Mutagenetix > Incidental Mutation

Incidental Mutation 'R0611:Stk38'

54767

Institutional Source

Beutler Lab

Gene Symbol

Stk38

Ensembl Gene

ENSMUSG00000024006

Gene Name

serine/threonine kinase 38

Synonyms

5830476G13Rik, Ndr1, 9530097A09Rik

MMRRC Submission

038800-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.516) question?

Stock #

R0611 (G1)

Quality Score

219

Status

Not validated

Chromosome

Chromosomal Location

29189854-29226969 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 29194907 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Valine at position 280 (F280V)

Ref Sequence

ENSEMBL: ENSMUSP00000113657 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000009138] [ENSMUST00000119274]

AlphaFold

Q91VJ4

Predicted Effect

possibly damaging
Transcript: ENSMUST00000009138
AA Change: F280V

PolyPhen 2 Score 0.721 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000009138
Gene: ENSMUSG00000024006
AA Change: F280V

Domain	Start	End	E-Value	Type
Blast:S_TKc	31	77	1e-9	BLAST
S_TKc	89	382	1.69e-94	SMART
S_TK_X	383	447	1.23e-2	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000119274
AA Change: F280V

PolyPhen 2 Score 0.721 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000113657
Gene: ENSMUSG00000024006
AA Change: F280V

Domain	Start	End	E-Value	Type
Blast:S_TKc	31	77	1e-9	BLAST
S_TKc	89	382	1.69e-94	SMART
S_TK_X	383	447	1.23e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125070

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126619

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126671

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126893

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140355

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000142923

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156732

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141431

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144299

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.5%
20x: 94.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the AGC serine/threonine kinase family of proteins. The kinase activity of this protein is regulated by autophosphorylation and phosphorylation by other upstream kinases. This protein has been shown to function in the cell cycle and apoptosis. This protein has also been found to regulate the protein stability and transcriptional activity of the MYC oncogene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to bacterial infection and altered TLR9-activated inflammatory responses. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca14	T	A	7: 119,851,479 (GRCm39)	M819K	possibly damaging	Het
Adamtsl3	T	G	7: 82,178,120 (GRCm39)	C528G	probably damaging	Het
Akap9	A	G	5: 4,004,870 (GRCm39)	K148E	probably benign	Het
Akr1b1	A	T	6: 34,286,577 (GRCm39)	D225E	probably benign	Het
Alms1	C	A	6: 85,655,653 (GRCm39)	Q2931K	possibly damaging	Het
Ano3	T	C	2: 110,715,346 (GRCm39)	K31E	possibly damaging	Het
Cdc37	A	G	9: 21,053,537 (GRCm39)	I242T	probably damaging	Het
Celsr1	T	A	15: 85,816,524 (GRCm39)	K1806N	possibly damaging	Het
Clpb	T	A	7: 101,436,956 (GRCm39)	I707N	possibly damaging	Het
Cntnap2	A	T	6: 47,072,483 (GRCm39)	Y1017F	possibly damaging	Het
Creb3l2	A	T	6: 37,311,416 (GRCm39)	S458T	probably benign	Het
Ctnnd2	C	A	15: 31,009,230 (GRCm39)	T1109K	possibly damaging	Het
Dcaf10	T	A	4: 45,373,011 (GRCm39)	L425Q	probably damaging	Het
Dlec1	A	G	9: 118,941,167 (GRCm39)	E239G	probably benign	Het
Dnah2	T	C	11: 69,390,020 (GRCm39)	K742E	probably damaging	Het
Dsp	A	T	13: 38,371,717 (GRCm39)	R889S	probably damaging	Het
Dync1h1	T	A	12: 110,599,222 (GRCm39)	M1859K	probably damaging	Het
Efcab7	T	A	4: 99,758,886 (GRCm39)	N361K	probably damaging	Het
Eps8l2	T	C	7: 140,935,646 (GRCm39)	V139A	probably damaging	Het
Fads3	T	G	19: 10,019,200 (GRCm39)	H35Q	probably damaging	Het
Fam163b	C	A	2: 27,003,583 (GRCm39)	V24F	probably damaging	Het
Gm14496	A	T	2: 181,636,904 (GRCm39)	T121S	probably benign	Het
Gm4799	C	T	10: 82,790,563 (GRCm39)		noncoding transcript	Het
Gm7168	A	T	17: 14,169,797 (GRCm39)	D388V	probably benign	Het
Gmeb1	A	T	4: 131,953,386 (GRCm39)	L460*	probably null	Het
Gpc6	T	G	14: 118,212,430 (GRCm39)	F534V	probably null	Het
Hectd3	A	G	4: 116,853,241 (GRCm39)	D156G	possibly damaging	Het
Itga6	T	C	2: 71,650,404 (GRCm39)	I150T	possibly damaging	Het
Kansl1	A	G	11: 104,229,012 (GRCm39)	M863T	probably benign	Het
Kcnb2	A	T	1: 15,780,664 (GRCm39)	Y512F	probably benign	Het
Klhdc2	A	T	12: 69,347,053 (GRCm39)	M73L	probably benign	Het
Ktn1	A	G	14: 47,932,073 (GRCm39)	T667A	probably benign	Het
Lgsn	A	C	1: 31,242,736 (GRCm39)	I273L	probably benign	Het
Lilra5	A	G	7: 4,245,232 (GRCm39)	D292G	probably benign	Het
Mrps27	C	T	13: 99,541,582 (GRCm39)	R229C	probably damaging	Het
Muc5b	T	G	7: 141,416,173 (GRCm39)	S3040A	probably benign	Het
Nat14	T	C	7: 4,926,275 (GRCm39)	S7P	probably damaging	Het
Nfia	A	G	4: 97,671,694 (GRCm39)	I135V	possibly damaging	Het
Nkd1	G	A	8: 89,248,944 (GRCm39)	A30T	probably damaging	Het
Nup205	A	G	6: 35,202,903 (GRCm39)	D1370G	probably null	Het
Or1j15	C	G	2: 36,459,568 (GRCm39)		probably null	Het
Or4k15c	G	A	14: 50,321,310 (GRCm39)	T276I	probably damaging	Het
Or51k2	T	C	7: 103,596,400 (GRCm39)	L209P	probably damaging	Het
Or5p79	T	A	7: 108,221,494 (GRCm39)	N158K	possibly damaging	Het
Or8s10	T	C	15: 98,336,168 (GRCm39)	S273P	possibly damaging	Het
Orc1	C	T	4: 108,459,229 (GRCm39)	A466V	probably benign	Het
Otud7a	T	A	7: 63,385,638 (GRCm39)	D367E	possibly damaging	Het
Pcdhb4	A	G	18: 37,441,263 (GRCm39)	Y191C	probably damaging	Het
Pclo	T	C	5: 14,762,828 (GRCm39)	V3767A	unknown	Het
Pclo	T	C	5: 14,728,789 (GRCm39)		probably benign	Het
Prmt1	A	T	7: 44,628,225 (GRCm39)		probably null	Het
Ralgapa1	A	G	12: 55,842,483 (GRCm39)	F62S	probably damaging	Het
Rangrf	T	C	11: 68,863,518 (GRCm39)	S163G	probably benign	Het
Rgs12	C	A	5: 35,176,804 (GRCm39)	A65E	probably damaging	Het
Rrbp1	T	C	2: 143,830,436 (GRCm39)	N577S	probably damaging	Het
Septin11	A	G	5: 93,315,393 (GRCm39)	H374R	probably damaging	Het
Serpina5	T	G	12: 104,070,046 (GRCm39)	N314K	probably benign	Het
Sgce	T	C	6: 4,689,621 (GRCm39)	D395G	probably damaging	Het
Slc26a9	A	T	1: 131,690,499 (GRCm39)	N501I	probably damaging	Het
Slc9c1	A	G	16: 45,401,965 (GRCm39)	D784G	possibly damaging	Het
Snapc2	A	G	8: 4,305,676 (GRCm39)	D207G	probably benign	Het
Stard9	G	T	2: 120,529,738 (GRCm39)	M1998I	probably benign	Het
Tas2r126	A	G	6: 42,412,025 (GRCm39)	K186R	probably damaging	Het
Tdp1	A	C	12: 99,875,970 (GRCm39)	D307A	probably benign	Het
Tead2	A	G	7: 44,866,674 (GRCm39)	D11G	probably damaging	Het
Tmco4	C	A	4: 138,747,383 (GRCm39)	L211I	probably damaging	Het
Tmem183a	A	G	1: 134,280,115 (GRCm39)	F255S	probably damaging	Het
Tmem87a	C	T	2: 120,205,929 (GRCm39)	G349S	possibly damaging	Het
Tpte	G	A	8: 22,826,549 (GRCm39)	E377K	possibly damaging	Het
Trim32	T	C	4: 65,531,893 (GRCm39)	F150S	possibly damaging	Het
Trpc7	T	A	13: 57,035,636 (GRCm39)	K99M	probably damaging	Het
Ttc22	A	G	4: 106,491,381 (GRCm39)	K195E	probably damaging	Het
Txn2	G	A	15: 77,811,917 (GRCm39)	P7S	probably damaging	Het
Ubxn2a	G	A	12: 4,930,700 (GRCm39)	T220I	probably damaging	Het
Ufd1	A	G	16: 18,633,626 (GRCm39)	N17S	possibly damaging	Het
Unc13a	A	G	8: 72,102,509 (GRCm39)	S958P	probably damaging	Het
Vmn1r202	T	A	13: 22,685,824 (GRCm39)	M198L	probably damaging	Het
Vmn2r84	G	A	10: 130,221,991 (GRCm39)	A743V	probably damaging	Het
Washc5	A	G	15: 59,213,007 (GRCm39)	F891S	probably damaging	Het
Zfp708	T	C	13: 67,218,375 (GRCm39)	T495A	probably benign	Het
Zfp81	A	G	17: 33,553,593 (GRCm39)	I407T	probably benign	Het
Zswim5	T	C	4: 116,843,874 (GRCm39)		probably null	Het

Other mutations in Stk38

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02364:Stk38	APN	17	29,210,390 (GRCm39)	missense	probably benign
IGL03279:Stk38	APN	17	29,203,179 (GRCm39)	splice site	probably benign
R0029:Stk38	UTSW	17	29,201,112 (GRCm39)	missense	probably benign	0.00
R0276:Stk38	UTSW	17	29,211,390 (GRCm39)	critical splice donor site	probably null
R1554:Stk38	UTSW	17	29,198,206 (GRCm39)	missense	possibly damaging	0.87
R4583:Stk38	UTSW	17	29,201,130 (GRCm39)	missense	probably damaging	1.00
R5191:Stk38	UTSW	17	29,193,344 (GRCm39)	missense	probably benign	0.19
R5686:Stk38	UTSW	17	29,201,103 (GRCm39)	missense	probably damaging	1.00
R6366:Stk38	UTSW	17	29,193,338 (GRCm39)	missense	probably benign	0.01
R6468:Stk38	UTSW	17	29,203,086 (GRCm39)	missense	probably benign	0.35
R6830:Stk38	UTSW	17	29,218,981 (GRCm39)	critical splice donor site	probably null
R7237:Stk38	UTSW	17	29,193,620 (GRCm39)	missense	possibly damaging	0.49
R8000:Stk38	UTSW	17	29,211,422 (GRCm39)	missense	probably benign
R8263:Stk38	UTSW	17	29,203,161 (GRCm39)	missense	probably damaging	1.00
R8551:Stk38	UTSW	17	29,207,199 (GRCm39)	missense	probably damaging	1.00
R8805:Stk38	UTSW	17	29,219,094 (GRCm39)	missense	probably benign	0.00
R9529:Stk38	UTSW	17	29,207,210 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGTTCACCTCCAAGCAATTCCCTG -3'
(R):5'- AGGTGTAGAGCCTGCTTCCTAACG -3'

Sequencing Primer
(F):5'- GCAATTCCCTGTAACAGCAATG -3'
(R):5'- AACGGGTGCTTAGTCACTTAC -3'

Posted On

2013-07-11