Busch Lab

ZMP

LOC792554

Ensembl ID:
ENSDARG00000007265
Human Orthologue:
RGS13
Human Description:
regulator of G-protein signaling 13 [Source:HGNC Symbol;Acc:9995]
Mouse Orthologue:
Rgs13
Mouse Description:
regulator of G-protein signaling 13 Gene [Source:MGI Symbol;Acc:MGI:2180585]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa43844 Nonsense Mutation detected in F1 DNA Not yet available
sa43845 Nonsense Mutation detected in F1 DNA Not yet available
sa13389 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa43844
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007901 Nonsense 48 183 3 5
Genomic Location (Zv9):
Chromosome 22 (position 23540496)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24241360
GRCz11 22 24267924
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTAATCCGGTCAACTAATCAAACCTGTCTGATCCCATCAGGCTAAGTT[T/A]AGAAGACACCCAACAATGGTCTCAGTCTCTGGAGCGACTCCTCGGGTCCA
Long Flanking Sequence:
TATTTGAACATGCAACAAAAAGAACTTCAAAACCACAAAAACCAATACAAAAACACATTTAAAATACTTTTTAATCATTTATACCGTATAAAGATAAGTTACTTTATTAAAAAGTTCAAAACTTTACTTATTTTTATCAGGTATCTTTTTAAGTTAAACAAATTATAACTTGACGTTTTAGTCATTTTAATTGGTGTAAGTTGAAATTAAGTAAGTTCAATTTGATACAACTCAAAAATTGAATACAGCAGCAAATGTTTTGCATAAATATAATTAAAAACATTAATTAAATTAACATTAAAGACATTTAAGACCTGGAGCACAACAACAAAGTGCGATTTAAGACTTTTTAAAGGCCTAACATTTTAATTCTGGCATTGATTTCAGGCATGTTAAGACCTGTGGAAACCCTGTGTGAGGTCAAAAATAGTTTGAGACAAGAGATATTGCTTGTAATCCGGTCAACTAATCAAACCTGTCTGATCCCATCAGGCTAAGTT[T/A]AGAAGACACCCAACAATGGTCTCAGTCTCTGGAGCGACTCCTCGGGTCCAAATGTAAGGCCTTTTTTTTTGTAAGTCTATTTTTGGCACTGGTAAACTGGAACATAAATTAAAGAGGTGCTGTTTGCCTCCTCCAGATGGCCTGGCAACTTTCCGCACCTTTCTGAAATCAGAGTTTAGCGATGAAAATATCGAATTCTGGTTGACCTGCGAGGATTATAAGACGATCACGTCATCCCATAAGATGAGCTCTAAGGCCAGGAAGATCTTTGAACAGTTTGTTGAAGCAGAGTCTCCGAAAGAGGTAAAAGACACAACACTGTTGATCTGCAGACTGTCATTTATAATGGTAAAAATGCTTTTACTTAGTACCTAAATGCACACATGTCAGTACCAAAAGGTCCATATTGGTACCTTAAAGTACATACTAGTACCTTTCGAATGGGTACCAGCTTTTATAATTGCTGAGAGTGATTAATTATTGACGCCATTTACAATAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43845
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007901 Nonsense 53 183 3 5
Genomic Location (Zv9):
Chromosome 22 (position 23540510)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24241346
GRCz11 22 24267910
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTAATCAAACCTGTCTGATCCCATCAGGCTAAGTTTAGAAGACACCCAA[C/T]AATGGTCTCAGTCTCTGGAGCGACTCCTCGGGTCCAAATGTAAGGCCTTT
Long Flanking Sequence:
ACAAAAAGAACTTCAAAACCACAAAAACCAATACAAAAACACATTTAAAATACTTTTTAATCATTTATACCGTATAAAGATAAGTTACTTTATTAAAAAGTTCAAAACTTTACTTATTTTTATCAGGTATCTTTTTAAGTTAAACAAATTATAACTTGACGTTTTAGTCATTTTAATTGGTGTAAGTTGAAATTAAGTAAGTTCAATTTGATACAACTCAAAAATTGAATACAGCAGCAAATGTTTTGCATAAATATAATTAAAAACATTAATTAAATTAACATTAAAGACATTTAAGACCTGGAGCACAACAACAAAGTGCGATTTAAGACTTTTTAAAGGCCTAACATTTTAATTCTGGCATTGATTTCAGGCATGTTAAGACCTGTGGAAACCCTGTGTGAGGTCAAAAATAGTTTGAGACAAGAGATATTGCTTGTAATCCGGTCAACTAATCAAACCTGTCTGATCCCATCAGGCTAAGTTTAGAAGACACCCAA[C/T]AATGGTCTCAGTCTCTGGAGCGACTCCTCGGGTCCAAATGTAAGGCCTTTTTTTTTGTAAGTCTATTTTTGGCACTGGTAAACTGGAACATAAATTAAAGAGGTGCTGTTTGCCTCCTCCAGATGGCCTGGCAACTTTCCGCACCTTTCTGAAATCAGAGTTTAGCGATGAAAATATCGAATTCTGGTTGACCTGCGAGGATTATAAGACGATCACGTCATCCCATAAGATGAGCTCTAAGGCCAGGAAGATCTTTGAACAGTTTGTTGAAGCAGAGTCTCCGAAAGAGGTAAAAGACACAACACTGTTGATCTGCAGACTGTCATTTATAATGGTAAAAATGCTTTTACTTAGTACCTAAATGCACACATGTCAGTACCAAAAGGTCCATATTGGTACCTTAAAGTACATACTAGTACCTTTCGAATGGGTACCAGCTTTTATAATTGCTGAGAGTGATTAATTATTGACGCCATTTACAATAGAAATGCTATGCAGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13389
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
Order Allele From EZRC
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007901 Essential Splice Site 66 183 4 5
Genomic Location (Zv9):
Chromosome 22 (position 23540631)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24241225
GRCz11 22 24267789
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCACTGGWAAACTGGAACATAAATTAAAGAGGTGCTGTTTGCCTCCTCC[A/T]GRTGGCCTGGCAACTTTCCGCACCTTTCTGAAATCAGAGTTTAGCGATGA
Long Flanking Sequence:
ATCAGGTATCTTTTTAAGTTAAACAAATTATAACTTGACGTTTTAGTCATTTTAATTGGTGTAAGTTGAAATTAAGTAAGTTCAATTTGATACAACTCAAAAATTGAATACAGCAGCAAATGTTTTGCATAAATATAATTAAAAACATTAATTAAATTAACATTAAAGACATTTAAGACCTGGAGCACAACAACAAAGTGCGATTTAAGACTTTTTAAAGGCCTAACATTTTAATTCTGGCATTGATTTCAGGCATGTTAAGACCTGTGGAAACCCTGTGTGAGGTCAAAAATAGTTTGAGACAAGAGATATTGCTTGTAATCCGGTCAACTAATCAAACCTGTCTGATCCCATCAGGCTAAGTTTAGAAGACACCCAACAATGGTCTCAGTCTCTGGAGCGACTCCTCGGGTCCAAATGTAAGGCCTTTTTTTTTGTAAGTCTATTTTTGGCACTGGTAAACTGGAACATAAATTAAAGAGGTGCTGTTTGCCTCCTCC[A/T]GATGGCCTGGCAACTTTCCGCACCTTTCTGAAATCAGAGTTTAGCGATGAAAATATCGAATTCTGGTTGACCTGCGAGGATTATAAGACGATCACGTCATCCCATAAGATGAGCTCTAAGGCCAGGAAGATCTTTGAACAGTTTGTTGAAGCAGAGTCTCCGAAAGAGGTAAAAGACACAACACTGTTGATCTGCAGACTGTCATTTATAATGGTAAAAATGCTTTTACTTAGTACCTAAATGCACACATGTCAGTACCAAAAGGTCCATATTGGTACCTTAAAGTACATACTAGTACCTTTCGAATGGGTACCAGCTTTTATAATTGCTGAGAGTGATTAATTATTGACGCCATTTACAATAGAAATGCTATGCAGATAATTTTATATGTTCAATATTTAAATAACTCAAATATGCATTAATATTTAGTCAAAATGTACTGTTACAATTTAACAATACAATAAAAATGTGTATAAACAATTGCAATATGCTAATACATA
Associated Phenotype:
Not determined