ZMP
c10orf119
Ensembl ID:
ZFIN ID:
Description:
c10orf119 homolog [Source:RefSeq peptide;Acc:NP_997743]
Human Orthologue:
C10orf119
Human Description:
chromosome 10 open reading frame 119 [Source:HGNC Symbol;Acc:25782]
Mouse Orthologue:
1110007A13Rik
Mouse Description:
RIKEN cDNA 1110007A13 gene Gene [Source:MGI Symbol;Acc:MGI:1920977]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22305 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22305
Status:
Available for shipment
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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 |
|---|---|---|---|---|---|
| ENSDART00000077655 | Nonsense | 21 | 631 | 2 | 16 |
| ENSDART00000135788 | Nonsense | 21 | 631 | 2 | 16 |
The following transcripts of ENSDARG00000055314 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 25772408)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 25418068 |
| GRCz11 | 13 | 25548518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTATATTGTAAATAACCTACGTTTTTTTGCTTTATGCTCCCACAGCC[C/T]AGAGTAACTCCAGTCCAGACTGGGAGAAGAAAGTTGTGGAGTATTTCAAA
Long Flanking Sequence:
AAATTTAATGCATTTATAATTATAGATTTTGATGTATTTAAATAATTTATTCCAGGAAAGAGTAATAAAGTAAATCAGTTTCTGCAGTTGCTACAATGCAAATCGGTGAACTACTGCCAAGTCTACACAGGGCAGCGAATGCAGGCACGTTGGTCACGTGTTAGTTTCATGACGCAATTTTCCCGCCACGGTGTATTGTGCCGTGCTAAACTCTGAAACGTGTTTACTGTAGTACACGTCAAAGGAGTATTACTTTTAACTTTGGTCTGTTTCTGAATCCTGCAGCGATGCCCACTACTCATGACTGGATCAATAACCCGCTGGGTGTTGTTGACGGGCTGTTTGGTAAGACAAAATGTGTGTTTTTGTACTAATATATGCAGTTCAGAGATGAGCCATGTGACCCGTGTCATGCTATGCTTTTAAATCGCTCTGTACATGTGCTGACAGTAATTATATTGTAAATAACCTACGTTTTTTTGCTTTATGCTCCCACAGCC[C/T]AGAGTAACTCCAGTCCAGACTGGGAGAAGAAAGTTGTGGAGTATTTCAAAGAGAAACTGAAACTAAACGACGCTCATACATGGGTAACTGTCATAAAGCAAATGTTTTTGTATATTTTGATACATATGAATAACTTTATGCGATATTCTGGCAAGATTATGTGGATATGCTTAATTTTAGGATGTTCAAATTTATTGTTCTATATAATTAAGCTTTCTGGAAATTATATTATTACATTGCAATAAACCGGTTTCTTTTGTTATGTAGACTTGCCTGGTCCTAATCTATCATTCTATTCTGCACAGCTTTGTGTAAACACAGGGTTGTAAGGGTAGCCATGATAATTGTCCATAATGAATGGTTATGGTGAGGGATCACATGTTTGACTGTGGTTTCTTTAGGTTCCTTCTCTGAATGATGTTCCTCTGCACTACCTAAAGCCCAACAGCCTTGTAAAATTTCGTTGCATGGTCCAGGATATGTTTGATCCAGAGTTTTTC
Associated Phenotype:
Not determined