Mutagenetix > Incidental Mutation

Incidental Mutation 'R5583:Suv39h2'

486863

Institutional Source

Beutler Lab

Gene Symbol

Suv39h2

Ensembl Gene

ENSMUSG00000026646

Gene Name

suppressor of variegation 3-9 2

Synonyms

4930507K23Rik, D2Ertd544e, Suv39h histone methyltransferase, KMT1B

MMRRC Submission

043137-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5583 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

3456852-3476068 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to A at 3475890 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027956] [ENSMUST00000060618] [ENSMUST00000127540]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000027956
AA Change: T32S

SMART Domains

Protein: ENSMUSP00000027956
Gene: ENSMUSG00000026646
AA Change: T32S

Domain	Start	End	E-Value	Type
low complexity region	2	47	N/A	INTRINSIC
CHROMO	117	169	2.44e-11	SMART
Pfam:Pre-SET	212	309	4.4e-18	PFAM
SET	317	446	4.05e-41	SMART
PostSET	461	477	7.05e-4	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000060618
AA Change: T32S

SMART Domains

Protein: ENSMUSP00000054169
Gene: ENSMUSG00000026646
AA Change: T32S

Domain	Start	End	E-Value	Type
low complexity region	2	47	N/A	INTRINSIC
SET	70	226	6.61e-23	SMART
PostSET	241	257	7.05e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000100458

SMART Domains

Protein: ENSMUSP00000098026
Gene: ENSMUSG00000026646

Domain	Start	End	E-Value	Type
CHROMO	6	67	2e-7	SMART
Pfam:Pre-SET	110	207	1.3e-17	PFAM
SET	215	344	4.05e-41	SMART
PostSET	359	375	7.05e-4	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000127540
AA Change: T32S

SMART Domains

Protein: ENSMUSP00000125485
Gene: ENSMUSG00000026646
AA Change: T32S

Domain	Start	End	E-Value	Type
low complexity region	2	47	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149932

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.4%
20x: 95.4%

Validation Efficiency

97% (60/62)

MGI Phenotype

PHENOTYPE: Less than 5% of mice either heterozygous or homozygous for a reporter/null allele develop late-onset B cell lymphomas. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A1bg	A	T	15: 60,793,083 (GRCm39)	L8Q	probably damaging	Het
Abca4	T	C	3: 121,942,550 (GRCm39)	V1681A	probably damaging	Het
Abce1	G	T	8: 80,416,922 (GRCm39)	A363E	probably benign	Het
Adgrl2	T	C	3: 148,564,800 (GRCm39)	Y256C	probably damaging	Het
Afm	T	C	5: 90,695,740 (GRCm39)	C416R	probably damaging	Het
Ahnak	T	A	19: 8,984,281 (GRCm39)	V1855D	probably damaging	Het
Alb	A	T	5: 90,616,452 (GRCm39)	H319L	probably benign	Het
Ankrd35	G	T	3: 96,592,219 (GRCm39)	R835L	probably damaging	Het
Atg2b	T	C	12: 105,615,414 (GRCm39)	D1014G	possibly damaging	Het
Cdk6	T	A	5: 3,394,436 (GRCm39)	Y24N	probably damaging	Het
Chd7	T	A	4: 8,752,473 (GRCm39)	N323K	probably damaging	Het
Cops9	A	T	1: 92,567,489 (GRCm39)		probably benign	Het
Crybg1	T	C	10: 43,879,506 (GRCm39)	T561A	probably benign	Het
Dcdc5	T	C	2: 106,195,778 (GRCm39)		noncoding transcript	Het
Dnah7b	G	T	1: 46,281,359 (GRCm39)	A2807S	probably benign	Het
Fam149b	A	G	14: 20,413,368 (GRCm39)	T196A	possibly damaging	Het
Fam217a	C	A	13: 35,094,280 (GRCm39)	C402F	probably damaging	Het
Fat2	A	T	11: 55,144,715 (GRCm39)	V4053E	probably benign	Het
Fcgbp	T	C	7: 27,791,004 (GRCm39)	V755A	probably damaging	Het
Fxr1	C	A	3: 34,123,125 (GRCm39)	S641R	probably benign	Het
Gata5	A	T	2: 179,976,047 (GRCm39)	M39K	probably benign	Het
Gon4l	T	A	3: 88,807,278 (GRCm39)	D1658E	probably damaging	Het
Gpr180	C	T	14: 118,400,110 (GRCm39)	T426M	probably damaging	Het
Gtf2h3	C	T	5: 124,722,360 (GRCm39)	T121I	probably benign	Het
Helq	T	C	5: 100,910,459 (GRCm39)	E1039G	probably damaging	Het
Hibch	T	A	1: 52,940,406 (GRCm39)	Y192N	probably damaging	Het
Hp1bp3	A	G	4: 137,949,426 (GRCm39)	I41M	probably damaging	Het
Itpripl2	G	T	7: 118,089,101 (GRCm39)	P486Q	probably benign	Het
Kcnj6	T	C	16: 94,634,060 (GRCm39)	D17G	probably benign	Het
Kprp	T	A	3: 92,731,643 (GRCm39)	Y469F	unknown	Het
Kremen2	T	C	17: 23,961,229 (GRCm39)	T373A	probably benign	Het
Lgi4	A	G	7: 30,760,562 (GRCm39)	Y39C	possibly damaging	Het
Lgr5	T	C	10: 115,314,409 (GRCm39)	D176G	probably benign	Het
Lrp1	T	C	10: 127,424,332 (GRCm39)	S785G	probably benign	Het
Ltbp1	A	T	17: 75,598,325 (GRCm39)	Q920L	probably benign	Het
Map2	A	G	1: 66,455,196 (GRCm39)	E1362G	probably damaging	Het
Nkx2-6	T	C	14: 69,409,272 (GRCm39)	S8P	probably damaging	Het
Or2h1b	T	C	17: 37,462,485 (GRCm39)	Q126R	probably benign	Het
Pde4dip	C	T	3: 97,654,892 (GRCm39)	R888Q	possibly damaging	Het
Per1	A	G	11: 68,994,271 (GRCm39)	H494R	probably damaging	Het
Pira2	A	G	7: 3,845,545 (GRCm39)	F280L	probably benign	Het
Plekhm3	C	T	1: 64,977,145 (GRCm39)	W108*	probably null	Het
Ptcd3	A	G	6: 71,879,920 (GRCm39)	S113P	probably damaging	Het
Scarf1	T	C	11: 75,404,842 (GRCm39)	L42P	possibly damaging	Het
Scart2	G	A	7: 139,876,739 (GRCm39)	C710Y	probably damaging	Het
Skint1	A	C	4: 111,876,253 (GRCm39)	Q58P	probably damaging	Het
Spata7	A	T	12: 98,635,590 (GRCm39)	N438I	probably damaging	Het
Spdya	C	A	17: 71,876,126 (GRCm39)	D164E	probably damaging	Het
Speer3	G	A	5: 13,844,782 (GRCm39)		probably null	Het
Ssc4d	A	T	5: 135,999,050 (GRCm39)	L51H	probably damaging	Het
Steap1	A	G	5: 5,790,579 (GRCm39)	I123T	possibly damaging	Het
Styx	T	A	14: 45,608,483 (GRCm39)	F147I	possibly damaging	Het
Tfb2m	A	G	1: 179,373,446 (GRCm39)	V84A	probably benign	Het
Tlcd1	T	G	11: 78,069,762 (GRCm39)	V25G	probably benign	Het
Tmem79	T	C	3: 88,239,870 (GRCm39)	Y280C	probably damaging	Het
Trim5	T	A	7: 103,926,042 (GRCm39)	N173I	probably damaging	Het
Ttc17	A	T	2: 94,208,027 (GRCm39)	D194E	probably damaging	Het
Zfp2	T	C	11: 50,790,984 (GRCm39)	E353G	possibly damaging	Het

Other mutations in Suv39h2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01380:Suv39h2	APN	2	3,465,296 (GRCm39)	splice site	probably benign
IGL03408:Suv39h2	APN	2	3,460,913 (GRCm39)	missense	probably damaging	1.00
R0060:Suv39h2	UTSW	2	3,465,953 (GRCm39)	missense	probably damaging	1.00
R0060:Suv39h2	UTSW	2	3,465,953 (GRCm39)	missense	probably damaging	1.00
R0511:Suv39h2	UTSW	2	3,473,616 (GRCm39)	missense	probably damaging	0.99
R1892:Suv39h2	UTSW	2	3,460,805 (GRCm39)	missense	probably damaging	1.00
R1919:Suv39h2	UTSW	2	3,465,353 (GRCm39)	missense	probably damaging	1.00
R3888:Suv39h2	UTSW	2	3,465,845 (GRCm39)	missense	probably benign	0.09
R6770:Suv39h2	UTSW	2	3,473,588 (GRCm39)	missense	possibly damaging	0.52
R6801:Suv39h2	UTSW	2	3,465,458 (GRCm39)	missense	probably benign	0.16
R7607:Suv39h2	UTSW	2	3,475,866 (GRCm39)	missense	unknown
R7914:Suv39h2	UTSW	2	3,465,453 (GRCm39)	nonsense	probably null
R9557:Suv39h2	UTSW	2	3,475,451 (GRCm39)	missense
R9781:Suv39h2	UTSW	2	3,463,631 (GRCm39)	missense	probably benign	0.01
X0062:Suv39h2	UTSW	2	3,465,822 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- CAAAGTTTCCCGGAGCTCAG -3'
(R):5'- GTCAAAGCGAGTAACAAGCC -3'

Sequencing Primer
(F):5'- TCGAACGCAGGCACCAG -3'
(R):5'- TCTCCGCTGACGTCAGAAC -3'

Posted On

2017-09-06