ZMP
exoc4
Ensembl ID:
ZFIN ID:
Description:
exocyst complex component 4 [Source:RefSeq peptide;Acc:NP_001025305]
Human Orthologue:
EXOC4
Human Description:
exocyst complex component 4 [Source:HGNC Symbol;Acc:30389]
Mouse Orthologue:
Exoc4
Mouse Description:
exocyst complex component 4 Gene [Source:MGI Symbol;Acc:MGI:1096376]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa312 | Nonsense | F2 line generated | Not yet available |
| sa8527 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa312
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000021384 | Nonsense | 92 | 968 | 3 | 18 |
| ENSDART00000101619 | Nonsense | 92 | 487 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 4 (position 14678787)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 15614640 |
| GRCz11 | 4 | 15613395 |
KASP Assay ID:
554-3181.1 (used for ordering genotyping assays)
KASP Sequence:
TCAAGTGTGAACTTTCACCTTTTCCTCACGTGGGTTTCTCTGCTCAGGTC[A/T]AGGAGAACCTGCTGTCCTGTAAGATGCTCCTCCACTGTAAGCGGGATGAA
Long Flanking Sequence:
CAAGGACTCTAATAAAAGCGCTTCCCTTTGTGTCTCAATTTGCATGTGTGTGAGCTTGAGAGGGAAAATGGAAGACATAAAGCCAACACAGCCAATGGAACGCAACAATGTTCATTAATTTTGCTGTTTGTTTATCCAGCTTTGGGATTTGCTCACGTTTTGTAAGCTCTTTTATGAACACTAAAAAATGAACTAATTACCGCTTCCCCTGCCACCTAAAACGGGGCTGCGAAACATGGTGAGCCATCATAAAAGCAACATTAGGAATCACTAGTAATTGTCTTCGATGTCTGAAATAATATCCTTGTAAATTAGCCGCTAAGCTTGGGTTTTAATCTACGGCAAAATGTTTGTTTATCATCTTCTCCCCTGCTGCTGACACGCTTGAAAATAATTATGCAGAGAATAAAGCGCTGGGAAAGGAGAAGGGAATACACGATGCTCGTTTCATCAAGTGTGAACTTTCACCTTTTCCTCACGTGGGTTTCTCTGCTCAGGTC[A/T]AGGAGAACCTGCTGTCCTGTAAGATGCTCCTCCACTGTAAGCGGGATGAACTGAGGAAGCTGTGGATTGAGGGTGTCGAGCACAAGCATGTCCTTAGCCTGTTGGATGAGATCGAAAACATCAAACAGGTGCCTCAGAAATTGGAGGCGTCCATGGCCAGCAAGCATTACCTGCATGCGACGGATATGCTGGTAAGTGAATGTTCCAGTGTGTTAGTAGGGGACGTTTGATTGCATGGTTAGGTGCATGACACCTTTTTTCAGCTTGTCTCTGATATATTTTTAAAAATATTTAAAGTCTTTACCGTGAGCTTTGTTATATTGTGATGTTTCTCGAAATTACTTTCTCTATAATATTAGGGTGTTTTGAGTTATTTTATTTAACAGACCGGCACAAATATGCAAACAAAGAGTTTCTGAGTTCTCTCAGTCTGCTCTCATGTAATCCTGGAACACATTCAGTGCTGGGAATACATTGTAAAAGCATGCCCTGCTTATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8527
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 |
|---|---|---|---|---|---|
| ENSDART00000021384 | Essential Splice Site | 777 | 968 | 15 | 18 |
| ENSDART00000101619 | None | None | 487 | None | 10 |
Genomic Location (Zv9):
Chromosome 4 (position 14860593)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 15796446 |
| GRCz11 | 4 | 15795201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCAAGACAKCRCTGACCGCTGCCTGCTGGTGCTGCATCTGGAGGTTAG[G/A]TAGGTCTGACCACTTCATCTAAATCCRAGAAGAWGCCAGATGCATGTATT
Long Flanking Sequence:
GTCATCCTCTGGCTGTGTGTCTCATTGAATAGGCTGTAAAATATGCTAAATAAAGATTATTAGAGTACATTTACAAGTTTTTTTAGTTAAAATGCAATGTTTATTTCTGATGTTTCTTGCTGTTTGTTTATAAAATGACCTAGCAAGTTTTAATAGTTAGCAAGTTTATGCTATGCATTCATGAATTATGCAAGCTGGATCTATTCTACGTGGCCAAAAGTAAAAACAAAATCTATAATATAGTCAATTGTTAAATTTCATAAGAAATTCAGGAAGCTATTCTACTTGTTGTCAGTATATTGGCTATAAATCTGTTTTTCAGGTTTTTTTTATGGCTCTTATTTGGTCTTTTGTGTAGGTGTATCCCCAGGCTCAGATGCACAGGTGAACAGTGAGAGCGTTCGCAGCCGAGAGCAGATTCTCCAGACGTTGACTGACCTCTCCAGATCATTTCAAGACATCGCTGACCGCTGCCTGCTGGTGCTGCATCTGGAGGTTAG[G/A]TAGGTCTGACCACTTCATCTAAATCCGAGAAGATGCCAGATGCATGTATTAAAGGGATCGTTCCCCCAAAAAATGATTGCCGAGGCTCTTGCTCTTACAGCCTTCTTGCTGTGAGGCAACAGTGCCGCAGTTTATTTCATGTAAAGTTTTATTTTTCTTATAATGTGTGTGCTTTAATAGTAAGTTGGATTGAACATTTTTTCCAGTTAATTTCTTTTGTTCAGTCCGTCAAAGTCAGTCATGAGTGAAACGAGCAGAGAGCTGCTATATGAGAAACTAAAGTTATAATTCTAATATGCTACAATATTCGTTTTGCTATGACTAGATACTTTCTTAAAGCTACATTCTACTTTTTGAGAGTAAAACAGTTAAGTTTTGCCTTTTTTCCCATTCAAATGATCTCTGGGTCTGACAGGATGACTTTTAGTTTAGCTTAGCTTAGCATAGATCATGCTACCATAAACGGAAACACTTTATTTTGATGGTGCATTTGAGTATTA
Associated Phenotype:
Not determined