Mutagenetix > Incidental Mutations

Incidental Mutation 'R1458:Hspa12b'

161848

Institutional Source

Beutler Lab

Gene Symbol

Hspa12b

Ensembl Gene

ENSMUSG00000074793

Gene Name

heat shock protein 12B

Synonyms

2700081N06Rik

MMRRC Submission

039513-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.061) question?

Stock #

R1458 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

131127280-131146321 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to C at 131145192 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Proline at position 678 (A678P)

Ref Sequence

ENSEMBL: ENSMUSP00000096950 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028800] [ENSMUST00000099349] [ENSMUST00000103188] [ENSMUST00000127862] [ENSMUST00000133602] [ENSMUST00000184121] [ENSMUST00000184535]

AlphaFold

Q9CZJ2

Predicted Effect

probably benign
Transcript: ENSMUST00000028800

SMART Domains

Protein: ENSMUSP00000028800
Gene: ENSMUSG00000027327

Domain	Start	End	E-Value	Type
Pfam:DUF4517	30	177	1.6e-56	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000099349
AA Change: A678P

PolyPhen 2 Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000096950
Gene: ENSMUSG00000074793
AA Change: A678P

Domain	Start	End	E-Value	Type
low complexity region	15	30	N/A	INTRINSIC
SCOP:d1bupa1	62	248	3e-14	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000103188

SMART Domains

Protein: ENSMUSP00000099477
Gene: ENSMUSG00000027327

Domain	Start	End	E-Value	Type
Pfam:DUF4517	27	174	1.1e-55	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000127862

Predicted Effect

probably benign
Transcript: ENSMUST00000133602

SMART Domains

Protein: ENSMUSP00000115000
Gene: ENSMUSG00000027327

Domain	Start	End	E-Value	Type
Pfam:DUF4517	27	140	3.5e-30	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136838

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152961

Predicted Effect

probably benign
Transcript: ENSMUST00000184121

Predicted Effect

probably benign
Transcript: ENSMUST00000184535

Meta Mutation Damage Score

0.4485

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.3%
20x: 92.8%

Validation Efficiency

98% (95/97)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains an atypical heat shock protein 70 (Hsp70) ATPase domain and is therefore a distant member of the mammalian Hsp70 family. This gene may be involved in susceptibility to atherosclerosis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]

Allele List at MGI

Other mutations in this stock

Total: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700036A12Rik	A	G	9: 60,769,761		noncoding transcript	Het
A430110L20Rik	T	A	1: 181,227,858		noncoding transcript	Het
Abce1	T	C	8: 79,707,235	K63R	possibly damaging	Het
Acp6	A	G	3: 97,173,788		probably benign	Het
Adamts13	T	A	2: 26,988,354	L579Q	probably damaging	Het
Adamtsl3	T	A	7: 82,523,320	M497K	probably damaging	Het
Adgrb2	T	A	4: 130,014,591	M1042K	possibly damaging	Het
Akap12	A	T	10: 4,353,693	S168C	probably damaging	Het
Akap3	A	T	6: 126,865,554	M379L	probably damaging	Het
Aldh6a1	C	T	12: 84,439,663	M135I	probably null	Het
Arhgef12	A	G	9: 42,988,998	S860P	probably damaging	Het
Atp11b	A	C	3: 35,789,558	T185P	probably damaging	Het
Bcas1	T	C	2: 170,387,951	D243G	probably damaging	Het
Cdhr2	T	A	13: 54,717,872	S228T	probably damaging	Het
Cic	T	C	7: 25,279,737		probably benign	Het
Cmya5	T	A	13: 93,065,327	I3376L	probably benign	Het
Ctrc	C	A	4: 141,846,224		probably null	Het
D230025D16Rik	T	C	8: 105,246,556		probably null	Het
Dchs1	G	T	7: 105,755,244	P2697Q	probably damaging	Het
Dmbt1	A	G	7: 131,044,487		probably benign	Het
Drd2	G	A	9: 49,402,212	R227H	probably damaging	Het
Dscc1	C	A	15: 55,086,764	C195F	probably damaging	Het
Dzip1	T	A	14: 118,922,713	M28L	probably benign	Het
Edar	A	T	10: 58,607,366	S313T	probably benign	Het
Eef1e1	C	A	13: 38,656,123	A69S	probably damaging	Het
Fbn1	A	G	2: 125,301,929	V2760A	probably benign	Het
Fez1	GACAAACA	GACA	9: 36,870,549		probably null	Het
Fgl1	C	G	8: 41,210,459	A11P	possibly damaging	Het
Fras1	T	C	5: 96,600,733	V689A	probably benign	Het
Fry	T	A	5: 150,380,859	D571E	probably damaging	Het
Gm11232	T	A	4: 71,757,213	R104*	probably null	Het
Gm1527	A	G	3: 28,918,050	I439V	possibly damaging	Het
Gm4922	C	A	10: 18,783,892	G361*	probably null	Het
Gm7052	T	A	17: 22,040,466		probably benign	Het
Gm7534	T	C	4: 134,196,833	D467G	probably benign	Het
Gpatch8	A	T	11: 102,481,229	S494R	unknown	Het
Gria2	A	T	3: 80,732,045	V220E	possibly damaging	Het
Grik4	G	A	9: 42,521,122	H860Y	probably benign	Het
Gtpbp1	A	C	15: 79,707,729	S93R	probably damaging	Het
Gucy2g	C	A	19: 55,215,036		probably benign	Het
Hist1h2ae	C	A	13: 23,571,047		probably benign	Het
Hmcn1	G	A	1: 150,609,700	R4384C	probably damaging	Het
Igsf21	T	A	4: 140,028,124	N407Y	probably damaging	Het
Insig2	A	G	1: 121,307,156	Y174H	probably benign	Het
Itpr3	T	A	17: 27,118,372	M2413K	probably benign	Het
Kalrn	A	T	16: 34,174,487	I1322N	probably damaging	Het
Klk1b24	T	A	7: 44,191,466	M106K	possibly damaging	Het
Krt81	G	T	15: 101,460,317	Q352K	probably benign	Het
Lca5l	A	T	16: 96,159,859	S468T	possibly damaging	Het
Lvrn	T	C	18: 46,882,385		probably benign	Het
Mcpt1	T	A	14: 56,019,164		probably benign	Het
Med13l	T	C	5: 118,738,459	M900T	probably benign	Het
Med16	A	G	10: 79,907,478		probably benign	Het
Megf6	G	T	4: 154,177,121	V68L	probably benign	Het
Mep1a	T	C	17: 43,491,672	H154R	probably damaging	Het
Mrc2	A	T	11: 105,337,772	D659V	probably benign	Het
Mroh8	T	A	2: 157,221,304	E799V	probably damaging	Het
Mrpl21	A	G	19: 3,284,808	Y50C	possibly damaging	Het
Msl1	A	G	11: 98,803,982		probably benign	Het
Myo1a	C	A	10: 127,719,937	Q932K	probably benign	Het
Nav3	A	C	10: 109,720,044	S1675R	probably damaging	Het
Neurl2	A	G	2: 164,832,746	V232A	possibly damaging	Het
Nfatc1	T	A	18: 80,665,267		probably benign	Het
Odf3l2	A	T	10: 79,645,558		probably benign	Het
Olfr1362	C	T	13: 21,611,822	C49Y	probably benign	Het
Olfr175-ps1	T	A	16: 58,824,676	E11V	probably null	Het
P4hb	A	G	11: 120,562,555		probably benign	Het
Papss1	T	G	3: 131,605,854	I281S	probably damaging	Het
Pde10a	A	T	17: 8,964,708	D832V	probably damaging	Het
Pfkfb2	A	T	1: 130,708,190	Y35N	possibly damaging	Het
Phf20l1	T	A	15: 66,604,813	F253Y	probably damaging	Het
Pkhd1l1	G	A	15: 44,516,115	V1046I	probably benign	Het
Plin3	C	T	17: 56,284,337	A148T	probably benign	Het
Ppp1r8	T	C	4: 132,840,631		probably benign	Het
Ppp2r3a	A	G	9: 101,211,312	L604P	probably damaging	Het
Prdm5	T	C	6: 65,883,601	V239A	probably damaging	Het
Prickle1	A	G	15: 93,500,638	S770P	probably damaging	Het
Prl2c5	T	A	13: 13,190,725	I155N	probably benign	Het
Prom1	T	C	5: 44,032,932		probably benign	Het
Psg25	C	T	7: 18,529,587	G104R	probably damaging	Het
Rbm19	T	C	5: 120,144,029	V817A	probably benign	Het
Ryr2	T	A	13: 11,727,022	Y2091F	probably damaging	Het
Slc16a4	A	G	3: 107,300,932	T253A	probably benign	Het
Smg7	A	T	1: 152,855,843		probably null	Het
Spink5	C	A	18: 44,007,719	H662N	probably benign	Het
Taf2	A	T	15: 55,059,915	M322K	probably damaging	Het
Tmc2	T	C	2: 130,248,762	F676S	probably damaging	Het
Tmem177	A	G	1: 119,910,185	S255P	possibly damaging	Het
Trim46	A	T	3: 89,235,068		probably null	Het
Tubb1	T	A	2: 174,450,803		probably null	Het
Upf1	T	C	8: 70,344,254	T110A	probably benign	Het
Vmn2r9	T	A	5: 108,848,984	I140L	probably benign	Het
Zfp638	T	A	6: 83,944,656	H588Q	probably damaging	Het
Zfp780b	T	A	7: 27,964,827	N101I	probably damaging	Het

Other mutations in Hspa12b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00235:Hspa12b	APN	2	131134120	missense	probably damaging	1.00
IGL01643:Hspa12b	APN	2	131142697	missense	probably damaging	1.00
IGL02145:Hspa12b	APN	2	131143735	unclassified	probably benign
IGL02441:Hspa12b	APN	2	131138595	missense	probably null	1.00
R0356:Hspa12b	UTSW	2	131144799	missense	possibly damaging	0.78
R1618:Hspa12b	UTSW	2	131140929	missense	probably benign
R1734:Hspa12b	UTSW	2	131138536	missense	possibly damaging	0.82
R2149:Hspa12b	UTSW	2	131143057	missense	probably damaging	0.98
R4091:Hspa12b	UTSW	2	131133488	splice site	probably null
R4234:Hspa12b	UTSW	2	131139012	missense	probably benign	0.00
R4235:Hspa12b	UTSW	2	131139012	missense	probably benign	0.00
R4243:Hspa12b	UTSW	2	131141858	missense	possibly damaging	0.90
R5133:Hspa12b	UTSW	2	131139508	missense	possibly damaging	0.86
R5134:Hspa12b	UTSW	2	131139508	missense	possibly damaging	0.86
R5228:Hspa12b	UTSW	2	131142964	missense	possibly damaging	0.82
R6358:Hspa12b	UTSW	2	131137066	critical splice donor site	probably benign
R7555:Hspa12b	UTSW	2	131138476	missense	probably damaging	1.00
R8035:Hspa12b	UTSW	2	131140939	missense	probably damaging	1.00
R8117:Hspa12b	UTSW	2	131138469	missense	possibly damaging	0.79
R8721:Hspa12b	UTSW	2	131141002	missense	probably benign	0.01
R8807:Hspa12b	UTSW	2	131145183	missense	probably benign	0.04
R9233:Hspa12b	UTSW	2	131134116	missense	probably damaging	1.00
X0065:Hspa12b	UTSW	2	131144561	splice site	probably null

Predicted Primers

PCR Primer
(F):5'- TCATCAATCTGTACTGCTGCGCTG -3'
(R):5'- TGCTGTGTCCACATCTCCAAACTG -3'

Sequencing Primer
(F):5'- GCTTCATCACTGACCCTGG -3'
(R):5'- ACCTCAAGTTCAGGTCAGTG -3'

Posted On

2014-03-14