Mutagenetix > Incidental Mutation

Incidental Mutation 'R7972:Zcwpw1'

650657

Institutional Source

Beutler Lab

Gene Symbol

Zcwpw1

Ensembl Gene

ENSMUSG00000037108

Gene Name

zinc finger, CW type with PWWP domain 1

Synonyms

LOC381678

MMRRC Submission

046015-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.139) question?

Stock #

R7972 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

137786060-137820883 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 137799323 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 230 (I230T)

Ref Sequence

ENSEMBL: ENSMUSP00000048730 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035852]

AlphaFold

Q6IR42

Predicted Effect

probably benign
Transcript: ENSMUST00000035852
AA Change: I230T

PolyPhen 2 Score 0.129 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000048730
Gene: ENSMUSG00000037108
AA Change: I230T

Domain	Start	End	E-Value	Type
Pfam:zf-CW	246	293	7.3e-18	PFAM
Pfam:PWWP	306	401	6.9e-22	PFAM
coiled coil region	440	462	N/A	INTRINSIC
low complexity region	587	598	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

98% (48/49)

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abhd16a	T	A	17: 35,320,287 (GRCm39)	V384E	probably damaging	Het
Acacb	C	T	5: 114,364,918 (GRCm39)	R1533*	probably null	Het
Alox12	T	A	11: 70,133,513 (GRCm39)	M604L	probably benign	Het
Amotl2	C	T	9: 102,600,968 (GRCm39)	T345I	probably benign	Het
Brdt	A	T	5: 107,496,415 (GRCm39)	I176F	possibly damaging	Het
Cdk5	G	T	5: 24,624,656 (GRCm39)	T245K	probably benign	Het
Chd9	A	T	8: 91,732,395 (GRCm39)	R1304S	unknown	Het
Clpsl2	G	A	17: 28,769,702 (GRCm39)	G55R	probably damaging	Het
Cyp2j11	T	A	4: 96,185,871 (GRCm39)	E438V	probably damaging	Het
Dao	AGG	AG	5: 114,153,270 (GRCm39)		probably benign	Het
Dnah10	T	C	5: 124,803,949 (GRCm39)	V92A	probably benign	Het
Evl	C	T	12: 108,647,783 (GRCm39)	R295*	probably null	Het
Fam184a	A	T	10: 53,514,355 (GRCm39)	L1022Q	probably damaging	Het
Foxd4	T	C	19: 24,877,594 (GRCm39)	H202R	probably damaging	Het
Fry	T	C	5: 150,233,861 (GRCm39)	V16A	probably benign	Het
Gstcd	A	T	3: 132,777,894 (GRCm39)	F306I	probably benign	Het
H2bc13	A	G	13: 21,899,977 (GRCm39)	S113P	possibly damaging	Het
Hivep3	T	C	4: 119,954,711 (GRCm39)	V1009A	possibly damaging	Het
Hoxd12	G	T	2: 74,506,269 (GRCm39)	R227L	probably damaging	Het
Ifi208	T	A	1: 173,506,556 (GRCm39)	M113K	possibly damaging	Het
Ift70a1	A	T	2: 75,810,802 (GRCm39)	M427K	probably damaging	Het
Kcnh4	T	G	11: 100,643,278 (GRCm39)	T330P	probably damaging	Het
Kctd17	CAGCTGGAGGAGC	CAGC	15: 78,321,113 (GRCm39)		probably benign	Het
Lin28a	G	A	4: 133,733,574 (GRCm39)	P158S	probably damaging	Het
Muc16	C	A	9: 18,557,060 (GRCm39)	E3078*	probably null	Het
Naaladl1	A	G	19: 6,156,274 (GRCm39)	N120S	probably damaging	Het
Nol10	G	A	12: 17,402,648 (GRCm39)	R40H	probably benign	Het
Ntng1	G	A	3: 110,042,802 (GRCm39)	S8L	probably benign	Het
Or4a71	T	G	2: 89,357,948 (GRCm39)	I269L	probably benign	Het
Or4c107	T	A	2: 88,789,177 (GRCm39)	Y122*	probably null	Het
Pacsin1	T	A	17: 27,927,613 (GRCm39)	F319I	unknown	Het
Pla2g4d	G	A	2: 120,109,413 (GRCm39)	T212I	probably benign	Het
Ppp4r1	T	A	17: 66,140,093 (GRCm39)	C664S	possibly damaging	Het
Prodh2	T	C	7: 30,210,580 (GRCm39)	I377T	probably damaging	Het
Prss57	A	T	10: 79,619,230 (GRCm39)	L243H	probably benign	Het
Pxdn	C	T	12: 30,056,601 (GRCm39)	L1271F	probably damaging	Het
Ros1	G	A	10: 52,030,926 (GRCm39)	R581*	probably null	Het
Rps6kc1	C	T	1: 190,531,321 (GRCm39)	G894S	probably benign	Het
Sirt7	A	G	11: 120,510,016 (GRCm39)	S183P	unknown	Het
Slc12a4	G	A	8: 106,678,237 (GRCm39)	R319W	possibly damaging	Het
Son	AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG	AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG	16: 91,457,222 (GRCm39)		probably benign	Het
Styxl2	T	A	1: 165,926,708 (GRCm39)	E968V	probably damaging	Het
Tbc1d8	A	G	1: 39,431,250 (GRCm39)	F374S	probably damaging	Het
Tdrd1	T	A	19: 56,837,134 (GRCm39)	D489E	probably damaging	Het
Tiprl	T	A	1: 165,064,543 (GRCm39)		probably benign	Het
Tpt1	T	C	14: 76,085,539 (GRCm39)	*173Q	probably null	Het
Trim17	A	G	11: 58,859,394 (GRCm39)	I203V	probably benign	Het
Trim43b	T	A	9: 88,973,361 (GRCm39)	H124L	probably damaging	Het
Triobp	T	C	15: 78,852,186 (GRCm39)	I780T	probably damaging	Het
Tyrobp	G	A	7: 30,114,063 (GRCm39)	G101R		Het
Vmn1r181	A	T	7: 23,683,871 (GRCm39)	H112L	probably benign	Het
Wdr19	A	G	5: 65,381,193 (GRCm39)	N406D	probably damaging	Het
Zc3h12a	T	C	4: 125,013,728 (GRCm39)	K379E	probably benign	Het
Zfhx4	A	G	3: 5,477,533 (GRCm39)	T3383A	probably benign	Het

Other mutations in Zcwpw1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01296:Zcwpw1	APN	5	137,795,061 (GRCm39)	missense	probably benign	0.42
IGL02316:Zcwpw1	APN	5	137,808,272 (GRCm39)	unclassified	probably benign
IGL02336:Zcwpw1	APN	5	137,808,376 (GRCm39)	missense	probably damaging	0.96
R0103:Zcwpw1	UTSW	5	137,808,375 (GRCm39)	nonsense	probably null
R0103:Zcwpw1	UTSW	5	137,808,375 (GRCm39)	nonsense	probably null
R0295:Zcwpw1	UTSW	5	137,815,734 (GRCm39)	missense	probably damaging	1.00
R0514:Zcwpw1	UTSW	5	137,794,945 (GRCm39)	missense	probably benign	0.26
R0685:Zcwpw1	UTSW	5	137,797,854 (GRCm39)	missense	probably benign	0.00
R0698:Zcwpw1	UTSW	5	137,815,783 (GRCm39)	missense	probably benign
R0727:Zcwpw1	UTSW	5	137,809,069 (GRCm39)	unclassified	probably benign
R1677:Zcwpw1	UTSW	5	137,795,022 (GRCm39)	missense	probably damaging	0.99
R1780:Zcwpw1	UTSW	5	137,794,914 (GRCm39)	missense	probably damaging	0.98
R1938:Zcwpw1	UTSW	5	137,809,884 (GRCm39)	missense	probably damaging	0.99
R2875:Zcwpw1	UTSW	5	137,808,304 (GRCm39)	missense	probably damaging	1.00
R4177:Zcwpw1	UTSW	5	137,798,395 (GRCm39)	missense	probably damaging	0.99
R5073:Zcwpw1	UTSW	5	137,793,781 (GRCm39)	start codon destroyed	probably null	0.81
R5913:Zcwpw1	UTSW	5	137,798,269 (GRCm39)	missense	probably benign	0.31
R6224:Zcwpw1	UTSW	5	137,810,298 (GRCm39)	missense	possibly damaging	0.63
R6542:Zcwpw1	UTSW	5	137,810,282 (GRCm39)	missense	probably damaging	0.98
R7204:Zcwpw1	UTSW	5	137,810,346 (GRCm39)	missense	probably damaging	0.98
R7542:Zcwpw1	UTSW	5	137,817,785 (GRCm39)	missense	probably benign	0.00
R7600:Zcwpw1	UTSW	5	137,798,396 (GRCm39)	nonsense	probably null
R7911:Zcwpw1	UTSW	5	137,795,032 (GRCm39)	missense	probably null	1.00
R7988:Zcwpw1	UTSW	5	137,815,753 (GRCm39)	missense	possibly damaging	0.69
R8174:Zcwpw1	UTSW	5	137,817,839 (GRCm39)	critical splice donor site	probably null
R8713:Zcwpw1	UTSW	5	137,797,794 (GRCm39)	missense	probably benign	0.06
R8851:Zcwpw1	UTSW	5	137,820,626 (GRCm39)	missense	probably damaging	1.00
R9016:Zcwpw1	UTSW	5	137,798,340 (GRCm39)	missense	probably damaging	0.98
R9131:Zcwpw1	UTSW	5	137,809,182 (GRCm39)	missense	probably damaging	1.00
R9337:Zcwpw1	UTSW	5	137,799,274 (GRCm39)	missense	probably benign	0.37
X0021:Zcwpw1	UTSW	5	137,809,869 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGCAGCCTACAACTTCCTGC -3'
(R):5'- AGATGAAGTCTTTCTGCTTCGTCC -3'

Sequencing Primer
(F):5'- CAGGCTTGGGGCTTCCTG -3'
(R):5'- GTCCTCTTTCCTTATCTCCTAAGAAG -3'

Posted On

2020-09-15