ZMP

si:ch211-51l3.1

Ensembl ID:

ENSDARG00000051899

ZFIN ID:

ZDB-GENE-061207-36

Description:

Exocyst complex component 3-like protein [Source:UniProtKB/Swiss-Prot;Acc:A2AV37]

Human Orthologue:

EXOC3L

Human Description:

exocyst complex component 3-like [Source:HGNC Symbol;Acc:27540]

Mouse Orthologue:

Exoc3l

Mouse Description:

exocyst complex component 3-like Gene [Source:MGI Symbol;Acc:MGI:3041195]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa1667	Nonsense	Available for shipment	Available now
sa6799	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa1667

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103957	Nonsense	142	780	3	13

The following transcripts of ENSDARG00000051899 do not overlap with this mutation:

ENSDART00000141594

Genomic Location (Zv9):

Chromosome 25 (position 14692368)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	14335291
GRCz11	25	14431691

KASP Assay ID:

554-1614.1 (used for ordering genotyping assays)

KASP Sequence:

AGATTTCTGTCAGTCACTGTCAGCTTCTTGCTGCAGTAAGCAACCTGCCT[C/T]GACTCTACAAAGGTTAGGGACTGCCCACTCATTATGCACATTATGTCTAG

Long Flanking Sequence:

ATATTTTTTTTTTTTCAATTTTGATTGACAGAGGCCCTTGTCCCAGTCGAGGTGTGGCAAGAGCTGGAAAGGGCTGAATGTTTGGCACGGGGTGCTGCGCTGAAATGGGCTTCAGGTGTCTTTTGTCGTCCAGAGCATCTGGAGAAACTTGGGCAGTACAAGAAAAGAGAGAGTCAGCGAACTGCATCAATTCAGTCAAGGTTAAAGGTAAGTACTGATAATTGGTCAATTAGAAAGCCTTTAAAAATCTTTGCATAAAAAATGTCAATTAATCTTATACATTTTTTCTTTAGTCAGTTGTACAGTCCTACCTGGAGGGTGTTGACTGGGGTCTTGGTCAATTGCGAGAGGCACGAGCTGAGCTAAGAGGTGTGTCACATGACTTGTACAAGGCAAACTTGGAGTCCAGGAAAAATTCTGAAGAAGTAACTACACTGGAAACACTTCGGGAGATTTCTGTCAGTCACTGTCAGCTTCTTGCTGCAGTAAGCAACCTGCCT[C/T]GACTCTACAAAGGTTAGGGACTGCCCACTCATTATGCACATTATGTCTAGATTACATCCTCTTTATGGAATTATGCCTTGGATCTCTTAGAGAGGATGTGTCCAGTCCTTGATCTGTATAATATAGCTGCAACTTGTTCCAGCATACCTGTCTGGAGAAGAGTAATGAATAAATGAATAAATTAGTTTGCTTAATTAAATTAAGGGCGCTAAATCTTGCAGGATAGCAACCTGGAGGACACACTCTTGCCTAACATCAGGTCTATATATTACATACATATGAAATTGTTCTCTGTTGAGTTTTCTACAAAGTCTACAAAGCCAGAACAAGAATATTGACATTAAAACTGACATGTTTATTGTTAGACAGCTGATAACACTGGCCATCACCCACTGAAATATCAAGGTTTTTACACTAATGCAAAACTATTTGCTGTTCTTCTCTATTTTATTAGTACGGAGTATGGTGCTAGAGACAGAAAGGCTAGTGGAGTCTCGGAG

Associated Phenotype:

Normal

Stage	Entity	Quality	Tag
Larval:Day 5 ZFS:0000037	whole organism ZFA:0001094	quality PATO:0000001	normal PATO:0000461

Mutation Details

Allele Name:

sa6799

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
ENSDART00000103957	Essential Splice Site	532	780	None	13

The following transcripts of ENSDARG00000051899 do not overlap with this mutation:

ENSDART00000141594

Genomic Location (Zv9):

Chromosome 25 (position 14690283)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	14333206
GRCz11	25	14429606

KASP Assay ID:

554-4976.1 (used for ordering genotyping assays)

KASP Sequence:

TCTACCTCCATTACCTCCTGGCCTGCATCAACAACTGCATCATTCTCAAG[T/C]GAGATGGTGTACAAGTATCTTTTTACAGTATGTCTGTATTTATGTGAAGC

Long Flanking Sequence:

CGTCTCGGAGTGGATGCAAAAGGCTCTAGAAGTGGAGCTAACAGACTGGCAGAGGGATCAGGAACCAGATATTGACCATGAGGGCTACTACCACACTAGCCTTCCAACTATCATCACTCAGGTACTTTATGGCTTGATCTACAGTAAGCAAGATTTTGTCTGATTTCACCACTGATATTTATGAATCTGGATTGATAGATGCTAGAAGAGAATGCACGAGTGGCCTTGATGATAAGTGAAGCTCTGCGGGACCAGACAATCCAAATGGGTCTTTATGAGATGGAGAAGCTCCTCAGTCGGTTTGTATGTTTAGCAATACCAGGATATCACAATTATAACGGTTGAGTTTCAATGTTTTTGTGATTTTTCTCTCGCTACATCTAAACAGATTTCGAGACGCAGTCATAGAATTTGGTAAGGAGCATCGCAAGGATCCAACTGTTAACAAGTTCTACCTCCATTACCTCCTGGCCTGCATCAACAACTGCATCATTCTCAAG[T/C]GAGATGGTGTACAAGTATCTTTTTACAGTATGTCTGTATTTATGTGAAGCTTGTTTGAAAATGTGCGTTTCAAGCACTTTTATAAGTGTTTAAATTTGTACTTTAAATGCACATCCAGAACCTCTACAGAAAGTCTGCAGCAGCAGATTTGCTCCTTCGTTTCAAACCGGTATTCACGTATCCCACTTGGACCTCTGGCTGCCCTGGACCGTGCTGTAAGAAAGGCATGTCGTTTAGTTATGGATCATCTCTTGTTTGAGTTGCAACCACATCTACAAGAGCTCCTCTCTAGTACCTGGCTGGACCAGGGAGATGTGACCCTAAATATGTGTGGGGTTCTAGAACGTCACTGTGAACTTTACAACAGAGTGCGACAACCTTGTCGCCAGGTTAGTGTTTACTGAAATGACAGTCTTAAAAACTACTCCTATAAGTGAGAAATGAACCCTAAATGCAATCTCTATCATCTACAGAGGTTAAAGGAGGAATGCCAGTGGCTA

Associated Phenotype:

Not determined