ZMP
zgc:55794
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC327593 [Source:RefSeq peptide;Acc:NP_956128]
Human Orthologue:
C15orf44
Human Description:
chromosome 15 open reading frame 44 [Source:HGNC Symbol;Acc:25372]
Mouse Orthologue:
2010321M09Rik
Mouse Description:
RIKEN cDNA 2010321M09 gene Gene [Source:MGI Symbol;Acc:MGI:1917132]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa706 | Essential Splice Site | Available for shipment | Available now |
| sa36624 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa706
Status:
Available for shipment
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:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060731 | Essential Splice Site | None | 518 | 1 | 12 |
| ENSDART00000129776 | Essential Splice Site | None | 435 | 1 | 12 |
| ENSDART00000135800 | None | None | 518 | None | 11 |
The following transcripts of ENSDARG00000041429 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 18786543)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 19016766 |
| GRCz11 | 18 | 19005832 |
KASP Assay ID:
554-0614.1 (used for ordering genotyping assays)
KASP Sequence:
TTATTACGGTGCGCNNTTGGTGAAGAAGAAGAGAGGATTTGCAGAAATGG[G/A]TAAACATTTTAACGCTTTTTNNNAAACGAAGGTTGTTATGCTTACCTWCG
Long Flanking Sequence:
ACCTGAAGTCTTTTAAGAGGATTAGATGTACTCTCACCCCACACTCTCATTACTCCTCCAGCCATTTTAGCACAATTATTCTGATCATTTGCGTCTCATTCACAATTCCCAGAAATTGAACGTCGATGTAAAGTGGCTAGAAAAATACAAATCGAAGGCTAACAATTACTTCGAGAAAATAATTTCTCTTTTGTAATTATTGGTAATTATCTTTATGAACTATGGATTACAGATTAGTATTAAAATTGTAAATATATTTTTTATTCCCGGGGTGATATTAGGCTTATAGGTTTCAGGACATGCAATTTTTTACTCGTTTTCCATCTTTACACTTTTTAAAACAAACAAACACAAAGTGAGAGAGTGATAGTTTCACACAACTTTTTAGAATCTCTCTCGTTTCCGAGTAGGAACGGATTGGTAGGCTTCTTTTGTTCCCCACCGGTCTGCTTATTACGGTGCGCGCTTGGTGAAGAAGAAGAGAGGATTTGCAGAAATGG[G/A]TAAACATTTTAACGCTTTTTCATAAACGAAGGTTGTTATGCTTACCTACGCGTTGTATTAAAAATATCAAGAATTTATTGTATTTATACTTTTATGATCATTTAATGTTTTTCAGGGTGAACGTTTGGTCACTGACGTTTGGTCACTGATAATGTAACTCTCATTACATTACATATTTTGTTTTGGTTGCTCTACTACCTTTAAAAAAGTATTAAAATATATTTTAAAACGTTTTATATGTACCTAGCTGAGAAACCAGATTTAAACACCCTGAGATGATTTCTTGGCCTTTCAGTGGGTTGGTTTTGGAAACTATGAGCTGTAAACTCGGAGACCAGTTAATCAAACAACTAGAAAACTTCAAAGCCTCTTTCCTGTTTATTCGCATATTAAAGCACAAACGCGATTAATGTAGTATATTTCTACCATGCTCAAAAATTAAAGTTTACTCAACATTTACCCATCCTTAATTTTTTTCCCAACCTTTGAGCTTATTTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36624
Status:
Available for shipment
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:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060731 | Essential Splice Site | 110 | 518 | 3 | 12 |
| ENSDART00000129776 | Essential Splice Site | 110 | 435 | 3 | 12 |
| ENSDART00000135800 | Essential Splice Site | 110 | 518 | 2 | 11 |
The following transcripts of ENSDARG00000041429 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 18784541)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 19014764 |
| GRCz11 | 18 | 19003830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTAGTAATGTAGTACAGCAGGAGTGGGGATCTGCTTGTCCATGCCAG[G/A]TAAATCAACATACAAATATTATTTATGTAATATACATATACTATGTAAAA
Long Flanking Sequence:
AACCTGTGCTTTTGTTTTCCGCAGATATCTCCTATATTCATTCATAACTGTTCTTCAGCGTGTAAAGAGAACAGCTTGCAAACATGCCCACGGTGGTTCTTATGGACTCGTCGCTGTCCATGACGCGACCGGTGTCAGTGGAGGGCAGTGAAGAGTTTCAGAGGAAGAACCTGGCAGTTCATGGACTAACCATGCTGTTTGAGCACATGGCCACAAACTACAAGCTGGAGTTCACTTCACTTGTGGCCTTTTCCTCGCTTTGGGAGCTAATGGTGCCTTTCACTAGAGACTACAATACATTGCAGGTAAAATAAAAAGTGTGTGTCGTGTTGCATGAAAGAAAAATGTACATGCTATAGCTGAAACCTAAATCAAGATCTTATTTCTTCCAGGAAGCCTTGAATAACCTTGAAGACTATGATAAAACCTGCCTGGAAGGAGCTTTACAAGGTGTTAGTAATGTAGTACAGCAGGAGTGGGGATCTGCTTGTCCATGCCAG[G/A]TAAATCAACATACAAATATTATTTATGTAATATACATATACTATGTAAAACATGTATACGTGTGGTGTGTAATGTAGTTTTAATAAATAATTGCAACATCATTAGGTTGATTTAAAATGGCAATCTCTGTTACAATTGTTTTTATACAAACAAAAATCATGCACATATAGTATAAGAATCATTAGATTACATTAAAAAGGTAACAGTGCAGCTCCAAAATACTAATTTGATTTGTCAGTAATGTATAATTCAAACCAAGCTTTAATCCATATGTAAGAAAAACATTTCAATAATTTAGCATTCAATACAATTTAGTATGCTCACTTATTCTTTTAGGTGTTTTAATAAGTACACATCAGAATAAATATGTTTCATCTCTATATTCTGACATTTTTCACAGTAGTTATTTTTTTGGTAACACTAAAGTAGGCATTTTACTTCAACTTTGTATGCTTTGCATGAATATAAAATCAGTTTGGTACATTTAATTTGATGTGAAC
Associated Phenotype:
Not determined