Mutagenetix > Incidental Mutation

Incidental Mutation 'R7810:Brsk2'

652008

Institutional Source

Beutler Lab

Gene Symbol

Brsk2

Ensembl Gene

ENSMUSG00000053046

Gene Name

BR serine/threonine kinase 2

Synonyms

SAD-A, 4833424K13Rik

MMRRC Submission

045865-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7810 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

141503488-141557981 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to A at 141539157 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000134201 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000018971] [ENSMUST00000075528] [ENSMUST00000078200] [ENSMUST00000105989] [ENSMUST00000172652] [ENSMUST00000173705] [ENSMUST00000174309] [ENSMUST00000174405] [ENSMUST00000174499]

AlphaFold

Q69Z98

Predicted Effect

probably null
Transcript: ENSMUST00000018971

SMART Domains

Protein: ENSMUSP00000018971
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
S_TKc	20	271	3.65e-99	SMART
low complexity region	410	429	N/A	INTRINSIC
low complexity region	456	475	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000075528

SMART Domains

Protein: ENSMUSP00000074969
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
S_TKc	20	271	3.65e-99	SMART
low complexity region	410	429	N/A	INTRINSIC
low complexity region	456	475	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000078200

SMART Domains

Protein: ENSMUSP00000077330
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
S_TKc	20	271	3.65e-99	SMART
low complexity region	410	429	N/A	INTRINSIC
low complexity region	456	475	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000105989

SMART Domains

Protein: ENSMUSP00000101610
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
S_TKc	20	271	3.65e-99	SMART
low complexity region	410	429	N/A	INTRINSIC
low complexity region	456	475	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000172652

SMART Domains

Protein: ENSMUSP00000133438
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
S_TKc	20	271	3.65e-99	SMART
low complexity region	432	451	N/A	INTRINSIC
low complexity region	478	497	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000172967

SMART Domains

Protein: ENSMUSP00000133750
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
S_TKc	3	240	6.78e-85	SMART
low complexity region	379	398	N/A	INTRINSIC
low complexity region	425	444	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000173705

SMART Domains

Protein: ENSMUSP00000134170
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
Pfam:Pkinase_Tyr	1	111	4.4e-10	PFAM
Pfam:Pkinase	1	113	2e-24	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000173924

SMART Domains

Protein: ENSMUSP00000134153
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
Pfam:Pkinase_Tyr	1	98	3.7e-13	PFAM
Pfam:Pkinase	1	209	2.6e-29	PFAM
low complexity region	239	258	N/A	INTRINSIC
low complexity region	285	304	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000174309

SMART Domains

Protein: ENSMUSP00000134310
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
Pfam:Pkinase	1	82	7.1e-13	PFAM
low complexity region	221	240	N/A	INTRINSIC
low complexity region	267	286	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000174405

SMART Domains

Protein: ENSMUSP00000134289
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
Pfam:Pkinase	20	92	1e-13	PFAM
Pfam:Pkinase_Tyr	20	92	1.1e-8	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000174499

SMART Domains

Protein: ENSMUSP00000134201
Gene: ENSMUSG00000053046

Domain	Start	End	E-Value	Type
S_TKc	20	271	3.65e-99	SMART
low complexity region	410	429	N/A	INTRINSIC
low complexity region	456	475	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

99% (91/92)

MGI Phenotype

PHENOTYPE: Homozygous mutant mice are healthy and fertile. Mice homozygous for a condition allele activated in sensory and motor neurons exhibit partial neonatal lethality, hypokinesis, absnece of gastric milk and abnormal type Ia proprioceptive sensory neuron projections [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam34	T	C	8: 44,105,045 (GRCm39)	E200G	probably benign	Het
Ankfy1	C	T	11: 72,645,281 (GRCm39)	Q787*	probably null	Het
Birc6	T	A	17: 74,855,815 (GRCm39)	H208Q	probably damaging	Het
Cabp5	T	A	7: 13,132,263 (GRCm39)	F11I	possibly damaging	Het
Ccdc88a	T	C	11: 29,435,964 (GRCm39)	Y1296H	probably damaging	Het
Ccdc88b	A	G	19: 6,826,454 (GRCm39)	V1087A	probably benign	Het
Cct3	C	T	3: 88,228,442 (GRCm39)	T508I	probably damaging	Het
Ceacam9	T	A	7: 16,457,658 (GRCm39)	M57K	possibly damaging	Het
Ces1f	T	C	8: 93,983,546 (GRCm39)	E487G	probably damaging	Het
Chd5	A	G	4: 152,443,032 (GRCm39)	K278E	probably damaging	Het
Cntnap3	T	A	13: 64,941,122 (GRCm39)	H286L	possibly damaging	Het
Dnai7	T	G	6: 145,140,312 (GRCm39)	D163A	probably benign	Het
Efr3a	G	T	15: 65,659,022 (GRCm39)		probably benign	Het
Fastkd2	T	A	1: 63,770,851 (GRCm39)	I69N	possibly damaging	Het
Flg2	T	C	3: 93,107,548 (GRCm39)	I11T	possibly damaging	Het
Folr2	T	C	7: 101,490,102 (GRCm39)	M84V	possibly damaging	Het
Galnt12	T	C	4: 47,113,786 (GRCm39)	F360S	probably damaging	Het
Galr2	T	C	11: 116,173,946 (GRCm39)	V192A	probably benign	Het
Gas6	A	T	8: 13,516,809 (GRCm39)	I563N	probably damaging	Het
Gbe1	T	C	16: 70,324,085 (GRCm39)	F567L	possibly damaging	Het
Gm12695	G	A	4: 96,619,608 (GRCm39)	H423Y	probably damaging	Het
Gm6902	T	C	7: 22,973,243 (GRCm39)	T95A	probably benign	Het
Gpr155	G	T	2: 73,212,296 (GRCm39)	A109D	probably damaging	Het
Hsdl1	T	C	8: 120,294,711 (GRCm39)	D5G	probably damaging	Het
Hyal1	C	T	9: 107,455,628 (GRCm39)	P313S	probably damaging	Het
Igfn1	G	A	1: 135,902,527 (GRCm39)	T390M	probably damaging	Het
Irx1	C	A	13: 72,107,917 (GRCm39)	R255L	probably benign	Het
Itga2	T	A	13: 115,002,715 (GRCm39)	T592S	probably benign	Het
Kit	C	A	5: 75,769,982 (GRCm39)	S131R	probably benign	Het
Map1b	T	C	13: 99,568,390 (GRCm39)	T1444A	unknown	Het
Mapk8ip1	C	T	2: 92,219,496 (GRCm39)	E112K	probably benign	Het
Marveld3	T	C	8: 110,681,266 (GRCm39)	I210V	probably damaging	Het
Masp1	T	A	16: 23,295,068 (GRCm39)	I398L	probably benign	Het
Mmrn1	T	C	6: 60,953,309 (GRCm39)	I530T	probably benign	Het
Mtss2	A	G	8: 111,452,833 (GRCm39)	Y26C	probably damaging	Het
Myo5a	T	A	9: 75,067,747 (GRCm39)	S600R	probably benign	Het
Myo5a	A	G	9: 75,076,292 (GRCm39)	I836V	probably benign	Het
Naaladl1	A	G	19: 6,159,694 (GRCm39)	D375G	probably damaging	Het
Napepld	T	A	5: 21,888,263 (GRCm39)	D62V	possibly damaging	Het
Nedd9	A	C	13: 41,465,483 (GRCm39)	I719S	possibly damaging	Het
Nes	T	A	3: 87,882,923 (GRCm39)	M394K	probably benign	Het
Nlrc5	A	T	8: 95,231,772 (GRCm39)	Y1288F	possibly damaging	Het
Nlrp14	T	A	7: 106,791,782 (GRCm39)	C822*	probably null	Het
Noa1	A	C	5: 77,457,071 (GRCm39)	L278R	probably damaging	Het
Nop16	A	G	13: 54,737,889 (GRCm39)		probably benign	Het
Odr4	T	C	1: 150,268,659 (GRCm39)		probably benign	Het
Or11h7	A	T	14: 50,891,450 (GRCm39)	Y252F	probably benign	Het
Or5b12	A	G	19: 12,897,229 (GRCm39)	V148A	probably benign	Het
Osbpl10	C	T	9: 114,890,962 (GRCm39)	H117Y	probably benign	Het
Oxct1	A	T	15: 4,077,058 (GRCm39)	E130D	probably benign	Het
Padi2	A	G	4: 140,676,575 (GRCm39)	E571G	possibly damaging	Het
Pcdhac2	G	A	18: 37,278,717 (GRCm39)	V566M	probably benign	Het
Pdcd11	G	A	19: 47,086,659 (GRCm39)	E222K	possibly damaging	Het
Pira12	C	A	7: 3,897,204 (GRCm39)	C544F	probably damaging	Het
Plekha2	A	G	8: 25,578,356 (GRCm39)		probably null	Het
Pogz	T	C	3: 94,777,418 (GRCm39)	L366P	probably benign	Het
Ppp4r3b	A	G	11: 29,138,086 (GRCm39)	I145V	probably benign	Het
Prkcd	A	G	14: 30,320,407 (GRCm39)		probably null	Het
Ptprk	T	A	10: 28,468,853 (GRCm39)	H1438Q	probably damaging	Het
Rbm4	A	T	19: 4,842,650 (GRCm39)	V63E	possibly damaging	Het
Sbk2	T	A	7: 4,961,938 (GRCm39)	H116L	probably damaging	Het
Sdk1	A	G	5: 141,923,434 (GRCm39)	T352A	probably benign	Het
Septin9	T	A	11: 117,250,264 (GRCm39)	C529*	probably null	Het
Setx	T	A	2: 29,038,663 (GRCm39)	V1716D	probably benign	Het
Slc19a3	C	T	1: 82,997,162 (GRCm39)	V349I	probably benign	Het
Slc27a4	C	A	2: 29,695,722 (GRCm39)	R86S	probably benign	Het
Slc4a8	A	G	15: 100,696,059 (GRCm39)	H613R	possibly damaging	Het
Smoc2	A	G	17: 14,545,884 (GRCm39)	R58G	probably damaging	Het
Sphkap	T	A	1: 83,254,021 (GRCm39)	N1243Y	probably damaging	Het
Srsf5	T	C	12: 80,996,720 (GRCm39)	S261P	unknown	Het
Tab1	A	T	15: 80,042,999 (GRCm39)	T398S	possibly damaging	Het
Tas2r131	T	A	6: 132,934,705 (GRCm39)	T35S	probably benign	Het
Tasor2	T	C	13: 3,625,714 (GRCm39)	K1412R	possibly damaging	Het
Tigd4	T	A	3: 84,502,310 (GRCm39)	V409E	possibly damaging	Het
Tlr12	T	C	4: 128,510,501 (GRCm39)	Q583R	probably benign	Het
Tmprss9	T	A	10: 80,733,145 (GRCm39)	C894S	unknown	Het
Topaz1	T	A	9: 122,578,250 (GRCm39)	S387T	probably benign	Het
Tsfm	T	C	10: 126,847,558 (GRCm39)	R178G	probably benign	Het
Ttll13	T	C	7: 79,902,875 (GRCm39)	I181T	probably damaging	Het
Ttyh3	T	A	5: 140,610,896 (GRCm39)	K97N		Het
Ubr4	A	G	4: 139,142,394 (GRCm39)	E38G		Het
Ugt2b37	T	C	5: 87,402,118 (GRCm39)	Y171C	probably damaging	Het
Unc5b	C	A	10: 60,601,020 (GRCm39)	M935I	probably benign	Het
Usp34	T	C	11: 23,362,314 (GRCm39)	S1606P		Het
Vmn1r195	T	C	13: 22,463,244 (GRCm39)	L238P	probably damaging	Het
Vmn2r85	T	A	10: 130,261,081 (GRCm39)	M419L	probably benign	Het
Washc2	G	T	6: 116,236,020 (GRCm39)	A1164S	probably benign	Het
Wdfy3	A	T	5: 102,042,940 (GRCm39)	M1937K	probably benign	Het
Wdfy3	A	T	5: 102,099,265 (GRCm39)	L261*	probably null	Het
Wdr64	A	T	1: 175,559,092 (GRCm39)	Y285F	probably benign	Het
Wtap	A	G	17: 13,199,797 (GRCm39)	L62P	probably damaging	Het
Zfp1007	A	C	5: 109,825,170 (GRCm39)	Y93*	probably null	Het
Zfp94	C	A	7: 24,002,498 (GRCm39)	V315F	probably benign	Het
Zhx1	A	T	15: 57,911,798 (GRCm39)		probably null	Het

Other mutations in Brsk2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01576:Brsk2	APN	7	141,535,292 (GRCm39)	missense	possibly damaging	0.53
IGL02243:Brsk2	APN	7	141,547,036 (GRCm39)	missense	probably damaging	1.00
R0400:Brsk2	UTSW	7	141,552,290 (GRCm39)	missense	probably damaging	1.00
R0609:Brsk2	UTSW	7	141,552,229 (GRCm39)	missense	probably damaging	0.99
R0972:Brsk2	UTSW	7	141,547,441 (GRCm39)	splice site	probably benign
R1699:Brsk2	UTSW	7	141,539,200 (GRCm39)	missense	probably damaging	0.97
R3928:Brsk2	UTSW	7	141,552,155 (GRCm39)	missense	probably damaging	1.00
R5357:Brsk2	UTSW	7	141,538,248 (GRCm39)	missense	possibly damaging	0.55
R5411:Brsk2	UTSW	7	141,554,594 (GRCm39)	missense	probably benign	0.03
R5461:Brsk2	UTSW	7	141,541,643 (GRCm39)	missense	probably damaging	1.00
R6813:Brsk2	UTSW	7	141,556,214 (GRCm39)	missense	probably benign	0.00
R6966:Brsk2	UTSW	7	141,538,270 (GRCm39)	missense	possibly damaging	0.48
R7560:Brsk2	UTSW	7	141,554,597 (GRCm39)	missense	probably benign	0.00
R7922:Brsk2	UTSW	7	141,546,957 (GRCm39)	missense	possibly damaging	0.63
R8254:Brsk2	UTSW	7	141,538,153 (GRCm39)	missense	probably damaging	1.00
R8336:Brsk2	UTSW	7	141,538,211 (GRCm39)	missense	probably damaging	1.00
R8798:Brsk2	UTSW	7	141,541,601 (GRCm39)	missense	probably damaging	1.00
R8859:Brsk2	UTSW	7	141,552,415 (GRCm39)	missense	probably damaging	1.00
R9225:Brsk2	UTSW	7	141,547,039 (GRCm39)	missense	probably damaging	1.00
R9296:Brsk2	UTSW	7	141,552,375 (GRCm39)	missense	probably benign	0.09
R9347:Brsk2	UTSW	7	141,552,133 (GRCm39)	missense	probably damaging	0.97
R9445:Brsk2	UTSW	7	141,538,149 (GRCm39)	missense	probably damaging	1.00
R9466:Brsk2	UTSW	7	141,536,800 (GRCm39)	missense	probably benign	0.01
R9494:Brsk2	UTSW	7	141,555,955 (GRCm39)	missense	possibly damaging	0.84
R9516:Brsk2	UTSW	7	141,546,852 (GRCm39)	missense	probably benign	0.29

Predicted Primers

PCR Primer
(F):5'- GGGCACACTTTTATTGAGCC -3'
(R):5'- TGCCAGATGTCGGCAGTATG -3'

Sequencing Primer
(F):5'- TCTCTCCTGGGTCTAAGCAGAG -3'
(R):5'- CAGTATGCAAGGTAGGGGTATC -3'

Posted On

2020-09-23