Mutagenetix > Incidental Mutation

Incidental Mutation 'R8269:Mapk4'

639522

Institutional Source

Beutler Lab

Gene Symbol

Mapk4

Ensembl Gene

ENSMUSG00000024558

Gene Name

mitogen-activated protein kinase 4

Synonyms

p63Mapk, A330097D03Rik, Erk3-related

MMRRC Submission

067693-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8269 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

74061557-74198430 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to C at 74063622 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 533 (F533L)

Ref Sequence

ENSEMBL: ENSMUSP00000089462 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000091851] [ENSMUST00000159162] [ENSMUST00000162863]

AlphaFold

Q6P5G0

Predicted Effect

probably damaging
Transcript: ENSMUST00000091851
AA Change: F533L

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000089462
Gene: ENSMUSG00000024558
AA Change: F533L

Domain	Start	End	E-Value	Type
S_TKc	20	312	3.81e-79	SMART
low complexity region	462	478	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000159162

SMART Domains

Protein: ENSMUSP00000123922
Gene: ENSMUSG00000024558

Domain	Start	End	E-Value	Type
Pfam:Pkinase	20	232	2.3e-58	PFAM
Pfam:Pkinase_Tyr	22	232	5.5e-30	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000162863

SMART Domains

Protein: ENSMUSP00000124408
Gene: ENSMUSG00000024558

Domain	Start	End	E-Value	Type
Pfam:Pkinase	20	192	1.7e-41	PFAM
Pfam:Pkinase_Tyr	22	189	5.9e-25	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

100% (51/51)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Mitogen-activated protein kinase 4 is a member of the mitogen-activated protein kinase family. Tyrosine kinase growth factor receptors activate mitogen-activated protein kinases which then translocate into the nucleus and phosphorylate nuclear targets. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
PHENOTYPE: Mice homozygous for a knock-out allele are viabel and fertile. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acox2	T	C	14: 8,246,325 (GRCm38)	T489A	probably benign	Het
Adgra3	A	T	5: 50,121,079 (GRCm39)	C850S	probably damaging	Het
Ago3	T	A	4: 126,270,721 (GRCm39)	K258*	probably null	Het
Akap11	G	A	14: 78,750,818 (GRCm39)	T523I		Het
Amigo2	G	T	15: 97,144,112 (GRCm39)	N103K	possibly damaging	Het
Arfgap3	A	C	15: 83,194,542 (GRCm39)	S377A	probably benign	Het
Arhgap39	G	T	15: 76,635,942 (GRCm39)	Q98K	probably benign	Het
Atp1a4	T	C	1: 172,059,892 (GRCm39)	D779G	probably damaging	Het
Bckdhb	T	C	9: 84,004,417 (GRCm39)	I388T	probably benign	Het
Ccpg1	G	A	9: 72,913,001 (GRCm39)	R179H	probably damaging	Het
Cd109	A	G	9: 78,572,964 (GRCm39)	K496R	probably benign	Het
Cnot1	A	G	8: 96,478,389 (GRCm39)	F979L	probably damaging	Het
Cyb5r1	T	A	1: 134,334,803 (GRCm39)		probably benign	Het
D130040H23Rik	T	A	8: 69,755,800 (GRCm39)	S402T	probably benign	Het
Dmtf1	A	T	5: 9,182,500 (GRCm39)	Y211*	probably null	Het
Dnah6	A	G	6: 73,145,810 (GRCm39)		probably null	Het
Emc10	G	T	7: 44,141,408 (GRCm39)	Q227K	possibly damaging	Het
Epha8	G	T	4: 136,665,897 (GRCm39)	L420M	probably damaging	Het
Exosc4	A	T	15: 76,211,732 (GRCm39)	I14L	probably benign	Het
Fat2	T	C	11: 55,173,535 (GRCm39)	T2393A	possibly damaging	Het
Flg2	A	T	3: 93,109,187 (GRCm39)	H405L	possibly damaging	Het
Gin1	T	A	1: 97,710,929 (GRCm39)	M204K	probably damaging	Het
Gm57858	A	T	3: 36,100,862 (GRCm39)	N103K	possibly damaging	Het
Gnal	A	G	18: 67,268,693 (GRCm39)	D193G	possibly damaging	Het
Itpr3	G	T	17: 27,312,258 (GRCm39)	R554L	possibly damaging	Het
Lipc	A	G	9: 70,727,655 (GRCm39)	L149P	probably damaging	Het
Lrrc37a	A	G	11: 103,388,724 (GRCm39)	Y2234H	unknown	Het
Lsm14b	T	C	2: 179,674,407 (GRCm39)	S317P	probably damaging	Het
Mgll	T	A	6: 88,790,930 (GRCm39)	Y183*	probably null	Het
Mrrf	T	A	2: 36,037,973 (GRCm39)	D81E	possibly damaging	Het
Ncan	T	A	8: 70,560,330 (GRCm39)	Q879L	probably benign	Het
Nox4	T	G	7: 86,955,930 (GRCm39)		probably benign	Het
Or4p18	A	T	2: 88,232,381 (GRCm39)	V299D	probably damaging	Het
Or5p67	A	T	7: 107,922,776 (GRCm39)	C36S	probably benign	Het
Pcdhb10	A	G	18: 37,547,062 (GRCm39)	K713E	probably benign	Het
Phkb	A	G	8: 86,756,211 (GRCm39)	D835G	probably benign	Het
Pld1	A	G	3: 28,079,388 (GRCm39)	N63D	probably benign	Het
Pls1	G	T	9: 95,644,023 (GRCm39)	T491K	probably damaging	Het
Plscr1	A	G	9: 92,145,095 (GRCm39)	D35G	unknown	Het
Slc28a2b	C	T	2: 122,352,169 (GRCm39)	H336Y	probably damaging	Het
Slc3a1	A	G	17: 85,339,982 (GRCm39)	K180R	probably benign	Het
Suv39h1	G	T	X: 7,937,270 (GRCm39)	Q129K	probably benign	Het
Tbc1d8	A	G	1: 39,465,169 (GRCm39)	V73A	probably benign	Het
Tmem161a	T	A	8: 70,634,608 (GRCm39)	V421E	probably benign	Het
Topbp1	C	A	9: 103,205,792 (GRCm39)	P810Q	possibly damaging	Het
Ttc28	G	A	5: 111,425,325 (GRCm39)	V1717M	probably benign	Het
Vmn2r55	T	A	7: 12,404,585 (GRCm39)	T273S	possibly damaging	Het
Vwa5b2	A	G	16: 20,423,188 (GRCm39)	D1062G	probably damaging	Het
Zcrb1	A	G	15: 93,295,056 (GRCm39)	Y27H	probably benign	Het
Zfp128	G	A	7: 12,624,663 (GRCm39)	G344R	probably damaging	Het

Other mutations in Mapk4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02396:Mapk4	APN	18	74,067,068 (GRCm39)	splice site	probably null
IGL02621:Mapk4	APN	18	74,103,346 (GRCm39)	missense	probably damaging	1.00
IGL03068:Mapk4	APN	18	74,103,415 (GRCm39)	missense	probably damaging	1.00
R0041:Mapk4	UTSW	18	74,068,109 (GRCm39)	missense	probably damaging	1.00
R0519:Mapk4	UTSW	18	74,103,392 (GRCm39)	missense	probably damaging	1.00
R0636:Mapk4	UTSW	18	74,063,525 (GRCm39)	missense	probably benign
R0918:Mapk4	UTSW	18	74,103,408 (GRCm39)	missense	probably damaging	1.00
R1654:Mapk4	UTSW	18	74,064,010 (GRCm39)	missense	probably damaging	1.00
R2913:Mapk4	UTSW	18	74,068,236 (GRCm39)	missense	probably benign	0.34
R2914:Mapk4	UTSW	18	74,068,236 (GRCm39)	missense	probably benign	0.34
R4089:Mapk4	UTSW	18	74,063,530 (GRCm39)	missense	probably damaging	1.00
R4414:Mapk4	UTSW	18	74,063,609 (GRCm39)	missense	possibly damaging	0.76
R4487:Mapk4	UTSW	18	74,064,046 (GRCm39)	missense	probably damaging	1.00
R4792:Mapk4	UTSW	18	74,070,321 (GRCm39)	missense	probably damaging	0.98
R5445:Mapk4	UTSW	18	74,064,073 (GRCm39)	missense	probably benign	0.00
R5597:Mapk4	UTSW	18	74,070,341 (GRCm39)	missense	probably benign	0.12
R5654:Mapk4	UTSW	18	74,103,365 (GRCm39)	missense	probably damaging	1.00
R6700:Mapk4	UTSW	18	74,063,882 (GRCm39)	missense	probably damaging	1.00
R6793:Mapk4	UTSW	18	74,063,539 (GRCm39)	missense	probably damaging	1.00
R7200:Mapk4	UTSW	18	74,063,990 (GRCm39)	missense	possibly damaging	0.92
R7335:Mapk4	UTSW	18	74,070,338 (GRCm39)	missense	possibly damaging	0.75
R8010:Mapk4	UTSW	18	74,063,647 (GRCm39)	missense	probably benign	0.04
R8736:Mapk4	UTSW	18	74,103,396 (GRCm39)	missense	probably benign	0.01
Z1176:Mapk4	UTSW	18	74,070,255 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTTCTGCTAACCCCAACG -3'
(R):5'- TGTGTCACGTGAGGATGAGC -3'

Sequencing Primer
(F):5'- CAGCTTTCTGGATGGGGATCC -3'
(R):5'- GATGAGCCAGCAAGCCTCTTTC -3'

Posted On

2020-07-28