ZMP

si:ch73-212j7.3

Ensembl ID:

ENSDARG00000058835

ZFIN ID:

ZDB-GENE-081104-259

Description:

Novel protein similar to vertebrate pleckstrin homology domain containing, family G (With RhoGef dom

Human Orthologue:

PLEKHG3

Human Description:

pleckstrin homology domain containing, family G (with RhoGef domain) member 3 [Source:HGNC Symbol;Ac

Mouse Orthologue:

Plekhg3

Mouse Description:

pleckstrin homology domain containing, family G (with RhoGef domain) member 3 Gene [Source:MGI Symbo

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23626	Nonsense	Available for shipment	Available now
sa36947	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23626

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
ENSDART00000081781	Nonsense	43	973	1	23
ENSDART00000131697	None	None	527	None	2
ENSDART00000134137	None	None	188	None	6

Genomic Location (Zv9):

Chromosome 20 (position 3216889)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	3170751
GRCz11	20	3183838

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACCTACTTGGACCGTGTGGTTATGGAGATCATTGAGACCGAACGAATGTA[T/A]GTGAGAGATCTGCGGAGTATTGTTGAGGTAAGCATAAGCCTTTCAAATCC

Long Flanking Sequence:

TCAAAACTATGCCTGTTTTCAGTGTGTGATAAACGTATTATAACATGCAGAAAAATGACTCTCGACTCACCTTCCCTTGTTGCTGTTTCTTTTTCAGAATCGCCTCGATTGTCCATCGCCTCTCTTGGCAGTAATGACCGCTCCTCCATTACTACGCTGTCTGATTGCTCTGACTTCACAGACGTCCAGAGGCCCGTAAGCGTAGTCTCCAACATATCATCTGGGTCCGGTTCCTCTCGGGACGACGTTCCCTTGTCAGGTGTTGTGTCCGCTGCTGTACCAATCGAGGACAATGTGGATCTAGAGCTGACACCTGCTGCCAATCCGACTGAACCTAATCTTACCCAAACATCCAGTCACTTCCTCCAGCAAAACAGCAGCAACACTGTTAACAACAATACCAGTTTCTCTCCATTTGCTGCCAACACCATGGCACCCAACCCCGAGCTCACCTACTTGGACCGTGTGGTTATGGAGATCATTGAGACCGAACGAATGTA[T/A]GTGAGAGATCTGCGGAGTATTGTTGAGGTAAGCATAAGCCTTTCAAATCCTTCCCCCTAAAAACTTTATTTACATTATATGCTTAATCAATCAATCAATCATATAGCAATTCACATATTTTAATAATTAAAATAAATACATTATTATAGACAAGTAAATAGATGATGGATCGGTTATTATCTCAACACATTGGCTTAAACTGATTATAGACTGCTCCTAAAACACTGAACACAATGTATTGGTCTTCAGTTGAGGTTGTGTGTGGTATATCAGTGGACACTTGCAGATAAAGTACATTACTGTCGTGTTGTTCTGCAGTCTATCATTAATGATTTTCATTTATAGCTTCTAAGTTAACGGTTGTTATGGTTTGTTCCACAGTGTAGATTAGCATGTAGGTGTACTTGACTTTTAACATACATGCTATAGGTTCACTCTTTTCTGTCAGTCTGGAAAGTGACCAGCTAAAACCATTTAAAACCAGCTTGACCAGCCTGGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36947

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
ENSDART00000081781	Nonsense	935	973	23	23
ENSDART00000131697	Nonsense	362	527	1	2
ENSDART00000134137	None	None	188	None	6

Genomic Location (Zv9):

Chromosome 20 (position 3184581)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	3138443
GRCz11	20	3151283

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATGGCAGAAAGAAGGTAGACTCCTTAGCGCTCTAGCCCCCAGAGTCATC[C/T]AGTTAAGAGCAGAATCTGAATATGAGAGAGGCACAGGAGCTCAGTCAGCT

Long Flanking Sequence:

TATCAGAAGCCACTTCGAGTGCAAATTCATCCCGTCAGGAACAACCTGTTGTCAGCGCTTCCACAAATCCCACAGGGTTCAATGTAGATGGTTCTGTGAAACCTCAGTCTACCTATATTCAAGCTGAGAGTGAACAGAACGAGGTTTTCCATCCCTCCTCTGAGATGATCAAAGTATGGCAAGATATGGAAAGAGAGGTCACTAGATGTCAAGGAGACGTCAAAGCACTGGTGCCCAGAGGAAATCCTTATTTCAGAGGGATCTGTCCCAACCTTATCAGGAGGGATCCAAACCAGGACGAAAAGACTGAAGCCAAAGGAAACAAAGGACTGATTGCATTTGAAGATTCAGATTTGAGCACTATCAAAGAAGAGTCCTTCACACCATCACCGTTAATAGAAAAAGAAAACAGTGAAGCCATTAGTAGGAATGATGCCATCAGACAAAAACAATGGCAGAAAGAAGGTAGACTCCTTAGCGCTCTAGCCCCCAGAGTCATC[C/T]AGTTAAGAGCAGAATCTGAATATGAGAGAGGCACAGGAGCTCAGTCAGCTGAAGATGGAGATTCAGCCCAAAGCAAGGTTTTAAATCTTGCAAGGAAATACAGTCAGCGCATCAAGTGCACTCAACCCATGCTGAGACAGAGGAGTCAGGAGTCAGGAGAAACAGGGTTGACCAAGAGGAACATGCTGTCGGTGGTGGATGAAAAGCCAGAGGAGGTCAAAGGTAAGACTGATCACCTTTGCCTACATCAGAGGTTCTCAAAGTGGGGGTCGGGACCCCCCGAGGGGTCGCGGGACAATGAAGGGGGGTCGCCTGGTGATTTTCAAAAATCAATTAATTTTTATTAAACCTTAAGACTTACTGTATTTTATCAATAACCTACTGAAGAGAAAAAATAGTTGTTTATAGTTACTATAAACTATATGGTTTCTATAGTAGCTTATAGTTAATAGTTCTATTGGATTGCGACTTCTTGGGTAATTACATTATACTTAAGACAC

Associated Phenotype:

Not determined