ZMP
zgc:92765
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC436832 [Source:RefSeq peptide;Acc:NP_001002559]
Human Orthologue:
C2orf18
Human Description:
chromosome 2 open reading frame 18 [Source:HGNC Symbol;Acc:26055]
Mouse Orthologue:
4930471M23Rik
Mouse Description:
RIKEN cDNA 4930471M23 gene Gene [Source:MGI Symbol;Acc:MGI:1922169]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12824 | Essential Splice Site | Available for shipment | Available now |
| sa39279 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12824
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016864 | Essential Splice Site | 217 | 374 | 5 | 6 |
| ENSDART00000016864 | Essential Splice Site | 217 | 374 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 25937056)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 26008359 |
| GRCz11 | 20 | 25907449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTTTACAAGCATAATGTGCATCCACTCAAGGCTGTTGGGACTGAAGG[T/A]AAAGTTTTAGAATTATTCATTTTCACATAAAGCCACTGACTAATTTGATC
Long Flanking Sequence:
TGTTTTTTTCTGTCTCTAGCACTTAACATGACCAGCGCTTCCAGTTTCCAGATGTTGCGAGGAGCTGTGATCATCTTCACTGGACTGCTATCTGTAGCATTTTTAGGACGCCGGCTGAAACCTAGCCAGTGGTTTGGGATACTAATCACCATTCTTGGTCTGGTGGTGGTTGGACTGGCTGACTTTGTAAGCGGCCATGGTGACGACTCCCATAAACTTAGTGAAATTATCACAGGTAACTGGTGTTGCTTAAAATATGTAGTCATAAAGAATGATGCAATTTGTCTACACATTCTCACATGAGGATGTTTTTCTTCTAATCGATAGCACTCTGCATCTTTATCTGTTTGGAATGTTGCACTGATTACCTATTGATCTTGTCTGCTAGGAGACCTTTTGATCATCATGGCTCAGATCATTGTTGCTGTTCAGATGGTCTTGGAGGAGAAGTTTGTTTACAAGCATAATGTGCATCCACTCAAGGCTGTTGGGACTGAAGG[T/A]AAAGTTTTAGAATTATTCATTTTCACATAAAGCCACTGACTAATTTGATCAAAGTATATGGATAGCTTCAGTCATGAAAACACAAATGAGTGATTTGCAACATGTTTCACTCTTTTTTTTCTTCTATAGGGTTTTCGTATTGTGGGTAAAATAGGTTATGTGGTAAACTACATGCTTTTACAAACTGTACAGATACCATAAATATTCTTATGCAGCAAATTATCAAAAATCTATGTGTTTTAAAATTAATGCAAATGTATGTTTTCAGTATGGATGTGTGTAGTTAACATCATGGAGCAAAACATTAAAGAATCATCAAGTTTATTTACCAGGTTTGAAGAAGTTTTGGAAAACAGTAAAGCAGACTTTCTGGTTTTATCTTCATAGCTTAATTGGTGCTACCTAATAATAATTTATAATAAGTTGTAAAACATAAAGACTATTGTTCAAATGTTAGAAATTTAATAAAATAAAAATAGAAGAAGTTCATCAGGGCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39279
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 |
|---|---|---|---|---|---|
| ENSDART00000016864 | Essential Splice Site | 217 | 374 | 5 | 6 |
| ENSDART00000016864 | Essential Splice Site | 217 | 374 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 25937056)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 26008359 |
| GRCz11 | 20 | 25907449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTTACAAGCATAATGTGCATCCACTCAAGGCTGTTGGGACTGAAGG[T/C]AAAGTTTTAGAATTATTCATTTTCACATAAAGCCACTGACTAATTTGATC
Long Flanking Sequence:
TGTTTTTTTCTGTCTCTAGCACTTAACATGACCAGCGCTTCCAGTTTCCAGATGTTGCGAGGAGCTGTGATCATCTTCACTGGACTGCTATCTGTAGCATTTTTAGGACGCCGGCTGAAACCTAGCCAGTGGTTTGGGATACTAATCACCATTCTTGGTCTGGTGGTGGTTGGACTGGCTGACTTTGTAAGCGGCCATGGTGACGACTCCCATAAACTTAGTGAAATTATCACAGGTAACTGGTGTTGCTTAAAATATGTAGTCATAAAGAATGATGCAATTTGTCTACACATTCTCACATGAGGATGTTTTTCTTCTAATCGATAGCACTCTGCATCTTTATCTGTTTGGAATGTTGCACTGATTACCTATTGATCTTGTCTGCTAGGAGACCTTTTGATCATCATGGCTCAGATCATTGTTGCTGTTCAGATGGTCTTGGAGGAGAAGTTTGTTTACAAGCATAATGTGCATCCACTCAAGGCTGTTGGGACTGAAGG[T/C]AAAGTTTTAGAATTATTCATTTTCACATAAAGCCACTGACTAATTTGATCAAAGTATATGGATAGCTTCAGTCATGAAAACACAAATGAGTGATTTGCAACATGTTTCACTCTTTTTTTTCTTCTATAGGGTTTTCGTATTGTGGGTAAAATAGGTTATGTGGTAAACTACATGCTTTTACAAACTGTACAGATACCATAAATATTCTTATGCAGCAAATTATCAAAAATCTATGTGTTTTAAAATTAATGCAAATGTATGTTTTCAGTATGGATGTGTGTAGTTAACATCATGGAGCAAAACATTAAAGAATCATCAAGTTTATTTACCAGGTTTGAAGAAGTTTTGGAAAACAGTAAAGCAGACTTTCTGGTTTTATCTTCATAGCTTAATTGGTGCTACCTAATAATAATTTATAATAAGTTGTAAAACATAAAGACTATTGTTCAAATGTTAGAAATTTAATAAAATAAAAATAGAAGAAGTTCATCAGGGCTGCA
Associated Phenotype:
Not determined