Busch Lab

ZMP

zgc:153610

Ensembl ID:
ENSDARG00000069489
ZFIN ID:
ZDB-GENE-060929-132
Description:
hypothetical protein LOC767763 [Source:RefSeq peptide;Acc:NP_001070198]
Human Orthologue:
EXOC6B
Human Description:
exocyst complex component 6B [Source:HGNC Symbol;Acc:17085]
Mouse Orthologue:
Exoc6b
Mouse Description:
exocyst complex component 6B Gene [Source:MGI Symbol;Acc:MGI:1923164]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa34065 Nonsense Available for shipment Available now
sa40885 Nonsense Mutation detected in F1 DNA Not yet available
sa40886 Nonsense Mutation detected in F1 DNA Not yet available
sa34066 Nonsense Mutation detected in F1 DNA Not yet available
sa20933 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa34065
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052773 Nonsense 129 224 5 7
ENSDART00000101188 Nonsense 158 804 6 22
Genomic Location (Zv9):
Chromosome 7 (position 26338733)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 24900485
GRCz11 7 25171642
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACCCTTCCTACACCAGATACTACCCAGCACTACGGACCCTGGAACAGT[T/A]GGAGGAGAGCTGTTTGCCTCAAGCAGGATCCTATCGTTTCTGCACCATCA
Long Flanking Sequence:
TTCATAACTATTATAACAGTCTGTTGTGCGTATGTTTAGTTTTTTAAGTTATGTTGAAAAAAATGTATGTATACAATTAGGGTCTGCTTGTTTTTGACACATTATTTAAAAAGTGTTGCTAAGAAATAGGTTATTATTATAGTTTTTTGATGGGGCAAGTGCATTTTTTTTCTGCTGGGCCATTAAAAAATCCTAAGCATTTAGCCCTATATAAGTCTGAAATTTCATTCTTCCTGGTCTTAAAAAGATCTTAAAGTCTTACATTTGACTTGGTAAAATCTGCAGAAAACCTGCTAAAACAAACCTGTTTCTTTGTGGCTGCTGAAAACGGAACACTGAACTAGAAATCAAACATTTTTTCCATTGAGCCACCAGAAAAAATGCATTACCATTCATCATAATGTAATCAAAATGCCATGTATATGCAACATTTCCTGTATCCATAATTTCTGACCCTTCCTACACCAGATACTACCCAGCACTACGGACCCTGGAACAGT[T/A]GGAGGAGAGCTGTTTGCCTCAAGCAGGATCCTATCGTTTCTGCACCATCATGGCAGAGAATATCCCACGTCTGCGCACGCACATCAGAGACGTCTCCATGTCTGACCTCAAAGACTTCCTGGAGAGCATCCGCAAGCATTCGGATAAGATCGGAGAGACTGCCATGAAACAGGTGTTTGTTTGTGTGTGCGTGTGTGTGTGTGTGTGAGTGTGAGTTTGTGTTAGTAAGCGCTCATGTCTGAATGAAGCCTGAAGGTGCATCACAGCTAGTGTTTGACAGCTGCATCATGCGCTCGCGTCTGACCCGACGGTCACAGCTGGCTTTCAACATGAGTTCTCTGAGGGAAGGACAAAGGCCTTGTTCTTCTTTAGTTTAATGCACTTTTCCCAGTTTTTCCTTTCATCTTATCTCTGACCATCTAGTCATCTAGTCTGGAGGAAAGAGAGAGCTACCAATCTGTTCTGAATCAAAGATCGTTTTAGGTCGCTTTTGTTGATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40885
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052773 None None 224 None 7
ENSDART00000101188 Nonsense 418 804 13 22
Genomic Location (Zv9):
Chromosome 7 (position 26386205)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 24947957
GRCz11 7 25219114
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTTGCAGGGTTATGGCTTTCCAGTAAACCAGTTGTTCGACATGTTGT[T/A]GGAGATGAGGGATCAATATGGAGAGATCCTGCTGAAAAAGTGGTCCCAGT
Long Flanking Sequence:
CAGGCCTGTGCTTTTCCTCCTCTTCATTTAAAAGGCTCACCAAAGCGGTATCATCTGCATACTTTACAAAATATCTATTTTTAAATGAACTCATGCAAGAATTTGCATGTAAAAATAAATAATAACAGAGATAAAACACAACCCTGGGAGCTCCGACTGAAGTACACCTTTTATCTGAAATAAAACATGCCATTTTATTCTGTTGGATTCTAGAGCTAAGAAAATTGGTCACCCTGGCATTATTTTATTGTCTAATAAAAAATATTTTGCAAGTGTAGCAACTAATATGCTAGGAGAAATACACTCAAACGCCATAGAGAATTGTAGAAAAATAATTATTTAATGTGATGCTTGAAAAAAAAATTATGTGAACAAATGTGTAAACCCAATTTTGCCTGGTATTCGACTGAGGGCTACATTCATTTAGTTCTTGCTTTCATCTTACTATCTCTCTTTGCAGGGTTATGGCTTTCCAGTAAACCAGTTGTTCGACATGTTGT[T/A]GGAGATGAGGGATCAATATGGAGAGATCCTGCTGAAAAAGTGGTCCCAGTCCTTCAGGTGATTTCCTGCTTTTTTTAATCATCTCTATACTACGATTTGTCATGCGAGTCAGAATAATGATGATTTGGTTATCACCTTATGACCCTTGCGAAATCCATACTGAAGGAATTAGGCTAATAGGGTTATGCCCAAACATAAGATGCGTTCAGCGTAAATCAGATTGTGTTTACTGTACGTCATTTGCTCTGCAATTCAATACTAGTTAACCATACATCCATTTTTTTAATGAGATATCCATTTTAATGCCCTATATCAAAGTACCATTTAGGGAAATTGCCTGAATCTGATACCTGCAGTGCTCCAAGATTTATATTCGGACAGCTGAAGGACAGCGAAATGCTGTCCGGCCAAACCATCTGAAATCTCTGATCAAATTACCCCCATATGACTAAATCATATTGCTTGAAGGACAAATATTTTCTTCGTTTCAGTTCTGGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40886
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052773 None None 224 None 7
ENSDART00000101188 Nonsense 536 804 16 22
Genomic Location (Zv9):
Chromosome 7 (position 26398242)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 24959988
GRCz11 7 25231145
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGTAAATCTACAAATCTCCTGCTTACGCGAACTCTTAGCCACTGCCTA[C/T]AGTATGCCATTAAGAAGAAAAACGTAGGACTGGCAGAGGTGAGTTTCTTT
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATAATCAATATAACTTATCTCTAATAAAACAACAAACTCTGTATCGTTTCAGATGTCATTCCCTCGCTGTAAATGCTAGCGCTAACAGGGTTTTTTTTGCAACCTCGCTGCGTATGCATCCTGATTGTTTACAAACTGGTAATTCATCTATACTGTAAGGATTAGCATCTAGCTTAAGTTTTTTCCTTTTAAAAAACTGACAACAAAAAAATAAAACAGTAGTGTATGCAATTTAAGATAAGCATGTTCAACATTAAAAATCTCCCCAGCTTTTTTAGTCCACTGATACAGTCTCTGTGAACTCAGAATGCTGAACATCTTTATAGAAAATGTACCCAAGTCATGAATATATGTATTTCAATCCTAATTAGATCATTTTTCATTTTCAGCTCTACAGAAATTGATGACATGATTCGTAAATCTACAAATCTCCTGCTTACGCGAACTCTTAGCCACTGCCTA[C/T]AGTATGCCATTAAGAAGAAAAACGTAGGACTGGCAGAGGTGAGTTTCTTTTTACTTCTTATTTTATGTGTATTTACTAAACATCCTTGTTGTCCCATGTCTTTTAATGCCACATCACCAATCCAGCATCAACAGAGAGGAAAATTTGTATGGGCTGTTTGTTTTCTGTGTGCTAAGTTACACTTGAAATGTGTGAATTGAGTTTCATCAATCTCCACATCGTGTAGACTTGTTGCACTTTATTTTCATGGTTGACTTTAGCCACTTTAAACTAACTGATTTAAAATTAACCAATCCCAAAAGGAATGACCACTTACCATTTTTTAATCAGACCCTTACCTGTTCAATTTGTTTGTGCATTATTTTTCATATATATATTTCATGAGTTGGTAAATAAAGTGTAACCCATAGACCCCTTGGGAACTCCAGCAATCCATTCATTTGGATATTCATACTTCATTTATTTATTCATTTTAAAAAGTTATTTTAGATCACTGTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34066
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052773 None None 224 None 7
ENSDART00000101188 Nonsense 634 804 18 22
Genomic Location (Zv9):
Chromosome 7 (position 26402657)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 24964403
GRCz11 7 25235560
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGATTATGATTGGACAGCAGCACAGGGTGGTGGGCAGGCCAGTGACTA[C/A]CTGAGTGACCTCATCGCTTTTCTCTGTAGCACCTTTGCAGTGTTTACTCA
Long Flanking Sequence:
TGCTTGTTGTTGTATAAAAATATATACATACCCAAACATATGAGAAGTAATCTATTTCAGTCTCTGTTATAAAACTTGCACAAAACTTAAATTATAACAAGTTATAATTTGAAAATGTATTTGATACCCCAAGTTGGTGCAGATCATCATCAACACCACTCACCTGGAGCAGTCCTGTCATTATCTAGAAGAGTTCATCTCCAACATAACTAATGTGCCTCCTGACACCATCAATGCCACAAAGCTCTATGGAACCTCCACCTTCAAGGTACTTCTTTTCTCCCAAAGAATATATGAATTATGATTTAATATTATAGCAATACCAGTTGTATCTAGTCAGGATCTCTGGTTAGTCATTGTTTGCTTCTCTCTGTTTAGGATGCAAGGCACGCCGCTGAAGAAGAGATTTATACTAACCTGAATCAGAAGATTGACCAGTTTCTGCAGCTGGCCGATTATGATTGGACAGCAGCACAGGGTGGTGGGCAGGCCAGTGACTA[C/A]CTGAGTGACCTCATCGCTTTTCTCTGTAGCACCTTTGCAGTGTTTACTCACCTGCCTGTAAGTATTTCATCCACAGATGCATTCAAATTATTGTTAAGTTTTAAATTGAATCAATTAAATTTTTTTGATAGTTTTTTACTCCTGATTACATAGTTACTTAGGATAAATAAAATATTTAGGACAGTAAAAGGACAGATTATGGTTCTAGCTGTTGTTTGTGGGACCGGTCAAAAAATGTTCTTGGTGGTAAATATACACATTTTTTATTTATTTATTTTTTATTTGTGGCGTTTACTCTCTCTCTCTCTCGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATCTATCTACCTATCTACCTATATATATATATATATATATATATATATATATATATTTATATATATATATTAATCATTTTATTTCCGTGATGACAGCTAATTTTGTTTTAAGCAGTCATCATAGTGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20933
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
ENSDART00000052773 None None 224 None 7
ENSDART00000101188 Essential Splice Site 700 804 19 22
Genomic Location (Zv9):
Chromosome 7 (position 26418684)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 24980430
GRCz11 7 25251587
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTATGGGAGCCCTGCAGCAGTTCAACGTGGACGTCAAAGAATGTGAAA[G/A]TAAGTTTGACTTTTAGCAACAAAAACCCATCTTAAACCTGATTGCATGAC
Long Flanking Sequence:
CAGCGAATGTGTATTGATGTTTAAACAGCACTGCAGTTCTCCCGGCTTAAATGTCCACCCGAGTGCTACTAAGCCTCACTCTTTTTTTTTTTTTTTGAGATTGCATGTAAGCATAGACTTTCAGGATTGTAAATTCAGTCTGAAATGTGGTTGCATATATGAAGTCTACATTAGAGACCAGAATGCAGAATATTGTGCTGGTCAAGAGAATCCAACACAATTCACTCTGACAGATAGAAAATAAGTGGAGAAACATGCAAACAGTTATAAACAGTTAAATATCCATAGTTTCACCACCTGCTAGAGAAGGTCCTGCTGGAAAATACATCATTTGTTTTTCTTCATTCTTTGTCTGTAGGGAAAGGTGGCTCAGACAGCATGTATGTCAGCCTGTAAACACCTCTCCACCTCCTTGCTGCAGCTGCTGTTGGAGGCTGATGTCAGGCAAGTGTCTATGGGAGCCCTGCAGCAGTTCAACGTGGACGTCAAAGAATGTGAAA[G/A]TAAGTTTGACTTTTAGCAACAAAAACCCATCTTAAACCTGATTGCATGACTGTTCTTCATCCTGGTGTGTCCCAATTGAAAATTTCATAAACTGCCCCAGAGACTTTTTATTGTGGCACAAATTGTTGCATCCACTGTAACAAACTTCCCCATGGCTTTCTCAAAACTGGCTGAATGTTGGAGAAAAAGGTGAGAAGAGACGAGTATGCACTTTTGGCTAGTGCCTAAGATTTGTCGCTTGGCTCATCTCTCCTCACGGCTTTGTGTGTGACCACAGCTAAAACTGCCTTTGAGCTCCTAACCCCAGATGGTTGATGGATTTCCCATGATCCTCATCCAGCACACACTATTGCACATGGGTTACAAGCAAAGAAAGTTTGACCCCATCACCAAACGGTCACATCAGTCACACTGTATGCTGCGTTTTTGGTGTGGTTTGCTTTGGGCTTAACAAACAGGCTGATAAGTACCATATCAGTTCATTTTAATTTTTTTTTTAT
Associated Phenotype:
Not determined