Mutagenetix > Incidental Mutation

Incidental Mutation 'R7197:Acad8'

574637

Institutional Source

Beutler Lab

Gene Symbol

Acad8

Ensembl Gene

ENSMUSG00000031969

Gene Name

acyl-Coenzyme A dehydrogenase family, member 8

Synonyms

2310016C19Rik

MMRRC Submission

045276-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.101) question?

Stock #

R7197 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

26885431-26910862 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to T at 26888967 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000112908 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000060513] [ENSMUST00000120367] [ENSMUST00000128923] [ENSMUST00000132293]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000060513

SMART Domains

Protein: ENSMUSP00000054370
Gene: ENSMUSG00000031969

Domain	Start	End	E-Value	Type
Pfam:Acyl-CoA_dh_N	40	151	1e-28	PFAM
Pfam:Acyl-CoA_dh_M	155	207	1.8e-23	PFAM
Pfam:Acyl-CoA_dh_1	261	411	2.9e-47	PFAM
Pfam:Acyl-CoA_dh_2	276	399	1.8e-22	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000120367

SMART Domains

Protein: ENSMUSP00000112908
Gene: ENSMUSG00000031969

Domain	Start	End	E-Value	Type
Pfam:Acyl-CoA_dh_N	40	151	7.8e-29	PFAM
Pfam:Acyl-CoA_dh_M	155	249	3.7e-28	PFAM
Pfam:Acyl-CoA_dh_1	261	411	5.7e-45	PFAM
Pfam:Acyl-CoA_dh_2	276	400	2.9e-20	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000128923

Predicted Effect

probably benign
Transcript: ENSMUST00000132293

Predicted Effect

probably benign
Transcript: ENSMUST00000215693

Meta Mutation Damage Score

0.9756

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

97% (77/79)

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 that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. The encoded protein is a mitochondrial enzyme that functions in catabolism of the branched-chain amino acid valine. Defects in this gene are the cause of isobutyryl-CoA dehydrogenase deficiency.[provided by RefSeq, Nov 2009]
PHENOTYPE: Mice homozygous for an ENU-induced allele exhibit cold intolerance at young age with a progressive hepatic steatosis and abnormal mitochondria. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017B05Rik	AGCTTCCCTGCTT	AGCTT	9: 57,165,505 (GRCm39)		probably null	Het
Aars2	T	C	17: 45,819,885 (GRCm39)	Y221H	probably damaging	Het
Abca8b	G	A	11: 109,836,648 (GRCm39)	R1216*	probably null	Het
Acer2	A	G	4: 86,805,287 (GRCm39)	T84A	probably null	Het
Adgrb2	A	G	4: 129,903,315 (GRCm39)	N613S	probably damaging	Het
Arap2	T	C	5: 62,798,729 (GRCm39)	D1300G	possibly damaging	Het
Castor1	T	C	11: 4,168,949 (GRCm39)	C39R	probably damaging	Het
Ccl11	A	T	11: 81,948,665 (GRCm39)		probably benign	Het
Cfh	A	T	1: 140,016,505 (GRCm39)	Y1151*	probably null	Het
Cobll1	A	G	2: 64,928,882 (GRCm39)	S815P	probably benign	Het
Cryz	T	C	3: 154,327,205 (GRCm39)	S240P	probably damaging	Het
Csmd2	A	G	4: 128,404,826 (GRCm39)	Y2404C		Het
F13a1	T	C	13: 37,100,860 (GRCm39)	D428G	probably damaging	Het
Fbxo42	A	G	4: 140,927,396 (GRCm39)	S559G	probably benign	Het
Fry	A	G	5: 150,393,232 (GRCm39)	S263G		Het
Fshr	C	T	17: 89,292,897 (GRCm39)	A594T	probably damaging	Het
Gm1527	A	G	3: 28,980,690 (GRCm39)	M597V	probably null	Het
Gpr158	A	T	2: 21,815,412 (GRCm39)	T602S	probably damaging	Het
Hmgxb4	C	A	8: 75,756,624 (GRCm39)	T583K	probably damaging	Het
Igkv8-30	C	T	6: 70,094,069 (GRCm39)	C114Y	probably damaging	Het
Igsf5	T	A	16: 96,204,546 (GRCm39)	N366K	probably damaging	Het
Kif15	T	C	9: 122,838,991 (GRCm39)		probably null	Het
Klk1b26	T	A	7: 43,665,821 (GRCm39)		probably null	Het
Lama1	G	T	17: 68,044,700 (GRCm39)	E200*	probably null	Het
Lpar5	C	T	6: 125,059,347 (GRCm39)	T356I	probably benign	Het
Lrch3	A	T	16: 32,810,665 (GRCm39)	T538S	probably damaging	Het
Mansc4	A	G	6: 146,977,203 (GRCm39)	S138P	probably damaging	Het
Mief1	T	C	15: 80,134,061 (GRCm39)	S373P	possibly damaging	Het
Nbas	G	T	12: 13,570,751 (GRCm39)	V2053F	possibly damaging	Het
Nek11	T	C	9: 105,121,614 (GRCm39)	E435G	probably damaging	Het
Nynrin	A	T	14: 56,109,380 (GRCm39)	I1496F	probably benign	Het
Odf1	A	T	15: 38,219,794 (GRCm39)	M41L	probably benign	Het
Or10a5	A	G	7: 106,635,364 (GRCm39)	M8V	probably benign	Het
Or4c115	A	G	2: 88,927,626 (GRCm39)	V215A	probably benign	Het
Or4c29	A	T	2: 88,740,708 (GRCm39)	F10I	probably benign	Het
Or7h8	T	G	9: 20,123,851 (GRCm39)	S69A	probably benign	Het
Oxnad1	T	C	14: 31,818,473 (GRCm39)	V106A	possibly damaging	Het
Padi4	C	A	4: 140,488,969 (GRCm39)	E157*	probably null	Het
Parp10	A	T	15: 76,126,616 (GRCm39)	F217L	probably damaging	Het
Pcdhb18	T	A	18: 37,623,436 (GRCm39)	S255R	probably benign	Het
Pde4c	G	T	8: 71,197,978 (GRCm39)	G102W	probably damaging	Het
Pde6a	T	C	18: 61,391,295 (GRCm39)	Y547H	probably damaging	Het
Phf11b	A	T	14: 59,563,507 (GRCm39)	L137I	probably benign	Het
Pigh	A	C	12: 79,130,463 (GRCm39)	I134S	probably damaging	Het
Pigt	G	A	2: 164,344,436 (GRCm39)	V362M	probably damaging	Het
Pld1	A	G	3: 28,078,401 (GRCm39)	D20G	probably damaging	Het
Pou3f2	T	C	4: 22,487,288 (GRCm39)	R282G	probably damaging	Het
Ppp2r5d	A	G	17: 46,996,527 (GRCm39)	V382A	probably damaging	Het
Prdm16	T	C	4: 154,425,967 (GRCm39)	E606G	probably damaging	Het
Psg28	A	G	7: 18,164,509 (GRCm39)	Y68H	probably damaging	Het
Qpctl	C	A	7: 18,882,944 (GRCm39)	W56L	probably damaging	Het
Rab11fip5	G	A	6: 85,319,137 (GRCm39)	P584L	probably damaging	Het
Sde2	C	T	1: 180,678,843 (GRCm39)	H36Y	probably benign	Het
Sema4d	T	C	13: 51,856,872 (GRCm39)	S787G	probably benign	Het
Sgca	C	T	11: 94,864,014 (GRCm39)		probably null	Het
Shroom3	A	G	5: 93,090,463 (GRCm39)	E1071G	probably damaging	Het
Skint5	A	G	4: 113,437,679 (GRCm39)		probably null	Het
Slc44a3	T	A	3: 121,319,411 (GRCm39)	D110V	probably benign	Het
Slc4a4	A	C	5: 89,082,433 (GRCm39)		probably benign	Het
Slc4a8	A	G	15: 100,688,857 (GRCm39)	D389G	probably damaging	Het
Sp3	C	G	2: 72,809,953 (GRCm39)	E11Q	probably benign	Het
Srrm2	A	G	17: 24,037,198 (GRCm39)	S1281G	unknown	Het
Tat	A	T	8: 110,723,459 (GRCm39)	I316F	probably benign	Het
Thoc5	A	G	11: 4,865,563 (GRCm39)	T381A	probably benign	Het
Tiam1	T	C	16: 89,681,826 (GRCm39)	Y384C	probably damaging	Het
Tmem45a	A	T	16: 56,632,026 (GRCm39)	F197L	probably damaging	Het
Trav8d-1	A	G	14: 53,016,435 (GRCm39)	Y107C	probably damaging	Het
Trim10	T	A	17: 37,187,846 (GRCm39)	V354D	probably damaging	Het
Unc45b	A	T	11: 82,831,013 (GRCm39)		probably null	Het
Unc79	A	G	12: 103,078,765 (GRCm39)	I1643M	probably benign	Het
Unc80	G	T	1: 66,560,725 (GRCm39)	G818*	probably null	Het
Usp15	A	T	10: 122,966,910 (GRCm39)	M470K	possibly damaging	Het
Vldlr	T	C	19: 27,212,241 (GRCm39)	V85A	probably benign	Het
Vma21-ps	A	G	4: 52,496,994 (GRCm39)	V84A	probably benign	Het
Vmn2r67	C	T	7: 84,785,774 (GRCm39)	V744I	possibly damaging	Het
Wdr73	A	G	7: 80,542,946 (GRCm39)	C221R	probably benign	Het
Zxdc	C	T	6: 90,355,819 (GRCm39)	H443Y	probably damaging	Het

Other mutations in Acad8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01081:Acad8	APN	9	26,901,890 (GRCm39)	missense	probably damaging	1.00
IGL01721:Acad8	APN	9	26,903,563 (GRCm39)	splice site	probably benign
R1473:Acad8	UTSW	9	26,890,337 (GRCm39)	missense	probably benign	0.00
R2102:Acad8	UTSW	9	26,896,861 (GRCm39)	nonsense	probably null
R3030:Acad8	UTSW	9	26,890,355 (GRCm39)	missense	probably benign	0.04
R4023:Acad8	UTSW	9	26,890,481 (GRCm39)	missense	probably benign	0.02
R4276:Acad8	UTSW	9	26,889,745 (GRCm39)	missense	probably null	0.47
R4667:Acad8	UTSW	9	26,901,923 (GRCm39)	missense	probably damaging	1.00
R4668:Acad8	UTSW	9	26,901,923 (GRCm39)	missense	probably damaging	1.00
R4669:Acad8	UTSW	9	26,901,923 (GRCm39)	missense	probably damaging	1.00
R4898:Acad8	UTSW	9	26,889,698 (GRCm39)	missense	probably damaging	1.00
R5418:Acad8	UTSW	9	26,896,853 (GRCm39)	missense	probably damaging	1.00
R5486:Acad8	UTSW	9	26,910,791 (GRCm39)	start codon destroyed	probably null
R5549:Acad8	UTSW	9	26,896,847 (GRCm39)	missense	probably damaging	1.00
R5887:Acad8	UTSW	9	26,890,620 (GRCm39)	splice site	probably null
R5943:Acad8	UTSW	9	26,910,740 (GRCm39)	missense	probably benign	0.00
R7150:Acad8	UTSW	9	26,889,750 (GRCm39)	missense	probably damaging	1.00
R7226:Acad8	UTSW	9	26,889,726 (GRCm39)	nonsense	probably null
R7561:Acad8	UTSW	9	26,890,538 (GRCm39)	missense	probably benign	0.03
R7812:Acad8	UTSW	9	26,890,476 (GRCm39)	missense	probably damaging	1.00
R8360:Acad8	UTSW	9	26,890,352 (GRCm39)	missense	possibly damaging	0.94
R8752:Acad8	UTSW	9	26,896,853 (GRCm39)	missense	probably damaging	1.00
R8868:Acad8	UTSW	9	26,890,544 (GRCm39)	missense	probably damaging	1.00
R8919:Acad8	UTSW	9	26,910,785 (GRCm39)	missense	probably benign	0.00
R9300:Acad8	UTSW	9	26,888,928 (GRCm39)	missense	probably damaging	1.00
R9396:Acad8	UTSW	9	26,887,041 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTAGCCACAGAGCAGTGAC -3'
(R):5'- CTGGTTCAGTAGGATGCCCTTG -3'

Sequencing Primer
(F):5'- CTGACATAGGCTTGGAAAAGC -3'
(R):5'- GCGTCTGACCACTTAGAATCTGGAG -3'

Posted On

2019-09-26