Mutagenetix > Incidental Mutation

Incidental Mutation 'R1862:Srpk2'

204008

Institutional Source

Beutler Lab

Gene Symbol

Srpk2

Ensembl Gene

ENSMUSG00000062604

Gene Name

serine/arginine-rich protein specific kinase 2

Synonyms

WBP6, mSRPK2

MMRRC Submission

039885-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1862 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

23708262-23889615 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 23729148 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Arginine at position 497 (K497R)

Ref Sequence

ENSEMBL: ENSMUSP00000085734 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000088392] [ENSMUST00000196388] [ENSMUST00000196929]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000088392
AA Change: K497R

PolyPhen 2 Score 0.316 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000085734
Gene: ENSMUSG00000062604
AA Change: K497R

Domain	Start	End	E-Value	Type
low complexity region	5	46	N/A	INTRINSIC
Pfam:Pkinase	79	228	1.3e-22	PFAM
Pfam:Pkinase_Tyr	79	228	1e-9	PFAM
coiled coil region	263	314	N/A	INTRINSIC
coiled coil region	339	373	N/A	INTRINSIC
low complexity region	393	406	N/A	INTRINSIC
Pfam:Pkinase	506	680	1.9e-18	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000196388

SMART Domains

Protein: ENSMUSP00000143453
Gene: ENSMUSG00000062604

Domain	Start	End	E-Value	Type
S_TKc	3	129	7.2e-6	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000196929

SMART Domains

Protein: ENSMUSP00000143216
Gene: ENSMUSG00000062604

Domain	Start	End	E-Value	Type
Pfam:Pkinase_Tyr	1	131	2.6e-8	PFAM
Pfam:Pkinase	2	130	2.3e-18	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200173

Coding Region Coverage

1x: 97.5%
3x: 96.8%
10x: 94.9%
20x: 90.5%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a targeted allele exhibit normal phenotype. [provided by MGI curators]

Allele List at MGI

All alleles(39) : Targeted(3) Gene trapped(36)

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acox2	T	A	14: 8,241,416 (GRCm38)	E565D	probably benign	Het
Adam30	A	T	3: 98,069,429 (GRCm39)	K421*	probably null	Het
Atp6v1b1	A	G	6: 83,726,834 (GRCm39)		probably null	Het
Cacna1a	A	T	8: 85,142,559 (GRCm39)	I96F	possibly damaging	Het
Card10	G	A	15: 78,664,714 (GRCm39)	R747W	probably damaging	Het
Cdh8	T	A	8: 99,917,026 (GRCm39)	D363V	probably damaging	Het
Cecr2	T	C	6: 120,734,902 (GRCm39)	Y685H	probably damaging	Het
Cibar1	C	T	4: 12,155,717 (GRCm39)	V306I	possibly damaging	Het
Cmklr1	T	C	5: 113,752,468 (GRCm39)	T178A	probably damaging	Het
Col16a1	G	A	4: 129,986,575 (GRCm39)		probably null	Het
Col4a1	C	T	8: 11,276,439 (GRCm39)		probably benign	Het
Coro2a	T	A	4: 46,548,797 (GRCm39)	I166F	possibly damaging	Het
Cry2	T	C	2: 92,254,911 (GRCm39)	H148R	probably damaging	Het
Crygd	T	C	1: 65,101,133 (GRCm39)	Y154C	probably benign	Het
Cubn	T	C	2: 13,313,372 (GRCm39)	Y3066C	probably damaging	Het
Defb15	C	T	8: 22,420,002 (GRCm39)	E42K	possibly damaging	Het
Dnah12	A	G	14: 26,418,553 (GRCm39)	D147G	probably benign	Het
Dnah12	A	T	14: 26,430,412 (GRCm39)	Y340F	probably benign	Het
Dot1l	G	T	10: 80,619,373 (GRCm39)	R193L	probably damaging	Het
Dusp29	A	G	14: 21,736,757 (GRCm39)	V115A	probably benign	Het
Esd	A	C	14: 74,979,514 (GRCm39)	Y119S	probably damaging	Het
Esp36	A	G	17: 38,730,330 (GRCm39)		probably benign	Het
Etfbkmt	T	A	6: 149,045,649 (GRCm39)	M1K	probably null	Het
Exph5	A	G	9: 53,287,548 (GRCm39)	H1543R	probably benign	Het
Fbxo16	A	G	14: 65,508,252 (GRCm39)	T23A	probably damaging	Het
Gorasp2	C	A	2: 70,509,808 (GRCm39)	H136Q	probably damaging	Het
Hdc	T	A	2: 126,439,853 (GRCm39)	I367F	probably benign	Het
Hmcn1	C	T	1: 150,514,651 (GRCm39)	V3574M	probably benign	Het
Ilvbl	A	G	10: 78,419,958 (GRCm39)	D592G	probably benign	Het
Inmt	G	A	6: 55,151,868 (GRCm39)	A34V	probably damaging	Het
Ints9	A	C	14: 65,263,862 (GRCm39)	H378P	probably benign	Het
Kcnh7	T	A	2: 62,618,098 (GRCm39)	I464L	possibly damaging	Het
Kcnt2	T	A	1: 140,353,068 (GRCm39)	V259D	probably damaging	Het
Lipo3	A	G	19: 33,762,092 (GRCm39)	F135S	probably damaging	Het
Lrba	T	C	3: 86,680,510 (GRCm39)		probably null	Het
Mapk1	T	A	16: 16,844,293 (GRCm39)	S22T	probably benign	Het
Mbd3l2	T	C	9: 18,356,217 (GRCm39)	S181P	possibly damaging	Het
Mgat5	C	T	1: 127,387,706 (GRCm39)	P554L	probably damaging	Het
Mki67	T	C	7: 135,301,090 (GRCm39)	T1315A	probably benign	Het
Mprip	C	T	11: 59,649,047 (GRCm39)	T917M	possibly damaging	Het
Mroh3	T	A	1: 136,113,726 (GRCm39)	I688F	probably benign	Het
Myo1d	A	T	11: 80,553,874 (GRCm39)	Y536N	probably damaging	Het
Neb	C	T	2: 52,052,199 (GRCm39)		probably null	Het
Noc2l	A	G	4: 156,322,165 (GRCm39)	R161G	probably benign	Het
Nup54	T	A	5: 92,567,426 (GRCm39)	I375L	possibly damaging	Het
Nup93	T	C	8: 95,032,730 (GRCm39)	F539L	probably damaging	Het
Or10x1	T	A	1: 174,197,018 (GRCm39)	H178Q	probably damaging	Het
Or2n1e	A	G	17: 38,586,235 (GRCm39)	E191G	probably damaging	Het
Or5p57	A	C	7: 107,665,932 (GRCm39)	Y24*	probably null	Het
Or8b12	T	A	9: 37,658,264 (GRCm39)	M278K	probably benign	Het
Panx1	A	T	9: 14,918,724 (GRCm39)	D378E	probably damaging	Het
Papss1	T	A	3: 131,288,945 (GRCm39)	V170D	possibly damaging	Het
Pcnx1	T	C	12: 81,965,506 (GRCm39)	S558P	probably damaging	Het
Pde3a	G	T	6: 141,433,239 (GRCm39)	A757S	probably damaging	Het
Pde3a	T	A	6: 141,196,079 (GRCm39)	I255N	probably damaging	Het
Pdzph1	A	G	17: 59,229,578 (GRCm39)	Y1027H	probably damaging	Het
Pkhd1	G	T	1: 20,621,244 (GRCm39)	R805S	probably benign	Het
Polr1a	G	A	6: 71,886,187 (GRCm39)	G14D	probably damaging	Het
Prg4	T	A	1: 150,336,420 (GRCm39)	D60V	probably damaging	Het
Ptgr3	T	C	18: 84,113,443 (GRCm39)	V373A	possibly damaging	Het
Ptprc	T	C	1: 138,039,965 (GRCm39)	S311G	probably benign	Het
Rapgefl1	G	A	11: 98,733,035 (GRCm39)	R205K	probably benign	Het
Rcan2	A	T	17: 44,347,980 (GRCm39)		probably null	Het
Rock1	A	G	18: 10,079,207 (GRCm39)	I1087T	probably damaging	Het
Sectm1b	A	G	11: 120,945,768 (GRCm39)	I191T	possibly damaging	Het
Septin4	A	G	11: 87,458,061 (GRCm39)	H145R	possibly damaging	Het
Setd1b	T	C	5: 123,285,676 (GRCm39)	S241P	unknown	Het
Slco1a8	T	C	6: 141,949,149 (GRCm39)	M76V	possibly damaging	Het
Sspo	T	C	6: 48,467,940 (GRCm39)	S4296P	probably damaging	Het
Syne4	T	C	7: 30,016,308 (GRCm39)	V168A	probably benign	Het
Tank	T	C	2: 61,480,256 (GRCm39)	F264S	probably damaging	Het
Ticrr	T	C	7: 79,344,955 (GRCm39)	S1607P	probably damaging	Het
Trim30a	A	G	7: 104,060,405 (GRCm39)	V457A	probably damaging	Het
Trim43b	T	A	9: 88,967,624 (GRCm39)	K336N	probably damaging	Het
Trim47	T	C	11: 115,996,963 (GRCm39)	Q598R	probably damaging	Het
Tspan12	T	C	6: 21,851,022 (GRCm39)	N18S	probably damaging	Het
Ubap2	A	G	4: 41,221,607 (GRCm39)	S231P	probably benign	Het
Vit	A	G	17: 78,930,175 (GRCm39)	D380G	probably damaging	Het
Vmn2r2	T	C	3: 64,041,942 (GRCm39)	N258D	possibly damaging	Het
Vmn2r52	C	T	7: 9,907,333 (GRCm39)	C131Y	possibly damaging	Het
Zfp58	A	T	13: 67,639,307 (GRCm39)	F395I	probably damaging	Het
Zfp940	C	A	7: 29,544,435 (GRCm39)	G491C	probably damaging	Het

Other mutations in Srpk2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00697:Srpk2	APN	5	23,745,377 (GRCm39)	missense	probably benign	0.10
IGL02057:Srpk2	APN	5	23,723,705 (GRCm39)	missense	probably damaging	0.99
IGL02217:Srpk2	APN	5	23,750,568 (GRCm39)	missense	probably damaging	1.00
IGL03115:Srpk2	APN	5	23,729,616 (GRCm39)	splice site	probably null
FR4737:Srpk2	UTSW	5	23,750,194 (GRCm39)	splice site	probably null
P0008:Srpk2	UTSW	5	23,718,976 (GRCm39)	missense	probably damaging	1.00
R0142:Srpk2	UTSW	5	23,732,928 (GRCm39)	missense	probably damaging	0.97
R0462:Srpk2	UTSW	5	23,723,424 (GRCm39)	missense	probably damaging	1.00
R0992:Srpk2	UTSW	5	23,750,541 (GRCm39)	missense	probably damaging	0.99
R1569:Srpk2	UTSW	5	23,719,024 (GRCm39)	missense	probably damaging	1.00
R1677:Srpk2	UTSW	5	23,730,748 (GRCm39)	splice site	probably null
R1696:Srpk2	UTSW	5	23,753,492 (GRCm39)	nonsense	probably null
R1752:Srpk2	UTSW	5	23,733,017 (GRCm39)	missense	probably damaging	1.00
R1989:Srpk2	UTSW	5	23,723,421 (GRCm39)	missense	probably damaging	1.00
R2173:Srpk2	UTSW	5	23,723,613 (GRCm39)	splice site	probably null
R4096:Srpk2	UTSW	5	23,745,500 (GRCm39)	intron	probably benign
R4271:Srpk2	UTSW	5	23,753,513 (GRCm39)	missense	possibly damaging	0.95
R4894:Srpk2	UTSW	5	23,750,527 (GRCm39)	missense	probably damaging	1.00
R5043:Srpk2	UTSW	5	23,729,515 (GRCm39)	missense	probably benign
R5044:Srpk2	UTSW	5	23,729,390 (GRCm39)	missense	possibly damaging	0.91
R5309:Srpk2	UTSW	5	23,730,716 (GRCm39)	missense	probably damaging	0.97
R5478:Srpk2	UTSW	5	23,729,181 (GRCm39)	missense	possibly damaging	0.71
R5568:Srpk2	UTSW	5	23,730,697 (GRCm39)	missense	possibly damaging	0.73
R5665:Srpk2	UTSW	5	23,723,475 (GRCm39)	missense	probably damaging	0.99
R5678:Srpk2	UTSW	5	23,729,604 (GRCm39)	frame shift	probably null
R6364:Srpk2	UTSW	5	23,745,465 (GRCm39)	missense	probably damaging	1.00
R7201:Srpk2	UTSW	5	23,712,626 (GRCm39)	missense	possibly damaging	0.64
R7597:Srpk2	UTSW	5	23,753,517 (GRCm39)	missense	possibly damaging	0.96
R8251:Srpk2	UTSW	5	23,729,266 (GRCm39)	missense	probably benign
R8477:Srpk2	UTSW	5	23,718,986 (GRCm39)	missense	probably benign	0.03
R9348:Srpk2	UTSW	5	23,719,671 (GRCm39)	missense	probably damaging	0.98
R9606:Srpk2	UTSW	5	23,729,604 (GRCm39)	missense	probably benign
R9745:Srpk2	UTSW	5	23,880,874 (GRCm39)	intron	probably benign
RF035:Srpk2	UTSW	5	23,730,573 (GRCm39)	utr 3 prime	probably benign
RF042:Srpk2	UTSW	5	23,730,573 (GRCm39)	utr 3 prime	probably benign

Predicted Primers

PCR Primer
(F):5'- AAGCCCAGGGATAGGATTTCAG -3'
(R):5'- AGCAGCTCCTATGAACAATTCAATG -3'

Sequencing Primer
(F):5'- TTTCAGAGAGTAAGAGCAAGCC -3'
(R):5'- TCAATGGTGAATTGCCAAATGGAC -3'

Posted On

2014-06-23