ZMP
rgs9
Ensembl ID:
Description:
hypothetical protein LOC767636 [Source:RefSeq peptide;Acc:NP_001070045]
Human Orthologue:
RGS9
Human Description:
regulator of G-protein signaling 9 [Source:HGNC Symbol;Acc:10004]
Mouse Orthologue:
Rgs9
Mouse Description:
regulator of G-protein signaling 9 Gene [Source:MGI Symbol;Acc:MGI:1338824]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33239 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9502 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33239
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000123630 | None | None | 334 | None | 11 |
| ENSDART00000130128 | Essential Splice Site | 229 | 334 | 11 | 12 |
| ENSDART00000130591 | None | None | 480 | None | 17 |
| ENSDART00000131018 | None | None | 418 | None | 17 |
Genomic Location (Zv9):
Chromosome 3 (position 36385023)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 36256307 |
| GRCz11 | 3 | 36385707 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTGTGATCTGTATGTTTAGTGAAGTATTTAGAATGGATCTTTTTAAT[A/T]TAACGTAACAGAATTGAACATTTCTGAGCTCTGTATTTCTTCTTAGGTTT
Long Flanking Sequence:
AGTATTGGCTTTAAATTGCTTAAACCCTGAAAATTGCTGCTTGCAGCTACAGCATATTTCTGTTTACTATTCCTATAGGCACTAGAACATGTGTTTCTTTTCATCTACAGGTGAGAATTTAGCTTTCTGGGAAGCTGCTGAGGAGTTAAAATTTGGCTCAGCAGCTACAATGTCAGAAAAAGCTGAACAAGTTTTCAAGTGAGTTTGTATTGCCTTAATGTATGGCAATTTATACAACTGGTCTCTATAGCTGAACATTTCTCTCTTTTTTTAAATTTTGCAGAACGTTTTTGGCCCCAGGAGCTCCACGCTGGATCAACATTGACGGCAGGACAATGGGTCTTACAGTAAAGGGACTGGAGCATCCTCACCGCTATGTGCTGGAGGCGGCACAGACTCACATCTTCATGCTCATGAAGAAGGTTTGATCGTATTCTTGGAGAGTTTTTTTTTGTGTGATCTGTATGTTTAGTGAAGTATTTAGAATGGATCTTTTTAAT[A/T]TAACGTAACAGAATTGAACATTTCTGAGCTCTGTATTTCTTCTTAGGTTTGGCAATTTGTTGTGACTTTTATCATTTTTTAATTTAGCTGTACTTTATGCTCATGTCAGTTTTAGTCATTTAATTACTGAAACTTATTTTTATAAAAAAGAAACATAACAAAAGCATTGTTCATTTGTGAACTTTTAGGATACCTTTTATCGCTACTTGAAGTCACCAGTTTATAAGGACATACAGAAAAAGGCCATTTCACCTGCACCACACAACTTCACGTAAGTTTTGAAACATTTTTAAAAATGTATAACAGTTTGAAATATTTTCACCAATAATTAATCCTTTAATGCTTTTTCCCTGATTTAATTCTGAATTTATGCTTTTTAGTTTTATGTTTATTATAAGTAATTTTTCTTGTGTGCTTCTGTCATTTTTAAAAAAAAGTTTTACTTAATGTTAATGTTGAAATATTTTTAATCTTATGGTTATTTAGATACTATTATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9502
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000123630 | None | None | 334 | None | 11 |
| ENSDART00000130128 | Essential Splice Site | 229 | 334 | 11 | 12 |
| ENSDART00000130591 | None | None | 480 | None | 17 |
| ENSDART00000131018 | None | None | 418 | None | 17 |
Genomic Location (Zv9):
Chromosome 3 (position 36385024)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 36256308 |
| GRCz11 | 3 | 36385708 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGTGATCTGTATGTTTAGTGAAGTATTTAGAATGGATCTTTTTAATA[T/G]AAYGTAACAGAATTGAACATTTCTGAGCTCTGTATTTCTTNNNNNGTTTG
Long Flanking Sequence:
GTATTGGCTTTAAATTGCTTAAACCCTGAAAATTGCTGCTTGCAGCTACAGCATATTTCTGTTTACTATTCCTATAGGCACTAGAACATGTGTTTCTTTTCATCTACAGGTGAGAATTTAGCTTTCTGGGAAGCTGCTGAGGAGTTAAAATTTGGCTCAGCAGCTACAATGTCAGAAAAAGCTGAACAAGTTTTCAAGTGAGTTTGTATTGCCTTAATGTATGGCAATTTATACAACTGGTCTCTATAGCTGAACATTTCTCTCTTTTTTTAAATTTTGCAGAACGTTTTTGGCCCCAGGAGCTCCACGCTGGATCAACATTGACGGCAGGACAATGGGTCTTACAGTAAAGGGACTGGAGCATCCTCACCGCTATGTGCTGGAGGCGGCACAGACTCACATCTTCATGCTCATGAAGAAGGTTTGATCGTATTCTTGGAGAGTTTTTTTTTGTGTGATCTGTATGTTTAGTGAAGTATTTAGAATGGATCTTTTTAATA[T/G]AACGTAACAGAATTGAACATTTCTGAGCTCTGTATTTCTTCTTAGGTTTGGCAATTTGTTGTGACTTTTATCATTTTTTAATTTAGCTGTACTTTATGCTCATGTCAGTTTTAGTCATTTAATTACTGAAACTTATTTTTATAAAAAAGAAACATAACAAAAGCATTGTTCATTTGTGAACTTTTAGGATACCTTTTATCGCTACTTGAAGTCACCAGTTTATAAGGACATACAGAAAAAGGCCATTTCACCTGCACCACACAACTTCACGTAAGTTTTGAAACATTTTTAAAAATGTATAACAGTTTGAAATATTTTCACCAATAATTAATCCTTTAATGCTTTTTCCCTGATTTAATTCTGAATTTATGCTTTTTAGTTTTATGTTTATTATAAGTAATTTTTCTTGTGTGCTTCTGTCATTTTTAAAAAAAAGTTTTACTTAATGTTAATGTTGAAATATTTTTAATCTTATGGTTATTTAGATACTATTATTATAT
Associated Phenotype:
Not determined