Mutagenetix > Incidental Mutation

Incidental Mutation 'R6805:Acot10'

533555

Institutional Source

Beutler Lab

Gene Symbol

Acot10

Ensembl Gene

ENSMUSG00000047565

Gene Name

acyl-CoA thioesterase 10

Synonyms

MT-ACT48, p48, Acate3

MMRRC Submission

044918-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.116) question?

Stock #

R6805 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

20665214-20666750 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 20665366 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Proline at position 430 (T430P)

Ref Sequence

ENSEMBL: ENSMUSP00000051333 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052910]

AlphaFold

Q32MW3

Predicted Effect

probably benign
Transcript: ENSMUST00000052910
AA Change: T430P

PolyPhen 2 Score 0.417 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000051333
Gene: ENSMUSG00000047565
AA Change: T430P

Domain	Start	End	E-Value	Type
SCOP:d1lo7a_	108	222	1e-4	SMART
PDB:4IEN\|D	277	400	3e-6	PDB

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.8%
20x: 97.1%

Validation Efficiency

98% (62/63)

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410089E03Rik	T	C	15: 8,244,306 (GRCm38)	V2591A	probably benign	Het
4930407I10Rik	A	G	15: 82,062,543 (GRCm38)	T214A	possibly damaging	Het
A930009A15Rik	G	T	10: 115,579,905 (GRCm38)		probably benign	Het
Aadac	A	C	3: 60,037,336 (GRCm38)	D143A	probably benign	Het
Adgrb3	T	C	1: 25,826,172 (GRCm38)	T197A	possibly damaging	Het
B230118H07Rik	T	C	2: 101,566,459 (GRCm38)	K192E	probably benign	Het
Bbs1	A	G	19: 4,900,615 (GRCm38)	I200T	probably damaging	Het
C1ra	G	A	6: 124,517,725 (GRCm38)	E316K	probably benign	Het
Cadps	G	A	14: 12,467,103 (GRCm38)	A943V	probably damaging	Het
Cc2d2a	A	G	5: 43,681,331 (GRCm38)	E48G	probably damaging	Het
Clca1	A	T	3: 145,018,667 (GRCm38)	C211S	probably damaging	Het
Col18a1	A	G	10: 77,054,239 (GRCm38)	L1429P	probably damaging	Het
Cul2	T	G	18: 3,421,263 (GRCm38)	Y196D	probably damaging	Het
D630023F18Rik	T	C	1: 65,117,206 (GRCm38)	S43G	probably benign	Het
Ddx39	G	A	8: 83,723,137 (GRCm38)	R427Q	probably damaging	Het
Def6	A	G	17: 28,223,717 (GRCm38)	T285A	probably damaging	Het
Defb21	T	A	2: 152,574,869 (GRCm38)	D88E	probably benign	Het
Defb6	A	G	8: 19,228,101 (GRCm38)	K63R	probably benign	Het
Dnph1	T	C	17: 46,498,744 (GRCm38)	S112P	probably damaging	Het
Dock10	T	A	1: 80,586,690 (GRCm38)	I467L	probably benign	Het
Dspp	C	A	5: 104,175,850 (GRCm38)	H286Q	probably benign	Het
Eya1	T	A	1: 14,183,277 (GRCm38)	T459S	probably benign	Het
Faf1	T	C	4: 109,861,852 (GRCm38)	L385P	probably damaging	Het
Fbxw21	C	A	9: 109,157,565 (GRCm38)	R82L	probably damaging	Het
Fryl	A	G	5: 73,065,094 (GRCm38)	V2048A	probably benign	Het
Galnt5	A	T	2: 58,035,299 (GRCm38)	D864V	possibly damaging	Het
Gata6	T	G	18: 11,054,460 (GRCm38)	S130A	possibly damaging	Het
Gbf1	G	T	19: 46,262,507 (GRCm38)	R434L	probably damaging	Het
Gga3	A	G	11: 115,585,762 (GRCm38)	F709L	probably damaging	Het
Hcar1	A	G	5: 123,879,130 (GRCm38)	V166A	probably benign	Het
Hexa	T	A	9: 59,563,937 (GRCm38)	N491K	possibly damaging	Het
Hpse2	A	T	19: 43,294,321 (GRCm38)	C164*	probably null	Het
Ifi202b	T	C	1: 173,974,989 (GRCm38)	Y93C	probably damaging	Het
Iscu	T	A	5: 113,775,243 (GRCm38)	I79N	probably damaging	Het
Jmjd7	T	A	2: 120,031,323 (GRCm38)	Y182*	probably null	Het
Jup	A	T	11: 100,383,458 (GRCm38)	D135E	probably benign	Het
Kit	T	A	5: 75,652,808 (GRCm38)	I881N	probably damaging	Het
Llgl1	T	A	11: 60,702,865 (GRCm38)	S55T	probably benign	Het
Lonp2	G	A	8: 86,709,096 (GRCm38)	M653I	probably benign	Het
Lrp8	T	C	4: 107,854,320 (GRCm38)	Y307H	probably damaging	Het
Med13	A	T	11: 86,278,796 (GRCm38)	M1914K	possibly damaging	Het
Ms4a1	A	G	19: 11,253,173 (GRCm38)		probably null	Het
Naip1	A	G	13: 100,427,341 (GRCm38)	S439P	probably benign	Het
Nrg1	T	C	8: 31,821,264 (GRCm38)	R476G	probably damaging	Het
Olfr1129	T	A	2: 87,574,918 (GRCm38)		probably null	Het
Olfr835	G	T	9: 19,035,301 (GRCm38)	M59I	probably damaging	Het
Pds5b	T	A	5: 150,805,561 (GRCm38)		probably null	Het
Phf12	G	A	11: 78,027,373 (GRCm38)	G804R	probably damaging	Het
Pou6f2	T	C	13: 18,239,489 (GRCm38)	T234A		Het
Prune2	A	T	19: 17,120,590 (GRCm38)	I1153L	probably benign	Het
Ptprc	C	T	1: 138,067,885 (GRCm38)		probably null	Het
Qpctl	T	C	7: 19,149,154 (GRCm38)	Q11R	probably benign	Het
Rfx4	A	G	10: 84,840,228 (GRCm38)	K103E	possibly damaging	Het
Srcin1	T	A	11: 97,551,980 (GRCm38)		probably null	Het
St6galnac1	G	T	11: 116,768,944 (GRCm38)	A181D	probably damaging	Het
Stk36	T	C	1: 74,622,239 (GRCm38)	V475A	probably benign	Het
Tbc1d21	T	C	9: 58,361,288 (GRCm38)	T263A	possibly damaging	Het
Tex24	A	T	8: 27,345,000 (GRCm38)	K185N	probably damaging	Het
Tnxb	T	A	17: 34,698,153 (GRCm38)	V2174E	possibly damaging	Het
Tollip	A	G	7: 141,890,845 (GRCm38)	S57P	probably benign	Het
Zbtb49	A	G	5: 38,213,241 (GRCm38)		probably benign	Het
Zfp758	A	G	17: 22,361,669 (GRCm38)	T30A	probably benign	Het

Other mutations in Acot10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01306:Acot10	APN	15	20,665,965 (GRCm38)	missense	probably benign	0.11
IGL01610:Acot10	APN	15	20,665,695 (GRCm38)	missense	probably damaging	1.00
IGL02457:Acot10	APN	15	20,666,143 (GRCm38)	missense	possibly damaging	0.88
IGL02587:Acot10	APN	15	20,665,797 (GRCm38)	missense	possibly damaging	0.93
IGL02951:Acot10	APN	15	20,665,782 (GRCm38)	missense	probably benign	0.36
ANU23:Acot10	UTSW	15	20,665,965 (GRCm38)	missense	probably benign	0.11
PIT4151001:Acot10	UTSW	15	20,666,598 (GRCm38)	missense	probably damaging	0.98
R0026:Acot10	UTSW	15	20,666,236 (GRCm38)	missense	probably benign	0.10
R0026:Acot10	UTSW	15	20,666,236 (GRCm38)	missense	probably benign	0.10
R0462:Acot10	UTSW	15	20,666,626 (GRCm38)	missense	possibly damaging	0.85
R1312:Acot10	UTSW	15	20,666,499 (GRCm38)	missense	probably benign	0.00
R1495:Acot10	UTSW	15	20,665,507 (GRCm38)	missense	probably damaging	0.99
R2128:Acot10	UTSW	15	20,666,626 (GRCm38)	missense	probably benign	0.00
R3779:Acot10	UTSW	15	20,665,542 (GRCm38)	missense	probably damaging	0.98
R4110:Acot10	UTSW	15	20,666,526 (GRCm38)	missense	probably damaging	1.00
R4111:Acot10	UTSW	15	20,666,526 (GRCm38)	missense	probably damaging	1.00
R4464:Acot10	UTSW	15	20,665,744 (GRCm38)	nonsense	probably null
R4668:Acot10	UTSW	15	20,665,942 (GRCm38)	missense	probably benign
R4933:Acot10	UTSW	15	20,666,330 (GRCm38)	missense	possibly damaging	0.88
R5255:Acot10	UTSW	15	20,665,932 (GRCm38)	missense	probably benign	0.01
R5885:Acot10	UTSW	15	20,666,104 (GRCm38)	missense	probably benign	0.01
R6190:Acot10	UTSW	15	20,665,785 (GRCm38)	missense	possibly damaging	0.80
R6301:Acot10	UTSW	15	20,666,262 (GRCm38)	missense	probably benign	0.05
R7334:Acot10	UTSW	15	20,665,543 (GRCm38)	missense	possibly damaging	0.86
R7601:Acot10	UTSW	15	20,665,629 (GRCm38)	missense	probably damaging	1.00
R8400:Acot10	UTSW	15	20,666,172 (GRCm38)	missense	possibly damaging	0.56
R9195:Acot10	UTSW	15	20,665,431 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGGCAAATTTGTGAACAGGTTC -3'
(R):5'- ATGTTTCAGAAGCCTGTTGAAGTTG -3'

Sequencing Primer
(F):5'- GTGAACAGGTTCTTAAAATTCCATG -3'
(R):5'- GGTATGCTTCACCCAGGGTAATTAC -3'

Posted On

2018-09-12