ZMP
LOC100331813
Ensembl ID:
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 are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36713 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30705 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10677 | Nonsense | Available for shipment | Available now |
sa43161 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36713
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000114993 | Nonsense | 218 | 823 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 18 (position 39434028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 41146420 |
GRCz11 | 18 | 41136612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACAATGTTTCTGAAGGTAACAAGGTCAAGCAGTTACAAAGGGAGGTCA[C/T]AGTTTCATGTAGAGGAGGAGGACATAGAGAAACTGGAGATCAAGTGAGTT
Long Flanking Sequence:
GTACGCCACAGTAACACTCGTAGGACCCACCAGGTGAGTTTATTAACACTTGAAGTCGTCATATATAAGGTGCCCTTACATCACAAGGCTTACTGTAAAGGAACAGAAGTTTGCGTAAAGCAAAATGTTTTCTAATGAAGGTACTTACTGAAAACAGCCAACAGGCATGATTGTGATTTGCTTCTAAAATCAGTCTGTCATAAGTCAGTTTCAGCCTCTGTCTCTGATCTAGTTTGAAATGAGTACATAACATCCGCTCTGATTCAATAATAACATCCTGCTCTGTCTTTCTGTTTCTCTCACACTCTCTTACAGGTCAGACCAGAAGAAAACTAAAGTGAAGAAGAAAACCAGCGACCCTCAGTTTGACGAGACCTTTCATTTTGAGGTACTCCCTCATCCATTCATTGATCTTTAAATCATTTGAATGATAGATACAGTGTGCATAATCCACAATGTTTCTGAAGGTAACAAGGTCAAGCAGTTACAAAGGGAGGTCA[C/T]AGTTTCATGTAGAGGAGGAGGACATAGAGAAACTGGAGATCAAGTGAGTTCTTCCTATCTCTTGTTTTGTTTTATTCATCAGTTTTATTATATTATTGGGGTCAAATGATTTATCACGATTAATCGCATCCAAAATAAAAGTACATATTCACAAAAAATATTTGCCCCCACTATGTATATTTTTGTGTATATAAATATATGCATATTATGCAAACACAAACTATGGCTATGGATGCGATTAATCATTTGAGATAGTTTTAATTTAAATCGATATAATTTTATATTTTTAATTTCTCTCCATTTTTTTAACTGGTGTTTTGTTTTAAGCCTTATATTTTCACTAGCTATGTTTCCAACCAAGAATGCAAATTAGATTTATGCTCAAAACTGGAATATCGCTTAAAACATTCGTGAATAAAGCACCGTTTTCATTCAGCAAGTCAAAAAGAACAAAATAATCACTTTCTGATAATCTGGTGCCAAAGATCAAATAGAAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30705
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114993 | Nonsense | 366 | 823 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 18 (position 39420550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 41132942 |
GRCz11 | 18 | 41123134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCACAACCGCCTGCTGCCCTTTCTCACTGCTGTTGCTGCACTGGAGCTG[G/T]AGAATACACAGTTCAGTATCACAGTTACATAGTTAAAAAAAAAATCATGA
Long Flanking Sequence:
TGAAAAAAAGATAAATGTTTTCCTGCAAAAACATCTTTAAATCTGTTTTATAAGACATGCGTTAACCCCCTTGCAGTGTATAGGTTTGTTTTACGATGGGTTTATGCACTTTTGGATGCTTCAAAATAAAAGCCACTATCCAACACCATTATATAGCATTGAAGAGCTAAAATGTAAAACTACACCAACAATGTCTTCATCTGAAAGAAGAAAGTTATATACACAAAAAAATGGCTTGAGGGTGTCTAAGTTAAGAGGTGATTTAAATTTTTGTTTAAACTATTGCTTTAGGACTGGCAACCGTGTTTAACGTTCTGTTTGTTTGTAACTTCTGTTTATTTCTTTTGTGTGTGTAGCCGATCTCAGCATCAGCAGCTCATGTTCTGGGAGATATTTGCAGGGAGGGTGTCGGATATGATGCACTGCTCCCTGTGGTCAGACTGCTGCTTCATCACAACCGCCTGCTGCCCTTTCTCACTGCTGTTGCTGCACTGGAGCTG[G/T]AGAATACACAGTTCAGTATCACAGTTACATAGTTAAAAAAAAAATCATGATCAACAGTTCTTTAGCTTTTTTGGTTTCTTTTATTTGTTAATATGCACATAGTCCTTATTTTAGTAGTTTATTTTGTTTTGTTAATGTGCATATATCTATTGTTTTTATTTTGTATATTTGTTCATATTTTAAAAAAACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATATATGTATATATTGCTGGATAAGTTGGAGAGTCATACCGCTGTGGCGACCACCTGATGAATGAAGGGACTAAGCTAGAGGAAAATGAATGAATGAATTTATTATTATATATTTTGTTGTTGTTGTTGTTGCTATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10677
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
Mutation Details
Allele Name:
sa43161
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000114993 | Nonsense | 740 | 823 | 22 | 24 |
Genomic Location (Zv9):
Chromosome 18 (position 39395324)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 41107791 |
GRCz11 | 18 | 41097983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGTTGGCTAATATTCAACTGGATATCGACTGTGACCGGGAAACAGAG[C/T]GAATCTTCTCCTTCTTCTCCACCTACCGCTCCAGACTACAGAAGATGGAG
Long Flanking Sequence:
TCAATCTTGCACACTGCACCTTTAAGCAAAGTTAACAAATGATACTTTCCAGTGTATATCACACAATCAGTCTGACCCCAGCAATAATTATTCCAAACATTTGATCTGTATGTAAATGTAACACACTCCTCTACCCTGTTTTGTTTTGCAGATGTTTCAGGTAATCCACTCAGAGAAGCCCCTGTACGTCCAGGCGAGTAACTGTGTAGAGACCAACAGCTGGATTGAGGTGTTGAGTCAGGTCAGCCGGTGTAACCCGGGACGCCTCAGCACATTTCACCTCTCTGCATACGTCGGTGGATCCTGGTTATGCTGTAAGGAGCCCAATGAAAGTGCTCCAGGCTGCAAACCCTGCACTGCGTAAGAAATCATATTAATTTGCACATTTAGTTTATATACAAAAATGTACCTGGTGCCATTATTTTTTATGTTCGACTTCACAATATAGGACAGTGTTGGCTAATATTCAACTGGATATCGACTGTGACCGGGAAACAGAG[C/T]GAATCTTCTCCTTCTTCTCCACCTACCGCTCCAGACTACAGAAGATGGAGGGTGTGTAGCCTTATAACATTGAGAAACATCCCCGTTTACTGTTCATGATTGATTAAAACATACAGTTTATATTAGTCATTAATGTTTAGTCATTAATTCCTTTATATTATGCAAACAAATCATTTTTTTGTATGGTAAAATGATTGGTTTATCACAAGGACGATGATTAAAGCTATGAAACTTGGAGGATATTTCACCAGCAAATTGGGTTTATCTTGTTATCATGACCCCCATAAAATGTACTGATTTGTTTGTGCTGGTCTCTGCAGACGTCTGTGCCGGTATGTCAGTGTATCTTGGGCAGCAGGAGGAGTGTTCGGCCTTCACTATACAGGACCCTAAAGAGACCTTCCGCACCATTAAAGAGCTCGGAGAGGTGCTGGACGAGCTGCAGTCTCACCATGACTCAAAGGGGGCACTAACTGATGAACCAGGCACTATGTAAGGCA
Associated Phenotype:
Not determined