ZMP
rgs11
Ensembl ID:
ZFIN ID:
Description:
regulator of G-protein signaling 11 [Source:RefSeq peptide;Acc:NP_001104631]
Human Orthologue:
RGS11
Human Description:
regulator of G-protein signaling 11 [Source:HGNC Symbol;Acc:9993]
Mouse Orthologue:
Rgs11
Mouse Description:
regulator of G-protein signaling 11 Gene [Source:MGI Symbol;Acc:MGI:1354739]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25529 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32597 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19433 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25529
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 |
|---|---|---|---|---|---|
| ENSDART00000054829 | Essential Splice Site | 21 | 477 | 1 | 18 |
| ENSDART00000054833 | Essential Splice Site | 21 | 359 | 1 | 16 |
| ENSDART00000135702 | Essential Splice Site | 21 | 471 | 1 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 8963174)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9202979 |
| GRCz11 | 1 | 9887090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTCAGCCAGGATGGCGTGCAGAGACAGCAAATGCCCTGTTTGACCAAG[G/A]TAAACCCCACAAAATATGATTTATTTAACCATTCCATATCAAATGTCTGC
Long Flanking Sequence:
CAACTGACCCAGCCGAGGCTCGAATCGGCGACTTTCTTGCTGTGAGGCGATCTTGCTACTCTGCTACCGTGAGGCCCTATTGTAATTTCAAGTGTTTATTTATTTATTCATTTATTAATTTGCTTAGGCCTTAATATTTTATTTTAATTTACGTTAATTCATTCCCAGTTAAAAACAAAAAAATATGATTTAATTTAAATAATATCCCTGCTGTCAAACTGCAGTGCACGTTTGATTTTTGAAGTGTCACTTTAAATAAGTTTCCACCGAGAGGCGCTGTTTTACACCTGGATCTAAGTTATCTGAATAATGTTATGGCGCCACCCCGTCATCGTCTCCTCCTCAGCTTCACTTCTGACGGGACAGCAGACTCCGAGCAGCAGCACAAACAAACCCGTCCAGCTCTCTTCAACTTTACATCCACAGCAGCAGAAAACATGACCATCAACACACTCAGCCAGGATGGCGTGCAGAGACAGCAAATGCCCTGTTTGACCAAG[G/A]TAAACCCCACAAAATATGATTTATTTAACCATTCCATATCAAATGTCTGCTTTAGGACGGGTATTTTTGCAAACTAGCTATATTTATAATTCTCTTGTTGTTTTTAGTCAGTATCTTATAGTAATACAACTGAAAATATGTAAAAAATGATTGAAAGACGTCAATTAGTCAAACATAAAAAAGCATCAGCTGTTTTGACTGGAAACACTAACACTGTTCTTGAACATTTTTCATGATGATAGTGTGTTTTGTGAACATGCATGATAGTGGTATCATATTTTCAGTCATTGCTATTACAATTCACATTTTATTTCAATTTTGTTTAATGAATTTTAAGATGTTGATGCTTCAAATCACATGATTATATTATTAGACAAACTGTGAAAATGAGAAATATGAAAGACATTAGTATTTATTGGACATGCATTATGGTGATACCCTGATTATAATCATTGCTATTTATTCATTCATTTTCGACTTAGTCTCTTTATTAACCTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32597
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 |
|---|---|---|---|---|---|
| ENSDART00000054829 | Essential Splice Site | 128 | 477 | 5 | 18 |
| ENSDART00000054833 | Essential Splice Site | 123 | 359 | 5 | 16 |
| ENSDART00000135702 | Essential Splice Site | 123 | 471 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 8969878)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9209683 |
| GRCz11 | 1 | 9893794 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGTATTACTGGATGTCTACACGCTGGCCTGCTTCAGAACTAGACTATG[G/A]TAAGTGAAATTCTCACTTATTAACTCTTATGTTATTCCAAAAAGCATTTC
Long Flanking Sequence:
AGGTCTTTCAGTCTCTGCTAATGTGCTGATGATCTGAATCAGGTGTGTTTGGTTAAGGAGACATGGTAAATGTGCAGGGCTGGTGATCCTCCAGGAACGCGGTTGAGAACAACTGTTTTAGTAAACTTGATGAACTAAAATAAACACTATTATCAGTTTGGAGTGCACATTCTAGTTTTGTTTCCATCTAGTAAATTCTTAATAACTTTTTCTGAAATGAGAATGCATGATCATTTATTTGTTCTTATTTAGAAGCAGCGCACATTGGACAGTTTCTCGTGAAGTATGGCTACATTTACCCTTTAAAAGAACCCAGAAACCTTATTCTGAAAGCTGACGAATCAGCATATCGTTTTCAGGTCAATACACACAAATGTACACTATGTTGTATCAGCATAAAATTCTATATTCAAAAAACGACACCTTTTTAATTCTCTGCCTTTCTCAGACACCGTATTACTGGATGTCTACACGCTGGCCTGCTTCAGAACTAGACTATG[G/A]TAAGTGAAATTCTCACTTATTAACTCTTATGTTATTCCAAAAAGCATTTCTTTGCATTAAGAATACAAAATCCTGACATTTCGGAAGGCATGTTTTATTTATATATCTATCTATATGTGTTTTAGCAATCTACCTGGCCAAGAAGAATATCAGAAAACAAGGAGAATTAATCGAGTATGAAAAGGTATGTGGGTAAATGCAAAACCACACCATTTGGCAGTGGTGTATACAGTACTTAAAAGCCAGACTTGAGTAAAAGTAGAGATACCTTACTTGAAAATGACTTTGGTGAAAGTTTAAGTCACTGTTTGGCATATTACTTGACTAAAAATACAGATATTTTACTAGAAAATGACTAAGGTAAAAGTTAAAATCACTGTATAGAATTTTACTGGAGTAAAAGTACAGAAGGGGCGAAGGAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCGAGCCTCGGCTCAGTTGGCGTTTCTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19433
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 |
|---|---|---|---|---|---|
| ENSDART00000054829 | Nonsense | 172 | 477 | 7 | 18 |
| ENSDART00000054833 | Nonsense | 167 | 359 | 7 | 16 |
| ENSDART00000135702 | Nonsense | 167 | 471 | 7 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 8972253)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 9212058 |
| GRCz11 | 1 | 9896169 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAACGTATCAACCACACCTGGGACTTTGTTGTGATGCAGGCAAGAGAG[C/T]AGCTCAGGTAACTCTACGTTTCCATCACACACACGCGCACACACACACAT
Long Flanking Sequence:
TGTTTTTGTGTTTTTTTTACTAATTTTTATTTGTTTTTATTTTTATTTTACTTGTTTCTTTTATTCCTGTTTTTGTAAAGCACTTTGAATTGCCACTGTGTATGAAATGTGCTATATAAATAAACTTGCCTTGCCTTGCCTTGCCTTACCAATTCTACATGGTGAAATCATATTAGCAGCCAATGTCTATCAAAGTTGTTCACAGTCAAATAAACAGTGCTAATGTTGTTTTGAAGTCATACTTGCATTTGAATTTGGATTAAATATTCAACAACAATATAGGGAGCTTGTCACTGAACTATTGTACAAATATAAAACCAACCTTCAGAAACCGCAACACTCAAGTAAAGTATAGATACTCACAAAAAAATGCTTAAGAACATTACACCTGTACAATGTTAACCCGTTGTTTATGTCTCTGTCTTTGTAAGGAGTGCTATAATGCTTTACATAAACGTATCAACCACACCTGGGACTTTGTTGTGATGCAGGCAAGAGAG[C/T]AGCTCAGGTAACTCTACGTTTCCATCACACACACGCGCACACACACACATACACACACACACACAAAACACTTAGGATCAGATTAACTAAACAGGGAAAATCCCACAGATGGGAGTGGAAATTTCTACAAGTAATCCACTGACGCTGCATGAATTACAGAGCATAGATGCAGCCGCTTATTTTCATAATGTCTAACGCAGCACATAAACCTGCACAAACAAGGGGGTAAACAGCAGAGCTGATGGTAATAAATCGCATGTATACTAATAACAACATCTAGTAGGTGCCAAATGCCAGAATGAGCTTGCCTTCTTCTTTCAGTTGCACCTCCCTTTTAAACATATGTGACACCAGATCCACCAATCACTTTGAAATGATTTAAATGATTTCTGAAGGCCTGTGTGACACCGATGCTGTGTTGATGCCAAAAATTCATATCACAGGAATAAATTAAATTGTAGTGTACAGTTAAAGTCAGAATTATTAGCCCCCTTTGAATT
Associated Phenotype:
Not determined