATATATTTACTAATAAACTAATAAAATGTTGTTTTTCAGGCATCAGCAGTGCGACTCCCACTGAGGAGATGAACGGCGCCGGGAACCTGATGGACTTCTTAGATGAACCATTTCCAGATGTTGGCACTTA[T/A]GAGGACTTTCACACCATCGACTGGCTCCGAGAGAAGTCCAAAGACACAGACAGACACCGCAAGGTAAAGCCGACCGCCTGACGCTCATATGCTGATTTTAGGGCTGCATGATACTGGACAAATCTGACATTATGATATTTTGTTTTTATGCAATATATATTGCAATATGAATACATTTTCACTATATGACTTGAATAGCTGTATTTGGAAAGAATTGTATAGTAAAATGTAAAATAGTACTAGTTTATATTCTTATTTTGTAGTTAAATTTTTCCTCATTAAAGTTGTGCTTTTTTGTTCCTGAATGCTTTAGGGTGCTTTCACACCTACACTTTTGTTTGGGAACGTGTCTCGTTTGCCCAGTTAGCGCGGTTCGTTTGGCATATGTGAACAGGGCAATCACGCTCTGTTCCGCGCCACAGTAATCGCTCCGAGATCGCTTGAGTGAGGTGGTCTCGGCTGGATTGAAACGAACCCTGTAGCGGTTCGATTACAGTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41919
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 |
|---|---|---|---|---|---|
| ENSDART00000047126 | Nonsense | 652 | 768 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 11 (position 45244019)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 43846286 |
| GRCz11 | 11 | 44148314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACACCGACTACAACGGCTTCCCGGTGGTGGTGTCCCGCGAGTCTGAG[C/T]GACTCATCGGCTTCGTGCAGAGACGAGACCTGATCCTGGCTATCAGTATG
Long Flanking Sequence:
CCCAGTACTGGGTTGTGACTGTAAGGGCATCTGCTGCATAAAACACATGCTGAAATAATTGCTGGTTCATTCTGCTGTGGCGCCCCCTGATAAATAAGCCGAAGGAAAGTGAATGAATGAATATAAAGGAGCAAAGCCTCTGTCCTGCAGGCGGTGTGACCCGTATGACGGTGTCTCTGGTGGTCATCATGTTCGAGCTGACGGGCGGACTCGAGTATATCGTCCCTCTGATGGCGGCGGCGGTCACCAGTAAATGGGTGGCGGACGCGTTTGGGAAGGAGGGGATCTACGAGGCGCACATCCAGCTGAACGGCTACCCGTACCTGGACCAGGACGAGTTCACACACCGCACGCTGGCCACTGACGTGATGCGCCCACGCCGCAGCGAGCCACCGCTGTCTGTCCTCACGCAGGACAGCAGCACGCTGGAGGAGGCCGAGGCGCTCATCACACACACCGACTACAACGGCTTCCCGGTGGTGGTGTCCCGCGAGTCTGAG[C/T]GACTCATCGGCTTCGTGCAGAGACGAGACCTGATCCTGGCTATCAGTATGACACACACACACTATACACACACTATACACACCTGATCCTGCTCATCAGTACGACACACACACTATACACACACACCTGATCCTGCTCATCAGTACTACACACACAATATACACACACACTATACACACCTGATCCTGCTCATCAGTACTACACACACACTATACACACACTATACACACCTGATCCTGCTCATCAGTACTACACACACACTATACACACACTATACACACCTGATCCTGCTCATCAGTACTACACACACACTATACACACACTATACACACCTGATCCTGCTCATCAGTACTACACACACACTATACACACACTATACACACCTGATCCTGCTCATCAGTACAACACACACACTATACACACACACTATACACACCTGATCCTGCTCATCAGTACTACACACACACTATACACACACACTATACACACCTGATCCTGCT
Associated Phenotype:
Not determined