Mutagenetix > Incidental Mutations

Incidental Mutation 'R0884:Prrg4'

81009

Institutional Source

Beutler Lab

Gene Symbol

Prrg4

Ensembl Gene

ENSMUSG00000027171

Gene Name

proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)

Synonyms

9930111I18Rik, TMG4

MMRRC Submission

039051-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.110) question?

Stock #

R0884 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

104830741-104849876 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 104839362 bp

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 137 (Y137N)

Ref Sequence

ENSEMBL: ENSMUSP00000121788 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028593] [ENSMUST00000126824]

Predicted Effect

probably damaging
Transcript: ENSMUST00000028593
AA Change: Y137N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000028593
Gene: ENSMUSG00000027171
AA Change: Y137N

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
GLA	33	97	1.71e-18	SMART
transmembrane domain	118	140	N/A	INTRINSIC
low complexity region	203	210	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000126824
AA Change: Y137N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000121788
Gene: ENSMUSG00000027171
AA Change: Y137N

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
GLA	33	97	1.71e-18	SMART
transmembrane domain	118	140	N/A	INTRINSIC

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.4%
20x: 94.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc4	A	T	14: 118,553,288	I844N	possibly damaging	Het
Acbd3	CGAGGAGGAGGAGGAGGA	CGAGGAGGAGGAGGA	1: 180,747,059		probably benign	Het
Adam6b	A	T	12: 113,490,995	R477S	probably damaging	Het
Aqp7	T	A	4: 41,034,929	T175S	possibly damaging	Het
Bclaf1	A	T	10: 20,322,076	R22*	probably null	Het
Bend7	A	T	2: 4,744,244	K57N	probably damaging	Het
Bicc1	A	C	10: 70,958,847	V160G	probably damaging	Het
Cacna2d4	C	T	6: 119,307,286	R745W	probably damaging	Het
Cep72	A	G	13: 74,054,881		probably null	Het
Cobl	A	G	11: 12,375,908	I196T	possibly damaging	Het
Cux1	T	G	5: 136,307,835	D941A	probably damaging	Het
Cyp2a12	T	C	7: 27,032,542	I236T	probably benign	Het
Depdc5	T	A	5: 32,917,978	V500D	possibly damaging	Het
Dhx35	T	C	2: 158,831,711	I354T	probably damaging	Het
Dnase1l2	A	G	17: 24,441,880	V170A	possibly damaging	Het
Eif4g3	C	A	4: 138,151,776	N588K	possibly damaging	Het
Epsti1	A	T	14: 77,931,275	R117S	probably damaging	Het
Fam53a	T	C	5: 33,600,816	E321G	probably benign	Het
Fat4	C	A	3: 38,982,858	T3553K	possibly damaging	Het
Fer1l4	T	C	2: 156,019,313	T1978A	possibly damaging	Het
Gabarapl2	A	T	8: 111,942,505	I32F	probably damaging	Het
Gje1	G	T	10: 14,716,740	S99R	possibly damaging	Het
Gm13083	A	G	4: 143,615,184	D61G	probably benign	Het
Gosr1	A	G	11: 76,730,146	I239T	probably benign	Het
Gpnmb	T	C	6: 49,047,913	V293A	possibly damaging	Het
Hyi	T	A	4: 118,360,217	I62N	probably damaging	Het
Il4ra	A	G	7: 125,574,663	I267V	probably damaging	Het
Kcnd2	A	T	6: 21,216,541	Q81H	probably benign	Het
Ksr1	A	T	11: 79,021,503	H675Q	possibly damaging	Het
Lpcat4	A	G	2: 112,242,732	N208S	probably damaging	Het
Muc3	T	A	5: 137,142,298	T162S	possibly damaging	Het
Mup3	T	A	4: 62,087,174	I20F	possibly damaging	Het
Nebl	A	C	2: 17,411,118	S327A	probably benign	Het
Nfatc4	A	C	14: 55,826,644	D126A	probably damaging	Het
Nmt2	A	T	2: 3,314,785	R271*	probably null	Het
Nol7	G	A	13: 43,400,615	V133I	probably benign	Het
Olfr376	A	T	11: 73,374,889	I47F	probably benign	Het
Olfr610	C	T	7: 103,506,862	W28*	probably null	Het
Pde4d	A	T	13: 109,950,940	I670L	probably damaging	Het
Phlpp1	T	A	1: 106,389,665		probably null	Het
Pigz	A	G	16: 31,941,976		probably null	Het
Rbm28	A	T	6: 29,155,154	S217T	possibly damaging	Het
Ryr2	T	C	13: 11,554,529	D4963G	probably damaging	Het
Slc35b2	T	A	17: 45,566,825	F293I	probably damaging	Het
Slc35f1	A	T	10: 53,089,347	Y286F	probably damaging	Het
Slc6a18	G	T	13: 73,667,037	A384D	probably damaging	Het
St5	A	G	7: 109,557,345	L66P	probably damaging	Het
Syt9	A	G	7: 107,436,561	I262V	probably damaging	Het
Tln2	C	A	9: 67,370,733	R333L	probably damaging	Het
Tnrc6b	ACAGCAGCAGCAGCAGCAGCAG	ACAGCAGCAGCAGCAGCAG	15: 80,902,555		probably benign	Het
Ttn	G	A	2: 76,751,066	T14834I	possibly damaging	Het
Uggt1	T	C	1: 36,175,078	S177G	probably benign	Het
Zfp454	A	G	11: 50,873,937	S223P	probably benign	Het
Zmat4	A	G	8: 24,015,127	T128A	probably benign	Het

Other mutations in Prrg4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01804:Prrg4	APN	2	104832690	missense	probably damaging	1.00
R1624:Prrg4	UTSW	2	104832682	missense	probably damaging	0.97
R1647:Prrg4	UTSW	2	104832743	missense	probably benign	0.00
R1648:Prrg4	UTSW	2	104832743	missense	probably benign	0.00
R2151:Prrg4	UTSW	2	104839388	missense	probably damaging	1.00
R5592:Prrg4	UTSW	2	104832778	missense	probably benign	0.22
R5898:Prrg4	UTSW	2	104845033	missense	probably benign	0.00
R7158:Prrg4	UTSW	2	104832613	missense	probably damaging	1.00
R7203:Prrg4	UTSW	2	104839442	missense	possibly damaging	0.63
R7727:Prrg4	UTSW	2	104839378	missense	probably benign	0.00

Predicted Primers

Posted On

2013-11-07