Mutagenetix > Incidental Mutation

Incidental Mutation 'R0032:Zfp120'

18626

Institutional Source

Beutler Lab

Gene Symbol

Zfp120

Ensembl Gene

ENSMUSG00000068134

Gene Name

zinc finger protein 120

Synonyms

E030042N05Rik, MZF31

MMRRC Submission

038326-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.080) question?

Stock #

R0032 (G1) of strain 731

Quality Score

Status

Validated

Chromosome

Chromosomal Location

149956327-149978598 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 149959512 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 270 (V270E)

Ref Sequence

ENSEMBL: ENSMUSP00000092116 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000089207] [ENSMUST00000094538] [ENSMUST00000109931] [ENSMUST00000122859]

AlphaFold

Q8BZW4

Predicted Effect

probably benign
Transcript: ENSMUST00000089207
AA Change: V292E

PolyPhen 2 Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000086615
Gene: ENSMUSG00000068134
AA Change: V292E

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
KRAB	28	91	1.7e-17	SMART
ZnF_C2H2	156	178	9.08e-4	SMART
ZnF_C2H2	184	206	3.44e-4	SMART
ZnF_C2H2	212	234	9.58e-3	SMART
ZnF_C2H2	240	262	1.95e-3	SMART
ZnF_C2H2	268	288	1.26e1	SMART
ZnF_C2H2	296	318	4.17e-3	SMART
ZnF_C2H2	324	346	5.29e-5	SMART
ZnF_C2H2	352	374	1.4e-4	SMART
ZnF_C2H2	408	430	2.71e-2	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000094538
AA Change: V270E

PolyPhen 2 Score 0.938 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000092116
Gene: ENSMUSG00000068134
AA Change: V270E

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
KRAB	28	89	1.01e-19	SMART
ZnF_C2H2	134	156	9.08e-4	SMART
ZnF_C2H2	162	184	3.44e-4	SMART
ZnF_C2H2	190	212	9.58e-3	SMART
ZnF_C2H2	218	240	1.95e-3	SMART
ZnF_C2H2	246	266	1.26e1	SMART
ZnF_C2H2	274	296	4.17e-3	SMART
ZnF_C2H2	302	324	5.29e-5	SMART
ZnF_C2H2	330	352	1.4e-4	SMART
ZnF_C2H2	386	408	2.71e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000109931

SMART Domains

Protein: ENSMUSP00000105557
Gene: ENSMUSG00000068134

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
KRAB	28	89	1.01e-19	SMART
internal_repeat_1	96	130	3.31e-8	PROSPERO

Predicted Effect

probably benign
Transcript: ENSMUST00000122859

SMART Domains

Protein: ENSMUSP00000114205
Gene: ENSMUSG00000068134

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
KRAB	28	80	1.68e-16	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000142792

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 80.9%
3x: 73.4%
10x: 52.4%
20x: 32.5%

Validation Efficiency

94% (87/93)

Allele List at MGI

Other mutations in this stock

Total: 40 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acss3	T	A	10: 106,959,156 (GRCm39)	T97S	probably benign	Het
Adcy1	T	C	11: 7,094,729 (GRCm39)	S552P	possibly damaging	Het
C2cd3	T	A	7: 100,093,652 (GRCm39)		probably benign	Het
Cd86	A	T	16: 36,441,235 (GRCm39)	S77R	probably damaging	Het
Cfap54	C	T	10: 92,768,559 (GRCm39)	R188H	probably benign	Het
Cpne8	T	A	15: 90,453,771 (GRCm39)		probably benign	Het
Ctsg	T	A	14: 56,339,196 (GRCm39)	I21F	probably damaging	Het
Cyp2j9	T	G	4: 96,457,043 (GRCm39)	N476T	possibly damaging	Het
Dcaf4	G	A	12: 83,582,762 (GRCm39)		probably benign	Het
Dennd4c	T	C	4: 86,746,387 (GRCm39)		probably null	Het
Dicer1	A	T	12: 104,671,057 (GRCm39)	L995*	probably null	Het
Dnah10	A	G	5: 124,877,955 (GRCm39)	K2623R	possibly damaging	Het
Dnajc21	G	T	15: 10,461,963 (GRCm39)	T146K	probably benign	Het
Dnmbp	A	C	19: 43,891,158 (GRCm39)	L203R	probably damaging	Het
Eif4g1	C	T	16: 20,504,648 (GRCm39)	S829F	probably damaging	Het
Enkur	T	C	2: 21,194,115 (GRCm39)	I153V	probably benign	Het
Erf	T	C	7: 24,944,500 (GRCm39)	Y277C	possibly damaging	Het
Fcsk	G	A	8: 111,618,735 (GRCm39)	T341M	possibly damaging	Het
Fstl5	T	A	3: 76,555,742 (GRCm39)		probably benign	Het
Grm3	A	G	5: 9,561,452 (GRCm39)		probably null	Het
Il11ra1	A	G	4: 41,768,187 (GRCm39)	E366G	probably damaging	Het
Ipo8	A	G	6: 148,712,209 (GRCm39)	C261R	probably damaging	Het
Itga11	T	C	9: 62,681,377 (GRCm39)	F998L	probably benign	Het
Krt74	T	A	15: 101,669,887 (GRCm39)		noncoding transcript	Het
Me2	T	G	18: 73,927,596 (GRCm39)	M219L	probably benign	Het
Mlh3	A	G	12: 85,292,523 (GRCm39)		probably benign	Het
Nfx1	T	A	4: 41,015,321 (GRCm39)	V842E	probably benign	Het
Oma1	T	A	4: 103,223,209 (GRCm39)	S465T	possibly damaging	Het
Opa1	A	T	16: 29,433,887 (GRCm39)	H574L	probably damaging	Het
Pcsk5	T	C	19: 17,542,179 (GRCm39)	N804S	possibly damaging	Het
Pde4a	C	A	9: 21,112,728 (GRCm39)		probably benign	Het
Pilra	T	A	5: 137,829,527 (GRCm39)	D179V	probably damaging	Het
Piwil1	G	A	5: 128,820,344 (GRCm39)	S247N	probably benign	Het
Prss58	T	G	6: 40,872,633 (GRCm39)	T158P	probably benign	Het
Slc35e3	T	C	10: 117,580,837 (GRCm39)	M156V	probably benign	Het
Slit2	G	A	5: 48,414,198 (GRCm39)	R938Q	probably damaging	Het
Syt8	T	C	7: 141,992,926 (GRCm39)	V152A	probably benign	Het
Tppp2	G	T	14: 52,156,866 (GRCm39)	R81L	possibly damaging	Het
Trpc3	A	G	3: 36,698,405 (GRCm39)	I618T	probably damaging	Het
Zc3h4	T	A	7: 16,168,565 (GRCm39)	D891E	unknown	Het

Other mutations in Zfp120

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00586:Zfp120	APN	2	149,961,748 (GRCm39)	missense	possibly damaging	0.88
IGL03033:Zfp120	APN	2	149,961,794 (GRCm39)	missense	probably benign	0.32
R0032:Zfp120	UTSW	2	149,959,512 (GRCm39)	missense	possibly damaging	0.94
R1165:Zfp120	UTSW	2	149,961,849 (GRCm39)	missense	probably damaging	1.00
R1965:Zfp120	UTSW	2	149,959,318 (GRCm39)	missense	probably damaging	1.00
R1966:Zfp120	UTSW	2	149,959,318 (GRCm39)	missense	probably damaging	1.00
R4418:Zfp120	UTSW	2	149,960,105 (GRCm39)	missense	possibly damaging	0.79
R4902:Zfp120	UTSW	2	149,961,440 (GRCm39)	utr 3 prime	probably benign
R4910:Zfp120	UTSW	2	149,959,872 (GRCm39)	missense	probably damaging	0.96
R5108:Zfp120	UTSW	2	149,961,862 (GRCm39)	missense	probably damaging	0.98
R5521:Zfp120	UTSW	2	149,959,499 (GRCm39)	nonsense	probably null
R6280:Zfp120	UTSW	2	149,959,964 (GRCm39)	missense	possibly damaging	0.84
R8389:Zfp120	UTSW	2	149,959,327 (GRCm39)	missense	probably damaging	1.00
R8530:Zfp120	UTSW	2	149,959,168 (GRCm39)	missense	probably benign
R8871:Zfp120	UTSW	2	149,959,995 (GRCm39)	missense	probably benign	0.00
R9281:Zfp120	UTSW	2	149,959,615 (GRCm39)	missense	probably damaging	1.00
R9720:Zfp120	UTSW	2	149,959,197 (GRCm39)	missense	probably benign	0.00

Posted On

2013-03-25