ZMP
zgc:64141
Ensembl ID:
ZFIN ID:
Description:
chloride channel Kb [Source:RefSeq peptide;Acc:NP_956676]
Human Orthologues:
CLCNKA, CLCNKB
Human Descriptions:
chloride channel Ka [Source:HGNC Symbol;Acc:2026]
chloride channel Kb [Source:HGNC Symbol;Acc:2027]
chloride channel Kb [Source:HGNC Symbol;Acc:2027]
Mouse Orthologues:
Clcnka, Clcnkb
Mouse Descriptions:
chloride channel Ka Gene [Source:MGI Symbol;Acc:MGI:1329026]
chloride channel Kb Gene [Source:MGI Symbol;Acc:MGI:1930643]
chloride channel Kb Gene [Source:MGI Symbol;Acc:MGI:1930643]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8872 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18332 | Nonsense | Available for shipment | Available now |
sa37699 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32442 | Essential Splice Site | Available for shipment | Available now |
sa37700 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1792 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8872
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 |
---|---|---|---|---|---|
ENSDART00000029974 | Essential Splice Site | 140 | 693 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 24562125)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24348601 |
GRCz11 | 23 | 24275142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGCTCTGTCCACCAGCTTCGCCCACAGCGTCTGCCCATRCTCTGCAG[G/A]TTACACAGCACTWAGAAATTAGGGCAATMATTTTGTTTCATTTAATTTWA
Long Flanking Sequence:
TAATGTTAATGTATGTGTCTGTATTTGTATCTGTTATGTGTATGTGTTTGCATCTGGCCAGAGTGTGTGCTGAATGTGAAGAAGCTCCTGGTGTCTCTCGCCAGCATGGAGTGGTACTGTTATGCTCTGTTAGGGATCATCACAGCTCTAATGAGCTTCTTCATGGACATGACTGTGGCGAAGCTGCTAAACGGTGAGCGGTTCCACCATGTCACTCAGAAAGCGTTTGGTAAATAATTTACATAGAGATGAATGCAGGTCGGCTAACTGTTTGAGTCGTTCTAGCAGCTGAATGTTGCAAGGTCTTTCAAAAACAGGTTTGACCTTACAGTTTCTCACCTCGGTCTGTGTCCTTCTCTCTCTCTTATTAGCCCACCAGTGGCTGTACGGCTGTCTGAAGGGTCACCACCTGCTGCAGTTCCTCTGCTGGACGCTTTACCCAGCCTGCCTCTGTGCTCTGTCCACCAGCTTCGCCCACAGCGTCTGCCCATACTCTGCAG[G/A]TTACACAGCACTAAGAAATTAGGGCAATCATTTTGTTTCATTTAATTTTATTTTATTTTTATTCAGTACATTAAAAAAAAGTTACACATTAAATTAATTTCAGGTCTACCAAATTTTGTCATCACTTTAGATACTTCTTACTTACAGTATAGGCATGTTTAATACAGTGTATGTGTAATTATTTAAATCTGTCAAACTATATATAAAAAAAGAAAAAAAAAGGGGAAGCCGATCTAAAATGAAAATGGAGTTACCTCACCTGCTTTGCACATTAGAACAAAAACATTTAACACACAGAAAAATAAAACATGTAGTCAGTTTTTGCCTTTTTAAAATTAAAAATGCTCTGCTTTACTTTACCAGTTTGATTTATACAATCTGAGAATACTGATATATAACTTCCTAGAAGTTGGAAGAATGAAAAGCATAATTATTGTCCATAATAATATGTACTAAAACAGTTATCATGGGCAGATTTACAACATGCACAAATATTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18332
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029974 | Nonsense | 193 | 693 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 24564288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24350764 |
GRCz11 | 23 | 24277305 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATAWATTGACCTTAAACTTATTATCTYAATAGGGCCCATTTGTCCATT[T/G]WTCTATCATGGTTGGTGCATTTATGAAYCGTCTGCATGTCTCCTGTCGTG
Long Flanking Sequence:
AGTAAGCATAATTTTCAAATATATAATTTCATAAAAATTACATTTAATCCACTTGACCCAATCAGTCAGCTCTGCATGGGCCTGACACCCTCGTAAGCAAAGCTGCTGTGAGTGACAGGGACAATTGCATTGGGATTAAGCTGAGGCAATATGAAACATGGACATGTTTAATCATAAACGTCGAGTATTGCTTGAGTAGGTCCGTCAGGTCCATTTGCTCATGCATAATGTTTTTCTCTCGACCCCTCAGGCTCTGGTGTTCCTGAAGCGAGGGCTATTCTCTTAGGAGTGGACATGCCAGATTACCTGTCTCTCTCCAATCTGTTTGCTAAAATGTTTGGCCTGATATGCACACTAGCCGCTGGCAGCACTGTGTTTCTTGGCAAAGTGGTAAAAAAATCTTATATGCAAATGAGGATGTGAAGATTAATCAAAAAATGACATGCTGCTGAATATATTGACCTTAAACTTATTATCTTAATAGGGCCCATTTGTCCATT[T/G]ATCTATCATGGTTGGTGCATTTATGAACCGTCTGCATGTCTCCTGTCGTGGCGGAAAGCAGGTAGCTAAACTGTAATATAATACATGAACCATACAGTCCACTTTTATTTTATTTTATGAAAACCAGATGGGAATTGTATAGAAGGCTACTTATGCTAATGACTCTTGTGGTGTCATTCATTTGCATCTGGCAGAGAGCAGCTAAAGGAGAAATGTTGGTTGTGGCATCAGCGGTGGGAGTTGCGAGCTGTTTTGGGGCTCCAATAAGCGGTGAGTTCAAGTGTTTACATGACATAATTTTCAACCAAAAAAAGAAAAAAATTGGCAACACTTCACTTGAAATGGTGTTCATAAGGCTATCATGAAACATTCATAATCATGACATTAAATATGTGACATAAATATGGGTCATTCACTCAGTTGTCATTTTAAATGCAAAGATGACATTAGCTGTGTTTCATTTTAGAGGCTGCATCCTCCGAAGGATGCAGACTTCAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37699
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029974 | Essential Splice Site | 239 | 693 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 24564560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24351036 |
GRCz11 | 23 | 24277577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCATCAGCGGTGGGAGTTGCGAGCTGTTTTGGGGCTCCAATAAGCGG[T/A]GAGTTCAAGTGTTTACATGACATAATTTTCAACCAAAAAAAGAAAAAAAT
Long Flanking Sequence:
GGCTATTCTCTTAGGAGTGGACATGCCAGATTACCTGTCTCTCTCCAATCTGTTTGCTAAAATGTTTGGCCTGATATGCACACTAGCCGCTGGCAGCACTGTGTTTCTTGGCAAAGTGGTAAAAAAATCTTATATGCAAATGAGGATGTGAAGATTAATCAAAAAATGACATGCTGCTGAATATATTGACCTTAAACTTATTATCTTAATAGGGCCCATTTGTCCATTTATCTATCATGGTTGGTGCATTTATGAACCGTCTGCATGTCTCCTGTCGTGGCGGAAAGCAGGTAGCTAAACTGTAATATAATACATGAACCATACAGTCCACTTTTATTTTATTTTATGAAAACCAGATGGGAATTGTATAGAAGGCTACTTATGCTAATGACTCTTGTGGTGTCATTCATTTGCATCTGGCAGAGAGCAGCTAAAGGAGAAATGTTGGTTGTGGCATCAGCGGTGGGAGTTGCGAGCTGTTTTGGGGCTCCAATAAGCGG[T/A]GAGTTCAAGTGTTTACATGACATAATTTTCAACCAAAAAAAGAAAAAAATTGGCAACACTTCACTTGAAATGGTGTTCATAAGGCTATCATGAAACATTCATAATCATGACATTAAATATGTGACATAAATATGGGTCATTCACTCAGTTGTCATTTTAAATGCAAAGATGACATTAGCTGTGTTTCATTTTAGAGGCTGCATCCTCCGAAGGATGCAGACTTCAAAGGTGAGTCCTTCCAAGTCCACACAAGCCGAACCGAGTGTTTTGAAATGAGACGATCTAGCCTACAGAGGACTGATCTCGTCACCAGGCAACCGTAACAGCTGCTGTTAATAGGCGCTAATAACATTTGTAATGACTTTTTTCCAAGTGATTTTAAAACTTACTTAAGCGATCTGAAGGCAAAACAAGATTTACAGAAGCTGGAAATATATTTTCTTTGATCCATACATGTACACATAAAACTGTAAACTGTCTATAAAATCACTCTTTAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32442
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029974 | Essential Splice Site | 280 | 693 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 24567087)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24353563 |
GRCz11 | 23 | 24280104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCGGCGCCATCACCTTCAGGCTGCTTTCTGTCTGTATTGGAGATCAAG[G/A]TAAGAGCTTTACACTTCCTACAGCGCCACCTAATGGATGCTTTTGCTGTC
Long Flanking Sequence:
CATCTATGATGACTTCAGGGTGAGTAAATTATGGGGTAATTTTAATTTTTGGGTGAACTACTCCTTTAAGATGGAAAAAAAAAGTCAGTGTGTGTTCAATCAAATTTTATTTATTTTAAAAGGTTTTTGGCCCCAATAACAGTTCATACTAGCGTATATGTGTAAAGCCCCGAGGGTGCTTTGGGTTTTAGAAGAAATCAATAAATTACAAATAATTTATTGAAATCTTTGTCAATAATATGGAGTCATGAAAGTGTAGTCTGATTTAATATTTTAAATTGTATTTACCATTTAAAATTCAAATGACAATCAGTTGGTAGCCAGCACTGTCAGCTGACCTTTGGCTCATGTTTATCTCTGTCTCATTGTCACAGGCGTTCTCTTCAGTATAGAGGTGATGGGGACTCATTATTCAGTCAGCGATTATTGCCCCTGCTTCTTTGCAGCGGCGTGCGGCGCCATCACCTTCAGGCTGCTTTCTGTCTGTATTGGAGATCAAG[G/A]TAAGAGCTTTACACTTCCTACAGCGCCACCTAATGGATGCTTTTGCTGTCTTTGCAGTAATCTCATTTACCGCTGTGCTTTTAGATTGCATTAGGGGATGCTATGAATTGACATTATTGAATTTAGATATGATTACACAGCCTGAAGGATATACGAGAGAAATTATTCAATACTTATTTAATCTCTTTCCGCAGACACAATCCAAGCCCTGTTTAAGACCAGCTTTTCTACTGATCTGCCTTTTCAGCCTTTTGAAATAATAATTTTTGCTCTGCTTGGGTAAGCTTGTGGTTAAGAGATTGGCAACAGACAGTGAAAAGTTAAATACAACTTACTCATATCTGTAACCTTATGGGTATTTATGAAAGAGTAACTGTTCTAATGGTTTTTTTCTCTCTCTCTCTGATTCAGGCTGTTTTGCAGTATTCTCAGCTGTATTTACTTACTCTGTCATCGCTGGGCTCTGCGTTTTGTCAAAACAAACAAACCCATCAGCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37700
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029974 | Nonsense | 530 | 693 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 24573238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24359612 |
GRCz11 | 23 | 24286153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTCCCGCTCTGGTGGCGACGCTCGTGTCCAATGCTGTGGCTCGGGCT[A/T]AACACAGGCCGTCTTTCTATGATGGCATATCGCTTATTAAACGGCTCCCG
Long Flanking Sequence:
AGGCGATTTGCTTTGTGTCCTCGTAATTTATAACTGTTTATAAACAGCTCATAACGTTAGCTAAGTTTTTTTTACATTCAAAATTTGGATTTCCGGGGTGTGGTAGGGCCATAGGCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATATATATGTATATGTATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATATATTTATTTTTTTATTTTTTTATTTTTTAACTATAACATACGCCTACGGAGAGTCATAAATCTCAAAAACCAACCTGTGTGTGTTTTCAGGAGCGGCTGCTTTCTCCGGGGCCGTGACACACACACTTTCTCCTGCCCTGCTGGCGGTGGAGATGACCGGTCAGTGTTCCTATGCTGTTCCCGCTCTGGTGGCGACGCTCGTGTCCAATGCTGTGGCTCGGGCT[A/T]AACACAGGCCGTCTTTCTATGATGGCATATCGCTTATTAAACGGCTCCCGCACCTGCCGTCTCTAATCCGCGCATGTCCGAAGTGAGTAAAGCGTCGATCAATCATCTGCCTTCAGGCGCCGGTGGAAATTAAACTGCATTTTTCTTGAGGTGACACTGCCTCATAGTGCTTTCTGCCATTCATGATTCTGAGGGGAGACATGGTTTGAAATCAGAGTTAATCATAGGCTGTTTTATGTTCGTAAGAGATACTGTGACTCTTTCATTGTGGCGATGTCACTGCCATTGCATTCATATCGCAATACATGTAGCAGAAAGACCGCAGTTAAATGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNATGCATTTTCACATGGTTTAATAGCATTCTTTGGGAAATAAATCTTGGATTAGGGCAGATTATGGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1792
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029974 | Essential Splice Site | 682 | 693 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 24578539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24365115 |
GRCz11 | 23 | 24291656 |
KASP Assay ID:
554-1784.1 (used for ordering genotyping assays)
KASP Sequence:
AACACAGAGCTCATACATTACAATTCATTATAAAATCTGATTTTTCTTCC[A/G]GATGAAAAAAATTATTGAAGAGATGGCAAAGGAGGTCTGATGAATAAAGG
Long Flanking Sequence:
TATTTTAATTTCTGTTAGTATTACTGAATGGATTTAGCTAAGAAAGTTGCACCTGGAAGCTTCTCTGCATCACTAAATCTTCTTGCAGGATTCATGTAAACAGCTTGAAGAAGTGTGTTGTGTTCAGCCTGTGCGTCTTCATCTGACTCCTGACAGCACAGTAAAGCAGGTGTGCAGTGAGAATCAGCTTACCACTATTATGTTTCCTTCACATTATCTCCATGTTTTGTTCCGGTTTGCCTCGACATGATGAGTGCTTGTGTGTGTGTGTGTGCGTGTTCTGTCAGGCTCATTGCATCATGAGCATCACGGGTGAGCAGCGTCTGTTTATAACAGAGAGTGGGCGACTGTGTGGCGTCATCACATGGAAAGAGGTGACAAGAGCAGCCTGCAAGAACAAACATAAACACATCCACACACACATCTATACTCCAATCAAATACACCAATGAACACAGAGCTCATACATTACAATTCATTATAAAATCTGATTTTTCTTCC[A/G]GATGAAAAAAATTATTGAAGAGATGGCAAAGGAGGTCTGATGAATAAAGGGTGCATCAATTTGCGCTTGTCATTTTAATTCTATAAGTTGTTTACTGAAAATAAAAGTCAAACCTTCTGAAATGGCCAGTTTTATAATCAGAATTGTGAATGGTTTCCAGCCTGTCCAGTTCTCTTTGTTTGTTTAGTACTTTCTCTCATGTTATTTTGTGGATGAATTGGATTCCTTGTGGACTATTCACTTATTTTAAATTAAAATAAAGTTAAAAGCTACATTTAGATCCTCTTGGCGAATCCTTATTTTACCTCATTGTAGCGTACAAGTACACCCACAGGCCACTTTACTAGGTACACCTTACTAGTACTGGGTTGGACCCCCTTCAGAACTGCCTAGATCCTTCATAGCACAGATTCAACAAGGTACTGGAATTATTCCTCAGAGATTTTGGTCCATATTGACATGATAGCAGCATGTAATTGCTGCACAACCATGATGTGAAT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |