Mutagenetix > Incidental Mutation

Incidental Mutation 'R6159:Gm43302'

489747

Institutional Source

Beutler Lab

Gene Symbol

Gm43302

Ensembl Gene

ENSMUSG00000079362

Gene Name

predicted gene 43302

Synonyms

MMRRC Submission

044306-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.056) question?

Stock #

R6159 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

105362773-105441561 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 105436894 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 71 (S71P)

Ref Sequence

ENSEMBL: ENSMUSP00000142518 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000050011] [ENSMUST00000196520] [ENSMUST00000200045]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000050011
AA Change: S71P

PolyPhen 2 Score 0.108 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000062528
Gene: ENSMUSG00000079362
AA Change: S71P

Domain	Start	End	E-Value	Type
Pfam:GBP	16	279	7.6e-118	PFAM
Pfam:GBP_C	281	575	2.1e-117	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000196520
AA Change: S71P

PolyPhen 2 Score 0.108 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000142518
Gene: ENSMUSG00000104713
AA Change: S71P

Domain	Start	End	E-Value	Type
Pfam:GBP	16	279	2.8e-124	PFAM
Pfam:GBP_C	281	575	2.1e-117	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000199944

Predicted Effect

probably benign
Transcript: ENSMUST00000200045

SMART Domains

Protein: ENSMUSP00000142994
Gene: ENSMUSG00000104713

Domain	Start	End	E-Value	Type
Pfam:GBP	16	62	7.4e-19	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 98.0%
20x: 94.2%

Validation Efficiency

96% (54/56)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahcyl2	A	C	6: 29,908,457 (GRCm39)	N609T	possibly damaging	Het
Ankzf1	G	A	1: 75,170,888 (GRCm39)	C98Y	probably damaging	Het
Atg101	T	A	15: 101,188,519 (GRCm39)	M208K	possibly damaging	Het
Baiap2l2	A	G	15: 79,143,930 (GRCm39)	I388T	probably benign	Het
Cabs1	C	T	5: 88,127,613 (GRCm39)	T88I	possibly damaging	Het
Chrnd	T	A	1: 87,118,812 (GRCm39)	D56E	probably benign	Het
Col28a1	A	T	6: 8,162,247 (GRCm39)		probably null	Het
Col4a1	G	T	8: 11,270,007 (GRCm39)	P899Q	probably damaging	Het
Cts3	C	A	13: 61,714,655 (GRCm39)	A217S	probably damaging	Het
Dab2	A	G	15: 6,465,941 (GRCm39)	N495S	possibly damaging	Het
Dnah2	T	A	11: 69,349,368 (GRCm39)	I2423F	probably damaging	Het
Dnah2	C	T	11: 69,349,746 (GRCm39)	R2399Q	probably benign	Het
Dock6	T	C	9: 21,733,041 (GRCm39)	H1053R	probably benign	Het
Eif1ad14	G	A	12: 87,886,521 (GRCm39)	A36V	probably damaging	Het
Fam184a	G	A	10: 53,574,869 (GRCm39)	L191F	probably damaging	Het
Fbxl9	T	C	8: 106,049,925 (GRCm39)	Y33C	probably damaging	Het
Fip1l1	C	T	5: 74,752,608 (GRCm39)	R472W	probably damaging	Het
Gbp2	T	C	3: 142,338,018 (GRCm39)	F378S	probably damaging	Het
Ggt1	A	T	10: 75,420,799 (GRCm39)	E388V	probably damaging	Het
Gm14496	A	G	2: 181,638,050 (GRCm39)	T375A	probably benign	Het
Gnrhr	G	T	5: 86,330,216 (GRCm39)	T268K	probably damaging	Het
Htt	T	C	5: 34,962,020 (GRCm39)	V335A	probably benign	Het
Klhl20	A	T	1: 160,933,037 (GRCm39)	L257H	probably damaging	Het
Med27	C	A	2: 29,414,376 (GRCm39)		probably null	Het
Muc5ac	T	A	7: 141,369,323 (GRCm39)	C2433S	possibly damaging	Het
Nasp	A	G	4: 116,461,086 (GRCm39)		probably null	Het
Nipal2	A	C	15: 34,600,172 (GRCm39)	V215G	probably damaging	Het
Or10al5	A	T	17: 38,063,038 (GRCm39)	I98F	probably damaging	Het
Or9i1b	C	T	19: 13,897,104 (GRCm39)	T240I	probably damaging	Het
Oxct2b	G	A	4: 123,011,244 (GRCm39)	R388H	probably damaging	Het
Pbrm1	A	G	14: 30,774,240 (GRCm39)	I469V	possibly damaging	Het
Phyhip	A	G	14: 70,704,294 (GRCm39)	H171R	possibly damaging	Het
Pigs	C	T	11: 78,219,326 (GRCm39)	T9M	probably benign	Het
Plek	T	C	11: 16,935,539 (GRCm39)	D256G	probably damaging	Het
Prss50	T	C	9: 110,693,371 (GRCm39)	V369A	probably benign	Het
Psmc5	A	G	11: 106,152,088 (GRCm39)	K82E	possibly damaging	Het
Qrsl1	A	T	10: 43,758,189 (GRCm39)	F301L	probably benign	Het
Rasal1	T	C	5: 120,797,673 (GRCm39)	L135P	probably damaging	Het
Rbm47	A	G	5: 66,184,159 (GRCm39)	V148A	probably damaging	Het
Scyl1	T	A	19: 5,814,785 (GRCm39)	D381V	probably benign	Het
Selplg	G	T	5: 113,957,162 (GRCm39)	D381E	probably benign	Het
Sh3rf2	C	A	18: 42,289,200 (GRCm39)	Q674K	probably damaging	Het
Sned1	A	G	1: 93,210,659 (GRCm39)	T987A	probably benign	Het
Sntb1	A	G	15: 55,539,698 (GRCm39)		probably null	Het
Synj2	A	T	17: 6,036,327 (GRCm39)	I14F	probably damaging	Het
Taf2	A	T	15: 54,926,440 (GRCm39)	M170K	possibly damaging	Het
Tg	A	G	15: 66,607,096 (GRCm39)	E211G	possibly damaging	Het
Thnsl1	G	T	2: 21,217,016 (GRCm39)	E257*	probably null	Het
Tlr4	A	G	4: 66,758,070 (GRCm39)	R288G	possibly damaging	Het
Trbc1	T	C	6: 41,515,385 (GRCm39)		probably benign	Het
Trim37	G	A	11: 87,107,374 (GRCm39)		probably null	Het
Txnrd3	T	C	6: 89,640,176 (GRCm39)		probably null	Het
Tyk2	C	A	9: 21,021,800 (GRCm39)	Q875H	probably damaging	Het
Vmn2r55	A	G	7: 12,385,698 (GRCm39)	Y761H	probably damaging	Het
Zswim5	T	C	4: 116,836,876 (GRCm39)	L720P	probably damaging	Het

Other mutations in Gm43302

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0033:Gm43302	UTSW	5	105,424,710 (GRCm39)	missense	probably benign	0.12
R0066:Gm43302	UTSW	5	105,438,766 (GRCm39)	missense	probably damaging	1.00
R0764:Gm43302	UTSW	5	105,428,355 (GRCm39)	missense	probably benign
R1400:Gm43302	UTSW	5	105,422,622 (GRCm39)	missense	probably damaging	1.00
R1421:Gm43302	UTSW	5	105,365,215 (GRCm39)	missense	probably benign
R1539:Gm43302	UTSW	5	105,422,635 (GRCm39)	missense	probably benign	0.02
R1774:Gm43302	UTSW	5	105,423,660 (GRCm39)	missense	probably benign	0.01
R1842:Gm43302	UTSW	5	105,425,602 (GRCm39)	missense	probably benign	0.01
R2011:Gm43302	UTSW	5	105,438,846 (GRCm39)	missense	probably damaging	1.00
R2131:Gm43302	UTSW	5	105,422,610 (GRCm39)	missense	probably damaging	0.99
R2174:Gm43302	UTSW	5	105,422,216 (GRCm39)	missense	probably benign	0.12
R3687:Gm43302	UTSW	5	105,428,132 (GRCm39)	missense	probably damaging	1.00
R5322:Gm43302	UTSW	5	105,365,347 (GRCm39)	missense	probably benign	0.00
R5396:Gm43302	UTSW	5	105,427,955 (GRCm39)	nonsense	probably null
R5668:Gm43302	UTSW	5	105,423,678 (GRCm39)	missense	probably benign
R5723:Gm43302	UTSW	5	105,365,352 (GRCm39)	missense	possibly damaging	0.89
R6073:Gm43302	UTSW	5	105,438,825 (GRCm39)	missense	probably damaging	0.96
R6225:Gm43302	UTSW	5	105,425,605 (GRCm39)	nonsense	probably null
R6483:Gm43302	UTSW	5	105,423,726 (GRCm39)	missense	probably benign	0.01
R6537:Gm43302	UTSW	5	105,438,861 (GRCm39)	missense	possibly damaging	0.94
R6678:Gm43302	UTSW	5	105,438,820 (GRCm39)	missense	probably benign	0.14
R6889:Gm43302	UTSW	5	105,428,004 (GRCm39)	missense	probably benign	0.00
R7163:Gm43302	UTSW	5	105,441,493 (GRCm39)	splice site	probably null
R7790:Gm43302	UTSW	5	105,425,691 (GRCm39)	missense	probably benign	0.03
R7893:Gm43302	UTSW	5	105,436,891 (GRCm39)	nonsense	probably null
R8047:Gm43302	UTSW	5	105,422,623 (GRCm39)	missense	possibly damaging	0.74
R8350:Gm43302	UTSW	5	105,422,573 (GRCm39)	critical splice donor site	probably null
R8450:Gm43302	UTSW	5	105,422,573 (GRCm39)	critical splice donor site	probably null
R8495:Gm43302	UTSW	5	105,424,570 (GRCm39)	missense	possibly damaging	0.79
R8728:Gm43302	UTSW	5	105,438,793 (GRCm39)	missense	probably benign	0.30
R8856:Gm43302	UTSW	5	105,438,739 (GRCm39)	missense	probably damaging	1.00
R8956:Gm43302	UTSW	5	105,425,602 (GRCm39)	missense	possibly damaging	0.79
R9009:Gm43302	UTSW	5	105,427,974 (GRCm39)	missense	probably benign	0.01
RF014:Gm43302	UTSW	5	105,422,623 (GRCm39)	missense	possibly damaging	0.94
Z1177:Gm43302	UTSW	5	105,424,662 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GCAGTTCAGTCAGAATTCACAC -3'
(R):5'- GACTGGCTTCACAAAAGAGAC -3'

Sequencing Primer
(F):5'- GTTCAGTCAGAATTCACACATAGATC -3'
(R):5'- GACTGAGTTATAACCTTCAAAATCCC -3'

Posted On

2017-10-10