ZMP
zgc:113159
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC503773 [Source:RefSeq peptide;Acc:NP_001013369]
Human Orthologue:
C16orf7
Human Description:
chromosome 16 open reading frame 7 [Source:HGNC Symbol;Acc:13526]
Mouse Orthologue:
1300018I17Rik
Mouse Description:
RIKEN cDNA 1300018I17 gene Gene [Source:MGI Symbol;Acc:MGI:1914143]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36596 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36596
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 |
|---|---|---|---|---|---|
| ENSDART00000019809 | Essential Splice Site | 112 | 493 | 5 | 12 |
| ENSDART00000090846 | Essential Splice Site | 243 | 598 | 9 | 17 |
| ENSDART00000133834 | Essential Splice Site | 304 | 659 | 9 | 17 |
| ENSDART00000138995 | Essential Splice Site | 121 | 232 | 5 | 7 |
| ENSDART00000147351 | Essential Splice Site | 121 | 502 | 5 | 12 |
The following transcripts of ENSDARG00000019195 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 14234953)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 14680371 |
| GRCz11 | 18 | 14648883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCAAATGATCCTGCACTGGTTTCCGGTCTTATCGCCTGCCTTCTCAG[G/A]TAATTTCATAGTGTTAGATAAATTGTTAGAAGGTAATAAATTTATTCAAT
Long Flanking Sequence:
TGTTTAAAATGTTCTGAAAGACACCTTTTCTTAGCAAATCTGTAATTATTTGATTCAAAAATACATTATATTATAACATTATAGCTATATATTTTAAATATAAAATATATGCAATTTTATTGTCAAATATAATTGCAATTTTAAATAAGTTTCCAATCATTTTTATATATTTTAAAATTATTTTGTGGCAGTAAACTAATATTTGTTGCAGAAGAAACATTTTTACAGCTCAACACTCAGGCATATACATTTTTTGTGGAAACATTTTTATTTTAAATCTAAAGAACAACATTAATTTGAAATGTAAATATTTAGCAACTACAGTTTTTATACGCATGATATGTTTACTGCATCTTTTCTGAATGAAAACCAATGTGTACATTTCCTCTAATTATTTAAACAATTTAATCTCAGGAGTGGCCAAAAATTTGGAAAGCCAAGCTTAAAAAGTCTCCAAATGATCCTGCACTGGTTTCCGGTCTTATCGCCTGCCTTCTCAG[G/A]TAATTTCATAGTGTTAGATAAATTGTTAGAAGGTAATAAATTTATTCAATGACTTAAACCATCTGTTTCCATCCATTTTACAATCCCAGCTATCCAGATCACCCAGTCATGAAGTTGCTGAAGAGGCTTCAGTATCGGGTATATAACAGACTGTATCCTATAGTGAGCCAGTGCTCTCCTCTAAACACAACATCTGGTCACTCTCTATCCTTAAAGCCTTCCCGAAGTGCCCATAGCCTCCTCCTCTCAGACTGTCCCATCTCTCCACATCATCAGCAGAGCCCCTTCAAATCAGCCCTGACACACAGCTTATCGGATGCCTCCATCTCCCTTTCCCCATCCCGTGATCTCAACGCCAACGACACCAAGTCTGAGGCCGACCCTGACGATTCCTCAAGTCTCCTCACCACGGACAGAGAAAACTCTTTTGAGGATCTGGAGAAGTTTCTAACTCAGCTGGACTGGGTTCCTTCTCACAGTGGTGATGATGATGATACAGA
Associated Phenotype:
Not determined