Mutagenetix > Incidental Mutation

Incidental Mutation 'R6112:Hspa14'

484881

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

044261-MU

Accession Numbers

Essential gene?

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

Stock #

R6112 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

3489891-3513851 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 3499105 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Tyrosine at position 230 (H230Y)

Ref Sequence

ENSEMBL: ENSMUSP00000027961 (fasta)

Gene Model

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

AlphaFold

Q99M31

Predicted Effect

probably benign
Transcript: ENSMUST00000027961
AA Change: H230Y

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000027961
Gene: ENSMUSG00000109865
AA Change: H230Y

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135157

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139485

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 95.1%

Validation Efficiency

98% (54/55)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc1	A	G	16: 14,278,780 (GRCm39)	Y1030C	probably damaging	Het
Adh5	G	T	3: 138,157,029 (GRCm39)	V197F	probably damaging	Het
Ankmy1	A	T	1: 92,798,684 (GRCm39)	F936I	probably damaging	Het
Aoc1	A	T	6: 48,885,625 (GRCm39)	D710V	probably damaging	Het
Aplp1	T	C	7: 30,134,902 (GRCm39)	E622G	probably damaging	Het
Arhgap20	T	C	9: 51,740,684 (GRCm39)	Y219H	probably damaging	Het
Bag3	A	G	7: 128,143,556 (GRCm39)	D184G	probably damaging	Het
Cacna1g	C	T	11: 94,300,072 (GRCm39)	A2216T	probably damaging	Het
Cbarp	T	C	10: 79,971,205 (GRCm39)		probably null	Het
Cep250	C	A	2: 155,836,503 (GRCm39)	L2211I	possibly damaging	Het
Cfap65	A	G	1: 74,942,298 (GRCm39)	I1752T	probably benign	Het
Col4a4	A	G	1: 82,431,604 (GRCm39)	V1560A	unknown	Het
Dapk3	A	T	10: 81,019,864 (GRCm39)	Q6L	probably benign	Het
Dctn5	A	G	7: 121,732,460 (GRCm39)		probably benign	Het
Eef1akmt1	A	T	14: 57,787,330 (GRCm39)	I182N	possibly damaging	Het
Eef1g	T	C	19: 8,954,955 (GRCm39)	F346S	probably damaging	Het
Erap1	G	T	13: 74,794,398 (GRCm39)	W19L	probably benign	Het
Gm10801	A	G	2: 98,494,409 (GRCm39)	H162R	probably benign	Het
Gpm6a	G	A	8: 55,507,845 (GRCm39)	A194T	probably benign	Het
Grip1	C	A	10: 119,829,137 (GRCm39)	N32K	probably benign	Het
Hmcn1	A	G	1: 150,494,687 (GRCm39)	I4134T	probably damaging	Het
Ift172	T	C	5: 31,414,241 (GRCm39)	T1435A	probably benign	Het
Igsf3	T	A	3: 101,358,322 (GRCm39)	Y738N	probably damaging	Het
Lcor	T	C	19: 41,547,520 (GRCm39)	V368A	possibly damaging	Het
Lmna	C	A	3: 88,393,928 (GRCm39)	E217*	probably null	Het
Lrp1b	C	T	2: 41,231,894 (GRCm39)	G337E	probably benign	Het
Maf1	A	G	15: 76,236,312 (GRCm39)		probably benign	Het
Magi1	T	C	6: 93,722,571 (GRCm39)	I436V	probably damaging	Het
Muc4	C	T	16: 32,596,157 (GRCm39)	T3123I	possibly damaging	Het
Muc5b	T	A	7: 141,417,042 (GRCm39)	H3329Q	probably benign	Het
Noa1	C	T	5: 77,457,593 (GRCm39)	R104Q	probably benign	Het
Odc1	T	G	12: 17,599,473 (GRCm39)	S267A	probably benign	Het
Or5p60	T	A	7: 107,724,369 (GRCm39)	I34F	probably benign	Het
Pam	A	G	1: 97,762,193 (GRCm39)	Y691H	probably damaging	Het
Pamr1	T	C	2: 102,441,953 (GRCm39)	Y181H	probably damaging	Het
Pcdhga2	T	A	18: 37,802,612 (GRCm39)	I152N	probably damaging	Het
Pigt	C	T	2: 164,348,365 (GRCm39)	Q437*	probably null	Het
Prx	T	C	7: 27,215,973 (GRCm39)	L158P	probably damaging	Het
Ptprh	T	A	7: 4,600,922 (GRCm39)	T152S	probably benign	Het
Pum1	G	A	4: 130,457,591 (GRCm39)	R201H	probably damaging	Het
Rad51ap2	T	C	12: 11,507,290 (GRCm39)	I404T	probably benign	Het
Radil	C	T	5: 142,529,399 (GRCm39)	R99H	probably damaging	Het
Rc3h2	C	T	2: 37,268,899 (GRCm39)	V856I	possibly damaging	Het
Slx4ip	T	A	2: 136,888,664 (GRCm39)	V115E	probably damaging	Het
Snx3	C	A	10: 42,402,042 (GRCm39)	S85R	probably benign	Het
Sppl2c	A	T	11: 104,077,963 (GRCm39)	E254D	probably benign	Het
Srms	C	A	2: 180,849,780 (GRCm39)	E237*	probably null	Het
Tenm1	C	T	X: 41,916,072 (GRCm39)	G404E	probably damaging	Het
Trank1	T	C	9: 111,220,805 (GRCm39)	L2514P	probably damaging	Het
Trib1	C	T	15: 59,523,487 (GRCm39)	R174*	probably null	Het
Usp4	A	G	9: 108,233,703 (GRCm39)	Y108C	probably damaging	Het
Vmn2r60	A	T	7: 41,844,847 (GRCm39)	I737F	probably damaging	Het
Zfp600	A	T	4: 146,131,701 (GRCm39)	H123L	probably benign	Het
Zfp646	G	T	7: 127,478,190 (GRCm39)	R122S	possibly damaging	Het
Znfx1	A	G	2: 166,880,126 (GRCm39)	Y553H	probably benign	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
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
R7692:Hspa14	UTSW	2	3,497,643 (GRCm39)	missense	probably damaging	1.00
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'- CTCTATAAGAGGCTGAGCTACCTCC -3'
(R):5'- ACGAATGGCTTCAAAAGTACAG -3'

Sequencing Primer
(F):5'- TGAGCTACCTCCCCAGC -3'
(R):5'- TGGCTTCAAAAGTACAGTCTGGC -3'

Posted On

2017-08-16