Mutagenetix > Incidental Mutation

Incidental Mutation 'R4599:Prmt7'

345442

Institutional Source

Beutler Lab

Gene Symbol

Prmt7

Ensembl Gene

ENSMUSG00000060098

Gene Name

protein arginine N-methyltransferase 7

Synonyms

MMRRC Submission

041815-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.914) question?

Stock #

R4599 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

106210936-106252794 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 106250329 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Glycine at position 558 (S558G)

Ref Sequence

ENSEMBL: ENSMUSP00000071521 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000067512] [ENSMUST00000071592] [ENSMUST00000212896]

AlphaFold

Q922X9

PDB Structure

Crystal structure of mouse protein arginine methyltransferase 7 in complex with SAH [X-RAY DIFFRACTION]

Predicted Effect

probably benign
Transcript: ENSMUST00000067512

SMART Domains

Protein: ENSMUSP00000069255
Gene: ENSMUSG00000031906

Domain	Start	End	E-Value	Type
transmembrane domain	15	37	N/A	INTRINSIC
transmembrane domain	57	79	N/A	INTRINSIC
low complexity region	178	189	N/A	INTRINSIC
Pfam:Exo_endo_phos	321	639	1.2e-15	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000071592
AA Change: S558G

PolyPhen 2 Score 0.801 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000071521
Gene: ENSMUSG00000060098
AA Change: S558G

Domain	Start	End	E-Value	Type
Pfam:PrmA	53	148	1.6e-7	PFAM
internal_repeat_1	382	652	1.71e-8	PROSPERO

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000180410

Predicted Effect

probably benign
Transcript: ENSMUST00000212896

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Arginine methylation is an apparently irreversible protein modification catalyzed by arginine methyltransferases, such as PMT7, using S-adenosylmethionine (AdoMet) as the methyl donor. Arginine methylation is implicated in signal transduction, RNA transport, and RNA splicing (Miranda et al., 2004 [PubMed 15044439]).[supplied by OMIM, Mar 2008]

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca14	T	C	7: 120,255,403	V930A	probably benign	Het
Ankrd13b	T	C	11: 77,471,668	R677G	probably benign	Het
Apc	T	A	18: 34,317,987	Y2611*	probably null	Het
Apold1	A	G	6: 134,984,069	Y162C	probably damaging	Het
Atp6v0a4	T	C	6: 38,078,802	I325V	probably benign	Het
Cab39	A	G	1: 85,848,329	Y249C	probably damaging	Het
Cd22	T	A	7: 30,875,900	H239L	probably damaging	Het
Chrna7	A	G	7: 63,103,790	M327T	probably damaging	Het
Clock	T	C	5: 76,235,810	M499V	probably benign	Het
Clspn	A	G	4: 126,581,460	E1002G	probably benign	Het
Clta	C	T	4: 44,012,819	P10S	probably damaging	Het
Col5a3	A	G	9: 20,774,559		probably null	Het
Coq6	T	C	12: 84,362,139	V30A	probably benign	Het
Csmd2	G	T	4: 127,988,128	R20L	probably benign	Het
D430041D05Rik	A	T	2: 104,208,183	V1547D	probably damaging	Het
Dapk1	C	T	13: 60,718,047	P153S	probably benign	Het
Dock2	T	A	11: 34,239,536	Y1545F	probably damaging	Het
Dpp6	G	T	5: 27,634,548	G354C	probably damaging	Het
Dyrk1b	T	C	7: 28,182,431	L105P	probably damaging	Het
Epor	A	G	9: 21,961,859	S86P	probably benign	Het
Fam166b	T	C	4: 43,427,574	H250R	possibly damaging	Het
Gale	C	A	4: 135,967,837	S341*	probably null	Het
Galnt4	T	A	10: 99,109,493	V360E	probably damaging	Het
Gart	A	T	16: 91,622,945	C24*	probably null	Het
Gcnt2	G	T	13: 40,887,490	V42L	probably benign	Het
Herc6	A	G	6: 57,659,713	I805V	probably benign	Het
Ints12	T	A	3: 133,098,453	I67N	probably benign	Het
Irx1	C	A	13: 71,960,113	R150L	probably damaging	Het
Kif26b	A	G	1: 178,530,459	Y45C	unknown	Het
Krt35	T	C	11: 100,094,008	T275A	probably damaging	Het
Laptm5	G	T	4: 130,916,005		probably benign	Het
Lin7a	T	C	10: 107,412,166	S111P	unknown	Het
Med27	A	G	2: 29,524,458	D159G	probably damaging	Het
Msh2	A	G	17: 87,708,578	K546R	probably damaging	Het
Myo1a	A	T	10: 127,720,151		probably null	Het
Myo1c	T	C	11: 75,668,193	F604L	probably damaging	Het
Myrip	A	G	9: 120,464,784	K782E	probably damaging	Het
Ndc80	T	C	17: 71,521,068	D88G	probably damaging	Het
Nrxn2	A	G	19: 6,455,252	D375G	probably damaging	Het
Olfr1380	T	C	11: 49,564,718	S266P	probably damaging	Het
Olfr676	A	G	7: 105,036,073	I292V	probably benign	Het
Padi3	T	C	4: 140,798,111	H187R	probably damaging	Het
Pcdhgb1	A	T	18: 37,681,557	N367I	probably damaging	Het
Pdrg1	T	C	2: 153,012,390	I77V	probably benign	Het
Pfas	T	C	11: 68,991,069	E930G	probably benign	Het
Pik3cb	C	T	9: 99,061,764	R662Q	probably benign	Het
Pla2g4e	T	G	2: 120,186,382	H226P	possibly damaging	Het
Plxnd1	A	T	6: 115,994,276	V177E	probably damaging	Het
Pspc1	A	C	14: 56,777,789		probably null	Het
Rilp	T	C	11: 75,512,760	S343P	probably benign	Het
Ror1	A	G	4: 100,407,910	M194V	probably damaging	Het
Rsu1	T	C	2: 13,170,004	Y225C	probably damaging	Het
Rundc1	A	G	11: 101,433,926	N486S	probably damaging	Het
Sema6d	T	A	2: 124,654,231	I65N	probably damaging	Het
Slc5a11	A	G	7: 123,258,378	E230G	probably benign	Het
Spint1	T	C	2: 119,246,460	S342P	probably damaging	Het
Stard3nl	A	G	13: 19,367,753	S214P	probably damaging	Het
Tcp10a	A	C	17: 7,336,924	T271P	probably damaging	Het
Tie1	A	G	4: 118,472,634	Y1091H	probably benign	Het
Tlr12	T	C	4: 128,617,332	Y375C	probably benign	Het
Tmem107	T	A	11: 69,071,448	M77K	probably damaging	Het
Tns2	C	T	15: 102,108,934	R281C	probably damaging	Het
Tns3	T	C	11: 8,531,747	K202E	probably damaging	Het
Tspoap1	C	T	11: 87,779,521	P1634L	probably damaging	Het
Ttc7b	G	A	12: 100,500,117	R79C	probably damaging	Het
Ush2a	A	G	1: 188,911,647	N4402S	probably benign	Het
Vmn2r13	A	T	5: 109,156,456	I703N	probably damaging	Het
Xrcc4	A	G	13: 90,062,007		probably null	Het
Zp3	A	T	5: 135,984,235	K168*	probably null	Het

Other mutations in Prmt7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01080:Prmt7	APN	8	106237214	splice site	probably benign
IGL01565:Prmt7	APN	8	106250409	missense	probably damaging	0.97
IGL02245:Prmt7	APN	8	106237305	missense	probably benign	0.10
R0104:Prmt7	UTSW	8	106237350	missense	probably damaging	0.99
R0255:Prmt7	UTSW	8	106227207	splice site	probably benign
R1432:Prmt7	UTSW	8	106237284	nonsense	probably null
R1551:Prmt7	UTSW	8	106237382	missense	probably benign
R1848:Prmt7	UTSW	8	106237008	missense	probably benign
R2117:Prmt7	UTSW	8	106227298	missense	probably damaging	0.96
R3784:Prmt7	UTSW	8	106242136	missense	probably benign	0.01
R4940:Prmt7	UTSW	8	106237278	missense	probably benign	0.01
R4983:Prmt7	UTSW	8	106250363	missense	probably damaging	1.00
R5285:Prmt7	UTSW	8	106248359	missense	probably benign	0.15
R6015:Prmt7	UTSW	8	106235008	intron	probably benign
R6520:Prmt7	UTSW	8	106234884	missense	probably damaging	1.00
R7097:Prmt7	UTSW	8	106235100	missense	unknown
R7122:Prmt7	UTSW	8	106235100	missense	unknown
R7233:Prmt7	UTSW	8	106220010	missense	probably damaging	0.99
R7538:Prmt7	UTSW	8	106237386	missense	probably benign	0.02
R7577:Prmt7	UTSW	8	106242203	missense	probably damaging	1.00
R7659:Prmt7	UTSW	8	106237286	missense	probably benign	0.00
R7858:Prmt7	UTSW	8	106244688	missense	possibly damaging	0.47
R8991:Prmt7	UTSW	8	106217242	critical splice acceptor site	probably null
R9041:Prmt7	UTSW	8	106236828	missense	possibly damaging	0.87
R9188:Prmt7	UTSW	8	106234854	missense	probably damaging	1.00
R9338:Prmt7	UTSW	8	106235033	missense	unknown
R9406:Prmt7	UTSW	8	106243803	missense	probably damaging	1.00
R9517:Prmt7	UTSW	8	106227298	missense	probably damaging	0.96

Predicted Primers

PCR Primer
(F):5'- GAGAAATTGGCTCTTGTGACCAG -3'
(R):5'- AGAGTCTCCAGGCTGTTTGTC -3'

Sequencing Primer
(F):5'- TCTTGTGACCAGGAGCCCAG -3'
(R):5'- AGGCTGTTTGTCCTTCACAATTG -3'

Posted On

2015-09-25