Mutagenetix > Incidental Mutation

Incidental Mutation 'R9114:Zfp457'

692437

Institutional Source

Beutler Lab

Gene Symbol

Zfp457

Ensembl Gene

ENSMUSG00000055341

Gene Name

zinc finger protein 457

Synonyms

Rslcan-6

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.084) question?

Stock #

R9114 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

67440514-67454476 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 67442068 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 169 (D169G)

Ref Sequence

ENSEMBL: ENSMUSP00000053879 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049705] [ENSMUST00000224325]

AlphaFold

L7N1X4

Predicted Effect

probably benign
Transcript: ENSMUST00000049705
AA Change: D169G

PolyPhen 2 Score 0.160 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000053879
Gene: ENSMUSG00000055341
AA Change: D169G

Domain	Start	End	E-Value	Type
KRAB	5	65	1.55e-29	SMART
ZnF_C2H2	81	103	2.75e-3	SMART
ZnF_C2H2	109	131	1.1e-2	SMART
ZnF_C2H2	165	187	3.63e-3	SMART
ZnF_C2H2	193	215	2.4e-3	SMART
ZnF_C2H2	221	243	1.12e-3	SMART
ZnF_C2H2	249	271	6.32e-3	SMART
ZnF_C2H2	277	299	6.32e-3	SMART
ZnF_C2H2	305	327	3.52e-1	SMART
ZnF_C2H2	333	355	3.89e-3	SMART
ZnF_C2H2	361	383	7.26e-3	SMART
ZnF_C2H2	389	411	1.2e-3	SMART
ZnF_C2H2	417	439	7.67e-2	SMART
ZnF_C2H2	445	467	1.05e1	SMART
ZnF_C2H2	473	495	3.11e-2	SMART
ZnF_C2H2	501	523	5.9e-3	SMART
ZnF_C2H2	529	551	9.08e-4	SMART
ZnF_C2H2	585	607	5.72e-1	SMART
transmembrane domain	624	646	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000224325
AA Change: D73G

PolyPhen 2 Score 0.380 (Sensitivity: 0.90; Specificity: 0.89)

Predicted Effect

probably benign
Transcript: ENSMUST00000225338

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb1a	T	A	5: 8,788,702 (GRCm39)	L1027*	probably null	Het
Actl11	T	A	9: 107,808,509 (GRCm39)	M944K	possibly damaging	Het
Afap1l2	T	C	19: 56,906,427 (GRCm39)	K491E	probably damaging	Het
Ahr	A	T	12: 35,561,164 (GRCm39)	D150E	probably damaging	Het
Arhgef1	T	A	7: 24,607,304 (GRCm39)	L17Q	probably damaging	Het
Bysl	A	G	17: 47,915,242 (GRCm39)	S169P		Het
C4b	A	T	17: 34,948,404 (GRCm39)	F1610I	probably damaging	Het
Chtf8	C	A	8: 107,612,481 (GRCm39)	A153S	probably benign	Het
Ciapin1	C	T	8: 95,558,400 (GRCm39)		probably null	Het
Cnnm1	A	G	19: 43,429,395 (GRCm39)	E171G	possibly damaging	Het
Crybb3	T	C	5: 113,225,407 (GRCm39)	N155S	probably benign	Het
Dclk3	T	A	9: 111,317,683 (GRCm39)	M773K	probably benign	Het
Ddx18	A	T	1: 121,489,267 (GRCm39)	V260D	probably damaging	Het
Dmxl2	T	A	9: 54,307,321 (GRCm39)	N2216Y		Het
Epn2	T	C	11: 61,437,446 (GRCm39)	E42G	probably damaging	Het
Esrrg	C	A	1: 187,878,605 (GRCm39)	P229T	probably benign	Het
Esrrg	C	A	1: 187,878,606 (GRCm39)	P229Q	possibly damaging	Het
Ethe1	G	T	7: 24,305,643 (GRCm39)	R130L	probably benign	Het
Fgl2	G	A	5: 21,580,363 (GRCm39)	C235Y	probably damaging	Het
Fmnl1	C	T	11: 103,087,327 (GRCm39)	T890M	unknown	Het
Fsip2	C	G	2: 82,807,301 (GRCm39)	P1207A	probably benign	Het
Gc	C	T	5: 89,593,165 (GRCm39)	D85N	possibly damaging	Het
Gfi1	G	A	5: 107,869,370 (GRCm39)	R287W	probably damaging	Het
Gm3629	T	C	14: 17,834,566 (GRCm39)		probably null	Het
Hapln3	A	G	7: 78,771,712 (GRCm39)	F59S	probably benign	Het
Il24	G	A	1: 130,813,483 (GRCm39)	T38I	possibly damaging	Het
Izumo1	A	G	7: 45,276,583 (GRCm39)	D382G	probably benign	Het
Kdm5a	T	A	6: 120,382,887 (GRCm39)	Y739*	probably null	Het
Kif2b	T	A	11: 91,466,538 (GRCm39)	I582F	possibly damaging	Het
Klhdc1	A	G	12: 69,288,783 (GRCm39)	Y31C	probably damaging	Het
Lama1	G	A	17: 68,128,669 (GRCm39)	E3009K		Het
Mad2l1bp	G	A	17: 46,458,958 (GRCm39)	R191C	probably damaging	Het
Mark1	A	C	1: 184,644,261 (GRCm39)	S468A	probably damaging	Het
Mknk2	T	A	10: 80,504,823 (GRCm39)	N236Y	probably damaging	Het
Muc2	T	A	7: 141,287,983 (GRCm39)	C251*	probably null	Het
Nacad	T	C	11: 6,552,252 (GRCm39)	D313G	probably damaging	Het
Neb	G	T	2: 52,099,599 (GRCm39)	D4750E	probably benign	Het
Nlrp6	T	C	7: 140,506,332 (GRCm39)	S758P	probably damaging	Het
Nxt2	C	T	X: 141,020,747 (GRCm39)	A118V	possibly damaging	Het
Or13a28	A	C	7: 140,218,282 (GRCm39)	I223L	probably benign	Het
Or51b4	T	C	7: 103,530,569 (GRCm39)	T294A	possibly damaging	Het
Or8b3b	A	G	9: 38,583,892 (GRCm39)	F283L	probably benign	Het
Oxtr	A	G	6: 112,466,481 (GRCm39)	V93A	probably damaging	Het
Pbx3	C	A	2: 34,103,271 (GRCm39)	D234Y	probably damaging	Het
Pde4b	A	T	4: 102,459,826 (GRCm39)	T554S	probably damaging	Het
Peg10	GC	GCTCC	6: 4,756,452 (GRCm39)		probably benign	Het
Pid1	A	T	1: 84,015,955 (GRCm39)	Y151N	probably damaging	Het
Plcd4	A	G	1: 74,591,307 (GRCm39)	E234G	possibly damaging	Het
Pou6f1	A	G	15: 100,478,789 (GRCm39)	V373A	probably benign	Het
Ppp1r12c	T	C	7: 4,485,792 (GRCm39)	K685E	possibly damaging	Het
Rnf34	T	A	5: 122,999,957 (GRCm39)	V71D	probably damaging	Het
Rpap2	T	G	5: 107,746,156 (GRCm39)	H11Q	possibly damaging	Het
Skint2	A	G	4: 112,496,834 (GRCm39)	T247A	probably benign	Het
Stat5b	T	A	11: 100,692,350 (GRCm39)	N145Y	probably damaging	Het
Sv2b	A	G	7: 74,856,017 (GRCm39)	L91P	probably damaging	Het
Syt1	A	G	10: 108,340,376 (GRCm39)	I314T	probably damaging	Het
Tlk1	A	T	2: 70,572,502 (GRCm39)	N355K	probably benign	Het
Tnc	C	A	4: 63,890,973 (GRCm39)	M1636I	probably benign	Het
Trank1	C	A	9: 111,162,843 (GRCm39)	A34D	probably damaging	Het
Unc13c	A	G	9: 73,719,665 (GRCm39)	I1001T	probably benign	Het
Vdr	T	C	15: 97,765,136 (GRCm39)	D201G	probably benign	Het
Vmn2r115	A	T	17: 23,564,307 (GRCm39)	I160L	probably benign	Het
Wdr81	C	A	11: 75,335,250 (GRCm39)	R1772L	probably damaging	Het

Other mutations in Zfp457

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01329:Zfp457	APN	13	67,442,330 (GRCm39)	missense	possibly damaging	0.46
IGL02259:Zfp457	APN	13	67,444,471 (GRCm39)	missense	possibly damaging	0.88
R0055:Zfp457	UTSW	13	67,442,098 (GRCm39)	missense	probably damaging	0.99
R0055:Zfp457	UTSW	13	67,442,098 (GRCm39)	missense	probably damaging	0.99
R0149:Zfp457	UTSW	13	67,440,710 (GRCm39)	missense	probably damaging	0.97
R0211:Zfp457	UTSW	13	67,441,211 (GRCm39)	missense	probably benign	0.01
R0211:Zfp457	UTSW	13	67,441,211 (GRCm39)	missense	probably benign	0.01
R0230:Zfp457	UTSW	13	67,442,180 (GRCm39)	missense	possibly damaging	0.91
R0270:Zfp457	UTSW	13	67,441,991 (GRCm39)	missense	probably damaging	1.00
R0361:Zfp457	UTSW	13	67,440,710 (GRCm39)	missense	probably damaging	0.97
R0561:Zfp457	UTSW	13	67,442,134 (GRCm39)	missense	probably damaging	1.00
R0679:Zfp457	UTSW	13	67,441,655 (GRCm39)	missense	probably damaging	1.00
R0826:Zfp457	UTSW	13	67,441,378 (GRCm39)	missense	possibly damaging	0.85
R1136:Zfp457	UTSW	13	67,441,846 (GRCm39)	missense	probably damaging	1.00
R1175:Zfp457	UTSW	13	67,441,748 (GRCm39)	missense	probably damaging	1.00
R1523:Zfp457	UTSW	13	67,441,501 (GRCm39)	missense	probably damaging	1.00
R1616:Zfp457	UTSW	13	67,444,375 (GRCm39)	missense	possibly damaging	0.95
R2348:Zfp457	UTSW	13	67,441,468 (GRCm39)	missense	probably benign	0.33
R4930:Zfp457	UTSW	13	67,442,164 (GRCm39)	missense	probably damaging	1.00
R4964:Zfp457	UTSW	13	67,441,342 (GRCm39)	missense	probably damaging	1.00
R4966:Zfp457	UTSW	13	67,441,342 (GRCm39)	missense	probably damaging	1.00
R5040:Zfp457	UTSW	13	67,440,899 (GRCm39)	missense	probably benign	0.03
R5129:Zfp457	UTSW	13	67,441,420 (GRCm39)	missense	probably benign	0.00
R5714:Zfp457	UTSW	13	67,444,490 (GRCm39)	missense	possibly damaging	0.85
R6017:Zfp457	UTSW	13	67,441,763 (GRCm39)	missense	probably damaging	1.00
R6052:Zfp457	UTSW	13	67,442,015 (GRCm39)	missense	probably damaging	1.00
R6132:Zfp457	UTSW	13	67,441,360 (GRCm39)	nonsense	probably null
R6184:Zfp457	UTSW	13	67,440,976 (GRCm39)	missense	possibly damaging	0.89
R6313:Zfp457	UTSW	13	67,440,746 (GRCm39)	missense	probably damaging	1.00
R7038:Zfp457	UTSW	13	67,441,997 (GRCm39)	missense	probably benign	0.00
R7170:Zfp457	UTSW	13	67,442,241 (GRCm39)	nonsense	probably null
R7184:Zfp457	UTSW	13	67,442,065 (GRCm39)	missense	possibly damaging	0.69
R7859:Zfp457	UTSW	13	67,454,445 (GRCm39)	start gained	probably benign
R7973:Zfp457	UTSW	13	67,441,882 (GRCm39)	missense	probably benign	0.20
R8308:Zfp457	UTSW	13	67,441,663 (GRCm39)	missense	probably benign	0.00
R8346:Zfp457	UTSW	13	67,441,862 (GRCm39)	nonsense	probably null
R9205:Zfp457	UTSW	13	67,441,965 (GRCm39)	missense	probably benign	0.00
R9525:Zfp457	UTSW	13	67,441,492 (GRCm39)	missense	probably damaging	1.00
R9765:Zfp457	UTSW	13	67,440,874 (GRCm39)	missense	probably benign	0.10

Predicted Primers

PCR Primer
(F):5'- GGATCATGGAAGGTTTTGTCACA -3'
(R):5'- GGCTTTCACCTATGCTGTGTTG -3'

Sequencing Primer
(F):5'- TGGAAGGTTTTGTCACATAATTCAC -3'
(R):5'- TCCTTCTTCACCAGGGGGAAAATG -3'

Posted On

2021-12-30