Busch Lab

ZMP

exoc6

Ensembl ID:
ENSDARG00000020521
ZFIN ID:
ZDB-GENE-040426-2511
Description:
exocyst complex component 6 [Source:RefSeq peptide;Acc:NP_998465]
Human Orthologue:
EXOC6
Human Description:
exocyst complex component 6 [Source:HGNC Symbol;Acc:23196]
Mouse Orthologue:
Exoc6
Mouse Description:
exocyst complex component 6 Gene [Source:MGI Symbol;Acc:MGI:1351611]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa45452 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41967 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa30956 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35215 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa45452
Status:
Mutation detected in F1 DNA
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
ENSDART00000022163 Essential Splice Site 517 708 15 19
ENSDART00000125230 Essential Splice Site 515 810 15 22
Genomic Location (Zv9):
Chromosome 12 (position 9775674)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 8983629
GRCz11 12 9021472
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGTTTATTTATGCCAGCTTGAAGTTCTCCGAGTCACTCCATCGCAGG[T/C]GAGCAGATGCCATCGACACCCTCCACATCAGCAGACACATTCAGCACTCA
Long Flanking Sequence:
ATTTGTTTTTGTTTTTAAATTAAAACTCCTTTCATTGTAGCCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAGTATTATAGGAAATACTGTGCAAAATTTTTTGCTCTGTTAATCATCTTTTGGGAAATTAAAATAAAAAGAAAGGCTAATAATTGTGACTTCAACTGTAGTTTGTAGTGGTAGATTTCTGTTTTTACATACAGAATAGTTGGGCATCATCACCATATTGTTGGGTATAATCAATAGCTGGGTGTATTCACCAAATGCGATTCACAAGTTTGATTCGTAACTGCATGAAAACAATGCATATATGTCACAGAAATTAAATGAGTTGTGTATGTAATTTCTTTTTGACTAGTTTGAATCTTTCCTTATTAAACAGCAACAATTCCCAAAGAAGCTGCCCATGTCCCAGTCAGTGCCTCAGATCTACTCTCAAGTGAAGGAGTTTATTTATGCCAGCTTGAAGTTCTCCGAGTCACTCCATCGCAGG[T/C]GAGCAGATGCCATCGACACCCTCCACATCAGCAGACACATTCAGCACTCAATTGTTGGTCAGTGGATATTGAATGAAAACATTGAATAATCATGGTAAGGAAGGGGGTGTTCATGAGATTGTCATGAAACTTTTATTCATCCATTTATTCATTCATTTTCCTTAGTCCCTTATTTATCAGAGGTCGCCACAGAGGAATGAATCGCCAAATATTCCAGCATATGTTTTACGTAGCGGATGCCCTTCCAGCCACAACCCAGTCCTGGGGAACATCCATACATTCTCTCTCTCTCTCTCTCTCACACACACATACACACACACACACAGTCACACACAAAACCACTTAAGCCAATTTAATTCATCCAATTCGCTTATACCGCATGTCTTTGGACTGTGGAGGAAACCGGAGCACCCAGAGCAAACCCACGCAAACACGGAGAACATGTAAGCTCCACACAGAAACGGCAACTGGTTCAGCTGGGACTCAGCCTTTATTTGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41967
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022163 Essential Splice Site 659 708 18 19
ENSDART00000125230 Essential Splice Site 657 810 18 22
ENSDART00000022163 Essential Splice Site 659 708 18 19
ENSDART00000125230 Essential Splice Site 657 810 18 22
Genomic Location (Zv9):
Chromosome 12 (position 9761585)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 8969540
GRCz11 12 9007383
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCATTAACTTCCTGCGCAGCACCTTCCAGGTCTTCACCCACCTTCCGG[T/A]AAGTTCCACACCATCCTATCCACCAGGAGTCAGTCTCGTCACGGATTTGT
Long Flanking Sequence:
TATTTCAGACATAAGGACATATTGGATAAATAGAGCAAAGCCACACCACACGCAACTTGATCTTCCATTGTTGTATGAATTTGATAAGAAGTGCGCAACATTTTCACGCTAGAAACATGTTTTATGCAGGAATGTAACTGATATGCTGCAACGGCTCCTTTAAATATGAGATTATTGTAGCGAGTTTTGACGCTCTCGCCGCCGGAGCTGAAGGCAGAGAGCGTTATCGCCAGGGCGGCCAGAGCGACCTTGGACGCTCTCGCCGCTTTCGGTGTGAACGTACGGTTAAGAATTCATATGCACATTTTCTTATTGTCAGGATGCCAGACATGCAGCTGAAGGGGAAATCTACACTAAACTCAACCAGAAGATCGACGAGTTCATTCAGCTGGCGGATTATGAATGGGGAATGGCGGAGTCGGATGGCAGGGCCAGCGGCTACCTCATGGACCTCATTAACTTCCTGCGCAGCACCTTCCAGGTCTTCACCCACCTTCCGG[T/A]AAGTTCCACACCATCCTATCCACCAGGAGTCAGTCTCGTCACGGATTTGTGATCAATCACCAGTCAATGTGTGTTATTGCATGTGTTCCGTCAAAACCACTGTGGCGTTTATCGGTGTTTTGACGTAGGCAAAAGGTTGTAGGACATTTTTTAGTTTGCACAATTCAAGTCAAAACATACACTGCAAACAATGCTTTTCCCCACCTAGATTTTTTGTCTTGTTTCTAGTCCAAATATCTAAACATTCTTAAATCAAGAAGAATTTTCTAGACCAGCAAAAATGTGCTCTTGTTTTAGGAAATAATCTTCCAAATAAGTTTTTCCTTAAAAACAAGCTAAGTAATCTGCCAATGGTGTAAGGGAAATTTACACAATTGTTTCGCCTTTTGACATACGAATACTTACCCCATTGGCAGATTATTTTGCTTGATTTTAATGGAAAACTCACTTATTTTTGACATTTTTCTCAAAACAAAACAATATTTTGTCTGAGCACATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30956
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022163 Essential Splice Site 659 708 18 19
ENSDART00000125230 Essential Splice Site 657 810 18 22
ENSDART00000022163 Essential Splice Site 659 708 18 19
ENSDART00000125230 Essential Splice Site 657 810 18 22
Genomic Location (Zv9):
Chromosome 12 (position 9761585)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 8969540
GRCz11 12 9007383
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCATTAACTTCCTGCGCAGCACCTTCCAGGTCTTCACCCACCTTCCGG[T/A]AAGTTCCACACCATCCTATCCACCAGGAGTCAGTCTCGTCACGGATTTGT
Long Flanking Sequence:
TATTTCAGACATAAGGACATATTGGATAAATAGAGCAAAGCCACACCACACGCAACTTGATCTTCCATTGTTGTATGAATTTGATAAGAAGTGCGCAACATTTTCACGCTAGAAACATGTTTTATGCAGGAATGTAACTGATATGCTGCAACGGCTCCTTTAAATATGAGATTATTGTAGCGAGTTTTGACGCTCTCGCCGCCGGAGCTGAAGGCAGAGAGCGTTATCGCCAGGGCGGCCAGAGCGACCTTGGACGCTCTCGCCGCTTTCGGTGTGAACGTACGGTTAAGAATTCATATGCACATTTTCTTATTGTCAGGATGCCAGACATGCAGCTGAAGGGGAAATCTACACTAAACTCAACCAGAAGATCGACGAGTTCATTCAGCTGGCGGATTATGAATGGGGAATGGCGGAGTCGGATGGCAGGGCCAGCGGCTACCTCATGGACCTCATTAACTTCCTGCGCAGCACCTTCCAGGTCTTCACCCACCTTCCGG[T/A]AAGTTCCACACCATCCTATCCACCAGGAGTCAGTCTCGTCACGGATTTGTGATCAATCACCAGTCAATGTGTGTTATTGCATGTGTTCCGTCAAAACCACTGTGGCGTTTATCGGTGTTTTGACGTAGGCAAAAGGTTGTAGGACATTTTTTAGTTTGCACAATTCAAGTCAAAACATACACTGCAAACAATGCTTTTCCCCACCTAGATTTTTTGTCTTGTTTCTAGTCCAAATATCTAAACATTCTTAAATCAAGAAGAATTTTCTAGACCAGCAAAAATGTGCTCTTGTTTTAGGAAATAATCTTCCAAATAAGTTTTTCCTTAAAAACAAGCTAAGTAATCTGCCAATGGTGTAAGGGAAATTTACACAATTGTTTCGCCTTTTGACATACGAATACTTACCCCATTGGCAGATTATTTTGCTTGATTTTAATGGAAAACTCACTTATTTTTGACATTTTTCTCAAAACAAAACAATATTTTGTCTGAGCACATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35215
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022163 None None 708 None 19
ENSDART00000125230 Essential Splice Site 767 810 21 22
Genomic Location (Zv9):
Chromosome 12 (position 9731036)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 8938991
GRCz11 12 8976834
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAGTACCTGCGGGTGAACCCATCCACTGCGCTAGCACTTTTGGAGAA[G/A]TACGTATCATTTTCTTCTCTTTCAAGTGCAGAAATGTGAAAAACAAACTC
Long Flanking Sequence:
TATTATTGTACAATAACTGTTATTGTTATGCAATAACTGAAAGTAATTTTTTTTCAGCCAGCAAGTTTATGACCAGAAAGGCTTCTTCCAAAAGATAATAAGATGATCCACAAGAGGCATTATTTACATTTAAGCAAAAACTTAATTTTAAATAATTTTGGGCTTGACTGTAAGTCTCCTAAAATAAACCTCAAGTGTACTTGCAAATTCAGCATTGTATTAGTTAAATAAGACTGGCAGTGCTAATTATTATTGGCTAAATCAAATCTCCATTAAGTTCAATTTATTTTATTCTTCAGTATTCATTTCAAGCCTGTATATTTGGTTTGCTCAAAGTTTTGTATATCAGTCTTTGCTCACTTGAGACATCTGTGTTCTGTGTTTCAGCTCCTAGATCTGTTCATGGTGTGGGATTGGTCCACGTATCTGGCAGACTACGGGCAGCCAACCTCAAAGTACCTGCGGGTGAACCCATCCACTGCGCTAGCACTTTTGGAGAA[G/A]TACGTATCATTTTCTTCTCTTTCAAGTGCAGAAATGTGAAAAACAAACTCCTGGGAAATCAGTTCAACTTTCTAAAATGCTTAAAATAATTACATTTCTGACAAGAATGGGATTGAATCTGGAATGTCATTTTAAAATTATGTAACTTTGAATTGATTCTTCAAAAATACTAAAATATTAAACATATCTCCTGCTAACAATGAGTAAAAAAGCCATTGCAAAGAAATGGCTCAAAGACGATCCTCCATCTGTTGGTGAACGGCATGACATTGTAAAAGAGGTCTATGATATGGAAGTACTGACACTTCAGACAACAATCCTTTAAAATCTCTTCATGCCGGGGAAAGTGGCTATGTTTTAATTTTATTGCAGTGTTTTTATTTAGATGTATCTGAAATCCTCCTTCGAAGGCTTTTCAATCTTTTATATTTAACCCTTAACAGAACTTTGTATGGCAGGATCTGATCAAACATAAATACTTATGAATGTAAATAAGATTA
Associated Phenotype:
Not determined