ZMP
zgc:101814
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized protein C3orf26 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q5XJK9]
Human Orthologue:
C3orf26
Human Description:
chromosome 3 open reading frame 26 [Source:HGNC Symbol;Acc:28666]
Mouse Orthologue:
2610528E23Rik
Mouse Description:
RIKEN cDNA 2610528E23 gene Gene [Source:MGI Symbol;Acc:MGI:1913747]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34669 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa27413 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34669
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020743 | Essential Splice Site | 152 | 292 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 31023545)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 30179491 |
| GRCz11 | 9 | 29990237 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGCTGTAATGACCTCACACACAGCTTGTCTTCCTACCTCAAAGAAGG[T/C]AAATGCTTTATATGGACACCGTTTTTCTTTTTATATACTCTCTTAGTTTC
Long Flanking Sequence:
GACATGACAAAAAGAGCCAGACCAACTGCGGAGATGCTTTGATTTTGCCAAACATAATTGACAATATTTGCATTGCTGAAAAACCGACCTCTTCAATTATATTAGACGACAGCGCTTTTGCAAATTTATTCATTCCTCTTCTAGTCACTGTCTCTCCCACTGATGTGTTTTCTGTAAAACATGCTGGTGTTGCATAATTCTCCTTTGTCTTTAGAAGAAGAAAACTATCACAGATGTCCTGACAAGCTCTAAGCCTGTGCCCGGCTCTCCAGTTGACCTTGTGAGCCTTCTGAAGACTTACCACAGCCAGACCCGCTCTGTTATTGAGCAGGAGGAACTGACGTTACAAGGTGAGTATATGTATGTGTGTTTGTGTTTGTGTGTGTGTGTGTGTCTCTCAGTAATGAGGTTGAATTTGTGTGTCCTTTTTCTGTTTCAGATTCTTGTTTCCTCAGCTGTAATGACCTCACACACAGCTTGTCTTCCTACCTCAAAGAAGG[T/C]AAATGCTTTATATGGACACCGTTTTTCTTTTTATATACTCTCTTAGTTTCTTAAAGGCATGAAGTGCTTTGAAATATATATATATATTTTTTATTCCATGTTTGACTTAATCTCAACTGAAAATGAAGAGTGGGACATAGAGTAGCTCCTCCCCTATAAAAAATAGCCAATGACATTCTTGCCAATGGGAGTGGTGGGTAAACACCAACTTTCATAAATTTGGAGTCACTTTTTTTTTTCAGAAACCAGTCTAATATGCTGAAACATTTATTGTTATCATCCATGCTGAAAATGGCTTTGATGCTTAACATTTTTTCAGGATACTTTGATAAATACTGTATAAGGTTCTGAAGAGCTGGGCAAATTATAAATGCCTTTACTGTTGCTGATCAATTGAATGCATCCTTGATTAAAAGAAATAAATAAAAAATACACAAATAAATTCCCACTGATCCCAACATTTTAAACAGTATTGTACATAGTCGGGGGACTTTATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27413
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 |
|---|---|---|---|---|---|
| ENSDART00000020743 | Nonsense | 257 | 292 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 9 (position 31025641)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 30181587 |
| GRCz11 | 9 | 29992333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAAGGACTACGTTATCTGGTGCTGGACTGGAACTACAGAGACCAGAAG[C/T]AAAGGAGGATGGTGGATGTACCAGAGGTGCTGTCTGCAAATGGGGCACTT
Long Flanking Sequence:
CTAAAATGCAGAAACAGCACACCCAGACCAGCTCAGTGGTTTTGCTAATTGTTTGTGGATCTGCTTTAAGAACCATTGATCTCATTAAGTGAGTATTATTGTGTCTTACAGTCTTGTGAGTAATACAGCGTTTGCCTTCCCAAGTGATATTTTTTCCCCCAATCCTTTCTGTTAAAGGCAGCTGGTGACATTCAAAGGACAAGCTAAAGTGCTGAAGCTGTTTGCAAAACACATCAAAGTGGAAGAACAGATAAAGTCATTGAGTAAAGGTGTGACCCATATTGCTGTTGGAACTCCTGGGAGAATTTGCGCACTGTTAGAGAAAGGTTTGTTTTGATGCACAATTCTTGTAAATAGTTTTTTTATTTTTACTTTTGACATGCTCTTCAGTTTATAAAACCTCTTTTTTCTGCTTGGCTTGTTATCCTCATGCTTTAGAGGGATTGACTGTGCAAGGACTACGTTATCTGGTGCTGGACTGGAACTACAGAGACCAGAAG[C/T]AAAGGAGGATGGTGGATGTACCAGAGGTGCTGTCTGCAAATGGGGCACTTTTGTTTATATTGACAAAATATAGAACATTTTAATGAATTGTAATACTGATTTCAGTAAATATGAATTAATTTCAGTTGTTTTTTATCAAATATGTTGTCAAGCATTTTTAGAACAAGAATCATTTAATAGCAATTTAAAAGTCTTTAAGAATCAGTGCAACTGAAAATACTAAAAACATTTAATATTATATATAGTTTTACTCTTAAGACAAACTATCTTTCAAACCTCTAGTTTTTACTAATTTGTCACAGATTTTTAGGAATTCAGAATAAAATAATATTTAATGTTATCACTTGTTGCCATTTATAGATTTTAATAAATACTGATAAGAATAAGCCTTTTTTTAATAATATATTTTTATTTTCACCTTAAAGCAAAACAGAGCAATGCAAAACTATATAGACAGAAAAGAAAAGGCAAGCAAAACCAAAAAAAAAAAAAAAAAAGGC
Associated Phenotype:
Not determined