Mutagenetix > Incidental Mutation

Incidental Mutation 'R7233:Ccng2'

562619

Institutional Source

Beutler Lab

Gene Symbol

Ccng2

Ensembl Gene

ENSMUSG00000029385

Gene Name

cyclin G2

Synonyms

MMRRC Submission

045343-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7233 (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: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (75/75)

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: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acox3	A	G	5: 35,762,641 (GRCm39)	K505R	probably benign	Het
Arhgap24	A	G	5: 103,026,367 (GRCm39)	K263E	probably benign	Het
Ark2n	C	A	18: 77,722,882 (GRCm39)	V385F	probably damaging	Het
Armc2	A	T	10: 41,799,800 (GRCm39)	V686D	probably damaging	Het
Bhmt	T	A	13: 93,758,025 (GRCm39)	K229*	probably null	Het
Birc2	A	T	9: 7,827,009 (GRCm39)	C326S	probably damaging	Het
Blzf1	A	T	1: 164,123,512 (GRCm39)		probably null	Het
Camsap3	T	A	8: 3,650,371 (GRCm39)	F223Y	probably damaging	Het
Ccdc126	C	T	6: 49,316,775 (GRCm39)	T85M	probably damaging	Het
Ces2h	T	A	8: 105,744,088 (GRCm39)	C279S	probably damaging	Het
Cfap44	T	A	16: 44,242,771 (GRCm39)	L725Q	probably damaging	Het
Cibar2	A	G	8: 120,898,661 (GRCm39)	L131P	probably damaging	Het
Clip1	T	C	5: 123,749,922 (GRCm39)	E987G	probably damaging	Het
Cog1	G	T	11: 113,540,556 (GRCm39)	R57L	probably damaging	Het
Ctdspl	T	C	9: 118,849,114 (GRCm39)		probably null	Het
Dnaaf9	C	A	2: 130,648,708 (GRCm39)	R258L	unknown	Het
Dnttip2	T	C	3: 122,070,039 (GRCm39)	V418A	probably benign	Het
Dop1a	G	A	9: 86,403,749 (GRCm39)	A186T	probably benign	Het
Efcab3	T	C	11: 104,730,669 (GRCm39)	S1966P	possibly damaging	Het
Engase	T	A	11: 118,373,827 (GRCm39)	V323E	probably damaging	Het
Farsb	A	G	1: 78,447,718 (GRCm39)		probably null	Het
Fpr2	G	T	17: 18,113,766 (GRCm39)	W254L	probably damaging	Het
Frmd3	A	C	4: 73,932,023 (GRCm39)	H6P	probably benign	Het
Fscn1	C	T	5: 142,956,029 (GRCm39)	S366L	possibly damaging	Het
Galt	T	A	4: 41,758,267 (GRCm39)	I344N	probably benign	Het
Gfra4	A	T	2: 130,883,037 (GRCm39)	V194E	probably damaging	Het
Golgb1	T	C	16: 36,735,120 (GRCm39)	S1497P	possibly damaging	Het
Igfn1	A	C	1: 135,897,873 (GRCm39)	S898A	probably benign	Het
Igkv1-135	T	C	6: 67,587,332 (GRCm39)	S68P	probably benign	Het
Lama2	A	T	10: 27,107,659 (GRCm39)	C784S	probably damaging	Het
Lars2	G	T	9: 123,241,019 (GRCm39)	G229*	probably null	Het
Lats2	A	T	14: 57,960,151 (GRCm39)		probably null	Het
Lgr6	A	C	1: 134,928,214 (GRCm39)		probably null	Het
Lrp1	A	T	10: 127,430,930 (GRCm39)	I373N	probably damaging	Het
Maml2	A	T	9: 13,532,067 (GRCm39)	H427L		Het
Mansc1	A	G	6: 134,598,806 (GRCm39)	V37A	probably damaging	Het
Map4k3	A	G	17: 80,905,077 (GRCm39)	V738A	possibly damaging	Het
Mastl	A	G	2: 23,023,670 (GRCm39)	I351T	probably benign	Het
Mcmdc2	T	G	1: 10,002,408 (GRCm39)		probably null	Het
Mrgprd	A	G	7: 144,875,672 (GRCm39)	D181G	possibly damaging	Het
Msantd5f9	G	T	4: 73,835,808 (GRCm39)	L219M	probably benign	Het
Msra	T	C	14: 64,360,714 (GRCm39)	Y209C	probably damaging	Het
Musk	A	G	4: 58,373,307 (GRCm39)	E759G	possibly damaging	Het
Nab1	T	C	1: 52,498,378 (GRCm39)	*487W	probably null	Het
Or2z9	A	G	8: 72,853,900 (GRCm39)	T99A	probably benign	Het
Or5p66	T	A	7: 107,885,923 (GRCm39)	T137S	probably benign	Het
Pkdrej	A	G	15: 85,705,349 (GRCm39)	S196P	probably damaging	Het
Pln	A	G	10: 53,220,008 (GRCm39)	T17A	probably damaging	Het
Polrmt	A	T	10: 79,581,619 (GRCm39)		probably null	Het
Ppp1r14a	T	A	7: 28,988,949 (GRCm39)	Y64N	probably damaging	Het
Ppp1r9a	A	T	6: 5,134,804 (GRCm39)	H959L	probably benign	Het
Pramel42	A	T	5: 94,685,524 (GRCm39)	M395L	probably benign	Het
Prmt7	A	G	8: 106,946,642 (GRCm39)	T75A	probably damaging	Het
Prom1	T	C	5: 44,194,816 (GRCm39)	S319G	possibly damaging	Het
Prtg	G	A	9: 72,819,273 (GRCm39)	G1089S	probably benign	Het
Ptprd	T	C	4: 75,978,020 (GRCm39)	D596G	probably benign	Het
Rbm12	C	T	2: 155,937,894 (GRCm39)	G793S	unknown	Het
Rora	A	T	9: 69,104,804 (GRCm39)	R43*	probably null	Het
Sez6	T	C	11: 77,863,963 (GRCm39)	Y482H	probably damaging	Het
Skint2	A	T	4: 112,483,122 (GRCm39)	N176Y	probably damaging	Het
Slc44a2	G	T	9: 21,259,445 (GRCm39)		probably null	Het
Sox6	A	G	7: 115,089,044 (GRCm39)	V606A	possibly damaging	Het
Spa17	T	C	9: 37,514,587 (GRCm39)		probably null	Het
Syne1	A	C	10: 5,252,160 (GRCm39)	L2498R	probably damaging	Het
Synpo2	T	G	3: 122,911,333 (GRCm39)	H104P	probably benign	Het
Tapbp	G	T	17: 34,138,943 (GRCm39)	A46S	probably damaging	Het
Tbc1d30	C	A	10: 121,107,962 (GRCm39)	R480L	probably benign	Het
Tshz1	T	C	18: 84,032,944 (GRCm39)	D488G	possibly damaging	Het
Ulk1	A	G	5: 110,956,908 (GRCm39)	L70P	probably damaging	Het
Zcchc17	T	A	4: 130,221,116 (GRCm39)	D145V	probably damaging	Het
Zfp318	T	A	17: 46,716,978 (GRCm39)	L1037M	probably damaging	Het
Zfp324	C	T	7: 12,704,524 (GRCm39)	Q238*	probably null	Het
Zfp874a	A	G	13: 67,590,776 (GRCm39)	Y303H	possibly damaging	Het
Zfp975	T	C	7: 42,311,918 (GRCm39)	K232E	probably benign	Het
Zfp982	T	A	4: 147,597,718 (GRCm39)	N358K	probably benign	Het
Zmiz1	C	T	14: 25,650,092 (GRCm39)	P417S	possibly damaging	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
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
R7451: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'- TTTCACTTCCGTCAAAGCAAC -3'

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

Posted On

2019-06-26