Mutagenetix > Incidental Mutation

Incidental Mutation 'R3708:Cyp3a41a'

259437

Institutional Source

Beutler Lab

Gene Symbol

Cyp3a41a

Ensembl Gene

ENSMUSG00000075551

Gene Name

cytochrome P450, family 3, subfamily a, polypeptide 41A

Synonyms

steroid inducible, Cyp3a41

MMRRC Submission

040701-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.179) question?

Stock #

R3708 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

145630859-145656946 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to G at 145654733 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000091659 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000094111]

AlphaFold

Q9JMA7

Predicted Effect

probably null
Transcript: ENSMUST00000094111

SMART Domains

Protein: ENSMUSP00000091659
Gene: ENSMUSG00000075551

Domain	Start	End	E-Value	Type
Pfam:p450	38	494	1.7e-136	PFAM

Meta Mutation Damage Score

0.9481

Coding Region Coverage

1x: 99.0%
3x: 98.3%
10x: 96.5%
20x: 92.1%

Validation Efficiency

98% (51/52)

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700012B07Rik	G	T	11: 109,684,980 (GRCm39)	C172*	probably null	Het
Abcc5	G	T	16: 20,190,930 (GRCm39)	Q807K	probably benign	Het
Amfr	T	C	8: 94,709,948 (GRCm39)	H419R	probably benign	Het
Atp8b2	A	T	3: 89,852,459 (GRCm39)	F866I	probably damaging	Het
Atxn7l3	G	A	11: 102,182,705 (GRCm39)		probably benign	Het
Bcs1l	A	G	1: 74,629,264 (GRCm39)		probably benign	Het
Card11	G	A	5: 140,872,890 (GRCm39)	R608C	probably damaging	Het
Celf2	C	A	2: 6,629,489 (GRCm39)	K137N	probably damaging	Het
Cmya5	A	T	13: 93,231,874 (GRCm39)	Y1071*	probably null	Het
Cyp2d10	A	G	15: 82,287,217 (GRCm39)	F469L	possibly damaging	Het
Dnah8	A	T	17: 30,958,631 (GRCm39)	I2158L	probably damaging	Het
Dtnb	T	A	12: 3,639,156 (GRCm39)		probably null	Het
Dync1h1	T	C	12: 110,609,563 (GRCm39)	F2782L	probably damaging	Het
Ednrb	A	G	14: 104,054,516 (GRCm39)	Y439H	probably damaging	Het
Ferd3l	T	C	12: 33,978,748 (GRCm39)	V87A	probably benign	Het
Gphn	T	A	12: 78,579,467 (GRCm39)	S320T	probably benign	Het
Gpr39	C	T	1: 125,800,349 (GRCm39)	H367Y	probably damaging	Het
Hspa4l	A	T	3: 40,736,125 (GRCm39)	N582I	possibly damaging	Het
Ighv1-85	A	T	12: 115,963,836 (GRCm39)	W55R	probably damaging	Het
Lelp1	A	C	3: 92,042,714 (GRCm39)	C112G	unknown	Het
Lrba	A	G	3: 86,192,331 (GRCm39)	M82V	possibly damaging	Het
Macrod2	C	A	2: 141,652,549 (GRCm39)	T204K	probably damaging	Het
Map2	A	T	1: 66,455,714 (GRCm39)		probably benign	Het
Ncor1	T	C	11: 62,235,513 (GRCm39)	K647R	probably damaging	Het
Nr4a3	A	T	4: 48,056,699 (GRCm39)	Y417F	probably damaging	Het
Nup50l	G	A	6: 96,142,933 (GRCm39)	T37I	possibly damaging	Het
Obox7	C	A	7: 14,398,122 (GRCm39)	S54*	probably null	Het
Or2n1c	A	G	17: 38,519,174 (GRCm39)	I13V	probably benign	Het
Or52r1c	T	G	7: 102,735,501 (GRCm39)	Y254D	probably damaging	Het
Or8b101	T	C	9: 38,020,740 (GRCm39)	S253P	probably damaging	Het
Or9g20	T	A	2: 85,630,342 (GRCm39)	I91L	probably benign	Het
Pappa2	A	T	1: 158,662,488 (GRCm39)	Y1162*	probably null	Het
Pcdhb19	T	A	18: 37,630,442 (GRCm39)	I79K	probably benign	Het
Pi4k2a	C	T	19: 42,079,370 (GRCm39)	Q144*	probably null	Het
Pigc	T	A	1: 161,798,663 (GRCm39)	M215K	probably benign	Het
Pnma8a	T	A	7: 16,694,150 (GRCm39)	S2T	probably damaging	Het
Ppfia4	T	C	1: 134,237,398 (GRCm39)	E967G	probably damaging	Het
Ptch1	T	G	13: 63,672,773 (GRCm39)	E944A	probably benign	Het
Rims3	A	G	4: 120,740,352 (GRCm39)	T100A	probably damaging	Het
Serpinb9	A	T	13: 33,192,002 (GRCm39)	N61I	possibly damaging	Het
Sis	A	G	3: 72,850,856 (GRCm39)	M614T	probably benign	Het
Slc6a17	C	T	3: 107,400,401 (GRCm39)	V243I	probably benign	Het
Smad9	A	T	3: 54,693,602 (GRCm39)	Y177F	probably benign	Het
Vmn2r69	T	C	7: 85,061,029 (GRCm39)	D185G	probably damaging	Het
Vps36	G	T	8: 22,682,899 (GRCm39)	V5L	probably benign	Het
Vwa8	T	A	14: 79,300,136 (GRCm39)		probably benign	Het

Other mutations in Cyp3a41a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02284:Cyp3a41a	APN	5	145,641,673 (GRCm39)	splice site	probably benign
IGL03003:Cyp3a41a	APN	5	145,642,640 (GRCm39)	missense	probably benign
R0006:Cyp3a41a	UTSW	5	145,641,606 (GRCm39)	missense	probably benign	0.01
R0515:Cyp3a41a	UTSW	5	145,654,810 (GRCm39)	missense	probably damaging	1.00
R1052:Cyp3a41a	UTSW	5	145,642,621 (GRCm39)	missense	possibly damaging	0.49
R4049:Cyp3a41a	UTSW	5	145,650,350 (GRCm39)	missense	probably damaging	1.00
R4755:Cyp3a41a	UTSW	5	145,652,316 (GRCm39)	missense	probably damaging	1.00
R4975:Cyp3a41a	UTSW	5	145,656,858 (GRCm39)	start codon destroyed	probably null	1.00
R6519:Cyp3a41a	UTSW	5	145,652,308 (GRCm39)	missense	probably damaging	1.00
R6788:Cyp3a41a	UTSW	5	145,642,639 (GRCm39)	missense	probably benign	0.00
R7184:Cyp3a41a	UTSW	5	145,642,663 (GRCm39)	missense	probably benign	0.01
R7372:Cyp3a41a	UTSW	5	145,650,374 (GRCm39)	missense	possibly damaging	0.67
R7451:Cyp3a41a	UTSW	5	145,636,550 (GRCm39)	missense	probably benign	0.10
R7463:Cyp3a41a	UTSW	5	145,650,374 (GRCm39)	missense	probably damaging	1.00
R7766:Cyp3a41a	UTSW	5	145,654,827 (GRCm39)	missense	probably damaging	0.99
R9179:Cyp3a41a	UTSW	5	145,642,654 (GRCm39)	missense	probably benign
R9225:Cyp3a41a	UTSW	5	145,650,414 (GRCm39)	missense	probably benign	0.03
R9300:Cyp3a41a	UTSW	5	145,656,906 (GRCm39)	start gained	probably benign
R9308:Cyp3a41a	UTSW	5	145,656,858 (GRCm39)	start codon destroyed	probably null	1.00
R9403:Cyp3a41a	UTSW	5	145,639,008 (GRCm39)	missense	probably damaging	0.99
R9635:Cyp3a41a	UTSW	5	145,652,320 (GRCm39)	missense	possibly damaging	0.95
R9682:Cyp3a41a	UTSW	5	145,652,326 (GRCm39)	missense	possibly damaging	0.66

Predicted Primers

PCR Primer
(F):5'- GGACATTCTTATACGTGCAGATAC -3'
(R):5'- AGGATGGAGCCCAGTTGTTG -3'

Sequencing Primer
(F):5'- TCTTATACGTGCAGATACCCATATAC -3'
(R):5'- AGCCCAGTTGTTGATTTGTTTCAG -3'

Posted On

2015-01-23