ZMP
zgc:103710
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC494039 [Source:RefSeq peptide;Acc:NP_001008582]
Human Orthologue:
C3
Human Description:
complement component 3 [Source:HGNC Symbol;Acc:1318]
Mouse Orthologue:
C3
Mouse Description:
complement component 3 Gene [Source:MGI Symbol;Acc:MGI:88227]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39714 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38301 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39714
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064202 | Nonsense | 67 | 461 | 2 | 12 |
| ENSDART00000075469 | Nonsense | 67 | 320 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 56623800)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55407837 |
| GRCz11 | 1 | 56077198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGCTTAATCGTGAAGATCTCTGTAAAGAACCACCCGAGGAAGAACT[T/A]GGAGATCCTGTCGAAAACAGTAACACTGACCGACGAAAACAATTTCCAGA
Long Flanking Sequence:
AAGTTAAGCTTTACAGCTCTATTTACATGCCCCTCAATGTCAACTTCCTTCTGGAAGTAAATCGCTCAGCCCCTTTTTTCTACCCCCTCAAGAGAGTAGATGGCATAGGCATTTGTAGCTCCGCCCTCTTTTTTAAAAGAGCAGAATCTCATTTGAATTTAAAGCGACAGTCACCAAAACACCACAATTAGGATCAAAGCCTAAAAGGGTCCGTTTCAGAGTGTTATAAAACATTATTTATGTGCTGTTTTGAGCTGAAACTTCACACACACACACACACTCAGAGACTTATTTTACATCTTATAATGAAACGATATACAGTAGTAGGTCACCTTTTTAATGTAAAATATGACAATGATTTGATTTCCTCAGATATGTGCTGTCGGCTCCTAATCTGCTGAGAGTGGGTTCATCAGAGAATGTGTTTGTGGAGGCGCAGGATTACTCTGGAGGAAGCTTAATCGTGAAGATCTCTGTAAAGAACCACCCGAGGAAGAACT[T/A]GGAGATCCTGTCGAAAACAGTAACACTGACCGACGAAAACAATTTCCAGATCCTCGCAGATATAAAGGTGATGCCACTTTGACACACTTTGTTGTTATGCAAGAGATTGTGTGTGATTTTTAAAGGGCAAACTTCATATTTGAACAATCAGCTATTTTAGTTACAATTTCAATGTGTTAAAGCATGGAGAGGATATTTCATTATTAATTAGTGTTGTGCAGATTCCCAGTGATCGCGACTATTTCTCTGATGATCCTCTGGAGAAGCAGTATGTGTATCTGCAAGCTCAATTTCCAACTCACACTCTGGAGAAAGTGGTCATGCTGTCGTTTCAGTCTGGATATATATTTGTACAGACTGACAAGCCCATCTACACGCCTGGTAGCAACGGTAGGAATGAAGTATATGCCTAAACATTATAAGCTGCATTAGATATTATGTTAAAAAGCACAAAATAAACTATTTGCGGTTGAAAAAGTAACCATATGTCATAATAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38301
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064202 | Essential Splice Site | 170 | 461 | 4 | 12 |
| ENSDART00000075469 | Essential Splice Site | 170 | 320 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 56623215)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 55407252 |
| GRCz11 | 1 | 56076613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGGTCTGAAGCCACTTGAAAATGCTGGAGTATCAGTGGAAATCATG[G/A]TAATCTTACTAAAATCCACTTAAACCTTCCTAGACAGTGACATTATGGGA
Long Flanking Sequence:
CACTTTGTTGTTATGCAAGAGATTGTGTGTGATTTTTAAAGGGCAAACTTCATATTTGAACAATCAGCTATTTTAGTTACAATTTCAATGTGTTAAAGCATGGAGAGGATATTTCATTATTAATTAGTGTTGTGCAGATTCCCAGTGATCGCGACTATTTCTCTGATGATCCTCTGGAGAAGCAGTATGTGTATCTGCAAGCTCAATTTCCAACTCACACTCTGGAGAAAGTGGTCATGCTGTCGTTTCAGTCTGGATATATATTTGTACAGACTGACAAGCCCATCTACACGCCTGGTAGCAACGGTAGGAATGAAGTATATGCCTAAACATTATAAGCTGCATTAGATATTATGTTAAAAAGCACAAAATAAACTATTTGCGGTTGAAAAAGTAACCATATGTCATAATAATTTTTTTATGCAGTTCAATACAGGATCTTTTCACTGACATCTGGTCTGAAGCCACTTGAAAATGCTGGAGTATCAGTGGAAATCATG[G/A]TAATCTTACTAAAATCCACTTAAACCTTCCTAGACAGTGACATTATGGGAAGTCTGTCTTTCTGTTTTACATTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACAACCAAGAGCAACAATGAATAAGTGCTATAGACAAGTTTCAGGTCTGTAAAGTCTAAGAAGGGAAGTATTAGTAGTATTAGTAGGGATAATCCAGTTTGTGTCATGTTTCAACATGTTTGAAATTATTTTACAAATATATATTCGGTCATTGAATTTATTTCTCGGTTTAAATAAAATTAAGGAAAGTTTTATTGCTTTTTTTTGTAAGATTATCATTATTTTCACAGTGGAAATAATGATCATCTTACAAAAATGCACTAAAACTTCCTGAACAATGATATTTCTTCATGTGTTTGTTTATTCATTTATTTTCTAATAATTCAACGTCTCATTATCAGTTATTCCTTAC
Associated Phenotype:
Not determined