Mutagenetix > Incidental Mutation

Incidental Mutation 'R0015:Polr2g'

8248

Institutional Source

Beutler Lab

Gene Symbol

Polr2g

Ensembl Gene

ENSMUSG00000071662

Gene Name

polymerase (RNA) II (DNA directed) polypeptide G

Synonyms

Rpo2-7l, A230108L04Rik, RBP7, 2410046K11Rik

MMRRC Submission

038310-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.963) question?

Stock #

R0015 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

8770493-8775921 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 8771016 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 160 (I160T)

Ref Sequence

ENSEMBL: ENSMUSP00000093980 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096261]

AlphaFold

P62488

Predicted Effect

probably damaging
Transcript: ENSMUST00000096261
AA Change: I160T

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000093980
Gene: ENSMUSG00000071662
AA Change: I160T

Domain	Start	End	E-Value	Type
Pfam:SHS2_Rpb7-N	8	77	1e-18	PFAM
S1	80	162	1.75e-4	SMART

Meta Mutation Damage Score

0.4096

Coding Region Coverage

1x: 80.5%
3x: 72.2%
10x: 49.0%
20x: 28.4%

Validation Efficiency

90% (88/98)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the seventh largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The protein functions in transcription initiation, and is also thought to help stabilize transcribing polyermase molecules during elongation. [provided by RefSeq, Jan 2009]

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A130050O07Rik	A	G	1: 137,856,394 (GRCm39)	Y23C	unknown	Het
Aadat	C	T	8: 60,987,605 (GRCm39)		probably benign	Het
Adcy3	G	A	12: 4,245,260 (GRCm39)		probably null	Het
Armc3	A	G	2: 19,301,132 (GRCm39)		probably null	Het
Astn2	T	G	4: 66,184,619 (GRCm39)		probably null	Het
Borcs8	T	C	8: 70,593,017 (GRCm39)		probably benign	Het
Cacna1d	G	A	14: 29,836,928 (GRCm39)	T804I	probably benign	Het
Card19	A	G	13: 49,361,532 (GRCm39)	L33P	probably benign	Het
Ccny	A	C	18: 9,316,682 (GRCm39)		probably benign	Het
Cdh5	C	T	8: 104,867,559 (GRCm39)	T612I	probably benign	Het
Cfap58	A	G	19: 48,017,539 (GRCm39)	M800V	probably benign	Het
Clrn1	A	T	3: 58,753,848 (GRCm39)	I171K	probably damaging	Het
Cnp	T	A	11: 100,469,734 (GRCm39)		probably null	Het
Col12a1	T	C	9: 79,558,667 (GRCm39)	T1933A	probably damaging	Het
Cplane1	G	A	15: 8,215,668 (GRCm39)	R408H	probably damaging	Het
Cwf19l2	A	G	9: 3,454,666 (GRCm39)	S660G	probably benign	Het
Dync1i2	C	A	2: 71,044,828 (GRCm39)	R13S	probably damaging	Het
Fat4	T	A	3: 39,036,652 (GRCm39)	S3435T	probably damaging	Het
Fchsd1	A	G	18: 38,096,012 (GRCm39)	C533R	probably benign	Het
Fstl5	G	A	3: 76,229,498 (GRCm39)	V100M	probably damaging	Het
Gria2	C	T	3: 80,615,074 (GRCm39)	G469S	probably damaging	Het
Hsf5	C	A	11: 87,548,161 (GRCm39)	H615N	probably benign	Het
Ints2	T	C	11: 86,140,113 (GRCm39)	T240A	probably damaging	Het
Kcnn3	A	C	3: 89,570,080 (GRCm39)	D631A	probably damaging	Het
Lama4	C	T	10: 38,951,432 (GRCm39)	T1059M	possibly damaging	Het
Lgals8	A	G	13: 12,462,179 (GRCm39)	L226P	probably damaging	Het
Lonp1	T	A	17: 56,925,406 (GRCm39)	Q462L	probably benign	Het
Mark2	A	T	19: 7,263,142 (GRCm39)	Y231*	probably null	Het
Mdh1b	T	C	1: 63,760,959 (GRCm39)		probably benign	Het
Myh7b	C	T	2: 155,464,206 (GRCm39)	P569L	probably damaging	Het
Myl3	A	C	9: 110,596,997 (GRCm39)	D119A	probably damaging	Het
Ncapd3	C	A	9: 26,963,105 (GRCm39)	A470E	probably damaging	Het
Ndrg2	A	G	14: 52,147,902 (GRCm39)		probably benign	Het
Nprl2	A	T	9: 107,421,618 (GRCm39)	I209F	probably damaging	Het
Pcf11	T	A	7: 92,307,525 (GRCm39)	H881L	probably benign	Het
Pde10a	A	G	17: 9,196,029 (GRCm39)	D640G	probably damaging	Het
Pdxdc1	A	T	16: 13,705,547 (GRCm39)		probably benign	Het
Pter	G	A	2: 13,005,811 (GRCm39)	G328D	probably damaging	Het
Rad51	T	A	2: 118,946,808 (GRCm39)	M5K	probably benign	Het
Rbm43	T	A	2: 51,815,679 (GRCm39)	I181F	probably benign	Het
Rgs12	T	C	5: 35,180,120 (GRCm39)		probably benign	Het
Slc20a2	C	A	8: 23,025,361 (GRCm39)	A21E	probably damaging	Het
Sybu	T	C	15: 44,536,896 (GRCm39)	R349G	probably damaging	Het
Tmem161b	C	A	13: 84,370,533 (GRCm39)		probably null	Het
Xirp2	C	A	2: 67,341,243 (GRCm39)	Y1161*	probably null	Het
Zfand4	C	A	6: 116,305,258 (GRCm39)	T705K	probably damaging	Het

Other mutations in Polr2g

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01994:Polr2g	APN	19	8,771,740 (GRCm39)	splice site	probably benign
IGL02474:Polr2g	APN	19	8,775,820 (GRCm39)	splice site	probably null
IGL03346:Polr2g	APN	19	8,775,669 (GRCm39)	missense	probably damaging	1.00
R0014:Polr2g	UTSW	19	8,771,016 (GRCm39)	missense	probably damaging	0.99
R0015:Polr2g	UTSW	19	8,771,016 (GRCm39)	missense	probably damaging	0.99
R5372:Polr2g	UTSW	19	8,774,667 (GRCm39)	missense	probably damaging	1.00
R6073:Polr2g	UTSW	19	8,774,673 (GRCm39)	missense	probably damaging	0.99
R6177:Polr2g	UTSW	19	8,771,541 (GRCm39)	missense	probably damaging	1.00
R8213:Polr2g	UTSW	19	8,775,621 (GRCm39)	missense	probably damaging	1.00
R8963:Polr2g	UTSW	19	8,771,513 (GRCm39)	missense	probably damaging	1.00
R9325:Polr2g	UTSW	19	8,774,669 (GRCm39)	missense	probably benign	0.04
R9643:Polr2g	UTSW	19	8,774,631 (GRCm39)	missense	probably damaging	1.00

Posted On

2012-11-21