ZMP
C20orf26 (1 of 2)
Ensembl ID:
Description:
chromosome 20 open reading frame 26 [Source:HGNC Symbol;Acc:15872]
Human Orthologue:
C20orf26
Human Description:
chromosome 20 open reading frame 26 [Source:HGNC Symbol;Acc:15872]
Mouse Orthologue:
4930529M08Rik
Mouse Description:
RIKEN cDNA 4930529M08 gene Gene [Source:MGI Symbol;Acc:MGI:1926024]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39308 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43536 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16274 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39308
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057698 | Essential Splice Site | 60 | 500 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 49381886)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49269034 |
GRCz11 | 20 | 49076917 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGGCTCAACCTGGCTTTTCCATAGGTGGCGCTAAAGAGATATTCAGG[T/A]AAACTACTGTACTTTTTATCTAATATTCTGCCATTTCTTTTTTTTATTTT
Long Flanking Sequence:
AATATTTCCATATATGATATAGATCATTACAGGATTTTCCCAGTGCTGGGTTGCGGCTGGAAGGGCATCTGGTCTGTAAAACATATGCTGGAATAGTTTGCGGTTCATTCCGCAGTGGCGACCCCAGATAAATAAGGAAGATGAATGAATCGTTACAGGACATGTTTCTCTATTTTCATTGCAGTGAGAAAGCAAATTTAGCCGTGACCCTGAGCTCCAGTAAGAATGAAGTTTTGGCCCACGCATCTTTCTCAGATCACCCAATAGAAGAGCTGGTGGATCAGGCATGCTGGCAGAATCGGCTTCAAAATTACGCCAGTGCAGAGAAATTGACGGTAGGAAGAGTAAATAAAACCTGATGTCCATTAATACTCAAAATGTTTTTGGAGAGTTCCTGAGAATCTTGTTTTTCTATCCTCCAGCCCATGAACACTCTCTTCCTGCGGCTGTTTGTGGCTCAACCTGGCTTTTCCATAGGTGGCGCTAAAGAGATATTCAGG[T/A]AAACTACTGTACTTTTTATCTAATATTCTGCCATTTCTTTTTTTTATTTTAGTGTTATATTTGCACTTTTTATAAGCTGTAGTTTTAAAAATAGGGAGCTTGGAGGGAGATTTTTCTCTATTGGGGGCACTAAAGAGATCATGTAAACTACTGTACTTTTTATCTAATATTCTGCCCTTTCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGATATATATATATCTATAGAGAGCGATATAGAGATATATATATCTCTACGCACCCATTTTTTAAAACAAATGCATATAAAAAGAGAGAATATAACACAAAAATAAAAAAAAAAAATGACAGAATATGAGATAAAAAGTACATGTGTGTATCTGTATATCTCTCTATCTCTATATATATANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43536
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 |
---|---|---|---|---|---|
ENSDART00000057698 | Nonsense | 87 | 500 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 49379603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49266751 |
GRCz11 | 20 | 49075003 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTAAGACATTATTCTGTCATAATTGTCTTTATATTAGAGGCAGCGCTG[C/T]AGAAGATCTTTGAACCCATGACTTCTGTTACGGATGAAGCTCAGTATTCA
Long Flanking Sequence:
TACAAATATATATTTTAACTGACAAAGTACAATAACAGAAACATGTAATAATATTTTGGATGTCTTCTTTCTATCAAGCTGAATGAAAACACTTTATATATTTTGGGTCTCGGTTGAAATATGTTTTGTATTAGTTCACCTTCGAGCATTACATTTCTTCCCTATTGCTGCTCACTGGTTTATTTTTCATGTAATAAAGCGACAGTTATTGGGTTAGAGTGGATATGAATCTCGTTTTAGGCAGCACAAATTGCATTGGCTGTACAGCAATGCCATTCAGTCAGGTTATATCGGATTTGATCTTTATTTTCTTCCAGGACTGTTTTCAGTGCGGTTGTGGAGCTGGAACACATCTGTCTCCTGACCCCATACGGAGGTGCACTTGGTAGGAAATAAATGCACATGGACATATTTTGTATGCCGGCAGTGATGGCAAAATTGTTCAAATGATGTTAAGACATTATTCTGTCATAATTGTCTTTATATTAGAGGCAGCGCTG[C/T]AGAAGATCTTTGAACCCATGACTTCTGTTACGGATGAAGCTCAGTATTCAGCTTATGTTTGTCATCGACACGATCACTGTCCTCGACTGCACATCCGCAAAGCCAGGTTTACAAATCACCCAATCATTTATTTCCCTGCATTGTTACCTTTTGTGCATGCCAGTTAAGCACTTGCGTTTTTAAATATATTTAAAATACTTTTTTATATAAATATATTGAGAAAAAAATTATAATATATATTATAAAATATAATATATATTGGTTATTAAAAAGAGATTCAATATTTTAGCATTTTTCCTATAACTCTTATATAATTCTTATTGTTTTTATGTAAGCATGAAACTTGCCTTTTCAATTAGTTTATGATGTTTTTTATTTTGTTTGTTGTCAAAAAATACCTTCTGTAGTAATGTAGTTAAAAGCTAATTTAATAATTTATAAAATGTAATTTTATTATCTATCTTTTTTTTTTTAAGTTTAAACACTTGTAATAAAATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16274
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 |
---|---|---|---|---|---|
ENSDART00000057698 | Essential Splice Site | 369 | 500 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 49358781)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49245929 |
GRCz11 | 20 | 49054582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATGGATTTATTTGTGCTTCAGAAACCGTATAACTTTCTGTWTATTCTC[A/T]GGAGACTGGAGGTGCGTGTGGCGGTGTCGTCAGATATCCCAGCAGTCCAG
Long Flanking Sequence:
GCTTCAGTCCTTCATCAGAGTCGCTCCTCGTGACACCAGCACCTTCCCGCAGGAACTCTACCTGTGTCACAGATGGGGACTGACCAGGTACTGAATCATCTAATTGAGCTGACAAAGATACGAGATCAGTCGTAAGAGTTCAGTCAAACAAAAATATAAGATTTTTAAAAGGACTCGTGGCACCAAACCCCATCCCTAAACCCATCGTCATTGGGGATAAGCAATTTGTACTAAATTGTACAAAGAAGATCGTACAAATTCATTTGAATTAGCCACTAAATCAAAAAGTGGCCAAACTGCCGTCAGATATTGTTGGTTTACAGACCATTCACACACTGGCAATGAAAAAGTCATTCATACATCAAATGTTTAGAGACTTAACAAAATGTAAACAAATGAAACCTTATTGTAAAGTTATAACAAGTAAAACTTTAACAATACAGACCTGGATCATGGATTTATTTGTGCTTCAGAAACCGTATAACTTTCTGTATATTCTC[A/T]GGAGACTGGAGGTGCGTGTGGCGGTGTCGTCAGATATCCCAGCAGTCCAGAGTTTAACCGAAAGTCTCAGCCAGAGAGACTCCATCATTGAAGATCTGGATCTGTTCCTGCAGGCCCGAAAAAACTCGGTCTGTCAATGAAACCCACACACTTGATCTCAGACTGTAGACAGATGATTTAAACACTGTTTCTCCTCCTCAGGACGGAACTGCTCTTCAGGCATTTGTGGCTCATGTTGATGGCCGAGTTGTTGGTTTGATAATCACCAGAGACGAAGAGGTGAATATTTTGCTGATGAACATTCTAAGGTGTGCACATTATTTTCAGATAAATGCACAGCCAGCCAGGTCTTGACATCACGGATTTGTATCACTACACTGTAAAAATACTGGTTAATTGCATGATTAGCATTATTATGCTGGATGTTGACCTCTGCTCTGTCGACATTTGATATTGAAAAAAAATTCAACTCAGTTTATCAAAGTGACTTTTATTGGCAT
Associated Phenotype:
Not determined