ZMP

LOC796404

Ensembl ID:

ENSDARG00000089038

Human Orthologue:

PLEKHG5

Human Description:

pleckstrin homology domain containing, family G (with RhoGef domain) member 5 [Source:HGNC Symbol;Ac

Mouse Orthologue:

Plekhg5

Mouse Description:

pleckstrin homology domain containing, family G (with RhoGef domain) member 5 Gene [Source:MGI Symbo

Alleles

There are 7 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14396	Nonsense	Available for shipment	Available now
sa24392	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa14396

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
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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127492	Nonsense	266	1110	8	22

Genomic Location (Zv9):

Chromosome 23 (position 37761672)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	37739301
GRCz11	23	37670738

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGCTCGCTCAGCCTGCCCAACATCAAGCYGTCAGTAGGGGGCAGCGTCTA[C/A]ATCCTCACGCCRGCCACTGACAAACCAGAGCACAGTTCCCTGCCYCGCAG

Long Flanking Sequence:

TTGAAACGTATCTCATCCTGTTGTTCTAATCAACATCGGTACCAGTTTATCACAGGCACATGGTTGTATAGTCATGAATAGATGAAGCTACTACTGAAATGTCAATAAAATCACTTTGTTAAACTGTAGAGTTGAATTTGAACACCAAAATTCGACAGAGCAGAGTTCAACATCCTATAATGCAATTCACAACCGTAAATAAAACACTTGTTAATCACAAAACTGTTAATTTACAGATATTTTTAACAGTGTGTATTGCATTCTGATATGTATTTTTTTCTGCATTTTAAACATTTAATAACATTTATGCATTATTAAATATTGTTCGGTCTGTTTAGTAAGCAAAGCATTTTATAACATTGTTTGCTGTTGTAGTTGAATCTTTGTTTGTGTGTGTACACAGCTCGACCTGGCGATGAGCTGAAGGTGGAACAGAGTGTTAAGGATCTGCGCTCGCTCAGCCTGCCCAACATCAAGCCGTCAGTAGGGGGCAGCGTCTA[C/A]ATCCTCACGCCAGCCACTGACAAACCAGAGCACAGTTCCCTGCCCCGCAGAGACAGCGTCGACATACTGGTCAGTCATGCTGCTTTGTCTGTCTACACACACTCAAGCCTTTTACATCTTTTCTTTTTTTTCTCTCTCTCTCTATTTTTGGAGCATTCTGACTTTAACTGCTACTTATTATTATCTGATTTTATTTATTATTTATTTTCCCCCCACTTTATTTACATTTTCTGCAACTGAGCATGATTCACAATTACTATTACAGATAAAGAAAATACCTAAGATAGTTGACATGTATATGCACACACTTTATACAAATACCGTTAGTTTTGCACTGTTTATTTTTTCAACAGTGGTTAACTTTAGTGTTTTTAGTCATAATTTACTTTTATTTGTAATTTAGCTTTTTTACCCTGCAAAATAGTAGTTTTTTTATTTGGTTTTATTGAGTTGTAATATTTATTTATATTTTTGCATTTTTTACGATTACAAAATATTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24392

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
ENSDART00000127492	Nonsense	627	1110	15	22

Genomic Location (Zv9):

Chromosome 23 (position 37797731)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	37775360
GRCz11	23	37706797

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCAGATGCGCCAGCGGCAGGAGCAGCAGAAACTGGCAGCCACTTCAGCT[C/T]GAGTCGAGTCATACGAGGCCGTGGAGGGAGCCAGTGAGGAGGTGGAGAAG

Long Flanking Sequence:

CAGGCCTCCAGAGATGCTCTCAACAACATGGTGAGACACCAACATTTCTAAACTATCACAAAAACAGTTACAGCACAGTGTGTACAGTATACAGTTGAAGTCAGAATAATTTGCCCTCCTGAATTACTAGAATTATTATTCCTTATTTTCTGTTTAACAGAAAAAAGCCTTTTTCAACTCAATTCTATAGATATTAGTATTAATAACCAATTTCTAAAAACATATTTCTCAAGGGGGCTAATAACATAGACATTCAAATGGTTAAAATTAAAACAAATATTACATTTAATACTGTGGAAAATTCCTTGCTCTGTTAAACATCATTTGACAAATGTTTGAGAAAGAAGATAAATTCACAGGAAGGCTAGTAATTCTGACTCTATGCTGATCTGCATGTGTGTCCGTGTATTCAGGTTGCATGTGTGGAAGGCTTCATCAACGGTGTGGACTCTCAGATGCGCCAGCGGCAGGAGCAGCAGAAACTGGCAGCCACTTCAGCT[C/T]GAGTCGAGTCATACGAGGCCGTGGAGGGAGCCAGTGAGGAGGTGGAGAAGGTACTACACAGAGAATTCCCCATGTGATATGTGTAAAAAATGAAGATTACCCCATAAGTCACTCACCCTCGAGCCATTTTTGGTCTCATTTTACAATGAGGTTTCATTATTAGTCAATGTATTTACCATCTATGAACAACAATGATATAGCATTTATTAATCATAGTTCAACATTTCCTTAAACCCAAATTCATGCTGGTTAACATTACTTAATGCACTGAGTTAACAATGAATGACTGTATTTTCACTGACTAACATTAACAAGCATGAACACCGACCGTACTAAATGTATTGTTCAGTGTTTGTTGATGTTAGTAAATACATTAACTTACACAACCTTATTGTAAAGTGTTACCATGACTTTATTCTATCAGATGAACACAGTCTGAGTAGTTTTAAATGTTATCCTGGCTCTTCAATGATGCTGTTGGAGAGTGGCTTTTATTTTGA

Associated Phenotype:

Not determined