Mutagenetix > Incidental Mutation

Incidental Mutation 'R3809:Med15'

275131

Institutional Source

Beutler Lab

Gene Symbol

Med15

Ensembl Gene

ENSMUSG00000012114

Gene Name

mediator complex subunit 15

Synonyms

A230074L19Rik, Pcqap

MMRRC Submission

040766-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.959) question?

Stock #

R3809 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

17469072-17540811 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

C to T at 17473598 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000012259] [ENSMUST00000056962] [ENSMUST00000080936] [ENSMUST00000182117] [ENSMUST00000231674] [ENSMUST00000232236] [ENSMUST00000232645]

AlphaFold

Q924H2

Predicted Effect

unknown
Transcript: ENSMUST00000012259
AA Change: M452I

SMART Domains

Protein: ENSMUSP00000012259
Gene: ENSMUSG00000012114
AA Change: M452I

Domain	Start	End	E-Value	Type
Pfam:Med15	17	789	N/A	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000056962

SMART Domains

Protein: ENSMUSP00000049541
Gene: ENSMUSG00000041617

Domain	Start	End	E-Value	Type
low complexity region	12	34	N/A	INTRINSIC
Pfam:CCDC92	50	105	4.1e-24	PFAM
low complexity region	154	164	N/A	INTRINSIC
Pfam:CCDC74_C	209	326	1.4e-49	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000080936
AA Change: M412I

SMART Domains

Protein: ENSMUSP00000079737
Gene: ENSMUSG00000012114
AA Change: M412I

Domain	Start	End	E-Value	Type
Pfam:Med15	17	749	1.2e-276	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000182117

SMART Domains

Protein: ENSMUSP00000138657
Gene: ENSMUSG00000041617

Domain	Start	End	E-Value	Type
low complexity region	1	21	N/A	INTRINSIC
Pfam:CCDC92	36	97	2e-26	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000182671

Predicted Effect

probably benign
Transcript: ENSMUST00000183279

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000231231

Predicted Effect

unknown
Transcript: ENSMUST00000231674
AA Change: C47Y

Predicted Effect

unknown
Transcript: ENSMUST00000232236
AA Change: M452I

Predicted Effect

unknown
Transcript: ENSMUST00000232645
AA Change: M302I

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000231480

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000232012

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.6%
20x: 95.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	G	T	12: 71,211,320 (GRCm39)	E685*	probably null	Het
2700049A03Rik	A	T	12: 71,211,321 (GRCm39)	E685V	possibly damaging	Het
3425401B19Rik	T	C	14: 32,385,650 (GRCm39)	Y105C	possibly damaging	Het
Aoc1l3	C	T	6: 48,964,928 (GRCm39)	P312L	possibly damaging	Het
Apol7e	A	T	15: 77,602,262 (GRCm39)	T287S	probably benign	Het
Arhgap12	A	T	18: 6,037,057 (GRCm39)	N561K	probably benign	Het
Armc3	G	T	2: 19,305,476 (GRCm39)	A757S	probably damaging	Het
Baz2b	A	T	2: 59,799,240 (GRCm39)	S295T	probably benign	Het
Brd4	T	A	17: 32,430,244 (GRCm39)	K686N	possibly damaging	Het
Btnl6	T	C	17: 34,727,202 (GRCm39)	T443A	probably benign	Het
Cacna1g	T	C	11: 94,306,922 (GRCm39)	T1801A	probably damaging	Het
Celsr2	G	A	3: 108,310,555 (GRCm39)	T1509I	possibly damaging	Het
Cers1	A	G	8: 70,782,660 (GRCm39)	D10G	possibly damaging	Het
Cntnap3	A	G	13: 64,929,618 (GRCm39)	V527A	probably damaging	Het
Cog1	G	T	11: 113,545,836 (GRCm39)	M370I	probably benign	Het
Col6a6	C	G	9: 105,657,891 (GRCm39)	V774L	probably damaging	Het
Csf1r	T	A	18: 61,245,836 (GRCm39)	S264R	probably benign	Het
Ctnna2	A	T	6: 76,931,740 (GRCm39)	V620D	probably damaging	Het
Eif2b4	A	G	5: 31,348,512 (GRCm39)	S88P	possibly damaging	Het
Frmd4b	G	A	6: 97,300,690 (GRCm39)	L214F	possibly damaging	Het
Fstl1	T	A	16: 37,647,113 (GRCm39)	L161Q	probably damaging	Het
Hdac1	A	G	4: 129,418,113 (GRCm39)	F94S	probably damaging	Het
Hlf	T	C	11: 90,278,929 (GRCm39)	D45G	probably benign	Het
Hps3	A	T	3: 20,072,976 (GRCm39)	M501K	probably damaging	Het
Ighv14-4	A	G	12: 114,140,174 (GRCm39)	Y79H	probably damaging	Het
Ip6k1	T	A	9: 107,923,086 (GRCm39)	V406D	probably damaging	Het
Iqcf1	T	C	9: 106,379,077 (GRCm39)	S29P	probably benign	Het
Itga11	A	G	9: 62,678,664 (GRCm39)	T944A	probably benign	Het
Kcnj12	A	G	11: 60,961,103 (GRCm39)	N467S	probably benign	Het
Klhdc3	T	A	17: 46,988,858 (GRCm39)	N111Y	possibly damaging	Het
Kmt2c	T	C	5: 25,614,136 (GRCm39)	R195G	possibly damaging	Het
Lin9	A	G	1: 180,486,676 (GRCm39)	I81V	probably null	Het
Lrp2	T	C	2: 69,331,892 (GRCm39)	D1621G	probably damaging	Het
Neb	A	G	2: 52,146,801 (GRCm39)	I2821T	possibly damaging	Het
Or14j6	T	C	17: 38,214,464 (GRCm39)	V9A	probably benign	Het
Or2a25	A	T	6: 42,889,271 (GRCm39)	K271N	probably damaging	Het
Or4c112	G	T	2: 88,853,770 (GRCm39)	H192Q	probably benign	Het
Or56b1	A	T	7: 104,285,540 (GRCm39)	I220L	possibly damaging	Het
Or8b3b	C	T	9: 38,584,159 (GRCm39)	V207I	probably benign	Het
Paxip1	A	G	5: 27,977,027 (GRCm39)		probably benign	Het
Pfas	T	C	11: 68,880,779 (GRCm39)		probably benign	Het
Pfdn1	C	T	18: 36,584,145 (GRCm39)	G63D	probably damaging	Het
Pgghg	T	C	7: 140,525,208 (GRCm39)	F405L	probably damaging	Het
Plcd3	T	C	11: 102,992,209 (GRCm39)	M50V	probably null	Het
Plekha8	C	A	6: 54,596,334 (GRCm39)	S198R	probably benign	Het
Ppp4c	C	T	7: 126,386,499 (GRCm39)	G166D	probably damaging	Het
Rassf2	T	C	2: 131,840,180 (GRCm39)		probably null	Het
Rnf217	T	A	10: 31,379,804 (GRCm39)	I473F	possibly damaging	Het
Sec16a	G	C	2: 26,331,825 (GRCm39)	N63K	possibly damaging	Het
Sik3	A	G	9: 46,130,784 (GRCm39)	D1240G	probably benign	Het
Slamf1	A	G	1: 171,625,745 (GRCm39)	D307G	probably null	Het
Slc2a3	A	G	6: 122,709,388 (GRCm39)	I337T	probably benign	Het
Tent4a	A	G	13: 69,661,115 (GRCm39)	V51A	probably damaging	Het
Tinag	C	T	9: 76,859,187 (GRCm39)	D474N	probably benign	Het
Ublcp1	A	G	11: 44,349,109 (GRCm39)	F242L	probably benign	Het
Ucp1	C	A	8: 84,017,270 (GRCm39)	A20D	probably damaging	Het
Ugt1a7c	C	T	1: 88,023,104 (GRCm39)	R88W	possibly damaging	Het
Wipf3	A	G	6: 54,458,780 (GRCm39)	D45G	probably damaging	Het
Zfp592	G	A	7: 80,674,280 (GRCm39)	A415T	probably benign	Het

Other mutations in Med15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00235:Med15	APN	16	17,498,590 (GRCm39)	missense	probably damaging	0.96
IGL00780:Med15	APN	16	17,471,351 (GRCm39)	missense	probably damaging	1.00
IGL02365:Med15	APN	16	17,489,470 (GRCm39)	intron	probably benign
R0324:Med15	UTSW	16	17,515,476 (GRCm39)	missense	probably damaging	0.98
R1225:Med15	UTSW	16	17,540,652 (GRCm39)	missense	probably damaging	1.00
R1695:Med15	UTSW	16	17,540,644 (GRCm39)	missense	probably damaging	0.96
R1745:Med15	UTSW	16	17,473,570 (GRCm39)	unclassified	probably benign
R1801:Med15	UTSW	16	17,498,599 (GRCm39)	missense	possibly damaging	0.66
R1838:Med15	UTSW	16	17,471,426 (GRCm39)	missense	probably benign	0.11
R1901:Med15	UTSW	16	17,491,018 (GRCm39)	unclassified	probably benign
R2153:Med15	UTSW	16	17,503,315 (GRCm39)	critical splice donor site	probably null
R2974:Med15	UTSW	16	17,470,575 (GRCm39)	missense	probably damaging	1.00
R3808:Med15	UTSW	16	17,473,598 (GRCm39)	unclassified	probably benign
R4240:Med15	UTSW	16	17,473,358 (GRCm39)	missense	probably damaging	1.00
R4483:Med15	UTSW	16	17,489,428 (GRCm39)	intron	probably benign
R4484:Med15	UTSW	16	17,489,428 (GRCm39)	intron	probably benign
R4577:Med15	UTSW	16	17,492,379 (GRCm39)	nonsense	probably null
R5652:Med15	UTSW	16	17,473,055 (GRCm39)	missense	probably damaging	1.00
R6244:Med15	UTSW	16	17,470,609 (GRCm39)	nonsense	probably null
R6701:Med15	UTSW	16	17,489,447 (GRCm39)	intron	probably benign
R6793:Med15	UTSW	16	17,470,567 (GRCm39)	unclassified	probably benign
R7036:Med15	UTSW	16	17,516,019 (GRCm39)	start codon destroyed	probably null
R7038:Med15	UTSW	16	17,470,591 (GRCm39)	missense	possibly damaging	0.90
R7211:Med15	UTSW	16	17,515,977 (GRCm39)	missense	unknown
R7317:Med15	UTSW	16	17,489,507 (GRCm39)	missense	unknown
R7390:Med15	UTSW	16	17,540,626 (GRCm39)	missense	unknown
R7471:Med15	UTSW	16	17,540,729 (GRCm39)	missense	probably benign	0.03
R7726:Med15	UTSW	16	17,473,038 (GRCm39)	missense	possibly damaging	0.87
R8872:Med15	UTSW	16	17,470,605 (GRCm39)	missense	probably damaging	1.00
R9043:Med15	UTSW	16	17,470,582 (GRCm39)	missense	probably benign	0.07
R9084:Med15	UTSW	16	17,471,072 (GRCm39)	missense	probably damaging	0.99
R9089:Med15	UTSW	16	17,473,421 (GRCm39)	missense	unknown
R9363:Med15	UTSW	16	17,489,414 (GRCm39)	missense	unknown
Z1177:Med15	UTSW	16	17,471,096 (GRCm39)	missense	possibly damaging	0.81

Predicted Primers

PCR Primer
(F):5'- CTCTGAGAAGGCTGTGGTGAAG -3'
(R):5'- GATACCATGTGTTATGTGTGCCC -3'

Sequencing Primer
(F):5'- CTGTGGTGAAGGGCTAGGCAG -3'
(R):5'- TGCCCAGAGGTAAGGCTTG -3'

Posted On

2015-04-02