ZMP

LOC100331813

Ensembl ID:

ENSDARG00000078775

Human Orthologue:

RASA2

Human Description:

RAS p21 protein activator 2 [Source:HGNC Symbol;Acc:9872]

Mouse Orthologue:

Rasa2

Mouse Description:

RAS p21 protein activator 2 Gene [Source:MGI Symbol;Acc:MGI:2149960]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa10677	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa10677

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
ENSDART00000114993	Nonsense	448	823	14	24

Genomic Location (Zv9):

Chromosome 18 (position 39417234)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	41129626
GRCz11	18	41119818

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TNNAGGAGAATCTGCARGGTTATGTRCAGAAGGTTTTTACATCTATAACA[C/T]ARTCCAGCTCTAGCTGTCCCCCCCTCATGTGTGAYGTCTTCAGGTCACTC

Long Flanking Sequence:

CCAAATAATTTTGATGAACTCTGGGATTCCTGCAAGAACGCTTGTTTGTCATTTCAGATGACTTTATTAATAAGTTATTTGAGTCATTGCAGAGATGTATCGATGCTGTCCTCCATGCTCATGTAGTCATACACAATATTAATTATTTTTCCTCTGCACCATGACTTATATTCTAACATCAGATCTTACTGTACTAATTAAATAATTAAAAATCAAGACATGAGCGTATTTTATTTTTGGTAAAATAAGCGTAATCTAGAGGCGTTAGCCACTTCTGATACCAAATGATCAACTAGAAGTCAAGTTATTATTTGTTGTTTCTAAAACCTGGATAGGCGACAAGACTTTTGTCAGGTAGTGTAGTTCTTAATTAGCCCTTTAAGCCTATAGAGTTAAAAAAGGTCTAAAAAGTAAGTATTTATCTACATATAGTGTGCATTTCTGTGTGTGTTCAGGAGAATCTGCAAGGTTATGTACAGAAGGTTTTTACATCTATAACA[C/T]AGTCCAGCTCTAGCTGTCCCCCCCTCATGTGTGACGTCTTCAGGTCACTCCGACAACTCGCATCGAAACGCTTTCCAGGTGACACACTTTTACTCTCACTTTCATTCACATGTGCAAGCTTATGTTTAGTCTGGGATTCTTTCAGTGTTTGAATTTTGTCATGACCTCACCACTAGGAGGCGCTAGATACCCAATCATAACTAATAATCTGTGTTTGTGTGTCTCGCCACAGCTGATCCTCATGTTCAGTACTCGGCGGTCAGCAGTTTCATCTTTCTGAGGTTTTTTGCGGTGGCAGTTCTCTCTCCACACACTTTCCAGCTGAGATCCCATCATCCCGTGAGTGTGTGACAAAAACAGACATGCTAACAACAGTTATAGGCATAGGTTAAAAGGCATAGTTTACCCGTAAATGAGCATTTGCTTAACCTTAAAAGGTGCAAAAGGAGATCTTGGAAAATGCAAACATTAACCTGATAGCACTGTAAGCCTACGTACGT

Associated Phenotype:

Not determined