Mutagenetix > Incidental Mutation

Incidental Mutation 'R7283:Acad10'

565786

Institutional Source

Beutler Lab

Gene Symbol

Acad10

Ensembl Gene

ENSMUSG00000029456

Gene Name

acyl-Coenzyme A dehydrogenase family, member 10

Synonyms

2410021P16Rik

MMRRC Submission

045361-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7283 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

121759089-121798577 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 121787538 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 137 (V137G)

Ref Sequence

ENSEMBL: ENSMUSP00000031412 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031412] [ENSMUST00000111770]

AlphaFold

Q8K370

Predicted Effect

possibly damaging
Transcript: ENSMUST00000031412
AA Change: V137G

PolyPhen 2 Score 0.788 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000031412
Gene: ENSMUSG00000029456
AA Change: V137G

Domain	Start	End	E-Value	Type
Pfam:HAD_2	45	231	1.6e-14	PFAM
Pfam:Hydrolase	88	225	5e-8	PFAM
Pfam:APH	287	531	1.8e-52	PFAM
Pfam:Acyl-CoA_dh_N	660	787	1.7e-15	PFAM
Pfam:Acyl-CoA_dh_M	791	892	2.7e-20	PFAM
Pfam:Acyl-CoA_dh_1	904	1055	1.1e-35	PFAM
Pfam:Acyl-CoA_dh_2	919	1037	6.4e-13	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000111770
AA Change: V137G

PolyPhen 2 Score 0.788 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000107400
Gene: ENSMUSG00000029456
AA Change: V137G

Domain	Start	End	E-Value	Type
Pfam:HAD_2	45	231	2.3e-14	PFAM
Pfam:APH	287	523	3.2e-50	PFAM
Pfam:EcKinase	390	504	5.2e-8	PFAM
Pfam:Acyl-CoA_dh_N	660	787	3.4e-14	PFAM
Pfam:Acyl-CoA_dh_M	791	845	2.7e-13	PFAM
Pfam:Acyl-CoA_dh_1	904	1055	9.4e-36	PFAM
Pfam:Acyl-CoA_dh_2	919	1037	1.6e-14	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.5%

Validation Efficiency

100% (72/72)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes (ACADs), which participate in the beta-oxidation of fatty acids in mitochondria. The encoded enzyme contains a hydrolase domain at the N-terminal portion, a serine/threonine protein kinase catlytic domain in the central region, and a conserved ACAD domain at the C-terminus. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Nov 2008]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4833439L19Rik	A	G	13: 54,700,504 (GRCm39)	V278A	probably benign	Het
Abcc3	C	T	11: 94,247,873 (GRCm39)	A1207T	probably benign	Het
Abce1	C	A	8: 80,411,885 (GRCm39)	G592*	probably null	Het
Adcy3	A	G	12: 4,253,563 (GRCm39)	I672V	not run	Het
Adgrb1	A	T	15: 74,452,512 (GRCm39)	Q1166L	possibly damaging	Het
Ankrd44	A	T	1: 54,768,955 (GRCm39)	N465K	probably damaging	Het
Avpr1b	A	G	1: 131,537,469 (GRCm39)	T418A	probably benign	Het
Azin1	G	A	15: 38,501,652 (GRCm39)	T33I	probably damaging	Het
Bicra	T	C	7: 15,706,425 (GRCm39)	T1339A	probably damaging	Het
Bltp2	A	G	11: 78,165,654 (GRCm39)	Q1346R	probably damaging	Het
Cacna1s	A	G	1: 136,001,446 (GRCm39)	Y299C	probably damaging	Het
Clip1	A	C	5: 123,751,857 (GRCm39)	C641W		Het
Clip3	T	C	7: 30,005,237 (GRCm39)	S524P	probably damaging	Het
Cnpy4	A	T	5: 138,191,144 (GRCm39)	H240L	probably benign	Het
Cyp2b19	T	C	7: 26,466,339 (GRCm39)	Y381H	probably damaging	Het
Cyp3a13	T	A	5: 137,903,818 (GRCm39)	N280I	probably benign	Het
Diaph3	A	G	14: 87,104,020 (GRCm39)	F788S	probably damaging	Het
Drc7	A	G	8: 95,798,207 (GRCm39)	N484S	probably damaging	Het
Erap1	G	A	13: 74,821,903 (GRCm39)		probably null	Het
Fat4	A	T	3: 38,943,842 (GRCm39)	I912F	probably damaging	Het
Hsd3b3	T	A	3: 98,649,673 (GRCm39)	K217*	probably null	Het
Igkv12-89	A	G	6: 68,812,061 (GRCm39)	V36A	probably damaging	Het
Invs	T	A	4: 48,392,526 (GRCm39)		probably null	Het
Ipo8	T	A	6: 148,725,979 (GRCm39)	Y30F	possibly damaging	Het
Kctd14	T	C	7: 97,100,693 (GRCm39)	M1T	probably null	Het
Klrb1c	A	T	6: 128,761,220 (GRCm39)	C136S	probably benign	Het
Morn2	A	G	17: 80,604,688 (GRCm39)	E48G	probably damaging	Het
Myh1	A	T	11: 67,092,670 (GRCm39)		probably null	Het
Nbeal1	G	C	1: 60,276,310 (GRCm39)	V684L	probably benign	Het
Nfxl1	A	G	5: 72,686,393 (GRCm39)	S603P	probably benign	Het
Nlrc3	G	A	16: 3,765,741 (GRCm39)	A351V	probably benign	Het
Nlrp4f	G	A	13: 65,343,352 (GRCm39)	R76*	probably null	Het
Or1e1f	T	C	11: 73,855,634 (GRCm39)	S67P	probably damaging	Het
Or52n1	G	T	7: 104,382,800 (GRCm39)	T257K	probably damaging	Het
Or5h22	A	T	16: 58,894,555 (GRCm39)	M296K	probably benign	Het
Or7e176	A	C	9: 20,171,555 (GRCm39)	I140L	probably damaging	Het
Or8k41	A	T	2: 86,313,483 (GRCm39)	I201N	probably damaging	Het
Papolg	A	G	11: 23,817,394 (GRCm39)	V601A	not run	Het
Pde4dip	T	C	3: 97,666,198 (GRCm39)	T349A	probably benign	Het
Pdlim5	T	C	3: 142,017,741 (GRCm39)		probably null	Het
Pkhd1l1	A	G	15: 44,366,676 (GRCm39)	N718S	probably benign	Het
Plcxd3	A	G	15: 4,546,401 (GRCm39)	H135R	probably damaging	Het
Plxna2	A	T	1: 194,327,191 (GRCm39)	Y375F	probably damaging	Het
Prkca	C	T	11: 108,231,471 (GRCm39)		probably null	Het
Prkdc	A	G	16: 15,535,628 (GRCm39)	S1663G	probably benign	Het
Ptbp3	T	C	4: 59,514,384 (GRCm39)	T80A	probably benign	Het
Ptpn4	C	T	1: 119,610,261 (GRCm39)	V696I	possibly damaging	Het
Pygl	A	T	12: 70,263,342 (GRCm39)	W175R	possibly damaging	Het
Rftn1	A	G	17: 50,354,469 (GRCm39)	Y298H	probably damaging	Het
Rit2	A	G	18: 31,449,892 (GRCm39)		probably null	Het
Runx1t1	G	A	4: 13,846,935 (GRCm39)	G240R	probably damaging	Het
Scn10a	A	G	9: 119,493,845 (GRCm39)		probably null	Het
Serpina16	A	C	12: 103,638,691 (GRCm39)		probably null	Het
Slc17a3	A	T	13: 24,039,831 (GRCm39)	M290L		Het
Slc6a4	A	T	11: 76,901,522 (GRCm39)	M86L	probably benign	Het
Spag7	A	T	11: 70,556,139 (GRCm39)	V46E	probably benign	Het
Spata31h1	G	A	10: 82,127,131 (GRCm39)	R1960W	possibly damaging	Het
Sptlc1	T	C	13: 53,498,914 (GRCm39)	I271V	probably benign	Het
Stk17b	A	C	1: 53,796,674 (GRCm39)	H364Q	probably benign	Het
Strc	T	C	2: 121,209,933 (GRCm39)	H130R	probably damaging	Het
Stxbp1	T	A	2: 32,705,026 (GRCm39)	D148V	probably damaging	Het
Tirap	G	A	9: 35,100,225 (GRCm39)	P153L	probably damaging	Het
Tmco3	G	A	8: 13,369,605 (GRCm39)		probably null	Het
Tmem51	T	A	4: 141,759,094 (GRCm39)	D218V	probably damaging	Het
Trim40	A	T	17: 37,193,554 (GRCm39)	D218E	probably benign	Het
Ttc21b	T	C	2: 66,039,062 (GRCm39)	D934G	probably damaging	Het
Vmn2r26	T	C	6: 124,002,914 (GRCm39)	L108P	probably damaging	Het
Washc2	C	A	6: 116,204,379 (GRCm39)	P429Q	probably damaging	Het
Wipi1	A	G	11: 109,502,137 (GRCm39)	M1T	probably null	Het
Zfp438	A	G	18: 5,214,712 (GRCm39)	V82A	probably damaging	Het
Zfp853	G	C	5: 143,273,493 (GRCm39)	A724G	unknown	Het

Other mutations in Acad10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02379:Acad10	APN	5	121,760,106 (GRCm39)	missense	probably damaging	1.00
IGL02469:Acad10	APN	5	121,783,522 (GRCm39)	missense	probably damaging	1.00
IGL02526:Acad10	APN	5	121,784,923 (GRCm39)	missense	probably damaging	0.99
IGL02623:Acad10	APN	5	121,767,993 (GRCm39)	missense	possibly damaging	0.94
IGL02643:Acad10	APN	5	121,769,633 (GRCm39)	missense	probably benign
IGL02685:Acad10	APN	5	121,770,672 (GRCm39)	missense	probably benign
IGL03139:Acad10	APN	5	121,764,145 (GRCm39)	missense	probably benign
IGL03267:Acad10	APN	5	121,775,412 (GRCm39)	missense	probably benign	0.34
P0026:Acad10	UTSW	5	121,775,415 (GRCm39)	missense	probably damaging	1.00
R0099:Acad10	UTSW	5	121,759,353 (GRCm39)	missense	probably damaging	1.00
R0453:Acad10	UTSW	5	121,765,445 (GRCm39)	nonsense	probably null
R1051:Acad10	UTSW	5	121,764,143 (GRCm39)	missense	probably damaging	0.97
R1052:Acad10	UTSW	5	121,787,604 (GRCm39)	missense	possibly damaging	0.65
R1116:Acad10	UTSW	5	121,768,814 (GRCm39)	missense	probably damaging	1.00
R1548:Acad10	UTSW	5	121,764,104 (GRCm39)	splice site	probably benign
R1548:Acad10	UTSW	5	121,764,103 (GRCm39)	splice site	probably benign
R1571:Acad10	UTSW	5	121,759,411 (GRCm39)	missense	probably damaging	0.99
R1592:Acad10	UTSW	5	121,783,444 (GRCm39)	missense	probably damaging	0.99
R1741:Acad10	UTSW	5	121,785,899 (GRCm39)	missense	probably damaging	1.00
R1789:Acad10	UTSW	5	121,769,456 (GRCm39)	missense	possibly damaging	0.67
R1974:Acad10	UTSW	5	121,764,248 (GRCm39)	missense	possibly damaging	0.95
R2007:Acad10	UTSW	5	121,772,814 (GRCm39)	missense	probably damaging	1.00
R2085:Acad10	UTSW	5	121,787,523 (GRCm39)	missense	possibly damaging	0.79
R2351:Acad10	UTSW	5	121,767,990 (GRCm39)	missense	probably benign	0.23
R2511:Acad10	UTSW	5	121,769,630 (GRCm39)	missense	probably benign	0.02
R2570:Acad10	UTSW	5	121,768,267 (GRCm39)	missense	probably damaging	1.00
R3824:Acad10	UTSW	5	121,760,881 (GRCm39)	missense	probably benign
R3846:Acad10	UTSW	5	121,772,749 (GRCm39)	missense	probably benign	0.19
R4106:Acad10	UTSW	5	121,769,527 (GRCm39)	missense	probably damaging	0.98
R4107:Acad10	UTSW	5	121,769,527 (GRCm39)	missense	probably damaging	0.98
R4108:Acad10	UTSW	5	121,769,527 (GRCm39)	missense	probably damaging	0.98
R5569:Acad10	UTSW	5	121,764,143 (GRCm39)	missense	probably damaging	0.97
R5704:Acad10	UTSW	5	121,769,606 (GRCm39)	missense	probably benign	0.03
R5845:Acad10	UTSW	5	121,764,146 (GRCm39)	missense	probably benign
R5990:Acad10	UTSW	5	121,783,468 (GRCm39)	missense	probably damaging	1.00
R6019:Acad10	UTSW	5	121,772,864 (GRCm39)	missense	possibly damaging	0.88
R6145:Acad10	UTSW	5	121,760,096 (GRCm39)	missense	probably damaging	0.97
R6384:Acad10	UTSW	5	121,790,066 (GRCm39)	missense	probably benign	0.43
R6491:Acad10	UTSW	5	121,768,220 (GRCm39)	missense	probably damaging	1.00
R6608:Acad10	UTSW	5	121,770,555 (GRCm39)	missense	probably benign	0.02
R6941:Acad10	UTSW	5	121,787,420 (GRCm39)	missense	probably damaging	1.00
R7221:Acad10	UTSW	5	121,768,273 (GRCm39)	missense	probably damaging	1.00
R7355:Acad10	UTSW	5	121,768,780 (GRCm39)	nonsense	probably null
R7483:Acad10	UTSW	5	121,794,075 (GRCm39)	critical splice donor site	probably null
R7553:Acad10	UTSW	5	121,777,318 (GRCm39)	missense	probably damaging	1.00
R7721:Acad10	UTSW	5	121,784,929 (GRCm39)	splice site	probably null
R8075:Acad10	UTSW	5	121,790,148 (GRCm39)	missense	probably benign	0.00
R8400:Acad10	UTSW	5	121,764,268 (GRCm39)	missense	possibly damaging	0.82
R9171:Acad10	UTSW	5	121,767,981 (GRCm39)	missense	probably benign	0.14
X0061:Acad10	UTSW	5	121,760,876 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGCAGATATGTGAGTAGAAACCCAC -3'
(R):5'- ATCCAGGCAGCAATAGGATG -3'

Sequencing Primer
(F):5'- TGTGAGTAGAAACCCACTTCCTGG -3'
(R):5'- ATGCCAGGAATGGATTTGCC -3'

Posted On

2019-06-26