ZMP
CLPX (2 of 3)
Ensembl ID:
Description:
ClpX caseinolytic peptidase X homolog (E. coli) [Source:HGNC Symbol;Acc:2088]
Human Orthologue:
CLPX
Human Description:
ClpX caseinolytic peptidase X homolog (E. coli) [Source:HGNC Symbol;Acc:2088]
Mouse Orthologue:
Clpx
Mouse Description:
caseinolytic peptidase X (E.coli) Gene [Source:MGI Symbol;Acc:MGI:1346017]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34015 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18864 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15422 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34015
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124966 | Essential Splice Site | 19 | 224 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 14467107)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 13387167 |
GRCz11 | 7 | 13639887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACGTGTGCTATAGCAGCGAGAAAATTCATAAATTCAGCTCATAAAGG[T/C]AAGAAGAGATTCATATTTTGATAAATGTTGATGTTTGTTTATTTCTTAGC
Long Flanking Sequence:
TAATAAACAATAGCAAGCGTGCCACAACAGGCGTTATTTATTTGTCACACTTTGATTCACTGACTTCAATAGCGTATTGATTCATTCGATAAACGATTCTTTTTAATCTTTTCAGAATGATTCACCAATTCAAATGATTCCGTGTCCGAATGATTCAGTGAGTCAAGAGTGTCATCGGTTGTTTACTTGTATCACAGTGTCTAGTTCAGACAGCAGTGTGTGTGTGACACAGCTGTCCATAGCATCTCCCCGAACAACGTGTTTTGTAAATTCAGATGTACGATTGATTTTTATTTAACTTCGAAACTCAGCTAAATAGTTTTTATTATTGTCGGGCCTGTGTTGAATGGCTTTCAGCGGGTTAGCTCTCAGCTAGCGCTAACCTTCTAGCGCTCATCAAATTCAACCGGTTCAGTTCGTTAAAAACACACAACAGCACTGAAAATGTCGTGCACGTGTGCTATAGCAGCGAGAAAATTCATAAATTCAGCTCATAAAGG[T/C]AAGAAGAGATTCATATTTTGATAAATGTTGATGTTTGTTTATTTCTTAGCCTTAGTTTGGCTAGCACTGCTGCTAGTGCGCTCAACAATGTATAAACAAAACAAAACATTGATGTTTAGTTATATAAATAAGCTTTTATTTTAGACAGTTTGTTTTTTTAAAGGTAAAAATATACATAACATCGGATGATTGATAAGTAATTGTATCATATGTGCATCTGTGAGAGCGTTGTTTATGTAACCATTACCATACTGTAAAAATGACAACCTTCGAGTTGTTAATGAGTACTGTTGTTATATTAAACGTATTAAAATGTCAACCTACGATATAATAATGAATGTATTAAACGTACGAAGTTATTTTTTGGCTAGTTTATTTTGAAATGTGAAAAACATAGCTAAATTTTGTAAGACATGATTCTTGATAATTGTATATCCACACATAAGTTACGTGAGTTGTTTATGTAACCAGACTGTTTATTAAAATGACAACCTTCGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18864
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124966 | Essential Splice Site | 109 | 224 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 14471709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 13391769 |
GRCz11 | 7 | 13644489 |
KASP Assay ID:
2259-8506.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGCCCCAAATGCGGAGATCCCTGCACACATGTAGAAACATTTGTTTG[T/C]GAGTACTTGAATTACTTGTAGTTAACTTTGTATCATCCATTTTTAATATA
Long Flanking Sequence:
TAAGTTAGAAATTATATAATAAATTATAATAAATTATATAATAAATTAGTCATTAGAAATGAGCTAAAATGTATTAAATATAAATTTATATAAAATTTATTACATTTATATAAATAAATTTATAATTAGTTTAAAAATGTGTAGAAAAACTCCATTTAACAGCACCTGGGAAATATTTGAAAATTAAATTATAAATATTTCATTTCAGTAATTAAAATTAAATACATTTTGCCTTTAACTGTGAACATATATACAGCTTTACATCTTATACAATGATATGTTTCCTCCCAGACCTCAAGGGCCCTGAGGAGGAAATAAAAATGTCGTCCTCTTTCTGGAAATTCTTCCTCTTCCTTTTTAATCTGGGTCATTCTTTTTAAGAAATCTGTTGGTGAAGGAAGTGGAAAAAGAACCAGCTCTGGTAACTCTGGCAAAGGAGGAAGTCAGCTGAGGTGCCCCAAATGCGGAGATCCCTGCACACATGTAGAAACATTTGTTTG[T/C]GAGTACTTGAATTACTTGTAGTTAACTTTGTATCATCCATTTTTAATATACAGTTGAAGTCAAAATGATTCGCCCTCCTGTGAATTTTGTTTTCTTTGTGAAATATTTCCCAAATAACGTTTAACAGAGCAAAGAAAGTTTTCACAGTATTTCCTATAATAATTTTTCTTCTGTTGAAAGTTTTATTTGTTTTATTTTGGCTAGAATAAAATCAGCTTTTAATTTAAAACCATTTTAAGGTGAAAATTATTAGCCCCCTTAAGCAAAATTTTCTTCAGTTGTCTACAGAACAAACCATCGGTATACAATGACTTGCCTTATTTCCCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGAATACTATTATCTTGAAAAATATCTAGTAAACTATTATTTACTCTCATCATGTCAAGGATAAAAGAAATCATTTATAAGAAATTAGTTATTAAAACTATTATGTTTAGAAATGTGTTAGAAAAAAAAACTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15422
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 |
---|---|---|---|---|---|
ENSDART00000124966 | Nonsense | 164 | 224 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 14473714)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 13393774 |
GRCz11 | 7 | 13646494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGTASGTTGTAACGTCTCCGCTTTTGTTTTCTYSCAGATCTTTGCTTA[T/A]CTTGATAAGTWTGTTGTGGGTCAGGACCATRCTAAGAAGGTATTGTCAGT
Long Flanking Sequence:
TGTGGATTTAAAAATAAATAATATATATAAACTAGAGCACTACTGTGCTTCACTCAAAAAGATATATTTGGTTAAATCACAAACACTACAGGACATAAAAAGTGTTATAAGCAAATGAGGTTATGCCCTTTAAAGCATAAAACACTCATAAATAAAATATTATTTCTTTTTGCAGCATCAACACGGTTTGTGAAATGTGAGAAATGCCACCACTTCTTCGTCGTGCTGTCAGAGACGGACACTAAAAAGAGTCTGAGTAAAGACCCGGAGTCTGCGGCAGAAGCTGTCAAGTTGGCTTTCCAACAGAAACCTCCTCCACCACCTAAAAAGGTGTCTATTCATTTAATAACATTAGTAGAAGTAGTCATCTTTTAGTCCATTCATATGTTAATTTGGACAAAAGTGACAGCTAAATGACTAAATGTAAATATTTAGCTGCCGCTCATCTGTGTTGTAGGTTGTAACGTCTCCGCTTTTGTTTTCTCGCAGATCTTTGCTTA[T/A]CTTGATAAGTATGTTGTGGGTCAGGACCATGCTAAGAAGGTATTGTCAGTGGCAGTGTACAATCATTATAAACGCATCTACAACAACATGCCGGCGGGCTCCAGGCAGCAGCAGGTGGAGGTGGAGAAACAGGCCTCGCTCACTCCTCGAGGTTGGTCCTGCAGAGTGTGTGTGTTTGTGTAGAAACTGCATAGACTGTAGTATCAGGTGGTTTTCACTAAACGAGTCATATGTAAGAGACTCAGAGCCATTTGGAATTTAATCTATTAGTTGCATGATACTAATTTAATTGAGTGCTCTTGGAAAGCCTGGTTTCGCTCATATCAACTGAAAGTAAAATGAAGAAGTGACTCGTTGGTAAAATACAAAAACATATGCATCATATGTTACACACACACGGTAAAGTATCAGGAGTAACAGATGCATTTTGATGCAGTAGAGCATGTGCGCAACAGAGTTTACGCTTTGAATTGGCATGCTGTAAGGGAGAGTTCACCCAA
Associated Phenotype:
Not determined