Mutagenetix > Incidental Mutation

Incidental Mutation 'R0081:Gm14443'

44278

Institutional Source

Beutler Lab

Gene Symbol

Gm14443

Ensembl Gene

ENSMUSG00000078902

Gene Name

predicted gene 14443

Synonyms

MMRRC Submission

038368-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.077) question?

Stock #

R0081 (G1)

Quality Score

Status

Not validated

Chromosome

Chromosomal Location

175008048-175017664 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 175011729 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Valine at position 239 (G239V)

Ref Sequence

ENSEMBL: ENSMUSP00000104682 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109054]

AlphaFold

A2ARX0

Predicted Effect

probably damaging
Transcript: ENSMUST00000109054
AA Change: G239V

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

SMART Domains

Protein: ENSMUSP00000104682
Gene: ENSMUSG00000078902
AA Change: G239V

Domain	Start	End	E-Value	Type
KRAB	4	66	1.9e-15	SMART
ZnF_C2H2	78	97	1.38e2	SMART
ZnF_C2H2	103	123	3.05e1	SMART
ZnF_C2H2	131	153	1.25e-1	SMART
ZnF_C2H2	159	179	7.89e0	SMART
ZnF_C2H2	187	209	2.27e-4	SMART
ZnF_C2H2	215	237	4.54e-4	SMART
ZnF_C2H2	243	265	5.99e-4	SMART
ZnF_C2H2	271	293	4.54e-4	SMART
ZnF_C2H2	299	321	5.21e-4	SMART
ZnF_C2H2	327	349	3.95e-4	SMART
ZnF_C2H2	355	377	4.24e-4	SMART
ZnF_C2H2	383	405	5.21e-4	SMART
ZnF_C2H2	411	433	5.21e-4	SMART
ZnF_C2H2	439	461	3.95e-4	SMART
ZnF_C2H2	467	489	4.24e-4	SMART
ZnF_C2H2	495	517	5.21e-4	SMART
ZnF_C2H2	523	545	3.95e-4	SMART
ZnF_C2H2	551	573	5.21e-4	SMART
ZnF_C2H2	579	601	2.27e-4	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127251

Coding Region Coverage

1x: 99.0%
3x: 97.2%
10x: 88.5%
20x: 63.6%

Validation Efficiency

94% (159/169)

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam5	T	C	8: 25,271,703 (GRCm39)	D485G	probably damaging	Het
Adamts19	T	C	18: 59,036,137 (GRCm39)		probably null	Het
Adgrd1	A	T	5: 129,255,146 (GRCm39)	I598F	probably damaging	Het
Adh5	A	G	3: 138,157,174 (GRCm39)	D245G	probably benign	Het
Adra2b	T	C	2: 127,206,212 (GRCm39)	V238A	probably benign	Het
Ank1	G	A	8: 23,606,258 (GRCm39)	V1188I	possibly damaging	Het
Asap1	C	T	15: 63,971,413 (GRCm39)	G905D	probably damaging	Het
AW554918	T	C	18: 25,477,959 (GRCm39)	V428A	probably benign	Het
Birc6	T	A	17: 74,950,436 (GRCm39)	S3226T	probably benign	Het
Cdh17	A	T	4: 11,785,280 (GRCm39)		probably benign	Het
Cyfip2	A	T	11: 46,144,825 (GRCm39)	Y676*	probably null	Het
Dcaf17	T	A	2: 70,908,812 (GRCm39)		probably benign	Het
Dclre1a	A	G	19: 56,531,139 (GRCm39)	F736L	probably damaging	Het
Ddx41	A	T	13: 55,683,193 (GRCm39)	H171Q	possibly damaging	Het
Dennd5b	G	T	6: 148,895,257 (GRCm39)	Q1258K	probably benign	Het
Dock10	T	C	1: 80,584,295 (GRCm39)	D137G	probably damaging	Het
Dpyd	G	A	3: 118,737,904 (GRCm39)	V482I	probably benign	Het
Erich6	A	T	3: 58,543,547 (GRCm39)		probably benign	Het
Fam193b	A	G	13: 55,702,024 (GRCm39)		probably benign	Het
Foxp2	T	C	6: 15,405,643 (GRCm39)		probably benign	Het
Frmd4a	T	C	2: 4,577,252 (GRCm39)		probably null	Het
Gas2l2	A	G	11: 83,313,693 (GRCm39)	S540P	possibly damaging	Het
Glis2	T	C	16: 4,431,517 (GRCm39)	V348A	probably benign	Het
Gpr158	T	C	2: 21,831,528 (GRCm39)	V876A	probably damaging	Het
H1f8	A	G	6: 115,926,942 (GRCm39)	E273G	probably benign	Het
Hadh	C	T	3: 131,029,285 (GRCm39)	D245N	probably damaging	Het
Hk2	A	T	6: 82,711,957 (GRCm39)		probably benign	Het
Ice1	A	T	13: 70,767,163 (GRCm39)	Y108*	probably null	Het
Il10ra	T	G	9: 45,167,247 (GRCm39)	M435L	probably benign	Het
Inpp5k	GT	G	11: 75,521,973 (GRCm39)		probably null	Het
Kank4	G	T	4: 98,666,567 (GRCm39)	P627T	probably benign	Het
Kif16b	A	G	2: 142,549,346 (GRCm39)		probably benign	Het
Lipn	A	G	19: 34,054,376 (GRCm39)	I205V	probably benign	Het
Miox	C	T	15: 89,220,477 (GRCm39)	L189F	possibly damaging	Het
Myh1	T	C	11: 67,106,683 (GRCm39)	M1255T	probably benign	Het
Myl3	A	C	9: 110,596,997 (GRCm39)	D119A	probably damaging	Het
Myo1d	T	G	11: 80,448,349 (GRCm39)	K925N	probably benign	Het
Myoz1	T	A	14: 20,699,622 (GRCm39)	M239L	probably benign	Het
Ncoa6	TGC	TGCGC	2: 155,250,211 (GRCm39)		probably null	Het
Nf1	C	A	11: 79,344,805 (GRCm39)		probably benign	Het
Npepl1	C	T	2: 173,957,879 (GRCm39)	P239S	probably damaging	Het
Olfml1	A	G	7: 107,170,506 (GRCm39)	K131R	probably benign	Het
Or12k5	G	A	2: 36,895,462 (GRCm39)	L55F	probably damaging	Het
Or1e29	A	G	11: 73,667,935 (GRCm39)	F73L	possibly damaging	Het
Or1j15	T	A	2: 36,458,893 (GRCm39)	Y94*	probably null	Het
Or1j20	T	C	2: 36,760,022 (GRCm39)	L148S	possibly damaging	Het
Or4c10	T	A	2: 89,760,423 (GRCm39)	I90K	possibly damaging	Het
Or4f7	A	C	2: 111,644,213 (GRCm39)	I286S	probably damaging	Het
Or5p52	C	T	7: 107,502,212 (GRCm39)	T96I	probably benign	Het
Or6c202	C	T	10: 128,996,707 (GRCm39)	D49N	possibly damaging	Het
Pde7a	T	C	3: 19,295,697 (GRCm39)		probably benign	Het
Pik3c2g	T	C	6: 139,903,519 (GRCm39)	C591R	probably benign	Het
Pkn2	T	G	3: 142,559,343 (GRCm39)	K61Q	probably damaging	Het
Ppfia1	C	A	7: 144,058,711 (GRCm39)	G722C	probably damaging	Het
Ppp1cb	T	C	5: 32,644,958 (GRCm39)	V263A	probably damaging	Het
Rab11fip2	A	T	19: 59,895,567 (GRCm39)	N440K	possibly damaging	Het
Rbm34	T	A	8: 127,676,234 (GRCm39)	K340N	probably damaging	Het
Samd3	T	C	10: 26,147,399 (GRCm39)		probably benign	Het
Sfi1	TCGC	TC	11: 3,096,254 (GRCm39)		probably null	Het
Sigirr	T	C	7: 140,671,285 (GRCm39)	D399G	probably damaging	Het
Slc17a7	A	G	7: 44,824,371 (GRCm39)	E554G	probably benign	Het
Smc3	A	G	19: 53,589,993 (GRCm39)		probably benign	Het
Tdrd1	T	C	19: 56,819,703 (GRCm39)	Y68H	probably benign	Het
Tespa1	T	A	10: 130,196,719 (GRCm39)	L219Q	probably damaging	Het
Tmem144	G	A	3: 79,746,580 (GRCm39)		probably benign	Het
Ttc38	A	G	15: 85,740,673 (GRCm39)	S436G	probably benign	Het
Ttn	T	A	2: 76,581,423 (GRCm39)	I23157F	probably damaging	Het
Ubxn2b	T	A	4: 6,203,875 (GRCm39)		probably benign	Het
Vmn1r28	G	A	6: 58,242,702 (GRCm39)	A182T	probably benign	Het
Vmn2r72	T	C	7: 85,401,044 (GRCm39)	E125G	probably benign	Het
Vmn2r78	A	T	7: 86,572,235 (GRCm39)	D532V	probably benign	Het
Vwa8	C	A	14: 79,320,222 (GRCm39)	L1078I	probably benign	Het
Vwce	A	T	19: 10,641,453 (GRCm39)		probably null	Het
Zpr1	A	G	9: 46,190,995 (GRCm39)	D300G	probably damaging	Het

Other mutations in Gm14443

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02248:Gm14443	APN	2	175,012,107 (GRCm39)	missense	probably benign	0.01
R1312:Gm14443	UTSW	2	175,013,383 (GRCm39)	splice site	probably benign
R1958:Gm14443	UTSW	2	175,011,497 (GRCm39)	missense	probably benign	0.31
R4061:Gm14443	UTSW	2	175,011,402 (GRCm39)	missense	probably benign	0.01
R4089:Gm14443	UTSW	2	175,013,685 (GRCm39)	missense	probably damaging	1.00
R5306:Gm14443	UTSW	2	175,011,372 (GRCm39)	missense	possibly damaging	0.63
R5405:Gm14443	UTSW	2	175,013,644 (GRCm39)	missense	possibly damaging	0.55
R5417:Gm14443	UTSW	2	175,011,796 (GRCm39)	missense	probably damaging	1.00
R6422:Gm14443	UTSW	2	175,012,174 (GRCm39)	nonsense	probably null
R7410:Gm14443	UTSW	2	175,011,069 (GRCm39)	missense	possibly damaging	0.85
R7880:Gm14443	UTSW	2	175,011,163 (GRCm39)	missense	probably benign	0.08
R7962:Gm14443	UTSW	2	175,012,035 (GRCm39)	missense	probably benign	0.01
R8081:Gm14443	UTSW	2	175,012,238 (GRCm39)	nonsense	probably null
R8174:Gm14443	UTSW	2	175,011,468 (GRCm39)	missense	probably damaging	1.00
R8315:Gm14443	UTSW	2	175,013,640 (GRCm39)	critical splice donor site	probably null
R8725:Gm14443	UTSW	2	175,010,693 (GRCm39)	nonsense	probably null
R8804:Gm14443	UTSW	2	175,011,652 (GRCm39)	missense	probably damaging	0.98
R9109:Gm14443	UTSW	2	175,011,869 (GRCm39)	nonsense	probably null
R9298:Gm14443	UTSW	2	175,011,869 (GRCm39)	nonsense	probably null
R9332:Gm14443	UTSW	2	175,017,610 (GRCm39)	start gained	probably benign
R9624:Gm14443	UTSW	2	175,012,129 (GRCm39)	missense	possibly damaging	0.92
R9766:Gm14443	UTSW	2	175,012,248 (GRCm39)	missense	probably benign	0.03

Predicted Primers

Posted On

2013-06-11