Mutagenetix > Incidental Mutation

Incidental Mutation 'R2252:Gzf1'

241728

Institutional Source

Beutler Lab

Gene Symbol

Gzf1

Ensembl Gene

ENSMUSG00000027439

Gene Name

GDNF-inducible zinc finger protein 1

Synonyms

Zfp336, 8430437G08Rik

MMRRC Submission

040252-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.500) question?

Stock #

R2252 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

148522943-148534869 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 148525856 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Threonine at position 109 (M109T)

Ref Sequence

ENSEMBL: ENSMUSP00000028928 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028928] [ENSMUST00000131292]

AlphaFold

Q4VBD9

Predicted Effect

probably damaging
Transcript: ENSMUST00000028928
AA Change: M109T

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

SMART Domains

Protein: ENSMUSP00000028928
Gene: ENSMUSG00000027439
AA Change: M109T

Domain	Start	End	E-Value	Type
BTB	31	133	2.01e-20	SMART
low complexity region	199	213	N/A	INTRINSIC
coiled coil region	287	308	N/A	INTRINSIC
ZnF_C2H2	315	337	6.32e-3	SMART
ZnF_C2H2	346	369	1.2e-3	SMART
ZnF_C2H2	375	398	8.34e-3	SMART
ZnF_C2H2	405	427	7.78e-3	SMART
ZnF_C2H2	433	455	1.69e-3	SMART
ZnF_C2H2	461	483	1.43e-1	SMART
ZnF_C2H2	489	511	2.4e-3	SMART
ZnF_C2H2	517	539	1.47e-3	SMART
ZnF_C2H2	545	567	1.38e-3	SMART
ZnF_C2H2	573	595	1.04e-3	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000131292
AA Change: M109T

PolyPhen 2 Score 0.978 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000121799
Gene: ENSMUSG00000027439
AA Change: M109T

Domain	Start	End	E-Value	Type
BTB	31	133	2.01e-20	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151362

Coding Region Coverage

1x: 99.1%
3x: 98.6%
10x: 97.3%
20x: 95.1%

Validation Efficiency

Allele List at MGI

All alleles(5) : Gene trapped(5)

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700129C05Rik	G	A	14: 59,380,061 (GRCm39)	S79F	probably damaging	Het
Acaca	G	T	11: 84,262,358 (GRCm39)	V1987L	probably damaging	Het
B3gnt3	A	T	8: 72,145,462 (GRCm39)	M302K	probably damaging	Het
BC048507	T	C	13: 68,011,626 (GRCm39)	M1T	probably null	Het
Bckdk	C	A	7: 127,504,590 (GRCm39)	R105S	probably damaging	Het
Casp3	G	T	8: 47,090,990 (GRCm39)	W214L	probably damaging	Het
Cd180	A	T	13: 102,842,906 (GRCm39)	K651*	probably null	Het
Cdh15	T	A	8: 123,584,161 (GRCm39)	D87E	probably damaging	Het
Cldn24	G	T	8: 48,275,363 (GRCm39)	R62S	probably benign	Het
Cnot1	A	G	8: 96,489,814 (GRCm39)	V463A	probably benign	Het
Cspg4	C	T	9: 56,805,330 (GRCm39)	T2047I	probably damaging	Het
Cul2	A	T	18: 3,399,876 (GRCm39)	L3F	probably damaging	Het
Cwc27	A	T	13: 104,768,237 (GRCm39)	H419Q	probably damaging	Het
Dgkg	A	T	16: 22,441,010 (GRCm39)	M1K	probably null	Het
Dock5	A	T	14: 68,022,261 (GRCm39)	L1171H	probably damaging	Het
Drc1	G	T	5: 30,500,075 (GRCm39)	V103F	probably benign	Het
Ep400	A	T	5: 110,866,957 (GRCm39)	N1062K	unknown	Het
Faap20	A	C	4: 155,335,010 (GRCm39)	E37A	possibly damaging	Het
Foxa2	A	G	2: 147,886,086 (GRCm39)	F243S	probably damaging	Het
Itch	T	A	2: 155,054,259 (GRCm39)	M701K	probably benign	Het
Kpna1	T	C	16: 35,841,939 (GRCm39)	Y280H	possibly damaging	Het
L1td1	A	G	4: 98,625,874 (GRCm39)		probably null	Het
Lrrc37a	T	C	11: 103,392,293 (GRCm39)	Q1044R	probably benign	Het
Lrrc52	A	T	1: 167,293,937 (GRCm39)	I116N	probably damaging	Het
Mbd5	A	G	2: 49,147,698 (GRCm39)	E636G	probably damaging	Het
Mrpl40	T	C	16: 18,694,125 (GRCm39)	H29R	probably benign	Het
Nrip1	T	C	16: 76,088,173 (GRCm39)	Y1128C	probably damaging	Het
Or10d3	G	T	9: 39,461,273 (GRCm39)	A298D	probably damaging	Het
Or4g16	A	G	2: 111,136,655 (GRCm39)	Y35C	probably damaging	Het
Or5ak20	A	G	2: 85,184,202 (GRCm39)	S23P	possibly damaging	Het
Or8c8	A	G	9: 38,165,126 (GRCm39)	I135V	probably benign	Het
Pard3	A	T	8: 128,337,080 (GRCm39)	E1232V	probably damaging	Het
Pcif1	A	G	2: 164,732,799 (GRCm39)	E628G	probably benign	Het
Pcsk1	C	A	13: 75,274,845 (GRCm39)	A478D	probably benign	Het
Pkd1l2	T	C	8: 117,784,177 (GRCm39)	Y700C	probably damaging	Het
Pknox2	T	C	9: 36,821,816 (GRCm39)	N270D	probably benign	Het
Plcb2	T	C	2: 118,554,246 (GRCm39)	N69S	probably benign	Het
Reep1	T	A	6: 71,733,426 (GRCm39)		probably null	Het
Sash1	A	T	10: 8,605,741 (GRCm39)	M883K	probably benign	Het
Secisbp2l	C	T	2: 125,582,657 (GRCm39)	G933D	possibly damaging	Het
Septin4	A	G	11: 87,480,637 (GRCm39)	N405D	possibly damaging	Het
Serpinb3b	T	C	1: 107,083,208 (GRCm39)	I231M	possibly damaging	Het
Serping1	A	G	2: 84,600,195 (GRCm39)	S322P	probably damaging	Het
Slc7a2	T	C	8: 41,358,658 (GRCm39)	Y334H	probably benign	Het
Spink5	G	T	18: 44,153,891 (GRCm39)	E1013*	probably null	Het
Thoc3	A	T	13: 54,615,646 (GRCm39)	N139K	probably benign	Het
Tns2	C	T	15: 102,017,369 (GRCm39)	R281C	probably damaging	Het
Tubb2b	T	A	13: 34,314,198 (GRCm39)	I7F	possibly damaging	Het
Upf2	A	G	2: 5,966,271 (GRCm39)	D297G	unknown	Het
Vmn2r18	T	C	5: 151,508,441 (GRCm39)	I228V	possibly damaging	Het
Vmn2r98	A	C	17: 19,300,698 (GRCm39)	S567R	probably benign	Het
Vwa5a	T	C	9: 38,639,376 (GRCm39)	I369T	probably damaging	Het
Yjefn3	A	C	8: 70,342,095 (GRCm39)	F42V	probably damaging	Het
Zfp472	A	T	17: 33,195,257 (GRCm39)	R69*	probably null	Het
Zfp536	T	C	7: 37,178,814 (GRCm39)	S200G	probably benign	Het
Zfp970	T	A	2: 177,166,614 (GRCm39)		probably null	Het

Other mutations in Gzf1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01129:Gzf1	APN	2	148,532,916 (GRCm39)	missense	probably damaging	0.99
IGL01647:Gzf1	APN	2	148,525,570 (GRCm39)	missense	probably damaging	1.00
IGL01789:Gzf1	APN	2	148,525,981 (GRCm39)	missense	probably benign	0.41
IGL01791:Gzf1	APN	2	148,525,981 (GRCm39)	missense	probably benign	0.41
IGL01952:Gzf1	APN	2	148,525,981 (GRCm39)	missense	probably benign	0.41
IGL01954:Gzf1	APN	2	148,525,981 (GRCm39)	missense	probably benign	0.41
IGL01956:Gzf1	APN	2	148,525,981 (GRCm39)	missense	probably benign	0.41
IGL03391:Gzf1	APN	2	148,525,603 (GRCm39)	missense	probably damaging	1.00
I0000:Gzf1	UTSW	2	148,528,540 (GRCm39)	unclassified	probably benign
P0019:Gzf1	UTSW	2	148,525,900 (GRCm39)	missense	probably damaging	1.00
R0420:Gzf1	UTSW	2	148,525,753 (GRCm39)	missense	probably benign	0.30
R0725:Gzf1	UTSW	2	148,526,569 (GRCm39)	nonsense	probably null
R1131:Gzf1	UTSW	2	148,532,787 (GRCm39)	missense	probably benign	0.02
R2000:Gzf1	UTSW	2	148,526,531 (GRCm39)	missense	probably benign	0.16
R2211:Gzf1	UTSW	2	148,526,870 (GRCm39)	missense	probably damaging	1.00
R2251:Gzf1	UTSW	2	148,525,856 (GRCm39)	missense	probably damaging	1.00
R2253:Gzf1	UTSW	2	148,525,856 (GRCm39)	missense	probably damaging	1.00
R4233:Gzf1	UTSW	2	148,528,453 (GRCm39)	missense	possibly damaging	0.86
R5551:Gzf1	UTSW	2	148,526,248 (GRCm39)	missense	probably damaging	1.00
R6050:Gzf1	UTSW	2	148,526,158 (GRCm39)	missense	possibly damaging	0.89
R6891:Gzf1	UTSW	2	148,526,689 (GRCm39)	nonsense	probably null
R7457:Gzf1	UTSW	2	148,532,002 (GRCm39)	missense	probably damaging	0.99
R7735:Gzf1	UTSW	2	148,530,083 (GRCm39)	missense	possibly damaging	0.91
R7839:Gzf1	UTSW	2	148,525,815 (GRCm39)	nonsense	probably null
R8168:Gzf1	UTSW	2	148,526,686 (GRCm39)	missense	probably damaging	1.00
R8225:Gzf1	UTSW	2	148,532,764 (GRCm39)	missense	probably benign	0.02
R8432:Gzf1	UTSW	2	148,532,115 (GRCm39)	missense	probably benign	0.22
R9081:Gzf1	UTSW	2	148,525,317 (GRCm39)	intron	probably benign
R9761:Gzf1	UTSW	2	148,530,011 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AGACTTCATGGCCCATAAAGCAG -3'
(R):5'- ACAAGGCCATTGGAGTGAGC -3'

Sequencing Primer
(F):5'- CATGGCCCATAAAGCAGTGCTG -3'
(R):5'- ATTGGAGTGAGCATCCTCCC -3'

Posted On

2014-10-16