Busch Lab

ZMP

rgs11

Ensembl ID:
ENSDARG00000037646
ZFIN ID:
ZDB-GENE-080220-46
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.
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.
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.
Availability:
Order Allele From ZIRC
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

Mutation Details

This allele has been removed from public view.

Allele Name:
sa25530
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054829 Nonsense 176 477 8 18
ENSDART00000054833 Nonsense 171 359 8 16
ENSDART00000135702 Nonsense 171 471 8 17
Genomic Location (Zv9):
Chromosome 1 (position 8973715)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 9213520
GRCz11 1 9897631
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTAGTGTTCAGTGGTCTTGCTATGTTTTATTTCTTGTGTTAAGGGCAT[C/A]AAAACAGCGTCGGAAGGCAGATCGTATAGTGCTGGAGTGTCAGGAACAAG
Long Flanking Sequence:
TAATTCAGGGGGGCTAATAATTCTGACTTAAACTGTACATTAAAATATAAAAGAGCTATTTATGTCATTATATCGATTTTATATATGTTGTCTCTGAACATTAAGGACTTTTTTTTTTACAATTTTTCTCAAAGTCTTACTCAGCTTGAGGTACTTTTGAGTGGTAGAGTAGTAAATACTAAATTGTAAGCTGCTTAAATAATTTATAACAGGAAGCATAACATGGTAAGGGCAGTGTTCTCAGCAGGGGCTGCATCCAAATACCGTCACGATGCTTCTCACTTTAAGCAATTCCTCATTACAATCAATCATTCATAAAAATCTGCATGATTCAGCCTGATTGAAGTTTTATGCTGAAAGAAATATTAATCGTACACTCTGATGGTTATAAAAACAATACAAGCTGATCTAAAGGTTGTTGTCCCAACCTTTTTATAACTATTATTTCATGCTTAGTGTTCAGTGGTCTTGCTATGTTTTATTTCTTGTGTTAAGGGCAT[C/A]AAAACAGCGTCGGAAGGCAGATCGTATAGTGCTGGAGTGTCAGGAACAAGCGTTCTGGCTAGTGAACAGACCTCCTGTAAGTACTGAACTCTATAAAAGAAAAAACACTAGCAGAACCATAGCACCGTCACCTCACAGCAAGAAGGTTGATGGTTCTAGTCCCAGCTGGGTCAGTTTGCGTTTCGGTGTGGAGTTTGCATGTTCTCTATGTGTTCGCATGGGTTTCCTCCGGGTGCTCTGGTTTCCCCTACAGTACAAGGAGTGTGTATGGTTTTCCAGTACTGGGTTGCAACTGGAAAGACACTGTGTAAACATATGCTGGATAAGTTGGCGGTTCATTTTGCTGTGGCGACCCCAGATTAATAAAGCGACTAAGCTGAAGGAAAATAAATGAATGTCAATAAAAGTCACTTTGTTAAACCGTAGAGTTGAATTTTTAACATCAAATGTCGACAGAGCAGAGATCAACATCCCATAATGCAATTCACAACCGTAAATAA
Associated Phenotype:
Not determined