Busch Lab

ZMP

rgs12

Ensembl ID:
ENSDARG00000036774
ZFIN ID:
ZDB-GENE-031006-13
Description:
regulator of G-protein signaling 12 [Source:RefSeq peptide;Acc:NP_999889]
Human Orthologues:
RGS10, RGS12
Human Descriptions:
regulator of G-protein signaling 10 [Source:HGNC Symbol;Acc:9992]
regulator of G-protein signaling 12 [Source:HGNC Symbol;Acc:9994]
Mouse Orthologues:
Rgs10, Rgs12
Mouse Descriptions:
regulator of G-protein signaling 12 Gene [Source:MGI Symbol;Acc:MGI:1918979]
regulator of G-protein signalling 10 Gene [Source:MGI Symbol;Acc:MGI:1915115]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa10087 Nonsense Available for shipment Available now
sa31218 Nonsense Available for shipment Available now
sa19543 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa10087
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022546 Nonsense 578 1540 1 18
ENSDART00000101536 Nonsense 578 1183 1 17
ENSDART00000125886 Nonsense 578 1519 1 20
ENSDART00000125988 Nonsense 578 1183 1 15
ENSDART00000126853 Nonsense 578 1387 1 16

The following transcripts of ENSDARG00000036774 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 41666978)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 40583219
GRCz11 1 41286006
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACGTCCTGAGGGATTGGCGTCAGGGACACAGCAGTGATCAGGAGTCTTA[T/A]GCAGAGTCCACAGACGGATGGTCCAGTGCTAACTGTAGCACCCTGCCACC
Long Flanking Sequence:
GGTATGCGAGCTCGAGCTTTCCTTGATGGTGACTTAGATGCTCAGCAGAACAACAGCACAAGCAGCAACAGTGACAGCGGCATTGGGAACTTCTTGCCAGAGGAAAAGAACAACCGAGTCCTCTTGGTGGACTTGGGTGCAAATCCTAGTCGACATGTTCCTACAGGACCTTGGGAAAACCCTATGGGATCTTTTTGCCAGGGTGCCATAGGAGGTCTTCCGCCACCACCTCCTCCGCCACCGATCTCACATCGTAACGGATTTCGGCATGAGCAGTTTGTGGATCACCCTCAGCCCCATCCACATTCCCATGGAGACCCACCTCTGCTTTCTGGCAGGCATCTAAACTCCTCCTCACGGCTGGATGTGTCAGGCCTTCCTTCGCGCTCACACTATTCTGCTCATGGCAAGAAAGCGGCAGGGGCATCAGGCCAGCGCTGGCTGCCAGTTCACGTCCTGAGGGATTGGCGTCAGGGACACAGCAGTGATCAGGAGTCTTA[T/A]GCAGAGTCCACAGACGGATGGTCCAGTGCTAACTGTAGCACCCTGCCACCACCGATGAGCAAGATTCCAGCTGACCGGTACCGTGCTGCAGGCGAAATCGCCTCACAGCCTCACCGGCTTCATGCACAGAAGGATGAGTGGGCTAAGAAGCTGTTTGGGGAGAAGAACCTACGAGAGCATTCACAACAATCGAACAATGTCAGAAGAGCTAAAGATTCAGAAAAAAAGGTAAGATAATCAATCAAGTCACCATTGCAAGATTTGAGAACAATTTGTTTGAGATTACAATCTGTTAGCCTTCTTCATTCTTAACTGCAAATTAAAATGCATTTGTTTTTACAACACTGAACCTTAGGGATTAGGTAGAATGAGTGGGTACTGATTTTAAATGTGATCCCATTGCAGAAAACTTGTTAATCAGCTAGCGAGTGTGTTGTTCAAATCTTTGTTGTTTGCGTAAAATGTCCTTGCAAGCATAACCCAGCAAATAGTTTTGTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31218
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022546 Nonsense 646 1540 1 18
ENSDART00000101536 Nonsense 646 1183 1 17
ENSDART00000125886 Nonsense 646 1519 1 20
ENSDART00000125988 Nonsense 646 1183 1 15
ENSDART00000126853 Nonsense 646 1387 1 16

The following transcripts of ENSDARG00000036774 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 41666776)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 40583017
GRCz11 1 41285804
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGGGGAGAAGAACCTACGAGAGCATTCACAACAATCGAACAATGTC[A/T]GAAGAGCTAAAGATTCAGAAAAAAAGGTAAGATAATCAATCAAGTCACCA
Long Flanking Sequence:
GTGCCATAGGAGGTCTTCCGCCACCACCTCCTCCGCCACCGATCTCACATCGTAACGGATTTCGGCATGAGCAGTTTGTGGATCACCCTCAGCCCCATCCACATTCCCATGGAGACCCACCTCTGCTTTCTGGCAGGCATCTAAACTCCTCCTCACGGCTGGATGTGTCAGGCCTTCCTTCGCGCTCACACTATTCTGCTCATGGCAAGAAAGCGGCAGGGGCATCAGGCCAGCGCTGGCTGCCAGTTCACGTCCTGAGGGATTGGCGTCAGGGACACAGCAGTGATCAGGAGTCTTATGCAGAGTCCACAGACGGATGGTCCAGTGCTAACTGTAGCACCCTGCCACCACCGATGAGCAAGATTCCAGCTGACCGGTACCGTGCTGCAGGCGAAATCGCCTCACAGCCTCACCGGCTTCATGCACAGAAGGATGAGTGGGCTAAGAAGCTGTTTGGGGAGAAGAACCTACGAGAGCATTCACAACAATCGAACAATGTC[A/T]GAAGAGCTAAAGATTCAGAAAAAAAGGTAAGATAATCAATCAAGTCACCATTGCAAGATTTGAGAACAATTTGTTTGAGATTACAATCTGTTAGCCTTCTTCATTCTTAACTGCAAATTAAAATGCATTTGTTTTTACAACACTGAACCTTAGGGATTAGGTAGAATGAGTGGGTACTGATTTTAAATGTGATCCCATTGCAGAAAACTTGTTAATCAGCTAGCGAGTGTGTTGTTCAAATCTTTGTTGTTTGCGTAAAATGTCCTTGCAAGCATAACCCAGCAAATAGTTTTGTGTTTTATAGATGTCTAATAGACGTCAAAACGTAGCCAGCTTGGCTAAAACAAGGCTAAACATGGGCTGTCAGTGAAAATCTAATTGATATCTAAGAATAACCCAAAATTAGACTAGTTGTCAAGTAGACTTTATATGTGTAGTTATTAATTTGTGTTTATTGAATGACTAGTCTTGATTTCGCCTATTCTTAAACATCTATTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19543
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022546 Nonsense 832 1540 6 18
ENSDART00000101536 Nonsense 832 1183 6 17
ENSDART00000125886 Nonsense 832 1519 6 20
ENSDART00000125988 Nonsense 832 1183 6 15
ENSDART00000126853 Nonsense 832 1387 6 16

The following transcripts of ENSDARG00000036774 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 41609821)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 40526062
GRCz11 1 41228849
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGACGACATCCTCAACGCACCGAGGCCAGACATGTTTAAAGAGCAA[C/T]AGCTTCAGGTAAGACAGGAAACGCTCAGTCAGGATGTTTACTGAAACCCT
Long Flanking Sequence:
GGAATGAACCACCAACTTATCCAGGACATGATAACGAATCAATAAAATAAATAAATAAAAATATAAAAAGGAAAATACCAAAGAAATACGACACACATAAAAAGTGAACAATTGAATGAATTGCTTCTGGCATTTGTTTATAGGTCAGCATTAATTAATGACATCGTCAGATTATTACAAATGCTATTTGTACACCTGAAAATACTTTCTTTTATGACTTTTAATTTTATTCACTGTTTATTAGAACTTTTTTTCCCTCCATAGCAGTCCATTCAGGGTCCATGAATAGATCCTTTGTGTGGCCAGGATGAAACAAAGTTTTTCATTTGCTGTTTGATTGTGACCTTATACTGTTTGTCCTTCAGCTGTCCCAGCGGGCCAGAGAGATCTACAACAGCTTCCTGTCTAGTAAAGCTACCACACCCGTCAACATTGATAGTCAAGCTCAGCTGGCTGACGACATCCTCAACGCACCGAGGCCAGACATGTTTAAAGAGCAA[C/T]AGCTTCAGGTAAGACAGGAAACGCTCAGTCAGGATGTTTACTGAAACCCTCGGGTTACAACACTGTCCGGAAGACTATTAACAGAGCTTGAAAACGTCCCAGTGTTTATGTCAGGCATGTGGGCATCAGGACCATTCTAAAGACTTTGAAACTGTTGATTTATTTTCCTGACCACTTAATAAGGAATAACTGAGTGATGATTTTTAATTTGGGTATGTATTATTGTCCAATAATGAAATGGACCAGAGTCAGTTATTCCACTTATGATTAAAGATAGTAGTAATAATCTATGGTTAAAGATATTGGTCACACTTTACAATAAGGTTTCATTAGTTATTGGTAATTAATGTATTCACTTACATGAACTAAGCATGAACAAACTTCCACAGCATTTATTAATCACAGTTCAACATTTAATAATGCATTATTAAAATACTGGTCACACTTTATTTTGATGGTTTGTTGAATTTAAGTGACATTGCATCTACATGTCAACTAAT
Associated Phenotype:
Not determined