ZMP
LOC559312
Ensembl ID:
Human Orthologues:
ZC3H6, ZC3H8
Human Descriptions:
zinc finger CCCH-type containing 6 [Source:HGNC Symbol;Acc:24762]
zinc finger CCCH-type containing 8 [Source:HGNC Symbol;Acc:30941]
zinc finger CCCH-type containing 8 [Source:HGNC Symbol;Acc:30941]
Mouse Orthologues:
Zc3h6, Zc3h8
Mouse Descriptions:
zinc finger CCCH type containing 6 Gene [Source:MGI Symbol;Acc:MGI:1926001]
zinc finger CCCH type containing 8 Gene [Source:MGI Symbol;Acc:MGI:1930128]
zinc finger CCCH type containing 8 Gene [Source:MGI Symbol;Acc:MGI:1930128]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35589 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15241 | Nonsense | Available for shipment | Available now |
sa10803 | Nonsense | Available for shipment | Available now |
hu7905 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35589
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109978 | Nonsense | 111 | 1070 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 48806288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47538438 |
GRCz11 | 13 | 47829678 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGTGACTACAGTGAAGAAAAGTATGATTATGACGACGAAGACGATTA[C/A]TCAGAGGAGCTGTCCAAATACAAGCATGCTAAAGAGTCGTCTGGTCATGG
Long Flanking Sequence:
TCTAAATCTTAAGAGTAATGGGTTATCGATAATGGCAAAAAAAATCCATATCGGTGCATCTCTAATCACAATATATTGAAAATACTGAATTTTAGCATATCTTCACCTTGTTATTATAAGGTTCTATCTGCGTTCTGAATGATTTTGAGATATAGAGCTTTAAAGATTTTGCAATCCATAGCAAACAGTATGTGTGTAACATTTGTTTTTTTAAATAAAAAGTCTTAAAATGTAAACAACTTATAAAAACATCGCATAATGTAAATACGTTGTCATTTAATAAAAATATGTCAATAACTCAATTTTGACAAAAATTGTCAGATAGAACCTTATAATTCTAAGGTGACAATATGTCTATATAATTCCTCTTTCTATTCATGTCTCCAGCGGGAAAATGAACCCACAAAAATCCAGAGATCAATGCAGCATAAGAACAGTGATTTGGACAAATACAGTGACTACAGTGAAGAAAAGTATGATTATGACGACGAAGACGATTA[C/A]TCAGAGGAGCTGTCCAAATACAAGCATGCTAAAGAGTCGTCTGGTCATGGTAAAGGTGGGACACCTAAAGACCAGTCTAAGAGATCAAATATGAAGGGACAGCAAAAACAACAACAACAGCAGCAGCAGCAGCAGCAGTGTATGTTTGTTACTTTATTATATTATAGATGGGAATTAAATGGATGAATCTATAAATCTGAATCATGATGAATAAAGTTTTTGCATGTTATATAGTTGGTGGGCAGCGTGGCAGAGGTCGTGGTGGTGTTGTTGGTAGAGGACGAGGAATGCTGAACAAAAATAAGAAACTAAAGGGCAAGAACTGGGGCAGAGGCCGTGGTCGAGGAGGAGAGCAAATGGGAGGAGATGGGGTAAGAAATTCTCTCCCTTTTTTGGATTTACTTCCACCCAGTGTTGGGTAAATTACTTCAGAAAAAATATAATTTTAACTTGGTACAAATGTGTACATTAAAGATCTGGACTACATCTACTGACAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15241
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109978 | Nonsense | 166 | 1070 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 48806570)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47538720 |
GRCz11 | 13 | 47829960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WAGTTGGTGGGCAGCGTGGCAGAGGTCGTGGTGGTGTTRTTGGTAGAGGA[C/T]GAGGAATGCTGAACAAAAATAAGAAACTAAAGGGCAAGAACTGGGGCAGA
Long Flanking Sequence:
AAAATATGTCAATAACTCAATTTTGACAAAAATTGTCAGATAGAACCTTATAATTCTAAGGTGACAATATGTCTATATAATTCCTCTTTCTATTCATGTCTCCAGCGGGAAAATGAACCCACAAAAATCCAGAGATCAATGCAGCATAAGAACAGTGATTTGGACAAATACAGTGACTACAGTGAAGAAAAGTATGATTATGACGACGAAGACGATTACTCAGAGGAGCTGTCCAAATACAAGCATGCTAAAGAGTCGTCTGGTCATGGTAAAGGTGGGACACCTAAAGACCAGTCTAAGAGATCAAATATGAAGGGACAGCAAAAACAACAACAACAGCAGCAGCAGCAGCAGCAGTGTATGTTTGTTACTTTATTATATTATAGATGGGAATTAAATGGATGAATCTATAAATCTGAATCATGATGAATAAAGTTTTTGCATGTTATATAGTTGGTGGGCAGCGTGGCAGAGGTCGTGGTGGTGTTGTTGGTAGAGGA[C/T]GAGGAATGCTGAACAAAAATAAGAAACTAAAGGGCAAGAACTGGGGCAGAGGCCGTGGTCGAGGAGGAGAGCAAATGGGAGGAGATGGGGTAAGAAATTCTCTCCCTTTTTTGGATTTACTTCCACCCAGTGTTGGGTAAATTACTTCAGAAAAAATATAATTTTAACTTGGTACAAATGTGTACATTAAAGATCTGGACTACATCTACTGACAAATGCTTTATTGCACAAAGCAATGGTCAGGACCCAGAATGATTGCCTTTATTTGTATAATTGTATTCTGTTATAATTGATATATTTGATTATCATTTTATTGTTAATAGAATAGTTTTAAAATATATATTTTTTTAAATACAAAAAAAAAATTAGATTGTAGTTAAATTCAACTTTTCTAGTTACTTTGTCTGAAAACTGAAAATGTAACTATTTGACTTAATACAAAAAATTCACATAAATGTCAACACATAGGCAATAGAAATTAAATCTTCGATTCTTTAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10803
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109978 | Nonsense | 166 | 1070 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 48806570)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47538720 |
GRCz11 | 13 | 47829960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WAGTTGGTGGGCAGCGTGGCAGAGGTCGTGGTGGTGTTRTTGGTAGAGGA[C/T]GAGGAATGCTGAACAAAAATAAGAAACTAAAGGGCAAGAACTGGGGCAGA
Long Flanking Sequence:
AAAATATGTCAATAACTCAATTTTGACAAAAATTGTCAGATAGAACCTTATAATTCTAAGGTGACAATATGTCTATATAATTCCTCTTTCTATTCATGTCTCCAGCGGGAAAATGAACCCACAAAAATCCAGAGATCAATGCAGCATAAGAACAGTGATTTGGACAAATACAGTGACTACAGTGAAGAAAAGTATGATTATGACGACGAAGACGATTACTCAGAGGAGCTGTCCAAATACAAGCATGCTAAAGAGTCGTCTGGTCATGGTAAAGGTGGGACACCTAAAGACCAGTCTAAGAGATCAAATATGAAGGGACAGCAAAAACAACAACAACAGCAGCAGCAGCAGCAGCAGTGTATGTTTGTTACTTTATTATATTATAGATGGGAATTAAATGGATGAATCTATAAATCTGAATCATGATGAATAAAGTTTTTGCATGTTATATAGTTGGTGGGCAGCGTGGCAGAGGTCGTGGTGGTGTTGTTGGTAGAGGA[C/T]GAGGAATGCTGAACAAAAATAAGAAACTAAAGGGCAAGAACTGGGGCAGAGGCCGTGGTCGAGGAGGAGAGCAAATGGGAGGAGATGGGGTAAGAAATTCTCTCCCTTTTTTGGATTTACTTCCACCCAGTGTTGGGTAAATTACTTCAGAAAAAATATAATTTTAACTTGGTACAAATGTGTACATTAAAGATCTGGACTACATCTACTGACAAATGCTTTATTGCACAAAGCAATGGTCAGGACCCAGAATGATTGCCTTTATTTGTATAATTGTATTCTGTTATAATTGATATATTTGATTATCATTTTATTGTTAATAGAATAGTTTTAAAATATATATTTTTTTAAATACAAAAAAAAAATTAGATTGTAGTTAAATTCAACTTTTCTAGTTACTTTGTCTGAAAACTGAAAATGTAACTATTTGACTTAATACAAAAAATTCACATAAATGTCAACACATAGGCAATAGAAATTAAATCTTCGATTCTTTAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu7905
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109978 | Essential Splice Site | 991 | 1070 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 48816253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 47547879 |
GRCz11 | 13 | 47839119 |
KASP Assay ID:
554-2395.1 (used for ordering genotyping assays)
KASP Sequence:
ATYGAGGACTCTGAGAGCAATGCAAGTGTGTCGATTCCTCCAGTGCCTAC[A/T]GTAATGCCGGCGTCTCCTTGTTCTCCTSTWTTGGCGGCAGCTCCAGCAGT
Long Flanking Sequence:
GAGGGCGTCGTGCGGATTGGAAGTCCGCCTGGTAGGACTGTAGATCCTCGACATCAAGACAAGCCTACAGATCCACGCACTCATAAAGCGCTCGATCCCAGAATAAACCGCTCCGGAAGTCTAGACTCCAAGCTCCCGGTTGCTAAAGAGAGTCCAATCGAAAGAGTGGATCCGAGAATACAGCGTGCGTCCTCAAACCAACCGGTTAGTGTGGAAAAGTCTGAAAAGTTGCCTCCGTATGCACCACGTCTGGCTTCATCGATGGGTGCTGGTCTTGAAAGCCCAACCACATTGTTGGGTGGGATTAGTTTATATGATCCACGTAATCACAGCTTACTTTCTCCAAAACGGGAAAGCGAGGAGATGCCTAGAAAGTCAGGGATACTAAAGCCGCCGTCTACAAAGTTGTCTCCTCCTCATGAATCACCAGAAAAGGATGATAAAAACACTATCGAGGACTCTGAGAGCAATGCAAGTGTGTCGATTCCTCCAGTGCCTAC[A/T]GTAATGCCGGCGTCTCCTTGTTCTCCTGTTTTGGCGGCAGCTCCAGCAGTGCATAATTTACCCATTCAGGCACTGGCAGGACTGATACGGCCTGCATATACTGACCCACGGCAAAACAAACCTGTCGGCTCCACTGGTGCAAATGCACCGGAGGAAGAAGAGGACAAAGACAGTAAGAAGAAAGACAGGCCTTTAAGGGATGTCTTTAAAACATTTGACCCTACAGCATCACCATTCTGTCAGTAAACTCACACTAAATACACAGCAAAAAAATATTCGAGTTTCTTAGAGTTTTTGTCTTGTTTCTAGTCCAGAGATTTAAAAATAAATCTAGATTTAACAAATGTGTGAATTCTTCTTTAAAACAAGCTAAATAATCTGCCAATGGGATATGCAAAATAAACTTATTTCAAAAGTGATTGTAAGATTACCTTGCTTACTTCATTGGCAGATTATTTAGCTTGTTTTAAGGGAAAAACTCACTTAATTTTGACTAATTT
Associated Phenotype:
Not determined