Mutagenetix > Incidental Mutation

Incidental Mutation 'R6699:9530053A07Rik'

528680

Institutional Source

Beutler Lab

Gene Symbol

9530053A07Rik

Ensembl Gene

ENSMUSG00000078776

Gene Name

RIKEN cDNA 9530053A07 gene

Synonyms

MMRRC Submission

044817-MU

Accession Numbers

Essential gene?

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

Stock #

R6699 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

28129466-28164811 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 28144368 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 894 (T894A)

Ref Sequence

ENSEMBL: ENSMUSP00000114986 (fasta)

Gene Model

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

AlphaFold

E9PVG8

Predicted Effect

probably damaging
Transcript: ENSMUST00000059886
AA Change: T894A

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000056479
Gene: ENSMUSG00000078776
AA Change: T894A

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

noncoding transcript
Transcript: ENSMUST00000129051

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000130693

Predicted Effect

probably damaging
Transcript: ENSMUST00000150948
AA Change: T894A

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000114986
Gene: ENSMUSG00000078776
AA Change: T894A

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

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 95.1%

Validation Efficiency

100% (35/35)

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam39	A	G	8: 40,826,657 (GRCm38)	K695R	probably benign	Het
Agfg1	G	A	1: 82,858,454 (GRCm38)		probably null	Het
Ankrd44	G	A	1: 54,762,445 (GRCm38)	T241I	probably damaging	Het
Car15	T	C	16: 17,836,574 (GRCm38)	D166G	probably null	Het
Cpne2	G	A	8: 94,563,959 (GRCm38)	V391M	probably damaging	Het
Ddx27	C	T	2: 167,020,503 (GRCm38)	T155I	possibly damaging	Het
F830045P16Rik	T	C	2: 129,460,421 (GRCm38)	D417G	probably damaging	Het
Fam217b	T	G	2: 178,420,417 (GRCm38)	M58R	probably benign	Het
Ftmt	T	C	18: 52,331,665 (GRCm38)	S18P	possibly damaging	Het
Gm16494	C	T	17: 47,016,908 (GRCm38)	V17M	probably damaging	Het
Gm36864	A	T	7: 44,238,772 (GRCm38)	I342F	possibly damaging	Het
Grid2	C	G	6: 63,931,047 (GRCm38)	R224G	possibly damaging	Het
Hist1h4k	A	T	13: 21,750,504 (GRCm38)	M1K	probably null	Het
Hmgcr	T	C	13: 96,660,209 (GRCm38)	E191G	probably damaging	Het
Hrc	A	G	7: 45,335,695 (GRCm38)	D90G	possibly damaging	Het
Kbtbd7	A	G	14: 79,428,192 (GRCm38)	E488G	probably benign	Het
Krtap26-1	T	C	16: 88,647,715 (GRCm38)	N6S	unknown	Het
Mgat2	A	G	12: 69,184,781 (GRCm38)	D43G	probably damaging	Het
Mrps30	A	T	13: 118,380,598 (GRCm38)	S362T	probably damaging	Het
Olfr1124	A	T	2: 87,434,816 (GRCm38)	I110F	probably benign	Het
Olfr224	T	A	11: 58,567,205 (GRCm38)	I47L	possibly damaging	Het
Pcdhb11	T	A	18: 37,422,937 (GRCm38)	V440E	probably damaging	Het
Pcdhb18	T	A	18: 37,491,952 (GRCm38)	H778Q	probably benign	Het
Plekha7	T	C	7: 116,135,175 (GRCm38)	E1025G	probably damaging	Het
Rnf39	T	C	17: 36,947,229 (GRCm38)	W96R	probably damaging	Het
Rph3al	A	T	11: 75,900,837 (GRCm38)		probably benign	Het
Rrm1	T	A	7: 102,460,825 (GRCm38)	Y556N	probably damaging	Het
Saal1	A	T	7: 46,692,817 (GRCm38)	C401S	probably damaging	Het
Sec14l3	T	C	11: 4,075,193 (GRCm38)	S268P	possibly damaging	Het
Tmem54	A	G	4: 129,111,325 (GRCm38)	I199M	probably benign	Het
Tomm70a	A	G	16: 57,142,802 (GRCm38)	M395V	probably benign	Het
Topors	A	G	4: 40,262,300 (GRCm38)	V328A	probably damaging	Het
Vmn2r61	T	G	7: 42,300,156 (GRCm38)	S667A	probably benign	Het
Vmn2r68	G	A	7: 85,232,375 (GRCm38)	A499V	possibly damaging	Het
Zcchc14	A	T	8: 121,608,616 (GRCm38)		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
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
R9045:9530053A07Rik	UTSW	7	28,154,431 (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'- AGGGGCTTCACATTACACTACC -3'
(R):5'- AGGCCTCCTTACTCTAGGATTC -3'

Sequencing Primer
(F):5'- ACACTACCTTTGATGGCCG -3'
(R):5'- TGTTGAGGTCACACTTTCTCAC -3'

Posted On

2018-07-24