ZMP
rassf6
Ensembl ID:
ZFIN ID:
Description:
ras association domain-containing protein 6 [Source:RefSeq peptide;Acc:NP_001038804]
Human Orthologue:
RASSF6
Human Description:
Ras association (RalGDS/AF-6) domain family member 6 [Source:HGNC Symbol;Acc:20796]
Mouse Orthologue:
Rassf6
Mouse Description:
Ras association (RalGDS/AF-6) domain family member 6 Gene [Source:MGI Symbol;Acc:MGI:1920496]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21682 | Nonsense | Available for shipment | Available now |
| sa27575 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa12501 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21682
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 |
|---|---|---|---|---|---|
| ENSDART00000000887 | Nonsense | 101 | 338 | 5 | 11 |
| ENSDART00000136932 | Nonsense | 139 | 227 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 10 (position 13185038)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 13263129 |
| GRCz11 | 10 | 13221248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAATTATGTGTTTTGTGATTCGATCAACTGTGCCATTAGGGGTATGACA[C/T]GATGGGGAGAATTTGACAACCTTCACAATATTGCTGAACTGGAGGAAGCT
Long Flanking Sequence:
GACCCCGTATTAATAAAGGGACTAAACCGACAAGAAAATGAATAAGTTTAACATTTTCGTATGTAATGACTCAAGTAATGAAAGGAGGACTATTAGTTTTACATGCAATGACTTTTTAGCATTCAAGTTTAGTTAATTTTGACTAACATGACATAAGCTAATGATAATGTTATAAACAGAGAGAGTTGTGAAAGCAATTGATGCATGTCCAAAAGCTTTTGCAATTTGCTGGAAGGAATGAGAAACTGCTACTATGATGTGCACAAATGACTAATTGTTTTGAGAAATGCATTAACTGTCAGGCAAATGTAAATAGTGTTGTGAGAAATGCACAAAAGCCACTGAGAAAAACTGTAAGTGTTTGAATCCTATATTTATGTTTTTTAAAGCATGAAAGAGAATTAGTGCTGTTTTAGGCTTTGTTGAAGATTCTGTCTTATGTTTTCTAATTCAATTATGTGTTTTGTGATTCGATCAACTGTGCCATTAGGGGTATGACA[C/T]GATGGGGAGAATTTGACAACCTTCACAATATTGCTGAACTGGAGGAAGCTGGATCACCTGAAAATCCTACTGAAGGTTCAGTTTCTTTAACATTATTTGATGTTACAGTAGAATTTGGACTATGGTAACACAACTGATGGATCATATATGGTATTTCAGAAAATAAATGAATAAATATTAATTTACTTGAACACTTGTTCTCTTAGTAGAACATTAAAAAGGATATTTAGGCAAAATTGTGATTCTTGGTGAATAACAAAATACATATTCATGCAAAACAAAATTAATACTGTAATAATGTTTCCCTGAGAAGTTATAAAGGAAATCGATCAGTCTGTGTAACAAAGATCACAAAGAAGAAAGCATAACATTTAATCCATAGCTTTTAGTGCATCTATAAGAGTTATGGTTGTTAGGGATGGCCCAAATGGACTTAAAAGATTTATCACAATGTTTTTTGGCATTTGTGATAAGAATATCAATGGCAATATAATTCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27575
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000000887 | Essential Splice Site | 241 | 338 | 8 | 11 |
| ENSDART00000136932 | None | None | 227 | None | 7 |
Genomic Location (Zv9):
Chromosome 10 (position 13190316)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 13268407 |
| GRCz11 | 10 | 13226526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAACAGTCCAAATGAATTTTCCCTCTACTGCATTCATCAAACTGGAG[G/A]TATGTAGAACCCTCACTTTATTCCAAATCATACAAAAGCTGAAAAAAAAA
Long Flanking Sequence:
CTGAATTCACCTATGATACAAAATATCTATATTCATAAAATATAACTAAACAAACTGTATTAAAGTAAACAATAAAAACAATTTGGAGTAAATAAAACGTAAATAAATAAACTTCCTAACCTATTACTTCCTTTTTTCTGTAGAATTTAAAAGAAAATTTTAAAAAAATGTTTAAATTCTGAACACACCATTTTTCCTGATTTTTTTTTTCGATGACTTTGTTATTGTTTTTTTTTATAATTCTCTGAGTCATTTTGTTATTGTAGACATCTGTTTTCACACCATCATTTGGAGCAACCACAAATGTGCACATTAACAGCAGGATGACGACACAAGAGGTCATTACACAACTGCTACACAAATTTAAAGTAGGTACATGTATTATTACTGAAGGTTCGATACATAAGAACCACAGAGTTTACAGTTCCATTTAATTTTCTTTTTGCAGGTAGAAAACAGTCCAAATGAATTTTCCCTCTACTGCATTCATCAAACTGGAG[G/A]TATGTAGAACCCTCACTTTATTCCAAATCATACAAAAGCTGAAAAAAAAAGCTCAATCATTGACACCACCATTATTAAGACCAAACCAGAAAATATACAAAACAAAATGTGTACATGCTTTTAGGGTATTATGCTTGTTCAAACTACTTAATTAAAATGAGCTAAAACAACACAATTCTTGAGATTTCATTAGGACAACTTGTTTTATGTTTACTCTACAGAAATTTGTTGAAAGTGTTAAGGTAACTAAATGAATTTGTGTTGGGGTAATATGAATGAATTGTGTGGAACCCTACATTTTTTAGAGTGTATCCAAACCCAAAAAGTATCAAATGAATATAAATATAGATTAAGCTATATGTATAAGATAAGTATTAAAATTAATTCTATTGGATTTTCTAATGACAATATCATGCCTTTTTTTTTTTCTTATATTCTGTGCAAAATTCTTTACAGATACCCAGTCCTTAAAGACAAAAAAAAAAAAAAAAAAGAATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12501
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 |
|---|---|---|---|---|---|
| ENSDART00000000887 | Essential Splice Site | 281 | 338 | 9 | 11 |
| ENSDART00000136932 | None | None | 227 | None | 7 |
Genomic Location (Zv9):
Chromosome 10 (position 13198333)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 13276424 |
| GRCz11 | 10 | 13234543 |
KASP Assay ID:
2260-2994.1 (used for ordering genotyping assays)
KASP Sequence:
TTATGAAGATGTTCCTCATGGATACAGACGAAGAGGAAATTAGTCTTGAT[G/A]TAAGTCTAGCTCTTYAGGTATTACAGAAAGTGTATTYTAYTCAAATAAGC
Long Flanking Sequence:
TCCAAGTTTTTAAATATTGTCATGGCATTTTATTATTTATGTAAATAGAATAGAAATAAACATTCATTGAAAAAACTATATATTATAAGGCTGCTTTATTAGTATTGGTTTGTGGCTGGAAGGGCATCGGCTGCGTAAAGACATATGTTGGAATAGTTAGTGGTTCATTCCGCTAAGGCGATTCTTGATAAATAAGGGACTAAGCCTAAATAAAATGATTAAATTTATTCATGAAAGTTCATGACCCCTTTAATGAAACCAAAAGCTGTGAATGCCAAGTGTTCCAGGACTAAATGTACAAGTTATGTGGAGTGAACTACGAATGTGAACACGCCCAAAGTTTTCAGTCACATTTCTGATTATTATATCCATCTTTTATAGAGAAGAGAAGGTTGAGCAGTTCAGACCTGCCCTTGTGGGAGCGTGTTCTACAAGGACCATCAAACTTCATTATGAAGATGTTCCTCATGGATACAGACGAAGAGGAAATTAGTCTTGAT[G/A]TAAGTCTAGCTCTTCAGGTATTACAGAAAGTGTATTTTACTCAAATAAGCAAAACTAACGGGCCATTGCATTGATTTAACAGGTAGCTCAGTACCTCAATTTAGAAATGCCCATTTTGAAGGTTATCCTGCAGAAACTGGAAGAGCAAGAGAATCTGGAGATACAAAGGATAAAAGCAAAGTAAGTCTAAGGGTGTGTTGTTGTCTTTTTACAACTTTTACTTTCACAGTCATTCACTTAAAAAAATAAATAAATTGTATATAAAAGCATCTTGAGAGTGTGGTGAAGCCTACAGTATTGCTTAAGTGAGCCAATAAGTCAAGTTATTACTGCCAAAGAAATTCCTCTATTGATTTTAAAGATTATAATACACAATATAATTCAGTAACATTACACAAGCTTATATACAAACAAAAAGTTCCAACAAAGCCAGAGAAAAACATTTGTGTCTCAGAACAAAGTTGCAGAAATTCCTTCTTGTATGTATCTGTTTTAGAACA
Associated Phenotype:
Not determined