ZMP
rassf2
Ensembl ID:
ZFIN ID:
Description:
ras association domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_001004676]
Human Orthologue:
RASSF2
Human Description:
Ras association (RalGDS/AF-6) domain family member 2 [Source:HGNC Symbol;Acc:9883]
Mouse Orthologue:
Rassf2
Mouse Description:
Ras association (RalGDS/AF-6) domain family member 2 Gene [Source:MGI Symbol;Acc:MGI:2442060]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2417 | Essential Splice Site | F2 line generated | Not yet available |
| sa41277 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2417
Status:
F2 line generated
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048819 | Essential Splice Site | 94 | 325 | 4 | 10 |
| ENSDART00000142671 | Essential Splice Site | 94 | 129 | 4 | 5 |
| ENSDART00000146632 | Essential Splice Site | None | 61 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 45063755)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 43016537 |
| GRCz11 | 8 | 43023324 |
KASP Assay ID:
554-2535.1 (used for ordering genotyping assays)
KASP Sequence:
CTCCCTCCTCCACCTCCTGGCACTCGGGCTGTAATCTAGACAACCAGAGG[T/C]CAGATGGTGAACAAGCATATTTAAATGAGCTCTTTAACCTTCTAGAAGTC
Long Flanking Sequence:
GTTGTGCTCTGAAATACAACATTTGAATGTTTGTAAAAAACAAAAAAAAGCCAATGCACAATTGTACAATGCACTCATTATGTAGTTTCAAAATACAATATATTAGCATTTTAATGTAGAAAAAGCCAACGTAGGTCTCTTAAGGAAAAATACAGCAAATGGGCTCTTATATGCAGTTGTGTTATCACTCATATAGCAAGTCATATCTCTCCGGCCCTTCGTTTGGGATGCTTTTCATGAACCGGCCCCCATGACAAACTAATTGAACAGCCCTGGAATATAATAAGTAAAACACAGACAACATAACTTGATATAAGTTATCTTTATATTGTGTTTTTTGCCTGCAGGAAGAGGAGGAGCTGATCATGGAAGGACTCCTTAATATCTCATGGGGTTTGCGTCGACCAATCAGGCTTCAGATGCAGGATGACCATGAGCGAATCAAGCCTCCTCCCTCCTCCACCTCCTGGCACTCGGGCTGTAATCTAGACAACCAGAGG[T/C]CAGATGGTGAACAAGCATATTTAAATGAGCTCTTTAACCTTCTAGAAGTCAATATTTCTTCTGTTATGCATATGTTTATCAATGCTAATAAGGTTTATCTTGCGTTTGGAGTATTTTATTATGCTTTGACTGGAACAATAAGGTTTTTTCATATGTAAATATACAATACAGTCCTGTTCAAAAATGTCCAGTCTGTGAGATTTTTTAAAAAGGTTTTTGTCTTTTTAAATTTATTATGCTTGGTAAAGGCAGGATTTGTTTGTTTGAAAATACAGTAAAACAATAATATTGTAAATGATTCATGCAATTTTACATATATTACGCCCTAAGTCTAGGGGAAACAAAAAGGGCATAATAAACGAAGAAAAAACAAATGTGTTGGGGTGGTGGATTTCCCAAACTAAACAAAACTTAAAGCAAAAGATTCCCTTCGGTCGACAACCAAACTCACACACTCAATTGAGAGTATATATGAAGATATTTATTATAGAGAAATAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41277
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048819 | Nonsense | 149 | 325 | 6 | 10 |
| ENSDART00000142671 | None | None | 129 | None | 5 |
| ENSDART00000146632 | None | None | 61 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 45078646)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 43031428 |
| GRCz11 | 8 | 43038215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGATGTCTCCGCTCAGCTTCTCAGAACTAAGAGCGATGCAGGCGTAT[T/A]GAGGCGGGGCCGGAGACGGTCTCCTAGTGACCAGCGGAGAATCAGACGCC
Long Flanking Sequence:
ATATAAATTGTTTTAAAAAAGTCAGAACGTTTCATTAAGCAATTTAATCCAATACAAATGAACATCGACATTTGTAAATGTATAAAAATGAGTAAATTCACTTCATTAAAAATGTCAAACTTTTACTGTTCAGTTGACATTCCCTTATTAATACAATGTTGCTGATCAGATACAATATTGTTGTAGTCAAATAAATAAATAATAATCCTTATGTTTATGTTCAGTTATTTAGGTGTATAGGCAATGACACCAACCTATTCAACCTAAAACCTGAGGAAAATTAACATAAAATTTCAGGCAGCGCTCAGAGACTTTTGCATATAAACTTAATTGTTCTGAAAGATAACAGTCCTTCAGGCCCAAACAAAAATACTAAACTGATTTTAAACACGCAAATGTTCTGTGACTCATTTCCCTCCTCATTTCCCTTTTTTTTTCTCTGACAGAAGTGTGTGATGTCTCCGCTCAGCTTCTCAGAACTAAGAGCGATGCAGGCGTAT[T/A]GAGGCGGGGCCGGAGACGGTCTCCTAGTGACCAGCGGAGAATCAGACGCCACCGATTCTCCATCAACGGTCACTTCTACAACCACAAGGTGACAGGACGACAAACTGGTTCTCCATGTGTGATGGTTTGAGCATAACTTCCTTCTTCATGCAGTCTCTTCTTCCTCTTTTTAGACTGCTGTGTTCACTCCTGCATACGGTTCAGTCACAAACGTGCGGATCAACAGCTGTATGACCACGCCACAGGTGCTGCGGGTGCTGCTCAACAAGTTCAAGATCGAGAACAGTCCTGATGACTTTGCCCTGTACCTGGTTCATGCCAGTGGAGGTTTGTCTCTAACTGTTTTGTTTTCTTCTAAATTAGGGGTTTTCAACCTGTGGGGCTCCAATGCCTATTAAGGGGGACGTGAGAAATTGAGGCGTGTACTTGAGTAAATTGAACCTTCGCTAAGCCCTGTACTCTTTATTTACTGTTGTTATGCCTATCAAGCTTTCGTGTAT
Associated Phenotype:
Not determined