Mutagenetix > Incidental Mutations

Incidental Mutation 'R5892:Zfp963'

457249

Institutional Source

Beutler Lab

Gene Symbol

Zfp963

Ensembl Gene

ENSMUSG00000092260

Gene Name

zinc finger protein 963

Synonyms

MMRRC Submission

044093-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.064) question?

Stock #

R5892 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

69741639-69749970 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 69743377 bp

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 142 (D142G)

Ref Sequence

ENSEMBL: ENSMUSP00000119087 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000130458] [ENSMUST00000149782] [ENSMUST00000154063]

Predicted Effect

unknown
Transcript: ENSMUST00000126915
AA Change: D153G

SMART Domains

Protein: ENSMUSP00000122850
Gene: ENSMUSG00000092544
AA Change: D153G

Domain	Start	End	E-Value	Type
KRAB	16	73	1.96e-17	SMART
PDB:2I13\|B	104	210	3e-6	PDB
SCOP:d1fgja_	114	216	2e-6	SMART
Blast:KRAB	189	209	3e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000130458
AA Change: D142G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000119087
Gene: ENSMUSG00000092260
AA Change: D142G

Domain	Start	End	E-Value	Type
KRAB	4	61	1.96e-17	SMART
ZnF_C2H2	162	184	7.37e1	SMART
ZnF_C2H2	213	235	1.69e-3	SMART
ZnF_C2H2	240	262	8.47e-4	SMART
ZnF_C2H2	268	290	7.15e-2	SMART
ZnF_C2H2	296	318	3.83e-2	SMART
ZnF_C2H2	324	346	4.17e-3	SMART
ZnF_C2H2	352	374	5.99e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000149782

SMART Domains

Protein: ENSMUSP00000123252
Gene: ENSMUSG00000092544

Domain	Start	End	E-Value	Type
KRAB	80	139	1.2e-17	SMART
ZnF_C2H2	155	177	1.69e-3	SMART
ZnF_C2H2	182	204	8.47e-4	SMART
ZnF_C2H2	210	232	7.15e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000154063

SMART Domains

Protein: ENSMUSP00000117867
Gene: ENSMUSG00000092260

Domain	Start	End	E-Value	Type
KRAB	4	61	1.96e-17	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.6%
20x: 92.6%

Validation Efficiency

98% (56/57)

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930524J08Rik	G	T	5: 99,979,265		probably benign	Het
Abcb11	C	T	2: 69,261,500	A893T	probably damaging	Het
Adtrp	A	T	13: 41,828,206	N30K	probably benign	Het
Alms1	T	A	6: 85,620,903	S904T	probably damaging	Het
Cep170	T	A	1: 176,755,387		probably null	Het
Cntnap3	A	G	13: 64,799,180	V145A	probably damaging	Het
Dclre1a	T	C	19: 56,547,140	E4G	probably benign	Het
Depdc1a	G	C	3: 159,526,669	A686P	probably damaging	Het
Dnah7b	T	C	1: 46,337,593		probably null	Het
Enox1	A	G	14: 77,486,017		probably benign	Het
Fam107b	A	G	2: 3,778,564	E268G	probably damaging	Het
Fer1l6	A	G	15: 58,564,068	S437G	probably benign	Het
Flnb	C	A	14: 7,907,183	T1252K	probably damaging	Het
Fubp1	A	G	3: 152,218,314		probably benign	Het
Gm20402	G	A	3: 52,268,949	A50T	probably benign	Het
Gpr137b	T	C	13: 13,359,406	Y355C	probably damaging	Het
Gzmk	C	T	13: 113,173,922		probably null	Het
Ino80	A	T	2: 119,439,547		probably benign	Het
Ints8	T	C	4: 11,223,813	T677A	probably damaging	Het
Kat6a	A	G	8: 22,938,289	E1220G	probably damaging	Het
Lrfn5	A	G	12: 61,843,418	T498A	probably damaging	Het
Lrp2	T	A	2: 69,442,776	T4043S	probably benign	Het
Malrd1	A	G	2: 15,614,267	N314S	probably benign	Het
Mfsd1	A	G	3: 67,589,829		probably null	Het
Muc1	C	T	3: 89,230,993	P381S	probably benign	Het
Myh2	A	T	11: 67,185,176	K730*	probably null	Het
Nat3	T	A	8: 67,547,938	N156K	probably benign	Het
Nelfe	T	C	17: 34,854,669		probably benign	Het
Nlrp1a	A	T	11: 71,099,645	L927Q	probably damaging	Het
P4ha2	A	G	11: 54,120,188	Y343C	probably damaging	Het
Pclo	A	T	5: 14,521,171	Q190L	probably damaging	Het
Pde8a	A	G	7: 81,295,691	N183S	probably damaging	Het
Plekha2	C	T	8: 25,052,365	V278I	probably benign	Het
Plekha6	G	C	1: 133,272,307	R208P	possibly damaging	Het
Plxnb1	T	C	9: 109,111,707	L1550P	probably damaging	Het
Ppox	C	T	1: 171,277,461	V385I	probably damaging	Het
Prdm16	T	C	4: 154,323,259	D1170G	possibly damaging	Het
Prmt5	A	T	14: 54,509,911	S470T	probably damaging	Het
Robo2	T	A	16: 73,895,780		probably benign	Het
Siglecg	G	A	7: 43,412,204		probably benign	Het
Slc30a5	T	C	13: 100,813,302	N367S	probably damaging	Het
Tex29	C	T	8: 11,854,288		probably benign	Het
Tmem117	T	A	15: 94,638,139	V18E	probably damaging	Het
Tmtc2	C	T	10: 105,413,505	M122I	probably benign	Het
Tpr	T	A	1: 150,407,400	N287K	probably benign	Het
Unc93b1	A	T	19: 3,943,632	D358V	probably damaging	Het
Vrk2	A	T	11: 26,534,372		probably benign	Het
Wdr24	A	T	17: 25,827,986	Q671L	probably benign	Het
Zfp110	C	T	7: 12,848,478	T351I	probably benign	Het

Other mutations in Zfp963

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0220:Zfp963	UTSW	8	69743493	nonsense	probably null
R0220:Zfp963	UTSW	8	69743495	missense	probably benign	0.09
R0423:Zfp963	UTSW	8	69744506	missense	probably damaging	1.00
R1171:Zfp963	UTSW	8	69743019	missense	possibly damaging	0.86
R1630:Zfp963	UTSW	8	69744187	splice site	probably benign
R1750:Zfp963	UTSW	8	69743450	missense	possibly damaging	0.81
R2090:Zfp963	UTSW	8	69743346	nonsense	probably null
R2185:Zfp963	UTSW	8	69742911	missense	probably benign	0.43
R4484:Zfp963	UTSW	8	69744485	missense	probably benign	0.29
R4600:Zfp963	UTSW	8	69742860	splice site	probably null
R4617:Zfp963	UTSW	8	69743294	missense	probably benign	0.00
R5427:Zfp963	UTSW	8	69743456	missense	probably benign	0.01
R5917:Zfp963	UTSW	8	69742860	splice site	probably null
R6073:Zfp963	UTSW	8	69743203	nonsense	probably null
R7312:Zfp963	UTSW	8	69743109	missense	probably damaging	1.00
R7739:Zfp963	UTSW	8	69742883	missense	possibly damaging	0.59

Predicted Primers

PCR Primer
(F):5'- CCATAGTGGGGCTTCCTCCA -3'
(R):5'- TTCTGTGGGAGCCATGCTATAA -3'

Sequencing Primer
(F):5'- GTGCACAAACAGAGTTCTTTCC -3'
(R):5'- TCAGTGGTTCCATGTCAGAGACC -3'

Posted On

2017-02-15