Mutagenetix > Incidental Mutation

Incidental Mutation 'R7692:Hspa14'

593432

Institutional Source

Beutler Lab

Gene Symbol

Hspa14

Ensembl Gene

ENSMUSG00000109865

Gene Name

heat shock protein 14

Synonyms

HSP70L1, 70kDa, NST-1, Hsp70-4

MMRRC Submission

045756-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.201) question?

Stock #

R7692 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

3489891-3513851 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 3497643 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 283 (D283G)

Ref Sequence

ENSEMBL: ENSMUSP00000027961 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027961]

AlphaFold

Q99M31

Predicted Effect

probably damaging
Transcript: ENSMUST00000027961
AA Change: D283G

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

SMART Domains

Protein: ENSMUSP00000027961
Gene: ENSMUSG00000109865
AA Change: D283G

Domain	Start	End	E-Value	Type
Pfam:HSP70	3	509	6.3e-115	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam26b	G	A	8: 43,973,832 (GRCm39)	T390I	probably benign	Het
Adgb	A	G	10: 10,287,456 (GRCm39)		probably null	Het
Ado	G	T	10: 67,384,265 (GRCm39)	Y113*	probably null	Het
Angptl1	A	G	1: 156,672,885 (GRCm39)	E237G	probably damaging	Het
Arid2	T	A	15: 96,254,578 (GRCm39)	Y141*	probably null	Het
Clvs1	T	C	4: 9,350,739 (GRCm39)	I183T	probably benign	Het
Dnah1	T	C	14: 31,014,295 (GRCm39)	K1817E	probably benign	Het
Eif3e	C	A	15: 43,126,642 (GRCm39)	R271L	probably damaging	Het
Eml6	A	G	11: 29,703,085 (GRCm39)	V1611A	probably damaging	Het
Enpp3	G	T	10: 24,660,739 (GRCm39)	Y634*	probably null	Het
Evi5l	C	T	8: 4,250,886 (GRCm39)	R394W	probably damaging	Het
Fcgr3	A	C	1: 170,881,661 (GRCm39)	F156V	probably damaging	Het
Fmo1	T	A	1: 162,661,402 (GRCm39)	T294S	probably benign	Het
Gabrb3	A	G	7: 57,466,203 (GRCm39)	Q339R	probably damaging	Het
Gen1	T	A	12: 11,292,167 (GRCm39)	T606S	probably benign	Het
Gfod1	T	C	13: 43,354,528 (GRCm39)	Q149R	probably benign	Het
Golm1	A	G	13: 59,788,071 (GRCm39)	V276A	probably benign	Het
Hc	C	A	2: 34,914,161 (GRCm39)	V849F	probably damaging	Het
Hectd4	T	C	5: 121,459,627 (GRCm39)	I832T	possibly damaging	Het
Lztfl1	C	T	9: 123,541,536 (GRCm39)	W94*	probably null	Het
Lzts3	T	C	2: 130,477,306 (GRCm39)	S381G	probably benign	Het
Mgat2	A	G	12: 69,231,444 (GRCm39)	Y6C	probably damaging	Het
Mrpl30	T	C	1: 37,934,439 (GRCm39)	I27T	probably benign	Het
Muc5b	A	T	7: 141,406,966 (GRCm39)	T1045S	unknown	Het
Nlrp4a	G	A	7: 26,148,690 (GRCm39)	R99Q	probably benign	Het
Or10g1	T	C	14: 52,647,945 (GRCm39)	Y128C	probably damaging	Het
Or5b98	A	G	19: 12,931,006 (GRCm39)	T18A	possibly damaging	Het
Phlpp1	T	C	1: 106,209,132 (GRCm39)	L495P	probably damaging	Het
Pla2g4d	T	C	2: 120,109,776 (GRCm39)	D178G	possibly damaging	Het
Prl5a1	C	G	13: 28,333,997 (GRCm39)	L167V	probably damaging	Het
Sardh	A	G	2: 27,087,651 (GRCm39)	V740A	probably benign	Het
Sbno1	T	G	5: 124,543,709 (GRCm39)	T277P	probably benign	Het
Slc2a1	T	C	4: 118,993,462 (GRCm39)	V433A	probably damaging	Het
Slc4a10	T	C	2: 62,134,308 (GRCm39)	V1008A	possibly damaging	Het
Smarcal1	T	G	1: 72,625,179 (GRCm39)	S109A	probably benign	Het
Speg	A	G	1: 75,377,834 (GRCm39)	D864G	probably benign	Het
Steap4	T	C	5: 8,026,976 (GRCm39)	I313T	probably benign	Het
Tab2	A	T	10: 7,786,869 (GRCm39)	D614E	probably damaging	Het
Tenm4	A	G	7: 96,544,610 (GRCm39)	K2246E	probably damaging	Het
Timm23	A	G	14: 31,902,520 (GRCm39)	S208P	probably damaging	Het
Tmem229a	C	A	6: 24,955,211 (GRCm39)	C181F	probably benign	Het
Ugdh	T	C	5: 65,574,958 (GRCm39)	Y356C	probably damaging	Het
Ugt2a1	A	G	5: 87,634,586 (GRCm39)	L7P	probably damaging	Het
Uhrf1	A	G	17: 56,619,905 (GRCm39)	D272G	possibly damaging	Het
Vmn1r206	T	A	13: 22,804,827 (GRCm39)	I127F	probably damaging	Het
Vmn2r106	T	C	17: 20,505,490 (GRCm39)	Y68C	possibly damaging	Het
Zfand6	G	A	7: 84,283,141 (GRCm39)	P72L	not run	Het

Other mutations in Hspa14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00857:Hspa14	APN	2	3,503,796 (GRCm39)	missense	probably damaging	1.00
IGL02293:Hspa14	APN	2	3,512,071 (GRCm39)	missense	probably damaging	1.00
IGL02477:Hspa14	APN	2	3,497,661 (GRCm39)	missense	probably damaging	0.98
IGL02711:Hspa14	APN	2	3,503,557 (GRCm39)	missense	probably benign	0.15
R0522:Hspa14	UTSW	2	3,512,086 (GRCm39)	missense	probably damaging	1.00
R1169:Hspa14	UTSW	2	3,499,161 (GRCm39)	missense	possibly damaging	0.90
R1426:Hspa14	UTSW	2	3,509,858 (GRCm39)	missense	probably damaging	1.00
R1471:Hspa14	UTSW	2	3,492,645 (GRCm39)	missense	probably benign	0.01
R1846:Hspa14	UTSW	2	3,492,697 (GRCm39)	missense	possibly damaging	0.50
R1971:Hspa14	UTSW	2	3,490,804 (GRCm39)	missense	possibly damaging	0.51
R2353:Hspa14	UTSW	2	3,512,213 (GRCm39)	splice site	probably null
R3508:Hspa14	UTSW	2	3,492,045 (GRCm39)	missense	probably damaging	1.00
R3859:Hspa14	UTSW	2	3,495,616 (GRCm39)	nonsense	probably null
R4012:Hspa14	UTSW	2	3,513,675 (GRCm39)	missense	probably damaging	0.99
R4360:Hspa14	UTSW	2	3,503,560 (GRCm39)	missense	possibly damaging	0.89
R4938:Hspa14	UTSW	2	3,492,646 (GRCm39)	missense	probably benign	0.01
R5028:Hspa14	UTSW	2	3,499,206 (GRCm39)	missense	possibly damaging	0.72
R5326:Hspa14	UTSW	2	3,503,560 (GRCm39)	missense	possibly damaging	0.89
R5542:Hspa14	UTSW	2	3,503,560 (GRCm39)	missense	possibly damaging	0.89
R5881:Hspa14	UTSW	2	3,499,207 (GRCm39)	missense	probably benign	0.34
R6046:Hspa14	UTSW	2	3,490,801 (GRCm39)	missense	possibly damaging	0.91
R6076:Hspa14	UTSW	2	3,512,109 (GRCm39)	missense	probably benign	0.00
R6112:Hspa14	UTSW	2	3,499,105 (GRCm39)	missense	probably benign
R6334:Hspa14	UTSW	2	3,490,109 (GRCm39)	splice site	probably null
R7297:Hspa14	UTSW	2	3,499,179 (GRCm39)	missense	possibly damaging	0.76
R7424:Hspa14	UTSW	2	3,490,078 (GRCm39)	missense	possibly damaging	0.95
R7510:Hspa14	UTSW	2	3,499,159 (GRCm39)	missense	probably benign	0.01
R8394:Hspa14	UTSW	2	3,513,670 (GRCm39)	critical splice donor site	probably null
R9780:Hspa14	UTSW	2	3,490,741 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AAACTGCAGCAGCTATTGAGTC -3'
(R):5'- GAAGCCATGTTGCTACTTCTTG -3'

Sequencing Primer
(F):5'- GGAAAGCTGTTCACTGGA -3'
(R):5'- CATAATGGTGTTTAGAATTTGGTGAC -3'

Posted On

2019-11-12