Busch Lab

ZMP

clcn7

Ensembl ID:
ENSDARG00000019556
ZFIN ID:
ZDB-GENE-061103-196
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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