ZMP
rasa1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate RAS p21 protein activator (GTPase activating protein) 1 (RASA1)
Human Orthologue:
RASA1
Human Description:
RAS p21 protein activator (GTPase activating protein) 1 [Source:HGNC Symbol;Acc:9871]
Mouse Orthologue:
Rasa1
Mouse Description:
RAS p21 protein activator 1 Gene [Source:MGI Symbol;Acc:MGI:97860]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10485 | Nonsense | Available for shipment | Available now |
sa15062 | Nonsense | Available for shipment | Available now |
sa20521 | Nonsense | Available for shipment | Available now |
sa15906 | Essential Splice Site | Available for shipment | Available now |
sa33700 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9711 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10485
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051518 | Nonsense | 324 | 972 | 8 | 26 |
ENSDART00000139824 | Nonsense | 319 | 952 | 8 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 49709854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 47275552 |
GRCz11 | 5 | 47927063 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGATTAGCCCCACTCCCAACAATCAGTACATGATGGGAGGACGCTACTA[T/A]AACAGGTAGGAATGCAGGCTGRGGTTTAAATGCCTGAAAGCATCAACTGA
Long Flanking Sequence:
GGTTTTGGTTGTAGGATATGTTTTCTCATAATCTAAAGGCACACCAGGACGATTTTGAGTTAATACAAGGATTATGGAAGGAAAAAACAAATAATGACAAACGTAGACTGTTGGATTAAATATATATTTTTTAAATAATAAACAAATAATTAAAATAAAATATCCGTTAACCACTTCTGATTAATTTGTGTTTGACTGCAATTAGGCTCACATTAGCATAGATAACAAATGGTAAATATTCTTACAAGAATTAGAGGCAAATTGCGTACATTAGAGTATAAAAGAAACTGCCATTATTTCATAACTGCCTTTGAGGTTTACTCAAAAGCAGGTCTAACACTCTTTCTTCTCTTAGTTGGCCAGGTCTGCAGTTTTTTGGTCAGGCCCTCAGACAACACACCGGGCGATTACTCTCTCTTCTTTCGTACCAATGAGAACATCCAAAGGTTCAAGATTAGCCCCACTCCCAACAATCAGTACATGATGGGAGGACGCTACTA[T/A]AACAGGTAGGAATGCAGGCTGAGGTTTAAATGCCTGAAAGCATCAACTGACTTGAGAATAACCACTCATAACCCTAATAAATATATTGTTTTTCTTTATACTACAACATTTTTTTCAAGGCTATGTTTGTAATTTAACAAAAAAAAAAAAAATTATTTACATTCTTAATGGTCATTGTGATGATTGTATATATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTTTACTAACACTGACTTTTGTCTGTTTGCATAATATGCGAAGCGACAGAAGCATTTAAATACCACAGACATTCAGAAGCACAGAATAGTGCATTGCACTTGCAACTAAATAAACAAGTTTATAATTTAATTAATAAATCTTAAACCTCCTTAACATCACTAAAAGTACATGCTGGATGACTGATGACCCTGTTTGCCCTGATTTCTCAGATCTACCATTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15062
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051518 | Nonsense | 368 | 972 | 10 | 26 |
ENSDART00000139824 | Nonsense | 363 | 952 | 10 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 49715088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 47280786 |
GRCz11 | 5 | 47932297 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGCAAAAAGAGCAAGTTCTATCTGATTTGGTTGATGGCAGAGAAATATA[T/A]AACACTATTCGACGAAAAACAAAAGATGCTTTCTACAAAAACATCGTCAA
Long Flanking Sequence:
TATGAAATAAATAAACTTGCTAGAGAATAATATCTAAATGCAGATTAGAATATAATTTACCCACAAACATCATTTCTGTACAGACTCGTAACAGATTTCTCAGATTTTCATTTCCACTGCATGTCTCCACAAAGCATTTTAGAGATTAAACCTTGTCCCAAATATTGTGGCGCACAGCAAATTTAATTAAAATGCAATACTTTTTAATTTTCCACTCAGCAATGAAAAATCACAGAACTTTACTTTCAGACAGTCTCTAATTAAGTAATGCTTTTTTCCTCTCTTAGTGTTGATGATATTATCGAACGTTACCGAAAAGAGCAGATTGTAGAAGGATATACCCTGAAAGATCCTGTCCCAGTCCAGGTAAATGAATCTCACTGTAATATAATCAAATAATTTTATACCTCTTAATAACAGCCATGACATTGTGTTGTTTCTTTGTTGTATTAGCAAAAAGAGCAAGTTCTATCTGATTTGGTTGATGGCAGAGAAATATA[T/A]AACACTATTCGACGAAAAACAAAAGATGCTTTCTACAAAAACATCGTCAAGAAAGGATATCTTCTCTTCAACAAAGGTACCCATGATTACTTTTGTTTCCATCCAGCTGCTCTTCTCGCTGAGTTTGACTCTAGTAGTGTTTGTATTCGTCGCTCAGTGGGACTTGGACTGATCTTGAGAGGATGTGGGTAATTTGAAGCACATAAGCCCCATGCGAGTGTCTTTGATCTCCTGCGAAACGAAAAAGAGGGCTCTTTACAGACAGCTTAGGATGAGCCATGCTGAACAAAAAGAAAAAGCGTGTACCTTAACGCACACAGAGCTGTTCAGTTCAATGACACTGACTCTGCTTAATAAGAGATTTGGTTCTAGGTGGGGTTTGCTGCTGCTGATAAAAGTGTATTAGTCTGAATCGGTTCTGACACCCTGTCTGGTTATTATTCAGCTGTTGTTTGTATCTAATATCCAGATGGTTTAATAGGTGCTAAAACTTTTATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20521
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 |
---|---|---|---|---|---|
ENSDART00000051518 | Nonsense | 373 | 972 | 10 | 26 |
ENSDART00000139824 | Nonsense | 368 | 952 | 10 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 49715101)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 47280799 |
GRCz11 | 5 | 47932310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTTCTATCTGATTTGGTTGATGGCAGAGAAATATATAACACTATTCGA[C/T]GAAAAACAAAAGATGCTTTCTACAAAAACATCGTCAAGAAAGGATATCTT
Long Flanking Sequence:
AACTTGCTAGAGAATAATATCTAAATGCAGATTAGAATATAATTTACCCACAAACATCATTTCTGTACAGACTCGTAACAGATTTCTCAGATTTTCATTTCCACTGCATGTCTCCACAAAGCATTTTAGAGATTAAACCTTGTCCCAAATATTGTGGCGCACAGCAAATTTAATTAAAATGCAATACTTTTTAATTTTCCACTCAGCAATGAAAAATCACAGAACTTTACTTTCAGACAGTCTCTAATTAAGTAATGCTTTTTTCCTCTCTTAGTGTTGATGATATTATCGAACGTTACCGAAAAGAGCAGATTGTAGAAGGATATACCCTGAAAGATCCTGTCCCAGTCCAGGTAAATGAATCTCACTGTAATATAATCAAATAATTTTATACCTCTTAATAACAGCCATGACATTGTGTTGTTTCTTTGTTGTATTAGCAAAAAGAGCAAGTTCTATCTGATTTGGTTGATGGCAGAGAAATATATAACACTATTCGA[C/T]GAAAAACAAAAGATGCTTTCTACAAAAACATCGTCAAGAAAGGATATCTTCTCTTCAACAAAGGTACCCATGATTACTTTTGTTTCCATCCAGCTGCTCTTCTCGCTGAGTTTGACTCTAGTAGTGTTTGTATTCGTCGCTCAGTGGGACTTGGACTGATCTTGAGAGGATGTGGGTAATTTGAAGCACATAAGCCCCATGCGAGTGTCTTTGATCTCCTGCGAAACGAAAAAGAGGGCTCTTTACAGACAGCTTAGGATGAGCCATGCTGAACAAAAAGAAAAAGCGTGTACCTTAACGCACACAGAGCTGTTCAGTTCAATGACACTGACTCTGCTTAATAAGAGATTTGGTTCTAGGTGGGGTTTGCTGCTGCTGATAAAAGTGTATTAGTCTGAATCGGTTCTGACACCCTGTCTGGTTATTATTCAGCTGTTGTTTGTATCTAATATCCAGATGGTTTAATAGGTGCTAAAACTTTTATGCCTTCAATGCCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15906
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051518 | Essential Splice Site | 739 | 972 | 18 | 26 |
ENSDART00000139824 | Essential Splice Site | 734 | 952 | 18 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 49732880)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 47298578 |
GRCz11 | 5 | 47950089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTTAAAGACACCATACTGAAGATCATGGAGAGCAAGCAGTCMTGYGAG[G/A]TACAGCAAATAAACAAATAATAATATCCCACTTTTAAAAGGATAGTTCAG
Long Flanking Sequence:
AGAACTAGCAATAAAGGCACAGGCACAGCTACATTGTGTTCATAGCTGAAAATTATAAAATACTGTAAGCTGTAATAAATAATTTAATGGGTGTTTTGAGCTGGAACTTTACAGACACATTCTGGAGACACAAAAGATGTCTCTTAAATCTTGAAAAATGGGTAAAATAGTTGCCCTTGGGTTAGCAACATAAATTGTGACTTGTCACTGTAGCTTTTAATTTATTTATTTTTTTTGTCATATTCGACCTATAGTCCGAGAATTTTTTTTTTTTAATTTGAAATCAGTACACTTGTTAATTGCCTAGTGTTTACAACACACCTTTCTACATTATGTTGTTTGGTTTTGATGTTGCAGATGAGGCCACAACGCTGTTTCGTGCCACCACTCTGGCCAGTACATTGATGGAGCAGTACATGAAGGCCACGGCTACACCTTTCGTCCATCACGCTCTTAAAGACACCATACTGAAGATCATGGAGAGCAAGCAGTCATGTGAG[G/A]TACAGCAAATAAACAAATAATAATATCCCACTTTTAAAAGGATAGTTCAGCCAGAAAGAAAATTCAGTCATCAATTACTCATCCTCTGTTTATTCCAAACTTGTTTGAGTATTTTTTTTTTTTTTAACAAAAATGTAGATCTTAAAAAAGTTTTGAAACTGATAGTTGTTGACTTTTATACTATATATTCTTTTTGCTACCATGGAAGCCAATGACTACCAGTTTACAACATTCTTCAAAACATCTTTTGCATTTATCAGAAGAAATTAACTCATCAATGTTTTGTTTGAGGGTTAGTAAATGGGTGAACTGTTTCTTTTATCTCATGCTCTGTTACCTTAAGATCTGTAAGTGTTGTCTTCTGTTCCTCCTGATGTGTAGTGTATATTATATCTGCATCATGTTCTCTCCAAAGCTTTGGATAAATTGGCTTTTGTGTGATTTCTATGATTTTCATTGAATTGACTTCTTTTGTGAAGTAAAATTTTTATATGGAACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33700
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 |
---|---|---|---|---|---|
ENSDART00000051518 | Nonsense | 788 | 972 | 20 | 26 |
ENSDART00000139824 | Nonsense | 783 | 952 | 20 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 49736336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 47302034 |
GRCz11 | 5 | 47953545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGTCCATTTCCTGTCCCAGGACCCTGAGGTACATTTATGGCTGTCTT[C/T]AGAAGTCAGTGCAGCAGAAATGGCCGACCAACACTACAATGAGGACCCGA
Long Flanking Sequence:
ATCTGCTCTGTTCATCGGCTTACTGTAGACCGGGCAGAGCCAATAGCCTTGGACCTCAAGCTTAGAGGCTGAAATCATTCCACGTTAAAAGTAAAAAGTTCCAATAGCAAAAGGGAGATTAATTACTACATATGTGTATATTTATTTACTAATCACAAACAGAATATAGAACTTACTTTCTGTTTTTTATTTGCTAATGTCTTGTGGGCGAAAGCCAGGTTTGTTGTAACGCAAGCGTTACAGAACATGTACTGAGTAAAATATTTCTGAAAATGTATTATTAATGCCTTGCACTACTACGTTACAAGGAAAAAGAAATAAGTTACTGTAATACATTACTTTTATAATGCATTACTCCTAATTATTACTATATTTATTACTATATTACTGTCCTGTCAATGTCATATACATTGGACACTTACTTTTACAAAGCAGTTTATAGAGTTGGTTGATTGTCCATTTCCTGTCCCAGGACCCTGAGGTACATTTATGGCTGTCTT[C/T]AGAAGTCAGTGCAGCAGAAATGGCCGACCAACACTACAATGAGGACCCGAGTCGTGAGGTAACACCGTGCAAACACGCACAAATATAGCTTGACAAAGAACAGCCTCTTGCAAAGTGCTAAAATGTGTTTGTGTGTGTCCTCCAGTGGTTTCGTCTTCCTGAGACTCATCTGTCCAGCCATCCTCAACCCCAGAATGTTCAACATCATCGCTGGTAAGTGCAAAGCCTCACTCACAAGCTTATTTACCTGATGCAACACATTTACCTCAGGTAATCAGATTTTCACTCTGATTAAGAGTTATTTTTTAAATAAAATTGCACATTTAATACACATTTAGCATTTACAAAATTATAAAAAGGTTTTTAATATATTTATATAAATAACATATTCGTATCTAATATTTATAATATGTTATTTTCATTTTACTAAAATGTTAAAAAAATCTATACAGTAGTAATTTTATACATATACATTTTCAATAGTCTGTTGAAATCACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9711
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051518 | Essential Splice Site | 859 | 972 | 22 | 26 |
ENSDART00000139824 | Essential Splice Site | 854 | 952 | 22 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 49738700)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 47304398 |
GRCz11 | 5 | 47955909 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGCAAAGTCTGTGCAAAACTTGGCCAACCTGGTGGAGTTTGGTGCCAAG[G/T]TGTTTAGATTTTCACGCTSAGTTCTAAAATGATCTKTGCTGAGAGAATGC
Long Flanking Sequence:
TGCCTTTCTAACAGCTGGAAGGAGTATAGCCATTCTCCTCTGACATCAACAAGGCATTTGCAACCACCTAAATCACCTTCCTTCCCCATTCTGATGCTCGGTTTGAACTGCAGCAGATCATCTTGACGATGTCTACATGTCTAAATGCATTGAAATGCTGCCATGTGATTGGCTGATTAGAAATTTTGGTAACAAGCAGTTGGACCTGTGTACCTAATAAAGTGGCTGGTTAAGTGTATGTGCATGACATCATGCAATTTTAGACCCCCAAAACAATTAAAATGAAAAGCTCGAACACAAAGTTTTGTGTATTTTGTTGAACATTGTGTTGTGTAAATCCCCTCTAAAGATATACTGGTATCGGTCCAAACATAATATTAACGATGATGCAATCGTGTTTTGTCTTTTCAGATCCTCCATCCTCCACTGCAGGCCGGACGCTCACGCTGGTAGCAAAGTCTGTGCAAAACTTGGCCAACCTGGTGGAGTTTGGTGCCAAG[G/T]TGTTTAGATTTTCACGCTGAGTTCTAAAATGATCTGTGCTGAGAGAATGCTAATGTTGTGCTGATGTGTTTGTGTTGCAGGAGCCCTACATGGAGGGAGTCAATCCTTTCATCAAGAACAACAAACAAAGGATGATCATGTTTCTGGATGAGTTGGGGGTAAAGTTTCCTCTATTCATTTTTAAAGCAGCATGGCTCAGTTTATGAGTACTGTCTGAACCCATTTTCTCTGTTCTGCTCATCCAGAATGTTCCTGATCTCCCCGAATCCACCGAGCACTTTAGGACTGATCTGTCCCGTGACCTTGCTGCCCTGCACGAGATCTGTGCTACTCATTCGGACGAACTCCGCACCCTCAGCAACGAGAGAGGAGCACAGCAGGTATGGGTCTCTTTTGCAGGGCATGCTGGGAGGAAATATAGTGCATCCAGAAGTTTCTATTCATAGCGCTTCCCTTTTTAACATTTTTTTTATGTTACAGCCTTATTCCAAAATGGATAA
Associated Phenotype:
Not determined