Mutagenetix > Incidental Mutation

Incidental Mutation 'R7204:Gm9195'

560473

Institutional Source

Beutler Lab

Gene Symbol

Gm9195

Ensembl Gene

ENSMUSG00000109446

Gene Name

predicted gene 9195

Synonyms

MMRRC Submission

045282-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.093) question?

Stock #

R7204 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

72669100-72699094 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 72711626 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Serine at position 329 (P329S)

Ref Sequence

ENSEMBL: ENSMUSP00000146536 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000208955]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000208955
AA Change: P329S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

99% (75/76)

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700067K01Rik	T	C	8: 84,730,636 (GRCm39)	S227P	probably damaging	Het
Acot6	A	G	12: 84,153,301 (GRCm39)	H181R	probably benign	Het
Adam15	A	T	3: 89,254,244 (GRCm39)	H184Q	probably benign	Het
Agl	A	G	3: 116,587,469 (GRCm39)	F29L	probably benign	Het
Ak7	A	G	12: 105,708,502 (GRCm39)	Y319C	probably benign	Het
Ano8	C	A	8: 71,931,669 (GRCm39)	V813L	probably benign	Het
Apbb2	T	G	5: 66,608,946 (GRCm39)	K234Q	probably damaging	Het
Arfgef3	A	T	10: 18,522,210 (GRCm39)	D605E	probably damaging	Het
Bfsp2	C	A	9: 103,309,865 (GRCm39)	R340L	probably damaging	Het
Birc6	C	A	17: 74,947,103 (GRCm39)	P2956T	probably damaging	Het
C1rb	T	C	6: 124,554,386 (GRCm39)	I389T	probably benign	Het
Ccdc146	A	G	5: 21,513,624 (GRCm39)	F498S	probably benign	Het
Cdc14b	A	C	13: 64,358,012 (GRCm39)	V361G	possibly damaging	Het
Cdc25b	A	T	2: 131,033,552 (GRCm39)	I164F	probably damaging	Het
Col18a1	A	G	10: 76,921,110 (GRCm39)	S297P	unknown	Het
Col3a1	A	T	1: 45,361,578 (GRCm39)	I117F	unknown	Het
Cox4i2	AG	A	2: 152,602,618 (GRCm39)		probably null	Het
Crybg3	C	A	16: 59,379,253 (GRCm39)	G667V	probably benign	Het
Ctc1	A	G	11: 68,920,567 (GRCm39)	D623G	probably damaging	Het
Dennd1a	A	T	2: 37,929,215 (GRCm39)	H152Q	probably damaging	Het
Dgke	G	A	11: 88,932,306 (GRCm39)	P495S	probably damaging	Het
Dll3	A	T	7: 27,998,330 (GRCm39)	C212S	possibly damaging	Het
Dll4	A	T	2: 119,159,054 (GRCm39)	S235C	probably damaging	Het
Dnah12	G	A	14: 26,500,869 (GRCm39)		probably null	Het
Dnah12	A	T	14: 26,503,442 (GRCm39)	T1599S	probably damaging	Het
Elavl1	G	A	8: 4,361,712 (GRCm39)	T20M	probably damaging	Het
Epha3	T	C	16: 63,472,695 (GRCm39)	T397A	probably benign	Het
Fanca	A	T	8: 124,013,216 (GRCm39)	I859N	probably damaging	Het
Fzd1	A	T	5: 4,805,980 (GRCm39)	V534D	probably damaging	Het
Glmp	A	G	3: 88,233,917 (GRCm39)	Y258C	probably damaging	Het
Gpt	A	G	15: 76,583,199 (GRCm39)	R379G	probably benign	Het
Gsdmc2	T	C	15: 63,696,903 (GRCm39)	T423A	probably damaging	Het
Hemgn	T	C	4: 46,397,054 (GRCm39)	K61E	possibly damaging	Het
Ikzf4	A	T	10: 128,479,759 (GRCm39)	S56T	possibly damaging	Het
Jak1	T	C	4: 101,032,332 (GRCm39)	T425A	probably benign	Het
Jsrp1	T	C	10: 80,646,319 (GRCm39)	T80A	probably benign	Het
Klra9	T	A	6: 130,165,643 (GRCm39)	D124V	possibly damaging	Het
Lama5	A	T	2: 179,843,970 (GRCm39)	V397D	probably damaging	Het
Lrp2	A	G	2: 69,302,877 (GRCm39)	S2951P	probably benign	Het
Map7d1	A	G	4: 126,149,808 (GRCm39)		probably null	Het
Mcm6	A	T	1: 128,265,864 (GRCm39)	C636S	probably damaging	Het
Mia	T	C	7: 26,880,358 (GRCm39)	E39G	possibly damaging	Het
Mpeg1	T	A	19: 12,440,258 (GRCm39)	I572N	probably damaging	Het
Muc21	AGCTGGATGCAGTGGTGGTCAGGGTGGGTGTAGAGCCTGAGCCAGTGCTGGATACAGTGGTGGTC	AGCTGGATACAGTGGTGGTC	17: 35,932,105 (GRCm39)		probably benign	Het
Muc6	AGGCGCAGAAACCCTGGC	AGGC	7: 141,214,363 (GRCm39)		probably null	Het
Mup5	A	G	4: 61,751,992 (GRCm39)	Y86H	probably damaging	Het
Nckap5	A	T	1: 125,954,104 (GRCm39)	V816D	probably benign	Het
Nfib	T	C	4: 82,215,052 (GRCm39)		probably null	Het
Nlrc5	T	A	8: 95,218,153 (GRCm39)	V1056D	possibly damaging	Het
Nynrin	G	C	14: 56,110,190 (GRCm39)	E1766Q	probably damaging	Het
Or7d9	A	T	9: 20,197,100 (GRCm39)	Y43F	probably benign	Het
Oxct1	T	A	15: 4,123,524 (GRCm39)	L328Q	probably damaging	Het
Pax5	T	A	4: 44,679,485 (GRCm39)	I187F	possibly damaging	Het
Pcdhb4	A	T	18: 37,442,292 (GRCm39)	D534V	probably damaging	Het
Pebp4	C	T	14: 70,085,046 (GRCm39)	P35S	probably benign	Het
Pkhd1l1	T	A	15: 44,386,949 (GRCm39)	V1274E	possibly damaging	Het
Plcz1	A	T	6: 139,956,150 (GRCm39)	V373D	probably benign	Het
Plxnb1	C	T	9: 108,929,243 (GRCm39)	T33I	probably damaging	Het
Prag1	T	C	8: 36,613,915 (GRCm39)	C1156R	probably benign	Het
Ptprc	T	A	1: 138,045,600 (GRCm39)	I87F	probably benign	Het
Rbp4	G	A	19: 38,112,551 (GRCm39)	T138I	possibly damaging	Het
Semp2l2b	A	G	10: 21,943,785 (GRCm39)	L65P	probably damaging	Het
Slc12a1	A	T	2: 125,042,542 (GRCm39)	N733Y	possibly damaging	Het
Slc27a3	A	G	3: 90,297,033 (GRCm39)	V22A	probably benign	Het
Tcaf1	T	C	6: 42,651,973 (GRCm39)		probably null	Het
Tnc	T	C	4: 63,889,392 (GRCm39)		probably null	Het
Tspan31	A	T	10: 126,903,987 (GRCm39)	*211R	probably null	Het
Ttc17	A	T	2: 94,192,773 (GRCm39)	V86D	possibly damaging	Het
Ubr1	T	A	2: 120,734,558 (GRCm39)	N1114I	possibly damaging	Het
Ulk2	C	T	11: 61,674,457 (GRCm39)	G850R	probably benign	Het
Vmn1r13	T	A	6: 57,187,141 (GRCm39)	I100N	probably benign	Het
Zan	T	C	5: 137,426,240 (GRCm39)	D2512G	unknown	Het
Zc3h14	A	T	12: 98,737,615 (GRCm39)	N34I	probably damaging	Het
Zcwpw1	T	G	5: 137,810,346 (GRCm39)	L374R	probably damaging	Het
Zfp747l1	A	T	7: 126,983,518 (GRCm39)	I528K	possibly damaging	Het

Other mutations in Gm9195

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R6448:Gm9195	UTSW	14	72,671,451 (GRCm39)	missense	possibly damaging	0.81
R6617:Gm9195	UTSW	14	72,669,215 (GRCm39)	missense	probably damaging	0.99
R6833:Gm9195	UTSW	14	72,671,856 (GRCm39)	missense	possibly damaging	0.66
R6843:Gm9195	UTSW	14	72,678,651 (GRCm39)	missense	possibly damaging	0.90
R6994:Gm9195	UTSW	14	72,718,271 (GRCm39)	missense	probably damaging	1.00
R7082:Gm9195	UTSW	14	72,680,152 (GRCm39)	missense	probably benign	0.41
R7157:Gm9195	UTSW	14	72,718,221 (GRCm39)	missense	probably damaging	1.00
R7208:Gm9195	UTSW	14	72,689,192 (GRCm39)	missense	possibly damaging	0.93
R7319:Gm9195	UTSW	14	72,697,929 (GRCm39)	missense	probably benign	0.03
R7368:Gm9195	UTSW	14	72,717,496 (GRCm39)	missense	probably damaging	0.96
R7424:Gm9195	UTSW	14	72,673,217 (GRCm39)	missense	possibly damaging	0.89
R7481:Gm9195	UTSW	14	72,720,116 (GRCm39)	missense	probably benign	0.07
R7527:Gm9195	UTSW	14	72,711,310 (GRCm39)	missense	possibly damaging	0.83
R7573:Gm9195	UTSW	14	72,694,122 (GRCm39)	missense	probably null
R7618:Gm9195	UTSW	14	72,690,275 (GRCm39)	missense	probably damaging	1.00
R7700:Gm9195	UTSW	14	72,693,342 (GRCm39)	splice site	probably null
R7740:Gm9195	UTSW	14	72,678,113 (GRCm39)	missense	possibly damaging	0.62
R7896:Gm9195	UTSW	14	72,693,178 (GRCm39)	missense	unknown
R8005:Gm9195	UTSW	14	72,663,840 (GRCm39)	missense	probably benign	0.07
R8124:Gm9195	UTSW	14	72,680,063 (GRCm39)	missense	probably benign	0.41
R8177:Gm9195	UTSW	14	72,697,977 (GRCm39)	missense	possibly damaging	0.49
R8353:Gm9195	UTSW	14	72,678,201 (GRCm39)	missense	probably benign	0.41
R8371:Gm9195	UTSW	14	72,697,899 (GRCm39)	missense	probably benign	0.07
R8453:Gm9195	UTSW	14	72,678,201 (GRCm39)	missense	probably benign	0.41
R8700:Gm9195	UTSW	14	72,720,171 (GRCm39)	missense	probably damaging	1.00
R8821:Gm9195	UTSW	14	72,717,536 (GRCm39)	missense	possibly damaging	0.92
R8836:Gm9195	UTSW	14	72,695,830 (GRCm39)	missense	probably benign	0.07
R8880:Gm9195	UTSW	14	72,691,320 (GRCm39)	missense	unknown
R8977:Gm9195	UTSW	14	72,691,338 (GRCm39)	missense	unknown
R9111:Gm9195	UTSW	14	72,694,123 (GRCm39)	nonsense	probably null
R9157:Gm9195	UTSW	14	72,692,038 (GRCm39)	missense	unknown
R9172:Gm9195	UTSW	14	72,711,154 (GRCm39)	missense	probably damaging	0.99
R9234:Gm9195	UTSW	14	72,695,786 (GRCm39)	nonsense	probably null
R9246:Gm9195	UTSW	14	72,710,314 (GRCm39)	missense	probably benign	0.29
R9267:Gm9195	UTSW	14	72,700,546 (GRCm39)	missense	possibly damaging	0.92
R9341:Gm9195	UTSW	14	72,717,500 (GRCm39)	missense	probably damaging	0.96
R9343:Gm9195	UTSW	14	72,717,500 (GRCm39)	missense	probably damaging	0.96
R9446:Gm9195	UTSW	14	72,717,957 (GRCm39)	missense	probably damaging	1.00
R9546:Gm9195	UTSW	14	72,718,347 (GRCm39)	missense	possibly damaging	0.74
R9676:Gm9195	UTSW	14	72,709,667 (GRCm39)	missense	unknown
R9739:Gm9195	UTSW	14	72,690,264 (GRCm39)	missense	probably damaging	0.96
R9764:Gm9195	UTSW	14	72,699,885 (GRCm39)	missense	unknown
R9797:Gm9195	UTSW	14	72,687,705 (GRCm39)	missense	probably damaging	0.99
Z1177:Gm9195	UTSW	14	72,690,874 (GRCm39)	frame shift	probably null
Z1177:Gm9195	UTSW	14	72,680,442 (GRCm39)	missense	possibly damaging	0.90

Predicted Primers

PCR Primer
(F):5'- CTGGTCCCAGAAATTTGCCC -3'
(R):5'- AGGGGAATGTCCTGGGTATCTC -3'

Sequencing Primer
(F):5'- AGAAATTTGCCCCTTGGACC -3'
(R):5'- GGGTATCTCTCTCCGTGCAG -3'

Posted On

2019-06-26