Mutagenetix > Incidental Mutation

Incidental Mutation 'R7113:Cyp2d26'

551647

Institutional Source

Beutler Lab

Gene Symbol

Cyp2d26

Ensembl Gene

ENSMUSG00000022445

Gene Name

cytochrome P450, family 2, subfamily d, polypeptide 26

Synonyms

1300006E06Rik

MMRRC Submission

045205-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.090) question?

Stock #

R7113 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

82674302-82678495 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 82674403 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Phenylalanine at position 493 (Y493F)

Ref Sequence

ENSEMBL: ENSMUSP00000006094 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000006094] [ENSMUST00000229387] [ENSMUST00000229512]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000006094
AA Change: Y493F

PolyPhen 2 Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000006094
Gene: ENSMUSG00000022445
AA Change: Y493F

Domain	Start	End	E-Value	Type
transmembrane domain	10	27	N/A	INTRINSIC
Pfam:p450	37	497	3.5e-141	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000229387

Predicted Effect

probably benign
Transcript: ENSMUST00000229512

Meta Mutation Damage Score

0.0898

Coding Region Coverage

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

Validation Efficiency

95% (53/56)

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts6	T	C	13: 104,449,267 (GRCm39)	S226P	probably benign	Het
Adarb2	T	C	13: 8,781,881 (GRCm39)	Y586H	probably damaging	Het
Ano7	A	T	1: 93,313,342 (GRCm39)	E160V	probably benign	Het
Apob	G	C	12: 8,045,539 (GRCm39)	A895P	probably damaging	Het
Ccdc157	T	C	11: 4,098,889 (GRCm39)	T206A	possibly damaging	Het
Ceacam18	A	G	7: 43,291,400 (GRCm39)	N281D	probably benign	Het
Chil4	T	C	3: 106,110,083 (GRCm39)	D337G	probably damaging	Het
Chil4	T	G	3: 106,121,664 (GRCm39)	K62Q	probably benign	Het
Cic	A	T	7: 24,972,869 (GRCm39)	I867F	probably benign	Het
Cntln	A	G	4: 84,968,064 (GRCm39)	E761G	probably damaging	Het
Dync2h1	A	T	9: 7,075,788 (GRCm39)	F3026L	probably benign	Het
Ehd3	T	A	17: 74,137,179 (GRCm39)	D449E	probably benign	Het
Gpt2	G	A	8: 86,244,681 (GRCm39)	E325K	probably benign	Het
Herc2	T	G	7: 55,853,597 (GRCm39)	D3696E	probably damaging	Het
Hivep3	T	A	4: 119,955,566 (GRCm39)	I1294N	probably damaging	Het
Il19	T	C	1: 130,862,732 (GRCm39)	I139V	probably benign	Het
Jmjd1c	T	A	10: 66,993,780 (GRCm39)	I87N	probably damaging	Het
Kcnma1	A	G	14: 23,513,224 (GRCm39)	Y392H	probably damaging	Het
Kcnv2	T	C	19: 27,301,448 (GRCm39)	L433P	probably damaging	Het
Kif9	A	T	9: 110,335,732 (GRCm39)	N378Y	probably damaging	Het
Lonrf1	A	T	8: 36,697,664 (GRCm39)	V440E	probably benign	Het
Lrrc37	A	G	11: 103,509,625 (GRCm39)	I781T	unknown	Het
Manea	A	T	4: 26,336,718 (GRCm39)	L186Q	probably damaging	Het
Mas1	A	G	17: 13,061,324 (GRCm39)	I33T	probably benign	Het
Med13l	A	G	5: 118,864,330 (GRCm39)	S389G	probably benign	Het
Nxph3	T	C	11: 95,401,892 (GRCm39)	N174S	possibly damaging	Het
Or1l4	T	A	2: 37,091,568 (GRCm39)	F105Y	possibly damaging	Het
Or8g52	G	C	9: 39,630,973 (GRCm39)	C150S	probably benign	Het
Pcdha5	A	G	18: 37,094,757 (GRCm39)	D422G	probably benign	Het
Pias4	A	C	10: 80,990,287 (GRCm39)	V416G	possibly damaging	Het
Pik3cg	T	A	12: 32,255,666 (GRCm39)	Y107F	probably damaging	Het
Plcg1	T	A	2: 160,590,203 (GRCm39)	W156R	possibly damaging	Het
Plcl2	A	G	17: 50,913,492 (GRCm39)	D167G	probably damaging	Het
Podxl	T	A	6: 31,501,668 (GRCm39)		probably null	Het
Ppp1r2	T	C	16: 31,073,536 (GRCm39)	D197G	probably benign	Het
Ptprs	C	G	17: 56,758,697 (GRCm39)	V175L	probably benign	Het
Rad17	A	T	13: 100,766,025 (GRCm39)	S368T	probably benign	Het
Rdh8	G	T	9: 20,736,623 (GRCm39)	R230L	probably benign	Het
Rpl35	A	C	2: 38,894,168 (GRCm39)	L58R	probably damaging	Het
Rtp3	A	C	9: 110,815,767 (GRCm39)	C199W	probably damaging	Het
S100pbp	G	A	4: 129,075,896 (GRCm39)	T143I	probably damaging	Het
Scarf1	A	G	11: 75,416,904 (GRCm39)	E782G	probably damaging	Het
Slc30a9	T	C	5: 67,484,205 (GRCm39)	V114A	probably benign	Het
Speer1c	G	A	5: 10,292,977 (GRCm39)	P189S		Het
Stpg2	G	A	3: 139,407,535 (GRCm39)		probably null	Het
Tdpoz1	T	C	3: 93,578,113 (GRCm39)	S224G	possibly damaging	Het
Triml2	T	A	8: 43,636,370 (GRCm39)	Y52N	probably benign	Het
Trpm2	A	T	10: 77,783,765 (GRCm39)	I236N	probably damaging	Het
Unc5c	A	G	3: 141,507,054 (GRCm39)	D602G	probably benign	Het
Upk1a	A	G	7: 30,309,236 (GRCm39)	S29P	probably damaging	Het
Vmn2r54	A	G	7: 12,350,001 (GRCm39)	L527P	probably damaging	Het
Vmn2r72	A	T	7: 85,399,011 (GRCm39)		probably null	Het
Vstm2l	G	T	2: 157,756,649 (GRCm39)		probably benign	Het
Vwf	G	T	6: 125,632,007 (GRCm39)	G1952V		Het
Zfand6	A	C	7: 84,265,077 (GRCm39)	I208S	probably damaging	Het
Zfp236	A	G	18: 82,638,462 (GRCm39)	I1386T	possibly damaging	Het

Other mutations in Cyp2d26

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00559:Cyp2d26	APN	15	82,675,244 (GRCm39)	missense	probably benign	0.31
IGL00670:Cyp2d26	APN	15	82,675,942 (GRCm39)	missense	probably benign
IGL01646:Cyp2d26	APN	15	82,675,619 (GRCm39)	missense	probably benign	0.00
IGL01915:Cyp2d26	APN	15	82,674,450 (GRCm39)	missense	probably benign	0.06
IGL01940:Cyp2d26	APN	15	82,676,758 (GRCm39)	missense	probably benign	0.00
IGL02127:Cyp2d26	APN	15	82,675,307 (GRCm39)	missense	probably benign	0.09
IGL02452:Cyp2d26	APN	15	82,676,827 (GRCm39)	missense	probably benign	0.00
IGL03216:Cyp2d26	APN	15	82,677,462 (GRCm39)	missense	probably benign
IGL03377:Cyp2d26	APN	15	82,674,755 (GRCm39)	missense	possibly damaging	0.47
R0149:Cyp2d26	UTSW	15	82,676,968 (GRCm39)	missense	probably damaging	1.00
R0848:Cyp2d26	UTSW	15	82,674,434 (GRCm39)	missense	probably benign	0.00
R1165:Cyp2d26	UTSW	15	82,678,242 (GRCm39)	missense	probably damaging	1.00
R1217:Cyp2d26	UTSW	15	82,677,068 (GRCm39)	splice site	probably benign
R1780:Cyp2d26	UTSW	15	82,678,208 (GRCm39)	missense	probably damaging	1.00
R2048:Cyp2d26	UTSW	15	82,676,928 (GRCm39)	utr 3 prime	probably benign
R2152:Cyp2d26	UTSW	15	82,676,907 (GRCm39)	critical splice donor site	probably null
R2397:Cyp2d26	UTSW	15	82,678,236 (GRCm39)	missense	probably damaging	1.00
R4702:Cyp2d26	UTSW	15	82,676,648 (GRCm39)	intron	probably benign
R5157:Cyp2d26	UTSW	15	82,675,190 (GRCm39)	missense	probably benign	0.01
R5444:Cyp2d26	UTSW	15	82,676,739 (GRCm39)	missense	probably benign	0.18
R6017:Cyp2d26	UTSW	15	82,674,774 (GRCm39)	missense	possibly damaging	0.68
R6223:Cyp2d26	UTSW	15	82,675,918 (GRCm39)	missense	probably benign	0.04
R6390:Cyp2d26	UTSW	15	82,676,825 (GRCm39)	missense	possibly damaging	0.68
R6473:Cyp2d26	UTSW	15	82,675,968 (GRCm39)	missense	probably benign	0.02
R6858:Cyp2d26	UTSW	15	82,678,284 (GRCm39)	missense	probably damaging	1.00
R6912:Cyp2d26	UTSW	15	82,675,320 (GRCm39)	missense	probably benign	0.16
R6936:Cyp2d26	UTSW	15	82,676,741 (GRCm39)	missense	probably benign	0.14
R6960:Cyp2d26	UTSW	15	82,674,446 (GRCm39)	missense	probably damaging	0.98
R7053:Cyp2d26	UTSW	15	82,676,801 (GRCm39)	missense	probably benign	0.00
R7126:Cyp2d26	UTSW	15	82,678,209 (GRCm39)	missense	probably benign	0.00
R7272:Cyp2d26	UTSW	15	82,676,764 (GRCm39)	missense	probably benign
R7771:Cyp2d26	UTSW	15	82,675,947 (GRCm39)	missense	probably benign
R8695:Cyp2d26	UTSW	15	82,676,907 (GRCm39)	critical splice donor site	probably benign
R9466:Cyp2d26	UTSW	15	82,674,424 (GRCm39)	missense	probably benign	0.01
R9489:Cyp2d26	UTSW	15	82,674,672 (GRCm39)	missense	probably benign	0.00
R9605:Cyp2d26	UTSW	15	82,674,672 (GRCm39)	missense	probably benign	0.00
R9656:Cyp2d26	UTSW	15	82,677,059 (GRCm39)	missense	probably benign	0.03
X0021:Cyp2d26	UTSW	15	82,674,718 (GRCm39)	missense	probably benign	0.04

Predicted Primers

PCR Primer
(F):5'- ACAGCATCAAAGTTGTTCATGG -3'
(R):5'- AAGCCCCAATGAGGTCCTAG -3'

Sequencing Primer
(F):5'- AGCATCAAAGTTGTTCATGGGTTGG -3'
(R):5'- TGAGGTCCTAGACTAACTGAACC -3'

Posted On

2019-05-15