Mutagenetix > Incidental Mutation

Incidental Mutation 'R6384:Ccnj'

515528

Institutional Source

Beutler Lab

Gene Symbol

Ccnj

Ensembl Gene

ENSMUSG00000025010

Gene Name

cyclin J

Synonyms

D430039C20Rik

MMRRC Submission

044533-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.163) question?

Stock #

R6384 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

40819723-40837016 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 40834451 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 338 (V338A)

Ref Sequence

ENSEMBL: ENSMUSP00000113712 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025983] [ENSMUST00000119316] [ENSMUST00000120057]

AlphaFold

Q3TZI6

Predicted Effect

probably benign
Transcript: ENSMUST00000025983
AA Change: V350A

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

SMART Domains

Protein: ENSMUSP00000025983
Gene: ENSMUSG00000025010
AA Change: V350A

Domain	Start	End	E-Value	Type
CYCLIN	45	136	1.59e-13	SMART
Cyclin_C	145	282	7.02e-21	SMART
CYCLIN	153	248	2.1e0	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000119316
AA Change: V350A

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

SMART Domains

Protein: ENSMUSP00000112643
Gene: ENSMUSG00000025010
AA Change: V350A

Domain	Start	End	E-Value	Type
CYCLIN	45	136	1.59e-13	SMART
Cyclin_C	145	282	7.02e-21	SMART
CYCLIN	153	248	2.1e0	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000120057
AA Change: V338A

PolyPhen 2 Score 0.085 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000113712
Gene: ENSMUSG00000025010
AA Change: V338A

Domain	Start	End	E-Value	Type
CYCLIN	45	136	1.59e-13	SMART
Cyclin_C	145	270	6.99e-7	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 98.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acad10	T	A	5: 121,790,066 (GRCm39)	T97S	probably benign	Het
Adam34	T	A	8: 44,103,836 (GRCm39)	D603V	probably benign	Het
Adamts5	C	T	16: 85,659,716 (GRCm39)	V859I	probably benign	Het
Alb	T	A	5: 90,620,499 (GRCm39)	D536E	possibly damaging	Het
Amz2	A	G	11: 109,319,860 (GRCm39)	Y82C	probably damaging	Het
Asxl1	T	C	2: 153,233,744 (GRCm39)		probably null	Het
Bach1	C	T	16: 87,516,745 (GRCm39)	Q429*	probably null	Het
Bcl6	A	G	16: 23,793,615 (GRCm39)	Y111H	probably damaging	Het
Cdca3	C	T	6: 124,809,382 (GRCm39)	P174L	probably damaging	Het
Cdk17	T	C	10: 93,047,827 (GRCm39)	L25P	probably damaging	Het
Cdr2	G	A	7: 120,581,351 (GRCm39)		probably null	Het
Cyp2c38	A	T	19: 39,380,737 (GRCm39)		probably null	Het
Ednra	T	C	8: 78,415,723 (GRCm39)	N175D	probably damaging	Het
Elp3	T	C	14: 65,797,660 (GRCm39)	Y337C	probably damaging	Het
Eml2	G	A	7: 18,935,088 (GRCm39)	V432I	probably damaging	Het
Eps15l1	A	T	8: 73,122,554 (GRCm39)		probably null	Het
F11r	A	G	1: 171,288,508 (GRCm39)	N117S	probably benign	Het
Foxp2	C	T	6: 15,437,947 (GRCm39)	T716I	probably damaging	Het
Gnaq	A	G	19: 16,293,377 (GRCm39)		probably null	Het
Gpat2	G	C	2: 127,273,838 (GRCm39)	G294R	possibly damaging	Het
Gpr158	T	C	2: 21,831,099 (GRCm39)	M733T	probably damaging	Het
Hdac7	G	A	15: 97,709,387 (GRCm39)	Q48*	probably null	Het
Hmga2	G	A	10: 120,206,612 (GRCm39)		probably benign	Het
Itgb7	A	G	15: 102,132,886 (GRCm39)	V142A	probably benign	Het
Kif5a	T	C	10: 127,078,644 (GRCm39)	N334D	probably damaging	Het
Lrrc47	T	C	4: 154,100,317 (GRCm39)	S298P	probably benign	Het
Map3k1	A	T	13: 111,887,064 (GRCm39)	S1415R	probably damaging	Het
Mdn1	T	A	4: 32,670,607 (GRCm39)	L424Q	probably damaging	Het
Numb	A	C	12: 83,850,748 (GRCm39)	L154R	probably damaging	Het
Or8g27	T	C	9: 39,129,274 (GRCm39)	V207A	probably benign	Het
Or8k30	A	G	2: 86,339,381 (GRCm39)	K193E	probably benign	Het
Pdcd5	G	T	7: 35,346,334 (GRCm39)	A92E	possibly damaging	Het
Pdcl2	C	T	5: 76,478,855 (GRCm39)		probably null	Het
Rbfa	T	C	18: 80,235,996 (GRCm39)	Y251C	probably damaging	Het
Rgsl1	G	A	1: 153,703,291 (GRCm39)	T120I	possibly damaging	Het
Serpina3g	A	G	12: 104,206,655 (GRCm39)	Q152R	probably null	Het
Setx	T	C	2: 29,063,570 (GRCm39)	S2289P	probably damaging	Het
Slc6a16	A	G	7: 44,907,017 (GRCm39)		probably null	Het
Slco1a6	C	T	6: 142,055,105 (GRCm39)	D280N	probably benign	Het
Syde2	T	A	3: 145,704,568 (GRCm39)	Y240N	probably damaging	Het
Synpo2	G	A	3: 122,906,698 (GRCm39)	Q873*	probably null	Het
Tlr2	A	G	3: 83,744,301 (GRCm39)	V594A	probably benign	Het
Ttc16	C	T	2: 32,657,561 (GRCm39)	A512T	probably damaging	Het
Tubb5	T	C	17: 36,148,938 (GRCm39)	E3G	probably damaging	Het
Vmn2r112	T	C	17: 22,824,136 (GRCm39)	Y464H	probably damaging	Het
Xcr1	T	A	9: 123,684,847 (GRCm39)	H305L	probably damaging	Het
Yars1	T	G	4: 129,090,771 (GRCm39)		probably null	Het

Other mutations in Ccnj

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01903:Ccnj	APN	19	40,834,454 (GRCm39)	missense	probably damaging	1.00
IGL02584:Ccnj	APN	19	40,833,185 (GRCm39)	missense	probably benign	0.04
R0220:Ccnj	UTSW	19	40,833,254 (GRCm39)	missense	probably damaging	0.99
R0452:Ccnj	UTSW	19	40,833,508 (GRCm39)	splice site	probably null
R0693:Ccnj	UTSW	19	40,825,551 (GRCm39)	missense	probably damaging	1.00
R1600:Ccnj	UTSW	19	40,833,101 (GRCm39)	splice site	probably benign
R2237:Ccnj	UTSW	19	40,834,219 (GRCm39)	missense	probably benign	0.00
R2258:Ccnj	UTSW	19	40,834,277 (GRCm39)	missense	probably benign	0.00
R2879:Ccnj	UTSW	19	40,833,158 (GRCm39)	missense	probably damaging	1.00
R6162:Ccnj	UTSW	19	40,833,606 (GRCm39)	missense	probably damaging	1.00
R6528:Ccnj	UTSW	19	40,820,529 (GRCm39)	splice site	probably null
R6830:Ccnj	UTSW	19	40,833,636 (GRCm39)	missense	probably damaging	0.99
R7338:Ccnj	UTSW	19	40,825,477 (GRCm39)	missense	probably damaging	1.00
R7346:Ccnj	UTSW	19	40,833,394 (GRCm39)	missense	probably benign	0.28
R8472:Ccnj	UTSW	19	40,833,608 (GRCm39)	missense	probably damaging	0.97
R8977:Ccnj	UTSW	19	40,833,383 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTCACTTCCAGCAGCCTCAG -3'
(R):5'- CCCGTTGCATTGATGTACTG -3'

Sequencing Primer
(F):5'- GCCTCAGTATCTCCATCAGAG -3'
(R):5'- GATTGTATTCTTTCCTTCTGAAGAGG -3'

Posted On

2018-05-04