ZMP
si:ch211-215c18.6
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC791588 [Source:RefSeq peptide;Acc:NP_001038895]
Human Orthologue:
C9orf9
Human Description:
chromosome 9 open reading frame 9 [Source:HGNC Symbol;Acc:1367]
Mouse Orthologue:
1700026L06Rik
Mouse Description:
RIKEN cDNA 1700026L06 gene Gene [Source:MGI Symbol;Acc:MGI:1917237]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa26492 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33624 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26492
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 |
|---|---|---|---|---|---|
| ENSDART00000098336 | Nonsense | 48 | 220 | 2 | 4 |
The following transcripts of ENSDARG00000068130 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 31309626)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29070983 |
| GRCz11 | 5 | 29671136 |
KASP Assay ID:
2259-5942.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCAAGAGAACATGCAAGGGACAGAACAGAGCCTGTCTCCACCATAAAA[C/T]AGGTCATTATGATTTATTAACAGTTTTATAAAGTCATACAGTTCCCACGG
Long Flanking Sequence:
AGAGGGAGTGCGAGCTTCAACTCTAGTTGCTACGCAACATATGCGAAACAGAAAAAGAAGACACCGATTGTACAGGTATTTGATATGCTTCAGTATTAATACAGGTAAGTTCGAATAACGTACATGTGAATATTTGACAAATTGAAGACACAATTGGGCTAAAGTTACATTCCGTGAAAAAGCCCGCTCTTTAGTTTTACAACAAAGTTTTTTTTAAGTTTTAGCCGTAGTAGAATATCCTTAAGGTAATTACCTTAACGTTAACGTTACTCCTATTTATGAACAGTACTTCGTTTATTCTGTATTTTAATACTACTGTAACGTTATTCATCTTCAACAGGTTGAGCACTTTAACCGAGATGGCTGATGTCAGACAGCAGCTACTTTTCCTCGAGCAGAAATATAAACGTTTCAAACAACAACAGTTTATATTTATAAATGCTCTGGAGCGCTCAAGAGAACATGCAAGGGACAGAACAGAGCCTGTCTCCACCATAAAA[C/T]AGGTCATTATGATTTATTAACAGTTTTATAAAGTCATACAGTTCCCACGGCACCCAGTAAAGCTGTGATTATTAAAAAATGGGAGTAATCAAAGCGAACTGTTGTTAATTGTAAGAATGGCATGTTAATATTTTAAGCATAATTTATTGTCATGTTAACCTGGTGGAAATTAAACTGCTAATATTTTCAAGTAGCAACCCACTATTTTATTGTTGGTTGCAGTAACTATGCATACTTTTGAAGACACTGAAATTTTATTCATTAGTTCATTTTTGAATTTGTAAAGAATTAATTATTAAAATGTTTTTAATTTTTTTAAAACAAATCTTACAGCAAACTTGTGTAATTATAATCGGTAGTGTATATATTATTGGTTCAATACTGTTAAATAATATGTATTGCATGTATCAATAATGTAAAATTTAAACAAATAGAAAACATTGTTTTTCCGCAGGTCCAAAAGTACATGAATCACCATTGCAGCAATTCAACTGACAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33624
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098336 | Nonsense | 71 | 220 | 3 | 4 |
The following transcripts of ENSDARG00000068130 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 31309105)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29070462 |
| GRCz11 | 5 | 29670615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCACCATTGCAGCAATTCAACTGACAGGAGCATCTTTTTACTCTTTCTG[G/T]AAATTATTTCTGATCTTGAAGGTGTTTTAAAACAACTGGAGTCCTCAGTG
Long Flanking Sequence:
CAGTTTTATAAAGTCATACAGTTCCCACGGCACCCAGTAAAGCTGTGATTATTAAAAAATGGGAGTAATCAAAGCGAACTGTTGTTAATTGTAAGAATGGCATGTTAATATTTTAAGCATAATTTATTGTCATGTTAACCTGGTGGAAATTAAACTGCTAATATTTTCAAGTAGCAACCCACTATTTTATTGTTGGTTGCAGTAACTATGCATACTTTTGAAGACACTGAAATTTTATTCATTAGTTCATTTTTGAATTTGTAAAGAATTAATTATTAAAATGTTTTTAATTTTTTTAAAACAAATCTTACAGCAAACTTGTGTAATTATAATCGGTAGTGTATATATTATTGGTTCAATACTGTTAAATAATATGTATTGCATGTATCAATAATGTAAAATTTAAACAAATAGAAAACATTGTTTTTCCGCAGGTCCAAAAGTACATGAATCACCATTGCAGCAATTCAACTGACAGGAGCATCTTTTTACTCTTTCTG[G/T]AAATTATTTCTGATCTTGAAGGTGTTTTAAAACAACTGGAGTCCTCAGTGTCCAGCAGAAACACTTCATGTGAGGGATTGGAGACCTGCAAAGAGCTCCTGAACCCCAGCAGCAACATCAGTCAGCAAAGGGCACAGTTAAGTAACAGTAAAATTACACTACTTCTTACATAAATATAAACAATTGCTGTCTGAATGATTAACCTTCGGAATTTAACCCACTTTAAGGATGCGGGAGTCTCATTAAATAAAATCAGATGGTAACATAATGCTCAAGGCTCCCAAGAATCATTGCTTATTATTTGACTTAATCCCCTTTCTTTACAGCTATCCACACAATGTGATCAACCGGCTGAGCTGTGATGAAGCAAGAAATTTCTATGGTGGGATTGTGAGCATTATTCCACTGACTTTGGACCTTCTCGCTGCCTACATCAGAGGAAGTGCAAAACGTCTAAGTTCAGCATCTACAGTAACACCTAATCAAACGTTGACAAAGAA
Associated Phenotype:
Not determined