Mutagenetix > Incidental Mutation

Incidental Mutation 'R9447:Cyp2t4'

713997

Institutional Source

Beutler Lab

Gene Symbol

Cyp2t4

Ensembl Gene

ENSMUSG00000078787

Gene Name

cytochrome P450, family 2, subfamily t, polypeptide 4

Synonyms

LOC384724

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.071) question?

Stock #

R9447 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

26853139-26857989 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 26854717 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 66 (V66M)

Ref Sequence

ENSEMBL: ENSMUSP00000126779 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080058] [ENSMUST00000108382] [ENSMUST00000108385] [ENSMUST00000164093]

AlphaFold

E9PWV0

Predicted Effect

probably benign
Transcript: ENSMUST00000080058

SMART Domains

Protein: ENSMUSP00000078966
Gene: ENSMUSG00000058709

Domain	Start	End	E-Value	Type
low complexity region	4	18	N/A	INTRINSIC
low complexity region	64	73	N/A	INTRINSIC
Blast:P4Hc	75	136	3e-14	BLAST
low complexity region	154	174	N/A	INTRINSIC
P4Hc	201	387	9.71e-44	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000108382

SMART Domains

Protein: ENSMUSP00000104019
Gene: ENSMUSG00000058709

Domain	Start	End	E-Value	Type
low complexity region	4	18	N/A	INTRINSIC
low complexity region	64	73	N/A	INTRINSIC
Blast:P4Hc	75	136	3e-14	BLAST
low complexity region	154	174	N/A	INTRINSIC
P4Hc	201	387	9.71e-44	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000108385
AA Change: V58M

PolyPhen 2 Score 0.921 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000104022
Gene: ENSMUSG00000078787
AA Change: V58M

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:p450	35	492	5.3e-130	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000164093
AA Change: V66M

PolyPhen 2 Score 0.799 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000126779
Gene: ENSMUSG00000078787
AA Change: V66M

Domain	Start	End	E-Value	Type
transmembrane domain	13	32	N/A	INTRINSIC
Pfam:p450	43	500	2.6e-130	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl2fm2	T	A	3: 59,651,051 (GRCm39)	Y58N	probably damaging	Het
Ago4	G	A	4: 126,402,151 (GRCm39)	P572S	probably benign	Het
Akr1c19	A	G	13: 4,296,838 (GRCm39)	I295V	probably benign	Het
Cadps2	A	T	6: 23,323,297 (GRCm39)	I1007K	probably damaging	Het
Cd47	C	A	16: 49,715,822 (GRCm39)	T196K		Het
Cdrt4	T	G	11: 62,883,418 (GRCm39)	L40R	probably damaging	Het
Cox16	A	T	12: 81,406,109 (GRCm39)	C72S	probably benign	Het
Daxx	A	T	17: 34,132,247 (GRCm39)	D497V	unknown	Het
Ddt	A	G	10: 75,608,671 (GRCm39)	V62A	possibly damaging	Het
Dhx57	A	G	17: 80,549,523 (GRCm39)	V1294A	probably damaging	Het
Dnaaf5	A	G	5: 139,163,743 (GRCm39)	T667A	probably damaging	Het
Dnase2a	A	C	8: 85,635,786 (GRCm39)	S90R	probably damaging	Het
Dytn	A	G	1: 63,700,302 (GRCm39)	V276A		Het
Efcab8	G	C	2: 153,646,861 (GRCm39)	V397L	unknown	Het
Enpp6	A	T	8: 47,483,600 (GRCm39)	R131W	probably damaging	Het
Epm2a	C	T	10: 11,324,432 (GRCm39)	H174Y	possibly damaging	Het
Fcho1	A	G	8: 72,169,913 (GRCm39)	L70P	probably damaging	Het
Fhip1b	G	T	7: 105,034,155 (GRCm39)	T492K	probably benign	Het
Fstl4	G	T	11: 53,077,166 (GRCm39)	C641F	probably damaging	Het
Ganab	C	T	19: 8,886,894 (GRCm39)	H327Y	probably damaging	Het
Gkn1	A	G	6: 87,323,322 (GRCm39)	Y164H	probably benign	Het
Gm57858	A	G	3: 36,074,195 (GRCm39)	V318A	possibly damaging	Het
Hpf1	A	G	8: 61,348,618 (GRCm39)	D111G	probably damaging	Het
Hs3st2	C	T	7: 120,992,289 (GRCm39)	R113W	probably damaging	Het
Ighm	A	T	12: 113,384,794 (GRCm39)	L353Q		Het
Krbox5	A	G	13: 67,981,953 (GRCm39)	E55G	probably damaging	Het
Ksr1	T	C	11: 78,909,159 (GRCm39)	D782G	unknown	Het
Lpin2	A	G	17: 71,539,087 (GRCm39)	K392E	unknown	Het
Lrrc4	A	G	6: 28,830,650 (GRCm39)	S322P	probably benign	Het
Man2a1	T	C	17: 64,966,001 (GRCm39)	V313A	possibly damaging	Het
Mctp1	A	G	13: 76,727,904 (GRCm39)	S9G	probably benign	Het
Morn5	A	T	2: 35,969,525 (GRCm39)		probably null	Het
Mroh2b	C	T	15: 4,960,823 (GRCm39)	A795V	probably damaging	Het
Ncf4	G	T	15: 78,146,499 (GRCm39)	A310S	probably benign	Het
Nedd4	T	C	9: 72,577,381 (GRCm39)	Y69H	probably benign	Het
Nras	T	C	3: 102,967,673 (GRCm39)	F90L	possibly damaging	Het
Nrxn3	T	C	12: 89,221,678 (GRCm39)	F113L	probably benign	Het
Ntsr1	C	T	2: 180,180,540 (GRCm39)	T282I	probably benign	Het
Or1e1d-ps1	G	T	11: 73,819,617 (GRCm39)	C189F	probably benign	Het
Osbpl3	T	A	6: 50,321,857 (GRCm39)	K310*	probably null	Het
Pcca	T	C	14: 122,854,290 (GRCm39)	V194A	probably damaging	Het
Plekha5	A	G	6: 140,525,192 (GRCm39)	Y900C	probably damaging	Het
Prss22	T	C	17: 24,212,837 (GRCm39)	D300G	probably benign	Het
Rad17	A	T	13: 100,764,119 (GRCm39)	Y451N	probably damaging	Het
Rnf181	G	T	6: 72,337,570 (GRCm39)	T97K	probably damaging	Het
Sec24d	T	C	3: 123,084,162 (GRCm39)	S114P	probably benign	Het
Siae	C	A	9: 37,557,743 (GRCm39)	Q517K	probably benign	Het
Smurf2	A	T	11: 106,715,548 (GRCm39)	V653D	probably damaging	Het
Sqor	C	A	2: 122,649,520 (GRCm39)	T359K	possibly damaging	Het
Taf6	A	T	5: 138,176,970 (GRCm39)	*637R	probably null	Het
Tas2r109	A	C	6: 132,957,270 (GRCm39)	M220R	probably damaging	Het
Tlr2	T	A	3: 83,748,445 (GRCm39)		probably null	Het
Tm7sf3	C	T	6: 146,525,179 (GRCm39)	D89N	possibly damaging	Het
Tmem8b	T	G	4: 43,685,766 (GRCm39)	L179R	probably damaging	Het
Tnfrsf10b	T	A	14: 70,013,608 (GRCm39)	H179Q	probably damaging	Het
Trip11	T	A	12: 101,850,148 (GRCm39)	K1305N	probably damaging	Het
Ttn	C	A	2: 76,582,862 (GRCm39)	W22677L	probably damaging	Het
Ube2r2	T	C	4: 41,190,655 (GRCm39)	V183A	probably damaging	Het
Ubqln4	T	A	3: 88,464,124 (GRCm39)	D208E	probably benign	Het
Ugt2a3	T	A	5: 87,473,330 (GRCm39)	N529I	probably benign	Het
Vmn1r125	A	G	7: 21,006,627 (GRCm39)	N175S	probably benign	Het
Xirp2	T	A	2: 67,338,950 (GRCm39)	I397K	probably damaging	Het
Zfp821	G	A	8: 110,450,816 (GRCm39)	V270I	probably damaging	Het
Zfp935	A	G	13: 62,602,842 (GRCm39)	V99A	possibly damaging	Het

Other mutations in Cyp2t4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00088:Cyp2t4	APN	7	26,854,723 (GRCm39)	missense	probably benign	0.00
IGL00706:Cyp2t4	APN	7	26,854,583 (GRCm39)	missense	probably benign	0.01
IGL02926:Cyp2t4	APN	7	26,857,228 (GRCm39)	missense	probably damaging	1.00
R0560:Cyp2t4	UTSW	7	26,857,936 (GRCm39)	missense	probably damaging	0.99
R0632:Cyp2t4	UTSW	7	26,857,671 (GRCm39)	missense	possibly damaging	0.82
R0788:Cyp2t4	UTSW	7	26,854,588 (GRCm39)	missense	probably null
R1353:Cyp2t4	UTSW	7	26,856,055 (GRCm39)	missense	probably benign	0.03
R1652:Cyp2t4	UTSW	7	26,856,815 (GRCm39)	missense	possibly damaging	0.48
R1838:Cyp2t4	UTSW	7	26,857,841 (GRCm39)	missense	possibly damaging	0.92
R1997:Cyp2t4	UTSW	7	26,857,038 (GRCm39)	critical splice donor site	probably null
R2136:Cyp2t4	UTSW	7	26,857,585 (GRCm39)	missense	probably benign	0.32
R2963:Cyp2t4	UTSW	7	26,854,699 (GRCm39)	missense	possibly damaging	0.86
R6239:Cyp2t4	UTSW	7	26,856,900 (GRCm39)	missense	possibly damaging	0.73
R6634:Cyp2t4	UTSW	7	26,855,213 (GRCm39)	nonsense	probably null
R7251:Cyp2t4	UTSW	7	26,857,144 (GRCm39)	missense	possibly damaging	0.72
R7348:Cyp2t4	UTSW	7	26,856,676 (GRCm39)	missense	probably benign	0.01
R7436:Cyp2t4	UTSW	7	26,857,668 (GRCm39)	missense	probably damaging	0.99
R8350:Cyp2t4	UTSW	7	26,856,806 (GRCm39)	missense	possibly damaging	0.51
R8352:Cyp2t4	UTSW	7	26,857,162 (GRCm39)	missense	probably benign	0.04
R8405:Cyp2t4	UTSW	7	26,856,894 (GRCm39)	critical splice acceptor site	probably null
R8450:Cyp2t4	UTSW	7	26,856,806 (GRCm39)	missense	possibly damaging	0.51
R8452:Cyp2t4	UTSW	7	26,857,162 (GRCm39)	missense	probably benign	0.04
R9366:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9370:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9451:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9495:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9496:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9497:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9499:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9500:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9516:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9553:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9554:Cyp2t4	UTSW	7	26,854,717 (GRCm39)	missense	possibly damaging	0.80
R9682:Cyp2t4	UTSW	7	26,857,611 (GRCm39)	missense	probably damaging	1.00
R9732:Cyp2t4	UTSW	7	26,854,657 (GRCm39)	missense	probably damaging	0.97
Z1088:Cyp2t4	UTSW	7	26,857,171 (GRCm39)	missense	probably damaging	1.00
Z1177:Cyp2t4	UTSW	7	26,857,665 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGATCTTAGACAGGATGGTCACC -3'
(R):5'- GCATCAGCTCTTAGACACAGG -3'

Sequencing Primer
(F):5'- AGACAGGATGGTCACCTGCTTG -3'
(R):5'- TCTTAGACACAGGGGTCCAG -3'

Posted On

2022-06-15