Mutagenetix > Incidental Mutation

Incidental Mutation 'R4951:Setdb2'

382010

Institutional Source

Beutler Lab

Gene Symbol

Setdb2

Ensembl Gene

ENSMUSG00000071350

Gene Name

SET domain, bifurcated 2

Synonyms

KMT1F, LOC239122

MMRRC Submission

042548-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.544) question?

Stock #

R4951 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

59639458-59678329 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 59639752 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 713 (I713T)

Ref Sequence

ENSEMBL: ENSMUSP00000093450 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000095775] [ENSMUST00000161459]

AlphaFold

Q8C267

Predicted Effect

possibly damaging
Transcript: ENSMUST00000095775
AA Change: I713T

PolyPhen 2 Score 0.719 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000093450
Gene: ENSMUSG00000071350
AA Change: I713T

Domain	Start	End	E-Value	Type
Pfam:MBD	164	236	3.4e-10	PFAM
Pfam:Pre-SET	250	362	1.7e-17	PFAM
SET	370	694	9.33e-32	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159640

Predicted Effect

possibly damaging
Transcript: ENSMUST00000161459
AA Change: I697T

PolyPhen 2 Score 0.590 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000124696
Gene: ENSMUSG00000071350
AA Change: I697T

Domain	Start	End	E-Value	Type
Pfam:MBD	148	220	2.7e-9	PFAM
Pfam:Pre-SET	233	346	1.3e-19	PFAM
SET	354	678	9.33e-32	SMART

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.5%
20x: 93.1%

Validation Efficiency

98% (94/96)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of a family of proteins that contain a methyl-CpG-binding domain (MBD) and a SET domain and function as histone methyltransferases. This protein is recruited to heterochromatin and plays a role in the regulation of chromosome segregation. This region is commonly deleted in chronic lymphocytic leukemia. Naturally-occuring readthrough transcription occurs from this gene to the downstream PHF11 (PHD finger protein 11) gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]
PHENOTYPE: Mice homozygous for a hypomorphic allele exhibit altered response to infection and improved patology following superinfection of influenza virus-infected mice with S. pneumonia. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adcy1	G	A	11: 7,088,336 (GRCm39)	E452K	possibly damaging	Het
Adcy10	T	C	1: 165,391,532 (GRCm39)	L1263P	probably damaging	Het
Adgrg1	G	A	8: 95,731,874 (GRCm39)	V179M	probably damaging	Het
Agap1	T	A	1: 89,537,225 (GRCm39)	V77E	probably damaging	Het
Ahnak	A	T	19: 8,995,199 (GRCm39)	K5494N	probably damaging	Het
Arhgap19	A	G	19: 41,762,545 (GRCm39)	M437T	probably benign	Het
C2cd4c	C	A	10: 79,448,839 (GRCm39)	A103S	possibly damaging	Het
Clip1	A	T	5: 123,768,408 (GRCm39)	D776E	probably benign	Het
Cntn3	C	T	6: 102,145,986 (GRCm39)	V952M	possibly damaging	Het
Col6a6	A	G	9: 105,644,397 (GRCm39)		probably null	Het
Crtac1	C	T	19: 42,402,570 (GRCm39)	A13T	probably benign	Het
Ddx50	C	T	10: 62,469,899 (GRCm39)	A363T	probably damaging	Het
Dock9	A	G	14: 121,890,547 (GRCm39)	V241A	probably benign	Het
Dysf	T	C	6: 84,091,102 (GRCm39)		probably null	Het
Enpp3	A	T	10: 24,674,175 (GRCm39)	M375K	probably damaging	Het
Fam13c	G	A	10: 70,387,621 (GRCm39)		probably null	Het
Ftcd	C	T	10: 76,420,517 (GRCm39)	A417V	probably benign	Het
Gak	A	G	5: 108,730,584 (GRCm39)	S941P	probably benign	Het
Ganc	A	G	2: 120,286,528 (GRCm39)	T786A	probably benign	Het
Gfi1	A	C	5: 107,868,009 (GRCm39)	S420A	probably damaging	Het
Ghsr	A	T	3: 27,426,510 (GRCm39)	T189S	possibly damaging	Het
Glb1l	C	T	1: 75,185,019 (GRCm39)	G122D	probably damaging	Het
Gm10065	C	T	13: 21,663,421 (GRCm39)	S64N	unknown	Het
Gm5087	C	A	14: 13,158,749 (GRCm38)		noncoding transcript	Het
Gm973	G	A	1: 59,580,633 (GRCm39)		probably null	Het
Gm9930	A	T	10: 9,410,449 (GRCm39)		noncoding transcript	Het
H6pd	A	T	4: 150,066,044 (GRCm39)	Y781N	probably damaging	Het
Ide	G	A	19: 37,262,631 (GRCm39)	L695F	unknown	Het
Il17re	T	A	6: 113,445,868 (GRCm39)	V393E	probably damaging	Het
Lipo3	A	G	19: 33,759,621 (GRCm39)	V205A	probably benign	Het
Lipo5	C	T	19: 33,446,251 (GRCm39)	E49K	probably damaging	Het
Lonp1	A	T	17: 56,927,335 (GRCm39)	M306K	possibly damaging	Het
Lrig1	A	G	6: 94,640,959 (GRCm39)	L82P	probably damaging	Het
Lrp2	A	T	2: 69,366,332 (GRCm39)	C256S	probably damaging	Het
Map1b	A	T	13: 99,568,935 (GRCm39)	I1262K	unknown	Het
Mctp1	C	T	13: 76,975,894 (GRCm39)	P756S	probably damaging	Het
Mdn1	T	A	4: 32,707,459 (GRCm39)	W1583R	probably damaging	Het
Mis12	T	A	11: 70,916,473 (GRCm39)	Y169N	probably benign	Het
Mplkipl1	C	T	19: 61,164,364 (GRCm39)	G24R	unknown	Het
Msh5	G	A	17: 35,257,396 (GRCm39)	Q333*	probably null	Het
Necap2	A	T	4: 140,799,834 (GRCm39)		probably null	Het
Nfatc2	T	C	2: 168,412,992 (GRCm39)	D211G	probably damaging	Het
Nlrx1	A	G	9: 44,164,726 (GRCm39)	V906A	possibly damaging	Het
Or2ak7	G	A	11: 58,575,589 (GRCm39)	V297I	probably damaging	Het
Or4a2	T	A	2: 89,248,116 (GRCm39)	I214F	probably benign	Het
Or4l1	A	T	14: 50,166,515 (GRCm39)	L162*	probably null	Het
Or5b125-ps1	A	T	19: 13,056,620 (GRCm39)		noncoding transcript	Het
Or8g24	A	G	9: 38,989,555 (GRCm39)	F162S	probably benign	Het
Pate5	A	G	9: 35,750,732 (GRCm39)	V30A	probably damaging	Het
Pkhd1l1	T	A	15: 44,397,287 (GRCm39)	N2057K	possibly damaging	Het
Ppip5k2	T	C	1: 97,639,474 (GRCm39)	K1078R	possibly damaging	Het
Prdm11	A	G	2: 92,810,954 (GRCm39)	I215T	probably damaging	Het
Ptpn13	C	T	5: 103,735,912 (GRCm39)	P2137L	probably benign	Het
Rif1	T	A	2: 51,974,998 (GRCm39)		probably null	Het
Rnf17	T	C	14: 56,759,848 (GRCm39)	V1551A	probably benign	Het
Ror2	C	T	13: 53,271,183 (GRCm39)	V391I	probably benign	Het
Rps6ka2	A	T	17: 7,560,188 (GRCm39)	D542V	probably damaging	Het
Sema4g	A	G	19: 44,985,010 (GRCm39)		probably null	Het
Serpinb6d	T	G	13: 33,850,366 (GRCm39)	S64R	probably benign	Het
Serpine1	C	T	5: 137,098,205 (GRCm39)	R156K	probably benign	Het
Slamf7	A	G	1: 171,466,693 (GRCm39)	F171L	probably benign	Het
Slc15a5	A	G	6: 138,050,064 (GRCm39)	L117S	probably damaging	Het
Slc8a3	T	A	12: 81,362,760 (GRCm39)	T20S	probably damaging	Het
Slc8a3	T	A	12: 81,361,473 (GRCm39)	T449S	probably benign	Het
Smc2	G	A	4: 52,462,926 (GRCm39)	V639M	possibly damaging	Het
Sra1	A	T	18: 36,809,494 (GRCm39)	C223*	probably null	Het
Srgap1	A	T	10: 121,621,457 (GRCm39)	M1012K	probably benign	Het
Stk-ps2	A	T	1: 46,068,602 (GRCm39)		noncoding transcript	Het
Taar6	A	T	10: 23,861,106 (GRCm39)	S147T	probably benign	Het
Taf15	G	A	11: 83,375,637 (GRCm39)	G34D	possibly damaging	Het
Tarbp1	T	C	8: 127,174,184 (GRCm39)	E874G	possibly damaging	Het
Tob2	T	C	15: 81,735,924 (GRCm39)	Y15C	probably damaging	Het
Trim12a	A	G	7: 103,953,565 (GRCm39)	V182A	possibly damaging	Het
Trim67	A	G	8: 125,521,406 (GRCm39)	E256G	probably benign	Het
Trrap	T	A	5: 144,742,530 (GRCm39)	S1382T	possibly damaging	Het
Ttc39d	T	A	17: 80,523,462 (GRCm39)	S40R	probably benign	Het
Ttn	A	T	2: 76,779,406 (GRCm39)	V1158E	probably benign	Het
Vmn1r19	C	T	6: 57,381,927 (GRCm39)	T160I	probably benign	Het
Vmn2r100	T	C	17: 19,752,300 (GRCm39)	I781T	probably benign	Het
Vmn2r85	T	C	10: 130,261,113 (GRCm39)	E408G	probably damaging	Het
Vwde	T	C	6: 13,187,138 (GRCm39)	D783G	probably damaging	Het
Wdr27	A	T	17: 15,096,395 (GRCm39)	D796E	probably damaging	Het
Zfp365	C	T	10: 67,725,821 (GRCm39)		probably null	Het
Zfp9	T	G	6: 118,441,408 (GRCm39)	H418P	probably damaging	Het

Other mutations in Setdb2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00553:Setdb2	APN	14	59,653,241 (GRCm39)	missense	probably damaging	1.00
IGL01695:Setdb2	APN	14	59,639,742 (GRCm39)	utr 3 prime	probably benign
IGL01720:Setdb2	APN	14	59,660,885 (GRCm39)	missense	possibly damaging	0.76
IGL02003:Setdb2	APN	14	59,650,939 (GRCm39)	missense	probably damaging	0.98
IGL02023:Setdb2	APN	14	59,668,607 (GRCm39)	missense	probably damaging	1.00
IGL02108:Setdb2	APN	14	59,639,764 (GRCm39)	missense	probably damaging	1.00
IGL02113:Setdb2	APN	14	59,639,764 (GRCm39)	missense	probably damaging	1.00
IGL02114:Setdb2	APN	14	59,639,764 (GRCm39)	missense	probably damaging	1.00
IGL02115:Setdb2	APN	14	59,639,764 (GRCm39)	missense	probably damaging	1.00
IGL02116:Setdb2	APN	14	59,639,764 (GRCm39)	missense	probably damaging	1.00
IGL02117:Setdb2	APN	14	59,639,764 (GRCm39)	missense	probably damaging	1.00
IGL02141:Setdb2	APN	14	59,639,764 (GRCm39)	missense	probably damaging	1.00
IGL02148:Setdb2	APN	14	59,639,764 (GRCm39)	missense	probably damaging	1.00
R0419:Setdb2	UTSW	14	59,644,193 (GRCm39)	splice site	probably null
R0610:Setdb2	UTSW	14	59,654,919 (GRCm39)	missense	possibly damaging	0.55
R0636:Setdb2	UTSW	14	59,644,153 (GRCm39)	missense	probably benign	0.40
R0890:Setdb2	UTSW	14	59,656,669 (GRCm39)	missense	possibly damaging	0.89
R0931:Setdb2	UTSW	14	59,660,945 (GRCm39)	splice site	probably benign
R1355:Setdb2	UTSW	14	59,654,890 (GRCm39)	missense	probably damaging	1.00
R1553:Setdb2	UTSW	14	59,654,934 (GRCm39)	missense	probably benign	0.04
R1968:Setdb2	UTSW	14	59,656,858 (GRCm39)	missense	probably damaging	1.00
R2472:Setdb2	UTSW	14	59,656,903 (GRCm39)	missense	possibly damaging	0.49
R2894:Setdb2	UTSW	14	59,663,916 (GRCm39)	missense	probably benign	0.00
R3919:Setdb2	UTSW	14	59,656,616 (GRCm39)	missense	probably damaging	1.00
R4609:Setdb2	UTSW	14	59,653,153 (GRCm39)	missense	probably damaging	1.00
R4629:Setdb2	UTSW	14	59,646,808 (GRCm39)	missense	probably benign	0.13
R4816:Setdb2	UTSW	14	59,651,095 (GRCm39)	missense	probably benign	0.05
R4864:Setdb2	UTSW	14	59,646,715 (GRCm39)	missense	probably benign	0.01
R5040:Setdb2	UTSW	14	59,653,156 (GRCm39)	missense	probably damaging	0.99
R5245:Setdb2	UTSW	14	59,663,943 (GRCm39)	missense	probably null	0.00
R5358:Setdb2	UTSW	14	59,646,885 (GRCm39)	missense	probably benign	0.17
R5656:Setdb2	UTSW	14	59,656,567 (GRCm39)	missense	probably damaging	1.00
R5705:Setdb2	UTSW	14	59,660,814 (GRCm39)	missense	possibly damaging	0.80
R6103:Setdb2	UTSW	14	59,646,981 (GRCm39)	splice site	probably null
R6106:Setdb2	UTSW	14	59,660,898 (GRCm39)	nonsense	probably null
R6388:Setdb2	UTSW	14	59,662,146 (GRCm39)	missense	probably benign
R6431:Setdb2	UTSW	14	59,656,505 (GRCm39)	missense	probably damaging	1.00
R6494:Setdb2	UTSW	14	59,639,863 (GRCm39)	missense	probably benign	0.12
R6971:Setdb2	UTSW	14	59,653,189 (GRCm39)	missense	probably damaging	1.00
R7442:Setdb2	UTSW	14	59,656,700 (GRCm39)	missense	probably damaging	0.99
R7444:Setdb2	UTSW	14	59,660,794 (GRCm39)	nonsense	probably null
R7759:Setdb2	UTSW	14	59,656,813 (GRCm39)	missense	probably damaging	1.00
R8021:Setdb2	UTSW	14	59,660,833 (GRCm39)	nonsense	probably null
R8039:Setdb2	UTSW	14	59,639,824 (GRCm39)	missense	probably damaging	1.00
R8261:Setdb2	UTSW	14	59,651,141 (GRCm39)	splice site	probably benign
R8393:Setdb2	UTSW	14	59,650,180 (GRCm39)	missense	probably benign	0.04
R8513:Setdb2	UTSW	14	59,639,839 (GRCm39)	missense	probably damaging	1.00
R8700:Setdb2	UTSW	14	59,654,888 (GRCm39)	missense	probably damaging	1.00
R8707:Setdb2	UTSW	14	59,660,907 (GRCm39)	nonsense	probably null
R8940:Setdb2	UTSW	14	59,646,956 (GRCm39)	missense	probably damaging	1.00
R9217:Setdb2	UTSW	14	59,646,881 (GRCm39)	missense	possibly damaging	0.61
R9314:Setdb2	UTSW	14	59,650,240 (GRCm39)	missense	probably benign	0.02
R9336:Setdb2	UTSW	14	59,660,816 (GRCm39)	missense	unknown
R9442:Setdb2	UTSW	14	59,639,849 (GRCm39)	missense	probably damaging	1.00
R9525:Setdb2	UTSW	14	59,646,841 (GRCm39)	missense	probably benign	0.00
R9743:Setdb2	UTSW	14	59,651,002 (GRCm39)	missense	probably benign	0.00
X0017:Setdb2	UTSW	14	59,656,917 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTGTGATACTTGATGAGTGCCC -3'
(R):5'- TAGATTGACTTTAGGATGGCTGAC -3'

Sequencing Primer
(F):5'- ATACTTGATGAGTGCCCTTATTTTGC -3'
(R):5'- AGGATGGCTGACTTTGTTAATATG -3'

Posted On

2016-04-27