Mutagenetix > Incidental Mutation

Incidental Mutation 'R4583:Ern1'

343854

Institutional Source

Beutler Lab

Gene Symbol

Ern1

Ensembl Gene

ENSMUSG00000020715

Gene Name

endoplasmic reticulum (ER) to nucleus signalling 1

Synonyms

Ire1a, Ire1alpha, 9030414B18Rik, Ire1p

MMRRC Submission

041804-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4583 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

106394650-106487852 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 106407205 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 697 (S697T)

Ref Sequence

ENSEMBL: ENSMUSP00000001059 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000001059]

AlphaFold

Q9EQY0

PDB Structure

Crystal structure of murine IRE1 in complex with MKC9989 inhibitor [X-RAY DIFFRACTION]
Crystal structure of murine IRE1 in complex with OICR464 inhibitor [X-RAY DIFFRACTION]
Crystal structure of murine IRE1 in complex with OICR573 inhibitor [X-RAY DIFFRACTION]

Predicted Effect

probably damaging
Transcript: ENSMUST00000001059
AA Change: S697T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000001059
Gene: ENSMUSG00000020715
AA Change: S697T

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
PQQ	28	59	3.46e-5	SMART
PQQ	110	142	1.11e-3	SMART
PQQ	148	180	7.84e-4	SMART
PQQ	191	223	3.26e-1	SMART
PQQ	279	310	5.01e1	SMART
low complexity region	471	501	N/A	INTRINSIC
low complexity region	513	551	N/A	INTRINSIC
Pfam:Pkinase	571	832	1.8e-44	PFAM
Pfam:Pkinase_Tyr	572	829	8.7e-26	PFAM
PUG	895	952	5.25e-23	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000131895

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.2%
20x: 95.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is the ER to nucleus signalling 1 protein, a human homologue of the yeast Ire1 gene product. This protein possesses intrinsic kinase activity and an endoribonuclease activity and it is important in altering gene expression as a response to endoplasmic reticulum-based stress signals. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for null mutations display embryonic lethality during organogenesis. Homozygous mice may also display decreased embryo size, impaired hematopoiesis, and/or placental abnormalities. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 119 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310022A10Rik	T	C	7: 27,574,592	L86P	unknown	Het
Aimp1	C	T	3: 132,677,047	E23K	probably damaging	Het
Ap2b1	A	T	11: 83,397,779	N884I	probably benign	Het
Apoe	G	T	7: 19,697,498	Q65K	possibly damaging	Het
Arhgef1	T	A	7: 24,912,571	D93E	probably benign	Het
Arhgef12	G	T	9: 42,977,662	T1085K	probably damaging	Het
Arid5a	T	C	1: 36,317,664		probably null	Het
Atp9a	A	T	2: 168,689,360		probably null	Het
Baz1a	T	C	12: 54,922,540	I635V	probably damaging	Het
Bbs10	A	G	10: 111,301,134	K703E	probably benign	Het
Cckar	T	A	5: 53,699,782	M429L	probably benign	Het
Ccl3	A	T	11: 83,648,338	L65Q	probably benign	Het
Ccr3	A	G	9: 124,029,440	T271A	probably benign	Het
Cd8b1	T	A	6: 71,326,097	I52N	probably damaging	Het
Cdh15	G	A	8: 122,865,028	E551K	probably damaging	Het
Cdh17	A	G	4: 11,810,466	K719R	probably benign	Het
Cfap43	T	C	19: 47,837,216	R38G	probably null	Het
Chd6	T	C	2: 161,014,194	E715G	probably damaging	Het
Cldn34b2	T	A	X: 155,125,629	R68*	probably null	Het
Col19a1	T	G	1: 24,561,329	D44A	unknown	Het
Colgalt2	C	T	1: 152,506,876	S493F	probably damaging	Het
Cr1l	T	C	1: 195,129,831	I99M	probably damaging	Het
Crybg1	T	C	10: 43,997,620	E1164G	probably damaging	Het
Cym	G	T	3: 107,211,402	D367E	probably damaging	Het
Dennd2a	G	T	6: 39,522,842	T263K	probably damaging	Het
Dhx9	T	A	1: 153,460,303	M869L	probably damaging	Het
Dnm2	A	G	9: 21,504,446	H692R	probably damaging	Het
F12	G	A	13: 55,421,130	T273I	probably benign	Het
Fam151b	A	T	13: 92,468,109	L124Q	probably damaging	Het
Fancg	A	G	4: 43,002,991	V622A	probably benign	Het
Fbxo2	T	A	4: 148,164,899	N159K	possibly damaging	Het
Fgd2	C	A	17: 29,367,078	T212K	possibly damaging	Het
Fhl3	T	A	4: 124,707,549	D178E	probably benign	Het
Filip1	G	T	9: 79,815,809	A1176D	possibly damaging	Het
Fndc1	T	C	17: 7,739,249	Y1722C	probably damaging	Het
Frem3	T	C	8: 80,613,514	V812A	probably benign	Het
Fsip2	A	G	2: 82,978,673	I1779V	probably benign	Het
Gli2	C	T	1: 118,842,068	V585I	probably benign	Het
Gm15056	C	G	8: 20,900,681	S80T	probably benign	Het
Gm4951	T	C	18: 60,246,080	I229T	possibly damaging	Het
Gm5145	A	G	17: 20,570,453	E31G	probably benign	Het
Gmfg	A	G	7: 28,445,944	Y71C	probably damaging	Het
Grk1	A	G	8: 13,409,322	E291G	probably damaging	Het
Gtpbp1	A	G	15: 79,715,951	E393G	possibly damaging	Het
Gtpbp2	A	G	17: 46,161,145	D2G	probably damaging	Het
Hc	A	T	2: 35,028,177	V698E	probably benign	Het
Helz	G	A	11: 107,646,069	R249H	probably damaging	Het
Hmcn2	A	G	2: 31,413,265	I2973V	possibly damaging	Het
Hnrnpa3	A	G	2: 75,663,606	R286G	probably benign	Het
Hus1b	A	T	13: 30,947,518	W53R	probably damaging	Het
Hydin	C	T	8: 110,595,225	T4503I	probably benign	Het
Ighmbp2	G	C	19: 3,265,324	P699A	probably benign	Het
Igkv1-122	A	T	6: 68,017,458	Y110F	probably benign	Het
Igkv8-28	T	C	6: 70,143,620	Y113C	probably damaging	Het
Il16	A	G	7: 83,682,899	S158P	probably damaging	Het
Kalrn	T	A	16: 34,235,267	H876L	probably damaging	Het
Kdm5d	T	A	Y: 914,134	L357H	probably damaging	Het
Krt78	T	C	15: 101,946,620	T919A	possibly damaging	Het
L3mbtl2	T	C	15: 81,684,906	C594R	probably damaging	Het
Lcorl	A	T	5: 45,733,589	L474*	probably null	Het
Lgals3	A	T	14: 47,381,687		probably null	Het
Lnx1	C	T	5: 74,610,796	V350I	probably benign	Het
Lpcat3	T	G	6: 124,703,323	W429G	possibly damaging	Het
Lrp1	T	C	10: 127,541,372	T4149A	probably benign	Het
Memo1	G	A	17: 74,258,461	Q36*	probably null	Het
Micalcl	A	G	7: 112,412,947	N668S	probably benign	Het
Ms4a10	A	T	19: 10,968,189	I76N	possibly damaging	Het
Mthfr	T	G	4: 148,051,872	L362V	possibly damaging	Het
Myh3	T	A	11: 67,096,453	Y1376*	probably null	Het
Mymk	C	A	2: 27,062,280	V192F	probably benign	Het
Myo1c	A	G	11: 75,671,862	D966G	possibly damaging	Het
Ncam2	A	G	16: 81,517,557	N474D	probably damaging	Het
Nmnat1	T	C	4: 149,469,151	N168S	possibly damaging	Het
Nmur1	C	T	1: 86,386,645	V323M	possibly damaging	Het
Npr2	C	A	4: 43,633,522		probably null	Het
Nsd3	T	A	8: 25,710,676	M1265K	probably benign	Het
Olfr1206	G	T	2: 88,865,494	M296I	probably benign	Het
Olfr1212	T	A	2: 88,959,212	F249I	probably damaging	Het
Olfr1462	T	A	19: 13,190,698	F10L	probably damaging	Het
Olfr152	T	C	2: 87,783,221	V227A	possibly damaging	Het
Olfr155	A	G	4: 43,855,262	T318A	probably benign	Het
Olfr345	A	C	2: 36,640,614	T192P	probably damaging	Het
Olfr394	T	C	11: 73,887,803	T190A	probably damaging	Het
Olfr812	T	C	10: 129,842,475	D189G	probably damaging	Het
Otub1	G	A	19: 7,204,436	A25V	possibly damaging	Het
Paqr3	T	A	5: 97,108,210	R102*	probably null	Het
Patl2	A	G	2: 122,126,745	S103P	probably benign	Het
Pcdhb15	A	T	18: 37,475,575	H620L	possibly damaging	Het
Pdgfc	A	T	3: 81,141,528	D81V	possibly damaging	Het
Pdia2	T	C	17: 26,196,502	D447G	probably damaging	Het
Pold1	C	A	7: 44,538,913	A514S	probably damaging	Het
Pomgnt1	C	T	4: 116,158,494	T552I	probably benign	Het
Ppl	T	C	16: 5,104,536	E294G	probably benign	Het
Pramef8	A	G	4: 143,416,754	Y30C	probably damaging	Het
Prkcb	A	G	7: 122,457,224	S100G	probably benign	Het
Psg16	T	G	7: 17,095,172	I227S	probably benign	Het
Rbbp6	AAAGAAGAAGAAGAAGAAG	AAAGAAGAAGAAGAAG	7: 123,001,952		probably benign	Het
Reck	T	C	4: 43,931,062		probably null	Het
Rrbp1	C	T	2: 143,988,751	G499S	probably benign	Het
Sema6d	G	T	2: 124,664,162	R630L	probably damaging	Het
Slc29a1	A	G	17: 45,589,956	V94A	possibly damaging	Het
Slc35a1	T	A	4: 34,664,146	Q324L	probably benign	Het
Slc35c1	A	T	2: 92,458,921	L80Q	probably damaging	Het
Slc7a10	G	T	7: 35,197,952		probably null	Het
Srrm2	C	T	17: 23,819,619		probably benign	Het
Stk38	T	G	17: 28,982,156	D182A	probably damaging	Het
Tas2r104	C	T	6: 131,685,435	G104S	probably benign	Het
Tmem121b	T	C	6: 120,492,094	E554G	probably damaging	Het
Tor1aip2	A	G	1: 156,065,142	H398R	probably benign	Het
Tram2	C	T	1: 21,013,449	V83I	probably benign	Het
Ube3a	C	T	7: 59,286,063	T565I	probably damaging	Het
Ubr4	T	C	4: 139,380,853	V56A	possibly damaging	Het
Vmn1r128	T	C	7: 21,349,719	V116A	possibly damaging	Het
Vmn1r170	C	T	7: 23,606,662	T163I	probably benign	Het
Vmn2r75	T	A	7: 86,164,082	D504V	possibly damaging	Het
Vps36	G	A	8: 22,218,420	M363I	probably benign	Het
Wdsub1	A	G	2: 59,878,317	S71P	probably damaging	Het
Zdhhc12	A	G	2: 30,091,484	F189L	probably benign	Het
Zfp521	T	C	18: 13,844,330	M1009V	probably benign	Het

Other mutations in Ern1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00825:Ern1	APN	11	106421967	missense	probably benign	0.02
IGL01938:Ern1	APN	11	106411657	missense	probably benign
IGL02813:Ern1	APN	11	106423425	missense	probably damaging	1.00
IGL02928:Ern1	APN	11	106405879	splice site	probably benign
IGL02931:Ern1	APN	11	106423440	missense	probably damaging	1.00
IGL03153:Ern1	APN	11	106410098	missense	possibly damaging	0.63
Immoderate	UTSW	11	106420042	missense	possibly damaging	0.93
Militant	UTSW	11	106411652	missense	probably damaging	1.00
K7371:Ern1	UTSW	11	106400275	missense	probably damaging	1.00
R0090:Ern1	UTSW	11	106405823	missense	probably damaging	1.00
R0391:Ern1	UTSW	11	106407178	nonsense	probably null
R0411:Ern1	UTSW	11	106398586	missense	probably benign
R0627:Ern1	UTSW	11	106398693	missense	probably benign	0.00
R1416:Ern1	UTSW	11	106421980	splice site	probably benign
R1831:Ern1	UTSW	11	106399842	splice site	probably null
R1837:Ern1	UTSW	11	106458957	missense	probably damaging	1.00
R1944:Ern1	UTSW	11	106421950	missense	probably damaging	1.00
R1945:Ern1	UTSW	11	106421950	missense	probably damaging	1.00
R1954:Ern1	UTSW	11	106421974	splice site	probably benign
R1957:Ern1	UTSW	11	106426897	missense	probably damaging	1.00
R2192:Ern1	UTSW	11	106409924	missense	probably benign
R4276:Ern1	UTSW	11	106407181	missense	probably benign
R4277:Ern1	UTSW	11	106407181	missense	probably benign
R4471:Ern1	UTSW	11	106420042	missense	possibly damaging	0.93
R4731:Ern1	UTSW	11	106434850	intron	probably benign
R5177:Ern1	UTSW	11	106411775	missense	probably benign	0.01
R5489:Ern1	UTSW	11	106407529	missense	probably damaging	1.00
R5538:Ern1	UTSW	11	106421901	missense	possibly damaging	0.83
R5806:Ern1	UTSW	11	106398705	missense	probably damaging	0.96
R5922:Ern1	UTSW	11	106421730	missense	probably damaging	0.97
R5931:Ern1	UTSW	11	106426873	missense	possibly damaging	0.86
R5990:Ern1	UTSW	11	106411769	missense	probably benign
R6149:Ern1	UTSW	11	106405815	nonsense	probably null
R6253:Ern1	UTSW	11	106426908	missense	possibly damaging	0.89
R6721:Ern1	UTSW	11	106411652	missense	probably damaging	1.00
R6957:Ern1	UTSW	11	106403539	missense	probably damaging	1.00
R7362:Ern1	UTSW	11	106437123	missense	probably damaging	1.00
R7387:Ern1	UTSW	11	106421952	missense	probably damaging	0.98
R7494:Ern1	UTSW	11	106407535	missense	probably damaging	1.00
R7514:Ern1	UTSW	11	106409893	critical splice donor site	probably null
R7767:Ern1	UTSW	11	106400308	missense	probably damaging	1.00
R7811:Ern1	UTSW	11	106434868	missense	unknown
R7869:Ern1	UTSW	11	106459019	nonsense	probably null
R8750:Ern1	UTSW	11	106421950	missense	probably damaging	1.00
R9129:Ern1	UTSW	11	106410120	missense	probably benign
R9369:Ern1	UTSW	11	106414433	missense	probably benign	0.09
R9546:Ern1	UTSW	11	106410027	missense	probably benign	0.21
R9688:Ern1	UTSW	11	106459010	missense	possibly damaging	0.52
R9735:Ern1	UTSW	11	106421882	nonsense	probably null
X0021:Ern1	UTSW	11	106398606	missense	probably damaging	1.00
X0022:Ern1	UTSW	11	106458919	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTACAGGGTTGTCCTTACAGTC -3'
(R):5'- CTGACCTTCACAGGAGAAAGGG -3'

Sequencing Primer
(F):5'- ACAGGGTTGTCCTTACAGTCTTCAC -3'
(R):5'- CCTTCACAGGAGAAAGGGGTGTG -3'

Posted On

2015-09-24