Mutagenetix > Incidental Mutation

Incidental Mutation 'R2422:Zfp951'

249364

Institutional Source

Beutler Lab

Gene Symbol

Zfp951

Ensembl Gene

ENSMUSG00000072774

Gene Name

zinc finger protein 951

Synonyms

C230055K05Rik

MMRRC Submission

040384-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.073) question?

Stock #

R2422 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

104813169-104860070 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 104815277 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 141 (T141I)

Ref Sequence

ENSEMBL: ENSMUSP00000087350 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000089906] [ENSMUST00000186219]

AlphaFold

A0A087WRH0

Predicted Effect

probably benign
Transcript: ENSMUST00000089906
AA Change: T141I

PolyPhen 2 Score 0.145 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000087350
Gene: ENSMUSG00000072774
AA Change: T141I

Domain	Start	End	E-Value	Type
KRAB	28	90	2e-14	SMART
ZnF_C2H2	176	198	2.79e-4	SMART
ZnF_C2H2	204	226	4.11e-2	SMART
ZnF_C2H2	232	254	3.11e-2	SMART
ZnF_C2H2	260	282	3.16e-3	SMART
ZnF_C2H2	288	310	2.53e-2	SMART
ZnF_C2H2	316	338	2.95e-3	SMART
ZnF_C2H2	344	366	1.18e-2	SMART
ZnF_C2H2	372	394	2.95e-3	SMART
ZnF_C2H2	400	422	2.57e-3	SMART
ZnF_C2H2	428	450	2.4e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000186219
AA Change: T141I

PolyPhen 2 Score 0.066 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000140625
Gene: ENSMUSG00000072774
AA Change: T141I

Domain	Start	End	E-Value	Type
KRAB	28	90	2e-14	SMART
ZnF_C2H2	176	198	2.79e-4	SMART
ZnF_C2H2	204	226	4.11e-2	SMART
ZnF_C2H2	232	254	3.11e-2	SMART
ZnF_C2H2	260	282	3.16e-3	SMART
ZnF_C2H2	288	310	2.53e-2	SMART
ZnF_C2H2	316	338	2.95e-3	SMART
ZnF_C2H2	344	366	1.18e-2	SMART
ZnF_C2H2	372	394	2.95e-3	SMART
ZnF_C2H2	400	422	2.57e-3	SMART
ZnF_C2H2	428	450	2.4e-3	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.1%
20x: 94.5%

Validation Efficiency

99% (77/78)

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010300C02Rik	C	A	1: 37,613,475	V1084L	probably benign	Het
4933409G03Rik	A	T	2: 68,591,520	N47I	probably benign	Het
Actr5	T	C	2: 158,636,081	F457S	probably damaging	Het
Adamts3	A	G	5: 89,683,175	S1007P	probably damaging	Het
Adck2	C	T	6: 39,583,998	A440V	possibly damaging	Het
Birc6	T	A	17: 74,660,614	L301Q	probably damaging	Het
Ccdc18	A	C	5: 108,228,588	E1298D	probably damaging	Het
Ccdc77	A	G	6: 120,339,159	C186R	probably benign	Het
Cdk12	T	G	11: 98,219,074	S640R	probably benign	Het
Cdv3	T	C	9: 103,365,118		probably benign	Het
Celf2	G	A	2: 6,553,889	T364I	probably damaging	Het
Cmtr2	C	A	8: 110,222,781	S574R	probably benign	Het
Col14a1	T	C	15: 55,449,922	L56P	unknown	Het
Dctn1	C	T	6: 83,199,800	L1241F	possibly damaging	Het
Depdc5	T	C	5: 32,991,035	F1505S	probably damaging	Het
Dhcr24	G	T	4: 106,561,094		probably benign	Het
Dnajc21	A	G	15: 10,461,935	S127P	probably benign	Het
Entpd7	A	T	19: 43,728,088	Y507F	possibly damaging	Het
Fbp1	T	C	13: 62,871,306	K24E	probably benign	Het
Galr1	A	T	18: 82,405,923	N76K	probably damaging	Het
Glrb	A	G	3: 80,860,235	I226T	probably damaging	Het
Gm17421	T	A	12: 113,369,487		noncoding transcript	Het
Gm4950	T	A	18: 51,865,784	Q33L	probably benign	Het
Gm5415	C	T	1: 32,545,861	A323T	possibly damaging	Het
Gm6583	A	T	5: 112,355,118	V240D	probably damaging	Het
Gnat2	A	T	3: 108,095,539	M88L	probably damaging	Het
Gpr183	A	G	14: 121,954,177	Y311H	probably damaging	Het
H2-M10.5	A	G	17: 36,774,999	I308V	probably benign	Het
Hipk3	C	T	2: 104,471,485	G121R	probably benign	Het
Hjurp	A	G	1: 88,266,561		probably benign	Het
Homez	C	A	14: 54,857,574	V226F	probably benign	Het
Inf2	C	A	12: 112,610,824	A1034D	unknown	Het
Kcnc4	G	T	3: 107,445,547	P572T	probably benign	Het
Kmt2d	T	C	15: 98,862,266	E1037G	unknown	Het
Krt78	T	C	15: 101,947,264	E704G	probably damaging	Het
Lama1	A	T	17: 67,750,553	M541L	probably benign	Het
Lmbrd2	C	T	15: 9,194,765	T618M	possibly damaging	Het
Ly6g6e	G	A	17: 35,078,146	R121Q	probably benign	Het
Mettl22	T	C	16: 8,487,361	F293L	probably damaging	Het
Mib1	T	C	18: 10,751,906	S263P	probably damaging	Het
Ndufaf1	T	C	2: 119,655,737	E298G	probably damaging	Het
Nek1	T	C	8: 61,019,901	V152A	probably damaging	Het
Nlrp4d	T	A	7: 10,362,945	D876V	probably benign	Het
Olfr178	T	C	16: 58,889,965	E85G	probably benign	Het
Olfr235	A	T	19: 12,268,919	T230S	probably damaging	Het
Olfr740	T	C	14: 50,453,436	L128P	probably damaging	Het
Olfr975	A	G	9: 39,950,528	L81P	possibly damaging	Het
Pcdha11	G	T	18: 37,007,272	L651F	probably damaging	Het
Plekhg1	G	A	10: 3,958,048	M988I	probably benign	Het
Plxnb1	G	A	9: 109,108,438	R1169H	probably benign	Het
Ppp4r3a	A	G	12: 101,042,653		probably benign	Het
Pum2	A	T	12: 8,748,931	Q930L	possibly damaging	Het
Rbp4	T	C	19: 38,124,344	E67G	probably damaging	Het
Rgs9	C	A	11: 109,225,777		probably null	Het
Sipa1	A	T	19: 5,652,112	D923E	possibly damaging	Het
Smc1a	A	G	X: 152,047,975		probably benign	Het
Snx33	C	A	9: 56,918,538	M546I	probably benign	Het
Spag17	T	A	3: 100,027,619	W714R	probably benign	Het
Spata2	C	T	2: 167,484,206	R231Q	probably damaging	Het
Stard9	C	T	2: 120,700,284	R2341C	probably benign	Het
Tas2r116	A	T	6: 132,855,594	I53F	possibly damaging	Het
Tlk1	T	C	2: 70,770,005	E110G	probably damaging	Het
Tmem102	T	A	11: 69,804,537	E203V	probably benign	Het
Top2b	T	G	14: 16,409,189	I777M	probably damaging	Het
Ttc23l	CT	CTTGGATT	15: 10,537,562		probably benign	Het
Ttc23l	G	A	15: 10,537,566	S206L	probably benign	Het
Tyw5	A	G	1: 57,396,748	I82T	possibly damaging	Het
Uba6	A	G	5: 86,132,616		probably null	Het
Ugcg	C	T	4: 59,207,798	P46S	probably benign	Het
Unc13c	T	C	9: 73,931,547	Y674C	probably damaging	Het
Vmn2r105	T	A	17: 20,227,835	R242S	probably benign	Het
Vmn2r12	A	G	5: 109,086,532	Y605H	probably benign	Het
Wdr77	A	T	3: 105,960,021	K62*	probably null	Het
Zfhx4	C	A	3: 5,390,405	A1153E	probably benign	Het
Zfp266	C	A	9: 20,499,262	V540L	possibly damaging	Het
Zfp638	C	A	6: 83,966,439		probably benign	Het
Zfp644	A	G	5: 106,637,244	M479T	possibly damaging	Het

Other mutations in Zfp951

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01897:Zfp951	APN	5	104815283	missense	probably benign	0.00
R0594:Zfp951	UTSW	5	104814572	missense	possibly damaging	0.67
R1056:Zfp951	UTSW	5	104815285	missense	possibly damaging	0.90
R1857:Zfp951	UTSW	5	104814857	missense	probably damaging	0.97
R1967:Zfp951	UTSW	5	104817000	missense	possibly damaging	0.65
R4358:Zfp951	UTSW	5	104814675	missense	probably damaging	1.00
R4671:Zfp951	UTSW	5	104814701	missense	probably benign	0.01
R5539:Zfp951	UTSW	5	104814846	missense	probably damaging	0.99
R5634:Zfp951	UTSW	5	104815289	missense	probably benign	0.00
R7894:Zfp951	UTSW	5	104814972	missense	probably benign	0.00
R8058:Zfp951	UTSW	5	104814446	missense	probably damaging	1.00
R8125:Zfp951	UTSW	5	104815303	nonsense	probably null
Z1177:Zfp951	UTSW	5	104828955	start codon destroyed	probably null	0.01

Predicted Primers

PCR Primer
(F):5'- TCCAGTATGTGTCCTTTCATGG -3'
(R):5'- GTGACAATTGCATCTACAGGCATAAG -3'

Sequencing Primer
(F):5'- CATGGTTTTGAAGATCCCTGTGAC -3'
(R):5'- GCTAACGATTTTGTATGTCATAGGC -3'

Posted On

2014-11-12