Mutagenetix > Incidental Mutation

Incidental Mutation 'R9135:Swt1'

693878

Institutional Source

Beutler Lab

Gene Symbol

Swt1

Ensembl Gene

ENSMUSG00000052748

Gene Name

SWT1 RNA endoribonuclease homolog (S. cerevisiae)

Synonyms

1200016B10Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.180) question?

Stock #

R9135 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

151243450-151304206 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 151244239 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Glycine at position 899 (C899G)

Ref Sequence

ENSEMBL: ENSMUSP00000067516 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023918] [ENSMUST00000064771] [ENSMUST00000097543] [ENSMUST00000111883]

AlphaFold

Q9DBQ9

Predicted Effect

probably benign
Transcript: ENSMUST00000023918

SMART Domains

Protein: ENSMUSP00000023918
Gene: ENSMUSG00000023150

Domain	Start	End	E-Value	Type
BTB	32	129	1.89e-25	SMART
BACK	134	233	3.39e-8	SMART
low complexity region	325	338	N/A	INTRINSIC
Kelch	369	415	4.78e-15	SMART
Kelch	416	463	2.16e-13	SMART
Kelch	464	512	2.15e-8	SMART
Kelch	513	559	1.58e-15	SMART
Kelch	560	606	1.61e-12	SMART
Kelch	607	641	1.85e-1	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000064771
AA Change: C899G

PolyPhen 2 Score 0.612 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000067516
Gene: ENSMUSG00000052748
AA Change: C899G

Domain	Start	End	E-Value	Type
low complexity region	186	206	N/A	INTRINSIC
low complexity region	231	242	N/A	INTRINSIC
low complexity region	258	269	N/A	INTRINSIC
PINc	395	522	1.94e-9	SMART
low complexity region	783	793	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000097543

SMART Domains

Protein: ENSMUSP00000095150
Gene: ENSMUSG00000023150

Domain	Start	End	E-Value	Type
BTB	32	129	1.89e-25	SMART
Pfam:BACK	134	189	3.3e-8	PFAM
low complexity region	283	296	N/A	INTRINSIC
Kelch	327	373	4.78e-15	SMART
Kelch	374	421	2.16e-13	SMART
Kelch	422	470	2.15e-8	SMART
Kelch	471	517	1.58e-15	SMART
Kelch	518	564	1.61e-12	SMART
Kelch	565	599	1.85e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000111883

SMART Domains

Protein: ENSMUSP00000107514
Gene: ENSMUSG00000052748

Domain	Start	End	E-Value	Type
low complexity region	186	206	N/A	INTRINSIC
low complexity region	231	242	N/A	INTRINSIC
low complexity region	258	269	N/A	INTRINSIC
PINc	395	522	1.94e-9	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 116 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb9	T	C	5: 124,228,176 (GRCm39)	T22A	possibly damaging	Het
Abi3bp	A	G	16: 56,417,173 (GRCm39)	D419G	probably benign	Het
Acoxl	A	T	2: 127,696,691 (GRCm39)		probably benign	Het
Acvr1	T	C	2: 58,352,983 (GRCm39)	T326A	possibly damaging	Het
Adgra2	T	C	8: 27,610,979 (GRCm39)	L976P	probably damaging	Het
Adora2b	A	G	11: 62,155,886 (GRCm39)		probably null	Het
Ak1	A	T	2: 32,521,182 (GRCm39)	Q117L	probably damaging	Het
Akr1c14	T	A	13: 4,128,029 (GRCm39)	D143E	probably damaging	Het
Ap4e1	A	T	2: 126,861,242 (GRCm39)	H127L	probably damaging	Het
Asxl3	T	A	18: 22,649,670 (GRCm39)	I553N	probably damaging	Het
Asxl3	T	A	18: 22,657,481 (GRCm39)	N1830K	possibly damaging	Het
Atp11a	G	A	8: 12,863,144 (GRCm39)	A108T	probably damaging	Het
Bag6	A	G	17: 35,362,437 (GRCm39)	T582A	unknown	Het
Bbs9	T	C	9: 22,490,005 (GRCm39)	S259P	probably damaging	Het
Bean1	CT	C	8: 104,908,664 (GRCm39)		probably null	Het
Bltp3a	T	A	17: 28,104,902 (GRCm39)	L532*	probably null	Het
Blvrb	T	C	7: 27,165,210 (GRCm39)	S177P	probably damaging	Het
C1s2	T	A	6: 124,602,642 (GRCm39)	D523V	probably benign	Het
Cacna2d1	C	T	5: 16,558,850 (GRCm39)	T736I	probably damaging	Het
Card9	T	C	2: 26,242,397 (GRCm39)	N513S	probably benign	Het
Casp2	A	G	6: 42,245,882 (GRCm39)	T180A	probably benign	Het
Cenpf	A	T	1: 189,404,746 (GRCm39)	L361Q	probably damaging	Het
Cnbd2	T	C	2: 156,217,488 (GRCm39)	I659T	probably damaging	Het
Cped1	A	T	6: 21,987,012 (GRCm39)	D68V	probably damaging	Het
Cxcr1	T	C	1: 74,231,099 (GRCm39)	I308V	probably benign	Het
Dad1	A	G	14: 54,491,163 (GRCm39)	L46P	probably damaging	Het
Defb23	G	A	2: 152,301,422 (GRCm39)	A50V	probably benign	Het
Dhx33	C	T	11: 70,877,992 (GRCm39)	A684T	probably damaging	Het
Dnai3	T	C	3: 145,772,589 (GRCm39)	T486A	probably benign	Het
Epb41l4a	T	A	18: 33,965,729 (GRCm39)	N366I	probably benign	Het
Erich3	A	G	3: 154,467,912 (GRCm39)	E788G		Het
Fam241b	T	C	10: 61,944,892 (GRCm39)	N35S	probably benign	Het
Fbxo24	T	A	5: 137,622,526 (GRCm39)	Q80L	probably benign	Het
Foxk1	T	G	5: 142,434,497 (GRCm39)	F254V	probably benign	Het
Gm10801	C	CGTG	2: 98,494,152 (GRCm39)		probably null	Het
Gm12886	T	C	4: 121,274,743 (GRCm39)	I46V	probably benign	Het
Gm20834	G	T	Y: 10,323,354 (GRCm39)	H27Q	probably damaging	Het
Gm2888	A	G	14: 3,032,106 (GRCm38)	N138S	probably damaging	Het
Gm5773	T	C	3: 93,681,179 (GRCm39)	C284R	possibly damaging	Het
Gprin3	A	T	6: 59,330,273 (GRCm39)	M678K	probably benign	Het
Grm7	T	C	6: 111,472,729 (GRCm39)	V856A	probably benign	Het
Il18rap	C	T	1: 40,582,177 (GRCm39)	T366M	probably benign	Het
Immt	C	T	6: 71,851,403 (GRCm39)	T588I	probably damaging	Het
Ints1	G	C	5: 139,737,701 (GRCm39)	N2145K	possibly damaging	Het
Jade2	T	C	11: 51,715,951 (GRCm39)	D418G	probably benign	Het
Kdf1	T	C	4: 133,256,140 (GRCm39)	Y286H	probably damaging	Het
Kif18a	A	G	2: 109,171,506 (GRCm39)	Y861C	possibly damaging	Het
Lama2	T	A	10: 27,298,515 (GRCm39)	I194F	probably damaging	Het
Lhx8	A	G	3: 154,034,063 (GRCm39)	S33P	probably benign	Het
Lmo7	T	C	14: 102,118,297 (GRCm39)	I174T	probably damaging	Het
Lrfn2	A	T	17: 49,376,976 (GRCm39)	D19V	possibly damaging	Het
Lrrk1	A	T	7: 65,928,357 (GRCm39)	I1257N	probably damaging	Het
Malrd1	T	A	2: 15,802,516 (GRCm39)	H1076Q	unknown	Het
Map3k14	A	C	11: 103,128,364 (GRCm39)	M419R	probably damaging	Het
Mcm10	G	A	2: 5,011,372 (GRCm39)	R200C	probably benign	Het
Mertk	A	G	2: 128,604,035 (GRCm39)	N390D	probably benign	Het
Mitf	T	A	6: 97,990,680 (GRCm39)	I361N	probably damaging	Het
Mrgprb1	T	A	7: 48,097,046 (GRCm39)	I289F	possibly damaging	Het
Muc5ac	A	T	7: 141,352,218 (GRCm39)	D659V	probably damaging	Het
Nox4	G	A	7: 87,025,448 (GRCm39)	R525Q	probably benign	Het
Nphp3	T	G	9: 103,909,214 (GRCm39)	L808R	probably damaging	Het
Or14c42-ps1	G	A	7: 86,211,156 (GRCm39)	C72Y	unknown	Het
Or1e1	T	C	11: 73,245,316 (GRCm39)	S246P	probably damaging	Het
Or5an1	T	A	19: 12,260,808 (GRCm39)	L132Q	probably damaging	Het
Or5b113	T	A	19: 13,342,755 (GRCm39)	S254R	possibly damaging	Het
Pagr1a	T	C	7: 126,615,954 (GRCm39)	E47G	probably benign	Het
Papss2	G	T	19: 32,618,764 (GRCm39)	R274L	probably damaging	Het
Pcdhga10	C	A	18: 37,880,960 (GRCm39)	F240L	probably damaging	Het
Pcsk5	T	G	19: 17,563,472 (GRCm39)	E555A		Het
Peg10	C	CTCA	6: 4,756,453 (GRCm39)		probably benign	Het
Pgrmc2	T	A	3: 41,023,099 (GRCm39)	D206V	probably damaging	Het
Pkd1	T	C	17: 24,790,976 (GRCm39)	V1057A		Het
Plekha5	T	C	6: 140,480,239 (GRCm39)	I113T	probably damaging	Het
Prorp	T	A	12: 55,426,189 (GRCm39)	L513Q	probably damaging	Het
Prss32	C	T	17: 24,078,199 (GRCm39)	T295I	possibly damaging	Het
Ptprk	G	T	10: 28,456,413 (GRCm39)	V1072F	probably damaging	Het
Rasd2	T	A	8: 75,945,174 (GRCm39)	M1K	probably null	Het
Rhag	T	A	17: 41,139,302 (GRCm39)	M79K	probably damaging	Het
Rnf19a	C	A	15: 36,253,310 (GRCm39)		probably null	Het
Rnf213	G	T	11: 119,299,573 (GRCm39)	G101C		Het
Sap130	T	A	18: 31,780,116 (GRCm39)	D45E	probably benign	Het
Scel	T	A	14: 103,839,626 (GRCm39)	F510I	probably benign	Het
Sertad2	A	T	11: 20,598,425 (GRCm39)	E207V	probably benign	Het
Shoc2	T	A	19: 53,976,310 (GRCm39)	S67T	probably benign	Het
Slc22a3	T	C	17: 12,645,619 (GRCm39)	I441V	possibly damaging	Het
Slfn5	A	G	11: 82,851,503 (GRCm39)	D600G	probably benign	Het
Smim7	G	A	8: 73,324,757 (GRCm39)	T10M	probably damaging	Het
Sntb2	A	T	8: 107,662,831 (GRCm39)	Q133L	possibly damaging	Het
Steap3	A	C	1: 120,162,048 (GRCm39)	M408R	probably benign	Het
Supt4a	T	C	11: 87,633,624 (GRCm39)	I60T	probably benign	Het
Taok3	A	G	5: 117,344,744 (GRCm39)	E157G	probably damaging	Het
Taok3	C	T	5: 117,379,245 (GRCm39)	L427F	possibly damaging	Het
Taok3	T	C	5: 117,379,168 (GRCm39)	V401A	probably benign	Het
Tcf25	A	G	8: 124,108,182 (GRCm39)	E79G	probably benign	Het
Tigit	G	A	16: 43,479,876 (GRCm39)	L140F	possibly damaging	Het
Tmem143	G	T	7: 45,546,802 (GRCm39)		probably benign	Het
Tmem151b	C	T	17: 45,856,355 (GRCm39)	V362M	possibly damaging	Het
Tmem230	A	G	2: 132,085,989 (GRCm39)	F58L	probably benign	Het
Trim25	T	C	11: 88,899,988 (GRCm39)	M245T	probably benign	Het
Trim36	A	C	18: 46,302,410 (GRCm39)	V546G	probably benign	Het
Triml1	T	C	8: 43,583,624 (GRCm39)	N326D	probably damaging	Het
Trp53bp2	T	C	1: 182,286,328 (GRCm39)	V1056A	probably damaging	Het
Trpa1	C	A	1: 14,952,435 (GRCm39)	M865I	probably damaging	Het
Ttbk1	A	T	17: 46,790,132 (GRCm39)	Y104*	probably null	Het
Tubg1	T	A	11: 101,014,257 (GRCm39)	H139Q	probably damaging	Het
Ufsp2	A	G	8: 46,447,050 (GRCm39)		probably null	Het
Usp47	A	T	7: 111,652,431 (GRCm39)	N36I	probably benign	Het
Vmn1r32	G	A	6: 66,530,120 (GRCm39)	R219*	probably null	Het
Vmn2r59	G	A	7: 41,693,125 (GRCm39)	P492S	probably benign	Het
Vmn2r59	G	C	7: 41,693,127 (GRCm39)	A491G		Het
Wdr76	T	C	2: 121,364,592 (GRCm39)	Y299H	probably damaging	Het
Wnt5a	C	T	14: 28,240,309 (GRCm39)	A153V	probably benign	Het
Zfp202	T	C	9: 40,120,237 (GRCm39)	V226A	possibly damaging	Het
Zfp219	C	T	14: 52,244,598 (GRCm39)	R527H	probably damaging	Het
Zfp408	A	T	2: 91,475,528 (GRCm39)	L542H	probably damaging	Het
Zfyve9	A	T	4: 108,539,386 (GRCm39)	C271*	probably null	Het

Other mutations in Swt1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01109:Swt1	APN	1	151,286,890 (GRCm39)	missense	probably damaging	0.99
IGL01622:Swt1	APN	1	151,286,760 (GRCm39)	missense	probably benign	0.01
IGL01623:Swt1	APN	1	151,286,760 (GRCm39)	missense	probably benign	0.01
IGL01672:Swt1	APN	1	151,270,359 (GRCm39)	critical splice donor site	probably null
IGL01693:Swt1	APN	1	151,297,855 (GRCm39)	missense	probably benign	0.02
IGL02203:Swt1	APN	1	151,246,377 (GRCm39)	missense	probably benign	0.01
IGL03223:Swt1	APN	1	151,255,170 (GRCm39)	missense	possibly damaging	0.80
R0124:Swt1	UTSW	1	151,267,280 (GRCm39)	missense	probably damaging	1.00
R0496:Swt1	UTSW	1	151,287,021 (GRCm39)	missense	probably benign
R1037:Swt1	UTSW	1	151,246,320 (GRCm39)	splice site	probably benign
R1171:Swt1	UTSW	1	151,281,272 (GRCm39)	missense	probably damaging	1.00
R1270:Swt1	UTSW	1	151,260,142 (GRCm39)	missense	probably benign	0.00
R1883:Swt1	UTSW	1	151,299,284 (GRCm39)	nonsense	probably null
R2051:Swt1	UTSW	1	151,248,081 (GRCm39)	missense	probably damaging	1.00
R2110:Swt1	UTSW	1	151,279,636 (GRCm39)	missense	probably damaging	0.97
R2185:Swt1	UTSW	1	151,260,219 (GRCm39)	missense	probably damaging	1.00
R3688:Swt1	UTSW	1	151,267,240 (GRCm39)	missense	probably damaging	0.99
R3785:Swt1	UTSW	1	151,255,155 (GRCm39)	missense	probably benign	0.03
R4074:Swt1	UTSW	1	151,270,520 (GRCm39)	missense	probably benign
R4157:Swt1	UTSW	1	151,278,795 (GRCm39)	missense	probably damaging	1.00
R4660:Swt1	UTSW	1	151,283,348 (GRCm39)	missense	probably benign	0.18
R4761:Swt1	UTSW	1	151,276,853 (GRCm39)	missense	probably benign	0.43
R4972:Swt1	UTSW	1	151,299,293 (GRCm39)	missense	probably benign	0.22
R5141:Swt1	UTSW	1	151,287,145 (GRCm39)	missense	probably benign	0.04
R5227:Swt1	UTSW	1	151,278,727 (GRCm39)	nonsense	probably null
R5400:Swt1	UTSW	1	151,288,585 (GRCm39)	missense	probably benign	0.00
R5580:Swt1	UTSW	1	151,260,206 (GRCm39)	missense	probably benign	0.00
R5912:Swt1	UTSW	1	151,287,160 (GRCm39)	missense	probably damaging	1.00
R5945:Swt1	UTSW	1	151,286,921 (GRCm39)	missense	probably benign	0.01
R5973:Swt1	UTSW	1	151,278,700 (GRCm39)	splice site	probably null
R5979:Swt1	UTSW	1	151,283,339 (GRCm39)	missense	possibly damaging	0.94
R6242:Swt1	UTSW	1	151,283,365 (GRCm39)	missense	probably benign	0.41
R6283:Swt1	UTSW	1	151,260,084 (GRCm39)	missense	possibly damaging	0.78
R6951:Swt1	UTSW	1	151,273,019 (GRCm39)	missense	possibly damaging	0.88
R7009:Swt1	UTSW	1	151,246,381 (GRCm39)	missense	possibly damaging	0.94
R7165:Swt1	UTSW	1	151,264,428 (GRCm39)	missense	probably damaging	1.00
R7214:Swt1	UTSW	1	151,270,364 (GRCm39)	missense	possibly damaging	0.63
R7403:Swt1	UTSW	1	151,264,444 (GRCm39)	missense	probably benign	0.01
R7439:Swt1	UTSW	1	151,286,815 (GRCm39)	missense	probably benign	0.04
R7441:Swt1	UTSW	1	151,286,815 (GRCm39)	missense	probably benign	0.04
R7571:Swt1	UTSW	1	151,270,470 (GRCm39)	missense	probably benign	0.00
R8028:Swt1	UTSW	1	151,260,248 (GRCm39)	missense	probably benign	0.26
R8225:Swt1	UTSW	1	151,297,859 (GRCm39)	missense	possibly damaging	0.96
R9075:Swt1	UTSW	1	151,246,245 (GRCm39)	intron	probably benign
R9100:Swt1	UTSW	1	151,299,256 (GRCm39)	critical splice donor site	probably null
R9291:Swt1	UTSW	1	151,286,694 (GRCm39)	missense	probably damaging	0.96
R9292:Swt1	UTSW	1	151,278,787 (GRCm39)	missense	probably benign	0.00
R9368:Swt1	UTSW	1	151,286,767 (GRCm39)	missense	possibly damaging	0.90
X0062:Swt1	UTSW	1	151,287,190 (GRCm39)	missense	probably benign	0.43
Z1176:Swt1	UTSW	1	151,264,436 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- CTACACTAGATTCAATGAGATTGGTC -3'
(R):5'- AACACACCTAGCTGTAGAACTG -3'

Sequencing Primer
(F):5'- GAGATTGGTCAATACAACATTTTGG -3'
(R):5'- TGTCTAGACTGGAACTCCCTACATAG -3'

Posted On

2022-01-20