Mutagenetix > Incidental Mutation

Incidental Mutation 'R7767:Ern1'

598323

Institutional Source

Beutler Lab

Gene Symbol

Ern1

Ensembl Gene

ENSMUSG00000020715

Gene Name

endoplasmic reticulum to nucleus signalling 1

Synonyms

Ire1p, 9030414B18Rik, Ire1a, Ire1alpha

MMRRC Submission

045823-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7767 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

106285476-106378678 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 106291134 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 847 (D847G)

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: D847G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000001059
Gene: ENSMUSG00000020715
AA Change: D847G

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

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

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: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aox4	C	A	1: 58,274,366 (GRCm39)	S384Y	probably damaging	Het
Arhgef15	T	C	11: 68,844,673 (GRCm39)	E308G	probably damaging	Het
Asb15	A	G	6: 24,559,281 (GRCm39)	D142G	probably benign	Het
Atg13	A	G	2: 91,509,711 (GRCm39)	S394P	probably damaging	Het
Atp10a	G	C	7: 58,308,597 (GRCm39)	W132S	probably damaging	Het
Bltp1	G	T	3: 36,974,436 (GRCm39)		probably null	Het
Bod1l	T	A	5: 41,974,099 (GRCm39)	N2405I	probably benign	Het
Capsl	C	T	15: 9,462,770 (GRCm39)	R137C	probably damaging	Het
Cd109	T	A	9: 78,617,441 (GRCm39)	M1313K	probably damaging	Het
Chst13	G	A	6: 90,286,566 (GRCm39)	A132V	possibly damaging	Het
Cobl	T	C	11: 12,362,117 (GRCm39)		probably benign	Het
Coq9	A	T	8: 95,577,214 (GRCm39)	E193V	probably benign	Het
Cpd	T	A	11: 76,704,385 (GRCm39)	I410F	probably benign	Het
Cyth3	T	G	5: 143,693,229 (GRCm39)	V351G	probably damaging	Het
Dcdc2c	T	C	12: 28,520,256 (GRCm39)	K607E		Het
Dcp1a	T	C	14: 30,201,775 (GRCm39)		probably null	Het
Dennd3	A	G	15: 73,394,079 (GRCm39)	I35V	probably benign	Het
Dlgap4	C	T	2: 156,587,973 (GRCm39)	R606W	probably damaging	Het
Dnhd1	A	G	7: 105,343,817 (GRCm39)	I1720M	probably benign	Het
Erbin	A	G	13: 103,995,907 (GRCm39)	L265P	probably damaging	Het
Esyt3	T	G	9: 99,207,024 (GRCm39)	S342R	probably benign	Het
Exoc2	A	T	13: 31,060,752 (GRCm39)	I584K	probably benign	Het
Fam240a	T	C	9: 110,744,090 (GRCm39)	R50G	probably damaging	Het
Glis3	A	T	19: 28,241,360 (GRCm39)	M858K	probably benign	Het
Gls2	C	T	10: 128,030,998 (GRCm39)	R86C	unknown	Het
Gm10972	C	A	3: 94,550,901 (GRCm39)	Y25*	probably null	Het
H2-T10	A	T	17: 36,428,622 (GRCm39)	M350K	probably benign	Het
Has1	A	T	17: 18,070,792 (GRCm39)	V43D	probably damaging	Het
Herc2	T	A	7: 55,878,275 (GRCm39)	S4609R	probably benign	Het
Hmgcs2	A	C	3: 98,198,582 (GRCm39)	T162P	probably damaging	Het
Hspg2	G	T	4: 137,239,177 (GRCm39)	C368F	probably damaging	Het
Ighv11-1	A	G	12: 113,945,722 (GRCm39)	S44P	probably damaging	Het
Inppl1	A	G	7: 101,473,545 (GRCm39)	V1035A	probably benign	Het
Kmt2a	C	T	9: 44,730,295 (GRCm39)	V3341I	unknown	Het
Lrp1b	T	C	2: 40,691,517 (GRCm39)	N3434S		Het
Lrriq1	G	C	10: 103,051,815 (GRCm39)	S312R	probably damaging	Het
Map1a	G	A	2: 121,132,517 (GRCm39)	S1111N	probably damaging	Het
Myo15a	T	C	11: 60,392,922 (GRCm39)	V1029A		Het
Nol11	T	C	11: 107,069,908 (GRCm39)	H314R	possibly damaging	Het
Nphs1	A	T	7: 30,162,733 (GRCm39)	D404V	probably damaging	Het
Odr4	A	G	1: 150,247,788 (GRCm39)	V387A	probably benign	Het
Or51r1	A	T	7: 102,220,971 (GRCm39)		probably benign	Het
Pabpc2	T	C	18: 39,907,607 (GRCm39)	Y291H	possibly damaging	Het
Pcdh15	G	A	10: 74,322,088 (GRCm39)	A1020T	probably benign	Het
Pla2g4f	A	C	2: 120,135,490 (GRCm39)	S395A	possibly damaging	Het
Ppp1r18	A	G	17: 36,178,176 (GRCm39)	Q17R	probably damaging	Het
Prokr2	A	T	2: 132,215,996 (GRCm39)	V155D	probably damaging	Het
Pwwp2a	T	G	11: 43,596,696 (GRCm39)	C620W	probably damaging	Het
Rabepk	T	C	2: 34,675,605 (GRCm39)	D175G	probably damaging	Het
Rad54l	T	C	4: 115,956,866 (GRCm39)	Y485C	probably damaging	Het
Rasef	A	G	4: 73,652,771 (GRCm39)	S577P	probably damaging	Het
Rgma	C	A	7: 73,067,752 (GRCm39)	L446I	unknown	Het
Rnf212b	T	C	14: 55,079,825 (GRCm39)	S182P	probably damaging	Het
Rnf6	C	A	5: 146,147,986 (GRCm39)	R344I	probably damaging	Het
Rnf6	T	A	5: 146,147,987 (GRCm39)	R344*	probably null	Het
Sgo1	A	G	17: 53,986,639 (GRCm39)	I184T	possibly damaging	Het
Sgpl1	A	T	10: 60,953,502 (GRCm39)	I78N	possibly damaging	Het
Snx13	T	A	12: 35,157,483 (GRCm39)	Y510N	probably damaging	Het
Sptbn2	G	A	19: 4,784,171 (GRCm39)	E638K	possibly damaging	Het
Sspo	A	G	6: 48,428,316 (GRCm39)	T349A	probably damaging	Het
Sv2c	C	T	13: 96,126,223 (GRCm39)	S343N	probably damaging	Het
Syne1	C	A	10: 5,283,560 (GRCm39)	V1502F	possibly damaging	Het
Syne1	T	A	10: 5,283,632 (GRCm39)	I1478F	possibly damaging	Het
Tmem121	C	T	12: 113,151,992 (GRCm39)	A70V	probably damaging	Het
Tmem215	A	G	4: 40,474,042 (GRCm39)	I40V	possibly damaging	Het
Trim25	A	G	11: 88,899,943 (GRCm39)		probably null	Het
Trio	A	G	15: 27,889,504 (GRCm39)	V534A	unknown	Het
Tyr	T	A	7: 87,142,218 (GRCm39)	E114V	probably benign	Het
Ush2a	A	T	1: 188,285,457 (GRCm39)	T1998S	probably benign	Het
Usp40	G	T	1: 87,909,900 (GRCm39)	A518E	probably benign	Het
Usp48	T	A	4: 137,331,956 (GRCm39)		probably null	Het
Vash1	T	A	12: 86,733,767 (GRCm39)	F152L	probably damaging	Het
Vsig10l	C	A	7: 43,113,141 (GRCm39)	P31Q	probably damaging	Het
Xab2	C	T	8: 3,669,018 (GRCm39)	E43K	probably benign	Het
Zfp423	G	A	8: 88,507,512 (GRCm39)	S944F	probably damaging	Het
Zp2	A	T	7: 119,736,392 (GRCm39)	D350E	probably benign	Het
Zscan4e	T	G	7: 11,041,461 (GRCm39)	Q165P	probably damaging	Het

Other mutations in Ern1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00825:Ern1	APN	11	106,312,793 (GRCm39)	missense	probably benign	0.02
IGL01938:Ern1	APN	11	106,302,483 (GRCm39)	missense	probably benign
IGL02813:Ern1	APN	11	106,314,251 (GRCm39)	missense	probably damaging	1.00
IGL02928:Ern1	APN	11	106,296,705 (GRCm39)	splice site	probably benign
IGL02931:Ern1	APN	11	106,314,266 (GRCm39)	missense	probably damaging	1.00
IGL03153:Ern1	APN	11	106,300,924 (GRCm39)	missense	possibly damaging	0.63
Immoderate	UTSW	11	106,310,868 (GRCm39)	missense	possibly damaging	0.93
Militant	UTSW	11	106,302,478 (GRCm39)	missense	probably damaging	1.00
K7371:Ern1	UTSW	11	106,291,101 (GRCm39)	missense	probably damaging	1.00
R0090:Ern1	UTSW	11	106,296,649 (GRCm39)	missense	probably damaging	1.00
R0391:Ern1	UTSW	11	106,298,004 (GRCm39)	nonsense	probably null
R0411:Ern1	UTSW	11	106,289,412 (GRCm39)	missense	probably benign
R0627:Ern1	UTSW	11	106,289,519 (GRCm39)	missense	probably benign	0.00
R1416:Ern1	UTSW	11	106,312,806 (GRCm39)	splice site	probably benign
R1831:Ern1	UTSW	11	106,290,668 (GRCm39)	splice site	probably null
R1837:Ern1	UTSW	11	106,349,783 (GRCm39)	missense	probably damaging	1.00
R1944:Ern1	UTSW	11	106,312,776 (GRCm39)	missense	probably damaging	1.00
R1945:Ern1	UTSW	11	106,312,776 (GRCm39)	missense	probably damaging	1.00
R1954:Ern1	UTSW	11	106,312,800 (GRCm39)	splice site	probably benign
R1957:Ern1	UTSW	11	106,317,723 (GRCm39)	missense	probably damaging	1.00
R2192:Ern1	UTSW	11	106,300,750 (GRCm39)	missense	probably benign
R4276:Ern1	UTSW	11	106,298,007 (GRCm39)	missense	probably benign
R4277:Ern1	UTSW	11	106,298,007 (GRCm39)	missense	probably benign
R4471:Ern1	UTSW	11	106,310,868 (GRCm39)	missense	possibly damaging	0.93
R4583:Ern1	UTSW	11	106,298,031 (GRCm39)	missense	probably damaging	1.00
R4731:Ern1	UTSW	11	106,325,676 (GRCm39)	intron	probably benign
R5177:Ern1	UTSW	11	106,302,601 (GRCm39)	missense	probably benign	0.01
R5489:Ern1	UTSW	11	106,298,355 (GRCm39)	missense	probably damaging	1.00
R5538:Ern1	UTSW	11	106,312,727 (GRCm39)	missense	possibly damaging	0.83
R5806:Ern1	UTSW	11	106,289,531 (GRCm39)	missense	probably damaging	0.96
R5922:Ern1	UTSW	11	106,312,556 (GRCm39)	missense	probably damaging	0.97
R5931:Ern1	UTSW	11	106,317,699 (GRCm39)	missense	possibly damaging	0.86
R5990:Ern1	UTSW	11	106,302,595 (GRCm39)	missense	probably benign
R6149:Ern1	UTSW	11	106,296,641 (GRCm39)	nonsense	probably null
R6253:Ern1	UTSW	11	106,317,734 (GRCm39)	missense	possibly damaging	0.89
R6721:Ern1	UTSW	11	106,302,478 (GRCm39)	missense	probably damaging	1.00
R6957:Ern1	UTSW	11	106,294,365 (GRCm39)	missense	probably damaging	1.00
R7362:Ern1	UTSW	11	106,327,949 (GRCm39)	missense	probably damaging	1.00
R7387:Ern1	UTSW	11	106,312,778 (GRCm39)	missense	probably damaging	0.98
R7494:Ern1	UTSW	11	106,298,361 (GRCm39)	missense	probably damaging	1.00
R7514:Ern1	UTSW	11	106,300,719 (GRCm39)	critical splice donor site	probably null
R7811:Ern1	UTSW	11	106,325,694 (GRCm39)	missense	unknown
R7869:Ern1	UTSW	11	106,349,845 (GRCm39)	nonsense	probably null
R8750:Ern1	UTSW	11	106,312,776 (GRCm39)	missense	probably damaging	1.00
R9129:Ern1	UTSW	11	106,300,946 (GRCm39)	missense	probably benign
R9369:Ern1	UTSW	11	106,305,259 (GRCm39)	missense	probably benign	0.09
R9546:Ern1	UTSW	11	106,300,853 (GRCm39)	missense	probably benign	0.21
R9688:Ern1	UTSW	11	106,349,836 (GRCm39)	missense	possibly damaging	0.52
R9735:Ern1	UTSW	11	106,312,708 (GRCm39)	nonsense	probably null
X0021:Ern1	UTSW	11	106,289,432 (GRCm39)	missense	probably damaging	1.00
X0022:Ern1	UTSW	11	106,349,745 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTTTGACCAAGCCCACAAGG -3'
(R):5'- GAGGGATATATCTGCTCACGGG -3'

Sequencing Primer
(F):5'- TCCAAGAACAGGGATTTGGAATTCC -3'
(R):5'- TATATCTGCTCACGGGGAAAAAGTC -3'

Posted On

2019-11-26