Mutagenetix > Incidental Mutation

Incidental Mutation 'R5373:Zufsp'

428878

Institutional Source

Beutler Lab

Gene Symbol

Zufsp

Ensembl Gene

ENSMUSG00000039531

Gene Name

zinc finger with UFM1-specific peptidase domain

Synonyms

2700019D07Rik

MMRRC Submission

042949-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.105) question?

Stock #

R5373 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

33919142-33951269 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 33927466 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Aspartic acid at position 541 (N541D)

Ref Sequence

ENSEMBL: ENSMUSP00000151811 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048222] [ENSMUST00000218055] [ENSMUST00000218275] [ENSMUST00000218880] [ENSMUST00000219457] [ENSMUST00000219878]

AlphaFold

Q3T9Z9

Predicted Effect

possibly damaging
Transcript: ENSMUST00000048222
AA Change: N541D

PolyPhen 2 Score 0.456 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000037121
Gene: ENSMUSG00000039531
AA Change: N541D

Domain	Start	End	E-Value	Type
ZnF_C2H2	2	24	5.42e-2	SMART
ZnF_C2H2	29	52	1.13e1	SMART
ZnF_C2H2	153	176	2.47e1	SMART
ZnF_C2H2	192	214	6.23e-2	SMART
coiled coil region	236	267	N/A	INTRINSIC
Pfam:Peptidase_C78	334	550	1.2e-76	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000218055
AA Change: N541D

PolyPhen 2 Score 0.456 (Sensitivity: 0.89; Specificity: 0.90)

Predicted Effect

probably benign
Transcript: ENSMUST00000218275

Predicted Effect

probably benign
Transcript: ENSMUST00000218880

Predicted Effect

probably benign
Transcript: ENSMUST00000219457

Predicted Effect

probably benign
Transcript: ENSMUST00000219878

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000219935

Meta Mutation Damage Score

0.1793

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.2%
20x: 95.2%

Validation Efficiency

96% (74/77)

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	A	G	3: 138,067,635	S862G	probably benign	Het
2410089E03Rik	T	C	15: 8,270,803	V3198A	unknown	Het
Abcb5	G	T	12: 118,887,177	T887K	probably damaging	Het
Adgrf1	G	A	17: 43,291,005		probably benign	Het
Adss	T	G	1: 177,796,388	I3L	probably benign	Het
Anapc7	T	A	5: 122,438,217	D302E	probably benign	Het
Ank3	A	G	10: 69,953,476		probably null	Het
Arpp21	T	G	9: 112,067,268	M687L	probably benign	Het
Camkv	T	C	9: 107,946,889	S221P	probably benign	Het
Ccdc88a	C	T	11: 29,463,409	T649M	possibly damaging	Het
Cdh12	A	C	15: 21,583,912	S613R	probably damaging	Het
Chsy1	C	T	7: 66,110,076	Q56*	probably null	Het
Cisd2	A	G	3: 135,408,835	V125A	probably benign	Het
Cntnap2	T	A	6: 47,107,969	H1121Q	probably benign	Het
Corin	A	T	5: 72,304,953	C876S	probably damaging	Het
Cspp1	T	G	1: 10,134,126	L1038R	probably damaging	Het
Cwc15	A	G	9: 14,504,938	K147E	possibly damaging	Het
Dlgap2	A	G	8: 14,823,614	D739G	probably benign	Het
Dmxl2	A	G	9: 54,369,189		probably benign	Het
Dnajc6	T	C	4: 101,615,627	I317T	probably damaging	Het
Dpysl3	T	C	18: 43,361,036	Y193C	probably damaging	Het
Dtna	T	C	18: 23,651,613	Y730H	probably damaging	Het
Dusp3	A	G	11: 101,984,625	Y38H	possibly damaging	Het
Eif3m	A	T	2: 105,012,932	I151N	probably damaging	Het
Eml2	A	T	7: 19,179,263	D62V	possibly damaging	Het
Epb41l3	C	A	17: 69,286,800	H810N	probably damaging	Het
Evc2	C	T	5: 37,378,210	R410W	probably damaging	Het
Fam169b	T	C	7: 68,300,838	Y13H	probably damaging	Het
Fcrl5	A	G	3: 87,446,391	T348A	probably benign	Het
Fezf2	A	T	14: 12,344,803	V128E	possibly damaging	Het
Ighv3-5	A	G	12: 114,262,953	S18P	probably damaging	Het
Kcnq5	T	A	1: 21,961,571	H4L	unknown	Het
Kdm5d	C	T	Y: 927,995	P756S	probably benign	Het
Lig1	AG	A	7: 13,305,923		probably null	Het
Ly75	A	T	2: 60,311,771	L1332M	possibly damaging	Het
Med1	T	A	11: 98,163,963	K378N	probably damaging	Het
Mn1	A	G	5: 111,421,886		probably null	Het
Mpo	T	C	11: 87,803,611		probably null	Het
Mtfr2	G	T	10: 20,352,852	C48F	probably benign	Het
Nt5c	G	A	11: 115,490,817		probably null	Het
Pcdhga4	T	C	18: 37,685,596	V66A	probably damaging	Het
Pik3c3	T	C	18: 30,312,561	S534P	probably benign	Het
Pla2g4e	A	T	2: 120,186,395	C222S	probably benign	Het
Plch1	A	C	3: 63,698,078	H1468Q	probably benign	Het
Psd2	T	A	18: 36,007,503	W610R	probably damaging	Het
Ptgs1	A	T	2: 36,251,186	K548N	probably damaging	Het
Ptpn14	T	C	1: 189,850,963	M669T	probably benign	Het
Ptprf	G	T	4: 118,226,041	T923K	possibly damaging	Het
Ptprg	A	G	14: 12,213,665	N1011S	probably benign	Het
Ptprz1	T	A	6: 23,007,355	V1639E	probably damaging	Het
Rgsl1	C	T	1: 153,790,307	V986I	probably benign	Het
Rufy4	T	C	1: 74,147,663	C537R	probably damaging	Het
Rxfp2	A	G	5: 150,070,260	T596A	probably benign	Het
Serpina3j	A	G	12: 104,314,727	D53G	probably damaging	Het
Slc26a7	A	T	4: 14,546,447	I294N	probably damaging	Het
Slirp	T	C	12: 87,449,422	S96P	possibly damaging	Het
Snx6	T	C	12: 54,770,728	E128G	probably damaging	Het
Spata6	T	A	4: 111,822,834		probably null	Het
Stap1	A	G	5: 86,090,928	T152A	possibly damaging	Het
Susd5	G	A	9: 114,082,585	G188R	probably damaging	Het
Thap2	A	T	10: 115,372,839	Y125*	probably null	Het
Tnrc18	G	A	5: 142,740,156	R1793C	unknown	Het
Ugt1a10	T	A	1: 88,055,910	D143E	probably damaging	Het
Vmn1r85	A	T	7: 13,084,328	Y296*	probably null	Het
Vmn2r71	C	T	7: 85,618,542	T68I	possibly damaging	Het
Zc3h6	A	T	2: 129,002,156	I207F	possibly damaging	Het
Zfp518a	T	C	19: 40,913,510	S628P	probably benign	Het
Zfp85	T	C	13: 67,749,458	Y165C	probably damaging	Het

Other mutations in Zufsp

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02510:Zufsp	APN	10	33930154	critical splice donor site	probably null
IGL02586:Zufsp	APN	10	33935265	intron	probably benign
IGL03350:Zufsp	APN	10	33928111	missense	probably benign	0.04
R0145:Zufsp	UTSW	10	33943713	missense	probably damaging	0.96
R1156:Zufsp	UTSW	10	33949226	missense	probably benign	0.15
R1523:Zufsp	UTSW	10	33927440	missense	probably damaging	1.00
R1769:Zufsp	UTSW	10	33935176	missense	probably damaging	1.00
R1802:Zufsp	UTSW	10	33943718	missense	probably damaging	0.98
R2013:Zufsp	UTSW	10	33929824	missense	possibly damaging	0.75
R2014:Zufsp	UTSW	10	33929824	missense	possibly damaging	0.75
R2015:Zufsp	UTSW	10	33929824	missense	possibly damaging	0.75
R2017:Zufsp	UTSW	10	33927464	missense	possibly damaging	0.46
R2342:Zufsp	UTSW	10	33928117	missense	probably damaging	1.00
R2901:Zufsp	UTSW	10	33927612	missense	probably damaging	1.00
R2901:Zufsp	UTSW	10	33928063	missense	probably benign
R3813:Zufsp	UTSW	10	33940222	missense	possibly damaging	0.63
R4488:Zufsp	UTSW	10	33948964	missense	probably damaging	1.00
R4674:Zufsp	UTSW	10	33948984	missense	possibly damaging	0.92
R4883:Zufsp	UTSW	10	33949042	missense	probably damaging	0.98
R4926:Zufsp	UTSW	10	33949438	missense	probably damaging	1.00
R5163:Zufsp	UTSW	10	33949443	missense	probably damaging	1.00
R5374:Zufsp	UTSW	10	33927466	missense	possibly damaging	0.46
R5924:Zufsp	UTSW	10	33927547	missense	probably damaging	0.96
R5929:Zufsp	UTSW	10	33949047	nonsense	probably null
R5941:Zufsp	UTSW	10	33949462	missense	probably damaging	1.00
R6337:Zufsp	UTSW	10	33949256	missense	probably benign	0.00
R6663:Zufsp	UTSW	10	33949435	missense	possibly damaging	0.86
R6753:Zufsp	UTSW	10	33928029	missense	probably damaging	1.00
R7690:Zufsp	UTSW	10	33930155	critical splice donor site	probably null
R7772:Zufsp	UTSW	10	33921702	splice site	probably null
R7836:Zufsp	UTSW	10	33919319	missense	unknown
R7919:Zufsp	UTSW	10	33949112	missense	possibly damaging	0.92
R8054:Zufsp	UTSW	10	33940252	missense	probably damaging	1.00
R8943:Zufsp	UTSW	10	33919305	makesense	probably null
R9433:Zufsp	UTSW	10	33919359	missense	probably damaging	1.00
X0063:Zufsp	UTSW	10	33943687	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGAGTTAAACAACTGAAAGGCC -3'
(R):5'- GAATGTATACGTGCATGCATGTGTG -3'

Sequencing Primer
(F):5'- GTTAAACAACTGAAAGGCCATCTAAC -3'
(R):5'- TGTGTATGGATGTGACATATTAACTG -3'

Posted On

2016-09-06