Mutagenetix > Incidental Mutation

Incidental Mutation 'R7526:Hsp90aa1'

583017

Institutional Source

Beutler Lab

Gene Symbol

Hsp90aa1

Ensembl Gene

ENSMUSG00000021270

Gene Name

heat shock protein 90, alpha (cytosolic), class A member 1

Synonyms

Hspca, Hsp86-1, Hsp89, hsp4, Hsp90

MMRRC Submission

045598-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7526 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

110657470-110662829 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 110661728 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 96 (I96N)

Ref Sequence

ENSEMBL: ENSMUSP00000091921 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021698] [ENSMUST00000094361] [ENSMUST00000124156] [ENSMUST00000149189] [ENSMUST00000155242]

AlphaFold

P07901

Predicted Effect

unknown
Transcript: ENSMUST00000021698
AA Change: I96N

SMART Domains

Protein: ENSMUSP00000021698
Gene: ENSMUSG00000021270
AA Change: I96N

Domain	Start	End	E-Value	Type
HATPase_c	40	194	2.94e-11	SMART
Pfam:HSP90	196	733	6.7e-272	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000094361
AA Change: I96N

SMART Domains

Protein: ENSMUSP00000091921
Gene: ENSMUSG00000021270
AA Change: I96N

Domain	Start	End	E-Value	Type
HATPase_c	40	194	2.94e-11	SMART
Pfam:HSP90	196	728	2e-245	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000124156
AA Change: I96N

SMART Domains

Protein: ENSMUSP00000121138
Gene: ENSMUSG00000021270
AA Change: I96N

Domain	Start	End	E-Value	Type
PDB:3HHU\|B	1	103	1e-69	PDB
SCOP:d1byqa_	11	103	5e-48	SMART
Blast:HATPase_c	40	103	7e-39	BLAST

Predicted Effect

unknown
Transcript: ENSMUST00000149189
AA Change: I96N

SMART Domains

Protein: ENSMUSP00000114201
Gene: ENSMUSG00000021270
AA Change: I96N

Domain	Start	End	E-Value	Type
PDB:3HHU\|B	1	98	6e-66	PDB
SCOP:d1byqa_	11	98	2e-45	SMART
Blast:HATPase_c	40	98	2e-35	BLAST

Predicted Effect

unknown
Transcript: ENSMUST00000155242
AA Change: I96N

SMART Domains

Protein: ENSMUSP00000118189
Gene: ENSMUSG00000021270
AA Change: I96N

Domain	Start	End	E-Value	Type
HATPase_c	40	194	2.94e-11	SMART

Meta Mutation Damage Score

0.7853

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (74/74)

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 an inducible molecular chaperone that functions as a homodimer. The encoded protein aids in the proper folding of specific target proteins by use of an ATPase activity that is modulated by co-chaperones. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
PHENOTYPE: Mice homozygous for a gene trap allele exhibit male sterility associated with arrested male meiosis and male germ cell apoptosis. Mice homozygous for a transgenic gene disruption exhibit male sterility and small testis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700086D15Rik	A	T	11: 65,043,807 (GRCm39)	F85I	unknown	Het
Ankrd22	A	T	19: 34,126,765 (GRCm39)	W22R	possibly damaging	Het
Aqr	A	T	2: 113,938,590 (GRCm39)	H1287Q	probably damaging	Het
Armh1	C	A	4: 117,070,938 (GRCm39)	A396S	probably benign	Het
Atp8b5	A	G	4: 43,366,609 (GRCm39)	E791G	probably damaging	Het
Bicd1	T	G	6: 149,415,224 (GRCm39)	S646A	possibly damaging	Het
Bmpr1b	A	T	3: 141,562,360 (GRCm39)	Y276N	probably damaging	Het
Cadps2	T	C	6: 23,496,850 (GRCm39)	H465R	probably damaging	Het
Card11	A	T	5: 140,899,184 (GRCm39)		probably null	Het
Ccdc9	A	G	7: 16,016,325 (GRCm39)	L139P	probably damaging	Het
Cdk5rap3	A	T	11: 96,800,771 (GRCm39)	M355K	probably benign	Het
Cnot2	A	T	10: 116,342,985 (GRCm39)	V116E	probably benign	Het
Defb48	A	G	14: 63,215,280 (GRCm39)	V32A	possibly damaging	Het
Dmkn	A	G	7: 30,477,076 (GRCm39)	D460G	possibly damaging	Het
Dmxl2	A	G	9: 54,308,241 (GRCm39)	V2170A	possibly damaging	Het
Dnah1	A	T	14: 31,009,833 (GRCm39)	F1912I	possibly damaging	Het
Dok3	C	T	13: 55,675,306 (GRCm39)	V71I	probably benign	Het
Dzip3	A	T	16: 48,795,837 (GRCm39)	F178Y	probably damaging	Het
Enpp1	T	C	10: 24,550,308 (GRCm39)		probably null	Het
Eogt	A	G	6: 97,090,913 (GRCm39)	F409L	probably damaging	Het
Erich6	A	T	3: 58,538,110 (GRCm39)	L218H	probably damaging	Het
Fam186a	G	C	15: 99,839,796 (GRCm39)	I2149M	possibly damaging	Het
Fat1	G	A	8: 45,476,464 (GRCm39)	V1837I	probably damaging	Het
Flrt3	T	A	2: 140,502,126 (GRCm39)	T501S	probably damaging	Het
Fmn1	A	C	2: 113,518,479 (GRCm39)	E1365D	probably damaging	Het
Fzd5	G	T	1: 64,775,251 (GRCm39)	P170Q	probably benign	Het
Gm14326	G	A	2: 177,588,298 (GRCm39)	H233Y	probably damaging	Het
Gm19410	G	A	8: 36,257,766 (GRCm39)	V735M	probably damaging	Het
Gm21886	ACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGG	ACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAGG	18: 80,133,040 (GRCm39)		probably benign	Het
Gm2832	A	T	14: 41,002,919 (GRCm39)	I143L		Het
Greb1	G	A	12: 16,766,766 (GRCm39)	T344I	probably benign	Het
Grik2	A	T	10: 49,399,918 (GRCm39)	Y271N	possibly damaging	Het
Grin3b	A	G	10: 79,808,885 (GRCm39)	N212D	probably benign	Het
Hgsnat	A	G	8: 26,461,077 (GRCm39)	L187P	probably damaging	Het
Hmcn1	A	G	1: 150,532,324 (GRCm39)	I3152T	probably damaging	Het
Il18r1	T	A	1: 40,510,932 (GRCm39)	L6I	probably damaging	Het
Ing3	G	A	6: 21,953,798 (GRCm39)	V80I	probably damaging	Het
Kif18b	T	C	11: 102,805,493 (GRCm39)	I255V	probably damaging	Het
Kif2c	A	T	4: 117,039,629 (GRCm39)	N20K	possibly damaging	Het
Mfsd6l	T	C	11: 68,448,864 (GRCm39)	W572R	probably damaging	Het
Mybphl	A	G	3: 108,281,496 (GRCm39)	T71A	probably benign	Het
Myo7a	G	T	7: 97,734,655 (GRCm39)	T613K	possibly damaging	Het
Nfatc3	T	C	8: 106,805,715 (GRCm39)	S195P	probably damaging	Het
Nrg1	T	C	8: 32,308,351 (GRCm39)	N603S	probably benign	Het
Or52ae9	T	C	7: 103,389,607 (GRCm39)	Y280C	probably damaging	Het
Or8k22	A	T	2: 86,163,697 (GRCm39)	M1K	probably null	Het
Or8k37	A	G	2: 86,470,013 (GRCm39)	I13T	possibly damaging	Het
Parp8	T	C	13: 117,031,341 (GRCm39)	E457G	probably damaging	Het
Pclo	T	C	5: 14,571,076 (GRCm39)	F154L	probably benign	Het
Pear1	A	G	3: 87,659,875 (GRCm39)	S704P	probably damaging	Het
Pkib	A	G	10: 57,612,394 (GRCm39)	T92A	probably benign	Het
Pnpla7	A	G	2: 24,888,678 (GRCm39)	R376G	possibly damaging	Het
Pramel28	A	T	4: 143,692,387 (GRCm39)	C205S	probably benign	Het
Ptprd	T	A	4: 75,984,564 (GRCm39)	E527D	probably benign	Het
Pum1	T	C	4: 130,474,337 (GRCm39)	V469A	probably damaging	Het
Rnf148	G	A	6: 23,654,283 (GRCm39)	Q238*	probably null	Het
Scn9a	A	C	2: 66,313,990 (GRCm39)	N1909K	probably benign	Het
Sema3c	A	T	5: 17,932,594 (GRCm39)	H699L	possibly damaging	Het
Sema3f	A	T	9: 107,566,927 (GRCm39)	C201S	probably damaging	Het
Serinc2	T	A	4: 130,152,583 (GRCm39)	D206V	probably benign	Het
Serping1	A	T	2: 84,597,637 (GRCm39)	S415T	probably benign	Het
Sirpb1b	A	T	3: 15,613,932 (GRCm39)	L50Q	probably damaging	Het
Slc25a22	T	C	7: 141,011,296 (GRCm39)	E262G	probably benign	Het
Slc5a8	A	G	10: 88,738,353 (GRCm39)	I205M	probably damaging	Het
Sod2	G	T	17: 13,226,918 (GRCm39)		probably benign	Het
Tec	T	C	5: 72,943,362 (GRCm39)	I118V	probably benign	Het
Tenm3	A	T	8: 48,740,847 (GRCm39)	V1212E	probably damaging	Het
Tex44	G	A	1: 86,354,237 (GRCm39)	V49I	probably benign	Het
Tmem132d	A	T	5: 127,861,205 (GRCm39)	L972*	probably null	Het
Tpte	G	A	8: 22,815,563 (GRCm39)		probably null	Het
Trim6	T	A	7: 103,882,039 (GRCm39)	I456N	probably damaging	Het
Ubr4	G	C	4: 139,149,728 (GRCm39)	V520L	probably benign	Het
Ubxn8	A	T	8: 34,123,635 (GRCm39)	N101K	probably benign	Het
Vmn2r60	AG	A	7: 41,845,158 (GRCm39)		probably null	Het
Vmn2r83	A	G	10: 79,327,392 (GRCm39)	T667A	probably damaging	Het
Zpld2	T	C	4: 133,927,384 (GRCm39)		probably null	Het

Other mutations in Hsp90aa1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02056:Hsp90aa1	APN	12	110,660,449 (GRCm39)	unclassified	probably benign
IGL02243:Hsp90aa1	APN	12	110,661,525 (GRCm39)	missense	probably damaging	1.00
IGL02865:Hsp90aa1	APN	12	110,659,516 (GRCm39)	missense	probably benign	0.11
IGL02965:Hsp90aa1	APN	12	110,662,113 (GRCm39)	start codon destroyed	probably null	0.95
R0827:Hsp90aa1	UTSW	12	110,659,129 (GRCm39)	missense	probably benign	0.38
R1331:Hsp90aa1	UTSW	12	110,659,254 (GRCm39)	missense	probably damaging	1.00
R1498:Hsp90aa1	UTSW	12	110,662,122 (GRCm39)	splice site	probably null
R2039:Hsp90aa1	UTSW	12	110,660,216 (GRCm39)	missense	probably damaging	1.00
R2082:Hsp90aa1	UTSW	12	110,659,261 (GRCm39)	missense	probably damaging	1.00
R2102:Hsp90aa1	UTSW	12	110,660,566 (GRCm39)	missense	probably damaging	0.99
R2169:Hsp90aa1	UTSW	12	110,659,168 (GRCm39)	missense	probably damaging	0.99
R2194:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R2194:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R2359:Hsp90aa1	UTSW	12	110,661,003 (GRCm39)	critical splice donor site	probably null
R2364:Hsp90aa1	UTSW	12	110,659,187 (GRCm39)	missense	probably damaging	0.99
R2393:Hsp90aa1	UTSW	12	110,659,840 (GRCm39)	missense	probably damaging	1.00
R2398:Hsp90aa1	UTSW	12	110,658,755 (GRCm39)	missense	possibly damaging	0.86
R2435:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R2435:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R2924:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R2924:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R2925:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R2925:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R3176:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R3176:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R3177:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R3177:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R3276:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R3276:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R3277:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R3277:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R3615:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R3615:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R3616:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R3616:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R4033:Hsp90aa1	UTSW	12	110,662,114 (GRCm39)	start codon destroyed	possibly damaging	0.59
R4033:Hsp90aa1	UTSW	12	110,662,115 (GRCm39)	critical splice acceptor site	probably null
R4815:Hsp90aa1	UTSW	12	110,661,660 (GRCm39)	missense	possibly damaging	0.45
R4932:Hsp90aa1	UTSW	12	110,660,151 (GRCm39)	missense	probably damaging	1.00
R5117:Hsp90aa1	UTSW	12	110,661,698 (GRCm39)	missense	possibly damaging	0.71
R5555:Hsp90aa1	UTSW	12	110,659,168 (GRCm39)	missense	probably damaging	1.00
R6382:Hsp90aa1	UTSW	12	110,661,951 (GRCm39)	critical splice donor site	probably null
R7024:Hsp90aa1	UTSW	12	110,660,546 (GRCm39)	missense	possibly damaging	0.46
R7324:Hsp90aa1	UTSW	12	110,661,659 (GRCm39)	missense	unknown
R7447:Hsp90aa1	UTSW	12	110,658,562 (GRCm39)	missense	possibly damaging	0.94
R7732:Hsp90aa1	UTSW	12	110,659,852 (GRCm39)	missense	probably damaging	1.00
R8155:Hsp90aa1	UTSW	12	110,661,828 (GRCm39)	missense	unknown
R9004:Hsp90aa1	UTSW	12	110,659,045 (GRCm39)	missense	probably damaging	0.99
R9145:Hsp90aa1	UTSW	12	110,662,684 (GRCm39)	critical splice donor site	probably null
Z1177:Hsp90aa1	UTSW	12	110,659,900 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCTTCGTGATGACAGTCAC -3'
(R):5'- CGTGAGTATACCACTTGGAGG -3'

Sequencing Primer
(F):5'- GTGATGACAGTCACTTTCTCAGCAAC -3'
(R):5'- CCTGAAAATTTCACCTTGGGG -3'

Posted On

2019-10-17