ZMP
exoc2
Ensembl ID:
ZFIN ID:
Description:
exocyst complex component 2 [Source:RefSeq peptide;Acc:NP_956898]
Human Orthologue:
EXOC2
Human Description:
exocyst complex component 2 [Source:HGNC Symbol;Acc:24968]
Mouse Orthologue:
Exoc2
Mouse Description:
exocyst complex component 2 Gene [Source:MGI Symbol;Acc:MGI:1913732]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37041 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37041
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077962 | Nonsense | 880 | 918 | 27 | 28 |
| ENSDART00000134337 | None | None | 266 | None | 10 |
The following transcripts of ENSDARG00000055610 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 26603071)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 26674374 |
| GRCz11 | 20 | 26573464 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTTGTGTCTCAGCACTAGTTTTAAGCAGGCATTGGAAGCGCTTCCA[C/T]AGCTACAGAGTGGAGCTGACAAAAAGTAAGTTACACTTCAGTATAGTTAC
Long Flanking Sequence:
AAATACATTTTTAATTTTAAAATACTCTATTATGTAACTAATTCTTCATTTATTTGTAGCATAGGTCAACATAGATTTTCTGTATTCTTCTGTTTTTGCCCAGGTTTTCACAGTTTCCAAGGAGCTGGTTTCTCGTGTTCTTTCAAAGATCATCGAGGCTGTAGCAGAAGAAATGAGTCGCCTCATGCAGTGTGTGTCTTCTTTTAGTAAAAATGGTGCCTTGCAGGTATGGTAGCATCCTTCACATACACAATAAGCATTTGATCTGAAAATACTAAAATTGACATTACCCTTTTTATATTACTCTCTCGAGGCGCGTCTGGAGATCTGTGCTTTGCGAGATGCTATAGAGCCCTATCTCTCATCAGAGAGCTGGTAAGACATGCGACTGCAATGAGAAATTTAAACAGAAAAGGTGAAAACTGTTAGTATGTTAATGCTCATGATCTTTTCATTTGTGTCTCAGCACTAGTTTTAAGCAGGCATTGGAAGCGCTTCCA[C/T]AGCTACAGAGTGGAGCTGACAAAAAGTAAGTTACACTTCAGTATAGTTACAAACATGACTGAAACCTTGACACTGATAACACAAAACTATTTAATATTTAATACTAACTGCTATTAGAGATTATTAGAAATGGGGATGATGATTATTAAAACCATTTAATTGTGATAATTTAGGAATGACTTTATTATGCAGATTGGTGCTCTAGAAATCAAAAGTTGAAAATGGTTTTGCTGCTTATTTTTTCTGGAAATTCTCTGATTAAATGTTACTGTATCTTTTGATCAATAAGAGAGTTTACAAGTACAGCATTTGACGTTTTTTTAAACATTATAACCATTATTACTATCAATTTAATGTGTTTTTTCTGAACTCAATCCTCGTGACCTCAAAATTTCAAGTGGTTATGTTTATTTTTAAATAATAACATTTGTGGAGGGGTAGTGAAAATGCAAGGGCAAGTTAAAATGATAACTGTCAGGTTGGCTGGGCCAACACATCTT
Associated Phenotype:
Not determined