Mutagenetix > Incidental Mutation

Incidental Mutation 'R9190:Gm5134'

697694

Institutional Source

Beutler Lab

Gene Symbol

Gm5134

Ensembl Gene

ENSMUSG00000033255

Gene Name

predicted gene 5134

Synonyms

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.113) question?

Stock #

R9190 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

75790348-75845425 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 75844645 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 667 (H667R)

Ref Sequence

ENSEMBL: ENSMUSP00000097172 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099577]

AlphaFold

E9QAB5

Predicted Effect

probably damaging
Transcript: ENSMUST00000099577
AA Change: H667R

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

SMART Domains

Protein: ENSMUSP00000097172
Gene: ENSMUSG00000033255
AA Change: H667R

Domain	Start	End	E-Value	Type
Pfam:SSF	32	466	2.9e-119	PFAM
transmembrane domain	500	522	N/A	INTRINSIC
transmembrane domain	651	670	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (52/52)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930433I11Rik	C	T	7: 40,642,880 (GRCm39)	T183I	possibly damaging	Het
Abca13	T	A	11: 9,241,886 (GRCm39)	S1250T	probably damaging	Het
Adamts12	T	A	15: 11,336,446 (GRCm39)	S1510R	probably benign	Het
Adcy5	T	A	16: 35,089,364 (GRCm39)	C520*	probably null	Het
Arhgap21	A	T	2: 20,858,983 (GRCm39)	M1237K	probably null	Het
Atp8b4	T	A	2: 126,225,607 (GRCm39)	N541I	probably damaging	Het
Bbs12	G	T	3: 37,375,223 (GRCm39)	R557L	probably damaging	Het
Bcl7c	T	C	7: 127,266,200 (GRCm39)	T183A	probably benign	Het
Brd7	A	G	8: 89,081,274 (GRCm39)	S192P	probably damaging	Het
Calhm3	G	A	19: 47,146,121 (GRCm39)	A28V	probably benign	Het
Ccdc113	A	G	8: 96,263,101 (GRCm39)	N37S	probably damaging	Het
Cdh5	T	G	8: 104,867,337 (GRCm39)	V538G	probably damaging	Het
Cfap43	T	C	19: 47,726,293 (GRCm39)	E1639G	possibly damaging	Het
Clca3a2	C	T	3: 144,796,599 (GRCm39)	V203I	probably benign	Het
Clstn2	A	G	9: 97,414,815 (GRCm39)	F360L	probably damaging	Het
Cnst	GTGACACGCTTG	GTG	1: 179,407,039 (GRCm39)		probably benign	Het
Cog2	T	C	8: 125,260,058 (GRCm39)	Y234H	probably damaging	Het
Ddhd2	T	C	8: 26,244,495 (GRCm39)	S44G	probably benign	Het
Dync2i2	G	T	2: 29,922,211 (GRCm39)	H417N	probably benign	Het
Farp1	A	G	14: 121,492,988 (GRCm39)	E530G	probably damaging	Het
Fhad1	C	T	4: 141,646,058 (GRCm39)		probably null	Het
Foxj3	T	A	4: 119,477,538 (GRCm39)	C449*	probably null	Het
Fsbp	G	C	4: 11,584,005 (GRCm39)	V235L	probably benign	Het
Fuom	T	C	7: 139,681,252 (GRCm39)	E73G	probably benign	Het
Igsf21	A	G	4: 139,756,028 (GRCm39)	I361T	probably damaging	Het
Iws1	G	A	18: 32,213,213 (GRCm39)	E214K	possibly damaging	Het
Kmt2d	A	T	15: 98,749,896 (GRCm39)	V2599E	unknown	Het
Lama1	T	A	17: 68,111,514 (GRCm39)	M2255K		Het
Litafd	C	A	16: 8,501,647 (GRCm39)	P50T		Het
Lrrc32	A	G	7: 98,148,234 (GRCm39)	H338R	probably benign	Het
Map1b	C	A	13: 99,571,914 (GRCm39)	R269L	probably damaging	Het
Ms4a5	T	A	19: 11,256,733 (GRCm39)	I55F	probably damaging	Het
Muc5b	G	C	7: 141,411,939 (GRCm39)	L1628F	unknown	Het
Myo6	A	G	9: 80,195,384 (GRCm39)	Q918R	unknown	Het
Or1e25	T	A	11: 73,493,877 (GRCm39)	M157K	probably benign	Het
Or2t48	A	G	11: 58,420,161 (GRCm39)	V217A	possibly damaging	Het
Or5m11b	T	A	2: 85,805,884 (GRCm39)	I99N	possibly damaging	Het
Or9i1b	T	G	19: 13,896,967 (GRCm39)	N194K	probably benign	Het
Pals2	A	G	6: 50,157,219 (GRCm39)	R296G	probably damaging	Het
Plin5	A	G	17: 56,419,462 (GRCm39)	V320A	probably damaging	Het
Ptx4	A	T	17: 25,342,257 (GRCm39)	Q244L	possibly damaging	Het
Rab3gap1	A	G	1: 127,858,495 (GRCm39)	T535A	probably benign	Het
Ranbp2	T	C	10: 58,313,117 (GRCm39)	F1279S	probably damaging	Het
Rgl1	T	C	1: 152,428,362 (GRCm39)	H254R	probably damaging	Het
Rida	C	T	15: 34,487,909 (GRCm39)	A69T	probably damaging	Het
Scn2a	T	C	2: 65,511,346 (GRCm39)	F131L	probably benign	Het
Septin1	T	C	7: 126,816,092 (GRCm39)	I141V	probably benign	Het
Slc10a6	A	G	5: 103,765,571 (GRCm39)	S171P	probably damaging	Het
Slc18a1	A	G	8: 69,519,790 (GRCm39)		probably null	Het
Slc38a6	T	C	12: 73,388,526 (GRCm39)	S247P	possibly damaging	Het
Tet2	A	T	3: 133,187,147 (GRCm39)	I1094K	possibly damaging	Het
Tmem234	C	T	4: 129,501,333 (GRCm39)	S138L	probably benign	Het
Trpv1	T	A	11: 73,145,148 (GRCm39)		probably null	Het
Vmn2r60	T	A	7: 41,844,935 (GRCm39)	M766K	probably damaging	Het
Vmn2r84	T	C	10: 130,226,843 (GRCm39)	N332D	probably benign	Het
Zfp292	A	T	4: 34,819,563 (GRCm39)	I258N	probably damaging	Het
Zxdc	A	G	6: 90,375,773 (GRCm39)	K750E	probably damaging	Het

Other mutations in Gm5134

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00941:Gm5134	APN	10	75,836,255 (GRCm39)	missense	possibly damaging	0.70
IGL01371:Gm5134	APN	10	75,840,581 (GRCm39)	missense	probably damaging	0.99
IGL02140:Gm5134	APN	10	75,821,945 (GRCm39)	missense	probably benign	0.03
IGL02197:Gm5134	APN	10	75,790,536 (GRCm39)	critical splice donor site	probably null
IGL02233:Gm5134	APN	10	75,844,334 (GRCm39)	critical splice acceptor site	probably null
IGL02612:Gm5134	APN	10	75,828,323 (GRCm39)	missense	probably damaging	1.00
IGL02896:Gm5134	APN	10	75,810,058 (GRCm39)	missense	possibly damaging	0.82
R0021:Gm5134	UTSW	10	75,829,718 (GRCm39)	missense	probably damaging	1.00
R0021:Gm5134	UTSW	10	75,829,718 (GRCm39)	missense	probably damaging	1.00
R0035:Gm5134	UTSW	10	75,829,698 (GRCm39)	missense	probably benign	0.01
R0035:Gm5134	UTSW	10	75,829,698 (GRCm39)	missense	probably benign	0.01
R0110:Gm5134	UTSW	10	75,810,079 (GRCm39)	missense	probably benign	0.03
R0499:Gm5134	UTSW	10	75,828,359 (GRCm39)	missense	probably benign	0.00
R0510:Gm5134	UTSW	10	75,810,079 (GRCm39)	missense	probably benign	0.03
R1429:Gm5134	UTSW	10	75,814,215 (GRCm39)	missense	probably damaging	1.00
R1726:Gm5134	UTSW	10	75,828,361 (GRCm39)	missense	possibly damaging	0.83
R1918:Gm5134	UTSW	10	75,812,180 (GRCm39)	missense	possibly damaging	0.70
R1956:Gm5134	UTSW	10	75,840,680 (GRCm39)	missense	possibly damaging	0.89
R1993:Gm5134	UTSW	10	75,802,227 (GRCm39)	missense	probably damaging	0.96
R2049:Gm5134	UTSW	10	75,840,718 (GRCm39)	missense	possibly damaging	0.92
R2188:Gm5134	UTSW	10	75,831,670 (GRCm39)	missense	probably damaging	1.00
R3551:Gm5134	UTSW	10	75,836,281 (GRCm39)	missense	probably benign	0.08
R4074:Gm5134	UTSW	10	75,844,365 (GRCm39)	missense	probably damaging	1.00
R4435:Gm5134	UTSW	10	75,831,658 (GRCm39)	missense	probably damaging	1.00
R4466:Gm5134	UTSW	10	75,844,409 (GRCm39)	missense	probably benign	0.00
R5180:Gm5134	UTSW	10	75,812,200 (GRCm39)	missense	probably damaging	1.00
R5446:Gm5134	UTSW	10	75,831,670 (GRCm39)	missense	probably damaging	1.00
R5601:Gm5134	UTSW	10	75,821,786 (GRCm39)	missense	probably damaging	0.98
R5627:Gm5134	UTSW	10	75,821,942 (GRCm39)	missense	possibly damaging	0.93
R5777:Gm5134	UTSW	10	75,840,594 (GRCm39)	missense	probably benign	0.00
R5867:Gm5134	UTSW	10	75,844,450 (GRCm39)	missense	probably benign	0.00
R6145:Gm5134	UTSW	10	75,831,673 (GRCm39)	missense	probably damaging	0.99
R6232:Gm5134	UTSW	10	75,821,859 (GRCm39)	missense	possibly damaging	0.95
R6271:Gm5134	UTSW	10	75,831,643 (GRCm39)	missense	probably benign	0.32
R6329:Gm5134	UTSW	10	75,790,494 (GRCm39)	missense	possibly damaging	0.68
R6723:Gm5134	UTSW	10	75,844,453 (GRCm39)	missense	probably benign
R7049:Gm5134	UTSW	10	75,828,292 (GRCm39)	missense	probably damaging	0.97
R7305:Gm5134	UTSW	10	75,836,233 (GRCm39)	missense	probably damaging	1.00
R7579:Gm5134	UTSW	10	75,800,271 (GRCm39)	missense	probably damaging	1.00
R9716:Gm5134	UTSW	10	75,821,943 (GRCm39)	missense	probably benign	0.27
R9718:Gm5134	UTSW	10	75,828,331 (GRCm39)	missense	possibly damaging	0.90
X0050:Gm5134	UTSW	10	75,828,344 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCTGGAAGAAGGTTGTATCCAG -3'
(R):5'- TCAGAGAGGAGCACACATCC -3'

Sequencing Primer
(F):5'- GTTGTATCCAGCGACAGGTCAAC -3'
(R):5'- CCGCACAGTTTGTAAACACGGG -3'

Posted On

2022-02-07