Mutagenetix > Incidental Mutation

Incidental Mutation 'R9235:Sspo'

700417

Institutional Source

Beutler Lab

Gene Symbol

Sspo

Ensembl Gene

ENSMUSG00000029797

Gene Name

SCO-spondin

Synonyms

C79529, Scospondin

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9235 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

48425163-48478184 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 48466718 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 4078 (C4078S)

Ref Sequence

ENSEMBL: ENSMUSP00000131401 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000043676] [ENSMUST00000169350] [ENSMUST00000185370] [ENSMUST00000188970] [ENSMUST00000212740]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000043676
AA Change: C3935S

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000047991
Gene: ENSMUSG00000029797
AA Change: C3935S

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
low complexity region	126	135	N/A	INTRINSIC
Pfam:VWD	154	219	7.4e-11	PFAM
C8	267	346	2.3e-10	SMART
Pfam:TIL	349	404	3.2e-13	PFAM
VWC	406	448	2e-1	SMART
VWD	433	593	5.08e-29	SMART
C8	631	703	2.14e-28	SMART
Pfam:TIL	706	759	5.8e-11	PFAM
VWC	856	924	4.76e-2	SMART
VWD	883	1042	9.59e-48	SMART
C8	1076	1150	3.62e-26	SMART
Pfam:TIL	1153	1209	2.6e-13	PFAM
LDLa	1253	1291	2.29e-13	SMART
LDLa	1293	1328	1.87e-9	SMART
LDLa	1329	1366	5.77e-10	SMART
LDLa	1369	1408	1.52e-9	SMART
LDLa	1442	1479	2.55e-11	SMART
LDLa	1480	1520	5.6e-8	SMART
LDLa	1533	1574	2.29e-4	SMART
TSP1	1575	1626	6.47e-13	SMART
TSP1	1631	1686	1.35e-10	SMART
Pfam:TIL	1690	1746	3.1e-9	PFAM
TSP1	1774	1827	6.94e-2	SMART
VWC	1829	1886	4.95e-9	SMART
low complexity region	1901	1911	N/A	INTRINSIC
FA58C	1928	2085	1.4e-2	SMART
LDLa	2091	2128	1.48e-7	SMART
LDLa	2242	2279	5.68e-9	SMART
LDLa	2299	2336	5.77e-10	SMART
TSP1	2339	2389	1.42e-9	SMART
TSP1	2394	2446	6.36e-21	SMART
Pfam:TIL	2460	2511	5.7e-10	PFAM
VWC	2513	2567	2.48e-1	SMART
TSP1	2554	2605	3.07e-14	SMART
TSP1	2611	2664	4.05e-5	SMART
TSP1	2669	2719	1.83e-12	SMART
EGF_like	2733	2776	5.45e1	SMART
VWC	2783	2836	2.73e-11	SMART
TSP1	2823	2875	3.72e-13	SMART
TSP1	2878	2919	6.05e-4	SMART
Pfam:TIL	2926	2978	1.1e-11	PFAM
VWC	2980	3035	9.77e-2	SMART
TSP1	3022	3086	6.68e-6	SMART
TSP1	3091	3143	1.08e-14	SMART
Pfam:TIL	3147	3201	2.2e-9	PFAM
VWC	3203	3260	2.72e-1	SMART
TSP1	3247	3306	3.72e-4	SMART
TSP1	3311	3363	5.27e-4	SMART
Pfam:TIL	3365	3421	4.2e-9	PFAM
TSP1	3484	3529	1.87e-9	SMART
low complexity region	3591	3601	N/A	INTRINSIC
TSP1	3660	3713	5.02e-10	SMART
TSP1	3730	3779	2.95e-7	SMART
TSP1	3796	3849	1.99e-13	SMART
TSP1	3854	3906	2.51e-10	SMART
Pfam:TIL	3909	3964	3.4e-11	PFAM
VWC	3966	4022	1.26e0	SMART
TSP1	4009	4059	4.05e-5	SMART
TSP1	4103	4155	3.19e-12	SMART
TSP1	4161	4213	2.87e-2	SMART
TSP1	4218	4269	1.45e-6	SMART
Pfam:TIL	4273	4328	2.1e-10	PFAM
TSP1	4468	4516	7.56e-5	SMART
low complexity region	4551	4562	N/A	INTRINSIC
VWC	4578	4652	5.21e-1	SMART
TSP1	4619	4669	3.92e-12	SMART
Pfam:TIL	4671	4725	1.5e-11	PFAM
Pfam:TIL	4777	4835	3.1e-9	PFAM
VWC	4837	4892	1.8e-11	SMART
GHB	4904	4997	1.02e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000169350
AA Change: C4078S

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000131401
Gene: ENSMUSG00000029797
AA Change: C4078S

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
low complexity region	126	135	N/A	INTRINSIC
VWD	185	341	4.36e-28	SMART
C8	390	469	2.3e-10	SMART
Pfam:TIL	472	527	8.6e-13	PFAM
VWC	529	571	2e-1	SMART
VWD	556	716	5.08e-29	SMART
C8	754	826	2.14e-28	SMART
Pfam:TIL	829	882	1.6e-10	PFAM
VWC	979	1047	4.76e-2	SMART
VWD	1006	1165	9.59e-48	SMART
C8	1201	1275	3.62e-26	SMART
Pfam:TIL	1278	1334	7e-13	PFAM
LDLa	1378	1416	2.29e-13	SMART
LDLa	1418	1453	1.87e-9	SMART
LDLa	1454	1491	5.77e-10	SMART
LDLa	1494	1533	1.52e-9	SMART
LDLa	1567	1604	2.55e-11	SMART
LDLa	1605	1645	5.6e-8	SMART
LDLa	1658	1699	2.29e-4	SMART
TSP1	1700	1751	6.47e-13	SMART
TSP1	1756	1811	1.35e-10	SMART
Pfam:TIL	1815	1871	8.3e-9	PFAM
VWC	1873	1928	2.42e-1	SMART
TSP1	1915	1968	6.94e-2	SMART
VWC	1970	2027	4.95e-9	SMART
low complexity region	2042	2052	N/A	INTRINSIC
FA58C	2069	2226	1.4e-2	SMART
LDLa	2232	2269	1.48e-7	SMART
LDLa	2387	2424	5.68e-9	SMART
LDLa	2444	2481	5.77e-10	SMART
TSP1	2484	2534	1.42e-9	SMART
TSP1	2539	2591	6.36e-21	SMART
Pfam:TIL	2606	2656	1.8e-9	PFAM
VWC	2658	2712	2.48e-1	SMART
TSP1	2699	2750	3.07e-14	SMART
TSP1	2756	2809	4.05e-5	SMART
TSP1	2814	2864	1.83e-12	SMART
EGF_like	2878	2921	5.45e1	SMART
VWC	2928	2981	2.73e-11	SMART
TSP1	2968	3020	3.72e-13	SMART
TSP1	3023	3064	6.05e-4	SMART
Pfam:TIL	3071	3123	3e-11	PFAM
VWC	3125	3180	9.77e-2	SMART
TSP1	3167	3231	6.68e-6	SMART
TSP1	3236	3288	1.08e-14	SMART
Pfam:TIL	3292	3346	6e-9	PFAM
VWC	3348	3405	2.72e-1	SMART
TSP1	3392	3451	3.72e-4	SMART
TSP1	3456	3508	5.27e-4	SMART
Pfam:TIL	3510	3566	1.1e-8	PFAM
TSP1	3629	3674	1.87e-9	SMART
low complexity region	3734	3744	N/A	INTRINSIC
TSP1	3803	3856	5.02e-10	SMART
TSP1	3873	3922	2.95e-7	SMART
TSP1	3939	3992	1.99e-13	SMART
TSP1	3997	4049	2.51e-10	SMART
Pfam:TIL	4052	4107	9.1e-11	PFAM
VWC	4109	4165	1.26e0	SMART
TSP1	4152	4202	4.05e-5	SMART
TSP1	4246	4298	3.19e-12	SMART
TSP1	4304	4356	2.87e-2	SMART
TSP1	4361	4412	1.45e-6	SMART
Pfam:TIL	4416	4471	5.6e-10	PFAM
TSP1	4611	4659	7.56e-5	SMART
low complexity region	4694	4705	N/A	INTRINSIC
VWC	4721	4795	5.21e-1	SMART
TSP1	4762	4812	3.92e-12	SMART
Pfam:TIL	4814	4868	4e-11	PFAM
Pfam:TIL	4920	4978	8.4e-9	PFAM
VWC	4980	5035	1.8e-11	SMART
GHB	5050	5143	1.02e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000185370
AA Change: C109S

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000139484
Gene: ENSMUSG00000029797
AA Change: C109S

Domain	Start	End	E-Value	Type
TSP1	28	80	1.2e-12	SMART
Pfam:TIL	83	138	3.8e-9	PFAM
VWC	140	196	6e-3	SMART
TSP1	183	233	1.9e-7	SMART
TSP1	277	329	1.5e-14	SMART
TSP1	335	387	1.4e-4	SMART
TSP1	392	443	6.8e-9	SMART
Pfam:TIL	447	502	2e-8	PFAM
Blast:TSP1	549	637	2e-11	BLAST
TSP1	642	690	3.7e-7	SMART
Pfam:TIL	694	750	1.3e-7	PFAM
VWC_def	752	826	2.5e-3	SMART
TSP1	793	843	1.9e-14	SMART
Pfam:TIL	845	899	2.5e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000188970

SMART Domains

Protein: ENSMUSP00000140642
Gene: ENSMUSG00000029797

Domain	Start	End	E-Value	Type
Pfam:TSP_1	1	40	9.4e-5	PFAM
TSP1	105	155	1.9e-14	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000212740
AA Change: C4069S

PolyPhen 2 Score 0.949 (Sensitivity: 0.79; Specificity: 0.95)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.2%

Validation Efficiency

100% (59/59)

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921524L21Rik	T	A	18: 6,623,518 (GRCm39)	I76N	possibly damaging	Het
4930558K02Rik	T	C	1: 161,780,172 (GRCm39)	H114R	possibly damaging	Het
C2	T	C	17: 35,083,845 (GRCm39)	D414G	probably damaging	Het
Catsper4	C	T	4: 133,954,606 (GRCm39)	D15N	probably benign	Het
Ccnb2	A	G	9: 70,318,163 (GRCm39)	V203A	probably damaging	Het
Cd2	A	G	3: 101,195,159 (GRCm39)	F13L	probably benign	Het
Cwf19l1	G	A	19: 44,113,275 (GRCm39)	A227V	probably damaging	Het
Dis3l2	G	A	1: 86,749,061 (GRCm39)	D176N	possibly damaging	Het
Dmpk	T	G	7: 18,822,141 (GRCm39)	N366K	probably damaging	Het
Dnajb12	C	T	10: 59,728,799 (GRCm39)	T229I	probably benign	Het
Efcab3	A	G	11: 104,907,987 (GRCm39)	D4479G	probably benign	Het
Fat3	T	A	9: 15,833,674 (GRCm39)	E126V	probably null	Het
Fbxo27	T	A	7: 28,397,756 (GRCm39)	Y264*	probably null	Het
Fign	A	G	2: 63,810,907 (GRCm39)	M121T	probably damaging	Het
Flt3	T	C	5: 147,320,202 (GRCm39)	Y54C	possibly damaging	Het
Frmd4a	G	A	2: 4,599,366 (GRCm39)	R460H	probably damaging	Het
Igkv4-53	A	T	6: 69,626,301 (GRCm39)	I13N	possibly damaging	Het
Islr	T	A	9: 58,064,944 (GRCm39)	I188F	possibly damaging	Het
Klk15	C	T	7: 43,587,790 (GRCm39)	H73Y	possibly damaging	Het
Klra3	A	T	6: 130,311,218 (GRCm39)	C54*	probably null	Het
Klrb1b	A	G	6: 128,795,547 (GRCm39)	F140S	probably damaging	Het
Kmt2c	T	C	5: 25,504,997 (GRCm39)	E3437G	probably damaging	Het
Mdn1	C	A	4: 32,739,122 (GRCm39)	L3648I	probably benign	Het
Mlxipl	C	A	5: 135,157,541 (GRCm39)	T359K	possibly damaging	Het
Morc3	T	C	16: 93,659,321 (GRCm39)	W410R	probably damaging	Het
Mrpl49	G	A	19: 6,105,147 (GRCm39)	R105*	probably null	Het
Myom3	T	A	4: 135,541,653 (GRCm39)	Y1415N	probably damaging	Het
Nlgn3	T	C	X: 100,352,390 (GRCm39)	V179A	probably damaging	Het
Nrap	A	T	19: 56,330,760 (GRCm39)	Y1100*	probably null	Het
Or14a257	A	T	7: 86,138,306 (GRCm39)	V151E	probably benign	Het
Or5d43	A	T	2: 88,104,724 (GRCm39)	I223N	probably damaging	Het
Or5t5	T	C	2: 86,616,548 (GRCm39)	I158T	probably benign	Het
Or6c8b	G	T	10: 128,882,051 (GRCm39)	Q294K	probably benign	Het
Pank1	C	A	19: 34,856,197 (GRCm39)	A94S	probably benign	Het
Pikfyve	C	A	1: 65,299,188 (GRCm39)	T1613K	probably benign	Het
Plbd2	T	A	5: 120,626,554 (GRCm39)	I352L	probably benign	Het
Plec	T	C	15: 76,059,701 (GRCm39)	D3412G	probably damaging	Het
Plekhd1	T	A	12: 80,768,791 (GRCm39)	Y425N	possibly damaging	Het
Plscr5	A	G	9: 92,086,417 (GRCm39)	N129S	possibly damaging	Het
Prkdc	T	A	16: 15,651,751 (GRCm39)	M3796K	probably damaging	Het
Psme3	A	T	11: 101,211,594 (GRCm39)	E213D	possibly damaging	Het
Ptprn2	G	A	12: 117,233,271 (GRCm39)		probably null	Het
Sema5a	A	G	15: 32,619,034 (GRCm39)	S521G	probably benign	Het
Slc34a2	A	T	5: 53,226,667 (GRCm39)	M597L	probably benign	Het
Slc6a13	A	G	6: 121,301,984 (GRCm39)	R189G	probably damaging	Het
Smyd4	G	A	11: 75,295,689 (GRCm39)	E782K	probably benign	Het
Tmco1	C	T	1: 167,136,132 (GRCm39)		probably benign	Het
Trim28	G	A	7: 12,763,490 (GRCm39)	A544T	probably benign	Het
Ttc21a	G	T	9: 119,774,559 (GRCm39)	R271L	probably benign	Het
Ubr5	A	G	15: 38,045,982 (GRCm39)	L114P		Het
Ugt1a2	A	G	1: 88,128,488 (GRCm39)	R44G	possibly damaging	Het
Ulk4	G	A	9: 120,981,217 (GRCm39)	T907I	probably benign	Het
Unc13a	G	T	8: 72,115,912 (GRCm39)	L97I	probably benign	Het
Uqcc6	A	T	10: 82,458,586 (GRCm39)	C22S	possibly damaging	Het
Vmn1r25	A	G	6: 57,955,488 (GRCm39)	L267P	probably damaging	Het
Vmn2r101	T	A	17: 19,810,238 (GRCm39)	N341K	probably damaging	Het
Wdr3	T	A	3: 100,054,023 (GRCm39)	Q534L	probably benign	Het
Zfp28	A	T	7: 6,397,605 (GRCm39)	H680L	probably damaging	Het
Zfp986	T	A	4: 145,625,759 (GRCm39)	F140I	probably benign	Het

Other mutations in Sspo

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00333:Sspo	APN	6	48,447,387 (GRCm39)	missense	probably benign	0.02
IGL00339:Sspo	APN	6	48,460,680 (GRCm39)	splice site	probably benign
IGL00391:Sspo	APN	6	48,474,320 (GRCm39)	missense	probably damaging	0.96
IGL00433:Sspo	APN	6	48,466,970 (GRCm39)	missense	probably damaging	1.00
IGL00471:Sspo	APN	6	48,475,147 (GRCm39)	splice site	probably benign
IGL00500:Sspo	APN	6	48,474,355 (GRCm39)	nonsense	probably null
IGL00537:Sspo	APN	6	48,475,147 (GRCm39)	splice site	probably benign
IGL00540:Sspo	APN	6	48,475,147 (GRCm39)	splice site	probably benign
IGL01060:Sspo	APN	6	48,426,413 (GRCm39)	nonsense	probably null
IGL01090:Sspo	APN	6	48,467,059 (GRCm39)	missense	probably benign	0.08
IGL01125:Sspo	APN	6	48,469,822 (GRCm39)	missense	probably damaging	1.00
IGL01447:Sspo	APN	6	48,441,600 (GRCm39)	splice site	probably null
IGL01457:Sspo	APN	6	48,475,277 (GRCm39)	missense	probably benign	0.00
IGL01481:Sspo	APN	6	48,425,449 (GRCm39)	missense	probably benign	0.41
IGL01485:Sspo	APN	6	48,455,665 (GRCm39)	missense	probably damaging	1.00
IGL01544:Sspo	APN	6	48,467,953 (GRCm39)	missense	probably damaging	0.99
IGL01575:Sspo	APN	6	48,435,976 (GRCm39)	missense	probably benign	0.01
IGL01589:Sspo	APN	6	48,428,112 (GRCm39)	missense	probably damaging	1.00
IGL01601:Sspo	APN	6	48,463,313 (GRCm39)	missense	probably benign	0.33
IGL01644:Sspo	APN	6	48,429,436 (GRCm39)	missense	probably benign
IGL01659:Sspo	APN	6	48,451,377 (GRCm39)	missense	probably damaging	1.00
IGL01801:Sspo	APN	6	48,434,072 (GRCm39)	missense	probably damaging	1.00
IGL01872:Sspo	APN	6	48,431,623 (GRCm39)	missense	probably damaging	0.99
IGL01874:Sspo	APN	6	48,429,124 (GRCm39)	missense	probably damaging	1.00
IGL01936:Sspo	APN	6	48,452,821 (GRCm39)	missense	probably damaging	1.00
IGL01941:Sspo	APN	6	48,472,116 (GRCm39)	missense	probably benign	0.19
IGL01986:Sspo	APN	6	48,460,237 (GRCm39)	missense	probably benign	0.05
IGL01987:Sspo	APN	6	48,454,558 (GRCm39)	splice site	probably null
IGL02170:Sspo	APN	6	48,444,917 (GRCm39)	missense	possibly damaging	0.76
IGL02192:Sspo	APN	6	48,436,502 (GRCm39)	missense	possibly damaging	0.86
IGL02210:Sspo	APN	6	48,477,426 (GRCm39)	missense	probably damaging	1.00
IGL02225:Sspo	APN	6	48,461,268 (GRCm39)	missense	probably benign	0.09
IGL02280:Sspo	APN	6	48,473,165 (GRCm39)	missense	probably damaging	1.00
IGL02303:Sspo	APN	6	48,461,639 (GRCm39)	missense	possibly damaging	0.52
IGL02397:Sspo	APN	6	48,438,572 (GRCm39)	missense	probably benign	0.35
IGL02451:Sspo	APN	6	48,437,237 (GRCm39)	splice site	probably benign
IGL02500:Sspo	APN	6	48,455,313 (GRCm39)	nonsense	probably null
IGL02519:Sspo	APN	6	48,461,762 (GRCm39)	missense	probably damaging	1.00
IGL02549:Sspo	APN	6	48,428,707 (GRCm39)	missense	possibly damaging	0.81
IGL02562:Sspo	APN	6	48,467,056 (GRCm39)	splice site	probably null
IGL02673:Sspo	APN	6	48,475,709 (GRCm39)	critical splice donor site	probably null
IGL02673:Sspo	APN	6	48,452,794 (GRCm39)	missense	probably damaging	1.00
IGL02719:Sspo	APN	6	48,459,601 (GRCm39)	missense	probably benign	0.39
IGL02793:Sspo	APN	6	48,464,828 (GRCm39)	splice site	probably benign
IGL03003:Sspo	APN	6	48,432,021 (GRCm39)	missense	probably damaging	0.98
IGL03056:Sspo	APN	6	48,447,472 (GRCm39)	missense	probably benign	0.17
IGL03105:Sspo	APN	6	48,450,592 (GRCm39)	splice site	probably benign
IGL03116:Sspo	APN	6	48,471,035 (GRCm39)	missense	probably benign	0.32
IGL03163:Sspo	APN	6	48,461,266 (GRCm39)	missense	probably benign	0.19
IGL03198:Sspo	APN	6	48,454,516 (GRCm39)	missense	probably benign	0.31
IGL03365:Sspo	APN	6	48,436,349 (GRCm39)	missense	possibly damaging	0.82
Barrier	UTSW	6	48,472,146 (GRCm39)	missense	possibly damaging	0.58
R0312_sspo_280	UTSW	6	48,432,335 (GRCm39)	missense	possibly damaging	0.52
R3112_Sspo_731	UTSW	6	48,434,534 (GRCm39)	missense	probably damaging	1.00
R3498_Sspo_650	UTSW	6	48,444,914 (GRCm39)	missense	possibly damaging	0.58
R4180_Sspo_324	UTSW	6	48,475,329 (GRCm39)	critical splice donor site	probably null
spotsylvania	UTSW	6	48,453,505 (GRCm39)	nonsense	probably null
ANU74:Sspo	UTSW	6	48,437,893 (GRCm39)	missense	probably damaging	1.00
IGL02984:Sspo	UTSW	6	48,472,089 (GRCm39)	missense	probably benign	0.33
IGL03052:Sspo	UTSW	6	48,437,387 (GRCm39)	missense	probably damaging	1.00
IGL03134:Sspo	UTSW	6	48,427,999 (GRCm39)	missense	probably benign	0.28
PIT4531001:Sspo	UTSW	6	48,458,173 (GRCm39)	missense	probably benign
R0087:Sspo	UTSW	6	48,454,719 (GRCm39)	missense	probably damaging	1.00
R0122:Sspo	UTSW	6	48,450,910 (GRCm39)	missense	possibly damaging	0.95
R0129:Sspo	UTSW	6	48,432,352 (GRCm39)	missense	probably benign	0.00
R0164:Sspo	UTSW	6	48,471,128 (GRCm39)	splice site	probably benign
R0195:Sspo	UTSW	6	48,463,570 (GRCm39)	missense	probably benign
R0200:Sspo	UTSW	6	48,463,349 (GRCm39)	missense	probably null	0.01
R0201:Sspo	UTSW	6	48,432,686 (GRCm39)	missense	possibly damaging	0.64
R0241:Sspo	UTSW	6	48,438,429 (GRCm39)	missense	possibly damaging	0.82
R0241:Sspo	UTSW	6	48,438,429 (GRCm39)	missense	possibly damaging	0.82
R0243:Sspo	UTSW	6	48,470,120 (GRCm39)	missense	probably damaging	1.00
R0268:Sspo	UTSW	6	48,442,489 (GRCm39)	missense	probably benign	0.26
R0312:Sspo	UTSW	6	48,432,335 (GRCm39)	missense	possibly damaging	0.52
R0449:Sspo	UTSW	6	48,443,674 (GRCm39)	missense	probably damaging	1.00
R0523:Sspo	UTSW	6	48,428,794 (GRCm39)	missense	probably benign	0.20
R0576:Sspo	UTSW	6	48,441,876 (GRCm39)	splice site	probably null
R0671:Sspo	UTSW	6	48,467,325 (GRCm39)	splice site	probably benign
R0828:Sspo	UTSW	6	48,475,668 (GRCm39)	missense	probably damaging	1.00
R0880:Sspo	UTSW	6	48,452,869 (GRCm39)	missense	possibly damaging	0.69
R0903:Sspo	UTSW	6	48,432,242 (GRCm39)	critical splice acceptor site	probably null
R1051:Sspo	UTSW	6	48,468,389 (GRCm39)	nonsense	probably null
R1083:Sspo	UTSW	6	48,447,933 (GRCm39)	missense	possibly damaging	0.91
R1109:Sspo	UTSW	6	48,474,377 (GRCm39)	missense	probably damaging	1.00
R1118:Sspo	UTSW	6	48,436,352 (GRCm39)	missense	probably damaging	0.97
R1256:Sspo	UTSW	6	48,434,573 (GRCm39)	missense	probably damaging	1.00
R1342:Sspo	UTSW	6	48,438,569 (GRCm39)	missense	probably benign	0.07
R1355:Sspo	UTSW	6	48,425,560 (GRCm39)	missense	probably benign	0.41
R1370:Sspo	UTSW	6	48,425,560 (GRCm39)	missense	probably benign	0.41
R1469:Sspo	UTSW	6	48,467,916 (GRCm39)	missense	probably damaging	1.00
R1469:Sspo	UTSW	6	48,467,916 (GRCm39)	missense	probably damaging	1.00
R1476:Sspo	UTSW	6	48,440,334 (GRCm39)	critical splice donor site	probably null
R1566:Sspo	UTSW	6	48,443,804 (GRCm39)	critical splice donor site	probably null
R1630:Sspo	UTSW	6	48,434,658 (GRCm39)	missense	probably benign	0.01
R1686:Sspo	UTSW	6	48,437,334 (GRCm39)	missense	probably benign	0.00
R1707:Sspo	UTSW	6	48,454,811 (GRCm39)	missense	probably damaging	0.99
R1727:Sspo	UTSW	6	48,471,782 (GRCm39)	missense	probably damaging	1.00
R1822:Sspo	UTSW	6	48,469,820 (GRCm39)	missense	possibly damaging	0.75
R1831:Sspo	UTSW	6	48,466,720 (GRCm39)	missense	probably damaging	1.00
R1835:Sspo	UTSW	6	48,434,274 (GRCm39)	missense	probably damaging	0.97
R1862:Sspo	UTSW	6	48,467,940 (GRCm39)	missense	probably damaging	0.98
R1878:Sspo	UTSW	6	48,436,300 (GRCm39)	missense	possibly damaging	0.92
R1900:Sspo	UTSW	6	48,436,284 (GRCm39)	missense	probably benign	0.22
R1945:Sspo	UTSW	6	48,466,707 (GRCm39)	missense	possibly damaging	0.93
R1957:Sspo	UTSW	6	48,455,207 (GRCm39)	missense	probably damaging	0.99
R1990:Sspo	UTSW	6	48,427,984 (GRCm39)	missense	probably benign	0.00
R1996:Sspo	UTSW	6	48,452,424 (GRCm39)	missense	possibly damaging	0.50
R2049:Sspo	UTSW	6	48,440,465 (GRCm39)	missense	probably benign	0.36
R2049:Sspo	UTSW	6	48,437,697 (GRCm39)	splice site	probably benign
R2064:Sspo	UTSW	6	48,450,596 (GRCm39)	missense	probably damaging	0.99
R2072:Sspo	UTSW	6	48,450,451 (GRCm39)	missense	probably benign	0.01
R2096:Sspo	UTSW	6	48,438,608 (GRCm39)	missense	probably benign
R2106:Sspo	UTSW	6	48,443,250 (GRCm39)	missense	possibly damaging	0.96
R2230:Sspo	UTSW	6	48,477,437 (GRCm39)	missense	probably benign	0.11
R2230:Sspo	UTSW	6	48,425,606 (GRCm39)	missense	probably damaging	0.97
R2232:Sspo	UTSW	6	48,425,606 (GRCm39)	missense	probably damaging	0.97
R2351:Sspo	UTSW	6	48,441,803 (GRCm39)	missense	probably damaging	1.00
R2423:Sspo	UTSW	6	48,430,989 (GRCm39)	missense	probably benign	0.00
R2508:Sspo	UTSW	6	48,441,298 (GRCm39)	missense	probably damaging	1.00
R3110:Sspo	UTSW	6	48,434,534 (GRCm39)	missense	probably damaging	1.00
R3112:Sspo	UTSW	6	48,434,534 (GRCm39)	missense	probably damaging	1.00
R3413:Sspo	UTSW	6	48,457,631 (GRCm39)	missense	probably damaging	1.00
R3433:Sspo	UTSW	6	48,452,885 (GRCm39)	splice site	probably null
R3498:Sspo	UTSW	6	48,444,914 (GRCm39)	missense	possibly damaging	0.58
R3732:Sspo	UTSW	6	48,426,864 (GRCm39)	missense	probably damaging	1.00
R3816:Sspo	UTSW	6	48,458,037 (GRCm39)	missense	possibly damaging	0.77
R3818:Sspo	UTSW	6	48,458,037 (GRCm39)	missense	possibly damaging	0.77
R3819:Sspo	UTSW	6	48,458,037 (GRCm39)	missense	possibly damaging	0.77
R3838:Sspo	UTSW	6	48,457,754 (GRCm39)	missense	probably damaging	1.00
R3850:Sspo	UTSW	6	48,469,424 (GRCm39)	missense	probably damaging	1.00
R3880:Sspo	UTSW	6	48,471,874 (GRCm39)	missense	probably benign	0.38
R3893:Sspo	UTSW	6	48,453,505 (GRCm39)	nonsense	probably null
R4116:Sspo	UTSW	6	48,433,928 (GRCm39)	missense	probably damaging	0.99
R4179:Sspo	UTSW	6	48,475,329 (GRCm39)	critical splice donor site	probably null
R4180:Sspo	UTSW	6	48,475,329 (GRCm39)	critical splice donor site	probably null
R4207:Sspo	UTSW	6	48,455,227 (GRCm39)	missense	probably benign	0.00
R4210:Sspo	UTSW	6	48,441,835 (GRCm39)	missense	probably benign	0.00
R4223:Sspo	UTSW	6	48,428,091 (GRCm39)	missense	possibly damaging	0.54
R4224:Sspo	UTSW	6	48,428,091 (GRCm39)	missense	possibly damaging	0.54
R4225:Sspo	UTSW	6	48,428,091 (GRCm39)	missense	possibly damaging	0.54
R4229:Sspo	UTSW	6	48,467,868 (GRCm39)	missense	probably benign	0.00
R4230:Sspo	UTSW	6	48,467,868 (GRCm39)	missense	probably benign	0.00
R4363:Sspo	UTSW	6	48,475,665 (GRCm39)	missense	probably damaging	1.00
R4370:Sspo	UTSW	6	48,443,282 (GRCm39)	missense	probably null	0.14
R4407:Sspo	UTSW	6	48,437,454 (GRCm39)	missense	probably damaging	1.00
R4438:Sspo	UTSW	6	48,464,287 (GRCm39)	missense	probably damaging	1.00
R4454:Sspo	UTSW	6	48,464,159 (GRCm39)	missense	probably benign	0.05
R4455:Sspo	UTSW	6	48,442,450 (GRCm39)	missense	probably damaging	1.00
R4561:Sspo	UTSW	6	48,452,468 (GRCm39)	splice site	probably null
R4574:Sspo	UTSW	6	48,442,457 (GRCm39)	missense	probably damaging	1.00
R4578:Sspo	UTSW	6	48,440,307 (GRCm39)	missense	possibly damaging	0.58
R4653:Sspo	UTSW	6	48,455,580 (GRCm39)	missense	probably damaging	1.00
R4656:Sspo	UTSW	6	48,431,010 (GRCm39)	missense	possibly damaging	0.65
R4659:Sspo	UTSW	6	48,461,147 (GRCm39)	missense	probably damaging	1.00
R4664:Sspo	UTSW	6	48,450,468 (GRCm39)	missense	possibly damaging	0.82
R4685:Sspo	UTSW	6	48,469,828 (GRCm39)	missense	probably damaging	0.98
R4692:Sspo	UTSW	6	48,459,621 (GRCm39)	missense	probably damaging	1.00
R4703:Sspo	UTSW	6	48,477,387 (GRCm39)	missense	probably damaging	1.00
R4704:Sspo	UTSW	6	48,475,638 (GRCm39)	missense	probably damaging	1.00
R4738:Sspo	UTSW	6	48,455,330 (GRCm39)	missense	possibly damaging	0.78
R4766:Sspo	UTSW	6	48,447,514 (GRCm39)	missense	probably benign	0.04
R4771:Sspo	UTSW	6	48,437,813 (GRCm39)	missense	probably damaging	1.00
R4790:Sspo	UTSW	6	48,437,705 (GRCm39)	missense	probably benign	0.04
R4792:Sspo	UTSW	6	48,438,519 (GRCm39)	missense	probably benign	0.00
R4808:Sspo	UTSW	6	48,428,095 (GRCm39)	missense	probably damaging	1.00
R4812:Sspo	UTSW	6	48,467,444 (GRCm39)	missense	probably benign	0.00
R4883:Sspo	UTSW	6	48,437,756 (GRCm39)	missense	probably benign	0.00
R4906:Sspo	UTSW	6	48,442,664 (GRCm39)	critical splice acceptor site	probably null
R4934:Sspo	UTSW	6	48,442,486 (GRCm39)	missense	probably damaging	1.00
R4945:Sspo	UTSW	6	48,444,021 (GRCm39)	splice site	probably null
R4967:Sspo	UTSW	6	48,441,539 (GRCm39)	missense	probably damaging	0.97
R5016:Sspo	UTSW	6	48,429,214 (GRCm39)	nonsense	probably null
R5018:Sspo	UTSW	6	48,432,634 (GRCm39)	missense	probably damaging	1.00
R5034:Sspo	UTSW	6	48,457,757 (GRCm39)	missense	possibly damaging	0.93
R5044:Sspo	UTSW	6	48,443,889 (GRCm39)	critical splice acceptor site	probably null
R5055:Sspo	UTSW	6	48,441,729 (GRCm39)	missense	probably damaging	1.00
R5087:Sspo	UTSW	6	48,465,405 (GRCm39)	missense	possibly damaging	0.51
R5155:Sspo	UTSW	6	48,437,408 (GRCm39)	missense	probably benign	0.03
R5223:Sspo	UTSW	6	48,455,258 (GRCm39)	missense	probably damaging	1.00
R5249:Sspo	UTSW	6	48,470,244 (GRCm39)	missense	probably damaging	0.98
R5257:Sspo	UTSW	6	48,453,428 (GRCm39)	missense	probably damaging	1.00
R5258:Sspo	UTSW	6	48,453,428 (GRCm39)	missense	probably damaging	1.00
R5276:Sspo	UTSW	6	48,467,401 (GRCm39)	missense	probably damaging	1.00
R5307:Sspo	UTSW	6	48,431,784 (GRCm39)	missense	probably damaging	0.99
R5341:Sspo	UTSW	6	48,436,549 (GRCm39)	missense	probably damaging	1.00
R5361:Sspo	UTSW	6	48,443,247 (GRCm39)	missense	probably benign	0.02
R5385:Sspo	UTSW	6	48,439,187 (GRCm39)	missense	probably benign	0.18
R5394:Sspo	UTSW	6	48,472,194 (GRCm39)	missense	possibly damaging	0.52
R5477:Sspo	UTSW	6	48,475,327 (GRCm39)	missense	possibly damaging	0.60
R5490:Sspo	UTSW	6	48,470,214 (GRCm39)	missense	probably benign	0.33
R5512:Sspo	UTSW	6	48,432,605 (GRCm39)	missense	probably damaging	0.97
R5518:Sspo	UTSW	6	48,473,588 (GRCm39)	missense	possibly damaging	0.92
R5530:Sspo	UTSW	6	48,442,517 (GRCm39)	missense	probably damaging	0.97
R5538:Sspo	UTSW	6	48,429,112 (GRCm39)	missense	probably damaging	0.99
R5590:Sspo	UTSW	6	48,451,425 (GRCm39)	missense	probably damaging	1.00
R5613:Sspo	UTSW	6	48,431,978 (GRCm39)	missense	possibly damaging	0.79
R5638:Sspo	UTSW	6	48,469,825 (GRCm39)	missense	possibly damaging	0.86
R5809:Sspo	UTSW	6	48,436,979 (GRCm39)	missense	possibly damaging	0.59
R5810:Sspo	UTSW	6	48,460,832 (GRCm39)	missense	probably benign	0.02
R5814:Sspo	UTSW	6	48,428,818 (GRCm39)	missense	probably damaging	1.00
R5915:Sspo	UTSW	6	48,468,418 (GRCm39)	missense	possibly damaging	0.83
R5915:Sspo	UTSW	6	48,441,530 (GRCm39)	missense	probably benign	0.00
R5979:Sspo	UTSW	6	48,440,627 (GRCm39)	missense	probably benign	0.20
R5996:Sspo	UTSW	6	48,471,110 (GRCm39)	missense	possibly damaging	0.87
R6012:Sspo	UTSW	6	48,428,305 (GRCm39)	missense	probably benign	0.00
R6025:Sspo	UTSW	6	48,463,720 (GRCm39)	missense	possibly damaging	0.83
R6120:Sspo	UTSW	6	48,442,510 (GRCm39)	missense	probably damaging	1.00
R6150:Sspo	UTSW	6	48,463,313 (GRCm39)	missense	probably benign	0.33
R6221:Sspo	UTSW	6	48,440,639 (GRCm39)	missense	probably damaging	1.00
R6261:Sspo	UTSW	6	48,439,125 (GRCm39)	missense	possibly damaging	0.75
R6312:Sspo	UTSW	6	48,434,300 (GRCm39)	critical splice donor site	probably null
R6372:Sspo	UTSW	6	48,449,475 (GRCm39)	missense	probably damaging	1.00
R6456:Sspo	UTSW	6	48,428,740 (GRCm39)	missense	probably benign	0.08
R6497:Sspo	UTSW	6	48,472,142 (GRCm39)	missense	possibly damaging	0.71
R6501:Sspo	UTSW	6	48,472,146 (GRCm39)	missense	possibly damaging	0.58
R6617:Sspo	UTSW	6	48,467,980 (GRCm39)	missense	possibly damaging	0.93
R6825:Sspo	UTSW	6	48,442,459 (GRCm39)	missense	probably benign	0.04
R6831:Sspo	UTSW	6	48,461,767 (GRCm39)	missense	possibly damaging	0.68
R6861:Sspo	UTSW	6	48,464,889 (GRCm39)	missense	probably benign	0.15
R6961:Sspo	UTSW	6	48,440,811 (GRCm39)	missense	probably benign	0.05
R6967:Sspo	UTSW	6	48,466,728 (GRCm39)	missense	probably benign	0.21
R7016:Sspo	UTSW	6	48,426,098 (GRCm39)	missense	probably damaging	1.00
R7035:Sspo	UTSW	6	48,426,147 (GRCm39)	splice site	probably null
R7058:Sspo	UTSW	6	48,425,516 (GRCm39)	missense	probably damaging	1.00
R7072:Sspo	UTSW	6	48,431,913 (GRCm39)	missense	probably damaging	1.00
R7078:Sspo	UTSW	6	48,437,313 (GRCm39)	missense	probably damaging	1.00
R7082:Sspo	UTSW	6	48,455,543 (GRCm39)	critical splice acceptor site	probably null
R7120:Sspo	UTSW	6	48,442,505 (GRCm39)	missense	probably benign	0.05
R7127:Sspo	UTSW	6	48,426,446 (GRCm39)	missense	probably benign	0.02
R7146:Sspo	UTSW	6	48,478,029 (GRCm39)	missense	probably benign	0.15
R7220:Sspo	UTSW	6	48,453,540 (GRCm39)	nonsense	probably null
R7242:Sspo	UTSW	6	48,450,886 (GRCm39)	missense	probably benign
R7261:Sspo	UTSW	6	48,427,011 (GRCm39)	missense	possibly damaging	0.52
R7313:Sspo	UTSW	6	48,450,390 (GRCm39)	missense	probably benign	0.04
R7313:Sspo	UTSW	6	48,431,762 (GRCm39)	missense	probably damaging	1.00
R7323:Sspo	UTSW	6	48,438,581 (GRCm39)	missense	possibly damaging	0.93
R7330:Sspo	UTSW	6	48,452,396 (GRCm39)	missense	probably benign	0.00
R7351:Sspo	UTSW	6	48,441,855 (GRCm39)	missense	possibly damaging	0.89
R7467:Sspo	UTSW	6	48,463,237 (GRCm39)	missense	probably damaging	1.00
R7475:Sspo	UTSW	6	48,432,794 (GRCm39)	missense	probably benign	0.37
R7489:Sspo	UTSW	6	48,450,647 (GRCm39)	missense	probably damaging	0.99
R7508:Sspo	UTSW	6	48,443,633 (GRCm39)	missense	probably damaging	1.00
R7515:Sspo	UTSW	6	48,470,820 (GRCm39)	missense	probably damaging	1.00
R7564:Sspo	UTSW	6	48,426,434 (GRCm39)	missense	probably benign	0.04
R7607:Sspo	UTSW	6	48,466,661 (GRCm39)	missense	probably damaging	1.00
R7620:Sspo	UTSW	6	48,444,020 (GRCm39)	critical splice donor site	probably null
R7667:Sspo	UTSW	6	48,452,305 (GRCm39)	nonsense	probably null
R7691:Sspo	UTSW	6	48,461,163 (GRCm39)	missense	probably benign	0.12
R7707:Sspo	UTSW	6	48,438,461 (GRCm39)	missense	probably benign	0.01
R7723:Sspo	UTSW	6	48,441,572 (GRCm39)	missense	probably damaging	0.99
R7748:Sspo	UTSW	6	48,426,399 (GRCm39)	nonsense	probably null
R7767:Sspo	UTSW	6	48,428,316 (GRCm39)	missense	probably damaging	0.96
R7792:Sspo	UTSW	6	48,431,624 (GRCm39)	missense	probably damaging	0.98
R7878:Sspo	UTSW	6	48,469,460 (GRCm39)	missense	probably damaging	1.00
R7893:Sspo	UTSW	6	48,440,244 (GRCm39)	missense	probably benign	0.02
R7942:Sspo	UTSW	6	48,465,434 (GRCm39)	splice site	probably null
R7952:Sspo	UTSW	6	48,464,263 (GRCm39)	missense	probably damaging	1.00
R7981:Sspo	UTSW	6	48,445,428 (GRCm39)	missense	probably benign
R7995:Sspo	UTSW	6	48,469,823 (GRCm39)	missense	probably damaging	1.00
R8088:Sspo	UTSW	6	48,434,547 (GRCm39)	missense	probably damaging	1.00
R8129:Sspo	UTSW	6	48,443,959 (GRCm39)	missense	possibly damaging	0.79
R8145:Sspo	UTSW	6	48,444,683 (GRCm39)	missense	possibly damaging	0.49
R8202:Sspo	UTSW	6	48,434,534 (GRCm39)	missense	probably damaging	1.00
R8211:Sspo	UTSW	6	48,469,543 (GRCm39)	critical splice donor site	probably null
R8240:Sspo	UTSW	6	48,460,436 (GRCm39)	missense	possibly damaging	0.84
R8252:Sspo	UTSW	6	48,462,386 (GRCm39)	missense	probably damaging	0.99
R8270:Sspo	UTSW	6	48,426,897 (GRCm39)	missense	probably benign
R8272:Sspo	UTSW	6	48,425,453 (GRCm39)	missense	probably benign	0.03
R8316:Sspo	UTSW	6	48,459,622 (GRCm39)	missense	probably damaging	1.00
R8384:Sspo	UTSW	6	48,459,598 (GRCm39)	missense	probably damaging	1.00
R8390:Sspo	UTSW	6	48,444,896 (GRCm39)	missense	probably benign	0.00
R8770:Sspo	UTSW	6	48,451,206 (GRCm39)	missense	probably null	1.00
R8827:Sspo	UTSW	6	48,434,606 (GRCm39)	missense	possibly damaging	0.59
R8882:Sspo	UTSW	6	48,452,390 (GRCm39)	missense	probably damaging	1.00
R8886:Sspo	UTSW	6	48,458,201 (GRCm39)	missense	possibly damaging	0.92
R8946:Sspo	UTSW	6	48,434,071 (GRCm39)	missense	probably damaging	1.00
R8947:Sspo	UTSW	6	48,425,504 (GRCm39)	missense	probably damaging	1.00
R9028:Sspo	UTSW	6	48,473,087 (GRCm39)	missense	probably benign	0.38
R9043:Sspo	UTSW	6	48,470,214 (GRCm39)	missense	probably benign	0.07
R9056:Sspo	UTSW	6	48,450,608 (GRCm39)	missense	probably damaging	0.97
R9071:Sspo	UTSW	6	48,433,982 (GRCm39)	missense	probably benign	0.00
R9133:Sspo	UTSW	6	48,434,747 (GRCm39)	missense	possibly damaging	0.81
R9187:Sspo	UTSW	6	48,472,223 (GRCm39)	missense	probably damaging	1.00
R9205:Sspo	UTSW	6	48,432,806 (GRCm39)	missense	probably benign	0.03
R9213:Sspo	UTSW	6	48,440,869 (GRCm39)	missense	possibly damaging	0.91
R9214:Sspo	UTSW	6	48,440,869 (GRCm39)	missense	possibly damaging	0.91
R9215:Sspo	UTSW	6	48,440,869 (GRCm39)	missense	possibly damaging	0.91
R9254:Sspo	UTSW	6	48,464,928 (GRCm39)	missense	probably damaging	1.00
R9291:Sspo	UTSW	6	48,473,330 (GRCm39)	missense	probably damaging	1.00
R9312:Sspo	UTSW	6	48,445,396 (GRCm39)	missense	probably benign	0.00
R9357:Sspo	UTSW	6	48,443,989 (GRCm39)	missense	possibly damaging	0.77
R9480:Sspo	UTSW	6	48,470,820 (GRCm39)	missense	probably damaging	1.00
R9586:Sspo	UTSW	6	48,458,039 (GRCm39)	missense	probably benign	0.03
R9660:Sspo	UTSW	6	48,432,707 (GRCm39)	missense	probably damaging	1.00
R9661:Sspo	UTSW	6	48,455,272 (GRCm39)	nonsense	probably null
R9728:Sspo	UTSW	6	48,432,707 (GRCm39)	missense	probably damaging	1.00
R9776:Sspo	UTSW	6	48,439,269 (GRCm39)	missense	probably benign	0.00
RF009:Sspo	UTSW	6	48,436,919 (GRCm39)	nonsense	probably null
X0060:Sspo	UTSW	6	48,457,728 (GRCm39)	missense	probably damaging	1.00
X0060:Sspo	UTSW	6	48,443,228 (GRCm39)	missense	probably damaging	1.00
X0063:Sspo	UTSW	6	48,474,356 (GRCm39)	missense	probably damaging	0.96
X0065:Sspo	UTSW	6	48,438,618 (GRCm39)	missense	probably benign	0.00
Z1176:Sspo	UTSW	6	48,458,227 (GRCm39)	missense	probably damaging	1.00
Z1177:Sspo	UTSW	6	48,467,824 (GRCm39)	missense	probably damaging	1.00
Z1177:Sspo	UTSW	6	48,467,482 (GRCm39)	nonsense	probably null
Z1177:Sspo	UTSW	6	48,450,369 (GRCm39)	missense	probably damaging	0.99
Z1177:Sspo	UTSW	6	48,447,918 (GRCm39)	missense	probably benign	0.16
Z1177:Sspo	UTSW	6	48,441,750 (GRCm39)	missense	possibly damaging	0.72
Z1177:Sspo	UTSW	6	48,433,960 (GRCm39)	missense	probably benign	0.31
Z1186:Sspo	UTSW	6	48,445,441 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- CCTCTAGGAGTCCTGATAGGAAGG -3'
(R):5'- GTGCATTCACAGTGTCCAAC -3'

Sequencing Primer
(F):5'- TCTTGATTCACAGGCAGCAG -3'
(R):5'- AGTGTCCAACTGGCACAC -3'

Posted On

2022-02-07