ZMP
clcn7
Ensembl ID:
ZFIN ID:
Description:
H(+)/Cl(-) exchange transporter 7 [Source:RefSeq peptide;Acc:NP_001071005]
Human Orthologue:
CLCN7
Human Description:
chloride channel 7 [Source:HGNC Symbol;Acc:2025]
Mouse Orthologue:
Clcn7
Mouse Description:
chloride channel 7 Gene [Source:MGI Symbol;Acc:MGI:1347048]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20020 | Nonsense | Available for shipment | Available now |
sa14513 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20020
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 |
---|---|---|---|---|---|
ENSDART00000103660 | Nonsense | 119 | 795 | 5 | 25 |
ENSDART00000126533 | Nonsense | 119 | 795 | 5 | 26 |
ENSDART00000129235 | Nonsense | 119 | 795 | 5 | 26 |
The following transcripts of ENSDARG00000019556 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 27821367)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 27539406 |
GRCz11 | 3 | 27670248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCACAGGGCTTTAGATGCCTGGAGATCACACGATGGGTGATCTGCGGTT[T/A]GATTGGTTTACTCACCGGTCTCATCGCATGCTTGATAGACATTGCTGTGG
Long Flanking Sequence:
CAGATAGTGAAACAATCGCGTTGTACACTGCTGAGCTGTGCTTTTCTGTTTCTCCAAAAACCAAAAATGCTATTTAATAATTTAAACCTCTTTTTTAGAGAGTCTACAGGAAGATAAATGCTTGGACTTTTTCTGATCTTTTGATTTGTCAAAGTGCAATAAATATGCTCAATTTACATATCAATGTGTTCAAAGGCAACAGAAAATTATTCAAGGAGCAGCAGCTTTCATTTTAGCTCTGAGAGTCACAAAACTATGCCGAACATTGTTGTGTCAGAATTAGTATTGACTTGATTCGACATCTATATGTTAAGGCTTATCAGAACTGTAGTCACTGATAAGCTGTTTCCATGTAAAGACAATTTATTCAGCATACTCGCAGAACAGGGTCTGTTTTTCTTGTTATGCTTTAGTAATTTGTGGATTAACATTTAATGCTTCTCGATCTTAACCACAGGGCTTTAGATGCCTGGAGATCACACGATGGGTGATCTGCGGTT[T/A]GATTGGTTTACTCACCGGTCTCATCGCATGCTTGATAGACATTGCTGTGGAGAACCTTGCAGGACTTAAGTACTTTGCAGTCAAACTGAGTATCCTTCCCTGTACAATCCACTGAAATAATCATTTACTCGCATGAGGGAGTCATAGAGGTGCATTTGCTCTTAATTTAATTCAATTGAGCCAATACTCTGCTGTTCTAAAACTGGTTCACACTGTAATTTCATGCATTCCGTTTACATTTTGTTATATGGACTTTTGTCTAATCAGTTATCATTGAGGCTACATGAATAATTTGGCCATAAATCAGATTGCGGACGGATCGGAAACGTTTAATCTAATTGACGTTTTATTTAATGTCATCTGTCCAATTAGTTTGTTTCAATTTGCACTCAACTAAACTAAAATGTTAGTATTACCTCTTCTTTAGAGCAGCTACAGTTATTAAAATCAGGAGCTAATTTTATGAAGCCATAAATCATATTCATGATATAATGAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14513
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103660 | Essential Splice Site | 186 | 795 | 7 | 25 |
ENSDART00000126533 | Essential Splice Site | 186 | 795 | 8 | 26 |
ENSDART00000129235 | Essential Splice Site | 186 | 795 | 7 | 26 |
The following transcripts of ENSDARG00000019556 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 27823577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 27541616 |
GRCz11 | 3 | 27672458 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAAATAATGWGGTATTTTWCTTTGAASATGATYATTTATTTTTTCACA[G/T]CCCATTGCTGCAGGAAGTGGAAWCCCTCAAATAAAATGCTATCTGAATGG
Long Flanking Sequence:
TGAATAATTGAGTTTCCATCAAAGGAAAAAGTAAGTTTTAAAGTGTCTCTAGCTCTTTCTTCCTCTTTTAACTTCAATTACAAATCAAACTTGCTTTATTGACATGTCAAATGTTACACATGTATTGCCAAAGCATTTGTGATGTTTACATGAAAACAAATTACATAGTAGTATTGATATAAAACCAAAAACAATATTTAATATCATATTAAATGATTAACATTTTAGTATTAAATGATAATTAATAACAATAAACAGTATATAAAAAAATCAACATTTTAGGATTTATTTATAACAATTTAGAATTTAGTGTGTGTATCTGTGTCTTTCTCTCTATATAAATAATGTTCAGCAATATTGATAGTTTTAGTGAATTTTTGTCCTAAATAAATGGCAGGCAAAAGAAACCTCTTTCAAAAACCTTACTGTCTAATAAGTATGTTTTTTTTTTGTAAATAATGTGGTATTTTTCTTTGAAGATGATTATTTATTTTTTCACA[G/T]CCCATTGCTGCAGGAAGTGGAATCCCTCAAATAAAATGCTATCTGAATGGAGTAAAGGTTCCTCGTGTTGTTCGGCTTAAGGTGATGTCTTTTGGTTCATATATGATGTGTGATGGTGATGTATTTTATATACAGTTAGTCAGAATTATTAGCCCTCCTGAATTATCAGCCCCTCTGTATATCATTTCCCCAATTTTTGTTTAAAGGAGAGAAGATTGTTTCAACATGTTTTTAAGCATTATAGTTTTACTAACTCATTTCTAATAACTGATTTATTTTATCTTAGCCATGATGACAGTAAATAATTTTTTACTAGACACTTCTATATAATTTCCTAGAGATGGGTTGTGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCAGATTAAAAAAGGGACTAAGCCGACAAGAAAATGAATGAATGACTTCTATACAACTTAAAGTTAAATTTAAAGGCTTAACT
Associated Phenotype:
Not determined