ZMP
rassf2l
Ensembl ID:
ZFIN ID:
Description:
Ras association (RalGDS/AF-6) domain family 2, like [Source:RefSeq peptide;Acc:NP_001002195]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8593 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10991 | Essential Splice Site | Available for shipment | Available now |
sa34887 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8593
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064662 | Nonsense | 41 | 316 | 3 | 10 |
ENSDART00000142028 | Nonsense | 41 | 312 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 20726307)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 20687721 |
GRCz11 | 10 | 20645102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACATCTCAAAACATATAACGTGTATTTTGAAGGAGATGCCCTTCAGTTG[A/T]GWCACAGAGAGRTTGGTTATTTGGCAAGCTAYAGTCTRTTGTTTTGATGT
Long Flanking Sequence:
GGTTGACATTTGCACGCAATTGCTCAGTTATATCAGTAAATTGAAATCAAATTTAATAATAATAGACCTTTTTTTCTGTGTTTACAGGCTTTAATAGATTGATAGTATGTTTTGAGTTTGTTTAGCTTATTTATTTTTTGTTTTTTGTCGAGTTTGAGTGTGTGTTTCTGTGTGTGGGAATCTTGCCTGAGGTTATTTTGCGATTATGAGGCTTGAAGTCATGAGTTTTTCTTCTGGTCGCAGATAAACTTCATTACTTCATTCTTCCGTGTGTCTCCACTGACCCGACATGGAAAGTGTGGATTCAGACAAGATCCAGGTTGGAGAAAACAAATTTGTCAGCAAGTAAGTGCATCTCGTTGTGTGACTGTAAGCTTTCTTATTATCACTGTTTTCTTATATATGACATCACTTCCTTTTCTTTTTTTGGTCGCAGGAGTGTTATTCTCTCACATCTCAAAACATATAACGTGTATTTTGAAGGAGATGCCCTTCAGTTG[A/T]GACACAGAGAGGTTGGTTATTTGGCAAGCTATAGTCTGTTGTTTTGATGTGTTACACCACCAATGACTGTGATGTTATGTGGCTTTTAAAGGAGGAAGGAGAGCTGGTCATAGAGGGTTTGCTCAATGTTTTTTGGGGTGTGCGTCGACCAATCAGATTGCAGATGCAGGACGAGAAGGAGACTGGCAGGCCACGCCCCTTAGTGACACCACTGGACATCAATACAATAAAGTCAGATATTAACAATATGCTAACATGAGATTAATGTTATAGAAATGTATGTTTGCCTTGTTTTTAAAAAAATACATAAGGATTTATATGCTTGTTCTAAATTTTGGGGTTGGTAATATATTTTTTTAAAAAGTCTCTTCTGCTTAGCGTGTACAGGATTTGGTTTAGCGGGAAGTTATTTGGTTACAAAAAAACTGAAAAAAGAGAATAAATAATATTGTGAATGTAATAATTTTATATTTTGAGTTTTTCCATTTTTAAATAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10991
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 |
---|---|---|---|---|---|
ENSDART00000064662 | Essential Splice Site | 44 | 316 | 3 | 10 |
ENSDART00000142028 | Essential Splice Site | 44 | 312 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 20726295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 20687709 |
GRCz11 | 10 | 20645090 |
KASP Assay ID:
2260-3149.1 (used for ordering genotyping assays)
KASP Sequence:
CATATAACGTGTATTTTGAAGGAGATGCCCTTCAGTTGWGWCACAGAGAG[G/A]TTGGTTATTTGGCAAGCTAYAGTCTRTTGTTTTGATGTGTTACACCACCA
Long Flanking Sequence:
CACGCAATTGCTCAGTTATATCAGTAAATTGAAATCAAATTTAATAATAATAGACCTTTTTTTCTGTGTTTACAGGCTTTAATAGATTGATAGTATGTTTTGAGTTTGTTTAGCTTATTTATTTTTTGTTTTTTGTCGAGTTTGAGTGTGTGTTTCTGTGTGTGGGAATCTTGCCTGAGGTTATTTTGCGATTATGAGGCTTGAAGTCATGAGTTTTTCTTCTGGTCGCAGATAAACTTCATTACTTCATTCTTCCGTGTGTCTCCACTGACCCGACATGGAAAGTGTGGATTCAGACAAGATCCAGGTTGGAGAAAACAAATTTGTCAGCAAGTAAGTGCATCTCGTTGTGTGACTGTAAGCTTTCTTATTATCACTGTTTTCTTATATATGACATCACTTCCTTTTCTTTTTTTGGTCGCAGGAGTGTTATTCTCTCACATCTCAAAACATATAACGTGTATTTTGAAGGAGATGCCCTTCAGTTGAGACACAGAGAG[G/A]TTGGTTATTTGGCAAGCTATAGTCTGTTGTTTTGATGTGTTACACCACCAATGACTGTGATGTTATGTGGCTTTTAAAGGAGGAAGGAGAGCTGGTCATAGAGGGTTTGCTCAATGTTTTTTGGGGTGTGCGTCGACCAATCAGATTGCAGATGCAGGACGAGAAGGAGACTGGCAGGCCACGCCCCTTAGTGACACCACTGGACATCAATACAATAAAGTCAGATATTAACAATATGCTAACATGAGATTAATGTTATAGAAATGTATGTTTGCCTTGTTTTTAAAAAAATACATAAGGATTTATATGCTTGTTCTAAATTTTGGGGTTGGTAATATATTTTTTTAAAAAGTCTCTTCTGCTTAGCGTGTACAGGATTTGGTTTAGCGGGAAGTTATTTGGTTACAAAAAAACTGAAAAAAGAGAATAAATAATATTGTGAATGTAATAATTTTATATTTTGAGTTTTTCCATTTTTAAATAAAATTGTAATAATCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34887
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 |
---|---|---|---|---|---|
ENSDART00000064662 | Essential Splice Site | 223 | 316 | 8 | 10 |
ENSDART00000142028 | Essential Splice Site | 219 | 312 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 20724183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 20685597 |
GRCz11 | 10 | 20642978 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTTTTCTTTTGTTTGTGCAAGATAGTTCATTTTCATTTTGTCATTTA[G/A]AGAGGCATCAGCTGAAGCCCAATGATCATCCTTTGCTGGTTAGAGTTTTG
Long Flanking Sequence:
TTAACTTGTACTTTTGGCTGGAGTGGATTTAGTTATTCGGGGCCTGTAATAGTTTAATGAACACACTTGACTTAACAGAGCAACAGGATCACCTTTATTCTAGCTGAAAACATGTGAAGAACTTGCAAAGCATCATGGGTCGCATTGACCCCTTACCTCTCAATGTCATGACATAGTTCTTAAAGCTATACATACATTATTGGGACCCAAACCATTTTCAGCCATAGGGTCCATTTTGTGTGTGTTTAACTTTTATGCTACACTACTCCTATTGAACATGTCATTGACACTGCTGTGGTAAAACTTATGTTTTATGGGTTTTCATGGGTTGATGAATATAATTTGTTAATTCTAATAAATTATTTTATTATTTGGTGGATAAACCATGAGATTGACAATACTTCACTTTAACAGAAGCTACCATAATTCAAGCAAAGCATCATGGTGTCAATGGTTTTCTTTTGTTTGTGCAAGATAGTTCATTTTCATTTTGTCATTTA[G/A]AGAGGCATCAGCTGAAGCCCAATGATCATCCTTTGCTGGTTAGAGTTTTGCAAGGCCCTTGTGAACAGGTCAGCAAAATGTTTCTTATGGAGATGGACCAGGTGGAGGAGGTCACATATGATGTAAGAGACCAAATATCTCTGTCTGTTTGTCTATCTGTCTGTCTAACTGGCTGACTGATCATCTAGTCAAAATTAATCATCTACATATTTATAAAATCTAATAAGCACAATTCAACTATTAATAAATATTTACATTCTTTTTTAGAGGAAGAACATATATAATGCATTGCAGTAAAAGAATAAACAAAAATAATAATAATAATGCAAAAATTAATGCTTATTTATTTATTATTTTTATAGGGTCATGGGGAATGGGAAGCCAAATTACTCAAATGTAATTGTTAAGTGAATATGGATATATTTAAATAAATAATGATGAAACACATATTTGAATCATAAATTAAACAATTAATTAGTATTACCAAACAAATGAATTAA
Associated Phenotype:
Not determined