Mutagenetix > Incidental Mutation

Incidental Mutation 'R0427:Gm5141'

38778

Institutional Source

Beutler Lab

Gene Symbol

Gm5141

Ensembl Gene

ENSMUSG00000091183

Gene Name

predicted gene 5141

Synonyms

MMRRC Submission

038629-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R0427 (G1)

Quality Score

159

Status

Not validated

Chromosome

Chromosomal Location

62920014-62933622 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 62922525 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Glutamic Acid at position 215 (K215E)

Ref Sequence

ENSEMBL: ENSMUSP00000144368 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000167516] [ENSMUST00000201047]

AlphaFold

A0A0J9YUW3

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000116696

Predicted Effect

probably damaging
Transcript: ENSMUST00000167516
AA Change: K214E

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

SMART Domains

Protein: ENSMUSP00000126604
Gene: ENSMUSG00000091183
AA Change: K214E

Domain	Start	End	E-Value	Type
KRAB	3	65	2.32e-19	SMART
ZnF_C2H2	132	154	1.51e0	SMART
ZnF_C2H2	160	182	6.52e-5	SMART
ZnF_C2H2	188	210	5.42e-2	SMART
ZnF_C2H2	216	238	1.84e-4	SMART
ZnF_C2H2	244	266	1.3e-4	SMART
ZnF_C2H2	272	294	1.22e-4	SMART
ZnF_C2H2	300	322	1.82e-3	SMART
ZnF_C2H2	328	350	2.79e-4	SMART
ZnF_C2H2	356	378	3.89e-3	SMART
ZnF_C2H2	384	406	4.94e-5	SMART
ZnF_C2H2	412	434	5.67e-5	SMART
ZnF_C2H2	440	462	7.49e-5	SMART
ZnF_C2H2	468	490	5.21e-4	SMART
ZnF_C2H2	496	518	4.87e-4	SMART
ZnF_C2H2	524	546	1.22e-4	SMART
ZnF_C2H2	552	574	1.18e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000179519

Predicted Effect

probably damaging
Transcript: ENSMUST00000201047
AA Change: K215E

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

SMART Domains

Protein: ENSMUSP00000144368
Gene: ENSMUSG00000091183
AA Change: K215E

Domain	Start	End	E-Value	Type
KRAB	4	66	9.8e-22	SMART
ZnF_C2H2	133	155	6.5e-3	SMART
ZnF_C2H2	161	183	2.7e-7	SMART
ZnF_C2H2	189	211	2.4e-4	SMART
ZnF_C2H2	217	239	8.1e-7	SMART
ZnF_C2H2	245	267	5.6e-7	SMART
ZnF_C2H2	273	295	5.1e-7	SMART
ZnF_C2H2	301	323	7.9e-6	SMART
ZnF_C2H2	329	351	1.2e-6	SMART
ZnF_C2H2	357	379	1.7e-5	SMART
ZnF_C2H2	385	407	2.1e-7	SMART
ZnF_C2H2	413	435	2.4e-7	SMART
ZnF_C2H2	441	463	3.2e-7	SMART
ZnF_C2H2	469	491	2.2e-6	SMART
ZnF_C2H2	497	519	2.2e-6	SMART
ZnF_C2H2	525	547	5.4e-7	SMART
ZnF_C2H2	553	575	4.9e-5	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000202582

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.2%
20x: 92.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam34	T	G	8: 44,105,493 (GRCm39)	T51P	probably benign	Het
Alpk1	A	T	3: 127,464,720 (GRCm39)	V1186E	probably damaging	Het
Ankfn1	T	C	11: 89,296,423 (GRCm39)	D102G	probably damaging	Het
Armc2	A	G	10: 41,876,406 (GRCm39)	I127T	possibly damaging	Het
Atp6v1b2	T	C	8: 69,554,084 (GRCm39)	L87P	probably damaging	Het
Atp9a	T	A	2: 168,482,617 (GRCm39)		probably null	Het
BC048679	C	G	7: 81,144,993 (GRCm39)	V123L	probably benign	Het
Birc7	G	A	2: 180,571,307 (GRCm39)		probably null	Het
Btbd9	C	T	17: 30,493,916 (GRCm39)	D492N	possibly damaging	Het
Cacna1d	T	A	14: 30,068,774 (GRCm39)	N155I	probably damaging	Het
Cd300lg	T	C	11: 101,933,852 (GRCm39)	V33A	probably damaging	Het
Cep290	A	G	10: 100,352,041 (GRCm39)	D742G	probably benign	Het
Cep95	A	G	11: 106,681,578 (GRCm39)	N14S	probably benign	Het
Cfap74	A	T	4: 155,525,734 (GRCm39)	M728L	probably benign	Het
Ctsll3	T	A	13: 60,949,205 (GRCm39)	T9S	probably benign	Het
Cyp3a44	A	G	5: 145,716,412 (GRCm39)	S393P	possibly damaging	Het
Dmbt1	T	A	7: 130,642,632 (GRCm39)	L150*	probably null	Het
Dnah2	A	G	11: 69,343,705 (GRCm39)	I2868T	probably damaging	Het
Dop1a	A	G	9: 86,389,585 (GRCm39)	H505R	probably damaging	Het
Exo1	A	G	1: 175,733,519 (GRCm39)	K781R	probably damaging	Het
Fam184a	A	G	10: 53,566,211 (GRCm39)	Y459H	probably damaging	Het
Foxp1	C	T	6: 98,907,164 (GRCm39)	D540N	probably damaging	Het
Fstl5	T	A	3: 76,615,034 (GRCm39)	Y698*	probably null	Het
Grik5	C	A	7: 24,757,923 (GRCm39)	R386L	probably benign	Het
Ikbke	A	T	1: 131,185,647 (GRCm39)	S620R	possibly damaging	Het
Kcnh3	A	T	15: 99,131,180 (GRCm39)	M518L	probably benign	Het
Lrrcc1	G	T	3: 14,623,416 (GRCm39)	A748S	probably damaging	Het
Mbd5	T	G	2: 49,169,091 (GRCm39)	S1191A	probably benign	Het
Med27	T	C	2: 29,390,283 (GRCm39)	I70T	probably damaging	Het
Mplkipl1	A	G	19: 61,163,908 (GRCm39)	Y176H	probably damaging	Het
Myh4	A	G	11: 67,149,479 (GRCm39)	D1737G	probably damaging	Het
Myo5a	A	G	9: 75,081,478 (GRCm39)	D1021G	probably benign	Het
Ncor1	T	C	11: 62,301,746 (GRCm39)	E212G	probably damaging	Het
Neb	A	T	2: 52,133,896 (GRCm39)	N3362K	possibly damaging	Het
Neb	A	G	2: 52,134,081 (GRCm39)	S3301P	probably damaging	Het
Neurod1	T	G	2: 79,284,526 (GRCm39)	K286Q	probably damaging	Het
Noc3l	T	C	19: 38,778,095 (GRCm39)	Q773R	probably benign	Het
Nup205	T	A	6: 35,171,398 (GRCm39)	N420K	probably benign	Het
Olfml3	A	T	3: 103,644,330 (GRCm39)	V113E	probably benign	Het
Opa1	T	C	16: 29,430,279 (GRCm39)	V439A	probably damaging	Het
Or13c7	A	G	4: 43,854,417 (GRCm39)	Y36C	probably damaging	Het
Or14j7	A	T	17: 38,234,520 (GRCm39)	H21L	probably benign	Het
Or1j14	C	T	2: 36,417,994 (GRCm39)	S190L	probably damaging	Het
Or1o11	T	A	17: 37,756,593 (GRCm39)	D60E	probably damaging	Het
Pcdhb11	T	C	18: 37,555,818 (GRCm39)	S383P	probably damaging	Het
Pkd1	T	C	17: 24,812,476 (GRCm39)	V3803A	probably damaging	Het
Plekhg1	A	G	10: 3,914,235 (GRCm39)	D1319G	probably benign	Het
Polq	T	A	16: 36,882,355 (GRCm39)	C1227*	probably null	Het
Pramel22	A	T	4: 143,380,993 (GRCm39)	N343K	probably benign	Het
Psmc1	T	C	12: 100,085,487 (GRCm39)	F283L	probably damaging	Het
Psmd8	T	C	7: 28,875,552 (GRCm39)	N189S	probably damaging	Het
Ptger4	G	A	15: 5,272,382 (GRCm39)	T104I	probably benign	Het
Ptpro	T	G	6: 137,345,294 (GRCm39)	V100G	possibly damaging	Het
Rab11fip1	T	A	8: 27,644,520 (GRCm39)	T422S	probably damaging	Het
Rad54l2	A	G	9: 106,570,891 (GRCm39)	L1143P	possibly damaging	Het
Rnf148	A	G	6: 23,654,072 (GRCm39)	M308T	probably damaging	Het
Sbsn	T	A	7: 30,451,523 (GRCm39)		probably benign	Het
Scube2	T	A	7: 109,424,044 (GRCm39)	T487S	probably benign	Het
Sema4c	C	A	1: 36,592,892 (GRCm39)	E109*	probably null	Het
Sipa1l2	A	T	8: 126,207,071 (GRCm39)	L544Q	probably damaging	Het
Slc28a2	A	G	2: 122,288,702 (GRCm39)	T603A	probably benign	Het
Tbc1d7	T	A	13: 43,306,563 (GRCm39)	T138S	probably benign	Het
Timd4	A	T	11: 46,710,084 (GRCm39)	T239S	probably benign	Het
Trp53bp1	A	G	2: 121,066,498 (GRCm39)	S743P	probably damaging	Het
Tspan10	T	A	11: 120,335,120 (GRCm39)	Y77N	probably damaging	Het
Ttc14	T	C	3: 33,857,633 (GRCm39)	S245P	probably damaging	Het
Ttf1	T	A	2: 28,955,054 (GRCm39)	S139R	probably benign	Het
Tubd1	C	A	11: 86,448,616 (GRCm39)	Q279K	possibly damaging	Het
Twnk	A	G	19: 44,996,026 (GRCm39)	E153G	probably benign	Het
Ush2a	A	G	1: 188,132,478 (GRCm39)	D900G	probably damaging	Het
Usp54	A	G	14: 20,620,432 (GRCm39)	V691A	probably benign	Het
Usp8	T	C	2: 126,559,952 (GRCm39)		probably benign	Het
Vmn1r231	C	T	17: 21,110,490 (GRCm39)	V142I	probably benign	Het
Vmn2r15	C	T	5: 109,434,953 (GRCm39)	A584T	probably damaging	Het
Vmn2r6	A	G	3: 64,467,008 (GRCm39)	S164P	probably damaging	Het
Vps16	A	G	2: 130,280,770 (GRCm39)	Y233C	probably benign	Het
Vwf	C	G	6: 125,650,902 (GRCm39)	H2511D	probably benign	Het
Wipf3	T	G	6: 54,460,882 (GRCm39)	L110R	possibly damaging	Het
Zfp945	T	A	17: 23,084,226 (GRCm39)	N11I	probably benign	Het

Other mutations in Gm5141

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0220:Gm5141	UTSW	13	62,922,271 (GRCm39)	missense	probably damaging	1.00
R0534:Gm5141	UTSW	13	62,922,408 (GRCm39)	missense	probably damaging	1.00
R0652:Gm5141	UTSW	13	62,921,946 (GRCm39)	missense	probably damaging	1.00
R1495:Gm5141	UTSW	13	62,922,084 (GRCm39)	missense	probably damaging	1.00
R2079:Gm5141	UTSW	13	62,922,424 (GRCm39)	missense	probably benign	0.06
R4780:Gm5141	UTSW	13	62,922,764 (GRCm39)	missense	unknown
R5588:Gm5141	UTSW	13	62,921,584 (GRCm39)	missense	probably benign	0.06
R6292:Gm5141	UTSW	13	62,922,252 (GRCm39)	missense	probably damaging	1.00
R6455:Gm5141	UTSW	13	62,922,597 (GRCm39)	missense	probably damaging	1.00
R6605:Gm5141	UTSW	13	62,922,201 (GRCm39)	missense	probably damaging	1.00
R7091:Gm5141	UTSW	13	62,921,778 (GRCm39)	missense	possibly damaging	0.80
R7199:Gm5141	UTSW	13	62,924,877 (GRCm39)	missense	possibly damaging	0.92
R8933:Gm5141	UTSW	13	62,924,854 (GRCm39)	nonsense	probably null

Predicted Primers

Posted On

2013-05-23