Mutagenetix > Incidental Mutation

Incidental Mutation 'R8927:Rgs12'

690144

Institutional Source

Beutler Lab

Gene Symbol

Rgs12

Ensembl Gene

ENSMUSG00000029101

Gene Name

regulator of G-protein signaling 12

Synonyms

4632412M04Rik, 1200016K18Rik

MMRRC Submission

068771-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.243) question?

Stock #

R8927 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

35106789-35196988 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 35123633 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Leucine at position 472 (W472L)

Ref Sequence

ENSEMBL: ENSMUSP00000030984 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000030984] [ENSMUST00000087684]

AlphaFold

Q8CGE9

Predicted Effect

possibly damaging
Transcript: ENSMUST00000030984
AA Change: W472L

PolyPhen 2 Score 0.925 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000030984
Gene: ENSMUSG00000029101
AA Change: W472L

Domain	Start	End	E-Value	Type
PDZ	29	98	5.25e-18	SMART
PTB	224	373	5.05e-28	SMART
low complexity region	443	456	N/A	INTRINSIC
low complexity region	643	661	N/A	INTRINSIC
low complexity region	685	697	N/A	INTRINSIC
RGS	715	832	2.84e-41	SMART
low complexity region	849	865	N/A	INTRINSIC
low complexity region	868	880	N/A	INTRINSIC
low complexity region	911	928	N/A	INTRINSIC
RBD	962	1032	3.12e-28	SMART
RBD	1034	1104	2.44e-21	SMART
GoLoco	1187	1209	9.74e-9	SMART
low complexity region	1259	1280	N/A	INTRINSIC
low complexity region	1292	1308	N/A	INTRINSIC
low complexity region	1359	1378	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000087684
AA Change: W472L

PolyPhen 2 Score 0.847 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000084970
Gene: ENSMUSG00000029101
AA Change: W472L

Domain	Start	End	E-Value	Type
PDZ	29	98	5.25e-18	SMART
PTB	224	373	5.05e-28	SMART
low complexity region	443	456	N/A	INTRINSIC
low complexity region	643	661	N/A	INTRINSIC
low complexity region	685	697	N/A	INTRINSIC
RGS	715	832	2.84e-41	SMART
Pfam:RGS12_us1	836	953	4.3e-61	PFAM
RBD	962	1032	3.12e-28	SMART
RBD	1034	1104	2.44e-21	SMART
Pfam:RGS12_us2	1106	1180	2.4e-37	PFAM
GoLoco	1187	1209	9.74e-9	SMART
Pfam:RGS12_usC	1238	1379	9.2e-49	PFAM

Meta Mutation Damage Score

0.0675

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

99% (78/79)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the 'regulator of G protein signaling' (RGS) gene family. The encoded protein may function as a guanosine triphosphatase (GTPase)-activating protein as well as a transcriptional repressor. This protein may play a role in tumorigenesis. Multiple transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630089N07Rik	A	T	16: 97,867,367 (GRCm39)	H198Q	probably damaging	Het
Abcb9	T	C	5: 124,221,706 (GRCm39)	T223A	probably benign	Het
Actc1	T	A	2: 113,880,881 (GRCm39)	K115*	probably null	Het
Angptl2	G	A	2: 33,132,316 (GRCm39)	D308N	probably benign	Het
Arl4d	A	C	11: 101,557,892 (GRCm39)	Q139H	possibly damaging	Het
Aspm	T	A	1: 139,418,125 (GRCm39)	C2951*	probably null	Het
Atp23	A	T	10: 126,723,362 (GRCm39)	*247R	probably null	Het
B3gnt7	T	A	1: 86,232,839 (GRCm39)	S28R	probably benign	Het
Bmp7	C	T	2: 172,721,211 (GRCm39)	R288H	probably damaging	Het
Bsdc1	G	T	4: 129,355,439 (GRCm39)		probably benign	Het
Capn13	T	C	17: 73,631,761 (GRCm39)		probably null	Het
Ccdc146	T	C	5: 21,538,060 (GRCm39)	E88G	probably damaging	Het
Ccdc73	C	A	2: 104,822,542 (GRCm39)	D2E		Het
Cdc5l	C	A	17: 45,721,839 (GRCm39)	R477L		Het
Cdh22	T	A	2: 164,965,504 (GRCm39)	H529L	possibly damaging	Het
Chchd3	T	A	6: 32,780,951 (GRCm39)	E178D	probably benign	Het
Ciz1	A	T	2: 32,257,512 (GRCm39)	R186*	probably null	Het
Col4a2	A	G	8: 11,475,543 (GRCm39)		probably null	Het
Copa	T	A	1: 171,931,737 (GRCm39)	H329Q	probably null	Het
Dcaf7	A	G	11: 105,942,752 (GRCm39)	D233G	probably damaging	Het
Dclk2	G	T	3: 86,739,048 (GRCm39)	P317Q	probably damaging	Het
Dgat2	T	C	7: 98,818,710 (GRCm39)	Y90C	probably benign	Het
Dsc3	A	T	18: 20,107,234 (GRCm39)	H462Q	probably benign	Het
Fam151a	T	A	4: 106,603,242 (GRCm39)		probably benign	Het
Fn1	T	C	1: 71,638,535 (GRCm39)	N1998S	probably benign	Het
Fpr2	T	C	17: 18,113,724 (GRCm39)	L240S	possibly damaging	Het
Fzd9	A	T	5: 135,278,589 (GRCm39)	M432K	probably damaging	Het
Gm5862	T	A	5: 26,226,678 (GRCm39)	I75F	probably damaging	Het
Gpr45	T	A	1: 43,072,314 (GRCm39)	V319D	probably damaging	Het
H4c11	T	C	13: 21,919,525 (GRCm39)	V87A	possibly damaging	Het
Igfn1	T	A	1: 135,905,984 (GRCm39)	R275W	probably damaging	Het
Inafm1	G	A	7: 16,006,980 (GRCm39)	A79V	unknown	Het
Itfg1	C	T	8: 86,567,420 (GRCm39)		probably benign	Het
Kcnt2	T	A	1: 140,356,535 (GRCm39)		probably null	Het
Klhl35	T	G	7: 99,120,221 (GRCm39)	I366S	probably damaging	Het
Lysmd1	A	T	3: 95,045,831 (GRCm39)	I223F	probably damaging	Het
Mrps30	A	G	13: 118,523,205 (GRCm39)	L189P	probably damaging	Het
Ms4a4d	A	C	19: 11,533,574 (GRCm39)	T152P	probably benign	Het
Mtcl1	A	T	17: 66,755,628 (GRCm39)	I238K	probably benign	Het
Musk	T	C	4: 58,301,638 (GRCm39)	I132T	probably damaging	Het
Myh2	A	T	11: 67,079,509 (GRCm39)	M989L	probably benign	Het
Myh8	G	A	11: 67,174,081 (GRCm39)	R172H	probably benign	Het
Nt5c1a	C	T	4: 123,102,281 (GRCm39)	T69M	possibly damaging	Het
Nuak2	T	A	1: 132,255,916 (GRCm39)	D196E	probably damaging	Het
Or52h7	A	T	7: 104,214,229 (GRCm39)	H267L	probably damaging	Het
Or5ap2	A	T	2: 85,679,918 (GRCm39)	I41F	possibly damaging	Het
Or5t7	T	C	2: 86,507,630 (GRCm39)	T16A	probably benign	Het
Or8k53	T	C	2: 86,178,090 (GRCm39)	T7A	possibly damaging	Het
Or8s10	A	G	15: 98,336,519 (GRCm39)		probably benign	Het
Palb2	A	T	7: 121,723,821 (GRCm39)	C643S	probably damaging	Het
Pde5a	T	A	3: 122,633,249 (GRCm39)	I706N	probably damaging	Het
Pdlim4	T	C	11: 53,950,790 (GRCm39)	R100G	probably benign	Het
Pip5k1c	T	A	10: 81,128,906 (GRCm39)	V5E	possibly damaging	Het
Pira1	A	C	7: 3,742,358 (GRCm39)	N56K	probably benign	Het
Plekhm1	A	G	11: 103,268,039 (GRCm39)	V644A	probably benign	Het
Plk2	T	G	13: 110,535,750 (GRCm39)	V524G	probably damaging	Het
Ppl	T	A	16: 4,905,474 (GRCm39)	N1607I	probably benign	Het
Prag1	T	G	8: 36,614,360 (GRCm39)	V1304G	probably damaging	Het
Prex1	C	T	2: 166,426,995 (GRCm39)	V1077M	probably damaging	Het
Prmt6	T	C	3: 110,158,248 (GRCm39)	S14G	probably benign	Het
Psrc1	T	G	3: 108,293,973 (GRCm39)	S263R	probably damaging	Het
Qrfprl	C	A	6: 65,358,597 (GRCm39)	S107*	probably null	Het
Rbp7	A	T	4: 149,537,958 (GRCm39)	L36*	probably null	Het
Rrp8	C	A	7: 105,384,073 (GRCm39)	C143F	possibly damaging	Het
Sart1	T	C	19: 5,438,529 (GRCm39)	S43G	probably benign	Het
Setx	A	G	2: 29,016,971 (GRCm39)	T25A	possibly damaging	Het
Skint5	G	A	4: 113,341,099 (GRCm39)	T1414I	probably benign	Het
Sorbs2	T	A	8: 46,248,952 (GRCm39)	S734R	probably damaging	Het
Spata31g1	A	T	4: 42,972,251 (GRCm39)	Y528F	probably benign	Het
Spon1	T	C	7: 113,629,592 (GRCm39)		probably null	Het
Sptbn1	C	T	11: 30,088,962 (GRCm39)	V767I	probably damaging	Het
Srf	T	C	17: 46,860,095 (GRCm39)	I477V	probably damaging	Het
Tanc2	A	G	11: 105,701,331 (GRCm39)	Y282C	probably damaging	Het
Tbc1d23	A	G	16: 56,992,152 (GRCm39)	Y603H	probably damaging	Het
Tdpoz6	T	A	3: 93,599,950 (GRCm39)	T140S	probably benign	Het
Tfap4	T	C	16: 4,369,218 (GRCm39)	D134G	probably damaging	Het
Tmem200c	A	G	17: 69,148,733 (GRCm39)	T439A	probably benign	Het
Tmem63b	A	T	17: 45,975,908 (GRCm39)	M515K	probably damaging	Het
Tnc	A	T	4: 63,925,595 (GRCm39)	N980K	probably damaging	Het
Ttc23l	T	A	15: 10,530,720 (GRCm39)	L297F	probably damaging	Het
Vinac1	A	G	2: 128,882,789 (GRCm39)	S76P		Het
Vmn1r170	A	G	7: 23,305,814 (GRCm39)	N72S	possibly damaging	Het
Vmn2r8	T	C	5: 108,950,131 (GRCm39)	M239V		Het
Vopp1	A	G	6: 57,731,578 (GRCm39)	F138L	probably damaging	Het
Vps41	T	A	13: 18,929,501 (GRCm39)	F79I	probably benign	Het
Zfp317	T	C	9: 19,552,521 (GRCm39)	M1T	probably null	Het

Other mutations in Rgs12

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01443:Rgs12	APN	5	35,132,563 (GRCm39)	missense	probably benign	0.25
IGL02296:Rgs12	APN	5	35,123,464 (GRCm39)	missense	probably damaging	0.96
IGL02337:Rgs12	APN	5	35,177,697 (GRCm39)	missense	probably damaging	1.00
IGL02483:Rgs12	APN	5	35,187,861 (GRCm39)	missense	probably damaging	1.00
IGL02869:Rgs12	APN	5	35,183,227 (GRCm39)	missense	probably damaging	0.97
IGL02989:Rgs12	APN	5	35,122,463 (GRCm39)	missense	probably damaging	1.00
R0015:Rgs12	UTSW	5	35,180,120 (GRCm39)	unclassified	probably benign
R0015:Rgs12	UTSW	5	35,180,120 (GRCm39)	unclassified	probably benign
R0046:Rgs12	UTSW	5	35,122,664 (GRCm39)	missense	probably damaging	1.00
R0046:Rgs12	UTSW	5	35,122,664 (GRCm39)	missense	probably damaging	1.00
R0106:Rgs12	UTSW	5	35,124,008 (GRCm39)	missense	probably benign	0.03
R0106:Rgs12	UTSW	5	35,124,008 (GRCm39)	missense	probably benign	0.03
R0233:Rgs12	UTSW	5	35,187,842 (GRCm39)	missense	probably damaging	1.00
R0233:Rgs12	UTSW	5	35,187,842 (GRCm39)	missense	probably damaging	1.00
R0245:Rgs12	UTSW	5	35,187,424 (GRCm39)	missense	probably benign	0.01
R0611:Rgs12	UTSW	5	35,176,804 (GRCm39)	missense	probably damaging	1.00
R0704:Rgs12	UTSW	5	35,180,466 (GRCm39)	missense	possibly damaging	0.95
R0723:Rgs12	UTSW	5	35,181,710 (GRCm39)	unclassified	probably benign
R1174:Rgs12	UTSW	5	35,123,809 (GRCm39)	missense	probably benign	0.00
R1538:Rgs12	UTSW	5	35,178,511 (GRCm39)	missense	probably damaging	0.98
R1556:Rgs12	UTSW	5	35,196,626 (GRCm39)	missense	possibly damaging	0.67
R1774:Rgs12	UTSW	5	35,123,747 (GRCm39)	missense	probably benign	0.34
R1791:Rgs12	UTSW	5	35,123,456 (GRCm39)	missense	possibly damaging	0.86
R1866:Rgs12	UTSW	5	35,123,018 (GRCm39)	missense	probably damaging	1.00
R1872:Rgs12	UTSW	5	35,123,165 (GRCm39)	missense	probably damaging	1.00
R1923:Rgs12	UTSW	5	35,189,613 (GRCm39)	missense	probably damaging	1.00
R2012:Rgs12	UTSW	5	35,187,872 (GRCm39)	missense	probably benign	0.00
R2107:Rgs12	UTSW	5	35,124,079 (GRCm39)	missense	possibly damaging	0.68
R3730:Rgs12	UTSW	5	35,189,595 (GRCm39)	missense	probably damaging	1.00
R3731:Rgs12	UTSW	5	35,189,595 (GRCm39)	missense	probably damaging	1.00
R3808:Rgs12	UTSW	5	35,189,698 (GRCm39)	missense	probably damaging	1.00
R3826:Rgs12	UTSW	5	35,123,359 (GRCm39)	missense	possibly damaging	0.94
R3827:Rgs12	UTSW	5	35,123,359 (GRCm39)	missense	possibly damaging	0.94
R3829:Rgs12	UTSW	5	35,123,359 (GRCm39)	missense	possibly damaging	0.94
R3830:Rgs12	UTSW	5	35,123,359 (GRCm39)	missense	possibly damaging	0.94
R4392:Rgs12	UTSW	5	35,189,655 (GRCm39)	missense	probably damaging	1.00
R4617:Rgs12	UTSW	5	35,177,700 (GRCm39)	missense	probably damaging	1.00
R5132:Rgs12	UTSW	5	35,147,156 (GRCm39)	intron	probably benign
R5213:Rgs12	UTSW	5	35,122,664 (GRCm39)	missense	probably damaging	1.00
R5296:Rgs12	UTSW	5	35,178,448 (GRCm39)	unclassified	probably benign
R5480:Rgs12	UTSW	5	35,123,455 (GRCm39)	missense	probably benign	0.09
R5510:Rgs12	UTSW	5	35,123,383 (GRCm39)	missense	probably damaging	1.00
R5708:Rgs12	UTSW	5	35,123,696 (GRCm39)	missense	probably benign	0.41
R5987:Rgs12	UTSW	5	35,177,689 (GRCm39)	missense	probably damaging	1.00
R6053:Rgs12	UTSW	5	35,123,296 (GRCm39)	missense	probably benign	0.01
R6113:Rgs12	UTSW	5	35,177,667 (GRCm39)	missense	probably damaging	0.99
R6401:Rgs12	UTSW	5	35,177,676 (GRCm39)	missense	probably damaging	1.00
R6736:Rgs12	UTSW	5	35,180,436 (GRCm39)	missense	probably damaging	1.00
R6807:Rgs12	UTSW	5	35,180,515 (GRCm39)	missense	probably null	0.27
R6857:Rgs12	UTSW	5	35,187,366 (GRCm39)	nonsense	probably null
R7082:Rgs12	UTSW	5	35,124,050 (GRCm39)	missense	probably benign	0.00
R7250:Rgs12	UTSW	5	35,122,841 (GRCm39)	missense	probably damaging	1.00
R7276:Rgs12	UTSW	5	35,183,715 (GRCm39)	missense	probably benign	0.06
R7444:Rgs12	UTSW	5	35,183,287 (GRCm39)	missense	possibly damaging	0.65
R7632:Rgs12	UTSW	5	35,122,934 (GRCm39)	missense	probably damaging	1.00
R8049:Rgs12	UTSW	5	35,183,374 (GRCm39)	missense	possibly damaging	0.89
R8089:Rgs12	UTSW	5	35,177,692 (GRCm39)	missense	probably damaging	1.00
R8241:Rgs12	UTSW	5	35,123,117 (GRCm39)	missense	probably damaging	1.00
R8797:Rgs12	UTSW	5	35,186,915 (GRCm39)	missense
R8928:Rgs12	UTSW	5	35,123,633 (GRCm39)	missense	possibly damaging	0.93
R9073:Rgs12	UTSW	5	35,177,753 (GRCm39)	unclassified	probably benign
R9211:Rgs12	UTSW	5	35,123,165 (GRCm39)	missense	probably damaging	0.98
R9485:Rgs12	UTSW	5	35,189,614 (GRCm39)	missense	probably damaging	0.99
R9550:Rgs12	UTSW	5	35,196,665 (GRCm39)	missense	probably damaging	0.99
Z1176:Rgs12	UTSW	5	35,123,113 (GRCm39)	missense	probably damaging	1.00
Z1177:Rgs12	UTSW	5	35,183,696 (GRCm39)	missense	probably benign	0.44
Z1177:Rgs12	UTSW	5	35,122,198 (GRCm39)	start gained	probably benign

Predicted Primers

PCR Primer
(F):5'- TAGCACTAGCAGCAACAGTG -3'
(R):5'- ACACTGCCACTCTTGTAGCAC -3'

Sequencing Primer
(F):5'- ACAGTGACAGCGGCATC -3'
(R):5'- ACTCTTGTAGCACATGGACCG -3'

Posted On

2021-11-19