Mutagenetix > Incidental Mutation

Incidental Mutation 'R7457:Gm29106'

578177

Institutional Source

Beutler Lab

Gene Symbol

Gm29106

Ensembl Gene

ENSMUSG00000102030

Gene Name

predicted gene 29106

Synonyms

MMRRC Submission

045531-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.302) question?

Stock #

R7457 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

118104272-118130037 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 118126982 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 225 (S225P)

Ref Sequence

ENSEMBL: ENSMUSP00000141137 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000186264]

AlphaFold

A0A087WSP8

Predicted Effect

probably damaging
Transcript: ENSMUST00000186264
AA Change: S225P

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000141137
Gene: ENSMUSG00000102030
AA Change: S225P

Domain	Start	End	E-Value	Type
KRAB	8	66	2.8e-24	SMART
ZnF_C2H2	77	97	2.3e-2	SMART
ZnF_C2H2	105	127	4.5e-6	SMART
ZnF_C2H2	133	155	3.4e-6	SMART
ZnF_C2H2	161	183	3.2e-7	SMART
ZnF_C2H2	189	211	2.1e-4	SMART
ZnF_C2H2	217	239	6.3e-7	SMART
ZnF_C2H2	245	267	3.4e-6	SMART
ZnF_C2H2	273	295	3.2e-7	SMART
ZnF_C2H2	301	323	2.1e-4	SMART
ZnF_C2H2	329	351	6.3e-7	SMART
ZnF_C2H2	357	379	2.1e-4	SMART
ZnF_C2H2	385	407	7.8e-5	SMART
ZnF_C2H2	413	435	1.1e-7	SMART
ZnF_C2H2	441	463	4e-5	SMART
ZnF_C2H2	469	491	1.3e-6	SMART
ZnF_C2H2	497	519	2.4e-6	SMART
ZnF_C2H2	525	547	2.3e-4	SMART
ZnF_C2H2	553	575	1.4e-4	SMART
ZnF_C2H2	581	603	1.9e-6	SMART
ZnF_C2H2	609	631	5.2e-5	SMART
ZnF_C2H2	637	659	1.7e-5	SMART
ZnF_C2H2	665	687	9.4e-7	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (61/61)

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam32	A	T	8: 25,374,635 (GRCm39)	H452Q	probably damaging	Het
Adcy8	A	T	15: 64,792,529 (GRCm39)	N142K	possibly damaging	Het
Alkbh8	T	A	9: 3,343,056 (GRCm39)	S57R	probably damaging	Het
Atp4a	A	G	7: 30,420,192 (GRCm39)	T780A	probably benign	Het
Atp9b	A	T	18: 80,960,833 (GRCm39)		probably null	Het
Cdyl2	A	T	8: 117,305,935 (GRCm39)	V442E	probably damaging	Het
Ces2a	C	T	8: 105,464,021 (GRCm39)	R218C	possibly damaging	Het
Cfap57	A	T	4: 118,446,198 (GRCm39)	V688E	probably damaging	Het
Clec11a	T	C	7: 43,955,379 (GRCm39)	T139A	probably benign	Het
Clstn1	A	T	4: 149,719,373 (GRCm39)	T411S	probably benign	Het
Commd5	A	T	15: 76,784,824 (GRCm39)	S74C	probably damaging	Het
Cyp3a59	C	A	5: 146,041,560 (GRCm39)	P368Q	probably damaging	Het
Dennd4b	A	G	3: 90,176,622 (GRCm39)	M309V	probably benign	Het
Dhrs9	T	A	2: 69,231,611 (GRCm39)	V257E	probably benign	Het
Dhx16	T	C	17: 36,201,952 (GRCm39)	V993A	probably damaging	Het
Dok5	A	T	2: 170,712,735 (GRCm39)	Q247L	probably benign	Het
E330034G19Rik	A	T	14: 24,359,582 (GRCm39)	E331V	unknown	Het
Efs	A	G	14: 55,157,451 (GRCm39)	S287P	probably benign	Het
Fbn1	T	C	2: 125,193,667 (GRCm39)	N1384S	possibly damaging	Het
Flt4	A	G	11: 49,521,155 (GRCm39)	E388G	possibly damaging	Het
Fmn2	T	A	1: 174,331,303 (GRCm39)		probably null	Het
Fmo4	T	C	1: 162,621,672 (GRCm39)	Y513C	probably benign	Het
Gbp4	T	C	5: 105,267,419 (GRCm39)	E500G	probably damaging	Het
Gstt2	G	A	10: 75,668,354 (GRCm39)	R134W	probably damaging	Het
Gucy1b2	T	C	14: 62,630,401 (GRCm39)	T782A	probably benign	Het
Gzf1	G	T	2: 148,532,002 (GRCm39)	R543L	probably damaging	Het
H2-Eb2	G	A	17: 34,553,321 (GRCm39)	G169E	probably damaging	Het
Hdhd3	T	A	4: 62,418,027 (GRCm39)	R50W	probably damaging	Het
Hdlbp	T	C	1: 93,355,944 (GRCm39)	K407E	probably benign	Het
Isl2	A	G	9: 55,452,240 (GRCm39)	T271A	probably benign	Het
Kbtbd7	GTCTCTC	GTC	14: 79,665,364 (GRCm39)		probably null	Het
Kdm4b	T	A	17: 56,703,319 (GRCm39)	N671K	probably damaging	Het
Lats1	T	A	10: 7,586,655 (GRCm39)	L939H	probably damaging	Het
Map3k1	A	T	13: 111,892,789 (GRCm39)	M822K	probably damaging	Het
Mettl18	C	A	1: 163,824,330 (GRCm39)	T217N	probably damaging	Het
Nav3	A	T	10: 109,532,189 (GRCm39)	Y2083*	probably null	Het
Nckap1l	T	C	15: 103,362,233 (GRCm39)		probably benign	Het
Nkx2-3	A	G	19: 43,600,986 (GRCm39)	D16G	probably damaging	Het
Nlrx1	A	G	9: 44,167,807 (GRCm39)	S697P	probably benign	Het
Or14j4	T	C	17: 37,921,456 (GRCm39)	K62R	possibly damaging	Het
Or1e29	G	C	11: 73,667,652 (GRCm39)	S167C	probably benign	Het
Or4k6	A	T	14: 50,475,825 (GRCm39)	N172K	probably damaging	Het
Or6c75	T	C	10: 129,337,575 (GRCm39)	V266A	probably damaging	Het
Pappa	A	T	4: 65,107,503 (GRCm39)	D638V	probably damaging	Het
Pot1a	T	C	6: 25,771,621 (GRCm39)	D200G	probably benign	Het
Ptprs	G	T	17: 56,726,502 (GRCm39)	T1366K	probably damaging	Het
Sass6	A	T	3: 116,413,813 (GRCm39)	R505S	probably benign	Het
Slc30a6	T	C	17: 74,714,233 (GRCm39)	I84T	probably benign	Het
Sox10	A	T	15: 79,040,339 (GRCm39)	F400L	probably benign	Het
Spata31d1b	A	T	13: 59,864,723 (GRCm39)	I624F	probably damaging	Het
Stpg4	A	G	17: 87,735,006 (GRCm39)		probably null	Het
Tbc1d9	G	T	8: 83,963,309 (GRCm39)	K340N	probably damaging	Het
Tspan12	T	A	6: 21,772,682 (GRCm39)	H289L	probably benign	Het
Ubr1	T	A	2: 120,748,309 (GRCm39)	T809S	probably benign	Het
Vmn1r43	C	T	6: 89,847,172 (GRCm39)	V105M	probably damaging	Het
Vmn1r49	A	G	6: 90,049,534 (GRCm39)	V156A	probably benign	Het
Wnt5a	A	G	14: 28,240,236 (GRCm39)		probably null	Het
Wwp2	T	A	8: 108,244,592 (GRCm39)	S255T	probably benign	Het
Zbtb10	A	G	3: 9,316,538 (GRCm39)	T117A	possibly damaging	Het
Zfp800	C	T	6: 28,244,228 (GRCm39)	V246I	probably benign	Het
Zfp955a	G	T	17: 33,463,025 (GRCm39)	Y35*	probably null	Het

Other mutations in Gm29106

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R4985:Gm29106	UTSW	1	118,126,950 (GRCm39)	missense	probably benign	0.02
R4991:Gm29106	UTSW	1	118,106,121 (GRCm39)	missense	probably benign	0.01
R6029:Gm29106	UTSW	1	118,127,990 (GRCm39)	missense	probably damaging	1.00
R6922:Gm29106	UTSW	1	118,127,524 (GRCm39)	missense	probably damaging	0.98
R6954:Gm29106	UTSW	1	118,128,317 (GRCm39)	missense	probably damaging	1.00
R6961:Gm29106	UTSW	1	118,128,128 (GRCm39)	nonsense	probably null
R7232:Gm29106	UTSW	1	118,127,291 (GRCm39)	missense	probably damaging	1.00
R7337:Gm29106	UTSW	1	118,104,642 (GRCm39)	missense	unknown
R7662:Gm29106	UTSW	1	118,127,137 (GRCm39)	missense	possibly damaging	0.89
R7870:Gm29106	UTSW	1	118,126,885 (GRCm39)	missense	possibly damaging	0.55
R7894:Gm29106	UTSW	1	118,127,265 (GRCm39)	missense	probably damaging	1.00
R7986:Gm29106	UTSW	1	118,128,000 (GRCm39)	missense	possibly damaging	0.62
R8099:Gm29106	UTSW	1	118,126,521 (GRCm39)	missense	probably benign	0.00
R8377:Gm29106	UTSW	1	118,126,593 (GRCm39)	missense	probably damaging	0.99
R8498:Gm29106	UTSW	1	118,128,218 (GRCm39)	missense	probably damaging	1.00
R8553:Gm29106	UTSW	1	118,128,149 (GRCm39)	missense	probably damaging	1.00
R8980:Gm29106	UTSW	1	118,127,114 (GRCm39)	missense	possibly damaging	0.86
R9212:Gm29106	UTSW	1	118,127,270 (GRCm39)	missense	probably damaging	1.00
R9451:Gm29106	UTSW	1	118,127,644 (GRCm39)	missense	possibly damaging	0.66
R9746:Gm29106	UTSW	1	118,127,254 (GRCm39)	missense	possibly damaging	0.94

Predicted Primers

PCR Primer
(F):5'- TCGGGAAGCTCAAGATACTCTTTC -3'
(R):5'- CCTGGGTAAAAGATTTTCCACATTC -3'

Sequencing Primer
(F):5'- TCACCAGAGATTGCATACTGG -3'
(R):5'- TCATTACATTTGTAAGGTTTGTCTCC -3'

Posted On

2019-10-07