ZMP
exoc5
Ensembl ID:
ZFIN ID:
Description:
exocyst complex component 5 [Source:RefSeq peptide;Acc:NP_001107268]
Human Orthologue:
EXOC5
Human Description:
exocyst complex component 5 [Source:HGNC Symbol;Acc:10696]
Mouse Orthologue:
Exoc5
Mouse Description:
exocyst complex component 5 Gene [Source:MGI Symbol;Acc:MGI:2145645]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42993 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23168 | Nonsense | Available for shipment | Available now |
sa42992 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42993
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 |
---|---|---|---|---|---|
ENSDART00000130198 | Nonsense | 90 | 708 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 44479551)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44319229 |
GRCz11 | 17 | 44432994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAGCCAAGGAGTTTGCTCACAAGGTTCAAGACCTTCAAAGGAGCAAC[C/T]AAGTCAGTCGTCTTTACATTTGTTTGCATTTGTTTATTTTTTAACCTGTC
Long Flanking Sequence:
TTTTCACCCATGTTCATTAGTTACAAAGCAAACCTAAATGTTATGTTTAAGCCAACTTGTAAGGCTTATGGGACATGTATGTAATAATAAATGATAGTGGTAATATTGCATTCATGTACTTTGTGTCTGTTGGCACACTTTTACGTTTTAGAATATAGAAGTGTTGTGACACATAATTAGGTTTTTGCTGCAAATATGACATTGTAAATGGACTTCAGGGGAAAAAACGTAATGCCACAAATTGAACTGTAGGTTCATATTTGCTTTAAAGTGTTTAAAGTAATATAAATGCTTGTTAAGTCAGAAATTGTCTTTTGCTGCCTGCAGCTCTTTAATGTCAAATCTTTTGTTCCAGGTTGCTGGAAGAGTTTGTGAACCACATTGAGGAACTAAAACTGCTGGATGAAAGGATCCAGAGGAAAGTGGAGAAGTTAGAACAGCAGTGCCACCGTGAAGCCAAGGAGTTTGCTCACAAGGTTCAAGACCTTCAAAGGAGCAAC[C/T]AAGTCAGTCGTCTTTACATTTGTTTGCATTTGTTTATTTTTTAACCTGTCAATAGGTGTTTGAGTAACTATGTGTTACGTTATCATGAATGACGTTAAGGCCTAATTCAGATTTATACCTCTACGCCTTCCCCTTGGCCCTTAAAATAGAATGTAAAAGGGTTGGGATGAAAATATTCCCCTAATGGTTCGTTTCCACTGAGTGGTACAGTATGGTATGGGACCAGTCATCTTAATTAGGCTTGCATATCCACTGCCAAAAGGGTACCAATACCAATTTGGTGGGTATGGTGTAAGACAGAAAGTTTCAATGTCATTCTCGCTCTAGGAGATTTCAAACTAAAGCTGTACGGGTCATTCACATATCATACAAGAAACACATCTCACAAAACAGATGCTTTATACAGATAAATACTTGTGTAGAAATGTTCATTACTTAACCTTAATATGAATATGATTTGATTATAACTGCATATCAATGATAAGGCAAAATAGCCTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23168
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130198 | Nonsense | 377 | 708 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 44469427)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44309105 |
GRCz11 | 17 | 44422870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCGGCATGATTCTTCAGCGCTATTATGATTCCAAGAACCACCAAAAA[C/T]GACCTGTAGGCACTGGAAGGTGAGGAATTGTTGGTTTCTTTGGTTTCTTT
Long Flanking Sequence:
ATTCCATTATGAAGAAATAGATTACCCATGCTTGAACTGTTATTTATCTGTTATTTAAATAACCCTATTAACATATTTCATAACTTCAGGCTCATGTGAAAGAAAGACTAGATGAGACGCGCAACTCTGATGTGGAGCAATACCTCAAGAACCTCTATGACCTCTACACAAGGTATCAATGTATATTTCTTTTTAATTTCACAATTACTGCAATTGTTCAGTCTGCTATCATCAGCTTCCTCTGCCTAGAAAGCTTTAATGTGTCATTTATTTGCTTAACCCGTTTTGAACCGTTTTTTTTTTTTTTTAGGACGACAGCACTGGCTGCTAAACTCACAGACTATAACTTGGGCTCAGACAAGCACACATTTCTATCTAAGCTGATAAAGAATATCTTCTCCTGTTATCTGGAGAGCTATATAGACATGGAGCGGCAATATCTGCAGAACCGCAGCGGCATGATTCTTCAGCGCTATTATGATTCCAAGAACCACCAAAAA[C/T]GACCTGTAGGCACTGGAAGGTGAGGAATTGTTGGTTTCTTTGGTTTCTTTTTTTCTTATATTTCTCTTACCTTTATTTTCCATCTTCTCTTCTCATGTCAACAGTATCCAGGAGCTAAAAGAGAGAATCAGACAACGCACGAACTTGCCTCTGGGACCCAGTATTGACACACATGGAGAGACTTTGCTCTCACAAGAAGTTGTGGTCAACCTTTTGCAAGAAACAAGGCATGCCTTTGAGAGATGCAACAAGGTATAGGAATTTTCATCACTGCTTATGATACCTGAATTTAGAAGTTGTGGGCCTTAAACATTGGACTGTCTTTGTTGCAGTTGTCAGACCCAGCAGATCTGCCAAAGAATGCCTTCTCCATTTTCCTGATTTTGGTGGAGTACCTGTGTGTGGACCATATAGACTACGCCCTTGAGATTGGGCTGTCAGGTACAGTATAATGTTTATTGCAGGGTTCACACAACCATGGATTTTCTGGATTATCATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42992
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130198 | Nonsense | 633 | 708 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 44464638)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44304316 |
GRCz11 | 17 | 44418081 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTGCAGCAGTTCAGCTACAGCTCCATGGGTGGCATGCTGGCCATCTG[T/A]GATGTGGCAGAATACCGCCGCTCTGCCAAAGATTTCCGGGTAAGGACCGG
Long Flanking Sequence:
GTAAATGTTTTTCATCGATTTCTTTTGAATTGCAAATAAATGCAAAAATTAGATTTTACTCAAACGCATAACTATAAATTGCAAATCCTGTGTGTCAAAATAACTAAAACTACATGTTAAAAAAAGGTTAAACTGGTGTCACATAACCTCATTTTGGTGTATTGTCAACAACATGTCTAATTATAATGTTTGATTAATATTTCTGTACAAAACCATTTTAAAAATATGAAATCAGGGCTGAGAAAATTGTTCAGACCTAGGGATGAAGGTCATGCCTGATTATCCTGTGTTTAATACACCATCTTTTCTGTGCTCTTTTTCAAGGCATGCTCAAAGGTGTGCGCCTATGTGGGGAAGCAGGTGGAGCGTGTGCGGAGGTCCATGGATGGTAAGAATGTAGACACTGTTTTGACGGAGCTGGGAGTGCGCTTCCACAGGCTCATCCATGAGCACCTGCAGCAGTTCAGCTACAGCTCCATGGGTGGCATGCTGGCCATCTG[T/A]GATGTGGCAGAATACCGCCGCTCTGCCAAAGATTTCCGGGTAAGGACCGGTCAAAGGTCATGCCATTGTGTAAATTTGACCCTTTTATGATTTTAAATAATGAGTTTACCCCAAAATATTAATTCAGTCATTATTAACTTAATCTTATGTTGGTTTATAAGACTTTTGCTAATCTTTAAAACAAGAATGATTACATTTTTAATTATTTGAATTGAAAGAAGTTCCTTCTAAACTTTGACTCTTTAAATAGACTCTTAGAAGAACCACATTTGTGGCCCCACAGAACATTTCAGAACATTTTTTGAAATTATCATTTTTTTAGTGTTAAGAACATATAGAATATAGAATTTTTTAAATAAATTTTGTGGAGTCCTTTGAATTGTAGAGCGTGTTCTGGACCATTAATGCCAATAAAGAAGATTTATTCACTAAAAGTAAGATCTAATAAACATTCAAAAATGATCCATACTGTAAAGACTATATTTTGTAGAGCTACGTAA
Associated Phenotype:
Not determined