Mutagenetix > Incidental Mutation

Incidental Mutation 'R9045:9530053A07Rik'

687985

Institutional Source

Beutler Lab

Gene Symbol

9530053A07Rik

Ensembl Gene

ENSMUSG00000078776

Gene Name

RIKEN cDNA 9530053A07 gene

Synonyms

MMRRC Submission

068872-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.120) question?

Stock #

R9045 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

28129466-28164811 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 28154431 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 1607 (C1607S)

Ref Sequence

ENSEMBL: ENSMUSP00000056479 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000059886] [ENSMUST00000150948]

AlphaFold

E9PVG8

Predicted Effect

probably damaging
Transcript: ENSMUST00000059886
AA Change: C1607S

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

SMART Domains

Protein: ENSMUSP00000056479
Gene: ENSMUSG00000078776
AA Change: C1607S

Domain	Start	End	E-Value	Type
low complexity region	8	24	N/A	INTRINSIC
FOLN	27	49	1.23e-4	SMART
VWD	46	211	1.5e-40	SMART
C8	251	326	4.31e-33	SMART
Pfam:TIL	329	383	2e-13	PFAM
VWC	385	448	1.02e0	SMART
VWD	439	603	4.32e-32	SMART
C8	640	715	4.54e-9	SMART
Pfam:TIL	718	771	1.6e-12	PFAM
VWC	773	826	1.1e0	SMART
FOLN	805	827	6.87e1	SMART
VWD	825	988	7.92e-40	SMART
C8	1033	1108	5.1e-35	SMART
Pfam:TIL	1111	1164	7.6e-11	PFAM
VWC	1166	1224	1.1e-2	SMART
FOLN	1197	1219	9.55e-1	SMART
FOLN	1223	1245	5.38e1	SMART
VWD	1241	1410	9.04e-35	SMART
C8	1450	1526	9.54e-26	SMART
low complexity region	1540	1550	N/A	INTRINSIC
EGF_like	1557	1580	5.34e1	SMART
VWC	1588	1681	3.21e-3	SMART
VWD	1639	1806	7.3e-30	SMART
C8	1838	1913	2.44e-32	SMART
EGF_like	1941	1964	4.46e1	SMART
VWC	1971	2062	2.85e-1	SMART
VWD	2022	2178	1.32e-27	SMART
low complexity region	2199	2212	N/A	INTRINSIC
C8	2219	2294	1.43e-29	SMART
Pfam:TIL	2297	2350	1.1e-11	PFAM
FOLN	2383	2405	5.68e1	SMART
VWD	2402	2564	4.58e-4	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000150948
AA Change: C1607S

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

SMART Domains

Protein: ENSMUSP00000114986
Gene: ENSMUSG00000078776
AA Change: C1607S

Domain	Start	End	E-Value	Type
low complexity region	8	24	N/A	INTRINSIC
FOLN	27	49	1.23e-4	SMART
VWD	46	211	1.5e-40	SMART
C8	251	326	4.31e-33	SMART
Pfam:TIL	329	383	2e-13	PFAM
VWC	385	448	1.02e0	SMART
VWD	439	603	4.32e-32	SMART
C8	640	715	4.54e-9	SMART
Pfam:TIL	718	771	1.6e-12	PFAM
VWC	773	826	1.1e0	SMART
FOLN	805	827	6.87e1	SMART
VWD	825	988	7.92e-40	SMART
C8	1033	1108	5.1e-35	SMART
Pfam:TIL	1111	1164	7.6e-11	PFAM
VWC	1166	1224	1.1e-2	SMART
FOLN	1197	1219	9.55e-1	SMART
FOLN	1223	1245	5.38e1	SMART
VWD	1241	1410	9.04e-35	SMART
C8	1450	1526	9.54e-26	SMART
low complexity region	1540	1550	N/A	INTRINSIC
EGF_like	1557	1580	5.34e1	SMART
VWC	1588	1681	3.21e-3	SMART
VWD	1639	1806	7.3e-30	SMART
C8	1838	1913	2.44e-32	SMART
EGF_like	1941	1964	4.46e1	SMART
VWC	1971	2062	2.85e-1	SMART
VWD	2022	2178	1.32e-27	SMART
low complexity region	2199	2212	N/A	INTRINSIC
C8	2219	2294	1.43e-29	SMART
Pfam:TIL	2297	2350	1.1e-11	PFAM
FOLN	2383	2405	5.68e1	SMART
VWD	2402	2564	4.58e-4	SMART

Meta Mutation Damage Score

0.6329

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 97.6%

Validation Efficiency

100% (66/66)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5930422O12Rik	A	C	8: 33,429,334 (GRCm38)	M61L		Het
9130401M01Rik	G	T	15: 58,028,734 (GRCm38)	A223E	possibly damaging	Het
Adgra1	T	G	7: 139,852,650 (GRCm38)	L135V	possibly damaging	Het
Aida	A	G	1: 183,314,005 (GRCm38)	E127G	possibly damaging	Het
Ankrd31	T	A	13: 96,831,526 (GRCm38)	L557*	probably null	Het
Atxn7l3	T	A	11: 102,292,446 (GRCm38)	T221S	probably damaging	Het
Bbs7	A	G	3: 36,612,035 (GRCm38)	S27P	probably benign	Het
Cela3b	A	T	4: 137,424,799 (GRCm38)	C116S	possibly damaging	Het
Clstn3	A	C	6: 124,431,962 (GRCm38)	M909R	probably damaging	Het
Cnot2	T	C	10: 116,486,255 (GRCm38)	E523G	probably benign	Het
Col12a1	T	A	9: 79,674,752 (GRCm38)	T1406S	probably benign	Het
Cr2	A	T	1: 195,155,372 (GRCm38)	N763K	possibly damaging	Het
Csmd1	A	G	8: 16,234,074 (GRCm38)	F557L	probably damaging	Het
Cyth1	T	C	11: 118,182,264 (GRCm38)	H270R	possibly damaging	Het
Epg5	T	C	18: 77,948,799 (GRCm38)	L237P	probably damaging	Het
Fbxo36	G	A	1: 84,896,579 (GRCm38)	D99N	probably damaging	Het
Flot2	A	G	11: 78,059,197 (GRCm38)	I417M	probably benign	Het
Fryl	A	G	5: 73,024,775 (GRCm38)	L143P		Het
Gckr	A	G	5: 31,300,009 (GRCm38)	N122S	possibly damaging	Het
Gm14548	A	G	7: 3,894,548 (GRCm38)	I516T	possibly damaging	Het
Gm3250	T	A	10: 77,782,098 (GRCm38)	T149S	unknown	Het
Golga3	G	A	5: 110,193,097 (GRCm38)	M552I	probably benign	Het
Grip1	T	A	10: 120,035,451 (GRCm38)	D694E	probably damaging	Het
Heatr1	T	C	13: 12,413,352 (GRCm38)	V790A	probably benign	Het
Ighv1-54	G	A	12: 115,193,880 (GRCm38)	T49I	probably benign	Het
Iglv1	A	G	16: 19,085,303 (GRCm38)	V22A	probably benign	Het
Lama1	A	T	17: 67,753,843 (GRCm38)	Y722F		Het
Laptm5	A	T	4: 130,928,644 (GRCm38)	E91V		Het
Lrig1	A	G	6: 94,608,707 (GRCm38)		probably null	Het
Mcph1	T	G	8: 18,632,427 (GRCm38)	S527A	probably benign	Het
Med13l	G	T	5: 118,742,751 (GRCm38)	V1303L	probably benign	Het
Mindy4	A	G	6: 55,318,298 (GRCm38)	D741G	probably benign	Het
Myo15b	T	A	11: 115,892,352 (GRCm38)	*3034R	probably null	Het
Nfkbie	A	T	17: 45,562,033 (GRCm38)	K354I	probably damaging	Het
Npat	A	G	9: 53,563,476 (GRCm38)	N856S	possibly damaging	Het
Nr2c2ap	A	G	8: 70,133,158 (GRCm38)	D122G	probably damaging	Het
Nr4a3	C	A	4: 48,067,694 (GRCm38)	T430K	possibly damaging	Het
Olfr1145	C	A	2: 87,810,072 (GRCm38)	S84Y	probably damaging	Het
Olfr193	A	G	16: 59,110,002 (GRCm38)	S203P	probably benign	Het
Olfr599	T	G	7: 103,338,696 (GRCm38)	I214R	probably damaging	Het
Otud7b	A	G	3: 96,152,578 (GRCm38)	K397E	probably benign	Het
Pafah1b3	G	T	7: 25,297,473 (GRCm38)		probably benign	Het
Pcdhgc3	G	T	18: 37,807,616 (GRCm38)	V357L	probably damaging	Het
Pde2a	A	G	7: 101,503,291 (GRCm38)	T354A	unknown	Het
Rbfa	T	C	18: 80,192,811 (GRCm38)	H241R	probably damaging	Het
Rhox3c	C	T	X: 37,469,650 (GRCm38)		probably benign	Het
Rps6ka1	C	T	4: 133,872,839 (GRCm38)		probably benign	Het
S1pr2	T	C	9: 20,967,594 (GRCm38)	T313A	probably benign	Het
Sbno1	A	G	5: 124,405,657 (GRCm38)	V273A	probably benign	Het
Scg3	T	C	9: 75,663,240 (GRCm38)	N344S	probably damaging	Het
Serpinb1c	C	G	13: 32,882,044 (GRCm38)	G306A	probably benign	Het
Sh2d6	C	T	6: 72,515,621 (GRCm38)	G206D	probably benign	Het
Slamf9	G	A	1: 172,477,371 (GRCm38)	S184N	probably damaging	Het
Slc50a1	T	C	3: 89,268,735 (GRCm38)	T168A	probably damaging	Het
Tas2r124	G	C	6: 132,755,071 (GRCm38)	W114C	probably damaging	Het
Tgm4	C	T	9: 123,048,551 (GRCm38)	T206I	possibly damaging	Het
Tmem52	A	G	4: 155,469,442 (GRCm38)		probably null	Het
Vmn2r102	A	G	17: 19,660,579 (GRCm38)	K61E	probably benign	Het
Vmn2r58	T	C	7: 41,837,663 (GRCm38)	I603V	probably benign	Het
Vstm2l	G	T	2: 157,914,875 (GRCm38)	G22V	unknown	Het
Vwa5b1	T	A	4: 138,588,679 (GRCm38)	Y584F	probably damaging	Het
Wdfy3	A	T	5: 101,847,174 (GRCm38)	V3233D	probably damaging	Het
Wdhd1	A	G	14: 47,273,952 (GRCm38)	V101A	probably benign	Het
Zfc3h1	C	A	10: 115,427,414 (GRCm38)	Q1761K	possibly damaging	Het
Zfp180	G	A	7: 24,104,890 (GRCm38)	V245I	probably benign	Het
Zfp846	A	T	9: 20,593,893 (GRCm38)	I350L	probably benign	Het

Other mutations in 9530053A07Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00435:9530053A07Rik	APN	7	28,164,528 (GRCm38)	missense	probably damaging	1.00
IGL00757:9530053A07Rik	APN	7	28,154,445 (GRCm38)	missense	probably damaging	1.00
IGL01015:9530053A07Rik	APN	7	28,155,318 (GRCm38)	missense	probably damaging	1.00
IGL01079:9530053A07Rik	APN	7	28,139,778 (GRCm38)	missense	probably damaging	0.99
IGL01343:9530053A07Rik	APN	7	28,150,702 (GRCm38)	missense	probably benign	0.19
IGL01420:9530053A07Rik	APN	7	28,140,133 (GRCm38)	missense	probably benign	0.28
IGL01604:9530053A07Rik	APN	7	28,155,324 (GRCm38)	missense	probably benign	0.11
IGL01666:9530053A07Rik	APN	7	28,153,292 (GRCm38)	missense	probably damaging	1.00
IGL02002:9530053A07Rik	APN	7	28,152,796 (GRCm38)	missense	probably damaging	1.00
IGL02036:9530053A07Rik	APN	7	28,137,525 (GRCm38)	missense	possibly damaging	0.82
IGL02126:9530053A07Rik	APN	7	28,139,856 (GRCm38)	missense	probably damaging	1.00
IGL02150:9530053A07Rik	APN	7	28,146,779 (GRCm38)	nonsense	probably null
IGL02219:9530053A07Rik	APN	7	28,154,635 (GRCm38)	missense	probably damaging	1.00
IGL02563:9530053A07Rik	APN	7	28,157,892 (GRCm38)	missense	probably benign
IGL02804:9530053A07Rik	APN	7	28,153,370 (GRCm38)	missense	probably benign	0.00
IGL02830:9530053A07Rik	APN	7	28,162,923 (GRCm38)	missense	probably damaging	1.00
IGL02943:9530053A07Rik	APN	7	28,147,188 (GRCm38)	missense	probably damaging	1.00
IGL02977:9530053A07Rik	APN	7	28,164,372 (GRCm38)	missense	possibly damaging	0.83
IGL03231:9530053A07Rik	APN	7	28,153,722 (GRCm38)	missense	possibly damaging	0.95
IGL03304:9530053A07Rik	APN	7	28,142,242 (GRCm38)	missense	probably damaging	0.99
herz	UTSW	7	28,153,839 (GRCm38)	missense	possibly damaging	0.72
pulse	UTSW	7	28,153,749 (GRCm38)	missense	probably damaging	1.00
Sinusoidal	UTSW	7	28,140,130 (GRCm38)	missense	probably damaging	1.00
PIT4378001:9530053A07Rik	UTSW	7	28,154,464 (GRCm38)	missense	possibly damaging	0.61
R0023:9530053A07Rik	UTSW	7	28,153,412 (GRCm38)	missense	probably benign	0.00
R0131:9530053A07Rik	UTSW	7	28,137,615 (GRCm38)	missense	probably damaging	1.00
R0131:9530053A07Rik	UTSW	7	28,137,615 (GRCm38)	missense	probably damaging	1.00
R0132:9530053A07Rik	UTSW	7	28,137,615 (GRCm38)	missense	probably damaging	1.00
R0158:9530053A07Rik	UTSW	7	28,155,492 (GRCm38)	missense	probably damaging	1.00
R0230:9530053A07Rik	UTSW	7	28,156,825 (GRCm38)	missense	probably damaging	1.00
R0310:9530053A07Rik	UTSW	7	28,142,274 (GRCm38)	missense	probably benign	0.04
R0448:9530053A07Rik	UTSW	7	28,140,235 (GRCm38)	missense	probably benign	0.03
R0462:9530053A07Rik	UTSW	7	28,137,340 (GRCm38)	missense	probably damaging	1.00
R0481:9530053A07Rik	UTSW	7	28,153,749 (GRCm38)	missense	probably damaging	1.00
R0497:9530053A07Rik	UTSW	7	28,147,465 (GRCm38)	missense	probably damaging	1.00
R0556:9530053A07Rik	UTSW	7	28,159,378 (GRCm38)	missense	probably benign
R0562:9530053A07Rik	UTSW	7	28,162,690 (GRCm38)	missense	probably benign	0.30
R0586:9530053A07Rik	UTSW	7	28,137,091 (GRCm38)	missense	probably damaging	0.99
R0924:9530053A07Rik	UTSW	7	28,140,130 (GRCm38)	missense	probably damaging	1.00
R0930:9530053A07Rik	UTSW	7	28,140,130 (GRCm38)	missense	probably damaging	1.00
R1103:9530053A07Rik	UTSW	7	28,154,520 (GRCm38)	missense	probably damaging	1.00
R1213:9530053A07Rik	UTSW	7	28,157,673 (GRCm38)	missense	probably damaging	1.00
R1292:9530053A07Rik	UTSW	7	28,142,794 (GRCm38)	splice site	probably benign
R1368:9530053A07Rik	UTSW	7	28,159,478 (GRCm38)	missense	possibly damaging	0.89
R1451:9530053A07Rik	UTSW	7	28,137,157 (GRCm38)	missense	probably damaging	1.00
R1477:9530053A07Rik	UTSW	7	28,157,093 (GRCm38)	missense	probably benign	0.01
R1538:9530053A07Rik	UTSW	7	28,155,492 (GRCm38)	missense	probably damaging	1.00
R1655:9530053A07Rik	UTSW	7	28,147,110 (GRCm38)	missense	probably damaging	0.98
R1697:9530053A07Rik	UTSW	7	28,154,347 (GRCm38)	missense	probably damaging	1.00
R1741:9530053A07Rik	UTSW	7	28,157,854 (GRCm38)	missense	probably damaging	0.98
R1796:9530053A07Rik	UTSW	7	28,155,372 (GRCm38)	missense	probably damaging	1.00
R1853:9530053A07Rik	UTSW	7	28,155,546 (GRCm38)	nonsense	probably null
R1861:9530053A07Rik	UTSW	7	28,154,732 (GRCm38)	missense	probably damaging	1.00
R1909:9530053A07Rik	UTSW	7	28,144,348 (GRCm38)	missense	possibly damaging	0.52
R1971:9530053A07Rik	UTSW	7	28,131,512 (GRCm38)	missense	possibly damaging	0.90
R1990:9530053A07Rik	UTSW	7	28,154,360 (GRCm38)	missense	probably damaging	0.98
R2020:9530053A07Rik	UTSW	7	28,155,594 (GRCm38)	missense	probably benign
R2084:9530053A07Rik	UTSW	7	28,157,535 (GRCm38)	missense	probably damaging	1.00
R2125:9530053A07Rik	UTSW	7	28,158,022 (GRCm38)	missense	probably benign	0.00
R2132:9530053A07Rik	UTSW	7	28,155,474 (GRCm38)	missense	probably damaging	1.00
R2513:9530053A07Rik	UTSW	7	28,131,635 (GRCm38)	missense	probably damaging	0.99
R2913:9530053A07Rik	UTSW	7	28,164,307 (GRCm38)	missense	probably damaging	1.00
R3150:9530053A07Rik	UTSW	7	28,154,195 (GRCm38)	missense	probably benign	0.21
R3499:9530053A07Rik	UTSW	7	28,154,555 (GRCm38)	missense	probably benign	0.42
R3702:9530053A07Rik	UTSW	7	28,157,778 (GRCm38)	missense	probably damaging	1.00
R3881:9530053A07Rik	UTSW	7	28,140,038 (GRCm38)	nonsense	probably null
R3938:9530053A07Rik	UTSW	7	28,154,294 (GRCm38)	missense	probably damaging	1.00
R4050:9530053A07Rik	UTSW	7	28,152,985 (GRCm38)	missense	possibly damaging	0.55
R4152:9530053A07Rik	UTSW	7	28,156,897 (GRCm38)	missense	possibly damaging	0.47
R4168:9530053A07Rik	UTSW	7	28,137,109 (GRCm38)	missense	probably benign	0.05
R4235:9530053A07Rik	UTSW	7	28,156,648 (GRCm38)	missense	probably damaging	0.99
R4241:9530053A07Rik	UTSW	7	28,154,335 (GRCm38)	missense	probably damaging	1.00
R4363:9530053A07Rik	UTSW	7	28,146,906 (GRCm38)	missense	probably damaging	1.00
R4460:9530053A07Rik	UTSW	7	28,152,856 (GRCm38)	missense	probably benign	0.17
R4463:9530053A07Rik	UTSW	7	28,150,719 (GRCm38)	missense	probably benign
R4841:9530053A07Rik	UTSW	7	28,150,722 (GRCm38)	missense	probably damaging	1.00
R4842:9530053A07Rik	UTSW	7	28,150,722 (GRCm38)	missense	probably damaging	1.00
R4876:9530053A07Rik	UTSW	7	28,142,800 (GRCm38)	intron	probably benign
R4905:9530053A07Rik	UTSW	7	28,156,983 (GRCm38)	missense	possibly damaging	0.93
R4997:9530053A07Rik	UTSW	7	28,143,924 (GRCm38)	missense	possibly damaging	0.77
R5091:9530053A07Rik	UTSW	7	28,156,958 (GRCm38)	missense	probably benign	0.44
R5159:9530053A07Rik	UTSW	7	28,153,308 (GRCm38)	missense	probably benign	0.09
R5326:9530053A07Rik	UTSW	7	28,155,489 (GRCm38)	missense	probably damaging	0.98
R5396:9530053A07Rik	UTSW	7	28,140,183 (GRCm38)	missense	probably benign
R5441:9530053A07Rik	UTSW	7	28,156,914 (GRCm38)	missense	probably damaging	1.00
R5480:9530053A07Rik	UTSW	7	28,157,999 (GRCm38)	nonsense	probably null
R5542:9530053A07Rik	UTSW	7	28,155,489 (GRCm38)	missense	probably damaging	0.98
R5571:9530053A07Rik	UTSW	7	28,156,569 (GRCm38)	missense	probably damaging	0.99
R5613:9530053A07Rik	UTSW	7	28,142,878 (GRCm38)	intron	probably benign
R5637:9530053A07Rik	UTSW	7	28,152,852 (GRCm38)	missense	probably benign	0.00
R5766:9530053A07Rik	UTSW	7	28,137,329 (GRCm38)	nonsense	probably null
R6174:9530053A07Rik	UTSW	7	28,139,959 (GRCm38)	missense	probably damaging	0.96
R6233:9530053A07Rik	UTSW	7	28,131,460 (GRCm38)	missense	probably damaging	0.99
R6250:9530053A07Rik	UTSW	7	28,150,714 (GRCm38)	missense	probably damaging	1.00
R6379:9530053A07Rik	UTSW	7	28,157,592 (GRCm38)	missense	probably damaging	1.00
R6442:9530053A07Rik	UTSW	7	28,144,186 (GRCm38)	missense	possibly damaging	0.88
R6478:9530053A07Rik	UTSW	7	28,155,373 (GRCm38)	missense	probably damaging	1.00
R6699:9530053A07Rik	UTSW	7	28,144,368 (GRCm38)	missense	probably damaging	1.00
R6852:9530053A07Rik	UTSW	7	28,147,135 (GRCm38)	missense	probably damaging	1.00
R6883:9530053A07Rik	UTSW	7	28,152,835 (GRCm38)	missense	possibly damaging	0.89
R6902:9530053A07Rik	UTSW	7	28,137,213 (GRCm38)	missense	probably damaging	1.00
R6903:9530053A07Rik	UTSW	7	28,137,213 (GRCm38)	missense	probably damaging	1.00
R6904:9530053A07Rik	UTSW	7	28,137,213 (GRCm38)	missense	probably damaging	1.00
R6992:9530053A07Rik	UTSW	7	28,140,183 (GRCm38)	missense	probably benign	0.04
R7023:9530053A07Rik	UTSW	7	28,140,038 (GRCm38)	nonsense	probably null
R7039:9530053A07Rik	UTSW	7	28,140,148 (GRCm38)	missense	possibly damaging	0.80
R7171:9530053A07Rik	UTSW	7	28,154,519 (GRCm38)	nonsense	probably null
R7282:9530053A07Rik	UTSW	7	28,144,408 (GRCm38)	missense	probably benign	0.02
R7291:9530053A07Rik	UTSW	7	28,140,220 (GRCm38)	missense	probably benign
R7344:9530053A07Rik	UTSW	7	28,152,760 (GRCm38)	missense	possibly damaging	0.46
R7344:9530053A07Rik	UTSW	7	28,140,279 (GRCm38)	missense	possibly damaging	0.79
R7392:9530053A07Rik	UTSW	7	28,164,372 (GRCm38)	missense	possibly damaging	0.83
R7531:9530053A07Rik	UTSW	7	28,140,231 (GRCm38)	missense	probably benign
R7541:9530053A07Rik	UTSW	7	28,144,256 (GRCm38)	nonsense	probably null
R7577:9530053A07Rik	UTSW	7	28,154,423 (GRCm38)	missense	possibly damaging	0.65
R7594:9530053A07Rik	UTSW	7	28,131,460 (GRCm38)	missense	probably damaging	0.99
R7647:9530053A07Rik	UTSW	7	28,140,045 (GRCm38)	missense	probably benign	0.00
R7718:9530053A07Rik	UTSW	7	28,147,201 (GRCm38)	missense	probably damaging	1.00
R7733:9530053A07Rik	UTSW	7	28,139,965 (GRCm38)	missense	probably damaging	1.00
R7737:9530053A07Rik	UTSW	7	28,157,073 (GRCm38)	missense	probably damaging	1.00
R7908:9530053A07Rik	UTSW	7	28,147,496 (GRCm38)	missense	probably benign	0.12
R8013:9530053A07Rik	UTSW	7	28,137,541 (GRCm38)	missense	probably benign	0.14
R8014:9530053A07Rik	UTSW	7	28,137,541 (GRCm38)	missense	probably benign	0.14
R8151:9530053A07Rik	UTSW	7	28,153,341 (GRCm38)	missense	possibly damaging	0.95
R8175:9530053A07Rik	UTSW	7	28,164,448 (GRCm38)	nonsense	probably null
R8254:9530053A07Rik	UTSW	7	28,147,349 (GRCm38)	missense	possibly damaging	0.63
R8345:9530053A07Rik	UTSW	7	28,155,360 (GRCm38)	missense	probably damaging	1.00
R8414:9530053A07Rik	UTSW	7	28,142,733 (GRCm38)	missense	probably damaging	1.00
R8419:9530053A07Rik	UTSW	7	28,143,921 (GRCm38)	missense	probably damaging	1.00
R8496:9530053A07Rik	UTSW	7	28,143,952 (GRCm38)	missense	possibly damaging	0.81
R8691:9530053A07Rik	UTSW	7	28,153,839 (GRCm38)	missense	possibly damaging	0.72
R8785:9530053A07Rik	UTSW	7	28,154,707 (GRCm38)	missense	probably damaging	1.00
R8863:9530053A07Rik	UTSW	7	28,131,581 (GRCm38)	missense	probably damaging	1.00
R8926:9530053A07Rik	UTSW	7	28,154,444 (GRCm38)	missense	probably damaging	1.00
R8950:9530053A07Rik	UTSW	7	28,164,326 (GRCm38)	missense	probably benign	0.32
R9014:9530053A07Rik	UTSW	7	28,155,451 (GRCm38)	missense	probably damaging	1.00
R9115:9530053A07Rik	UTSW	7	28,154,329 (GRCm38)	missense	possibly damaging	0.74
R9233:9530053A07Rik	UTSW	7	28,140,094 (GRCm38)	missense	possibly damaging	0.83
R9330:9530053A07Rik	UTSW	7	28,156,985 (GRCm38)	missense	probably benign	0.02
R9426:9530053A07Rik	UTSW	7	28,143,856 (GRCm38)	missense	possibly damaging	0.92
R9477:9530053A07Rik	UTSW	7	28,152,840 (GRCm38)	missense	probably damaging	1.00
R9502:9530053A07Rik	UTSW	7	28,137,466 (GRCm38)	missense	probably benign	0.09
R9505:9530053A07Rik	UTSW	7	28,142,484 (GRCm38)	nonsense	probably null
R9601:9530053A07Rik	UTSW	7	28,154,380 (GRCm38)	missense	possibly damaging	0.78
R9630:9530053A07Rik	UTSW	7	28,137,199 (GRCm38)	missense	probably damaging	1.00
R9632:9530053A07Rik	UTSW	7	28,142,301 (GRCm38)	missense	probably benign
R9673:9530053A07Rik	UTSW	7	28,156,619 (GRCm38)	missense	probably benign	0.25
R9735:9530053A07Rik	UTSW	7	28,157,010 (GRCm38)	missense	probably damaging	1.00
Z1176:9530053A07Rik	UTSW	7	28,154,762 (GRCm38)	missense	probably benign	0.03
Z1176:9530053A07Rik	UTSW	7	28,142,386 (GRCm38)	missense	probably benign	0.06
Z1177:9530053A07Rik	UTSW	7	28,139,898 (GRCm38)	missense	probably benign	0.25
Z1186:9530053A07Rik	UTSW	7	28,156,986 (GRCm38)	missense	probably benign	0.01
Z1186:9530053A07Rik	UTSW	7	28,146,705 (GRCm38)	missense	probably benign	0.00
Z1186:9530053A07Rik	UTSW	7	28,131,572 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- AACAGCCACTACGAGCTCTG -3'
(R):5'- TGCCTTGGAAGTCAAACCG -3'

Sequencing Primer
(F):5'- ACTACGAGCTCTGTGGCC -3'
(R):5'- TTGGAAGTCAAACCGGTGCC -3'

Posted On

2021-11-19