ZMP
si:ch211-149l1.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JM07]
Human Orthologue:
C2orf55
Human Description:
chromosome 2 open reading frame 55 [Source:HGNC Symbol;Acc:33454]
Mouse Orthologue:
2010300C02Rik
Mouse Description:
RIKEN cDNA 2010300C02 gene Gene [Source:MGI Symbol;Acc:MGI:1919347]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38293 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19581 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38293
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 |
|---|---|---|---|---|---|
| ENSDART00000108523 | Essential Splice Site | 166 | 832 | 4 | 10 |
| ENSDART00000136747 | None | None | 134 | None | 5 |
| ENSDART00000140824 | Essential Splice Site | 166 | 775 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 50194880)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49044061 |
| GRCz11 | 1 | 49688481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCGGAAACCTACTTGTATGAGCGAGTGATGCATGGAGGCATTTACAAG[G/A]TTGCAGACTTTAACTTTGACCATTTGATTTGATTTGAGTTTAAACAAATA
Long Flanking Sequence:
TTTGGAAAATATTTGAAAAAGAAAAAAAATGAACAGGAGGGTGATTAATTGTGACTGTATGTAATATATTTGAATAGCAAATAGATTAATACAACTCACTGAATCTGATCTGCAGGTATCCACAGGGTCTGAGCCCCAGAGCGCTGTCTCATGATAGCATCTTCTTCACGGATCAAACCCAGAGCACAGAACCCACACGAGTGCTTTCACAAGAGAACGTTCACGGCAAAATTAAAGCCTTACAAGTAAGTAAATGTTCTTTGTCAGCGTATTTTTTGGATCTACTCTTTAAGCAAAGTGTGCATCAGATACAAGCTGTTTATATTTCGTTTTGGCAGCTAAAACTACAACAGCAGAACTTACATCTGGGTCCTCCTCCAATGCTGATTCCTGGAAAGCGCACAGAGGACTCGGGAGCCACTTCAGAGGATGATGGTTTACCTTGCAGCCCACCGGAAACCTACTTGTATGAGCGAGTGATGCATGGAGGCATTTACAAG[G/A]TTGCAGACTTTAACTTTGACCATTTGATTTGATTTGAGTTTAAACAAATAAATCATACACTTAAACAATTCTTTAAGCAAAATACATTTCATCATGGTCAAAATGGAGCGAAATGAAGCATAAACCTATTATTTTCCCCACCCCATTTCCAAACACATGCTTTTTCTGAAATGTAGCCCTATATACATTTCTGGAGATTGCGAATTATGTACCCAGAAGTAAGTATGGCTACATTTTATCTTTAAAACAAACGCTACAGGGTGGTATGATGCCATTCCTTTTTCGCGCTAGCAGCTTTCCGCTTACCACCGTATGGACGGCTTTCCCGCTGTTACCAGTTTGTCTAGTAGCTCGGTATGTGAAGTACGGACTGTACATGAGAGGAGAGGAGTTGACCATAACAACGGCAGGGCTTAATTTGTGTCGGAACAAGGATATGGATCCGGCACCTCTGAAATCTGATCCGGCACCTCATTTTACCGATCCCCCTCTAGACACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19581
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:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108523 | Splice Site, Nonsense | 745 | 832 | 9 | 10 |
| ENSDART00000136747 | None | None | 134 | None | 5 |
| ENSDART00000140824 | Splice Site, Nonsense | 745 | 775 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 1 (position 50204416)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49053597 |
| GRCz11 | 1 | 49698017 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTAAGCTTTGATCCAAAAATATACATTAAAAGGAAATGTATTCTGTTAG[C/T]AGGACAACAGTAGGAACAATACCACCGAAGATGACACGACAAAGAGAACA
Long Flanking Sequence:
CAGGATGTACACTGAAAGAAATAATCCTTAGACAACAAAATGTACAGATGCATAATAACAAATATAATAAAATATAATAATAAATCATTCATTCATTTTCTTTTCGCCTTAGTACCTTTATTAATCTAGGGTCACCACAGCGGAATGAACCACCAAATTATCCAGCATGTTTTATGCAGCGGATGTCCTTCCAGCTGCAACCCATCACTGGGAAACACCCATACACTCTCATTCACACATATACACTACGGATAATTTACCTTTCCCAATTCAACTAAAGCTAGTGTTTGAGCTGTGGGGAGCACCCGGAGGAAACCCACACCAACACAGGGAGAACATCCAAACTCCATACAGAAATACCCACTGGTACAGCTAAGACTCGAACCAGCGACCTTCTTGCTGTGAGGCAACAGTGCTAACCACTGAGCCACCGTGCTGCACTAAACAACATCTAAGCTTTGATCCAAAAATATACATTAAAAGGAAATGTATTCTGTTAG[C/T]AGGACAACAGTAGGAACAATACCACCGAAGATGACACGACAAAGAGAACAGCGACTATTAGTAAGATGGATTTCAATGCAAGACCTGTTCCACCTAACAGCAACACCGAAGGTAAACACCGCTTTAACTGTTATGTGTTAATGTTAGTGGTGTTGATATTAATGTGTGTGCATGTATTTTCCTACAATAGCTCTTACCATCACATCTGATCCTCCTCCAGCAACGTCATCATCGTCATCATCATCACCTTCATCTCCAGCAGATGCCGTTGGAGCTCAGCCGTCCTGGATGGAGCTCGCCAAGAGAAAGTCTTTAGCGTGGAGCGACAAAAAAACTCTAGAATGAAGAAGAGATAAACAGTTGGAGACTGATGAAGTTGTGCAATACTAATGTTACAGGGAATGAATGAAGGAATGTGTGTGTGAACATGACTGAGTGTGTGTGTGATTGAGTTACACAGTTTATCACTAATAGAGTTTTTTAATTCTTATTTTTGTGTG
Associated Phenotype:
Not determined