Incidental Mutation 'IGL02652:Rgsl1'
ID 302209
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rgsl1
Ensembl Gene ENSMUSG00000042641
Gene Name regulator of G-protein signaling like 1
Synonyms 4930415K13Rik, Rgsl2
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02652
Quality Score
Status
Chromosome 1
Chromosomal Location 153655127-153719888 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 153701236 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 441 (L441P)
Ref Sequence ENSEMBL: ENSMUSP00000139340 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000124558] [ENSMUST00000185164]
AlphaFold A0A5F8MPV0
Predicted Effect possibly damaging
Transcript: ENSMUST00000124558
AA Change: L406P

PolyPhen 2 Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000135642
Gene: ENSMUSG00000042641
AA Change: L406P

DomainStartEndE-ValueType
low complexity region 122 136 N/A INTRINSIC
low complexity region 242 254 N/A INTRINSIC
low complexity region 316 325 N/A INTRINSIC
Pfam:RGS 644 754 7.1e-12 PFAM
transmembrane domain 956 973 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134030
Predicted Effect probably benign
Transcript: ENSMUST00000184095
Predicted Effect probably damaging
Transcript: ENSMUST00000185164
AA Change: L441P

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000139340
Gene: ENSMUSG00000042641
AA Change: L441P

DomainStartEndE-ValueType
low complexity region 157 171 N/A INTRINSIC
low complexity region 277 289 N/A INTRINSIC
low complexity region 351 360 N/A INTRINSIC
Pfam:RGS 679 789 4.1e-11 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap28 A T 17: 68,191,795 (GRCm39) D139E probably benign Het
Asph C T 4: 9,529,984 (GRCm39) V347I probably benign Het
Ccdc138 A T 10: 58,348,901 (GRCm39) D149V probably benign Het
Cep192 A G 18: 67,991,921 (GRCm39) probably benign Het
Cnnm2 G A 19: 46,751,650 (GRCm39) R480Q probably damaging Het
Col24a1 C A 3: 145,198,056 (GRCm39) S1321* probably null Het
Cops6 T G 5: 138,159,700 (GRCm39) probably null Het
Crim1 G A 17: 78,623,106 (GRCm39) A435T probably damaging Het
Cttn G T 7: 143,995,468 (GRCm39) Q382K probably benign Het
Dhx38 A G 8: 110,282,761 (GRCm39) L635P probably damaging Het
Dmtf1 T A 5: 9,171,853 (GRCm39) T458S probably benign Het
Dnah5 T C 15: 28,366,333 (GRCm39) F2682S probably damaging Het
Dnah6 T A 6: 73,072,087 (GRCm39) Q2413L probably damaging Het
Dock10 T C 1: 80,570,561 (GRCm39) probably null Het
Engase C T 11: 118,369,776 (GRCm39) P63S probably damaging Het
Grik4 A G 9: 42,586,573 (GRCm39) V94A possibly damaging Het
Heatr6 T C 11: 83,660,558 (GRCm39) V566A probably damaging Het
Hydin A C 8: 111,316,154 (GRCm39) T4349P possibly damaging Het
Inpp4b G A 8: 82,497,429 (GRCm39) probably benign Het
Mertk A G 2: 128,643,190 (GRCm39) E863G probably benign Het
Muc19 T A 15: 91,762,009 (GRCm39) noncoding transcript Het
Myo9a T A 9: 59,771,211 (GRCm39) F928I probably damaging Het
Nyap2 T C 1: 81,219,435 (GRCm39) Y486H probably damaging Het
Oas1e T C 5: 120,933,470 (GRCm39) R32G probably damaging Het
Or14j2 A T 17: 37,885,836 (GRCm39) Y159* probably null Het
Or4k48 A G 2: 111,475,839 (GRCm39) F168L probably benign Het
Osbpl6 G A 2: 76,423,798 (GRCm39) R848Q probably damaging Het
Piezo2 G A 18: 63,157,546 (GRCm39) T2388I probably damaging Het
Prkdc A G 16: 15,600,951 (GRCm39) T2871A probably benign Het
Ptpn12 T C 5: 21,207,435 (GRCm39) K308E probably benign Het
Rictor T C 15: 6,805,668 (GRCm39) probably null Het
Scn2a T A 2: 65,532,382 (GRCm39) S665T possibly damaging Het
Scn8a A G 15: 100,911,357 (GRCm39) I926V probably damaging Het
Snrpg T C 6: 86,353,510 (GRCm39) I30T probably damaging Het
Spryd3 A T 15: 102,027,425 (GRCm39) probably null Het
Svil A G 18: 5,114,531 (GRCm39) D2036G probably damaging Het
Synj2 A T 17: 6,067,868 (GRCm39) I551F probably damaging Het
Tiam2 A T 17: 3,489,971 (GRCm39) probably benign Het
Tmem132b T C 5: 125,864,639 (GRCm39) F915S probably damaging Het
Try5 C A 6: 41,288,342 (GRCm39) V204L probably benign Het
Vmn2r6 T C 3: 64,463,749 (GRCm39) T362A probably benign Het
Other mutations in Rgsl1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01372:Rgsl1 APN 1 153,701,887 (GRCm39) missense probably damaging 1.00
IGL02253:Rgsl1 APN 1 153,669,513 (GRCm39) missense probably damaging 1.00
IGL02345:Rgsl1 APN 1 153,679,755 (GRCm39) splice site probably null
IGL02409:Rgsl1 APN 1 153,701,989 (GRCm39) missense possibly damaging 0.53
IGL02587:Rgsl1 APN 1 153,675,684 (GRCm39) missense probably damaging 1.00
IGL02797:Rgsl1 APN 1 153,683,454 (GRCm39) missense probably damaging 1.00
IGL03032:Rgsl1 APN 1 153,701,948 (GRCm39) missense possibly damaging 0.53
IGL03082:Rgsl1 APN 1 153,675,693 (GRCm39) missense possibly damaging 0.86
IGL03123:Rgsl1 APN 1 153,701,687 (GRCm39) missense probably damaging 1.00
IGL03213:Rgsl1 APN 1 153,701,587 (GRCm39) missense probably benign 0.12
IGL03410:Rgsl1 APN 1 153,669,501 (GRCm39) missense probably null 0.82
Bam UTSW 1 153,669,898 (GRCm39) missense probably benign 0.00
Candygram UTSW 1 153,697,245 (GRCm39) nonsense probably null
wham UTSW 1 153,678,038 (GRCm39) missense probably benign 0.02
IGL03050:Rgsl1 UTSW 1 153,701,422 (GRCm39) missense possibly damaging 0.60
PIT4519001:Rgsl1 UTSW 1 153,701,716 (GRCm39) missense possibly damaging 0.96
R0149:Rgsl1 UTSW 1 153,669,510 (GRCm39) missense probably damaging 1.00
R0536:Rgsl1 UTSW 1 153,701,927 (GRCm39) missense probably damaging 1.00
R0633:Rgsl1 UTSW 1 153,719,853 (GRCm39) missense possibly damaging 0.72
R0726:Rgsl1 UTSW 1 153,678,074 (GRCm39) missense probably damaging 1.00
R0839:Rgsl1 UTSW 1 153,677,980 (GRCm39) critical splice donor site probably null
R1240:Rgsl1 UTSW 1 153,660,937 (GRCm39) missense probably benign 0.18
R1355:Rgsl1 UTSW 1 153,683,507 (GRCm39) start codon destroyed probably null 0.23
R1491:Rgsl1 UTSW 1 153,701,672 (GRCm39) missense possibly damaging 0.93
R1688:Rgsl1 UTSW 1 153,680,422 (GRCm39) missense probably damaging 0.98
R1694:Rgsl1 UTSW 1 153,680,422 (GRCm39) missense probably damaging 0.98
R1842:Rgsl1 UTSW 1 153,675,543 (GRCm39) missense probably damaging 1.00
R2008:Rgsl1 UTSW 1 153,701,651 (GRCm39) missense possibly damaging 0.53
R2114:Rgsl1 UTSW 1 153,693,295 (GRCm39) missense probably benign
R2116:Rgsl1 UTSW 1 153,693,295 (GRCm39) missense probably benign
R2176:Rgsl1 UTSW 1 153,701,014 (GRCm39) splice site probably benign
R2229:Rgsl1 UTSW 1 153,698,104 (GRCm39) missense possibly damaging 0.72
R2895:Rgsl1 UTSW 1 153,703,294 (GRCm39) missense probably damaging 1.00
R3923:Rgsl1 UTSW 1 153,679,876 (GRCm39) critical splice acceptor site probably null
R4001:Rgsl1 UTSW 1 153,693,330 (GRCm39) missense probably damaging 1.00
R4434:Rgsl1 UTSW 1 153,678,087 (GRCm39) missense possibly damaging 0.52
R4489:Rgsl1 UTSW 1 153,703,282 (GRCm39) missense probably benign 0.27
R4649:Rgsl1 UTSW 1 153,693,328 (GRCm39) missense probably benign 0.01
R4925:Rgsl1 UTSW 1 153,688,023 (GRCm39) missense probably benign 0.01
R4928:Rgsl1 UTSW 1 153,669,514 (GRCm39) missense probably damaging 1.00
R5045:Rgsl1 UTSW 1 153,697,268 (GRCm39) nonsense probably null
R5304:Rgsl1 UTSW 1 153,703,238 (GRCm39) missense probably damaging 0.97
R5331:Rgsl1 UTSW 1 153,678,038 (GRCm39) missense probably benign 0.02
R5373:Rgsl1 UTSW 1 153,666,053 (GRCm39) missense probably benign 0.33
R5374:Rgsl1 UTSW 1 153,666,053 (GRCm39) missense probably benign 0.33
R5566:Rgsl1 UTSW 1 153,669,520 (GRCm39) missense probably damaging 1.00
R5649:Rgsl1 UTSW 1 153,701,639 (GRCm39) missense possibly damaging 0.93
R6062:Rgsl1 UTSW 1 153,675,618 (GRCm39) missense possibly damaging 0.72
R6142:Rgsl1 UTSW 1 153,687,984 (GRCm39) missense probably benign 0.01
R6158:Rgsl1 UTSW 1 153,679,767 (GRCm39) missense possibly damaging 0.72
R6184:Rgsl1 UTSW 1 153,703,194 (GRCm39) missense probably benign 0.08
R6273:Rgsl1 UTSW 1 153,703,211 (GRCm39) missense possibly damaging 0.96
R6384:Rgsl1 UTSW 1 153,703,291 (GRCm39) missense possibly damaging 0.86
R6419:Rgsl1 UTSW 1 153,698,117 (GRCm39) missense probably damaging 0.98
R6568:Rgsl1 UTSW 1 153,697,292 (GRCm39) missense possibly damaging 0.72
R6660:Rgsl1 UTSW 1 153,701,512 (GRCm39) missense possibly damaging 0.70
R6745:Rgsl1 UTSW 1 153,698,063 (GRCm39) missense probably benign 0.18
R6892:Rgsl1 UTSW 1 153,697,245 (GRCm39) nonsense probably null
R6974:Rgsl1 UTSW 1 153,675,568 (GRCm39) missense probably damaging 1.00
R7172:Rgsl1 UTSW 1 153,701,966 (GRCm39) missense possibly damaging 0.72
R7200:Rgsl1 UTSW 1 153,660,945 (GRCm39) missense probably benign 0.33
R7275:Rgsl1 UTSW 1 153,679,876 (GRCm39) critical splice acceptor site probably null
R7313:Rgsl1 UTSW 1 153,683,622 (GRCm39) critical splice acceptor site probably null
R7341:Rgsl1 UTSW 1 153,669,591 (GRCm39) missense probably benign 0.01
R7448:Rgsl1 UTSW 1 153,719,847 (GRCm39) critical splice donor site probably null
R7662:Rgsl1 UTSW 1 153,701,225 (GRCm39) missense probably benign
R7703:Rgsl1 UTSW 1 153,669,610 (GRCm39) missense possibly damaging 0.73
R7846:Rgsl1 UTSW 1 153,701,783 (GRCm39) missense possibly damaging 0.53
R8408:Rgsl1 UTSW 1 153,701,435 (GRCm39) missense possibly damaging 0.96
R8860:Rgsl1 UTSW 1 153,697,100 (GRCm39) nonsense probably null
R8894:Rgsl1 UTSW 1 153,698,119 (GRCm39) critical splice acceptor site probably null
R9043:Rgsl1 UTSW 1 153,717,567 (GRCm39) missense possibly damaging 0.73
R9187:Rgsl1 UTSW 1 153,669,613 (GRCm39) missense possibly damaging 0.53
R9280:Rgsl1 UTSW 1 153,669,898 (GRCm39) missense probably benign 0.00
R9326:Rgsl1 UTSW 1 153,679,768 (GRCm39) missense probably benign 0.01
R9388:Rgsl1 UTSW 1 153,693,355 (GRCm39) missense probably benign
R9479:Rgsl1 UTSW 1 153,657,445 (GRCm39) missense unknown
X0020:Rgsl1 UTSW 1 153,701,131 (GRCm39) missense probably benign 0.33
X0065:Rgsl1 UTSW 1 153,679,779 (GRCm39) missense possibly damaging 0.84
Z1177:Rgsl1 UTSW 1 153,701,734 (GRCm39) missense not run
Z1177:Rgsl1 UTSW 1 153,693,356 (GRCm39) missense possibly damaging 0.70
Posted On 2015-04-16