Mutagenetix > Incidental Mutation

Incidental Mutation 'R8762:Flywch1'

671877

Institutional Source

Beutler Lab

Gene Symbol

Flywch1

Ensembl Gene

ENSMUSG00000040097

Gene Name

FLYWCH-type zinc finger 1

Synonyms

MMRRC Submission

068622-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8762 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

23971767-23990576 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 23975731 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 504 (S504P)

Ref Sequence

ENSEMBL: ENSMUSP00000040022 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045517] [ENSMUST00000086325]

AlphaFold

Q8CI03

Predicted Effect

probably damaging
Transcript: ENSMUST00000045517
AA Change: S504P

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

SMART Domains

Protein: ENSMUSP00000040022
Gene: ENSMUSG00000040097
AA Change: S504P

Domain	Start	End	E-Value	Type
Pfam:FLYWCH_N	1	83	1.2e-24	PFAM
Pfam:FLYWCH	92	150	7e-17	PFAM
Pfam:FLYWCH	235	293	3.3e-17	PFAM
low complexity region	352	380	N/A	INTRINSIC
low complexity region	381	394	N/A	INTRINSIC
Pfam:FLYWCH	402	460	9.7e-18	PFAM
Pfam:FLYWCH	490	548	7.9e-18	PFAM
Pfam:FLYWCH	581	639	6.1e-17	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000086325
AA Change: S504P

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

SMART Domains

Protein: ENSMUSP00000083505
Gene: ENSMUSG00000040097
AA Change: S504P

Domain	Start	End	E-Value	Type
Pfam:FLYWCH_N	1	84	9.7e-10	PFAM
Pfam:FLYWCH	92	150	3.8e-17	PFAM
Pfam:FLYWCH	235	293	3.1e-17	PFAM
Pfam:FLYWCH_u	294	401	1.3e-30	PFAM
Pfam:FLYWCH	402	460	9.1e-18	PFAM
Pfam:FLYWCH	490	548	6.8e-18	PFAM
Pfam:FLYWCH_u	549	568	9.1e-3	PFAM
Pfam:FLYWCH	581	639	4.7e-17	PFAM
Pfam:FLYWCH_u	640	672	4.6e-4	PFAM

Predicted Effect

Meta Mutation Damage Score

0.5966

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

100% (66/66)

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aarsd1	A	G	11: 101,301,226 (GRCm39)	V272A	probably benign	Het
Acbd6	G	A	1: 155,562,706 (GRCm39)	E236K	probably damaging	Het
Actr1b	T	C	1: 36,748,909 (GRCm39)	N9S	probably benign	Het
Adam17	A	T	12: 21,401,595 (GRCm39)	D133E	probably benign	Het
Adam6b	G	A	12: 113,453,227 (GRCm39)	V15M	probably damaging	Het
Adam9	T	A	8: 25,457,235 (GRCm39)	N631I	probably damaging	Het
Albfm1	A	G	5: 90,714,461 (GRCm39)	N157S	probably benign	Het
Amy2a1	A	T	3: 113,325,276 (GRCm39)		probably benign	Het
Aplnr	A	T	2: 84,967,515 (GRCm39)	Y180F	probably benign	Het
Arhgef7	T	C	8: 11,831,216 (GRCm39)	V105A	probably benign	Het
Bambi	G	A	18: 3,511,277 (GRCm39)	D33N	probably damaging	Het
Bicc1	G	A	10: 70,779,216 (GRCm39)	T724I	probably benign	Het
Brd2	T	A	17: 34,335,934 (GRCm39)	Q93L	probably damaging	Het
Cacnb2	A	G	2: 14,972,759 (GRCm39)	D222G	possibly damaging	Het
Cdh1	G	T	8: 107,386,336 (GRCm39)	D420Y	probably damaging	Het
Cep162	T	C	9: 87,109,314 (GRCm39)	S430G	probably benign	Het
Cfap161	T	A	7: 83,443,282 (GRCm39)	R27S	possibly damaging	Het
Chek1	C	T	9: 36,629,636 (GRCm39)	A237T	probably benign	Het
Chrna3	T	A	9: 54,922,995 (GRCm39)	K271M	probably damaging	Het
Coro7	A	C	16: 4,452,203 (GRCm39)	V410G	probably benign	Het
Crmp1	C	A	5: 37,441,440 (GRCm39)	N507K	probably damaging	Het
Crocc	T	C	4: 140,761,369 (GRCm39)	R755G	possibly damaging	Het
Disc1	A	G	8: 125,881,796 (GRCm39)	D577G	probably damaging	Het
Dnah6	A	G	6: 73,156,811 (GRCm39)	Y649H	possibly damaging	Het
Fpr1	A	T	17: 18,097,851 (GRCm39)	V46D	probably damaging	Het
Fpr-rs7	C	T	17: 20,333,789 (GRCm39)	V234M	probably benign	Het
Ighv5-16	T	C	12: 113,802,288 (GRCm39)	N71D	probably benign	Het
Kash5	G	T	7: 44,845,481 (GRCm39)	D152E	probably damaging	Het
Kdm3b	A	G	18: 34,937,157 (GRCm39)	M480V	probably benign	Het
L3mbtl3	T	A	10: 26,152,121 (GRCm39)	D825V	probably damaging	Het
Lef1	T	A	3: 130,988,366 (GRCm39)	M311K	probably damaging	Het
Magi1	T	A	6: 93,792,789 (GRCm39)	R150*	probably null	Het
Magi3	C	T	3: 103,958,169 (GRCm39)	V639I	probably damaging	Het
Mocos	A	T	18: 24,812,554 (GRCm39)	R483W	probably damaging	Het
Mrps11	G	T	7: 78,438,487 (GRCm39)	V80F	possibly damaging	Het
Myh2	A	T	11: 67,084,578 (GRCm39)	R1706W	probably damaging	Het
Neurod6	T	A	6: 55,656,228 (GRCm39)	L136F	probably damaging	Het
Nfe2l1	A	T	11: 96,711,306 (GRCm39)	Y308N	probably damaging	Het
Nptn	T	A	9: 58,525,905 (GRCm39)		probably benign	Het
Or1e28-ps1	G	T	11: 73,615,307 (GRCm39)	T181N	unknown	Het
Or5g25	A	T	2: 85,478,034 (GRCm39)	S210R	probably damaging	Het
Oscar	A	G	7: 3,613,900 (GRCm39)	S227P	probably benign	Het
Phgdh	A	C	3: 98,247,024 (GRCm39)	I42R	possibly damaging	Het
Pla2g4a	C	T	1: 149,761,935 (GRCm39)	G174D	probably benign	Het
Plcd4	A	G	1: 74,591,213 (GRCm39)	T203A	possibly damaging	Het
Plk3	ACACTCAC	ACAC	4: 116,989,090 (GRCm39)		probably benign	Het
Plppr4	A	T	3: 117,119,482 (GRCm39)	V309D	probably damaging	Het
Pltp	T	C	2: 164,686,652 (GRCm39)	K324E	possibly damaging	Het
Pml	C	T	9: 58,154,348 (GRCm39)	R175H	probably damaging	Het
Psg20	C	A	7: 18,408,557 (GRCm39)	V388F	probably benign	Het
Qrfprl	T	C	6: 65,424,393 (GRCm39)	V182A	probably benign	Het
Rabgef1	A	G	5: 130,237,557 (GRCm39)	D209G	possibly damaging	Het
Rif1	A	T	2: 52,001,742 (GRCm39)	N90I		Het
Sec31a	T	C	5: 100,526,688 (GRCm39)	H57R		Het
Sidt1	T	C	16: 44,152,707 (GRCm39)	N62S	probably benign	Het
Slc18a2	T	A	19: 59,261,355 (GRCm39)	M172K	probably benign	Het
Slc34a3	T	C	2: 25,121,003 (GRCm39)	T362A	probably benign	Het
Smtn	T	G	11: 3,476,407 (GRCm39)	D158A	probably benign	Het
Spen	C	T	4: 141,200,261 (GRCm39)	V2789M	probably damaging	Het
Taf2	A	T	15: 54,910,849 (GRCm39)	N608K	probably benign	Het
Tctn3	A	G	19: 40,595,636 (GRCm39)	V383A	unknown	Het
Themis3	A	T	17: 66,866,676 (GRCm39)	M188K	probably benign	Het
Trpv5	A	G	6: 41,652,313 (GRCm39)	V124A	probably benign	Het
Tshr	G	A	12: 91,504,324 (GRCm39)	V421M	probably damaging	Het
Ttn	T	A	2: 76,539,426 (GRCm39)	D34520V	probably benign	Het
Ttn	A	C	2: 76,608,294 (GRCm39)	Y17876*	probably null	Het
Zrsr2-ps1	T	C	11: 22,923,694 (GRCm39)	L156P	probably benign	Het

Other mutations in Flywch1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01716:Flywch1	APN	17	23,982,000 (GRCm39)	missense	probably benign	0.01
IGL01843:Flywch1	APN	17	23,979,319 (GRCm39)	missense	possibly damaging	0.89
IGL02110:Flywch1	APN	17	23,982,066 (GRCm39)	splice site	probably null
IGL02586:Flywch1	APN	17	23,974,676 (GRCm39)	missense	probably benign	0.04
IGL02870:Flywch1	APN	17	23,974,876 (GRCm39)	missense	probably damaging	1.00
IGL02877:Flywch1	APN	17	23,979,388 (GRCm39)	missense	probably damaging	1.00
lubdub	UTSW	17	23,980,033 (GRCm39)	missense	possibly damaging	0.93
R0830:Flywch1	UTSW	17	23,981,344 (GRCm39)	missense	probably benign	0.00
R1411:Flywch1	UTSW	17	23,974,798 (GRCm39)	missense	probably damaging	1.00
R2044:Flywch1	UTSW	17	23,981,287 (GRCm39)	nonsense	probably null
R2153:Flywch1	UTSW	17	23,974,624 (GRCm39)	missense	probably benign	0.21
R2314:Flywch1	UTSW	17	23,982,000 (GRCm39)	missense	probably benign	0.01
R2497:Flywch1	UTSW	17	23,974,685 (GRCm39)	missense	probably benign	0.27
R3022:Flywch1	UTSW	17	23,982,082 (GRCm39)	missense	probably benign	0.00
R3625:Flywch1	UTSW	17	23,979,175 (GRCm39)	splice site	probably benign
R3691:Flywch1	UTSW	17	23,982,186 (GRCm39)	missense	probably damaging	0.96
R4805:Flywch1	UTSW	17	23,979,591 (GRCm39)	missense	probably benign	0.16
R5321:Flywch1	UTSW	17	23,975,625 (GRCm39)	missense	probably damaging	1.00
R7148:Flywch1	UTSW	17	23,974,649 (GRCm39)	missense	probably benign	0.01
R7200:Flywch1	UTSW	17	23,980,033 (GRCm39)	missense	possibly damaging	0.93
R7629:Flywch1	UTSW	17	23,974,744 (GRCm39)	missense	probably benign	0.06
R8362:Flywch1	UTSW	17	23,975,682 (GRCm39)	missense	probably damaging	1.00
RF003:Flywch1	UTSW	17	23,981,140 (GRCm39)	frame shift	probably null
RF007:Flywch1	UTSW	17	23,981,145 (GRCm39)	frame shift	probably null
RF007:Flywch1	UTSW	17	23,981,138 (GRCm39)	frame shift	probably null
RF009:Flywch1	UTSW	17	23,981,135 (GRCm39)	frame shift	probably null
RF010:Flywch1	UTSW	17	23,981,149 (GRCm39)	frame shift	probably null
RF013:Flywch1	UTSW	17	23,981,149 (GRCm39)	frame shift	probably null
RF018:Flywch1	UTSW	17	23,981,140 (GRCm39)	frame shift	probably null
RF022:Flywch1	UTSW	17	23,981,141 (GRCm39)	frame shift	probably null
RF027:Flywch1	UTSW	17	23,981,132 (GRCm39)	frame shift	probably null
RF031:Flywch1	UTSW	17	23,981,132 (GRCm39)	frame shift	probably null
RF038:Flywch1	UTSW	17	23,981,138 (GRCm39)	frame shift	probably null
RF040:Flywch1	UTSW	17	23,981,143 (GRCm39)	frame shift	probably null
RF041:Flywch1	UTSW	17	23,981,151 (GRCm39)	frame shift	probably null
RF041:Flywch1	UTSW	17	23,981,135 (GRCm39)	frame shift	probably null
RF046:Flywch1	UTSW	17	23,981,148 (GRCm39)	frame shift	probably null
RF046:Flywch1	UTSW	17	23,981,143 (GRCm39)	frame shift	probably null
RF049:Flywch1	UTSW	17	23,981,145 (GRCm39)	frame shift	probably null
RF058:Flywch1	UTSW	17	23,981,151 (GRCm39)	frame shift	probably null
X0009:Flywch1	UTSW	17	23,974,629 (GRCm39)	small deletion	probably benign
X0028:Flywch1	UTSW	17	23,980,069 (GRCm39)	missense	probably damaging	1.00
Z1176:Flywch1	UTSW	17	23,979,983 (GRCm39)	missense	probably benign	0.27

Predicted Primers

PCR Primer
(F):5'- AAGTTCTCCCTCTGCCGAAG -3'
(R):5'- GGTTTGAAGACAGGGCTATCTC -3'

Sequencing Primer
(F):5'- CCTGTGTGATAGCTCGG -3'
(R):5'- AGACAGGGCTATCTCACTGTG -3'

Posted On

2021-04-30