Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02247:Zfp648'

286247

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Zfp648

Ensembl Gene

ENSMUSG00000066797

Gene Name

zinc finger protein 648

Synonyms

Gm10178, LOC207678

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.091) question?

Stock #

IGL02247

Quality Score

Status

Chromosome

Chromosomal Location

154076933-154081435 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 154079923 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Arginine at position 27 (S27R)

Ref Sequence

ENSEMBL: ENSMUSP00000083370 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000086195]

AlphaFold

D3Z0W3

Predicted Effect

probably benign
Transcript: ENSMUST00000086195
AA Change: S27R

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000083370
Gene: ENSMUSG00000066797
AA Change: S27R

Domain	Start	End	E-Value	Type
ZnF_C2H2	236	258	1.82e-3	SMART
ZnF_C2H2	264	286	1.28e-3	SMART
ZnF_C2H2	292	315	1.2e-3	SMART
ZnF_C2H2	321	343	1.95e-3	SMART
ZnF_C2H2	349	371	8.94e-3	SMART
ZnF_C2H2	377	399	8.34e-3	SMART
ZnF_C2H2	405	427	4.54e-4	SMART
ZnF_C2H2	433	455	4.47e-3	SMART
ZnF_C2H2	461	483	5.81e-2	SMART
ZnF_C2H2	489	511	1.2e-3	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamtsl2	A	G	2: 26,974,905 (GRCm39)	R177G	probably damaging	Het
Ap3b1	T	C	13: 94,531,303 (GRCm39)		probably null	Het
Ascc3	A	C	10: 50,526,686 (GRCm39)	K595T	probably damaging	Het
Cnpy4	A	G	5: 138,191,125 (GRCm39)	T234A	probably benign	Het
Col13a1	T	C	10: 61,797,124 (GRCm39)	Y101C	probably damaging	Het
Crybg3	A	G	16: 59,323,513 (GRCm39)	I2809T	probably damaging	Het
Csgalnact1	C	A	8: 68,854,144 (GRCm39)	G219V	probably damaging	Het
Dgkz	T	C	2: 91,767,805 (GRCm39)	S824G	probably benign	Het
Dsg1c	T	A	18: 20,397,373 (GRCm39)	I27N	probably damaging	Het
Efhb	C	T	17: 53,708,652 (GRCm39)	V673I	probably benign	Het
Egr1	T	C	18: 34,995,916 (GRCm39)	Y233H	possibly damaging	Het
Fam184a	T	C	10: 53,551,256 (GRCm39)	E237G	probably damaging	Het
Galt	A	G	4: 41,755,623 (GRCm39)		probably benign	Het
Gm4795	T	C	10: 44,883,211 (GRCm39)		noncoding transcript	Het
Gm6563	G	A	19: 23,653,392 (GRCm39)	E61K	possibly damaging	Het
Igkv1-133	G	A	6: 67,702,590 (GRCm39)	V103M	probably damaging	Het
Iqcb1	T	A	16: 36,660,258 (GRCm39)	H140Q	probably benign	Het
Itpk1	G	T	12: 102,589,668 (GRCm39)	P74Q	probably damaging	Het
Itpr3	T	A	17: 27,317,153 (GRCm39)	W803R	probably damaging	Het
Lgr4	A	T	2: 109,832,846 (GRCm39)	D312V	probably benign	Het
Lgr4	C	T	2: 109,838,420 (GRCm39)		probably benign	Het
Lyst	G	A	13: 13,835,541 (GRCm39)	C1741Y	probably benign	Het
Mllt6	C	A	11: 97,561,158 (GRCm39)	A282E	probably benign	Het
Mtif2	T	C	11: 29,490,642 (GRCm39)	S449P	possibly damaging	Het
Nrg3	T	C	14: 38,093,269 (GRCm39)	I533M	probably damaging	Het
Nynrin	C	T	14: 56,109,167 (GRCm39)	Q1425*	probably null	Het
Or12e13	A	G	2: 87,663,873 (GRCm39)	I163M	probably damaging	Het
Or1e1f	A	T	11: 73,855,688 (GRCm39)	M85L	probably benign	Het
Or4n4b	T	A	14: 50,536,571 (GRCm39)	N65I	probably damaging	Het
Or4p22	C	T	2: 88,317,771 (GRCm39)	H232Y	probably benign	Het
Or56a3	T	A	7: 104,735,530 (GRCm39)	Y202*	probably null	Het
Or5b3	T	A	19: 13,388,831 (GRCm39)	S299R	probably benign	Het
Or7e175	G	A	9: 20,048,516 (GRCm39)	V35I	probably benign	Het
Plcb4	C	T	2: 135,836,245 (GRCm39)	T20I	possibly damaging	Het
Ppp1r12b	G	T	1: 134,763,721 (GRCm39)	T771K	probably benign	Het
Prss22	T	C	17: 24,215,363 (GRCm39)	T138A	probably benign	Het
Ros1	A	T	10: 52,005,677 (GRCm39)	S907T	probably damaging	Het
Rtel1	T	A	2: 180,993,134 (GRCm39)	Y521*	probably null	Het
Sacs	T	C	14: 61,429,984 (GRCm39)	F678S	probably damaging	Het
Smtnl1	A	T	2: 84,647,372 (GRCm39)		probably benign	Het
Sumf2	T	C	5: 129,888,986 (GRCm39)	V258A	probably damaging	Het
Tas1r2	A	T	4: 139,396,827 (GRCm39)	Y722F	probably damaging	Het
Tecpr1	A	G	5: 144,143,372 (GRCm39)	F668L	possibly damaging	Het
Timd4	T	C	11: 46,706,558 (GRCm39)	F120S	probably damaging	Het
Tnnt3	T	C	7: 142,062,062 (GRCm39)		probably benign	Het
Trp53bp1	G	A	2: 121,067,070 (GRCm39)	S552F	probably damaging	Het
Txlnb	G	A	10: 17,706,090 (GRCm39)	R333Q	possibly damaging	Het
Txlnb	A	G	10: 17,717,276 (GRCm39)		probably benign	Het
Uroc1	A	G	6: 90,324,910 (GRCm39)	E461G	probably benign	Het
Vps45	G	A	3: 95,950,236 (GRCm39)	T231I	probably damaging	Het

Other mutations in Zfp648

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00585:Zfp648	APN	1	154,079,935 (GRCm39)	missense	possibly damaging	0.88
IGL01150:Zfp648	APN	1	154,081,110 (GRCm39)	missense	probably damaging	1.00
IGL01557:Zfp648	APN	1	154,080,426 (GRCm39)	missense	probably benign
IGL01757:Zfp648	APN	1	154,080,671 (GRCm39)	missense	probably damaging	0.98
PIT4519001:Zfp648	UTSW	1	154,080,687 (GRCm39)	missense	probably damaging	0.98
R0001:Zfp648	UTSW	1	154,081,032 (GRCm39)	missense	probably damaging	1.00
R0256:Zfp648	UTSW	1	154,081,414 (GRCm39)	missense	probably benign	0.08
R0266:Zfp648	UTSW	1	154,080,632 (GRCm39)	missense	probably damaging	1.00
R0371:Zfp648	UTSW	1	154,080,413 (GRCm39)	missense	possibly damaging	0.66
R1498:Zfp648	UTSW	1	154,081,119 (GRCm39)	missense	probably damaging	1.00
R1562:Zfp648	UTSW	1	154,080,138 (GRCm39)	missense	probably benign
R1687:Zfp648	UTSW	1	154,079,988 (GRCm39)	missense	probably benign	0.15
R2128:Zfp648	UTSW	1	154,080,353 (GRCm39)	missense	probably benign
R2427:Zfp648	UTSW	1	154,080,819 (GRCm39)	missense	probably damaging	1.00
R2567:Zfp648	UTSW	1	154,080,695 (GRCm39)	missense	probably damaging	0.98
R2844:Zfp648	UTSW	1	154,080,881 (GRCm39)	nonsense	probably null
R3711:Zfp648	UTSW	1	154,080,304 (GRCm39)	missense	probably benign	0.30
R4491:Zfp648	UTSW	1	154,080,873 (GRCm39)	missense	probably damaging	1.00
R4693:Zfp648	UTSW	1	154,080,152 (GRCm39)	missense	probably benign	0.01
R5666:Zfp648	UTSW	1	154,079,963 (GRCm39)	missense	probably benign	0.00
R5670:Zfp648	UTSW	1	154,079,963 (GRCm39)	missense	probably benign	0.00
R7432:Zfp648	UTSW	1	154,080,783 (GRCm39)	missense	possibly damaging	0.84
R8069:Zfp648	UTSW	1	154,079,862 (GRCm39)	missense	probably benign	0.34
R8137:Zfp648	UTSW	1	154,081,110 (GRCm39)	missense	probably damaging	1.00
R8282:Zfp648	UTSW	1	154,080,535 (GRCm39)	missense	probably benign	0.25
R9023:Zfp648	UTSW	1	154,080,914 (GRCm39)	missense	probably damaging	0.98
R9489:Zfp648	UTSW	1	154,080,110 (GRCm39)	missense	probably benign	0.17
R9520:Zfp648	UTSW	1	154,081,221 (GRCm39)	missense	probably benign
R9605:Zfp648	UTSW	1	154,080,110 (GRCm39)	missense	probably benign	0.17
Z1088:Zfp648	UTSW	1	154,080,266 (GRCm39)	missense	probably benign	0.00

Posted On

2015-04-16