Mutagenetix > Incidental Mutation

Incidental Mutation 'R6594:Gm11437'

524803

Institutional Source

Beutler Lab

Gene Symbol

Gm11437

Ensembl Gene

ENSMUSG00000051452

Gene Name

predicted gene 11437

Synonyms

MMRRC Submission

044718-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.080) question?

Stock #

R6594 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

84039187-84058302 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 84055386 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Arginine at position 77 (G77R)

Ref Sequence

ENSEMBL: ENSMUSP00000056084 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000050771] [ENSMUST00000133811]

AlphaFold

Q5QR91

Predicted Effect

probably null
Transcript: ENSMUST00000050771
AA Change: G77R

PolyPhen 2 Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000056084
Gene: ENSMUSG00000051452
AA Change: G77R

Domain	Start	End	E-Value	Type
Pfam:DUF4711	1	226	7.4e-102	PFAM
low complexity region	227	238	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000133811

SMART Domains

Protein: ENSMUSP00000116174
Gene: ENSMUSG00000020532

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
PDB:2YL2\|B	115	157	2e-21	PDB

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.9%

Validation Efficiency

96% (52/54)

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aass	T	C	6: 23,113,432 (GRCm39)	N296S	probably benign	Het
Abca13	A	T	11: 9,244,632 (GRCm39)	N2165I	possibly damaging	Het
Anpep	T	A	7: 79,491,109 (GRCm39)		probably null	Het
Bcl2a1b	A	C	9: 89,089,647 (GRCm39)	I145L	probably benign	Het
Ccar2	G	A	14: 70,377,925 (GRCm39)	L687F	probably damaging	Het
Cd69	A	G	6: 129,246,537 (GRCm39)		probably null	Het
Chchd10	A	C	10: 75,772,158 (GRCm39)	Q43P	probably damaging	Het
Ddx55	A	G	5: 124,704,988 (GRCm39)	E415G	probably damaging	Het
Defa41	A	G	8: 21,692,471 (GRCm39)		probably null	Het
Dhx40	A	T	11: 86,676,599 (GRCm39)	C172S	possibly damaging	Het
Epha1	G	A	6: 42,341,625 (GRCm39)	T475I	probably benign	Het
Eri1	T	C	8: 35,949,687 (GRCm39)	T91A	probably damaging	Het
Fscn1	C	T	5: 142,955,783 (GRCm39)	A158V	probably benign	Het
Golm1	T	C	13: 59,812,041 (GRCm39)	N94D	possibly damaging	Het
Gpat2	G	C	2: 127,273,838 (GRCm39)	G294R	possibly damaging	Het
Haus4	C	A	14: 54,781,268 (GRCm39)	E269D	possibly damaging	Het
Hyou1	T	C	9: 44,300,619 (GRCm39)	M896T	probably benign	Het
Itpr2	T	A	6: 146,091,978 (GRCm39)	M2174L	possibly damaging	Het
Kars1	T	C	8: 112,720,299 (GRCm39)		probably benign	Het
Kif1a	T	C	1: 92,949,035 (GRCm39)	M1488V	probably benign	Het
Lrp2	T	C	2: 69,270,267 (GRCm39)	T4106A	possibly damaging	Het
Lrrc20	G	A	10: 61,318,225 (GRCm39)	V16I	possibly damaging	Het
Mecr	T	A	4: 131,582,004 (GRCm39)	V162E	probably damaging	Het
Ms4a4a	C	A	19: 11,363,778 (GRCm39)	A102E	probably damaging	Het
Mycn	T	C	12: 12,990,051 (GRCm39)	D115G	probably damaging	Het
Ninj2	A	T	6: 120,175,750 (GRCm39)	T138S	possibly damaging	Het
Oasl2	G	A	5: 115,044,836 (GRCm39)	V121I	probably benign	Het
Or10s1	T	C	9: 39,986,239 (GRCm39)	L216P	probably damaging	Het
Or2r11	A	T	6: 42,437,309 (GRCm39)	S215T	probably benign	Het
Or7g19	T	C	9: 18,856,127 (GRCm39)	F61S	probably damaging	Het
Pcdha11	A	C	18: 37,144,235 (GRCm39)	I109L	probably benign	Het
Pira1	T	A	7: 3,739,498 (GRCm39)	K457*	probably null	Het
Pon1	A	G	6: 5,185,314 (GRCm39)	L62P	probably damaging	Het
Rp1l1	A	T	14: 64,269,126 (GRCm39)	K1571*	probably null	Het
Sec24d	G	T	3: 123,087,412 (GRCm39)	G193C	probably damaging	Het
Sema3b	A	T	9: 107,476,025 (GRCm39)	M732K	probably benign	Het
Serpinb8	T	C	1: 107,525,201 (GRCm39)	M1T	probably null	Het
Sgip1	T	A	4: 102,819,676 (GRCm39)	V594E	probably damaging	Het
Slc3a2	T	C	19: 8,685,410 (GRCm39)	S197G	probably damaging	Het
Slc44a5	T	C	3: 153,964,660 (GRCm39)	V520A	possibly damaging	Het
Surf6	G	T	2: 26,792,761 (GRCm39)	D13E	possibly damaging	Het
Tmem94	G	A	11: 115,689,112 (GRCm39)	R1341H	probably damaging	Het
Tns2	G	A	15: 102,018,994 (GRCm39)	R395Q	probably benign	Het
Traf7	A	G	17: 24,728,813 (GRCm39)	V591A	possibly damaging	Het
Trim72	T	C	7: 127,609,220 (GRCm39)	S341P	probably damaging	Het
Trps1	A	G	15: 50,694,351 (GRCm39)	V398A	probably damaging	Het
Ube2m	C	A	7: 12,771,617 (GRCm39)	E14*	probably null	Het
Unc119	T	A	11: 78,238,046 (GRCm39)	Y10N	probably damaging	Het
Ush2a	T	C	1: 188,642,995 (GRCm39)	L4119P	possibly damaging	Het
Vcp	A	T	4: 42,993,826 (GRCm39)	I102N	probably damaging	Het
Vmn2r4	A	G	3: 64,296,731 (GRCm39)	S685P	probably damaging	Het
Vmn2r58	T	C	7: 41,486,535 (GRCm39)	M787V	possibly damaging	Het
Vmn2r72	T	C	7: 85,398,892 (GRCm39)	H487R	probably benign	Het
Xcr1	A	G	9: 123,685,309 (GRCm39)	I151T	probably benign	Het
Zfp658	T	C	7: 43,216,701 (GRCm39)	S24P	possibly damaging	Het
Zfyve16	T	C	13: 92,650,326 (GRCm39)	D886G	probably benign	Het

Other mutations in Gm11437

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00959:Gm11437	APN	11	84,039,448 (GRCm39)	intron	probably benign
IGL01354:Gm11437	APN	11	84,058,144 (GRCm39)	intron	probably benign
IGL02051:Gm11437	APN	11	84,043,592 (GRCm39)	missense	probably benign	0.00
IGL03184:Gm11437	APN	11	84,047,090 (GRCm39)	intron	probably benign
R0076:Gm11437	UTSW	11	84,039,462 (GRCm39)	missense	possibly damaging	0.91
R0076:Gm11437	UTSW	11	84,039,462 (GRCm39)	missense	possibly damaging	0.91
R1241:Gm11437	UTSW	11	84,055,454 (GRCm39)	missense	possibly damaging	0.93
R2135:Gm11437	UTSW	11	84,044,638 (GRCm39)	missense	probably damaging	0.97
R4065:Gm11437	UTSW	11	84,055,337 (GRCm39)	missense	probably benign	0.13
R4067:Gm11437	UTSW	11	84,055,337 (GRCm39)	missense	probably benign	0.13
R5356:Gm11437	UTSW	11	84,043,513 (GRCm39)	missense	possibly damaging	0.90
R6571:Gm11437	UTSW	11	84,047,038 (GRCm39)	missense	probably benign	0.13
R7173:Gm11437	UTSW	11	84,055,374 (GRCm39)	missense	probably benign	0.39
R7368:Gm11437	UTSW	11	84,058,298 (GRCm39)	intron	probably benign
R8918:Gm11437	UTSW	11	84,043,530 (GRCm39)	missense	probably benign	0.01
X0026:Gm11437	UTSW	11	84,056,153 (GRCm39)	missense	possibly damaging	0.92
X0028:Gm11437	UTSW	11	84,046,926 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- TGAGTGCCAACCTACCTCTG -3'
(R):5'- AGGGCCTGCACAGTTAGTAC -3'

Sequencing Primer
(F):5'- TCTGATCTCACTTTACCTGTTAGAAG -3'
(R):5'- GGCCTGCACAGTTAGTACCATAAAC -3'

Posted On

2018-06-22