ZMP
zgc:171819
Ensembl ID:
ZFIN ID:
Description:
Zgc:171819 protein [Source:UniProtKB/TrEMBL;Acc:A8KB83]
Human Orthologue:
C2orf3
Human Description:
chromosome 2 open reading frame 3 [Source:HGNC Symbol;Acc:1317]
Mouse Orthologue:
AW146020
Mouse Description:
expressed sequence AW146020 Gene [Source:MGI Symbol;Acc:MGI:2141656]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18029 | Essential Splice Site | Available for shipment | Available now |
| sa31013 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18029
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 |
|---|---|---|---|---|---|
| ENSDART00000112559 | None | None | 347 | None | 10 |
| ENSDART00000123399 | Essential Splice Site | 274 | 824 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 17 (position 32741843)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 32583574 |
| GRCz11 | 17 | 32536085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTGCACCCAAACCCAAAACTCTGAGAGAGASAATGGCTGAGAAGATGG[G/A]TGAGAAACGWGCACTATTTGTTTATGATAGAACATTCAAATTGGTTGAGA
Long Flanking Sequence:
GAACATAATGTATACTATGAGAAAATCAAATAAATAATGAACTTTGATGGATGTAAAGTAGCAGTAGGAAACCTCCCAAACAAAATTTGGAACATTTAAAATGTTAAATTGTCACTTTACAGGTTTTTTGTTGTTTTTTTTTGCTGTTGAAAAATGAAAAAACATCACAAGGTCCCTCAAGTCTCTGAAAATTCGGTTATTTCTTATGTTGTTTGTGTTACATTGTTGCTTAAATGTAAATGCACTTGTTTCCTTTATTGTTTGTCCAGTCATCATTCCTGATGCCAGAAAGATTCATGCTGCCAAAGAGAAAAGGAGACAAGCCAGAGCCCAGCAAGATTACATCTCTCTGGATTCACCTCGAACTCCTGGAAGCTTGAAGGAGGACGAGCTGAGCGATAAGGAACAAGACAGTGACAATGATCTGGATGATCATGAGCGCAGAATTGAGTTTGCACCCAAACCCAAAACTCTGAGAGAGAGAATGGCTGAGAAGATGG[G/A]TGAGAAACGTGCACTATTTGTTTATGATAGAACATTCAAATTGGTTGAGATATACAAAACATTTGCTGTGTTTGTCTTCTGTAGGGAGTGATAGTGAGGAGAGCTTTTCTGACAGCCAGGAGGAGGAAGAGCAGCAGATGTGGGAGGAACAACAGATTGGAAAAGGAGTCAAAAGGCACCAAGTGAGACCTTCTTATTGTGACACTTGATAACATTCAGTATTCAATATCTCGATATTTACTATCTTCTTATTACGCTTTGGTTTTATAGTGTTTCAAAGACCTTTCCTTATATTCCCAGAAGGAATGGCATGCTCCGAAAGCAGCCCGACAGAAGAGAGTGGAAATCCCAGAAACGCTTCCAGTAGTTAGTATTGGTGTCATTAAGAAGAGAATCACTGGAAAGTAAGTTGTAAAATATGGATTTGTTTTATAAGCCCCAAATGCTTTTGACCTCTTTTCACTTCCATTAGTGTGTAGTATGATAAAAGTCTGTAGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31013
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112559 | None | None | 347 | None | 10 |
| ENSDART00000123399 | Nonsense | 393 | 824 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 17 (position 32744190)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 32585921 |
| GRCz11 | 17 | 32538432 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAATGCAGATGAGCAGCTCCGATTTTACCGCACCATGAACGTTTTCT[C/A]ACAGAACCTGCTGGAATGCCTATCTGAGAAGGTAATCTTTGTCATTCAGT
Long Flanking Sequence:
TAGTTTGTATGAAAAAGAAATACAAAATGAAAATACCAAACAATACCAAACAATTGGTTACTGTGCAGCAATAAATAACGCTTTAAAGTGTGAGAAGTTTACATAAGATTTTTCTAAACTAGTAGAGTTTGGAAACTAATGAATGTATATTAATCGATATCACCATTAAACCATGATTATTCCTCAGACTATAATTGTACAACCAAAATCTATATCAGTTGCCTCCCTATAGTAAATGCATACTTATCGTAAAAAAACTAACTGCACAACCAACCTCAGACCTTTGTATGGTATTGTGAAGTCATAAATACAAATAAGGCATTAAAAAAATCAACCGATTTACTCCAGATTGGATTCGCTGAGGGAGGTACACAGGGCACGGGAGGCGCAGCTAAGGAGGATGCAGCTGGATGTGGAAATGGCCAAAACCTCTTTAGAGGGCCTTGAAAACAACAATGCAGATGAGCAGCTCCGATTTTACCGCACCATGAACGTTTTCT[C/A]ACAGAACCTGCTGGAATGCCTATCTGAGAAGGTAATCTTTGTCATTCAGTGTAGTTCTATAAAGATCCTCCATATGATATAATCCTCTAAAGTAGGTTTGTTTTATCTTTCAGATGGCTTTAATAAACTCAGTTGAGCTGGACATGCACGGTCTCTATATTGACCAGGCGGAGGCACTCTTGAGTCAGAGAAGAGAAGCATTACAAGAGGAGTCCTCTCGGATTCAGAAGTTAACTTGTAAGACTGCATCTGCATTCAGCCTTCTAGTTAGATAGATATAGTACAAATATTTTTCATTATCTTTTAAATCAGAACTCAAGAGACACCAGTTTAGTGTGACTTCCTTATTATAGTGCCTTGAGAGCCAACATACTGTTAAACTAATACTTATTATTCCTCCATATTCTTCTTATTAGACTATTTTAAAAACGCATCTCTTTCTAGACTGTTCATACTACAACCACAAAGCTAACTCCAAACCTCCAAACCATACTGAATTA
Associated Phenotype:
Not determined