Mutagenetix > Incidental Mutation

Incidental Mutation 'R1503:Ccpg1'

169461

Institutional Source

Beutler Lab

Gene Symbol

Ccpg1

Ensembl Gene

ENSMUSG00000034563

Gene Name

cell cycle progression 1

Synonyms

1700030B06Rik, D9Ertd392e, 1810073J13Rik, 9430028F23Rik

MMRRC Submission

039553-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1503 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

72985429-73016340 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 72999478 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 66 (N66S)

Ref Sequence

ENSEMBL: ENSMUSP00000082458 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037977] [ENSMUST00000085350] [ENSMUST00000124008] [ENSMUST00000140675] [ENSMUST00000149692] [ENSMUST00000150826] [ENSMUST00000156879]

AlphaFold

Q640L3

Predicted Effect

probably benign
Transcript: ENSMUST00000037977
AA Change: N66S

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000045669
Gene: ENSMUSG00000034563
AA Change: N66S

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
low complexity region	83	94	N/A	INTRINSIC
low complexity region	155	174	N/A	INTRINSIC
low complexity region	187	209	N/A	INTRINSIC
transmembrane domain	219	241	N/A	INTRINSIC
coiled coil region	296	450	N/A	INTRINSIC
low complexity region	566	572	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000085350
AA Change: N66S

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000082458
Gene: ENSMUSG00000034563
AA Change: N66S

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
low complexity region	83	94	N/A	INTRINSIC
low complexity region	155	174	N/A	INTRINSIC
low complexity region	187	209	N/A	INTRINSIC
transmembrane domain	219	241	N/A	INTRINSIC
coiled coil region	296	450	N/A	INTRINSIC
low complexity region	566	572	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000124008
AA Change: N66S

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000121059
Gene: ENSMUSG00000034563
AA Change: N66S

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
low complexity region	83	94	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000140675
AA Change: N66S

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000116976
Gene: ENSMUSG00000034563
AA Change: N66S

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
low complexity region	83	94	N/A	INTRINSIC
low complexity region	155	174	N/A	INTRINSIC
low complexity region	187	209	N/A	INTRINSIC
transmembrane domain	219	241	N/A	INTRINSIC
coiled coil region	296	450	N/A	INTRINSIC
low complexity region	566	572	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149551

Predicted Effect

probably benign
Transcript: ENSMUST00000149692

SMART Domains

Protein: ENSMUSP00000120629
Gene: ENSMUSG00000089865

Domain	Start	End	E-Value	Type
Pfam:CS	6	77	2.1e-9	PFAM
coiled coil region	101	161	N/A	INTRINSIC
Pfam:TPR_11	286	352	2e-14	PFAM
Pfam:TPR_1	322	352	5.6e-6	PFAM
Blast:TPR	364	386	1e-5	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000150826
AA Change: N66S

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000122966
Gene: ENSMUSG00000034563
AA Change: N66S

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
low complexity region	83	94	N/A	INTRINSIC
low complexity region	155	174	N/A	INTRINSIC
low complexity region	187	209	N/A	INTRINSIC
transmembrane domain	219	241	N/A	INTRINSIC
coiled coil region	296	450	N/A	INTRINSIC
low complexity region	566	572	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000156879
AA Change: N66S

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000117202
Gene: ENSMUSG00000034563
AA Change: N66S

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
low complexity region	83	94	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 96.1%
20x: 92.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgef6	T	C	X: 57,338,562	M5V	probably benign	Het
Atf7ip	G	T	6: 136,606,867	V1299L	probably damaging	Het
Atp12a	A	T	14: 56,373,424	N342Y	probably damaging	Het
Atp8b5	G	A	4: 43,344,430	G439D	probably damaging	Het
Bpifb2	G	A	2: 153,889,510	D269N	possibly damaging	Het
Btd	T	G	14: 31,667,655	C444W	probably damaging	Het
Cacna1a	A	G	8: 84,601,946	D1624G	probably benign	Het
Carmil3	A	C	14: 55,498,280	N563T	probably damaging	Het
Cars	T	C	7: 143,568,989	R538G	probably benign	Het
Catsperd	A	G	17: 56,654,525	K416E	possibly damaging	Het
Cc2d2a	A	T	5: 43,695,239	Y386F	probably damaging	Het
Cd48	T	A	1: 171,695,847	L86H	probably damaging	Het
Cdan1	A	T	2: 120,729,575	H369Q	probably damaging	Het
Chil4	T	C	3: 106,206,034	D189G	probably benign	Het
Cit	T	A	5: 115,873,900	Y189N	possibly damaging	Het
Cntn3	G	A	6: 102,464,565	Q7*	probably null	Het
Csn1s2a	A	T	5: 87,775,799	I5F	possibly damaging	Het
Ctnnd1	C	T	2: 84,605,179		probably null	Het
Dmxl2	A	T	9: 54,446,988	Y391*	probably null	Het
Dnah12	T	C	14: 26,773,692	S1426P	probably damaging	Het
Dnhd1	T	G	7: 105,693,660	S1404A	possibly damaging	Het
Drosha	T	A	15: 12,848,073	C484S	probably benign	Het
Dsg4	A	T	18: 20,449,679	I125F	probably damaging	Het
Egfr	T	A	11: 16,869,301	M277K	possibly damaging	Het
Eml5	G	T	12: 98,831,174	L1059I	probably damaging	Het
Erbb4	G	T	1: 68,346,546	H295N	probably benign	Het
Etl4	T	G	2: 20,743,874	V139G	possibly damaging	Het
Fam160a1	T	A	3: 85,672,477	Y807F	possibly damaging	Het
Frem3	A	T	8: 80,687,018	E1969D	probably damaging	Het
Gdf3	T	A	6: 122,606,337	D357V	probably damaging	Het
Gimap8	T	A	6: 48,647,529		probably null	Het
Gml2	C	A	15: 74,821,352	S68*	probably null	Het
Gphn	A	G	12: 78,504,629	I248V	possibly damaging	Het
Greb1	A	T	12: 16,724,819	Y192*	probably null	Het
Hmbs	A	C	9: 44,337,432	L215W	probably benign	Het
Iglon5	T	A	7: 43,479,025	T123S	probably benign	Het
Ints2	C	T	11: 86,226,781	R705H	probably damaging	Het
Ints8	A	T	4: 11,245,842	L212Q	probably damaging	Het
Itgad	A	G	7: 128,198,121	Y846C	probably benign	Het
Kcnj1	A	G	9: 32,396,492	T51A	probably damaging	Het
Kif1bp	A	G	10: 62,559,408	V485A	probably damaging	Het
Kif9	A	T	9: 110,510,438	K449N	possibly damaging	Het
Klk11	G	A	7: 43,778,909	W241*	probably null	Het
Krt32	T	C	11: 100,084,110		probably null	Het
Loxl1	A	G	9: 58,293,640	F513S	probably damaging	Het
Mapk8ip3	A	T	17: 24,904,923	S571T	probably damaging	Het
Mcam	C	T	9: 44,141,291	R606C	probably damaging	Het
Mtss1	T	C	15: 58,951,672	N282S	probably damaging	Het
Myh13	T	A	11: 67,353,674	D1012E	probably benign	Het
Myo16	A	G	8: 10,502,817	T952A	probably benign	Het
Neb	T	C	2: 52,298,620	D874G	probably damaging	Het
Nek11	A	G	9: 105,163,204	Y553H	probably damaging	Het
Nr2c2	T	A	6: 92,105,331	V9D	probably benign	Het
Nxf1	T	A	19: 8,762,436	F51L	probably benign	Het
Olfr1260	T	C	2: 89,978,528	V250A	probably damaging	Het
Olfr1347	T	C	7: 6,488,179	I232V	probably damaging	Het
Olfr1350	A	G	7: 6,570,471	N160S	probably damaging	Het
Olfr170	A	G	16: 19,606,312	S119P	probably benign	Het
Olfr344	A	T	2: 36,568,873	I92F	probably damaging	Het
Olfr397	T	G	11: 73,964,568		probably null	Het
Olfr750	A	G	14: 51,070,734	S220P	probably damaging	Het
Pcdhb8	A	T	18: 37,356,519	N76Y	probably damaging	Het
Pdzrn4	T	A	15: 92,399,804	F217I	probably damaging	Het
Ppp1r16a	T	A	15: 76,694,399	H434Q	probably benign	Het
Prpf19	T	A	19: 10,901,022	F291I	possibly damaging	Het
R3hdm2	G	T	10: 127,471,826	E319*	probably null	Het
Sel1l3	A	G	5: 53,137,929	Y777H	probably damaging	Het
Serpinb5	G	A	1: 106,870,289	A3T	possibly damaging	Het
Skp2	C	A	15: 9,127,911	V88F	probably damaging	Het
Slc25a16	T	C	10: 62,928,376	Y71H	probably damaging	Het
Slc6a6	T	A	6: 91,740,992	I304N	probably damaging	Het
Sned1	G	A	1: 93,281,654	V830M	possibly damaging	Het
Sox17	C	A	1: 4,491,928	G222C	probably damaging	Het
Trmu	T	A	15: 85,895,019	V289E	possibly damaging	Het
Vdac2	A	G	14: 21,837,877	E96G	probably damaging	Het
Wdhd1	A	T	14: 47,247,400	D885E	probably benign	Het
Zfp646	A	G	7: 127,880,136	N495S	probably damaging	Het
Zfp663	T	C	2: 165,352,653	T549A	probably damaging	Het
Zfp935	G	A	13: 62,455,137	A83V	possibly damaging	Het

Other mutations in Ccpg1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01665:Ccpg1	APN	9	73005877	missense	probably damaging	1.00
IGL01710:Ccpg1	APN	9	72997441	utr 3 prime	probably benign
IGL01818:Ccpg1	APN	9	72997453	missense	probably damaging	1.00
K7894:Ccpg1	UTSW	9	73001877	critical splice donor site	probably null
R0586:Ccpg1	UTSW	9	73001821	missense	probably benign	0.00
R1188:Ccpg1	UTSW	9	73012506	missense	possibly damaging	0.55
R1599:Ccpg1	UTSW	9	72999125	nonsense	probably null
R2130:Ccpg1	UTSW	9	73013158	missense	probably damaging	0.98
R2188:Ccpg1	UTSW	9	73013106	missense	probably benign	0.00
R3052:Ccpg1	UTSW	9	73005868	missense	probably damaging	1.00
R4155:Ccpg1	UTSW	9	73012167	missense	probably benign	0.38
R4156:Ccpg1	UTSW	9	73012167	missense	probably benign	0.38
R4157:Ccpg1	UTSW	9	73012167	missense	probably benign	0.38
R4257:Ccpg1	UTSW	9	73012627	missense	probably damaging	1.00
R4677:Ccpg1	UTSW	9	73015915	intron	probably benign
R5081:Ccpg1	UTSW	9	72999078	missense	possibly damaging	0.94
R5227:Ccpg1	UTSW	9	73012072	nonsense	probably null
R5288:Ccpg1	UTSW	9	73013044	missense	probably benign
R5385:Ccpg1	UTSW	9	73013044	missense	probably benign
R5386:Ccpg1	UTSW	9	73013044	missense	probably benign
R5412:Ccpg1	UTSW	9	73010306	missense	probably damaging	1.00
R5754:Ccpg1	UTSW	9	73013244	missense	possibly damaging	0.78
R6230:Ccpg1	UTSW	9	73012356	missense	probably benign	0.00
R7269:Ccpg1	UTSW	9	73013327	missense	probably benign	0.06
R7287:Ccpg1	UTSW	9	73015406	missense	probably benign	0.05
R7542:Ccpg1	UTSW	9	73012459	missense	probably damaging	1.00
R7882:Ccpg1	UTSW	9	73015505	missense	probably damaging	1.00
R8266:Ccpg1	UTSW	9	73005719	missense	probably damaging	1.00
R8268:Ccpg1	UTSW	9	73005719	missense	probably damaging	1.00
R8269:Ccpg1	UTSW	9	73005719	missense	probably damaging	1.00
R8345:Ccpg1	UTSW	9	73005719	missense	probably damaging	1.00
R8829:Ccpg1	UTSW	9	73010351	missense	probably benign	0.00
R9450:Ccpg1	UTSW	9	72997421	missense	unknown
R9648:Ccpg1	UTSW	9	73012030	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GAGAGCCTGTAATGAGTCACATTCCC -3'
(R):5'- CTTGCTTAGAGTCCTGTTCTGAAACCC -3'

Sequencing Primer
(F):5'- GAGTCACATTCCCTGTGTGAAATTG -3'
(R):5'- GAGTCCTGTTCTGAAACCCAAAAAAG -3'

Posted On

2014-04-13