Mutagenetix > Incidental Mutation

Incidental Mutation 'R6724:Trank1'

529770

Institutional Source

Beutler Lab

Gene Symbol

Trank1

Ensembl Gene

ENSMUSG00000062296

Gene Name

tetratricopeptide repeat and ankyrin repeat containing 1

Synonyms

A230061D21Rik, LOC235639, C030048J01Rik, Lba1

MMRRC Submission

044842-MU

Accession Numbers

Genbank: NM_001164659.1; Ensembl: ENSMUST00000078626

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6724 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

111311739-111395775 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to G at 111365916 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 1003 (R1003G)

Ref Sequence

ENSEMBL: ENSMUSP00000077697 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078626]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000078626
AA Change: R1003G

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

SMART Domains

Protein: ENSMUSP00000077697
Gene: ENSMUSG00000062296
AA Change: R1003G

Domain	Start	End	E-Value	Type
low complexity region	4	30	N/A	INTRINSIC
low complexity region	34	52	N/A	INTRINSIC
low complexity region	113	129	N/A	INTRINSIC
Blast:TPR	144	177	1e-15	BLAST
Blast:TPR	178	209	8e-13	BLAST
Blast:ANK	332	361	1e-6	BLAST
ANK	369	405	5.29e0	SMART
ANK	538	567	2.11e2	SMART
ANK	572	609	7.29e2	SMART
ANK	621	652	1.21e2	SMART
low complexity region	887	895	N/A	INTRINSIC
low complexity region	1152	1172	N/A	INTRINSIC
Blast:AAA	1351	1569	1e-6	BLAST
low complexity region	2166	2177	N/A	INTRINSIC
low complexity region	2395	2411	N/A	INTRINSIC
low complexity region	2636	2649	N/A	INTRINSIC
low complexity region	2966	2983	N/A	INTRINSIC

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.8%

Validation Efficiency

98% (63/64)

Allele List at MGI

All alleles(2) : Targeted, other(2)

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts5	T	A	16: 85,868,557 (GRCm38)	T619S	probably benign	Het
Adgra2	G	A	8: 27,114,182 (GRCm38)	A467T	possibly damaging	Het
AF366264	A	T	8: 13,837,083 (GRCm38)	L336Q	probably damaging	Het
Alox5	A	T	6: 116,414,548 (GRCm38)	I416N	probably damaging	Het
Blmh	A	G	11: 76,971,907 (GRCm38)		probably null	Het
Cftr	T	A	6: 18,255,974 (GRCm38)	Y567*	probably null	Het
Cnr1	T	A	4: 33,944,728 (GRCm38)	M372K	possibly damaging	Het
Col6a3	T	C	1: 90,779,152 (GRCm38)	T2080A	unknown	Het
Crybg3	A	T	16: 59,544,138 (GRCm38)	C2374S	probably benign	Het
Csmd2	A	G	4: 128,563,371 (GRCm38)	I3544V	probably damaging	Het
Dnah12	A	T	14: 26,796,223 (GRCm38)	D1809V	probably benign	Het
Dnah8	G	A	17: 30,748,568 (GRCm38)	D2585N	probably benign	Het
Dnajb12	A	G	10: 59,892,780 (GRCm38)	D190G	possibly damaging	Het
Dtnb	T	A	12: 3,686,817 (GRCm38)	V319D	probably damaging	Het
Ercc6	A	T	14: 32,566,331 (GRCm38)	E820V	probably benign	Het
Fip1l1	T	G	5: 74,591,774 (GRCm38)	V378G	probably damaging	Het
Gabrg1	T	A	5: 70,754,209 (GRCm38)	Y358F	possibly damaging	Het
Gcn1l1	T	G	5: 115,609,158 (GRCm38)		probably null	Het
Gm11011	T	A	2: 169,587,482 (GRCm38)	T28S	unknown	Het
Gm13762	T	G	2: 88,973,268 (GRCm38)	I208L	probably benign	Het
Gm14025	A	C	2: 129,038,056 (GRCm38)	V650G	probably benign	Het
Gm4027	A	T	12: 87,621,984 (GRCm38)	I129F	unknown	Het
Guf1	C	A	5: 69,566,393 (GRCm38)	N438K	probably damaging	Het
Hoxa7	T	C	6: 52,215,739 (GRCm38)	E223G	probably benign	Het
Hspg2	G	A	4: 137,515,307 (GRCm38)	G611E	probably damaging	Het
Ipo8	A	T	6: 148,809,975 (GRCm38)		probably null	Het
Isl2	A	G	9: 55,541,288 (GRCm38)	D3G	possibly damaging	Het
Kcnb2	A	G	1: 15,710,440 (GRCm38)	Y512C	probably damaging	Het
Kifc1	T	A	17: 33,886,733 (GRCm38)		probably null	Het
Klhdc10	A	G	6: 30,446,641 (GRCm38)	D183G	probably damaging	Het
Klra5	T	A	6: 129,906,680 (GRCm38)	K71N	probably benign	Het
Lrp6	T	C	6: 134,486,541 (GRCm38)	H559R	possibly damaging	Het
Maml3	T	C	3: 51,855,875 (GRCm38)	N556S	probably damaging	Het
Man2a1	A	G	17: 64,731,269 (GRCm38)	I83V	possibly damaging	Het
Mrgpra9	A	G	7: 47,235,038 (GRCm38)	S293P	probably damaging	Het
Nalcn	A	G	14: 123,298,067 (GRCm38)	S1282P	probably damaging	Het
Npepps	A	T	11: 97,206,002 (GRCm38)		probably benign	Het
Olfr1037	A	T	2: 86,085,357 (GRCm38)	V140E	possibly damaging	Het
Olfr1154	T	G	2: 87,903,602 (GRCm38)	S25R	probably benign	Het
Olfr1245	A	T	2: 89,574,965 (GRCm38)	F254I	probably benign	Het
Pkn3	C	A	2: 30,090,550 (GRCm38)	R818S	possibly damaging	Het
Plekha3	T	A	2: 76,687,401 (GRCm38)	H190Q	probably damaging	Het
Ppp2r3c	A	T	12: 55,288,496 (GRCm38)	S261T	probably benign	Het
Ptprj	T	C	2: 90,450,851 (GRCm38)	D1015G	probably benign	Het
Pus10	T	C	11: 23,729,037 (GRCm38)	M503T	possibly damaging	Het
Pvr	T	C	7: 19,918,679 (GRCm38)	R104G	possibly damaging	Het
Rubcnl	A	G	14: 75,052,010 (GRCm38)	R653G	probably benign	Het
Serpina1a	G	T	12: 103,860,420 (GRCm38)		probably benign	Het
Shank3	G	A	15: 89,532,453 (GRCm38)	R265Q	probably damaging	Het
Slc22a22	C	T	15: 57,247,532 (GRCm38)	R433H	probably damaging	Het
Slc22a26	A	G	19: 7,802,361 (GRCm38)	I30T	probably benign	Het
Spz1	A	T	13: 92,575,484 (GRCm38)	N161K	possibly damaging	Het
Tacc2	A	G	7: 130,728,762 (GRCm38)	R259G	probably damaging	Het
Top1	G	A	2: 160,712,696 (GRCm38)	V456M	probably damaging	Het
Tpcn2	G	A	7: 145,256,520 (GRCm38)	A649V	probably benign	Het
Tril	T	A	6: 53,819,574 (GRCm38)	H221L	possibly damaging	Het
Unc79	C	T	12: 103,104,861 (GRCm38)	T1305I	probably damaging	Het
Unc80	C	T	1: 66,683,191 (GRCm38)	A2988V	possibly damaging	Het
Vmn1r81	A	T	7: 12,260,672 (GRCm38)	M3K	probably damaging	Het
Vmn2r78	A	T	7: 86,954,258 (GRCm38)	D548V	probably damaging	Het
Vwa3b	G	A	1: 37,045,031 (GRCm38)	R95Q	probably damaging	Het
Wdr6	G	A	9: 108,574,894 (GRCm38)	H597Y	probably benign	Het
Yme1l1	C	T	2: 23,194,762 (GRCm38)	T624I	probably damaging	Het

Other mutations in Trank1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00234:Trank1	APN	9	111,392,609 (GRCm38)	missense	probably damaging	1.00
IGL00467:Trank1	APN	9	111,364,666 (GRCm38)	splice site	probably benign
IGL00569:Trank1	APN	9	111,345,511 (GRCm38)	missense	possibly damaging	0.69
IGL00585:Trank1	APN	9	111,349,290 (GRCm38)	missense	possibly damaging	0.82
IGL01070:Trank1	APN	9	111,366,793 (GRCm38)	missense	probably damaging	1.00
IGL01134:Trank1	APN	9	111,391,781 (GRCm38)	missense	probably benign
IGL01154:Trank1	APN	9	111,386,400 (GRCm38)	missense	probably benign	0.00
IGL01355:Trank1	APN	9	111,365,520 (GRCm38)	missense	possibly damaging	0.94
IGL01407:Trank1	APN	9	111,364,722 (GRCm38)	missense	probably damaging	0.99
IGL01410:Trank1	APN	9	111,365,049 (GRCm38)	missense	probably benign	0.00
IGL01410:Trank1	APN	9	111,365,259 (GRCm38)	missense	probably benign	0.00
IGL01504:Trank1	APN	9	111,373,544 (GRCm38)	missense	probably damaging	1.00
IGL01744:Trank1	APN	9	111,349,363 (GRCm38)	missense	probably damaging	1.00
IGL02043:Trank1	APN	9	111,363,960 (GRCm38)	missense	probably damaging	0.98
IGL02104:Trank1	APN	9	111,390,712 (GRCm38)	missense	possibly damaging	0.85
IGL02193:Trank1	APN	9	111,367,276 (GRCm38)	missense	probably benign	0.43
IGL02581:Trank1	APN	9	111,383,125 (GRCm38)	missense	probably benign	0.00
IGL02630:Trank1	APN	9	111,373,075 (GRCm38)	missense	possibly damaging	0.70
IGL02839:Trank1	APN	9	111,364,756 (GRCm38)	missense	probably damaging	1.00
IGL02897:Trank1	APN	9	111,367,517 (GRCm38)	missense	probably damaging	0.99
IGL03065:Trank1	APN	9	111,390,293 (GRCm38)	missense	possibly damaging	0.64
IGL03123:Trank1	APN	9	111,367,407 (GRCm38)	missense	probably damaging	1.00
IGL03143:Trank1	APN	9	111,366,087 (GRCm38)	missense	probably damaging	1.00
IGL03323:Trank1	APN	9	111,352,116 (GRCm38)	missense	probably damaging	1.00
1mM(1):Trank1	UTSW	9	111,392,981 (GRCm38)	missense	probably damaging	1.00
PIT4486001:Trank1	UTSW	9	111,390,107 (GRCm38)	missense	probably damaging	1.00
PIT4812001:Trank1	UTSW	9	111,347,912 (GRCm38)	missense	probably damaging	1.00
R0035:Trank1	UTSW	9	111,366,776 (GRCm38)	missense	probably benign	0.00
R0064:Trank1	UTSW	9	111,343,195 (GRCm38)	missense	probably damaging	1.00
R0064:Trank1	UTSW	9	111,343,195 (GRCm38)	missense	probably damaging	1.00
R0089:Trank1	UTSW	9	111,392,910 (GRCm38)	missense	probably benign	0.00
R0207:Trank1	UTSW	9	111,366,253 (GRCm38)	missense	probably damaging	1.00
R0255:Trank1	UTSW	9	111,366,024 (GRCm38)	missense	possibly damaging	0.92
R0334:Trank1	UTSW	9	111,392,940 (GRCm38)	missense	probably damaging	1.00
R0334:Trank1	UTSW	9	111,365,353 (GRCm38)	missense	probably benign	0.00
R0383:Trank1	UTSW	9	111,391,477 (GRCm38)	missense	probably benign	0.08
R0421:Trank1	UTSW	9	111,391,839 (GRCm38)	missense	probably damaging	1.00
R0494:Trank1	UTSW	9	111,391,293 (GRCm38)	missense	probably benign	0.19
R0518:Trank1	UTSW	9	111,333,808 (GRCm38)	missense	probably damaging	1.00
R0560:Trank1	UTSW	9	111,391,086 (GRCm38)	missense	possibly damaging	0.88
R0637:Trank1	UTSW	9	111,390,441 (GRCm38)	missense	probably damaging	1.00
R0731:Trank1	UTSW	9	111,365,488 (GRCm38)	missense	probably damaging	1.00
R0761:Trank1	UTSW	9	111,366,613 (GRCm38)	missense	probably damaging	1.00
R0766:Trank1	UTSW	9	111,347,469 (GRCm38)	missense	probably benign	0.45
R0827:Trank1	UTSW	9	111,349,417 (GRCm38)	unclassified	probably benign
R1005:Trank1	UTSW	9	111,333,721 (GRCm38)	missense	probably benign	0.13
R1108:Trank1	UTSW	9	111,365,307 (GRCm38)	missense	probably benign	0.00
R1155:Trank1	UTSW	9	111,366,970 (GRCm38)	missense	possibly damaging	0.95
R1470:Trank1	UTSW	9	111,343,232 (GRCm38)	missense	possibly damaging	0.91
R1470:Trank1	UTSW	9	111,343,232 (GRCm38)	missense	possibly damaging	0.91
R1596:Trank1	UTSW	9	111,366,290 (GRCm38)	missense	possibly damaging	0.93
R1601:Trank1	UTSW	9	111,373,477 (GRCm38)	missense	probably damaging	1.00
R1751:Trank1	UTSW	9	111,391,479 (GRCm38)	missense	probably benign
R1754:Trank1	UTSW	9	111,392,871 (GRCm38)	missense	probably benign	0.00
R1767:Trank1	UTSW	9	111,391,479 (GRCm38)	missense	probably benign
R1768:Trank1	UTSW	9	111,392,927 (GRCm38)	missense	probably damaging	0.96
R1809:Trank1	UTSW	9	111,392,825 (GRCm38)	missense	probably benign	0.34
R1912:Trank1	UTSW	9	111,390,709 (GRCm38)	missense	probably benign	0.00
R1920:Trank1	UTSW	9	111,347,928 (GRCm38)	critical splice donor site	probably null
R1960:Trank1	UTSW	9	111,391,628 (GRCm38)	missense	probably damaging	1.00
R1993:Trank1	UTSW	9	111,378,832 (GRCm38)	missense	probably benign	0.20
R2012:Trank1	UTSW	9	111,365,028 (GRCm38)	missense	probably benign
R2025:Trank1	UTSW	9	111,392,039 (GRCm38)	missense	probably benign	0.01
R2050:Trank1	UTSW	9	111,364,788 (GRCm38)	missense	probably damaging	1.00
R2857:Trank1	UTSW	9	111,366,933 (GRCm38)	missense	probably benign	0.00
R2912:Trank1	UTSW	9	111,392,483 (GRCm38)	missense	probably damaging	0.98
R2962:Trank1	UTSW	9	111,352,080 (GRCm38)	missense	probably damaging	1.00
R3030:Trank1	UTSW	9	111,391,530 (GRCm38)	missense	possibly damaging	0.63
R3821:Trank1	UTSW	9	111,378,819 (GRCm38)	missense	probably damaging	1.00
R3822:Trank1	UTSW	9	111,378,819 (GRCm38)	missense	probably damaging	1.00
R3892:Trank1	UTSW	9	111,364,759 (GRCm38)	missense	probably benign	0.03
R4105:Trank1	UTSW	9	111,352,197 (GRCm38)	missense	probably damaging	1.00
R4166:Trank1	UTSW	9	111,373,524 (GRCm38)	nonsense	probably null
R4237:Trank1	UTSW	9	111,367,035 (GRCm38)	missense	probably benign	0.04
R4239:Trank1	UTSW	9	111,367,035 (GRCm38)	missense	probably benign	0.04
R4394:Trank1	UTSW	9	111,365,197 (GRCm38)	missense	possibly damaging	0.86
R4417:Trank1	UTSW	9	111,365,968 (GRCm38)	missense	probably benign	0.17
R4611:Trank1	UTSW	9	111,362,261 (GRCm38)	missense	probably damaging	1.00
R4694:Trank1	UTSW	9	111,392,061 (GRCm38)	missense	probably benign	0.40
R4731:Trank1	UTSW	9	111,390,410 (GRCm38)	missense	probably damaging	1.00
R4843:Trank1	UTSW	9	111,366,078 (GRCm38)	missense	probably benign	0.00
R4852:Trank1	UTSW	9	111,391,895 (GRCm38)	missense	possibly damaging	0.68
R4859:Trank1	UTSW	9	111,365,010 (GRCm38)	missense	probably benign	0.17
R4868:Trank1	UTSW	9	111,365,641 (GRCm38)	missense	probably damaging	1.00
R5080:Trank1	UTSW	9	111,389,221 (GRCm38)	missense	probably damaging	0.99
R5156:Trank1	UTSW	9	111,390,694 (GRCm38)	missense	probably damaging	1.00
R5174:Trank1	UTSW	9	111,365,559 (GRCm38)	missense	probably benign	0.00
R5234:Trank1	UTSW	9	111,386,467 (GRCm38)	missense	probably damaging	1.00
R5386:Trank1	UTSW	9	111,362,402 (GRCm38)	missense	probably benign	0.12
R5419:Trank1	UTSW	9	111,391,301 (GRCm38)	missense	probably damaging	1.00
R5435:Trank1	UTSW	9	111,391,890 (GRCm38)	missense	probably benign	0.00
R5444:Trank1	UTSW	9	111,392,958 (GRCm38)	missense	probably benign	0.04
R5543:Trank1	UTSW	9	111,366,112 (GRCm38)	missense	probably damaging	0.97
R5560:Trank1	UTSW	9	111,390,567 (GRCm38)	missense	probably damaging	1.00
R5772:Trank1	UTSW	9	111,366,676 (GRCm38)	missense	possibly damaging	0.86
R5774:Trank1	UTSW	9	111,391,226 (GRCm38)	missense	probably damaging	1.00
R5843:Trank1	UTSW	9	111,365,860 (GRCm38)	missense	possibly damaging	0.59
R5858:Trank1	UTSW	9	111,392,536 (GRCm38)	missense	probably benign
R5878:Trank1	UTSW	9	111,366,685 (GRCm38)	missense	possibly damaging	0.93
R5900:Trank1	UTSW	9	111,391,716 (GRCm38)	missense	probably damaging	1.00
R5917:Trank1	UTSW	9	111,362,417 (GRCm38)	missense	probably benign	0.38
R5954:Trank1	UTSW	9	111,365,133 (GRCm38)	missense	probably benign	0.13
R6041:Trank1	UTSW	9	111,377,796 (GRCm38)	missense	possibly damaging	0.94
R6112:Trank1	UTSW	9	111,391,737 (GRCm38)	missense	probably damaging	1.00
R6165:Trank1	UTSW	9	111,391,872 (GRCm38)	missense	probably benign	0.00
R6255:Trank1	UTSW	9	111,352,246 (GRCm38)	critical splice donor site	probably null
R6395:Trank1	UTSW	9	111,367,200 (GRCm38)	missense	probably damaging	1.00
R6567:Trank1	UTSW	9	111,347,521 (GRCm38)	missense	probably benign	0.02
R6644:Trank1	UTSW	9	111,364,834 (GRCm38)	missense	possibly damaging	0.85
R6788:Trank1	UTSW	9	111,390,679 (GRCm38)	missense	probably damaging	1.00
R6831:Trank1	UTSW	9	111,377,899 (GRCm38)	missense	probably benign	0.00
R6934:Trank1	UTSW	9	111,373,090 (GRCm38)	missense	probably damaging	0.99
R7127:Trank1	UTSW	9	111,365,796 (GRCm38)	missense	possibly damaging	0.85
R7206:Trank1	UTSW	9	111,345,515 (GRCm38)	critical splice donor site	probably null
R7236:Trank1	UTSW	9	111,373,074 (GRCm38)	missense	possibly damaging	0.93
R7247:Trank1	UTSW	9	111,367,512 (GRCm38)	missense	probably damaging	1.00
R7292:Trank1	UTSW	9	111,377,870 (GRCm38)	missense	probably benign	0.02
R7310:Trank1	UTSW	9	111,367,126 (GRCm38)	missense	probably damaging	1.00
R7431:Trank1	UTSW	9	111,362,402 (GRCm38)	missense	probably benign	0.12
R7448:Trank1	UTSW	9	111,366,349 (GRCm38)	missense	probably benign	0.01
R7477:Trank1	UTSW	9	111,364,957 (GRCm38)	missense	probably benign	0.00
R7514:Trank1	UTSW	9	111,364,756 (GRCm38)	missense	probably damaging	1.00
R7595:Trank1	UTSW	9	111,365,991 (GRCm38)	missense	probably damaging	1.00
R7637:Trank1	UTSW	9	111,365,296 (GRCm38)	missense	possibly damaging	0.71
R7648:Trank1	UTSW	9	111,391,685 (GRCm38)	missense	probably benign
R7737:Trank1	UTSW	9	111,366,012 (GRCm38)	nonsense	probably null
R7784:Trank1	UTSW	9	111,364,103 (GRCm38)	missense	probably damaging	1.00
R7884:Trank1	UTSW	9	111,392,516 (GRCm38)	missense	probably benign
R7912:Trank1	UTSW	9	111,391,528 (GRCm38)	missense	probably benign	0.04
R7938:Trank1	UTSW	9	111,365,028 (GRCm38)	missense	probably benign
R7979:Trank1	UTSW	9	111,377,899 (GRCm38)	missense	probably benign	0.00
R8064:Trank1	UTSW	9	111,352,076 (GRCm38)	nonsense	probably null
R8100:Trank1	UTSW	9	111,392,793 (GRCm38)	missense	probably damaging	1.00
R8124:Trank1	UTSW	9	111,378,927 (GRCm38)	missense	probably benign	0.31
R8198:Trank1	UTSW	9	111,390,812 (GRCm38)	missense	probably benign	0.09
R8219:Trank1	UTSW	9	111,364,909 (GRCm38)	missense	probably damaging	1.00
R8223:Trank1	UTSW	9	111,365,889 (GRCm38)	missense	probably damaging	1.00
R8316:Trank1	UTSW	9	111,349,302 (GRCm38)	missense	probably benign	0.38
R8347:Trank1	UTSW	9	111,367,249 (GRCm38)	missense	probably damaging	1.00
R8436:Trank1	UTSW	9	111,391,382 (GRCm38)	missense	possibly damaging	0.86
R8489:Trank1	UTSW	9	111,390,275 (GRCm38)	missense	probably benign	0.01
R8682:Trank1	UTSW	9	111,365,344 (GRCm38)	missense	probably benign	0.01
R8768:Trank1	UTSW	9	111,389,276 (GRCm38)	missense	probably benign	0.00
R8770:Trank1	UTSW	9	111,390,824 (GRCm38)	missense	probably benign	0.00
R8829:Trank1	UTSW	9	111,347,523 (GRCm38)	missense	probably benign
R8838:Trank1	UTSW	9	111,364,905 (GRCm38)	missense	probably benign	0.03
R8855:Trank1	UTSW	9	111,312,221 (GRCm38)	missense	unknown
R8929:Trank1	UTSW	9	111,378,935 (GRCm38)	missense	possibly damaging	0.93
R9047:Trank1	UTSW	9	111,362,432 (GRCm38)	missense	probably damaging	0.99
R9090:Trank1	UTSW	9	111,345,479 (GRCm38)	missense	probably damaging	1.00
R9114:Trank1	UTSW	9	111,333,775 (GRCm38)	missense	probably damaging	1.00
R9133:Trank1	UTSW	9	111,391,702 (GRCm38)	missense	possibly damaging	0.93
R9177:Trank1	UTSW	9	111,392,511 (GRCm38)	missense	probably benign	0.00
R9178:Trank1	UTSW	9	111,367,200 (GRCm38)	missense	probably damaging	1.00
R9271:Trank1	UTSW	9	111,345,479 (GRCm38)	missense	probably damaging	1.00
R9314:Trank1	UTSW	9	111,365,981 (GRCm38)	missense	probably damaging	1.00
R9373:Trank1	UTSW	9	111,365,191 (GRCm38)	missense	probably benign	0.25
R9380:Trank1	UTSW	9	111,392,670 (GRCm38)	missense	probably benign	0.07
R9435:Trank1	UTSW	9	111,364,822 (GRCm38)	missense	probably benign	0.04
R9501:Trank1	UTSW	9	111,347,875 (GRCm38)	missense	probably benign	0.00
R9593:Trank1	UTSW	9	111,362,297 (GRCm38)	missense	probably benign	0.30
R9601:Trank1	UTSW	9	111,373,125 (GRCm38)	missense	probably benign	0.18
R9729:Trank1	UTSW	9	111,391,469 (GRCm38)	missense	probably damaging	1.00
X0064:Trank1	UTSW	9	111,343,236 (GRCm38)	missense	possibly damaging	0.57
Z1088:Trank1	UTSW	9	111,364,710 (GRCm38)	missense	probably damaging	0.99
Z1177:Trank1	UTSW	9	111,392,870 (GRCm38)	missense	possibly damaging	0.47
Z1177:Trank1	UTSW	9	111,367,377 (GRCm38)	missense	possibly damaging	0.83
Z1177:Trank1	UTSW	9	111,311,902 (GRCm38)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- GAGCTTGCCATCGACTTCTC -3'
(R):5'- TGGTACTGAAGCTGTGGAACTTC -3'

Sequencing Primer
(F):5'- CTCGGTGCAGTGAGAACTCTGAG -3'
(R):5'- AAGCTGTGGAACTTCATGATGC -3'

Posted On

2018-08-01