Mutagenetix > Incidental Mutation

Incidental Mutation 'R7451:Ccng2'

577708

Institutional Source

Beutler Lab

Gene Symbol

Ccng2

Ensembl Gene

ENSMUSG00000029385

Gene Name

cyclin G2

Synonyms

MMRRC Submission

045525-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7451 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

93415432-93424090 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to G at 93421202 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Arginine at position 237 (S237R)

Ref Sequence

ENSEMBL: ENSMUSP00000113278 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031331] [ENSMUST00000121127]

AlphaFold

O08918

Predicted Effect

probably benign
Transcript: ENSMUST00000031331
AA Change: S237R

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000031331
Gene: ENSMUSG00000029385
AA Change: S237R

Domain	Start	End	E-Value	Type
CYCLIN	61	147	3.06e-15	SMART
low complexity region	218	237	N/A	INTRINSIC
low complexity region	295	317	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000121127
AA Change: S237R

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000113278
Gene: ENSMUSG00000029385
AA Change: S237R

Domain	Start	End	E-Value	Type
CYCLIN	61	147	3.06e-15	SMART
low complexity region	218	237	N/A	INTRINSIC
low complexity region	295	317	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000130183

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149329

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152097

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153260

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

100% (84/84)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The eukaryotic cell cycle is governed by cyclin-dependent protein kinases (CDKs) whose activities are regulated by cyclins and CDK inhibitors. The 8 species of cyclins reported in mammals, cyclins A through H, share a conserved amino acid sequence of about 90 residues called the cyclin box. The amino acid sequence of cyclin G is well conserved among mammals. The nucleotide sequence of cyclin G1 and cyclin G2 are 53% identical. Unlike cyclin G1, cyclin G2 contains a C-terminal PEST protein destabilization motif, suggesting that cyclin G2 expression is tightly regulated through the cell cycle. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb6	A	G	1: 75,148,797 (GRCm39)	I794T	probably damaging	Het
Abcc5	T	A	16: 20,193,820 (GRCm39)	H767L	probably damaging	Het
Adgrb2	A	T	4: 129,908,350 (GRCm39)	M1031L	probably damaging	Het
Akna	T	A	4: 63,296,904 (GRCm39)	M891L	probably benign	Het
Aloxe3	C	A	11: 69,033,746 (GRCm39)	T620K	possibly damaging	Het
Amph	A	G	13: 19,261,538 (GRCm39)	Y63C	probably damaging	Het
Asprv1	A	G	6: 86,605,930 (GRCm39)	I259V	probably benign	Het
Atp7b	C	T	8: 22,504,700 (GRCm39)	W652*	probably null	Het
Atp8a2	C	T	14: 60,028,630 (GRCm39)	D946N	probably null	Het
BC024063	T	A	10: 81,944,576 (GRCm39)	N65K	probably benign	Het
Bean1	A	T	8: 104,940,628 (GRCm39)	M154L	probably benign	Het
Bltp1	G	T	3: 37,076,956 (GRCm39)		probably null	Het
Cacna1c	C	T	6: 118,570,981 (GRCm39)	V2181M	unknown	Het
Cacna1g	A	G	11: 94,319,901 (GRCm39)	I1425T	probably damaging	Het
Caskin2	A	G	11: 115,702,981 (GRCm39)		probably benign	Het
Cfap97d1	A	T	11: 101,882,283 (GRCm39)	N147I	possibly damaging	Het
Cfd	T	A	10: 79,727,362 (GRCm39)	V43E	probably damaging	Het
Chd9	GCCCC	GCCC	8: 91,760,418 (GRCm39)		probably null	Het
Chd9	T	A	8: 91,760,446 (GRCm39)	S2064T	probably benign	Het
Cpsf2	T	G	12: 101,967,051 (GRCm39)	V646G	possibly damaging	Het
Ctif	T	C	18: 75,652,874 (GRCm39)	D461G	possibly damaging	Het
Cyp3a41a	T	A	5: 145,636,550 (GRCm39)	E414D	probably benign	Het
Dagla	A	G	19: 10,230,719 (GRCm39)	V544A	probably damaging	Het
Dhx57	A	T	17: 80,554,542 (GRCm39)	V1228E	probably damaging	Het
Eif2b3	T	A	4: 116,909,993 (GRCm39)	L176*	probably null	Het
Fbxw26	T	A	9: 109,561,691 (GRCm39)	I168L	probably benign	Het
Flt3	T	A	5: 147,286,477 (GRCm39)	Y703F	probably damaging	Het
Frmpd1	C	T	4: 45,279,558 (GRCm39)	P761L	probably benign	Het
Gabrd	A	G	4: 155,472,916 (GRCm39)	V89A	possibly damaging	Het
Galnt14	A	T	17: 73,881,804 (GRCm39)	H98Q	probably benign	Het
Gli3	T	C	13: 15,900,876 (GRCm39)	V1421A	possibly damaging	Het
Gprin2	A	G	14: 33,917,762 (GRCm39)	S3P	probably damaging	Het
Ifi211	T	G	1: 173,727,058 (GRCm39)	D362A	probably damaging	Het
Lars1	G	T	18: 42,335,615 (GRCm39)	T1167K	probably benign	Het
Lce1b	T	C	3: 92,563,207 (GRCm39)	S109G	unknown	Het
Lrp2	T	G	2: 69,343,677 (GRCm39)	E894A	probably damaging	Het
Mamdc4	A	G	2: 25,454,473 (GRCm39)	V1081A	possibly damaging	Het
Mcub	T	C	3: 129,710,752 (GRCm39)	S227G	possibly damaging	Het
Mki67	A	G	7: 135,301,080 (GRCm39)	I1318T	probably benign	Het
Mybl2	C	T	2: 162,914,626 (GRCm39)	T248I	possibly damaging	Het
Myo9b	A	T	8: 71,804,832 (GRCm39)	H1441L	probably benign	Het
Nav2	T	A	7: 49,202,577 (GRCm39)		probably null	Het
Neb	C	T	2: 52,091,466 (GRCm39)	V5339I	probably benign	Het
Nktr	T	A	9: 121,558,722 (GRCm39)	S88T	probably damaging	Het
Nup155	C	T	15: 8,175,091 (GRCm39)	Q963*	probably null	Het
Oas1c	A	C	5: 120,940,207 (GRCm39)	L320V	possibly damaging	Het
Or10ak14	C	T	4: 118,610,884 (GRCm39)	A286T	probably benign	Het
Or10d1b	G	A	9: 39,613,423 (GRCm39)	T214I	probably damaging	Het
Or1o11	C	A	17: 37,757,196 (GRCm39)	S261R	probably damaging	Het
Or2t46	A	G	11: 58,472,516 (GRCm39)	Y282C	probably damaging	Het
Or4a81	A	G	2: 89,619,453 (GRCm39)	M81T	probably benign	Het
Or52b4i	T	C	7: 102,191,461 (GRCm39)	I106T	probably benign	Het
Pcdhga7	A	G	18: 37,849,057 (GRCm39)	S355G	possibly damaging	Het
Pde11a	C	T	2: 75,853,117 (GRCm39)	V834I	possibly damaging	Het
Pdzrn4	A	T	15: 92,667,948 (GRCm39)	D700V	possibly damaging	Het
Pif1	C	A	9: 65,495,630 (GRCm39)	P180Q	probably benign	Het
Pkig	G	T	2: 163,563,083 (GRCm39)	E5*	probably null	Het
Pla2r1	T	A	2: 60,365,346 (GRCm39)	M75L	probably damaging	Het
Pllp	T	C	8: 95,402,871 (GRCm39)	S157G	probably damaging	Het
Ppfia1	A	T	7: 144,061,947 (GRCm39)	H566Q	probably benign	Het
Ptpn13	A	G	5: 103,674,961 (GRCm39)	D646G	probably benign	Het
Rab11fip5	T	A	6: 85,318,538 (GRCm39)	T784S	probably benign	Het
Rad51ap2	T	G	12: 11,507,982 (GRCm39)	S635A	probably benign	Het
Ranbp17	A	T	11: 33,234,114 (GRCm39)		probably null	Het
Rce1	C	T	19: 4,675,081 (GRCm39)	G111D	probably damaging	Het
Rcor3	C	A	1: 191,822,173 (GRCm39)	G8V	probably damaging	Het
Rhox4d	G	A	X: 36,700,645 (GRCm39)	G191E	unknown	Het
Rimbp2	C	T	5: 128,865,435 (GRCm39)	V631I	probably benign	Het
Scai	T	C	2: 39,015,148 (GRCm39)	T94A	probably damaging	Het
Sfmbt1	G	A	14: 30,538,768 (GRCm39)	A796T	probably benign	Het
Slc6a11	C	A	6: 114,222,644 (GRCm39)	Y546*	probably null	Het
Slc7a2	T	C	8: 41,365,686 (GRCm39)	S506P	probably damaging	Het
Synj2	T	A	17: 6,080,066 (GRCm39)	N1098K	possibly damaging	Het
Tmem177	G	A	1: 119,837,971 (GRCm39)	A236V	probably damaging	Het
Togaram1	T	A	12: 65,043,749 (GRCm39)	D1249E	probably damaging	Het
Trav17	A	T	14: 54,044,096 (GRCm39)	M1L	probably damaging	Het
Trim25	C	A	11: 88,906,563 (GRCm39)	A433D	possibly damaging	Het
Trim69	T	C	2: 121,998,508 (GRCm39)	F160S	probably benign	Het
Trio	A	T	15: 27,747,999 (GRCm39)	V1407E	probably benign	Het
Trpm7	A	T	2: 126,668,657 (GRCm39)	M753K	probably damaging	Het
Ttc12	G	T	9: 49,383,179 (GRCm39)	A75E	probably benign	Het
Uchl4	A	T	9: 64,143,013 (GRCm39)	I165L	probably benign	Het
Uvrag	A	T	7: 98,790,120 (GRCm39)	L13Q	unknown	Het
Wwc2	G	A	8: 48,317,610 (GRCm39)	R656W	not run	Het

Other mutations in Ccng2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01148:Ccng2	APN	5	93,418,746 (GRCm39)	missense	probably damaging	0.99
IGL01289:Ccng2	APN	5	93,421,276 (GRCm39)	missense	probably null	0.88
R0133:Ccng2	UTSW	5	93,421,240 (GRCm39)	missense	probably benign	0.15
R0266:Ccng2	UTSW	5	93,419,148 (GRCm39)	splice site	probably benign
R0346:Ccng2	UTSW	5	93,418,753 (GRCm39)	missense	probably damaging	1.00
R0401:Ccng2	UTSW	5	93,421,272 (GRCm39)	missense	possibly damaging	0.52
R1087:Ccng2	UTSW	5	93,421,303 (GRCm39)	missense	probably benign	0.17
R1373:Ccng2	UTSW	5	93,418,914 (GRCm39)	splice site	probably benign
R1696:Ccng2	UTSW	5	93,421,241 (GRCm39)	missense	possibly damaging	0.90
R3727:Ccng2	UTSW	5	93,422,810 (GRCm39)	missense	probably damaging	1.00
R5395:Ccng2	UTSW	5	93,417,257 (GRCm39)	missense	possibly damaging	0.84
R6337:Ccng2	UTSW	5	93,418,780 (GRCm39)	missense	probably benign
R6611:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7077:Ccng2	UTSW	5	93,417,199 (GRCm39)	missense	possibly damaging	0.91
R7140:Ccng2	UTSW	5	93,416,614 (GRCm39)	missense	probably benign	0.00
R7161:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7193:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7233:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7235:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7269:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7270:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7271:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7449:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7567:Ccng2	UTSW	5	93,418,731 (GRCm39)	missense	probably benign	0.01
R7614:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7657:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7658:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7743:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7744:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7745:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7874:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7875:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7876:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7877:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R7884:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R8053:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R8279:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R8282:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R8492:Ccng2	UTSW	5	93,419,313 (GRCm39)	missense	probably damaging	1.00
R8503:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R8504:Ccng2	UTSW	5	93,421,202 (GRCm39)	missense	probably benign	0.00
R8528:Ccng2	UTSW	5	93,417,164 (GRCm39)	missense	possibly damaging	0.60
R9010:Ccng2	UTSW	5	93,416,616 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TCCTGTGTAAGTAATACTTGGAGTG -3'
(R):5'- TGTGGAAGACGCCTGCTTAC -3'

Sequencing Primer
(F):5'- GGAGTGTTATTTCAACCAGCAGTTCC -3'
(R):5'- GGAAGACGCCTGCTTACCTTTC -3'

Posted On

2019-10-07