Busch Lab

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