Mutagenetix > Incidental Mutation

Incidental Mutation 'R9659:Polr2a'

727462

Institutional Source

Beutler Lab

Gene Symbol

Polr2a

Ensembl Gene

ENSMUSG00000005198

Gene Name

polymerase (RNA) II (DNA directed) polypeptide A

Synonyms

Rpo2-1, 220kDa

MMRRC Submission

Accession Numbers

Essential gene?

Probably essential (E-score: 0.968) question?

Stock #

R9659 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

69624823-69649459 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 69625654 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 1832 (Y1832C)

Ref Sequence

ENSEMBL: ENSMUSP00000050771 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000058470] [ENSMUST00000071213]

AlphaFold

P08775

Predicted Effect

unknown
Transcript: ENSMUST00000058470
AA Change: Y1832C

SMART Domains

Protein: ENSMUSP00000050771
Gene: ENSMUSG00000005198
AA Change: Y1832C

Domain	Start	End	E-Value	Type
Blast:RPOLA_N	110	179	5e-37	BLAST
RPOLA_N	246	549	7.02e-203	SMART
Pfam:RNA_pol_Rpb1_4	716	823	3.6e-39	PFAM
Pfam:RNA_pol_Rpb1_5	830	1428	2e-101	PFAM
Pfam:RNA_pol_Rpb1_6	896	1079	1.7e-70	PFAM
Pfam:RNA_pol_Rpb1_7	1164	1299	1.7e-57	PFAM
Pfam:RNA_pol_Rpb1_R	1555	1568	2.1e-3	PFAM
Pfam:RNA_pol_Rpb1_R	1616	1629	8.8e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1630	1643	1.9e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1644	1657	2.3e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1658	1671	2.2e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1672	1685	2.4e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1686	1699	2.5e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1700	1713	2.5e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1714	1727	2.5e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1728	1741	2.6e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1742	1755	5.3e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1757	1769	5.8e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1784	1797	2.6e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1798	1811	4.8e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1826	1839	4.3e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1841	1853	2e-3	PFAM
Pfam:RNA_pol_Rpb1_R	1854	1867	6.9e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1868	1881	3.7e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1882	1895	1.2e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1896	1909	5e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1910	1923	2.5e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1924	1936	2e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1931	1954	2.6e-3	PFAM
Pfam:RNA_pol_Rpb1_R	1948	1960	2.5e-3	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000071213
AA Change: Y1794C

SMART Domains

Protein: ENSMUSP00000071200
Gene: ENSMUSG00000005198
AA Change: Y1794C

Domain	Start	End	E-Value	Type
Blast:RPOLA_N	110	179	5e-37	BLAST
RPOLA_N	246	549	7.02e-203	SMART
Pfam:RNA_pol_Rpb1_4	716	823	1.8e-41	PFAM
Pfam:RNA_pol_Rpb1_5	830	1428	4.8e-104	PFAM
Pfam:RNA_pol_Rpb1_6	896	1079	5.2e-74	PFAM
Pfam:RNA_pol_Rpb1_7	1164	1299	1.4e-55	PFAM
low complexity region	1503	1522	N/A	INTRINSIC
low complexity region	1524	1549	N/A	INTRINSIC
Pfam:RNA_pol_Rpb1_R	1578	1591	2.7e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1592	1605	2.5e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1606	1619	2.7e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1620	1633	2.5e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1634	1647	2.5e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1648	1661	2.4e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1662	1675	2.4e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1676	1689	2.6e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1690	1703	2.3e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1704	1717	5.2e-7	PFAM
Pfam:RNA_pol_Rpb1_R	1718	1731	5.5e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1732	1745	1.6e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1746	1759	8.6e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1760	1773	2e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1788	1801	3.3e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1802	1815	2.4e-4	PFAM
Pfam:RNA_pol_Rpb1_R	1816	1829	8.3e-7	PFAM
Pfam:RNA_pol_Rpb1_R	1830	1843	2.2e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1844	1857	1.6e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1858	1871	2.8e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1872	1885	6e-7	PFAM
Pfam:RNA_pol_Rpb1_R	1886	1899	4.6e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1893	1909	4.8e-5	PFAM
Pfam:RNA_pol_Rpb1_R	1903	1916	2.8e-6	PFAM
Pfam:RNA_pol_Rpb1_R	1910	1923	1.6e-4	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.2%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The product of this gene contains a carboxy terminal domain composed of heptapeptide repeats that are essential for polymerase activity. These repeats contain serine and threonine residues that are phosphorylated in actively transcribing RNA polymerase. In addition, this subunit, in combination with several other polymerase subunits, forms the DNA binding domain of the polymerase, a groove in which the DNA template is transcribed into RNA. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a reporter allele show prenatal lethality. Homozygotes for a small deletion in the C-terminal domain are viable, fertile and developmentally normal. Homozygotes for a larger deletion show reduced fetal size and partial postnatal lethality; survivors are small but otherwise normal. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A330070K13Rik	T	C	5: 130,407,876 (GRCm39)	I112V	unknown	Het
Adcy7	A	G	8: 89,045,733 (GRCm39)	T572A	probably benign	Het
Atad5	G	T	11: 79,980,542 (GRCm39)		probably benign	Het
C2cd2	A	G	16: 97,723,473 (GRCm39)	S15P	possibly damaging	Het
Cabp1	T	C	5: 115,311,187 (GRCm39)	D289G	possibly damaging	Het
Ccdc14	A	G	16: 34,541,913 (GRCm39)	I545V	probably damaging	Het
Cep295	C	A	9: 15,233,846 (GRCm39)	A2317S	probably benign	Het
Cerkl	T	C	2: 79,223,322 (GRCm39)	D133G	possibly damaging	Het
Cited4	T	G	4: 120,524,543 (GRCm39)	C182G	probably damaging	Het
Col6a5	T	A	9: 105,811,034 (GRCm39)	K828N	unknown	Het
Ear2	A	G	14: 44,340,705 (GRCm39)	Y121C	probably damaging	Het
Ect2l	C	T	10: 18,041,347 (GRCm39)	C369Y	possibly damaging	Het
Elapor1	G	A	3: 108,377,297 (GRCm39)	T387I	possibly damaging	Het
Ep300	A	G	15: 81,505,273 (GRCm39)	Y631C	unknown	Het
Ephb4	T	G	5: 137,363,743 (GRCm39)	Y583D	probably damaging	Het
Fbn2	C	G	18: 58,342,654 (GRCm39)	R75P	probably damaging	Het
Gabra2	T	C	5: 71,192,140 (GRCm39)	D63G	probably benign	Het
Gfra1	A	G	19: 58,441,652 (GRCm39)	M93T	probably damaging	Het
Gm21886	AGAGGCCTGCAGACAGTAGGTGCTCACTAGGGCCTGCAGACAGCAGGTGCTCACTGAGGCCTG	AGAGGCCTG	18: 80,132,776 (GRCm39)		probably benign	Het
Gm3604	A	T	13: 62,519,724 (GRCm39)	H10Q	possibly damaging	Het
Helz2	T	C	2: 180,882,025 (GRCm39)	D256G	probably benign	Het
Herc1	A	C	9: 66,307,185 (GRCm39)	I1002L	probably benign	Het
Hpgd	C	G	8: 56,772,075 (GRCm39)	C182W	probably damaging	Het
Htr5b	A	G	1: 121,455,428 (GRCm39)	L164P	possibly damaging	Het
Kmo	T	C	1: 175,486,085 (GRCm39)	F403L	probably damaging	Het
Ly75	C	A	2: 60,168,665 (GRCm39)	D748Y	probably damaging	Het
Mcm5	C	T	8: 75,844,168 (GRCm39)	S313F	probably benign	Het
Mipep	A	G	14: 61,083,893 (GRCm39)	T595A	probably damaging	Het
Muc6	T	C	7: 141,232,100 (GRCm39)	D968G	probably damaging	Het
Myo18b	T	C	5: 113,022,382 (GRCm39)	T337A	unknown	Het
Nlrp1b	T	A	11: 71,073,132 (GRCm39)	Q237L	possibly damaging	Het
Nr1h4	A	G	10: 89,314,638 (GRCm39)		probably null	Het
Nxph1	A	G	6: 9,247,418 (GRCm39)	T130A	probably damaging	Het
Or10al6	T	G	17: 38,082,880 (GRCm39)	F112C	probably damaging	Het
Or1l4	T	A	2: 37,091,897 (GRCm39)	C215S	possibly damaging	Het
Or4m1	A	G	14: 50,558,181 (GRCm39)	F37S	probably benign	Het
Or5p4	T	C	7: 107,680,745 (GRCm39)	V248A	probably damaging	Het
Or8g21	A	G	9: 38,906,296 (GRCm39)	V145A	possibly damaging	Het
Pcsk5	A	G	19: 17,455,245 (GRCm39)	Y1062H	probably benign	Het
Plch1	T	C	3: 63,681,136 (GRCm39)	I164V	probably benign	Het
Plekhh2	T	A	17: 84,854,892 (GRCm39)	M42K	possibly damaging	Het
Prpf4	G	A	4: 62,334,296 (GRCm39)		probably null	Het
Psg16	T	C	7: 16,824,524 (GRCm39)	S12P	possibly damaging	Het
Ptpn14	T	A	1: 189,587,174 (GRCm39)	M528K	probably benign	Het
Rb1cc1	T	A	1: 6,318,673 (GRCm39)	H697Q	probably benign	Het
Reg3a	T	G	6: 78,360,574 (GRCm39)	C171G	possibly damaging	Het
Slc22a26	G	A	19: 7,763,798 (GRCm39)	P412S	probably benign	Het
Spata31e5	G	T	1: 28,816,536 (GRCm39)	H499N	probably benign	Het
Tcstv2a	T	A	13: 120,725,754 (GRCm39)	D139E	probably damaging	Het
Tlk2	T	C	11: 105,131,263 (GRCm39)	I203T	probably benign	Het
Tmem120b	T	G	5: 123,253,788 (GRCm39)	H279Q	probably damaging	Het
Trip4	T	C	9: 65,740,702 (GRCm39)	E535G	probably benign	Het
Ttn	C	T	2: 76,715,357 (GRCm39)	E7912K	unknown	Het
Ubr5	A	T	15: 37,984,254 (GRCm39)	L2298I		Het
Utp20	A	G	10: 88,653,171 (GRCm39)	L303P	probably damaging	Het
Vcan	A	G	13: 89,839,860 (GRCm39)	Y1895H	probably damaging	Het
Vmn2r2	T	C	3: 64,041,942 (GRCm39)	N258D	possibly damaging	Het
Wdr20rt	A	T	12: 65,273,343 (GRCm39)	S269C	probably damaging	Het
Zfand4	T	G	6: 116,282,588 (GRCm39)	Y54D	probably damaging	Het
Zfp82	C	T	7: 29,755,963 (GRCm39)	R373H	probably damaging	Het
Zmiz2	A	G	11: 6,346,814 (GRCm39)	E141G	probably benign	Het

Other mutations in Polr2a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00987:Polr2a	APN	11	69,634,620 (GRCm39)	splice site	probably benign
IGL01067:Polr2a	APN	11	69,638,840 (GRCm39)	missense	possibly damaging	0.94
IGL01547:Polr2a	APN	11	69,635,768 (GRCm39)	missense	probably damaging	0.99
IGL01589:Polr2a	APN	11	69,632,020 (GRCm39)	missense	probably benign
IGL01955:Polr2a	APN	11	69,632,674 (GRCm39)	missense	probably damaging	1.00
IGL02457:Polr2a	APN	11	69,634,076 (GRCm39)	splice site	probably benign
IGL02526:Polr2a	APN	11	69,630,293 (GRCm39)	missense	probably benign	0.03
IGL02792:Polr2a	APN	11	69,636,938 (GRCm39)	missense	probably damaging	0.99
IGL03058:Polr2a	APN	11	69,635,873 (GRCm39)	splice site	probably null
IGL03083:Polr2a	APN	11	69,635,872 (GRCm39)	critical splice acceptor site	probably null
IGL03198:Polr2a	APN	11	69,638,107 (GRCm39)	splice site	probably null
IGL03201:Polr2a	APN	11	69,636,516 (GRCm39)	nonsense	probably null
Leastest	UTSW	11	69,638,118 (GRCm39)	splice site	probably null
PIT4260001:Polr2a	UTSW	11	69,626,793 (GRCm39)	missense	possibly damaging	0.93
R0126:Polr2a	UTSW	11	69,638,251 (GRCm39)	missense	probably damaging	0.99
R0254:Polr2a	UTSW	11	69,634,497 (GRCm39)	missense	possibly damaging	0.75
R0313:Polr2a	UTSW	11	69,625,906 (GRCm39)	missense	unknown
R0336:Polr2a	UTSW	11	69,627,719 (GRCm39)	missense	possibly damaging	0.92
R0453:Polr2a	UTSW	11	69,631,845 (GRCm39)	missense	possibly damaging	0.65
R0762:Polr2a	UTSW	11	69,625,943 (GRCm39)	missense	unknown
R1101:Polr2a	UTSW	11	69,638,897 (GRCm39)	missense	probably benign	0.23
R1509:Polr2a	UTSW	11	69,638,039 (GRCm39)	missense	possibly damaging	0.93
R1547:Polr2a	UTSW	11	69,625,381 (GRCm39)	missense	probably benign	0.39
R1567:Polr2a	UTSW	11	69,636,857 (GRCm39)	missense	probably benign	0.07
R1597:Polr2a	UTSW	11	69,630,755 (GRCm39)	missense	possibly damaging	0.88
R1614:Polr2a	UTSW	11	69,634,199 (GRCm39)	missense	possibly damaging	0.75
R1698:Polr2a	UTSW	11	69,630,703 (GRCm39)	critical splice donor site	probably null
R1735:Polr2a	UTSW	11	69,633,222 (GRCm39)	missense	probably damaging	0.99
R1743:Polr2a	UTSW	11	69,630,329 (GRCm39)	missense	probably damaging	0.96
R1899:Polr2a	UTSW	11	69,634,772 (GRCm39)	missense	probably damaging	0.99
R1900:Polr2a	UTSW	11	69,634,772 (GRCm39)	missense	probably damaging	0.99
R1931:Polr2a	UTSW	11	69,626,201 (GRCm39)	missense	unknown
R2217:Polr2a	UTSW	11	69,633,511 (GRCm39)	critical splice donor site	probably null
R2218:Polr2a	UTSW	11	69,633,511 (GRCm39)	critical splice donor site	probably null
R2245:Polr2a	UTSW	11	69,626,009 (GRCm39)	missense	unknown
R3123:Polr2a	UTSW	11	69,626,536 (GRCm39)	missense	possibly damaging	0.92
R3124:Polr2a	UTSW	11	69,626,536 (GRCm39)	missense	possibly damaging	0.92
R4018:Polr2a	UTSW	11	69,625,885 (GRCm39)	missense	unknown
R4025:Polr2a	UTSW	11	69,634,485 (GRCm39)	missense	possibly damaging	0.95
R4197:Polr2a	UTSW	11	69,626,162 (GRCm39)	missense	unknown
R4462:Polr2a	UTSW	11	69,637,229 (GRCm39)	missense	probably damaging	1.00
R4508:Polr2a	UTSW	11	69,633,385 (GRCm39)	critical splice acceptor site	probably null
R4746:Polr2a	UTSW	11	69,626,500 (GRCm39)	missense	probably benign	0.05
R5069:Polr2a	UTSW	11	69,627,561 (GRCm39)	splice site	probably null
R5102:Polr2a	UTSW	11	69,637,771 (GRCm39)	missense	possibly damaging	0.93
R5195:Polr2a	UTSW	11	69,634,905 (GRCm39)	missense	probably damaging	1.00
R5234:Polr2a	UTSW	11	69,627,666 (GRCm39)	missense	probably benign	0.03
R5330:Polr2a	UTSW	11	69,638,101 (GRCm39)	missense	probably benign	0.01
R5331:Polr2a	UTSW	11	69,638,101 (GRCm39)	missense	probably benign	0.01
R5896:Polr2a	UTSW	11	69,627,086 (GRCm39)	missense	probably damaging	0.99
R5910:Polr2a	UTSW	11	69,637,696 (GRCm39)	missense	probably damaging	0.99
R6128:Polr2a	UTSW	11	69,627,803 (GRCm39)	missense	probably damaging	1.00
R6238:Polr2a	UTSW	11	69,638,047 (GRCm39)	missense	possibly damaging	0.95
R6244:Polr2a	UTSW	11	69,635,052 (GRCm39)	missense	probably damaging	1.00
R6303:Polr2a	UTSW	11	69,637,739 (GRCm39)	missense	probably damaging	1.00
R6338:Polr2a	UTSW	11	69,630,505 (GRCm39)	splice site	probably null
R6361:Polr2a	UTSW	11	69,634,163 (GRCm39)	missense	probably damaging	0.99
R6374:Polr2a	UTSW	11	69,627,758 (GRCm39)	missense	probably damaging	0.98
R6630:Polr2a	UTSW	11	69,626,339 (GRCm39)	missense	possibly damaging	0.93
R6631:Polr2a	UTSW	11	69,626,339 (GRCm39)	missense	possibly damaging	0.93
R6633:Polr2a	UTSW	11	69,626,339 (GRCm39)	missense	possibly damaging	0.93
R6897:Polr2a	UTSW	11	69,626,787 (GRCm39)	missense	probably benign	0.12
R6923:Polr2a	UTSW	11	69,626,787 (GRCm39)	missense	probably benign	0.12
R6933:Polr2a	UTSW	11	69,630,293 (GRCm39)	missense	probably benign	0.03
R6933:Polr2a	UTSW	11	69,627,003 (GRCm39)	missense	probably damaging	0.99
R6953:Polr2a	UTSW	11	69,632,537 (GRCm39)	missense	probably damaging	0.99
R6974:Polr2a	UTSW	11	69,638,026 (GRCm39)	missense	probably damaging	0.98
R7033:Polr2a	UTSW	11	69,638,039 (GRCm39)	missense	possibly damaging	0.93
R7085:Polr2a	UTSW	11	69,634,706 (GRCm39)	missense	probably damaging	0.99
R7112:Polr2a	UTSW	11	69,626,135 (GRCm39)	missense	unknown
R7124:Polr2a	UTSW	11	69,628,288 (GRCm39)	nonsense	probably null
R7307:Polr2a	UTSW	11	69,638,118 (GRCm39)	splice site	probably null
R7319:Polr2a	UTSW	11	69,637,196 (GRCm39)	missense	possibly damaging	0.95
R7350:Polr2a	UTSW	11	69,631,886 (GRCm39)	missense	possibly damaging	0.92
R7369:Polr2a	UTSW	11	69,636,803 (GRCm39)	missense	probably benign	0.01
R7585:Polr2a	UTSW	11	69,630,828 (GRCm39)	missense	probably damaging	0.99
R7882:Polr2a	UTSW	11	69,627,000 (GRCm39)	missense	possibly damaging	0.86
R7935:Polr2a	UTSW	11	69,638,330 (GRCm39)	missense	probably benign	0.00
R8080:Polr2a	UTSW	11	69,625,874 (GRCm39)	missense	unknown
R8140:Polr2a	UTSW	11	69,637,202 (GRCm39)	missense	probably benign	0.12
R8221:Polr2a	UTSW	11	69,628,344 (GRCm39)	missense	probably benign	0.24
R8245:Polr2a	UTSW	11	69,630,779 (GRCm39)	missense	probably damaging	0.99
R8274:Polr2a	UTSW	11	69,638,882 (GRCm39)	missense	probably damaging	0.99
R8275:Polr2a	UTSW	11	69,638,882 (GRCm39)	missense	probably damaging	0.99
R8276:Polr2a	UTSW	11	69,638,882 (GRCm39)	missense	probably damaging	0.99
R8277:Polr2a	UTSW	11	69,638,882 (GRCm39)	missense	probably damaging	0.99
R8311:Polr2a	UTSW	11	69,628,282 (GRCm39)	missense	probably null	0.20
R8477:Polr2a	UTSW	11	69,626,312 (GRCm39)	missense	probably benign	0.00
R8677:Polr2a	UTSW	11	69,626,381 (GRCm39)	missense	possibly damaging	0.85
R8976:Polr2a	UTSW	11	69,638,037 (GRCm39)	missense	possibly damaging	0.92
R9296:Polr2a	UTSW	11	69,625,562 (GRCm39)	missense	probably benign	0.39
R9731:Polr2a	UTSW	11	69,638,043 (GRCm39)	missense	possibly damaging	0.88

Predicted Primers

PCR Primer
(F):5'- AGTACTTGGGAGAGGTCGGG -3'
(R):5'- CCAGTTACTCACCTACAAGTCCC -3'

Sequencing Primer
(F):5'- AGGTCGGGGTATAGACTGG -3'
(R):5'- TACTCACCTACAAGTCCCAACTATAC -3'

Posted On

2022-10-06