ZMP
chmp6b
Ensembl ID:
ZFIN ID:
Description:
Charged multivesicular body protein 6 [Source:UniProtKB/Swiss-Prot;Acc:Q503V0]
Human Orthologue:
CHMP6
Human Description:
chromatin modifying protein 6 [Source:HGNC Symbol;Acc:25675]
Mouse Orthologue:
Chmp6
Mouse Description:
chromatin modifying protein 6 Gene [Source:MGI Symbol;Acc:MGI:3583942]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42076 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42075 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22149 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42076
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 |
---|---|---|---|---|---|
ENSDART00000022767 | Nonsense | 33 | 188 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 35734236)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35487400 |
GRCz11 | 12 | 35588463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTGTGTGAGCAGCAACTGAAACAGCAGAGAGATAAACTGAAGCAGTA[T/A]CAGAAGAGGATCACGCTTCAGATGGACAAGGAGCGACAACTGGCCAAACA
Long Flanking Sequence:
ACACATACATACATCAGTGGCTTTTATTTTGAAGTACGTATCTTCCGGTAGGCTGGGTAGCTGTTTTCTTCTCCACACCTCAGACTTTAGTGTTTCTGTTATGGACTGACAGTATCGAGGCCTGTGGATTTAACATTTTCCGAATTTTAGAAACACCACCCCTGTCTGGACAGATAGTGGCGGGGATGCGGCATCGACATGGGAAATCTTTTCGGGAAAAAGAAAGCAACTCGGGTGACCGAGCAAGACAGAGCTGTGCTGGTGTGTTTGAAAACTGCTAACTGGCTAATCATTATGATTAGAGAACTTGTATATGTAAAACTCGGGTGTTATATTATCTTAATATGTTTATGTGTTTAAATTTGTATATCTTCAGGAAACGCACCTAAAGGACCGTTAGTCTACATATACCTCTCATTTTTAATATTAATATTAAATGTGTCACTTATTTATGTGTGTGAGCAGCAACTGAAACAGCAGAGAGATAAACTGAAGCAGTA[T/A]CAGAAGAGGATCACGCTTCAGATGGACAAGGAGCGACAACTGGCCAAACAGTTACTGAAAGATGGCAAGAAAGAGTGAGTACAGTCATGTATGACTTACTGTGACTTGTAGAACTAGAAGGTCAAGCTTTTCATAAAAACTACCTTCTAATGTTTTGTGTGTATAGTAAAGCACTCCTACTCCTGAAGAAGAAACGCTACCAGGATCAGTTACTGGAAAAGACAGAAAATCAAATTAGTAACCTGGAGCGAATGGTAAATAAAGCATTTTATGCTGAGGACATGATGAATGACACATGTTGACAAGACTGCAGCATTTATTGTATTTCTTTATTTTGGTTTTTACAGGTACAAGATATTGAATTTGCACAAATAGAGATGAAAGTTATTGAAGGATTGAAAGTTGGCAATGATTGCCTAAAGAAAATGCATGAGGTATGTAATGAGAAATGAGTTATACTTCATCACGTTTAGTACAATGTACTGGTAAATTTCACTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42075
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 |
---|---|---|---|---|---|
ENSDART00000022767 | Nonsense | 89 | 188 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 35733885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35487751 |
GRCz11 | 12 | 35588814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAAGACTGCAGCATTTATTGTATTTCTTTATTTTGGTTTTTACAGGTA[C/T]AAGATATTGAATTTGCACAAATAGAGATGAAAGTTATTGAAGGATTGAAA
Long Flanking Sequence:
TGTGTTTAAATTTGTATATCTTCAGGAAACGCACCTAAAGGACCGTTAGTCTACATATACCTCTCATTTTTAATATTAATATTAAATGTGTCACTTATTTATGTGTGTGAGCAGCAACTGAAACAGCAGAGAGATAAACTGAAGCAGTATCAGAAGAGGATCACGCTTCAGATGGACAAGGAGCGACAACTGGCCAAACAGTTACTGAAAGATGGCAAGAAAGAGTGAGTACAGTCATGTATGACTTACTGTGACTTGTAGAACTAGAAGGTCAAGCTTTTCATAAAAACTACCTTCTAATGTTTTGTGTGTATAGTAAAGCACTCCTACTCCTGAAGAAGAAACGCTACCAGGATCAGTTACTGGAAAAGACAGAAAATCAAATTAGTAACCTGGAGCGAATGGTAAATAAAGCATTTTATGCTGAGGACATGATGAATGACACATGTTGACAAGACTGCAGCATTTATTGTATTTCTTTATTTTGGTTTTTACAGGTA[C/T]AAGATATTGAATTTGCACAAATAGAGATGAAAGTTATTGAAGGATTGAAAGTTGGCAATGATTGCCTAAAGAAAATGCATGAGGTATGTAATGAGAAATGAGTTATACTTCATCACGTTTAGTACAATGTACTGGTAAATTTCACTTCACTTAACGTTTTTTTTGTAACCAGGTGCTGTCTATAGAGGAGGTGGAGAAAATCATGGATGAAACACATGATGCCATTGAGTATCAGAAGGTACATTTTACTTCTCACAATGTGAAAGGACCCCTTATATACACTGAGCTATACACTGACTGGGGTCCAACTGGGTACCTCTTTTGCATTTTTCCATACAAATAATGTTGTCAACATAATTATTGGAGTTAAAAAGCTGAATCAAAAAAATCTATGAAAAAATATTCATAAAATAAATTTAAAAATCCCAAAAGAAAACCTGGCTATTGAAGGAGCTTGCAAAAACTGTCACAAACTATTTCTTCATTTGACAGTCACATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22149
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 |
---|---|---|---|---|---|
ENSDART00000022767 | Essential Splice Site | 138 | 188 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 35733646)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35487990 |
GRCz11 | 12 | 35589053 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGAGAAAATCATGGATGAAACACATGATGCCATTGAGTATCAGAAG[G/A]TACATTTTACTTCTCACAATGTGAAAGGACCCCTTATATACACTGAGCTA
Long Flanking Sequence:
TATGACTTACTGTGACTTGTAGAACTAGAAGGTCAAGCTTTTCATAAAAACTACCTTCTAATGTTTTGTGTGTATAGTAAAGCACTCCTACTCCTGAAGAAGAAACGCTACCAGGATCAGTTACTGGAAAAGACAGAAAATCAAATTAGTAACCTGGAGCGAATGGTAAATAAAGCATTTTATGCTGAGGACATGATGAATGACACATGTTGACAAGACTGCAGCATTTATTGTATTTCTTTATTTTGGTTTTTACAGGTACAAGATATTGAATTTGCACAAATAGAGATGAAAGTTATTGAAGGATTGAAAGTTGGCAATGATTGCCTAAAGAAAATGCATGAGGTATGTAATGAGAAATGAGTTATACTTCATCACGTTTAGTACAATGTACTGGTAAATTTCACTTCACTTAACGTTTTTTTTGTAACCAGGTGCTGTCTATAGAGGAGGTGGAGAAAATCATGGATGAAACACATGATGCCATTGAGTATCAGAAG[G/A]TACATTTTACTTCTCACAATGTGAAAGGACCCCTTATATACACTGAGCTATACACTGACTGGGGTCCAACTGGGTACCTCTTTTGCATTTTTCCATACAAATAATGTTGTCAACATAATTATTGGAGTTAAAAAGCTGAATCAAAAAAATCTATGAAAAAATATTCATAAAATAAATTTAAAAATCCCAAAAGAAAACCTGGCTATTGAAGGAGCTTGCAAAAACTGTCACAAACTATTTCTTCATTTGACAGTCACATTGTAATGTTTTACATTTCTCATTTTATTTTGTTAAATGAAAAATTCAATGTGAATTTTATTGAAATATTTAAAAGCTTAAAATCTATTAAAACTAATCATTCAAATATAACATTCTAGTTGTCAAGCTCTAAAAATGTTAAGTAGAAATCATTATATGTAATTTAACATAAAAAACATTTAACTCAAAAACTAATCAAAAACTGAAATGTATCATTTATTATTAATAAAGCGGAAAAGTAT
Associated Phenotype:
Not determined