ZMP
zgc:91940
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized protein C17orf62 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6DGA7]
Human Orthologue:
C17orf62
Human Description:
chromosome 17 open reading frame 62 [Source:HGNC Symbol;Acc:28672]
Mouse Orthologue:
BC017643
Mouse Description:
cDNA sequence BC017643 Gene [Source:MGI Symbol;Acc:MGI:2384959]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30962 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42069 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30962
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 |
|---|---|---|---|---|---|
| ENSDART00000105562 | Essential Splice Site | 101 | 206 | 5 | 7 |
| ENSDART00000105562 | Essential Splice Site | 101 | 206 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 34951545)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 33355654 |
| GRCz11 | 12 | 33456637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTCTATACCATGTTGTTGACTCTGTGGAAAAGAGGGCACGAGAAAGG[T/C]GAGTTCAGCCTTAGCTGTCATCATTTGTATTTTTTCTTTTGTGAATTATA
Long Flanking Sequence:
GAAAGATACTTAAAAAATGTTAGAAACCTGTAACCATTGACTTCCATAGTTTTTGTTTTCTACTATAGAAATCAATGGTTAAGGGTTTTCAGCGTTTTTCTAAATAAAGTCGTTGTTGTTCAACAGAAGAAACTCAAAGATTTGCAACCACTCCAGAATGTTTATTTTTAGGTGAACGATCCCTTTTAGCGTATAAACTGTGTAAAGTCTCATTTGACCATCATTCCTGATAGAAGTAAACTTACATTTCTATTCTATTCTAGACAACATCTACATTCCTAAATGCATTGAGCTGCTGCCATGTGATTGGCTGATTATTTATGTAGAACATGTGTACTTAAATTGGCCAGCGAGTGTATGTTCAACTGTCATAACTAAAAATCTGGGTGGCTTTGCTCGTAGGAGGCAGTGTTTAATAAATCCAAGAACGAGATTGAACTGAAGACCTTCAGTCTCTATACCATGTTGTTGACTCTGTGGAAAAGAGGGCACGAGAAAGG[T/C]GAGTTCAGCCTTAGCTGTCATCATTTGTATTTTTTCTTTTGTGAATTATATCTGAGGCAAAGCGTTTGTTTTCTCCGGCTCAGTGCTGTTAGATCTGCGGCACCTGCGGGACGTCAGTGTTCAGGAGGAGAGAGTGAGGTATCTTGGAAAGGGTTACCTGGTAGTGCTGCGATTGGCTACGGGCTTCTCTTACCCGCTTACACAAAGTGCCACACTTGGGTCACGCAGGTATGAAAAGTAGTTCCTTTCAGAGTCCTATGATACGGTTAAAAAAACAACAACAAAAAAAACCCCCAGTAATTTATTCAGTAATAAAGTGTGTATATTTCAAACTACCAATAAGAGGTTGAGCTACTAATGTTTTTAATAATTAGTAATTAATATTTAAAAGATATTAGTAACTCCAAATCTCTTATTGGTTAGATATATGTATTTTAGTTACTAATAAAAGATTTGGATGTACTAATATTTTTATTAATTAGTTTCTATGTTTTTAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42069
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 |
|---|---|---|---|---|---|
| ENSDART00000105562 | Essential Splice Site | 101 | 206 | 5 | 7 |
| ENSDART00000105562 | Essential Splice Site | 101 | 206 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 34951545)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 33355654 |
| GRCz11 | 12 | 33456637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTCTATACCATGTTGTTGACTCTGTGGAAAAGAGGGCACGAGAAAGG[T/C]GAGTTCAGCCTTAGCTGTCATCATTTGTATTTTTTCTTTTGTGAATTATA
Long Flanking Sequence:
GAAAGATACTTAAAAAATGTTAGAAACCTGTAACCATTGACTTCCATAGTTTTTGTTTTCTACTATAGAAATCAATGGTTAAGGGTTTTCAGCGTTTTTCTAAATAAAGTCGTTGTTGTTCAACAGAAGAAACTCAAAGATTTGCAACCACTCCAGAATGTTTATTTTTAGGTGAACGATCCCTTTTAGCGTATAAACTGTGTAAAGTCTCATTTGACCATCATTCCTGATAGAAGTAAACTTACATTTCTATTCTATTCTAGACAACATCTACATTCCTAAATGCATTGAGCTGCTGCCATGTGATTGGCTGATTATTTATGTAGAACATGTGTACTTAAATTGGCCAGCGAGTGTATGTTCAACTGTCATAACTAAAAATCTGGGTGGCTTTGCTCGTAGGAGGCAGTGTTTAATAAATCCAAGAACGAGATTGAACTGAAGACCTTCAGTCTCTATACCATGTTGTTGACTCTGTGGAAAAGAGGGCACGAGAAAGG[T/C]GAGTTCAGCCTTAGCTGTCATCATTTGTATTTTTTCTTTTGTGAATTATATCTGAGGCAAAGCGTTTGTTTTCTCCGGCTCAGTGCTGTTAGATCTGCGGCACCTGCGGGACGTCAGTGTTCAGGAGGAGAGAGTGAGGTATCTTGGAAAGGGTTACCTGGTAGTGCTGCGATTGGCTACGGGCTTCTCTTACCCGCTTACACAAAGTGCCACACTTGGGTCACGCAGGTATGAAAAGTAGTTCCTTTCAGAGTCCTATGATACGGTTAAAAAAACAACAACAAAAAAAACCCCCAGTAATTTATTCAGTAATAAAGTGTGTATATTTCAAACTACCAATAAGAGGTTGAGCTACTAATGTTTTTAATAATTAGTAATTAATATTTAAAAGATATTAGTAACTCCAAATCTCTTATTGGTTAGATATATGTATTTTAGTTACTAATAAAAGATTTGGATGTACTAATATTTTTATTAATTAGTTTCTATGTTTTTAAATG
Associated Phenotype:
Not determined