ZMP
zgc:73189
Ensembl ID:
ZFIN ID:
Description:
regulator of G-protein signaling 9 [Source:RefSeq peptide;Acc:NP_957124]
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 |
---|---|---|---|
sa17031 | Nonsense | Available for shipment | Available now |
sa2644 | Essential Splice Site | F2 line generated | Not yet available |
sa17918 | Essential Splice Site | Available for shipment | Available now |
sa18091 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17031
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 |
---|---|---|---|---|---|
ENSDART00000034161 | Nonsense | 116 | 661 | 5 | 19 |
ENSDART00000127981 | Nonsense | 116 | 481 | 5 | 17 |
ENSDART00000143979 | Nonsense | 116 | 661 | 5 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 19718623)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18570784 |
GRCz11 | 12 | 18692658 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTTCCATACATTTCTTCCTCCAGACACCATATTTTTGGCCTGCACAG[C/T]AATGGCCGGTGGAAGAYACAGACTATGGTGTGTAATCATGRTTCAKTTTT
Long Flanking Sequence:
GTTTTTTTTTTTGCAGTAAGTAACTTTCTTTGTGTCTTAATCCTTAGAGGCCCGAGCTATGGGCACCATGATGGTGGCATTTGGATACATCTATCCACTACAAGACCATAAGAGACTTATCCTTAAACCAGACACATCCTTGTATCGCTTTCAGGTAACTTTTACAAACAACCTCAACATATTATACACACACACACATAGCCACTTAGGTATGGACACAAATGCAATACAATTTTTTTGCAATATTGAATAAATTATACCTATGGAGAATGCCCATAAACCACTAAACCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGTGTGTGCATGTGTGGAGTGAAGAATTTCCACAAATTTAGAAATGGCCTTTCCCTTATTACAGTTTACTTTGACACATTACAGTCCATATGCGTTTGTACTAATCATACCATTTCTTCCATACATTTCTTCCTCCAGACACCATATTTTTGGCCTGCACAG[C/T]AATGGCCGGTGGAAGATACAGACTATGGTGTGTAATCATGGTTCATTTTTCCATGCGTGCTGATAGGTTGTCATAGCAATATTTCACAGTGAGATTATTCATTATGGTTTCAAACAGCTGTCTGGGCTGAAGAATGTGATAAATTGCTTTCATGTTGAGTCACATTGCATCTTTAAATGGCTTTTACTGGGAGAGTCAGATGTTTACATGTGTATTTTCAGCAATATATTTGGCGAAAAGAAATATACGCAAGAAAGGGATGCTGGAGCTGTATGAACAGGTAACTGGATGTCAGAATGATAAATTATGACAAAATTTCATCACATCATCTGGTTGTTGCAAAATTATATAATGTAGTTTAACACAAGTGAAGATATTTTCAAATTAAATATAAGCAATTTTTGTCCATGTACTGAAGTTATATTCACCTAAAACTTTTTTGTCAAAGTCTTCTAAAGAGAAAATGATAAATATATAAAATTTTTGCTTTCATTAACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2644
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034161 | Essential Splice Site | 249 | 661 | 11 | 19 |
ENSDART00000127981 | Essential Splice Site | 249 | 481 | 11 | 17 |
ENSDART00000143979 | Essential Splice Site | 249 | 661 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 19725878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18578039 |
GRCz11 | 12 | 18699913 |
KASP Assay ID:
554-2926.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCAGTGCATCATGAGACCAAGGGTAAAGTCATCTGTGTCAATTGGAGC[G/A]TAAGTTACTGTTAAACTATAACTGCATTCATAAATTATTATAAAGCTACA
Long Flanking Sequence:
TTTTCTGTCTTTTGCTAATTTATTATATGAGACTTACCCTATTTACCAATTAAGTGGTTCTAATTGGATTTGTAGTGTAAACATTCAAATAAAAGTTAAATAGTTAATGTTTGTTTTTTTATGTGTTTAGCTTTAGTTAGCACTCTCTCAAAACCATTCGTCATGAATTCACAGATTTTTTACACAATTCTGTGAAAAAAAAAAAAAAAACGTCTGCAGATTCTGTCTGGCTTTTCTCATAAGGCCTACATGCTCAAATGTTAACAATTTTTTTTCACGAGTTTCTTTCTCTTCCTTTAAAACTTCTTCCAAATTGTTTTGCAGAAAAAAACATCTGACTACTACAGAAGAATTGTGAGTAAGAATTGGCTCAATTAAGTTCATTGTAAAAAGCCACAAAATCAATTAGAATCAATGAATCAATGTGTTTGCTTGCAGATCATGTTCACTCAGCAGTGCATCATGAGACCAAGGGTAAAGTCATCTGTGTCAATTGGAGC[G/A]TAAGTTACTGTTAAACTATAACTGCATTCATAAATTATTATAAAGCTACAATTCTTTAAAATATTTTTAAAATTCATGAAATTATTGTAAATTATGTTGTATTTTGACTTTATTTTGATATTTTGCAGAATTGTTAAGTACTCAACAACATACAAAGAGCACGACCCCTTTCTCCACCCGTGTCTTCCGAGTAGCCCCTGGTTAACTGATGATATTACATATTGGACTCTTAACATGCCAAAGTGAGCTGCAGTGTTTTAAAGCATTTCATTAGATTCCATGACTTTTTTGTTTTGTTATATGAGATTATGTTAAGTGGGAATGTAAAAAAGGGTTACAATATGTTTAAAGGAACACTCCACTTAAAAAATATAATAAAATAAAAACAATTTTCATGGTGCTGTATGTTTTTAACTCTTCTAAAGCATAAAAATACCCTAATATGTTTGCAGATATTTAAGAAATGTGCTAAGTGAACATTCTTGTTTATCTGTAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17918
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034161 | Essential Splice Site | 249 | 661 | 11 | 19 |
ENSDART00000127981 | Essential Splice Site | 249 | 481 | 11 | 17 |
ENSDART00000143979 | Essential Splice Site | 249 | 661 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 19725879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18578040 |
GRCz11 | 12 | 18699914 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGTGCATCATGAGACCAAGGGTAAAGTCMTCTGTGWCAATTGGAGCR[T/A]AAGTTACTGTTAAACTATAACTGCATTCATAAATTATTATAAAGCTACAANNN
Long Flanking Sequence:
TTTCTGTCTTTTGCTAATTTATTATATGAGACTTACCCTATTTACCAATTAAGTGGTTCTAATTGGATTTGTAGTGTAAACATTCAAATAAAAGTTAAATAGTTAATGTTTGTTTTTTTATGTGTTTAGCTTTAGTTAGCACTCTCTCAAAACCATTCGTCATGAATTCACAGATTTTTTACACAATTCTGTGAAAAAAAAAAAAAAAACGTCTGCAGATTCTGTCTGGCTTTTCTCATAAGGCCTACATGCTCAAATGTTAACAATTTTTTTTCACGAGTTTCTTTCTCTTCCTTTAAAACTTCTTCCAAATTGTTTTGCAGAAAAAAACATCTGACTACTACAGAAGAATTGTGAGTAAGAATTGGCTCAATTAAGTTCATTGTAAAAAGCCACAAAATCAATTAGAATCAATGAATCAATGTGTTTGCTTGCAGATCATGTTCACTCAGCAGTGCATCATGAGACCAAGGGTAAAGTCATCTGTGTCAATTGGAGCG[T/A]AAGTTACTGTTAAACTATAACTGCATTCATAAATTATTATAAAGCTACAATTCTTTAAAATATTTTTAAAATTCATGAAATTATTGTAAATTATGTTGTATTTTGACTTTATTTTGATATTTTGCAGAATTGTTAAGTACTCAACAACATACAAAGAGCACGACCCCTTTCTCCACCCGTGTCTTCCGAGTAGCCCCTGGTTAACTGATGATATTACATATTGGACTCTTAACATGCCAAAGTGAGCTGCAGTGTTTTAAAGCATTTCATTAGATTCCATGACTTTTTTGTTTTGTTATATGAGATTATGTTAAGTGGGAATGTAAAAAAGGGTTACAATATGTTTAAAGGAACACTCCACTTAAAAAATATAATAAAATAAAAACAATTTTCATGGTGCTGTATGTTTTTAACTCTTCTAAAGCATAAAAATACCCTAATATGTTTGCAGATATTTAAGAAATGTGCTAAGTGAACATTCTTGTTTATCTGTAAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18091
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034161 | Nonsense | 386 | 661 | 15 | 19 |
ENSDART00000127981 | Nonsense | 386 | 481 | 15 | 17 |
ENSDART00000143979 | Nonsense | 386 | 661 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 12 (position 19728740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18580901 |
GRCz11 | 12 | 18702775 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGAAAACAATGGAAATAAYAGTGAAGGGTTTGGGACACCCTCATCGTTA[T/A]GTACTGGATGCTGCCCAGACTCACATTTACATGCTCATGAAAAAGGTATC
Long Flanking Sequence:
GAACGTGTTAAGATCTGAAAACATGGTAAAAATCTGGCAAGGGCTTTTTCTTTTTCTTGATTATTTGTTAAAACTGTCAGTTGGGTTAAGGGCTAGAGGAGGGTGGGTCAGTCGATTGGTCAGTCAGTCAGTAAGTCAGTCGACAGCGGCCTCTGGTGGTTTTACGCGAGAACTGCAGGCTCGGATGGCACTTCAATGGCAAATTTGAGATCTCAAAAAGCAAAAACAGCAGCCTCTGGTGGATTCATGAAAACAAAAACTGCAAAAAAAATGTAGCTCCTGGGACATACTTGGTGACCAAATGTATATAACAGTACAATTTCTTAATTGGTCGGTTGGTTGGTTGGTTGATTTAAATGTTTACTTAAATTACATCAGCACTGACATTTTAACTTTTGTTTAATTAGGACCTTTTTGGCTCGTGGAGCTCCTCGTTGGATTAACATTGATGGGAAAACAATGGAAATAACAGTGAAGGGTTTGGGACACCCTCATCGTTA[T/A]GTACTGGATGCTGCCCAGACTCACATTTACATGCTCATGAAAAAGGTATCTAATCTCAAGTCAAATATTGCAACTCAATTGTCTGCAAACATGGAATTAATGCAAGTATGATCTTTCATCAAGGACTCATACGGGCGATATCTCAAGTCCCCGGTGTTTAAGGAAACTCAGAAGAAAGCCATTGCTCCTGAAGCACACAGATTCAGGTTAGATACGCCTTTATAAAATATATTAGACTGTGTTATTGTTCATAAGTGAGTATAAGATTTTCCTATTCTCCTACTTTAAAGGTTACTGTGTTGTTTTGGAAGTCTGCTTTAATAAGATTTACATCCATCATTTTTAAGTTTACATCTAAAAACAATTGAGGTTTCATATGATAAACAGTTGATTTTTACTGTCTAAAATTACAGATTTTGTCAAAATCATGTTAAACAGGAGTAGGCAAGCATACACAAATAATCCAAAGGGTGAATAATAAAAGAGGCGAATGGGCCAAG
Associated Phenotype:
Not determined