Mutagenetix > Incidental Mutations

Incidental Mutation 'R5951:Dgkq'

470881

Institutional Source

Beutler Lab

Gene Symbol

Dgkq

Ensembl Gene

ENSMUSG00000004815

Gene Name

diacylglycerol kinase, theta

Synonyms

110kDa, DAGK7, Dagk4, Dgkd, Dgk theta

MMRRC Submission

044141-MU

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5951 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

108646693-108669672 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 108654370 bp

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 443 (M443K)

Ref Sequence

ENSEMBL: ENSMUSP00000057859 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000053913] [ENSMUST00000132179] [ENSMUST00000132708] [ENSMUST00000153238]

Predicted Effect

probably damaging
Transcript: ENSMUST00000053913
AA Change: M443K

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000057859
Gene: ENSMUSG00000004815
AA Change: M443K

Domain	Start	End	E-Value	Type
C1	55	102	3.22e-14	SMART
C1	114	162	1.73e-2	SMART
C1	178	228	1.58e-13	SMART
low complexity region	267	275	N/A	INTRINSIC
RA	387	486	2.08e-20	SMART
DAGKc	580	707	4.79e-63	SMART
DAGKa	733	885	7e-88	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000123669

Predicted Effect

probably benign
Transcript: ENSMUST00000132179

SMART Domains

Protein: ENSMUSP00000118466
Gene: ENSMUSG00000004815

Domain	Start	End	E-Value	Type
C1	55	102	3.22e-14	SMART
Blast:C1	114	144	1e-12	BLAST
low complexity region	156	169	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000132708

SMART Domains

Protein: ENSMUSP00000122837
Gene: ENSMUSG00000004815

Domain	Start	End	E-Value	Type
Blast:C1	26	56	2e-13	BLAST
low complexity region	68	81	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139169

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139598

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144624

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145917

Predicted Effect

probably benign
Transcript: ENSMUST00000153238

SMART Domains

Protein: ENSMUSP00000118065
Gene: ENSMUSG00000004815

Domain	Start	End	E-Value	Type
C1	55	102	3.22e-14	SMART
Blast:C1	114	144	1e-12	BLAST
low complexity region	156	169	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153365

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156964

Meta Mutation Damage Score

0.5858

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.6%
20x: 92.4%

Validation Efficiency

100% (78/78)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains three cysteine-rich domains, a proline-rich region, and a pleckstrin homology domain with an overlapping Ras-associating domain. It is localized in the speckle domains of the nucleus, and mediates the regeneration of phosphatidylinositol (PI) from diacylglycerol in the PI-cycle during cell signal transduction. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930568D16Rik	T	A	2: 35,354,799	E180D	probably damaging	Het
Add3	A	G	19: 53,244,289		probably null	Het
Adgrv1	A	T	13: 81,442,501	I4396N	probably damaging	Het
Apc	C	T	18: 34,317,146	S2331L	possibly damaging	Het
Apoh	G	T	11: 108,395,903	C51F	probably damaging	Het
Arid4b	T	C	13: 14,143,063	V177A	possibly damaging	Het
Atp13a1	T	A	8: 69,797,285	I343N	probably damaging	Het
Bcar1	T	C	8: 111,713,400	D654G	probably benign	Het
Brox	T	C	1: 183,282,508	K245R	probably damaging	Het
Ccdc146	A	T	5: 21,319,579	S258R	possibly damaging	Het
Ccdc169	A	C	3: 55,140,141	K18Q	probably damaging	Het
Cenps	C	A	4: 149,130,201		probably benign	Het
Crot	C	A	5: 8,969,120	E478*	probably null	Het
Dhx32	A	T	7: 133,737,328	L326Q	probably damaging	Het
Dtwd1	A	G	2: 126,158,422	I93V	probably benign	Het
Ehmt2	C	T	17: 34,899,381	T44I	probably benign	Het
Enc1	T	C	13: 97,245,257	S92P	probably benign	Het
Epha5	T	C	5: 84,331,192		probably benign	Het
Eya4	T	A	10: 23,155,994	S244C	probably damaging	Het
Fmnl3	G	A	15: 99,325,910	R302W	probably damaging	Het
Fscn3	A	T	6: 28,436,174	I490F	possibly damaging	Het
Galntl6	A	G	8: 57,962,402	V239A	probably benign	Het
Glg1	T	C	8: 111,165,691	I841V	possibly damaging	Het
Gm15455	T	C	1: 33,837,812		noncoding transcript	Het
Gpd1l	C	T	9: 114,914,405	M142I	probably benign	Het
Helb	A	G	10: 120,091,748	V819A	possibly damaging	Het
Hnrnpul2	T	G	19: 8,824,891	F374C	probably damaging	Het
Hoxc10	G	A	15: 102,967,318	S154N	possibly damaging	Het
Ice2	A	T	9: 69,412,369	T367S	possibly damaging	Het
Iqca	A	T	1: 90,140,097		probably null	Het
Itgb4	C	T	11: 115,984,157	R447W	probably benign	Het
Klhl14	T	A	18: 21,651,620	H250L	probably damaging	Het
Kmt2c	A	T	5: 25,330,803	D1447E	probably benign	Het
Larp1	G	T	11: 58,049,939	M630I	probably benign	Het
Lrp2	A	G	2: 69,496,323		probably null	Het
Map4k3	G	T	17: 80,603,998	Q673K	probably benign	Het
Mettl16	A	G	11: 74,795,997	N201D	possibly damaging	Het
Mrpl15	C	A	1: 4,785,733		probably benign	Het
Mthfd1l	T	A	10: 4,048,222	V655D	probably damaging	Het
Odf1	T	C	15: 38,226,287	Y144H	probably damaging	Het
Olfr1093	G	T	2: 86,786,227	V166L	probably benign	Het
Olfr38	G	T	6: 42,762,559	C169F	probably damaging	Het
Padi1	T	C	4: 140,814,829	Y594C	probably damaging	Het
Palm3	T	A	8: 84,029,420	D520E	probably benign	Het
Paox	G	A	7: 140,127,654	C130Y	probably damaging	Het
Parpbp	T	A	10: 88,139,907	S115C	probably damaging	Het
Pcnx3	A	G	19: 5,671,680	V1438A	possibly damaging	Het
Pdlim2	T	A	14: 70,167,780	D212V	probably benign	Het
Pi4ka	A	G	16: 17,303,142	F53L	probably damaging	Het
Pik3c2a	A	T	7: 116,368,184	D839E	probably damaging	Het
Pou2f1	T	C	1: 165,883,056		probably benign	Het
Ppl	A	T	16: 5,088,628	Y1268N	probably benign	Het
Prelid3a	C	T	18: 67,464,941	S6L	probably benign	Het
Ptk2	T	G	15: 73,303,833	D285A	possibly damaging	Het
Rasd2	T	G	8: 75,222,183	Y246D	probably damaging	Het
Rhbdl2	A	G	4: 123,814,327	T110A	probably benign	Het
Rhobtb1	T	A	10: 69,270,255	F217I	probably damaging	Het
Serhl	T	C	15: 83,103,036		probably benign	Het
Sh3tc2	A	G	18: 61,990,007	E613G	probably damaging	Het
Slc26a3	A	G	12: 31,452,715		probably benign	Het
Steap4	T	C	5: 7,975,769	I110T	probably benign	Het
Syde1	C	A	10: 78,589,316	R287L	possibly damaging	Het
Tmem184c	C	T	8: 77,598,662		probably null	Het
Trmt44	C	A	5: 35,572,688		probably benign	Het
Ttbk2	G	T	2: 120,773,283	S256R	probably benign	Het
Ttll6	A	T	11: 96,145,510	I322F	probably damaging	Het
Ubap2	A	T	4: 41,205,753		probably null	Het
Wsb2	A	T	5: 117,377,535	T402S	probably damaging	Het

Other mutations in Dgkq

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00491:Dgkq	APN	5	108654582	missense	possibly damaging	0.72
IGL02364:Dgkq	APN	5	108656444	missense	probably benign	0.05
IGL02966:Dgkq	APN	5	108656421	splice site	probably null
IGL03297:Dgkq	APN	5	108650274	missense	probably damaging	1.00
R0179:Dgkq	UTSW	5	108658200	splice site	probably benign
R0194:Dgkq	UTSW	5	108654644	intron	probably benign
R0332:Dgkq	UTSW	5	108655099	splice site	probably benign
R0513:Dgkq	UTSW	5	108656495	missense	probably benign	0.02
R0525:Dgkq	UTSW	5	108654615	missense	probably damaging	1.00
R0673:Dgkq	UTSW	5	108655589	missense	probably damaging	0.97
R0801:Dgkq	UTSW	5	108660720	splice site	probably null
R0850:Dgkq	UTSW	5	108654578	missense	possibly damaging	0.82
R0944:Dgkq	UTSW	5	108656465	missense	probably damaging	1.00
R1069:Dgkq	UTSW	5	108656037	splice site	probably benign
R1411:Dgkq	UTSW	5	108650362	missense	probably damaging	1.00
R1488:Dgkq	UTSW	5	108650877	missense	probably damaging	1.00
R1858:Dgkq	UTSW	5	108653731	missense	probably benign	0.00
R1874:Dgkq	UTSW	5	108660595	missense	probably benign	0.07
R2210:Dgkq	UTSW	5	108660523	missense	probably damaging	1.00
R4499:Dgkq	UTSW	5	108649661	missense	possibly damaging	0.54
R5061:Dgkq	UTSW	5	108654123	missense	probably benign	0.02
R5474:Dgkq	UTSW	5	108649143	critical splice donor site	probably null
R5481:Dgkq	UTSW	5	108648810	splice site	probably null
R6193:Dgkq	UTSW	5	108655500	nonsense	probably null
R6429:Dgkq	UTSW	5	108653708	missense	probably damaging	1.00
R6458:Dgkq	UTSW	5	108654376	missense	possibly damaging	0.93
R7388:Dgkq	UTSW	5	108658246	missense	probably damaging	0.99
R7398:Dgkq	UTSW	5	108655190	missense	possibly damaging	0.90
R8098:Dgkq	UTSW	5	108652468	missense	probably damaging	1.00
R8244:Dgkq	UTSW	5	108648712	makesense	probably null

Predicted Primers

PCR Primer
(F):5'- AGGATCGTCCCTTCCACAAATAG -3'
(R):5'- GTGGTTCAAGAGGTTCTCCC -3'

Sequencing Primer
(F):5'- CAAATAGTTGCTCTAAGTCTCTGGG -3'
(R):5'- GGACAACAGGTATGTATCCTGTC -3'

Posted On

2017-03-31