Mutagenetix > Incidental Mutation

Incidental Mutation 'R0329:Hsp90b1'

65111

Institutional Source

Beutler Lab

Gene Symbol

Hsp90b1

Ensembl Gene

ENSMUSG00000020048

Gene Name

heat shock protein 90, beta (Grp94), member 1

Synonyms

ERp99, tumor rejection antigen (gp96) 1, Targ2, endoplasmin, Tra-1, Tra1, gp96, GRP94, 90 kDa

MMRRC Submission

038538-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0329 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

86690209-86705509 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 86694155 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 226 (E226G)

Ref Sequence

ENSEMBL: ENSMUSP00000122710 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000020238] [ENSMUST00000129413]

AlphaFold

P08113

Predicted Effect

probably damaging
Transcript: ENSMUST00000020238
AA Change: E550G

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000020238
Gene: ENSMUSG00000020048
AA Change: E550G

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
low complexity region	22	34	N/A	INTRINSIC
HATPase_c	96	255	4.96e-9	SMART
Pfam:HSP90	257	781	2.5e-233	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129178

Predicted Effect

probably damaging
Transcript: ENSMUST00000129413
AA Change: E226G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000122710
Gene: ENSMUSG00000020048
AA Change: E226G

Domain	Start	End	E-Value	Type
coiled coil region	9	35	N/A	INTRINSIC
Pfam:HSP90	39	373	3.8e-170	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134515

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152600

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000181587

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218095

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218106

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218691

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220419

Meta Mutation Damage Score

0.4683

Coding Region Coverage

1x: 98.9%
3x: 97.8%
10x: 95.0%
20x: 89.0%

Validation Efficiency

99% (107/108)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of a family of adenosine triphosphate(ATP)-metabolizing molecular chaperones with roles in stabilizing and folding other proteins. The encoded protein is localized to melanosomes and the endoplasmic reticulum. Expression of this protein is associated with a variety of pathogenic states, including tumor formation. There is a microRNA gene located within the 5' exon of this gene. There are pseudogenes for this gene on chromosomes 1 and 15. [provided by RefSeq, Aug 2012]
PHENOTYPE: Mice homozygous for a null mutation display embryonic lethality before somite formation with failure of primitive streak formation, absence of the chorion and amnion, and failure of mesoderm formation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 107 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700061G19Rik	A	T	17: 56,883,631	I400F	probably benign	Het
4833423E24Rik	T	A	2: 85,518,551	R72S	probably benign	Het
4931409K22Rik	T	C	5: 24,545,785		probably null	Het
Abca13	A	T	11: 9,399,430	H3668L	probably damaging	Het
Acvr1c	T	C	2: 58,284,838	T313A	probably damaging	Het
Adam28	T	C	14: 68,617,739	K651R	probably damaging	Het
Adamtsl3	A	T	7: 82,521,990	D417V	probably damaging	Het
Adgrf4	A	T	17: 42,667,313	C380S	probably damaging	Het
AI597479	T	G	1: 43,111,117	L129R	probably benign	Het
Anpep	C	T	7: 79,838,256	E518K	probably benign	Het
Anxa7	A	C	14: 20,469,498		probably null	Het
Arhgap22	A	G	14: 33,369,417	R650G	possibly damaging	Het
Atp8a1	T	A	5: 67,812,073		probably benign	Het
Bcr	C	T	10: 75,181,634	T1209I	possibly damaging	Het
Bmpr1a	C	T	14: 34,429,777	S185N	probably benign	Het
Calcoco1	A	T	15: 102,715,763	M246K	probably benign	Het
Casp12	T	A	9: 5,345,534		probably benign	Het
Ccno	T	A	13: 112,989,996	L333Q	probably damaging	Het
Cdhr2	T	A	13: 54,734,801		probably benign	Het
Cftr	T	A	6: 18,226,097	M318K	probably null	Het
Ckmt2	T	A	13: 91,863,203	D96V	possibly damaging	Het
Cnnm1	C	T	19: 43,441,910	P489L	probably damaging	Het
Cntnap1	A	T	11: 101,188,309	D1175V	probably damaging	Het
Cpne5	A	T	17: 29,211,660	L92H	probably damaging	Het
Crcp	C	A	5: 130,042,242	Q61K	possibly damaging	Het
Dcaf8	T	A	1: 172,187,411	D414E	probably benign	Het
Ddx28	T	C	8: 106,010,245	T394A	probably benign	Het
Ddx55	T	C	5: 124,559,147	F191L	probably benign	Het
Dnaaf1	T	C	8: 119,596,017		probably benign	Het
Dnaaf2	C	A	12: 69,197,744	R181L	probably damaging	Het
Elac2	A	G	11: 64,979,310	Y67C	probably damaging	Het
Elf5	A	G	2: 103,430,420		probably benign	Het
Emcn	T	A	3: 137,416,814		probably benign	Het
Erbb4	T	C	1: 68,298,280		probably benign	Het
Erbin	C	A	13: 103,868,865	C114F	probably damaging	Het
Etfdh	T	C	3: 79,609,844	I353V	probably benign	Het
Fam172a	T	A	13: 77,761,951		probably benign	Het
Fbxl12	C	T	9: 20,638,480	G316D	probably damaging	Het
Gbf1	G	A	19: 46,272,270		probably null	Het
Gbp2b	T	G	3: 142,608,176	S406A	probably benign	Het
Gli3	T	G	13: 15,723,558	L741R	probably damaging	Het
Gmip	G	T	8: 69,810,818	S70I	probably benign	Het
Gnptab	T	C	10: 88,440,309	S1153P	probably damaging	Het
Gp1ba	A	G	11: 70,640,409		probably benign	Het
Gramd1a	T	C	7: 31,138,254	D360G	possibly damaging	Het
Hectd4	T	C	5: 121,259,864	I285T	probably benign	Het
Hrh4	A	G	18: 13,007,245		probably benign	Het
Hspa13	A	T	16: 75,765,130	D60E	probably damaging	Het
Htt	T	A	5: 34,817,134		probably benign	Het
Ispd	C	T	12: 36,381,838	A22V	possibly damaging	Het
Kif14	G	C	1: 136,496,026		probably benign	Het
Kit	T	G	5: 75,652,829	V888G	probably damaging	Het
Lpin3	T	C	2: 160,905,305	V827A	probably benign	Het
Lrriq4	T	C	3: 30,655,724	S406P	probably benign	Het
Man2c1	T	C	9: 57,141,183	V777A	probably benign	Het
Mcm8	A	G	2: 132,819,994	K83E	possibly damaging	Het
Mep1a	A	G	17: 43,497,898		probably null	Het
Mtor	T	A	4: 148,484,380	V1119E	probably benign	Het
Mybpc2	C	T	7: 44,509,029	A710T	possibly damaging	Het
Myo9a	C	G	9: 59,923,677	T2368S	probably damaging	Het
Nbeal1	A	G	1: 60,268,063	Y1684C	probably damaging	Het
Npm3	A	G	19: 45,749,526	F11L	probably benign	Het
Nutf2	T	A	8: 105,876,363	S37T	probably damaging	Het
Obscn	T	A	11: 59,040,441	I5790F	probably damaging	Het
Obscn	A	T	11: 59,052,506	D4833E	probably damaging	Het
Olfr1015	T	A	2: 85,785,803	C97*	probably null	Het
Olfr123	A	T	17: 37,795,989	M182L	probably benign	Het
Olfr39	T	A	9: 20,285,857	S61T	possibly damaging	Het
Olfr955	T	C	9: 39,470,556	T57A	possibly damaging	Het
Pcdhb1	A	G	18: 37,267,024	D676G	possibly damaging	Het
Pcif1	G	T	2: 164,889,444	R466L	probably damaging	Het
Pdk1	T	C	2: 71,895,674		probably benign	Het
Phxr2	T	C	10: 99,126,117		probably benign	Het
Pidd1	A	T	7: 141,439,561		probably benign	Het
Plec	A	G	15: 76,191,418		probably null	Het
Polr1a	T	A	6: 71,966,416	C1212S	possibly damaging	Het
Pot1a	A	G	6: 25,778,831		probably benign	Het
Prdm5	T	C	6: 65,862,903		probably benign	Het
Primpol	A	T	8: 46,610,461	N53K	probably damaging	Het
Pyroxd1	A	G	6: 142,361,976	I491V	probably benign	Het
Serpinb3b	G	T	1: 107,159,703	N25K	probably damaging	Het
Slc9b1	C	T	3: 135,373,235	R218*	probably null	Het
Ssbp2	T	A	13: 91,680,579		probably null	Het
Stat4	A	G	1: 52,090,870		probably benign	Het
Steap4	T	C	5: 7,975,829	V130A	possibly damaging	Het
Stoml2	A	G	4: 43,030,238		probably null	Het
Syne2	G	T	12: 75,966,953	G2974C	probably benign	Het
Tfdp2	T	G	9: 96,306,893	F200V	probably damaging	Het
Tgm4	T	C	9: 123,048,557		probably null	Het
Tie1	C	A	4: 118,484,727	R175L	probably benign	Het
Tmem145	A	G	7: 25,308,674		probably benign	Het
Tsacc	A	G	3: 88,282,862	S94P	possibly damaging	Het
Tshz3	T	A	7: 36,770,033	D482E	probably benign	Het
Tspan33	T	C	6: 29,711,092		probably null	Het
Ugt2b35	A	G	5: 87,003,405	K290R	probably null	Het
Unc80	T	C	1: 66,674,087	L2788P	possibly damaging	Het
Usp10	T	A	8: 119,936,557	C39*	probably null	Het
Utp20	T	A	10: 88,817,979	T260S	probably benign	Het
Vmn2r118	G	T	17: 55,610,717	T265K	probably damaging	Het
Vmn2r7	C	A	3: 64,691,018	C797F	probably damaging	Het
Vmn2r98	A	C	17: 19,066,347	H369P	probably benign	Het
Vps39	A	T	2: 120,338,787	Y245N	possibly damaging	Het
Wdr27	A	G	17: 14,934,459		probably benign	Het
Ythdc2	A	G	18: 44,865,060		probably benign	Het
Zcwpw2	C	A	9: 118,014,055		noncoding transcript	Het
Zdhhc1	C	A	8: 105,483,543	A81S	probably benign	Het
Zfp729a	G	T	13: 67,620,354	H585Q	probably damaging	Het

Other mutations in Hsp90b1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01550:Hsp90b1	APN	10	86704370	missense	probably benign	0.40
IGL01671:Hsp90b1	APN	10	86704325	missense	probably benign	0.07
IGL01673:Hsp90b1	APN	10	86693432	missense	probably damaging	0.99
IGL02097:Hsp90b1	APN	10	86691684	unclassified	probably benign
IGL02124:Hsp90b1	APN	10	86705358	unclassified	probably benign
IGL02257:Hsp90b1	APN	10	86698589	missense	probably damaging	1.00
IGL02339:Hsp90b1	APN	10	86701814	missense	probably damaging	1.00
IGL02342:Hsp90b1	APN	10	86695739	critical splice acceptor site	probably null
R0330:Hsp90b1	UTSW	10	86694155	missense	probably damaging	1.00
R0735:Hsp90b1	UTSW	10	86695748	splice site	probably benign
R1531:Hsp90b1	UTSW	10	86696795	missense	probably benign	0.02
R1540:Hsp90b1	UTSW	10	86694042	missense	probably damaging	1.00
R1711:Hsp90b1	UTSW	10	86694525	missense	probably damaging	1.00
R1797:Hsp90b1	UTSW	10	86701745	missense	possibly damaging	0.86
R2128:Hsp90b1	UTSW	10	86695706	missense	probably damaging	1.00
R2129:Hsp90b1	UTSW	10	86695706	missense	probably damaging	1.00
R2903:Hsp90b1	UTSW	10	86703485	missense	probably damaging	1.00
R4735:Hsp90b1	UTSW	10	86693955	missense	probably damaging	1.00
R4749:Hsp90b1	UTSW	10	86701808	missense	probably damaging	1.00
R5011:Hsp90b1	UTSW	10	86696753	missense	probably benign	0.37
R5650:Hsp90b1	UTSW	10	86693503	missense	probably damaging	1.00
R5950:Hsp90b1	UTSW	10	86701745	missense	possibly damaging	0.86
R6731:Hsp90b1	UTSW	10	86701905	missense	probably benign	0.01
R6835:Hsp90b1	UTSW	10	86694085	missense	probably damaging	1.00
R7038:Hsp90b1	UTSW	10	86695866	missense	probably damaging	0.99
R7250:Hsp90b1	UTSW	10	86691708	missense	unknown
R7343:Hsp90b1	UTSW	10	86692183	missense	probably damaging	1.00
R8027:Hsp90b1	UTSW	10	86696730	missense	probably damaging	0.97
R8126:Hsp90b1	UTSW	10	86694382	missense	probably damaging	0.99
R8336:Hsp90b1	UTSW	10	86691104	makesense	probably null
R8768:Hsp90b1	UTSW	10	86705305	critical splice donor site	probably null
R9024:Hsp90b1	UTSW	10	86705310	missense	possibly damaging	0.85

Predicted Primers

Posted On

2013-08-08