ZMP
C1orf216
Ensembl ID:
Description:
chromosome 1 open reading frame 216 [Source:HGNC Symbol;Acc:26800]
Human Orthologue:
C1orf216
Human Description:
chromosome 1 open reading frame 216 [Source:HGNC Symbol;Acc:26800]
Mouse Orthologue:
5730409E04Rik
Mouse Description:
RIKEN cDNA 5730409E04Rik gene Gene [Source:MGI Symbol;Acc:MGI:3609248]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39261 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa5930 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39261
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 |
|---|---|---|---|---|---|
| ENSDART00000130929 | Nonsense | 55 | 309 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 50155167)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 47794584 |
| GRCz11 | 19 | 47939897 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCGAATGATGATGATACGATGATGATGATGATGATGGGAGATGAGAAT[C/T]GAAACCAGGTGCGTCCCAGAGCTCTAGGCAGAGATTTATCCTCCAATCAC
Long Flanking Sequence:
CAGGTTTATAAGTAAAGGATGAGTAAAGTTGGAGAAAATACTCATTTGTAGGTGAATTATCCATTTAAAGGGCCAGTTCACCCTAAAATGAATGTTTTGTTATACTTTACTCATCCTTCAGTTGTTCCAAATCTGAGTTTCTGTCTTATATTGAACACAAATGAGGATAAACTGAAGAGTGCTGTAAAGAAAGCAGTGTTATTTGGATGTCTACGACAACATTCTTCAAAATATCTTCTTTTGTGTCTCATTTGTGTTGTAGATATGTGATTTCTACCGTCAGATTTACACTAACAGTGTTTCTCCGATTCTAAAGGGCGAGTGAATCTCAAGCCAAAATGCTTCAGCAGCAGGATCATCGGGCGGCGAACCCCGAAGCGCCGCCGTCCATCAACCTGCGCATCAGTCAGAAGAGATGCACCGATAAAGATGGCAATTACAACTTCTTGGGTCCGAATGATGATGATACGATGATGATGATGATGATGGGAGATGAGAAT[C/T]GAAACCAGGTGCGTCCCAGAGCTCTAGGCAGAGATTTATCCTCCAATCACTACAACACCGGACCCTTTTCTCCACTGTCCCGCCTGCCAAGCTGGAGCCCTTTGGAGCCACTTCCGGAAATCGAAAGCGGGGATGATATGGGCGGACGAGTGCCTCCTGATGGAGCTGAAGAGGGGAAGGTGGATGAAGAGATGTGCAGGCTGACGGATGATGAGAAAAACGACTATGAAGACAGTCAGAAAGCTGAAGATCTCCTAGATGATGAAGAGGAGGAGGATGAGGATGATGATGATGTGATTGATTGGGGAAACAGCGATGATGAAGATTTCGAGTTCAGCTATAAGTCTGAGAGCTCCAGCATGGACAGCGCAGGAGCCAAGAACTCCATCTGGGAGCAGATCTGTGTGTCGGAGAGCTCCGAGAAGAAACCCAGACGCACAGCAGCGGGCCGCCGCGAGAGTGTGGAGGGGATGGACGCCGCTGGGTCGTCGGATTCGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5930
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000130929 | Nonsense | 168 | 309 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 50154826)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 47794243 |
| GRCz11 | 19 | 47940238 |
KASP Assay ID:
554-3837.1 (used for ordering genotyping assays)
KASP Sequence:
NNNNTGATTGATTGGGGAAACAGCGATGATGAAGATTTCGAGTTCAGCTA[T/G]AAGTCTGAGAGCTCCAGCATGGACAGCGCAGGAGCCAAGAACTCCATCTG
Long Flanking Sequence:
CTTCAGCAGCAGGATCATCGGGCGGCGAACCCCGAAGCGCCGCCGTCCATCAACCTGCGCATCAGTCAGAAGAGATGCACCGATAAAGATGGCAATTACAACTTCTTGGGTCCGAATGATGATGATACGATGATGATGATGATGATGGGAGATGAGAATCGAAACCAGGTGCGTCCCAGAGCTCTAGGCAGAGATTTATCCTCCAATCACTACAACACCGGACCCTTTTCTCCACTGTCCCGCCTGCCAAGCTGGAGCCCTTTGGAGCCACTTCCGGAAATCGAAAGCGGGGATGATATGGGCGGACGAGTGCCTCCTGATGGAGCTGAAGAGGGGAAGGTGGATGAAGAGATGTGCAGGCTGACGGATGATGAGAAAAACGACTATGAAGACAGTCAGAAAGCTGAAGATCTCCTAGATGATGAAGAGGAGGAGGATGAGGATGATGATGATGTGATTGATTGGGGAAACAGCGATGATGAAGATTTCGAGTTCAGCTA[T/G]AAGTCTGAGAGCTCCAGCATGGACAGCGCAGGAGCCAAGAACTCCATCTGGGAGCAGATCTGTGTGTCGGAGAGCTCCGAGAAGAAACCCAGACGCACAGCAGCGGGCCGCCGCGAGAGTGTGGAGGGGATGGACGCCGCTGGGTCGTCGGATTCGGACTGTGAGCCATGCGCGGAGCTGCCGGAGCTGATGGAGGCGGTGTGGACGCTGCAGGACCGGGAGAAGTTCAAGGCGCAGGAGATGGAGAAGCATCAGGTGCAGCTGAGCATGTACCGGCGGCTGGCGCTGATCCGCTGGCTGAGGACGCTGCAGAGCCGAGTGCAGGAGCAGCAGAACCGCCTGCAGAACAGCTTCGACATCATCCTCACACACAGGAAAGAGCTGCTGCGCATGGGGGCGGCGGCCAACACTGCTGCTGCGCAATAACACACACACACACACACACACACACACACACACATACAGTAAAGAGCTGCTGCGCATTAGGGTGTCCAACACTG
Associated Phenotype:
Not determined