Mutagenetix > Incidental Mutation

Incidental Mutation 'R2075:Stk3'

227567

Institutional Source

Beutler Lab

Gene Symbol

Stk3

Ensembl Gene

ENSMUSG00000022329

Gene Name

serine/threonine kinase 3

Synonyms

Ste20, 0610042I06Rik, Mst2, MST, mess1

MMRRC Submission

040080-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2075 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

34875645-35155990 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 34959195 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Valine at position 256 (M256V)

Ref Sequence

ENSEMBL: ENSMUSP00000064225 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000018476] [ENSMUST00000067033] [ENSMUST00000226555]

AlphaFold

Q9JI10

Predicted Effect

probably benign
Transcript: ENSMUST00000018476
AA Change: M326V

PolyPhen 2 Score 0.388 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000018476
Gene: ENSMUSG00000022329
AA Change: M326V

Domain	Start	End	E-Value	Type
low complexity region	7	19	N/A	INTRINSIC
S_TKc	27	278	4.16e-103	SMART
low complexity region	301	324	N/A	INTRINSIC
low complexity region	370	381	N/A	INTRINSIC
Pfam:Mst1_SARAH	443	490	9.6e-28	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000067033
AA Change: M256V

PolyPhen 2 Score 0.790 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000064225
Gene: ENSMUSG00000022329
AA Change: M256V

Domain	Start	End	E-Value	Type
Pfam:Pkinase_Tyr	5	205	2.1e-41	PFAM
Pfam:Pkinase	5	208	1.2e-56	PFAM
coiled coil region	217	256	N/A	INTRINSIC
low complexity region	300	311	N/A	INTRINSIC
Pfam:Mst1_SARAH	372	420	9.8e-30	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000128425

Predicted Effect

probably benign
Transcript: ENSMUST00000226555
AA Change: M324V

PolyPhen 2 Score 0.377 (Sensitivity: 0.90; Specificity: 0.89)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000226730

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a serine/threonine protein kinase activated by proapoptotic molecules indicating the encoded protein functions as a growth suppressor. Cleavage of the protein product by caspase removes the inhibitory C-terminal portion. The N-terminal portion is transported to the nucleus where it homodimerizes to form the active kinase which promotes the condensation of chromatin during apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
PHENOTYPE: Homozygous inactivation of this gene generally results in mice that are viable, fertile and developmentally normal. A small subset of mice homozygous for a knock-out allele develop mammary tumors in the absence of immunological defects. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	T	C	11: 9,472,382 (GRCm39)	F4263L	probably damaging	Het
Aebp2	G	A	6: 140,579,420 (GRCm39)	S219N	probably benign	Het
Anln	C	A	9: 22,244,464 (GRCm39)	W1083L	probably benign	Het
Atic	T	A	1: 71,615,286 (GRCm39)	D438E	probably benign	Het
Bahcc1	G	A	11: 120,162,515 (GRCm39)	C271Y	probably damaging	Het
Btbd17	A	T	11: 114,682,778 (GRCm39)		probably null	Het
Ccdc122	T	C	14: 77,306,391 (GRCm39)		probably null	Het
Ccdc149	A	G	5: 52,596,510 (GRCm39)	L34P	probably damaging	Het
Cd22	C	G	7: 30,569,123 (GRCm39)	C637S	probably damaging	Het
Ces1a	T	A	8: 93,774,703 (GRCm39)	N12Y	probably benign	Het
Chmp1a	A	T	8: 123,934,761 (GRCm39)	M65K	probably damaging	Het
Clec16a	G	A	16: 10,559,480 (GRCm39)	A918T	probably benign	Het
Clec2m	C	T	6: 129,303,666 (GRCm39)	E100K	probably benign	Het
Cnot1	G	T	8: 96,466,461 (GRCm39)	T1592K	possibly damaging	Het
Ddx10	A	T	9: 53,151,805 (GRCm39)	D73E	probably benign	Het
Dhx32	T	C	7: 133,323,021 (GRCm39)	N731S	probably benign	Het
Dmd	G	C	X: 83,356,089 (GRCm39)	A2257P	probably benign	Het
Dna2	A	G	10: 62,805,601 (GRCm39)	Q946R	probably benign	Het
Dnai4	G	A	4: 102,907,390 (GRCm39)	T632M	probably damaging	Het
Duox2	T	A	2: 122,125,639 (GRCm39)	S323C	probably damaging	Het
Esr2	A	G	12: 76,212,221 (GRCm39)		probably null	Het
Fbxo9	G	T	9: 77,991,798 (GRCm39)	H397N	possibly damaging	Het
Fsip2	T	A	2: 82,818,923 (GRCm39)	N4885K	possibly damaging	Het
Gm12695	T	C	4: 96,612,182 (GRCm39)	Y527C	possibly damaging	Het
Hivep1	A	G	13: 42,309,794 (GRCm39)	D678G	probably damaging	Het
Hmcn1	T	A	1: 150,453,074 (GRCm39)	I5414F	possibly damaging	Het
Hspb2	T	C	9: 50,662,646 (GRCm39)	Y67C	probably benign	Het
Kbtbd8	T	A	6: 95,103,664 (GRCm39)	C438S	possibly damaging	Het
Kif5a	T	C	10: 127,081,238 (GRCm39)	D232G	probably damaging	Het
Ky	A	G	9: 102,419,945 (GRCm39)	S651G	probably damaging	Het
Lgals12	T	C	19: 7,576,210 (GRCm39)	D238G	possibly damaging	Het
Lpcat3	T	A	6: 124,680,066 (GRCm39)	Y380N	probably damaging	Het
Mdn1	A	G	4: 32,716,058 (GRCm39)	H2080R	probably benign	Het
Mex3c	C	T	18: 73,722,840 (GRCm39)	S311L	probably benign	Het
Mlh3	A	T	12: 85,315,915 (GRCm39)	Y90*	probably null	Het
Mpped2	T	A	2: 106,575,147 (GRCm39)	Y77*	probably null	Het
Myo5a	A	T	9: 75,097,200 (GRCm39)	T49S	probably benign	Het
Nsd1	T	C	13: 55,458,313 (GRCm39)	V2142A	possibly damaging	Het
Or4a74	A	G	2: 89,439,822 (GRCm39)	V208A	probably benign	Het
Or51b17	T	A	7: 103,542,127 (GRCm39)	I272F	probably damaging	Het
Or51i2	T	A	7: 103,689,180 (GRCm39)	M59K	probably damaging	Het
Or5ac19	T	C	16: 59,089,274 (GRCm39)	Y252C	possibly damaging	Het
Pdgfra	T	C	5: 75,348,609 (GRCm39)	I883T	probably damaging	Het
Pdzd2	A	G	15: 12,385,905 (GRCm39)	L955P	probably damaging	Het
Phf24	A	G	4: 42,939,507 (GRCm39)	Y333C	possibly damaging	Het
Phlpp2	T	C	8: 110,655,124 (GRCm39)	S605P	possibly damaging	Het
Piezo2	C	T	18: 63,214,805 (GRCm39)	E1263K	probably damaging	Het
Pitrm1	A	G	13: 6,605,419 (GRCm39)	T149A	probably damaging	Het
Pkhd1l1	G	T	15: 44,422,035 (GRCm39)	A3102S	probably damaging	Het
Plch2	A	T	4: 155,074,366 (GRCm39)	L754Q	probably damaging	Het
Polr2c	A	G	8: 95,590,195 (GRCm39)	I267V	probably benign	Het
Potefam1	T	C	2: 111,030,763 (GRCm39)	E382G	probably damaging	Het
Prss8	C	A	7: 127,526,266 (GRCm39)	R148L	possibly damaging	Het
Ptpn2	T	A	18: 67,814,545 (GRCm39)	T155S	probably damaging	Het
Ptprn2	G	A	12: 117,211,337 (GRCm39)	V839I	probably benign	Het
Sbp	A	G	17: 24,164,132 (GRCm39)		probably null	Het
Sec16a	A	G	2: 26,330,251 (GRCm39)	I588T	probably damaging	Het
Six2	A	G	17: 85,994,933 (GRCm39)	S150P	probably damaging	Het
Slc5a5	C	T	8: 71,345,083 (GRCm39)	G75R	possibly damaging	Het
Slc6a20b	T	A	9: 123,424,099 (GRCm39)	T623S	probably benign	Het
Sqle	T	A	15: 59,195,750 (GRCm39)	V342E	probably damaging	Het
Tek	A	G	4: 94,715,966 (GRCm39)	I463V	probably benign	Het
Tex10	C	T	4: 48,456,800 (GRCm39)	R637Q	probably benign	Het
Tnc	G	A	4: 63,913,903 (GRCm39)	T1303M	possibly damaging	Het
Traf6	A	C	2: 101,527,398 (GRCm39)	I383L	probably benign	Het
Tubb3	C	T	8: 124,148,009 (GRCm39)	A314V	probably damaging	Het
Vmn1r199	A	T	13: 22,567,435 (GRCm39)	Y243F	probably damaging	Het
Vmn2r111	A	C	17: 22,778,043 (GRCm39)	N545K	probably damaging	Het
Vmn2r27	T	A	6: 124,177,510 (GRCm39)	Q498L	possibly damaging	Het
Vstm4	A	T	14: 32,639,811 (GRCm39)	S229C	probably damaging	Het
Wdr12	C	T	1: 60,130,222 (GRCm39)	R63Q	possibly damaging	Het
Wrn	T	A	8: 33,812,357 (GRCm39)	I187L	probably benign	Het
Xirp2	A	T	2: 67,340,545 (GRCm39)	I929L	probably benign	Het
Ywhae	T	A	11: 75,655,486 (GRCm39)	D252E	probably benign	Het
Zfp944	A	T	17: 22,558,178 (GRCm39)	C356*	probably null	Het

Other mutations in Stk3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00848:Stk3	APN	15	35,114,768 (GRCm39)	missense	possibly damaging	0.93
IGL02133:Stk3	APN	15	35,099,662 (GRCm39)	missense	probably damaging	1.00
IGL03121:Stk3	APN	15	35,099,572 (GRCm39)	splice site	probably benign
IGL03309:Stk3	APN	15	35,099,697 (GRCm39)	splice site	probably benign
R0276:Stk3	UTSW	15	35,099,615 (GRCm39)	missense	probably damaging	1.00
R0416:Stk3	UTSW	15	35,114,778 (GRCm39)	missense	probably benign	0.07
R1352:Stk3	UTSW	15	35,008,371 (GRCm39)	missense	probably damaging	1.00
R1633:Stk3	UTSW	15	34,959,206 (GRCm39)	missense	probably damaging	1.00
R1638:Stk3	UTSW	15	35,008,454 (GRCm39)	splice site	probably null
R1917:Stk3	UTSW	15	35,073,363 (GRCm39)	missense	probably damaging	1.00
R1919:Stk3	UTSW	15	35,073,363 (GRCm39)	missense	probably damaging	1.00
R2011:Stk3	UTSW	15	35,072,644 (GRCm39)	missense	probably damaging	1.00
R2072:Stk3	UTSW	15	34,959,195 (GRCm39)	missense	possibly damaging	0.79
R2073:Stk3	UTSW	15	34,959,195 (GRCm39)	missense	possibly damaging	0.79
R3158:Stk3	UTSW	15	35,008,387 (GRCm39)	missense	possibly damaging	0.83
R3402:Stk3	UTSW	15	34,945,144 (GRCm39)	splice site	probably benign
R4633:Stk3	UTSW	15	34,959,074 (GRCm39)	missense	probably damaging	0.99
R4672:Stk3	UTSW	15	35,099,603 (GRCm39)	missense	probably benign	0.06
R4687:Stk3	UTSW	15	35,114,711 (GRCm39)	missense	probably damaging	0.99
R4825:Stk3	UTSW	15	35,000,054 (GRCm39)	missense	probably benign	0.14
R4903:Stk3	UTSW	15	34,959,212 (GRCm39)	missense	probably damaging	0.99
R5390:Stk3	UTSW	15	35,114,706 (GRCm39)	nonsense	probably null
R5834:Stk3	UTSW	15	34,959,164 (GRCm39)	missense	probably damaging	1.00
R7208:Stk3	UTSW	15	35,073,262 (GRCm39)	missense	possibly damaging	0.76
R7266:Stk3	UTSW	15	34,959,182 (GRCm39)	missense	probably benign	0.05
R7862:Stk3	UTSW	15	35,115,732 (GRCm39)	missense	possibly damaging	0.90
R8354:Stk3	UTSW	15	34,876,870 (GRCm39)	missense	probably damaging	1.00
R8454:Stk3	UTSW	15	34,876,870 (GRCm39)	missense	probably damaging	1.00
R8996:Stk3	UTSW	15	34,945,208 (GRCm39)	missense	possibly damaging	0.51
R9160:Stk3	UTSW	15	35,099,611 (GRCm39)	missense	probably damaging	0.99
R9366:Stk3	UTSW	15	35,072,634 (GRCm39)	missense	probably damaging	1.00
R9777:Stk3	UTSW	15	35,114,791 (GRCm39)	missense	probably damaging	1.00
X0021:Stk3	UTSW	15	35,072,701 (GRCm39)	missense	probably damaging	1.00
X0060:Stk3	UTSW	15	35,114,679 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AGAGAAAGGGCTCCATACTTTTC -3'
(R):5'- TCAGCTATCTTCAAGAGGTCTTTG -3'

Sequencing Primer
(F):5'- AAGGGCTCCATACTTTTCATAGTTC -3'
(R):5'- ACTTACCCAGAATTCTAGTTGCAAGG -3'

Posted On

2014-09-17