ZMP

LOC100004252

Ensembl ID:

ENSDARG00000074740

Human Orthologue:

ARHGAP18

Human Description:

Rho GTPase activating protein 18 [Source:HGNC Symbol;Acc:21035]

Mouse Orthologue:

Arhgap18

Mouse Description:

Rho GTPase activating protein 18 Gene [Source:MGI Symbol;Acc:MGI:1921160]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa9512	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa9512

Status:

Available for shipment
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Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113237	Nonsense	283	546	6	11

Genomic Location (Zv9):

Chromosome 20 (position 2092795)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	2047181
GRCz11	20	2073887

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTGTGTCTCTGCTTTCKCAGGATTTTAAAGTGTCTCAGGATAAGACRGGA[C/T]AGACTAAAGTGGGCGATCTGTCGGCGGAGGACATGAAGAAGGTGCGCAGG

Long Flanking Sequence:

GGTCTTACACACACACACACACACACACACACACACAAATTATGAACAGAATTGGTGACAATGGGCAGCCCTGCTGGAGTCCAACATGCACTGGAAACAAGTCTGACTTATTGCCGGCAATGCGAACCAACCTCCTACTCTGTTCATACAGGCCCTTAACAGAGCACCCCATACTCCCAGAGCACCCTCCACAGAATGCCACAAGGGTCGAATGCCTTCTCCAAGTCCACAAAACACATGTGAACTGGTTGGGCATACTCCCATGAGCCCTTGAGCATCCTGCCGGGGGTATGGAGCTGGTAATCCAAAATGCTCCTAAAACTAAGCGGATGGAATCAAAGCTACTGAGCATCAGGGAATTCGACATTTGACTTAGACTGTGAACCAAGACTTCAGCATCACTCTACTGACCTCAGTGTTGTCCTGCAGCTCTCTGGGTCTGTTTGCTCACTGTGTCTCTGCTTTCTCAGGATTTTAAAGTGTCTCAGGATAAGACGGGA[C/T]AGACTAAAGTGGGCGATCTGTCGGCGGAGGACATGAAGAAGGTGCGCAGGCTGGTCCTAATAGAGATGAGCGCTCTGTTCGACACGTGCGGAGTCGAGGTCAAGGCTCATAAAGCACTCAAGGTCAAAGTCAGAGGTCGGTCAATCTGTTTTATTCATTAATTAATTACTTTTTTCGGCTTAGTCCGTTTATTAATCCGGGGTCGCCACAGCAGAATGAACCGCCAACTTATCCAGCATGTTTTTACGCAGCGGATGCCCTTCCAGCCGCAAATCTCTGGGAAACATCCACACAGACTCATCCACACTCATACACTATGGAAAATTTTGCCTCCCTGTACCACATGTTTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACATGAACGCAGGGAGAACATGCAAACTCCACACAGAAACAACAACTGATCCAGCCAAGACTGGAACCAGCAATCTTCTCGCTTTGAGGCGACTACCTACTGCGCCACTACG

Associated Phenotype:

Not determined