Busch Lab

ZMP

ENSDARG00000079791

Ensembl ID:
ENSDARG00000079791
Human Orthologue:
RASIP1
Human Description:
Ras interacting protein 1 [Source:HGNC Symbol;Acc:24716]
Mouse Orthologue:
Rasip1
Mouse Description:
Ras interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1917153]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa17863 Nonsense Available for shipment Available now
sa9151 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa19016 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21990 Missense Available for shipment Available now
sa41926 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17396 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa17863
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111976 Nonsense 102 1012 3 28
Genomic Location (Zv9):
Chromosome 12 (position 877214)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 674338
GRCz11 12 680279
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTTCTATTCCCGCAGGTATTCAGTGAGTAAAGCAGACGCGGGTGAGTA[T/A]GTGCTGTGYGATGTGATTGGCTGYGTGGTGAACCACAGCTGGAGGACGGA
Long Flanking Sequence:
ATTTATCTATCCATCCATCCATCCATTATCCAACCATATGTGTATCCATCCATCCATTCATTTACTTGTTTGCATATCCATCCATCCATCCATCCACCCATTAGTTTATTAATTTGCATATCCATCTATCCATCCATCCATTTATTTGTTTGCATATCCATACATCTATCCATTCATCCATCTATCATTCATCCATCCATCCATCCGTATGCATATCCATCCAGTCGTTTGCGTCTCTATCCATATGTGTATCCATCCATCCATTCGTATGCATATCCATCTATTGAACCATATGTACATCCATCCATCCATCAATTCATCCACCCATCTGTCCATCTGCTTATCCATCCATCTATGTGTAAATGTGTTAAGCTTAAAGGTGATGGAAATTACCCAAATTTAATTTAATTTAATTTAATTGTATTTTGTTTTGTTTTGTTTTGTCTTGTTTTGTTCTATTCCCGCAGGTATTCAGTGAGTAAAGCAGACGCGGGTGAGTA[T/A]GTGCTGTGCGATGTGATTGGCTGCGTGGTGAACCACAGCTGGAGGACGGAGTGTGTTCGCGCGCTCGGAGAAAATGAGAAACCGCTCCTGCTGCAGTCGCTCTGGAAACCCAGAGAAGGATTCGCTCGCCGGTTCGAGATCCAGCGCAAGGCCACGCTGGAGGAACAAAACTCCAGAGACGAGGACACGCTGACCGCTGGTACGACACACACAATGACAGTAATTAGCAGACAGCAGATTGTGTTTGTATGCTAAATGCTCGATATGTTTTGCTTATATTGAAATATTGTCATCTATTTGCATGCTGAATCATGATTGGTCTTAATTTTTTTCATCTCCTTGGATTCTGGATTGTGATTGGCTTTCATTTGTACATCTATTTGCATGCTGAATCATGATTGGTCATCAATCTTTCATCTGTTTGCGTTCTGAATTGTGATTGGCTTTCATTTAAACAACTATTTGCATGCCGCATTATGATTGGTCTTCATTTTGTCTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9151
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111976 Essential Splice Site 168 1012 3 28
Genomic Location (Zv9):
Chromosome 12 (position 877014)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 674138
GRCz11 12 680079
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCACGCTGGAGGAACAAMACTCCAGAGACGAGGACACGCKGACMGCTG[G/A]TACGACACACACAATRACAGTAATTAGCAGACAGCAGATTGTGTTTGTAT
Long Flanking Sequence:
CCATCCGTATGCATATCCATCCAGTCGTTTGCGTCTCTATCCATATGTGTATCCATCCATCCATTCGTATGCATATCCATCTATTGAACCATATGTACATCCATCCATCCATCAATTCATCCACCCATCTGTCCATCTGCTTATCCATCCATCTATGTGTAAATGTGTTAAGCTTAAAGGTGATGGAAATTACCCAAATTTAATTTAATTTAATTTAATTGTATTTTGTTTTGTTTTGTTTTGTCTTGTTTTGTTCTATTCCCGCAGGTATTCAGTGAGTAAAGCAGACGCGGGTGAGTATGTGCTGTGCGATGTGATTGGCTGCGTGGTGAACCACAGCTGGAGGACGGAGTGTGTTCGCGCGCTCGGAGAAAATGAGAAACCGCTCCTGCTGCAGTCGCTCTGGAAACCCAGAGAAGGATTCGCTCGCCGGTTCGAGATCCAGCGCAAGGCCACGCTGGAGGAACAAAACTCCAGAGACGAGGACACGCTGACCGCTG[G/A]TACGACACACACAATGACAGTAATTAGCAGACAGCAGATTGTGTTTGTATGCTAAATGCTCGATATGTTTTGCTTATATTGAAATATTGTCATCTATTTGCATGCTGAATCATGATTGGTCTTAATTTTTTTCATCTCCTTGGATTCTGGATTGTGATTGGCTTTCATTTGTACATCTATTTGCATGCTGAATCATGATTGGTCATCAATCTTTCATCTGTTTGCGTTCTGAATTGTGATTGGCTTTCATTTAAACAACTATTTGCATGCCGCATTATGATTGGTCTTCATTTTGTCTCCTGTTTGCATTTTGAACTGTGATTGGCTTTCATTCGTACGTCTATTTGCATGCTGCATCATGATTGGTCTGCATTTTTTCATCTGTTTGCACTCTGGATAGTGATTGGTCTTTATTCGTACATCTATTTGCATGCTGAATCATGATTGGTCATCAATCTTTTATCTGATTGCATTCTGAATTGTGATTGGCTTCCATTCGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19016
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111976 Essential Splice Site 305 1012 7 28
Genomic Location (Zv9):
Chromosome 12 (position 872564)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 669688
GRCz11 12 675629
KASP Assay ID:
2260-4762.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGCGTCACTGCTGCATCCGGCGAAAGGACATCAACACTGGACCCAG[G/T]TTATTATAGCTTATTTTGAAAAAAAGTTTTATTTTGATACTACACTGAAA
Long Flanking Sequence:
TAGCGGCACAGAGAAGAAATGGCAAATGTGGCCCAGTTATCTTAAAACACATGTGGGCCACTTTGGGCAAATATTCGGCACAGTTAGCTATGGCTAATGTGGCTCTGAACTTAATGTGGCCCAGAGAAGAAATGGCAAATGTGGCCCAGTTATCTTAAAACACATGTGAGCCAAATATTAGAGGAAACACTGTGAACAACTCCTGAATCTGTTCAAGAACATTTGGGAAATATTTGAAAGAAATTCACTGGAGGGCGAATCATTCTGACTTCCACTATCCGTACTGACTAACTCATATCTGCGTGTGCTGTTGTCAGTGATGATGTGTTTTCCCCTCAGGATCTGCTCCTGTATGCTCTGGTCAGCAGCTGCACGGTGTTCGGTCATCATGTGAATCTCTCTGACACTGAAAGCGATGTGAACGCTGTGTGTCTGTGGGATCCAGATCTGCTGGAGCGTCACTGCTGCATCCGGCGAAAGGACATCAACACTGGACCCAG[G/T]TTATTATAGCTTATTTTGAAAAAAAGTTTTATTTTGATACTACACTGAAATCAAATGCTTTTCCTACTTAGAGTTTTTGTGTTGTTTCTAGTATCAAGAATATAGTATCAATATCAAGAAGCATTTTCCAGACAAGTACAACATATTATGTTGTGAGCTGAAATTAAGTAAGATTTTTCTTAAAATGAGCAAAATAATCAGCAATGGGGTAAGCAAAATAATTTAAATAATTTAAATTGTTTATGGTTTGATTATTATTTCACTTACATCATTGGCAGATTATTTTGCTTATTATTTACAGATTATTTTCCTTGGGCAAAATAAATATTTAGATTAATCCTAAAATATAAAATAAAAAAACAAAAAAATTTAAGAGGAATTTATTAAAAAAATAAATATATCTTTGGGTTGTTCTAAAGCAAAATTATAATGCGATCTAAGGTAAAAAAAAAAAAAAAAAGTAACTTACTTAAATTTTTTAATTTAATTTTCTGATCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21990
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:
G > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111976 Missense 480 1012 15 28
Genomic Location (Zv9):
Chromosome 12 (position 868590)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 665714
GRCz11 12 671655
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTATTAATGTCTTCATCTGTCAGTAAATCTCTCCTCCTGCTGCTGCA[G/A]TGACCGTGAGCTGCTGGTGGCTCTGGAAGCGATGCTCTTCTGGATGTCTA
Long Flanking Sequence:
TTGTTTTGATCATGACTGAATCAAAGTTCTGAATGAATCACTTGAGTGAATGACTCACTCTTTAAGAGAGCCACTTGTTTTGTTCATGACTGAATCAAAGTTCTGAACAAATTAACTGAGCAAACAGCTCACTATTAAAGAGCCAAACATTTTGTTTGTGACTGAATCATATTGTTGAACAAACCAACTGAGTAAACGACTCACTCTTTAAGAGAGCCACTTGTTTTGTTTATGACTGAATCAAAGTTCTGAACGAATTTCCTGAGTGAACAACTCACTCTTAAAGAGCCACTCATCTTGTTCAAGACTGAGTTGAAGTGTTGAACAATACAACTGAGTGAATCATTTAATCATAAAGGTTTTGTTCATGACTGAATCAATTTGCTAAACGAACTAAAGAATGAGTGAATGAGTGAGTAAATGTTCGCTCTGTAAATAAACATTAGTGTACATGTATTAATGTCTTCATCTGTCAGTAAATCTCTCCTCCTGCTGCTGCA[G/A]TGACCGTGAGCTGCTGGTGGCTCTGGAAGCGATGCTCTTCTGGATGTCTAGCTCTCTGCAGCTCCTGTATTTCGTTCAGCAGGAGGTCCCGCGGCTCCAGAAACAGAAGCAGCCCTTCATCACAGCTCATTCAGACGCAGTGGAGCTGCACTTGGCCATTGAGGAGACGCTGAGCGTTCTGGAGGAGGTGTTCATGTTCTCCTTCCAGCAGTGCGTCTACTACATCACTAAGGTCAGAGCCACTGCACATATTATATTATTATGAGATATCTGTCAATAATGTGCAGCTGATATTCTACACATAATATCAGTCATTTAAAAATATAATAATAAACATACAATGTTGACGCAGTCGCGCAGTAGGTAGCGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCGAGCCTCGGCTGGGTCAGTGTGGAGTTTGCATGTTCTCCCCGTGTTGGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTTCAAACACATACG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41926
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111976 Essential Splice Site 627 1012 17 28
Genomic Location (Zv9):
Chromosome 12 (position 862082)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 659206
GRCz11 12 665147
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACACACACACACACACACACACACACACACACACTGTAGCTGTGTTTA[C/A]ATCCAAACATATCCCATCATAAAACATTTGAAATTTCAAAATGAAGATGT
Long Flanking Sequence:
CTGAATGCAGTGAGCTGCTGCCCTGTGATTGGCTGATTAGAAACTTGCGTTAACAAGCAGTTGGACAGGTGTACCTAATAAAGTGGCCGGTAAGTGTATATATACATACACATACACACATCTATCTGTCATATATAATATAATGTGTATATATATATTGTTGCATACAGTGCTGGTGCAACATAATTCCATTCTGCATTAAATGTGTGTGTGTGTTGTTCAGGTCCTGTACACACTCCTGCCGGCCGTTCTGGACAGTCATGCGTTCTCTGCGAGCGAGTGTGTGTCGGTGCAGCGGGTGCTGGAGGTGTTGATGCAGACGCTGCAGACACTCAGAGAACATCACCTTCATCCAGACGTCAGATCACAGCTCTTTTCATACCTGTTCTACTTCAGCAACACACTGCTGTTCAACCTGCTGATGGAGAGAGGTCACACACACACACACACACACACACACACACACACACACACACACACACACACTGTAGCTGTGTTTA[C/A]ATCCAAACATATCCCATCATAAAACATTTGAAATTTCAAAATGAAGATGTTTTCTTGTGTGTTTGTGCATGCATGTGTGTGTATGCACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTTGAATCTGGTGTGTATGTTTATGTGCACATGTGTTTGTGTCTTGAATGTGTGTGTGTGTGCATGCATGCATGTATGTGTGTGTGTGTGTTCAGGCTCAGGAGGAGGCTTCTTCTGCTGGTCTCGTGGTGTTCAGATCCGGGCAAATCTGGATCTGCTGCTGGACTGGACTGAAGCTTCTGGACTCTCAGATCTGGCTCAACATTTCCTGCTCAAACTCTCGTCAGCTGTCAATCTGCTGGCCACGCCCAGAGAAACCCTGCTGCAGGTCTGAATCCAGCCCACACACACACACACACACACACAGAAAACCAGCTTGTTCAACCCAGGCTCATTCTGAATATGTACCCGTGTATACATTTTAGGAGAGCTCCAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17396
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
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111976 Essential Splice Site 891 1012 25 28
Genomic Location (Zv9):
Chromosome 12 (position 858932)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 656056
GRCz11 12 661997
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACTTTTCTCTAATTGGTCAGATGGCYCMTACTCTCCTCTAATTGGTCA[G/A]ATGTCCAATRTTCTAAACTGATTGGTCAAATTACCCCACTCTACTTTAAT
Long Flanking Sequence:
TCCTGTTTGCTGACGCCACCGAACACCCCGAGACAAACTGAAGACGATGCAGAGCAGAGTGAGACCAACTCACACACACCATCAACATTCACTCAGACACAGCACACACACACTGACCCCGATGTTCTATTCAGAGATGATTTGATTGGATGTTTCTGCTTTTTGTCGTCTCTGATTGGTCAGATGGCCTCTTCTCTTTCCTAATAGGTCAGATGGCACCTAATCTACTCATATGGGTCAGATAGCCCATATTCTTGTCTGATTGGTCAGATGACCGCTACTGCACTCTAATTGGTCAGATGTCCCTTATTCTTCTCTAATTGGTCAGATGACCCATTTTCTTGTCTGATTGGTCAGATGATCGTACTCTTCTCTAATTGGTCAGATGGCCCTTGTTATTTTCTGATTCGTCAGATGACCCCTGTTCTTCTTTGACTGGTCAGATGTCCCCTACTTTTCTCTAATTGGTCAGATGGCTCATACTCTCCTCTAATTGGTCA[G/A]ATGTCCAATATTCTAAACTGATTGGTCAAATTACCCCACTCTACTTTAATGGGTCAGATGGCCCATATTGTCCTGTGATTGGTCAGATAGCCTTACTCTCCTCTGATTGGTCAGATAGCTTTATTCTCCTCTGGTCAAATAGCCTTAGCCTCCTGTGAGTGGTCAGATAGCATTACACTCGTCTGATTGGTCAGATAGCCTTAGTCTCCTGTGATTGGTTAGATAGCATTACACTCTTCTCGTTGGTCAGATAGCCTTAGTCTCCTGTGATTGGTCAGATAGCCTTAGTCTACTCTGATTGGTTAGATAGCATTACACTCTTCTCGTTGGTCAGATAGCCTTAGTCTCTCTGATTGGTCAGATATGCTTACTTTCCTATGATTGGTCGGATAGCCATACACTTCTGATTGGTCAGATAGCCTTAGCCTCTTGTGTTTGGTCAGACAGCCTTAGTCTTCTGTAATTGGTTAGATAGCTATACTGTCCTCTGATTGGTTAGA
Associated Phenotype:
Not determined