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
sa9277 Nonsense Mutation detected in F1 DNA Not yet available
sa19543 Nonsense Available for shipment Available now
sa1121 Nonsense F2 line generated Not yet available

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:
sa9277
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022546 Nonsense 651 1540 1 18
ENSDART00000101536 Nonsense 651 1183 1 17
ENSDART00000125886 Nonsense 651 1519 1 20
ENSDART00000125988 Nonsense 651 1183 1 15
ENSDART00000126853 Nonsense 651 1387 1 16

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

Genomic Location (Zv9):
Chromosome 1 (position 41666760)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 40583001
GRCz11 1 41285788
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTAMRAGAGCATTCACAACAATCGAACAATGTCAGAAGAGCTAAAGATT[C/A]AGAAAAAAAGGTAAGAKAAKCAATCAAGTCACCATTGCAAGATTTGAGAA
Long Flanking Sequence:
TCCGCCACCACCTCCTCCGCCACCGATCTCACATCGTAACGGATTTCGGCATGAGCAGTTTGTGGATCACCCTCAGCCCCATCCACATTCCCATGGAGACCCACCTCTGCTTTCTGGCAGGCATCTAAACTCCTCCTCACGGCTGGATGTGTCAGGCCTTCCTTCGCGCTCACACTATTCTGCTCATGGCAAGAAAGCGGCAGGGGCATCAGGCCAGCGCTGGCTGCCAGTTCACGTCCTGAGGGATTGGCGTCAGGGACACAGCAGTGATCAGGAGTCTTATGCAGAGTCCACAGACGGATGGTCCAGTGCTAACTGTAGCACCCTGCCACCACCGATGAGCAAGATTCCAGCTGACCGGTACCGTGCTGCAGGCGAAATCGCCTCACAGCCTCACCGGCTTCATGCACAGAAGGATGAGTGGGCTAAGAAGCTGTTTGGGGAGAAGAACCTACGAGAGCATTCACAACAATCGAACAATGTCAGAAGAGCTAAAGATT[C/A]AGAAAAAAAGGTAAGATAATCAATCAAGTCACCATTGCAAGATTTGAGAACAATTTGTTTGAGATTACAATCTGTTAGCCTTCTTCATTCTTAACTGCAAATTAAAATGCATTTGTTTTTACAACACTGAACCTTAGGGATTAGGTAGAATGAGTGGGTACTGATTTTAAATGTGATCCCATTGCAGAAAACTTGTTAATCAGCTAGCGAGTGTGTTGTTCAAATCTTTGTTGTTTGCGTAAAATGTCCTTGCAAGCATAACCCAGCAAATAGTTTTGTGTTTTATAGATGTCTAATAGACGTCAAAACGTAGCCAGCTTGGCTAAAACAAGGCTAAACATGGGCTGTCAGTGAAAATCTAATTGATATCTAAGAATAACCCAAAATTAGACTAGTTGTCAAGTAGACTTTATATGTGTAGTTATTAATTTGTGTTTATTGAATGACTAGTCTTGATTTCGCCTATTCTTAAACATCTATTAGACCTCTTTTAAAAACAA
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

Mutation Details

Allele Name:
sa1121
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000022546 Nonsense 1366 1540 16 18
ENSDART00000101536 None None 1183 15 17
ENSDART00000125886 Nonsense 1364 1519 17 20
ENSDART00000125988 None None 1183 15 15
ENSDART00000126853 Nonsense 1366 1387 16 16

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

Genomic Location (Zv9):
Chromosome 1 (position 41596864)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 40513105
GRCz11 1 41215892
KASP Assay ID:
554-1032.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGCTCTCTCCTTCACCAGTCCCCCATTCCTCTCCCTCCTTCCCCAGAG[C/T]GATCACACCTCCTGAAGGAGGACACTTGCCAGGACAGCTGGGCTCGATCA
Long Flanking Sequence:
AGCTCATATCCAAAGCACAGAGCAACAGAGCTGACGACCAGCGGGGTTTGCTGAACAAATCAGACCTTGTCCTGCCCGACTTCCTGCGCCTCGACACGGAAGCAGACGGCAACAACCTCAGCTCCACACCCATCTCCCACAAGACTCGACCACGATCCAAGGAGAATGGCTCTGCCCTCAGTGCCAGTCACCAAACGCAGAGCTTAGATTCAGCGGGGGAGGGCAAAGCACCCAGACGAGCACTAATGCCACCCAACAGTGCCCTCAGAAACACATCCAGCCGAATTCCGCCACCGTTCAGTTCCTCGCTCTCCCCAATCCCACATTCGCAAATGGGGGGCTCGTCCGGGATCACAGACTGGAGGAGTGACGGAGGGGTCCAGGCACTGGAGGAAGAGGAGAGCGGCATGGACCTGACTTTTGTTGCCGAAGGCGACATCACAAGCCCTAACAGCTCTCTCCTTCACCAGTCCCCCATTCCTCTCCCTCCTTCCCCAGAG[C/T]GATCACACCTCCTGAAGGAGGACACTTGCCAGGACAGCTGGGCTCGATCAGGTACCTCTCCTGTGTGAAGCAACTACGCTTGCATGTGATATCCTCATCTCTCTCTGGTCCCTCCTGAAGATGTGTGATTTCTGAGTGCTGTGGAATTGCTGTGGTCCTCGTTGTAAGCCCTCTGCCAAACTCTGGCAAAAGCAGCTCCTTCTCATGTACATTTGACACCCTTTAAGCACTTTAACGAAGAATCGAAAAAGAGACTTCTGTACCTACAATGCATATGATGGGTTATTTTTTTCCCTGAAAGTATTTTAAAACTAGCCACACAGAATCTTGACAATCATTAACTTCCATCGCTTTTATCCTCTGAGAGAAACAATAGAATTATTGTAGCAGTTTGACTGATTTGAGGTCAGTAACGAACTGAAGAGAACTTACTGGTTTTCTGCATATCTCTACCCTCTGGCTGATCACATGACGGCCTTAACAGGAGCCACAACTGACTG
Associated Phenotype:
Not determined