ZMP

exoc3

Ensembl ID:

ENSDARG00000014582

ZFIN ID:

ZDB-GENE-030131-5947

Description:

exocyst complex component 3 [Source:RefSeq peptide;Acc:NP_997880]

Human Orthologue:

EXOC3

Human Description:

exocyst complex component 3 [Source:HGNC Symbol;Acc:30378]

Mouse Orthologue:

Exoc3

Mouse Description:

exocyst complex component 3 Gene [Source:MGI Symbol;Acc:MGI:2443972]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa19896	Essential Splice Site	Available for shipment	Available now
sa39943	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa19896

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
ENSDART00000009347	Essential Splice Site	431	748	7	13

The following transcripts of ENSDARG00000014582 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 2 (position 50684107)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	50379639
GRCz11	2	50113869

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTTTAATCCCCCTACTTATACGAGTTCAACATGAGATCCTCCTCTTCA[G/A]ATGTTCGAGCAGAATCTTCAGGTCGCCGCTCAGATTAATGAGATCTTCAG

Long Flanking Sequence:

AGTGACCATTTTTTTCTTTATTTACTCACTGATTGTTTTTCTTCTGTTGAACACAAAGGAAGAAATTTAATGAGAGTTGAAGACCTGTAACCATTGACTTTCATAGTAGGGAAAAAATACTATGGAGGTTAATGGTGACCAGATTTCAGCTGTCTTCTTTTTTTGCTCAGAATAAGGAAACTTATAAAAGTTTGAAAATGCTTCAGTGTTTATAAATGTTCATTTTTGGGTGAACTATCCCTTTAATTTTAATGTTCATTGTCAATTCAGCTAGTCTTTGTTTCCCATCTGTCTTCAGTCAAACATCACAGGCTGGCTGCGTAAAGCTCTGGAAACAGATAAGAAAGACTGGCAGAAAGAGACGGAGCCTGAGGCCGATCAGGATGGCTACTACCAGACCACATTACCAGCTATTGTCTTCCAGGTACAACAACTTACTGACCGACTTCATGCTTTAATCCCCCTACTTATACGAGTTCAACATGAGATCCTCCTCTTCA[G/A]ATGTTCGAGCAGAATCTTCAGGTCGCCGCTCAGATTAATGAGATCTTCAGAGAGAAGGTGCTGGGCGTCTGTTTGAAGCAGATGAATTCATTCCTAAAAAGGTACTGTGATCTCATCCTGGCCACTTGTGTTGTTTTTTCCCACGGTAATGAGCCTGAAAAGGAAATTGCGTCCACATACAAAAAGCAAACTTCATAAAATGAGCTCCAATGTTGGTAGAAGAAACCTTTATTAATTTTCCAACTAATGGGACTGGATTAGATCTTTTTTACCAACTGTAGAGTCAGCCTGGAATCTGACCTTGGCTAAAAATATCACGGTTTCATGGTATTGTGATTACTGTTCTAAAATATGTCCTTTTTTAAATGTCTGGGTGAAAAACAGCAACTTTCTTTCCCCATTAAACGCAAAATATTTTAAGAAACATTTACAGTATTTTAGAGCAATAAACATGTCAGGCTAAAAAGAAGCTGACATCTGCTGTCTTTATTCATTTCAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39943

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000009347	Essential Splice Site	501	748	8	13

The following transcripts of ENSDARG00000014582 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 2 (position 50681564)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	50377096
GRCz11	2	50111326

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTACGTTCAGTATATGATCGCCATCATCAACAACTGCCAGACCTTCAA[G/A]TGAGTTTCTCTTATCAGTTTTTGATTTATTAATTTTGAAGTCGAACATTA

Long Flanking Sequence:

TCTAAATCTGAAGTATACATTTTTAAAACAAACAAACAGATTGCAGTATTGTTCTCTATTGTGAAGTATAGTACGTCTGGGTGAAATGCATTATTTTACAAGAGAAAAGTAGAATTGCCTGGATGTTTGTGGTGACAGTTCAATCCCTCCCTCTTTCTGGTAAACATGCTATTAGAGTAGAGATGAGATAAAAGAGGGAGGGAAGATTATTTTTATTAAAGATTGCAAGGATGCGCTTTTGATGTAAGGACGAATGATCTGCGCATATAAATCATTAATAATGTATATGTCAATGCTCCAATTAAATAATATGCGTTGTCCATTTTGATTTCATTGTGATGTCTGCTCTGTACCAAGCACATTTTCAGTTCTCCTGCATGTGTATGAAGGTACCGAGAGGAGGCGATCGTCTATAAGGAGGAACACCTGAAAGATCGTCAGCTCCCGCAGTGCTACGTTCAGTATATGATCGCCATCATCAACAACTGCCAGACCTTCAA[G/A]TGAGTTTCTCTTATCAGTTTTTGATTTATTAATTTTGAAGTCGAACATTACATTAATGCGGAATTCTGGGTCATATATCGTGCCTGCCTGCGTGCGTGCGTGCGTCTGTCTTTCTGTCTCTGTGTCTGTCTCTGTGTGCATCCGGAAAGGATTCACAGCGCTTCACATTTTTATGTTACAACCTCATTCCAAAATGGATTAAATTAATTTATTTCCTCAACATTCTACACACAATACCCCATAATGACAATGTGAAAAAAGAGTTTTTTATATTGTTGGAAAATTCATTTAAAAAAAAAAATCACATGTACAGAAGTATTTACAGCCTTTGCTCAATACTTTGTTGATGCACCTTCGGCAGCAGTTACAAGACTTTTTGAATATGATGCCACAAGCTTGGCACACCTGTCTTTGGGAATTTTTGCCCATTCCTCTGTGCAGAACCCCTCGAGCTCTAACAGGTTGGATGGGAAGCGACGGTGTACAGCCATTTTCAGATC

Associated Phenotype:

Not determined