Mutagenetix > Incidental Mutation

Incidental Mutation 'R3916:Acad12'

309732

Institutional Source

Beutler Lab

Gene Symbol

Acad12

Ensembl Gene

ENSMUSG00000042647

Gene Name

acyl-Coenzyme A dehydrogenase family, member 12

Synonyms

9330129D05Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

R3916 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

121736340-121757001 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 121737277 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 498 (V498A)

Ref Sequence

ENSEMBL: ENSMUSP00000046497 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041252]

AlphaFold

D3Z7X0

Predicted Effect

probably damaging
Transcript: ENSMUST00000041252
AA Change: V498A

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000046497
Gene: ENSMUSG00000042647
AA Change: V498A

Domain	Start	End	E-Value	Type
Pfam:Acyl-CoA_dh_N	151	278	7e-16	PFAM
Pfam:Acyl-CoA_dh_M	282	383	1.9e-18	PFAM
Pfam:Acyl-CoA_dh_1	395	536	1.5e-27	PFAM
Pfam:Acyl-CoA_dh_2	411	526	1.7e-13	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000131338

SMART Domains

Protein: ENSMUSP00000121904
Gene: ENSMUSG00000042647

Domain	Start	End	E-Value	Type
PDB:2WBI\|B	2	92	2e-26	PDB
SCOP:d1is2a3	3	58	3e-11	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197306

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198656

Meta Mutation Damage Score

0.8039

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932414N04Rik	T	G	2: 68,562,329 (GRCm39)	F319V	possibly damaging	Het
Adam19	A	G	11: 45,951,762 (GRCm39)	E37G	probably benign	Het
Anks3	A	G	16: 4,765,143 (GRCm39)	Y423H	probably damaging	Het
Arfgef1	A	T	1: 10,259,668 (GRCm39)	V600D	probably benign	Het
Arhgef18	T	C	8: 3,504,197 (GRCm39)	F939L	probably benign	Het
Arhgef2	A	G	3: 88,540,340 (GRCm39)	N127S	probably damaging	Het
Arid1b	A	G	17: 5,392,928 (GRCm39)	S2100G	probably benign	Het
Atp1b2	A	G	11: 69,493,901 (GRCm39)	V93A	probably damaging	Het
Atrnl1	T	C	19: 57,924,084 (GRCm39)	V1283A	possibly damaging	Het
Bpifb5	A	C	2: 154,070,101 (GRCm39)	K184Q	probably benign	Het
Cadps	C	T	14: 12,457,702 (GRCm38)	A1060T	probably benign	Het
Cant1	A	G	11: 118,299,572 (GRCm39)	V259A	probably damaging	Het
Ccdc89	A	G	7: 90,076,033 (GRCm39)	D81G	probably damaging	Het
Cd109	CATTTATTTATTTATTTATTTATTTATTTATTTAT	CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT	9: 78,619,782 (GRCm39)		probably benign	Het
Cntnap4	C	G	8: 113,602,165 (GRCm39)	P1190A	probably benign	Het
Colgalt2	T	A	1: 152,384,362 (GRCm39)	Y567*	probably null	Het
Cyp4f18	A	T	8: 72,749,881 (GRCm39)	F256Y	probably benign	Het
Ddx41	G	A	13: 55,682,293 (GRCm39)	R205W	possibly damaging	Het
Dop1a	G	A	9: 86,403,186 (GRCm39)	R1462H	probably damaging	Het
Dync1i2	A	G	2: 71,079,716 (GRCm39)	T377A	probably damaging	Het
F2	G	A	2: 91,455,833 (GRCm39)	T600M	probably damaging	Het
Fam91a1	C	T	15: 58,302,583 (GRCm39)	H308Y	probably damaging	Het
Fkbp2	C	A	19: 6,955,925 (GRCm39)		probably null	Het
Gabarapl2	T	A	8: 112,679,028 (GRCm39)	F115L	probably benign	Het
Heatr3	T	G	8: 88,876,999 (GRCm39)		probably null	Het
Ifi204	T	G	1: 173,583,341 (GRCm39)	K292N	possibly damaging	Het
Itpkc	A	T	7: 26,927,728 (GRCm39)	I62N	probably benign	Het
Kcnab1	G	A	3: 65,211,585 (GRCm39)		probably null	Het
Krt88	G	A	15: 101,350,809 (GRCm39)		probably null	Het
Larp4	C	T	15: 99,888,284 (GRCm39)	T107I	probably benign	Het
Lmo7	T	C	14: 102,166,778 (GRCm39)		probably benign	Het
Lrrc37a	T	C	11: 103,346,344 (GRCm39)	Y3174C	possibly damaging	Het
Lyzl4	T	A	9: 121,412,101 (GRCm39)	D105V	probably damaging	Het
Mst1	A	G	9: 107,961,494 (GRCm39)	I575V	probably benign	Het
Myh7	C	A	14: 55,211,503 (GRCm39)	E1555D	probably damaging	Het
Nwd1	T	A	8: 73,394,439 (GRCm39)	C608*	probably null	Het
Obox3	C	A	7: 15,361,151 (GRCm39)	C38F	probably benign	Het
P4ha2	A	G	11: 54,017,074 (GRCm39)	D441G	probably benign	Het
Pcdhb14	A	T	18: 37,581,598 (GRCm39)	I235F	possibly damaging	Het
Rasgrf2	A	G	13: 92,167,296 (GRCm39)	V259A	probably damaging	Het
Scn1a	T	C	2: 66,107,957 (GRCm39)	T1590A	probably damaging	Het
Sdk1	T	A	5: 142,036,999 (GRCm39)	D817E	probably damaging	Het
Sema3b	A	G	9: 107,477,657 (GRCm39)	F482S	probably damaging	Het
Slc35a5	G	C	16: 44,978,521 (GRCm39)		probably benign	Het
Slc6a3	A	G	13: 73,710,427 (GRCm39)	I346V	probably benign	Het
Slu7	G	T	11: 43,331,511 (GRCm39)		probably null	Het
Spns1	A	T	7: 125,970,711 (GRCm39)		probably null	Het
Supv3l1	T	C	10: 62,285,199 (GRCm39)	D89G	possibly damaging	Het
Taf1c	G	A	8: 120,327,244 (GRCm39)	R412W	probably damaging	Het
Tctn3	T	A	19: 40,596,093 (GRCm39)	T305S	possibly damaging	Het
Tekt1	A	G	11: 72,236,574 (GRCm39)	I296T	possibly damaging	Het
Tet2	T	C	3: 133,191,816 (GRCm39)	K873E	possibly damaging	Het
Thada	G	A	17: 84,749,210 (GRCm39)	A587V	possibly damaging	Het
Tmprss15	T	A	16: 78,782,884 (GRCm39)	N712Y	probably damaging	Het
Tnks	A	G	8: 35,320,515 (GRCm39)	S719P	probably damaging	Het
Tnrc6a	A	C	7: 122,780,607 (GRCm39)	Q1332H	probably damaging	Het
Trpv3	A	G	11: 73,174,560 (GRCm39)	D309G	possibly damaging	Het
Tti2	A	G	8: 31,643,547 (GRCm39)	K221E	possibly damaging	Het
Uba5	A	T	9: 103,931,389 (GRCm39)	C227S	probably damaging	Het
Ugcg	C	T	4: 59,207,798 (GRCm39)	P46S	probably benign	Het
Unc80	T	C	1: 66,716,654 (GRCm39)	C2925R	probably benign	Het
Vmn2r83	G	A	10: 79,314,744 (GRCm39)	G331R	probably benign	Het
Xirp2	G	T	2: 67,341,766 (GRCm39)	V1336F	probably benign	Het
Zbed5	T	C	5: 129,931,118 (GRCm39)	Y356H	possibly damaging	Het

Other mutations in Acad12

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00328:Acad12	APN	5	121,742,316 (GRCm39)	unclassified	probably benign
IGL02968:Acad12	APN	5	121,748,101 (GRCm39)	missense	probably benign	0.17
IGL03046:Acad12	UTSW	5	121,748,029 (GRCm39)	missense	probably benign	0.00
R0085:Acad12	UTSW	5	121,742,357 (GRCm39)	missense	possibly damaging	0.85
R0538:Acad12	UTSW	5	121,745,511 (GRCm39)	missense	possibly damaging	0.85
R1424:Acad12	UTSW	5	121,742,385 (GRCm39)	missense	probably benign	0.01
R1754:Acad12	UTSW	5	121,745,544 (GRCm39)	missense	probably benign	0.08
R1975:Acad12	UTSW	5	121,742,322 (GRCm39)	missense	probably benign
R3917:Acad12	UTSW	5	121,737,277 (GRCm39)	missense	probably damaging	1.00
R4531:Acad12	UTSW	5	121,736,964 (GRCm39)	missense	probably benign
R4531:Acad12	UTSW	5	121,736,962 (GRCm39)	missense	probably benign
R4676:Acad12	UTSW	5	121,745,234 (GRCm39)	missense	probably damaging	1.00
R5057:Acad12	UTSW	5	121,748,152 (GRCm39)	missense	probably benign	0.00
R5166:Acad12	UTSW	5	121,738,083 (GRCm39)	missense	probably benign	0.04
R5286:Acad12	UTSW	5	121,742,358 (GRCm39)	missense	probably benign	0.27
R5641:Acad12	UTSW	5	121,742,084 (GRCm39)	unclassified	probably benign
R5716:Acad12	UTSW	5	121,748,046 (GRCm39)	missense	probably benign	0.00
R5761:Acad12	UTSW	5	121,742,243 (GRCm39)	unclassified	probably benign
R6006:Acad12	UTSW	5	121,737,299 (GRCm39)	missense	possibly damaging	0.46
R6256:Acad12	UTSW	5	121,752,149 (GRCm39)	missense	probably benign	0.05
R6729:Acad12	UTSW	5	121,745,998 (GRCm39)	missense	probably damaging	1.00
R6785:Acad12	UTSW	5	121,747,908 (GRCm39)	missense	probably damaging	1.00
R7161:Acad12	UTSW	5	121,745,436 (GRCm39)	missense	probably damaging	1.00
R7571:Acad12	UTSW	5	121,745,257 (GRCm39)	nonsense	probably null
R8383:Acad12	UTSW	5	121,745,436 (GRCm39)	missense	probably damaging	1.00
R8473:Acad12	UTSW	5	121,745,538 (GRCm39)	missense	probably damaging	1.00
Z1177:Acad12	UTSW	5	121,737,257 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- AGTTCTAAGAGTGAATGCATGCTC -3'
(R):5'- ATGCCCAGGTCTAGCTTTGG -3'

Sequencing Primer
(F):5'- TGAATGCATGCTCAAAACAGCTG -3'
(R):5'- CCAGGTCTAGCTTTGGTCCAG -3'

Posted On

2015-04-17