Mutagenetix > Incidental Mutation

Incidental Mutation 'R5878:Trank1'

455663

Institutional Source

Beutler Lab

Gene Symbol

Trank1

Ensembl Gene

ENSMUSG00000062296

Gene Name

tetratricopeptide repeat and ankyrin repeat containing 1

Synonyms

LOC235639, C030048J01Rik, A230061D21Rik, Lba1

MMRRC Submission

044084-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5878 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

111140807-111224843 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 111195753 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 1259 (V1259A)

Ref Sequence

ENSEMBL: ENSMUSP00000077697 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000078626
AA Change: V1259A

PolyPhen 2 Score 0.932 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000077697
Gene: ENSMUSG00000062296
AA Change: V1259A

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: 97.9%
20x: 93.7%

Validation Efficiency

99% (66/67)

Allele List at MGI

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

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca12	A	T	1: 71,385,792 (GRCm39)	N275K	possibly damaging	Het
Abhd6	G	A	14: 8,028,286 (GRCm38)	V6I	probably benign	Het
Afap1l2	T	C	19: 56,904,107 (GRCm39)	T727A	probably benign	Het
Aggf1	T	C	13: 95,506,065 (GRCm39)	E174G	probably benign	Het
Ahnak	T	G	19: 8,985,706 (GRCm39)	L2330R	probably damaging	Het
Arb2a	T	A	13: 78,100,186 (GRCm39)	V129E	probably damaging	Het
Arfgef2	A	G	2: 166,712,137 (GRCm39)	T1205A	probably benign	Het
Ccdc3	T	C	2: 5,233,827 (GRCm39)	L217P	probably benign	Het
Cfap54	T	C	10: 92,800,423 (GRCm39)	D1595G	probably benign	Het
Cps1	G	T	1: 67,197,037 (GRCm39)		probably null	Het
Fam120b	A	G	17: 15,622,502 (GRCm39)	D160G	probably damaging	Het
Fezf1	C	A	6: 23,247,580 (GRCm39)	R165L	possibly damaging	Het
Fkbp15	A	T	4: 62,225,145 (GRCm39)	L838H	probably benign	Het
Frmd3	G	A	4: 74,071,847 (GRCm39)	G243D	probably damaging	Het
Gldc	A	T	19: 30,120,867 (GRCm39)		probably null	Het
Gm10188	T	C	1: 132,156,940 (GRCm39)		probably benign	Het
Gm5190	T	A	12: 113,360,859 (GRCm39)		noncoding transcript	Het
Gria1	T	C	11: 57,208,628 (GRCm39)		probably null	Het
Hdhd5	A	G	6: 120,491,485 (GRCm39)	L206P	probably damaging	Het
Herc2	A	G	7: 55,773,996 (GRCm39)	N1149S	probably benign	Het
Inca1	G	A	11: 70,586,808 (GRCm39)		probably benign	Het
Iqch	G	A	9: 63,455,272 (GRCm39)	S175F	probably damaging	Het
Itpr3	T	G	17: 27,329,836 (GRCm39)	D1543E	probably benign	Het
Khk	T	A	5: 31,088,219 (GRCm39)		probably null	Het
Kiz	C	T	2: 146,731,521 (GRCm39)	S337L	probably damaging	Het
Lzts3	G	A	2: 130,478,459 (GRCm39)	T213I	probably damaging	Het
Mab21l2	T	A	3: 86,454,025 (GRCm39)	D325V	probably damaging	Het
Mctp2	A	G	7: 71,863,856 (GRCm39)	S336P	probably benign	Het
Me3	T	A	7: 89,497,214 (GRCm39)	L405Q	probably benign	Het
Mgst2	A	T	3: 51,568,651 (GRCm39)		probably benign	Het
Myh2	A	G	11: 67,083,330 (GRCm39)	E1431G	probably damaging	Het
Naip6	A	G	13: 100,436,181 (GRCm39)	S781P	probably damaging	Het
Nr3c2	A	G	8: 77,634,897 (GRCm39)		probably null	Het
Or10ab5	A	T	7: 108,244,946 (GRCm39)	L279Q	probably damaging	Het
Or6s1	A	G	14: 51,308,449 (GRCm39)	Y134H	probably damaging	Het
Or6x1	C	T	9: 40,098,867 (GRCm39)	T152I	probably benign	Het
Otop1	G	T	5: 38,435,166 (GRCm39)	R132L	possibly damaging	Het
Parg	T	A	14: 31,939,619 (GRCm39)	D548E	possibly damaging	Het
Pcdhga4	G	T	18: 37,820,739 (GRCm39)	G763W	probably benign	Het
Pde10a	A	G	17: 9,168,204 (GRCm39)	N9S	possibly damaging	Het
Pi4k2a	T	C	19: 42,089,080 (GRCm39)	I147T	probably benign	Het
Polh	T	A	17: 46,505,251 (GRCm39)	T122S	probably damaging	Het
Ptpn13	T	C	5: 103,624,984 (GRCm39)	V96A	possibly damaging	Het
Ptpn6	C	A	6: 124,705,748 (GRCm39)	C132F	probably damaging	Het
Rbm19	T	A	5: 120,270,932 (GRCm39)	V585E	probably damaging	Het
Relch	T	A	1: 105,620,685 (GRCm39)	S387T	probably benign	Het
Rp1l1	C	T	14: 64,266,355 (GRCm39)	P647L	probably benign	Het
Rrp1b	A	G	17: 32,266,649 (GRCm39)	E72G	probably damaging	Het
Shcbp1	A	T	8: 4,798,742 (GRCm39)	H392Q	probably benign	Het
Skic2	C	T	17: 35,065,093 (GRCm39)	R371Q	possibly damaging	Het
Slc13a5	G	A	11: 72,144,217 (GRCm39)	T287I	possibly damaging	Het
Slc22a27	T	A	19: 7,904,122 (GRCm39)	E5V	probably benign	Het
Slc38a2	A	G	15: 96,590,465 (GRCm39)	V293A	probably damaging	Het
Slco6d1	T	A	1: 98,391,561 (GRCm39)		probably benign	Het
Sri	G	C	5: 8,109,353 (GRCm39)	D46H	probably damaging	Het
Tango6	A	G	8: 107,415,800 (GRCm39)	D207G	possibly damaging	Het
Tigd4	T	C	3: 84,501,749 (GRCm39)	M222T	probably benign	Het
Tmem229a	T	C	6: 24,955,172 (GRCm39)	D194G	probably benign	Het
Trdv5	T	C	14: 54,386,255 (GRCm39)	D70G	probably benign	Het
Trim52	T	A	14: 106,344,375 (GRCm39)	M11K	probably damaging	Het
Wdr62	A	G	7: 29,940,772 (GRCm39)	M882T	probably benign	Het
Ybx3	A	G	6: 131,344,726 (GRCm39)		probably null	Het
Zfand2b	A	G	1: 75,147,154 (GRCm39)		probably benign	Het
Zfp91	T	A	19: 12,747,684 (GRCm39)	T480S	possibly damaging	Het

Other mutations in Trank1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00234:Trank1	APN	9	111,221,677 (GRCm39)	missense	probably damaging	1.00
IGL00467:Trank1	APN	9	111,193,734 (GRCm39)	splice site	probably benign
IGL00569:Trank1	APN	9	111,174,579 (GRCm39)	missense	possibly damaging	0.69
IGL00585:Trank1	APN	9	111,178,358 (GRCm39)	missense	possibly damaging	0.82
IGL01070:Trank1	APN	9	111,195,861 (GRCm39)	missense	probably damaging	1.00
IGL01134:Trank1	APN	9	111,220,849 (GRCm39)	missense	probably benign
IGL01154:Trank1	APN	9	111,215,468 (GRCm39)	missense	probably benign	0.00
IGL01355:Trank1	APN	9	111,194,588 (GRCm39)	missense	possibly damaging	0.94
IGL01407:Trank1	APN	9	111,193,790 (GRCm39)	missense	probably damaging	0.99
IGL01410:Trank1	APN	9	111,194,117 (GRCm39)	missense	probably benign	0.00
IGL01410:Trank1	APN	9	111,194,327 (GRCm39)	missense	probably benign	0.00
IGL01504:Trank1	APN	9	111,202,612 (GRCm39)	missense	probably damaging	1.00
IGL01744:Trank1	APN	9	111,178,431 (GRCm39)	missense	probably damaging	1.00
IGL02043:Trank1	APN	9	111,193,028 (GRCm39)	missense	probably damaging	0.98
IGL02104:Trank1	APN	9	111,219,780 (GRCm39)	missense	possibly damaging	0.85
IGL02193:Trank1	APN	9	111,196,344 (GRCm39)	missense	probably benign	0.43
IGL02581:Trank1	APN	9	111,212,193 (GRCm39)	missense	probably benign	0.00
IGL02630:Trank1	APN	9	111,202,143 (GRCm39)	missense	possibly damaging	0.70
IGL02839:Trank1	APN	9	111,193,824 (GRCm39)	missense	probably damaging	1.00
IGL02897:Trank1	APN	9	111,196,585 (GRCm39)	missense	probably damaging	0.99
IGL03065:Trank1	APN	9	111,219,361 (GRCm39)	missense	possibly damaging	0.64
IGL03123:Trank1	APN	9	111,196,475 (GRCm39)	missense	probably damaging	1.00
IGL03143:Trank1	APN	9	111,195,155 (GRCm39)	missense	probably damaging	1.00
IGL03323:Trank1	APN	9	111,181,184 (GRCm39)	missense	probably damaging	1.00
1mM(1):Trank1	UTSW	9	111,222,049 (GRCm39)	missense	probably damaging	1.00
PIT4486001:Trank1	UTSW	9	111,219,175 (GRCm39)	missense	probably damaging	1.00
PIT4812001:Trank1	UTSW	9	111,176,980 (GRCm39)	missense	probably damaging	1.00
R0035:Trank1	UTSW	9	111,195,844 (GRCm39)	missense	probably benign	0.00
R0064:Trank1	UTSW	9	111,172,263 (GRCm39)	missense	probably damaging	1.00
R0064:Trank1	UTSW	9	111,172,263 (GRCm39)	missense	probably damaging	1.00
R0089:Trank1	UTSW	9	111,221,978 (GRCm39)	missense	probably benign	0.00
R0207:Trank1	UTSW	9	111,195,321 (GRCm39)	missense	probably damaging	1.00
R0255:Trank1	UTSW	9	111,195,092 (GRCm39)	missense	possibly damaging	0.92
R0334:Trank1	UTSW	9	111,222,008 (GRCm39)	missense	probably damaging	1.00
R0334:Trank1	UTSW	9	111,194,421 (GRCm39)	missense	probably benign	0.00
R0383:Trank1	UTSW	9	111,220,545 (GRCm39)	missense	probably benign	0.08
R0421:Trank1	UTSW	9	111,220,907 (GRCm39)	missense	probably damaging	1.00
R0494:Trank1	UTSW	9	111,220,361 (GRCm39)	missense	probably benign	0.19
R0518:Trank1	UTSW	9	111,162,876 (GRCm39)	missense	probably damaging	1.00
R0560:Trank1	UTSW	9	111,220,154 (GRCm39)	missense	possibly damaging	0.88
R0637:Trank1	UTSW	9	111,219,509 (GRCm39)	missense	probably damaging	1.00
R0731:Trank1	UTSW	9	111,194,556 (GRCm39)	missense	probably damaging	1.00
R0761:Trank1	UTSW	9	111,195,681 (GRCm39)	missense	probably damaging	1.00
R0766:Trank1	UTSW	9	111,176,537 (GRCm39)	missense	probably benign	0.45
R0827:Trank1	UTSW	9	111,178,485 (GRCm39)	unclassified	probably benign
R1005:Trank1	UTSW	9	111,162,789 (GRCm39)	missense	probably benign	0.13
R1108:Trank1	UTSW	9	111,194,375 (GRCm39)	missense	probably benign	0.00
R1155:Trank1	UTSW	9	111,196,038 (GRCm39)	missense	possibly damaging	0.95
R1470:Trank1	UTSW	9	111,172,300 (GRCm39)	missense	possibly damaging	0.91
R1470:Trank1	UTSW	9	111,172,300 (GRCm39)	missense	possibly damaging	0.91
R1596:Trank1	UTSW	9	111,195,358 (GRCm39)	missense	possibly damaging	0.93
R1601:Trank1	UTSW	9	111,202,545 (GRCm39)	missense	probably damaging	1.00
R1751:Trank1	UTSW	9	111,220,547 (GRCm39)	missense	probably benign
R1754:Trank1	UTSW	9	111,221,939 (GRCm39)	missense	probably benign	0.00
R1767:Trank1	UTSW	9	111,220,547 (GRCm39)	missense	probably benign
R1768:Trank1	UTSW	9	111,221,995 (GRCm39)	missense	probably damaging	0.96
R1809:Trank1	UTSW	9	111,221,893 (GRCm39)	missense	probably benign	0.34
R1912:Trank1	UTSW	9	111,219,777 (GRCm39)	missense	probably benign	0.00
R1920:Trank1	UTSW	9	111,176,996 (GRCm39)	critical splice donor site	probably null
R1960:Trank1	UTSW	9	111,220,696 (GRCm39)	missense	probably damaging	1.00
R1993:Trank1	UTSW	9	111,207,900 (GRCm39)	missense	probably benign	0.20
R2012:Trank1	UTSW	9	111,194,096 (GRCm39)	missense	probably benign
R2025:Trank1	UTSW	9	111,221,107 (GRCm39)	missense	probably benign	0.01
R2050:Trank1	UTSW	9	111,193,856 (GRCm39)	missense	probably damaging	1.00
R2857:Trank1	UTSW	9	111,196,001 (GRCm39)	missense	probably benign	0.00
R2912:Trank1	UTSW	9	111,221,551 (GRCm39)	missense	probably damaging	0.98
R2962:Trank1	UTSW	9	111,181,148 (GRCm39)	missense	probably damaging	1.00
R3030:Trank1	UTSW	9	111,220,598 (GRCm39)	missense	possibly damaging	0.63
R3821:Trank1	UTSW	9	111,207,887 (GRCm39)	missense	probably damaging	1.00
R3822:Trank1	UTSW	9	111,207,887 (GRCm39)	missense	probably damaging	1.00
R3892:Trank1	UTSW	9	111,193,827 (GRCm39)	missense	probably benign	0.03
R4105:Trank1	UTSW	9	111,181,265 (GRCm39)	missense	probably damaging	1.00
R4166:Trank1	UTSW	9	111,202,592 (GRCm39)	nonsense	probably null
R4237:Trank1	UTSW	9	111,196,103 (GRCm39)	missense	probably benign	0.04
R4239:Trank1	UTSW	9	111,196,103 (GRCm39)	missense	probably benign	0.04
R4394:Trank1	UTSW	9	111,194,265 (GRCm39)	missense	possibly damaging	0.86
R4417:Trank1	UTSW	9	111,195,036 (GRCm39)	missense	probably benign	0.17
R4611:Trank1	UTSW	9	111,191,329 (GRCm39)	missense	probably damaging	1.00
R4694:Trank1	UTSW	9	111,221,129 (GRCm39)	missense	probably benign	0.40
R4731:Trank1	UTSW	9	111,219,478 (GRCm39)	missense	probably damaging	1.00
R4843:Trank1	UTSW	9	111,195,146 (GRCm39)	missense	probably benign	0.00
R4852:Trank1	UTSW	9	111,220,963 (GRCm39)	missense	possibly damaging	0.68
R4859:Trank1	UTSW	9	111,194,078 (GRCm39)	missense	probably benign	0.17
R4868:Trank1	UTSW	9	111,194,709 (GRCm39)	missense	probably damaging	1.00
R5080:Trank1	UTSW	9	111,218,289 (GRCm39)	missense	probably damaging	0.99
R5156:Trank1	UTSW	9	111,219,762 (GRCm39)	missense	probably damaging	1.00
R5174:Trank1	UTSW	9	111,194,627 (GRCm39)	missense	probably benign	0.00
R5234:Trank1	UTSW	9	111,215,535 (GRCm39)	missense	probably damaging	1.00
R5386:Trank1	UTSW	9	111,191,470 (GRCm39)	missense	probably benign	0.12
R5419:Trank1	UTSW	9	111,220,369 (GRCm39)	missense	probably damaging	1.00
R5435:Trank1	UTSW	9	111,220,958 (GRCm39)	missense	probably benign	0.00
R5444:Trank1	UTSW	9	111,222,026 (GRCm39)	missense	probably benign	0.04
R5543:Trank1	UTSW	9	111,195,180 (GRCm39)	missense	probably damaging	0.97
R5560:Trank1	UTSW	9	111,219,635 (GRCm39)	missense	probably damaging	1.00
R5772:Trank1	UTSW	9	111,195,744 (GRCm39)	missense	possibly damaging	0.86
R5774:Trank1	UTSW	9	111,220,294 (GRCm39)	missense	probably damaging	1.00
R5843:Trank1	UTSW	9	111,194,928 (GRCm39)	missense	possibly damaging	0.59
R5858:Trank1	UTSW	9	111,221,604 (GRCm39)	missense	probably benign
R5900:Trank1	UTSW	9	111,220,784 (GRCm39)	missense	probably damaging	1.00
R5917:Trank1	UTSW	9	111,191,485 (GRCm39)	missense	probably benign	0.38
R5954:Trank1	UTSW	9	111,194,201 (GRCm39)	missense	probably benign	0.13
R6041:Trank1	UTSW	9	111,206,864 (GRCm39)	missense	possibly damaging	0.94
R6112:Trank1	UTSW	9	111,220,805 (GRCm39)	missense	probably damaging	1.00
R6165:Trank1	UTSW	9	111,220,940 (GRCm39)	missense	probably benign	0.00
R6255:Trank1	UTSW	9	111,181,314 (GRCm39)	critical splice donor site	probably null
R6395:Trank1	UTSW	9	111,196,268 (GRCm39)	missense	probably damaging	1.00
R6567:Trank1	UTSW	9	111,176,589 (GRCm39)	missense	probably benign	0.02
R6644:Trank1	UTSW	9	111,193,902 (GRCm39)	missense	possibly damaging	0.85
R6724:Trank1	UTSW	9	111,194,984 (GRCm39)	missense	probably damaging	1.00
R6788:Trank1	UTSW	9	111,219,747 (GRCm39)	missense	probably damaging	1.00
R6831:Trank1	UTSW	9	111,206,967 (GRCm39)	missense	probably benign	0.00
R6934:Trank1	UTSW	9	111,202,158 (GRCm39)	missense	probably damaging	0.99
R7127:Trank1	UTSW	9	111,194,864 (GRCm39)	missense	possibly damaging	0.85
R7206:Trank1	UTSW	9	111,174,583 (GRCm39)	critical splice donor site	probably null
R7236:Trank1	UTSW	9	111,202,142 (GRCm39)	missense	possibly damaging	0.93
R7247:Trank1	UTSW	9	111,196,580 (GRCm39)	missense	probably damaging	1.00
R7292:Trank1	UTSW	9	111,206,938 (GRCm39)	missense	probably benign	0.02
R7310:Trank1	UTSW	9	111,196,194 (GRCm39)	missense	probably damaging	1.00
R7431:Trank1	UTSW	9	111,191,470 (GRCm39)	missense	probably benign	0.12
R7448:Trank1	UTSW	9	111,195,417 (GRCm39)	missense	probably benign	0.01
R7477:Trank1	UTSW	9	111,194,025 (GRCm39)	missense	probably benign	0.00
R7514:Trank1	UTSW	9	111,193,824 (GRCm39)	missense	probably damaging	1.00
R7595:Trank1	UTSW	9	111,195,059 (GRCm39)	missense	probably damaging	1.00
R7637:Trank1	UTSW	9	111,194,364 (GRCm39)	missense	possibly damaging	0.71
R7648:Trank1	UTSW	9	111,220,753 (GRCm39)	missense	probably benign
R7737:Trank1	UTSW	9	111,195,080 (GRCm39)	nonsense	probably null
R7784:Trank1	UTSW	9	111,193,171 (GRCm39)	missense	probably damaging	1.00
R7884:Trank1	UTSW	9	111,221,584 (GRCm39)	missense	probably benign
R7912:Trank1	UTSW	9	111,220,596 (GRCm39)	missense	probably benign	0.04
R7938:Trank1	UTSW	9	111,194,096 (GRCm39)	missense	probably benign
R7979:Trank1	UTSW	9	111,206,967 (GRCm39)	missense	probably benign	0.00
R8064:Trank1	UTSW	9	111,181,144 (GRCm39)	nonsense	probably null
R8100:Trank1	UTSW	9	111,221,861 (GRCm39)	missense	probably damaging	1.00
R8124:Trank1	UTSW	9	111,207,995 (GRCm39)	missense	probably benign	0.31
R8198:Trank1	UTSW	9	111,219,880 (GRCm39)	missense	probably benign	0.09
R8219:Trank1	UTSW	9	111,193,977 (GRCm39)	missense	probably damaging	1.00
R8223:Trank1	UTSW	9	111,194,957 (GRCm39)	missense	probably damaging	1.00
R8316:Trank1	UTSW	9	111,178,370 (GRCm39)	missense	probably benign	0.38
R8347:Trank1	UTSW	9	111,196,317 (GRCm39)	missense	probably damaging	1.00
R8436:Trank1	UTSW	9	111,220,450 (GRCm39)	missense	possibly damaging	0.86
R8489:Trank1	UTSW	9	111,219,343 (GRCm39)	missense	probably benign	0.01
R8682:Trank1	UTSW	9	111,194,412 (GRCm39)	missense	probably benign	0.01
R8768:Trank1	UTSW	9	111,218,344 (GRCm39)	missense	probably benign	0.00
R8770:Trank1	UTSW	9	111,219,892 (GRCm39)	missense	probably benign	0.00
R8829:Trank1	UTSW	9	111,176,591 (GRCm39)	missense	probably benign
R8838:Trank1	UTSW	9	111,193,973 (GRCm39)	missense	probably benign	0.03
R8855:Trank1	UTSW	9	111,141,289 (GRCm39)	missense	unknown
R8929:Trank1	UTSW	9	111,208,003 (GRCm39)	missense	possibly damaging	0.93
R9047:Trank1	UTSW	9	111,191,500 (GRCm39)	missense	probably damaging	0.99
R9090:Trank1	UTSW	9	111,174,547 (GRCm39)	missense	probably damaging	1.00
R9114:Trank1	UTSW	9	111,162,843 (GRCm39)	missense	probably damaging	1.00
R9133:Trank1	UTSW	9	111,220,770 (GRCm39)	missense	possibly damaging	0.93
R9177:Trank1	UTSW	9	111,221,579 (GRCm39)	missense	probably benign	0.00
R9178:Trank1	UTSW	9	111,196,268 (GRCm39)	missense	probably damaging	1.00
R9271:Trank1	UTSW	9	111,174,547 (GRCm39)	missense	probably damaging	1.00
R9314:Trank1	UTSW	9	111,195,049 (GRCm39)	missense	probably damaging	1.00
R9373:Trank1	UTSW	9	111,194,259 (GRCm39)	missense	probably benign	0.25
R9380:Trank1	UTSW	9	111,221,738 (GRCm39)	missense	probably benign	0.07
R9435:Trank1	UTSW	9	111,193,890 (GRCm39)	missense	probably benign	0.04
R9501:Trank1	UTSW	9	111,176,943 (GRCm39)	missense	probably benign	0.00
R9593:Trank1	UTSW	9	111,191,365 (GRCm39)	missense	probably benign	0.30
R9601:Trank1	UTSW	9	111,202,193 (GRCm39)	missense	probably benign	0.18
R9729:Trank1	UTSW	9	111,220,537 (GRCm39)	missense	probably damaging	1.00
X0064:Trank1	UTSW	9	111,172,304 (GRCm39)	missense	possibly damaging	0.57
Z1088:Trank1	UTSW	9	111,193,778 (GRCm39)	missense	probably damaging	0.99
Z1177:Trank1	UTSW	9	111,221,938 (GRCm39)	missense	possibly damaging	0.47
Z1177:Trank1	UTSW	9	111,196,445 (GRCm39)	missense	possibly damaging	0.83
Z1177:Trank1	UTSW	9	111,140,970 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- CCATCAAAGTGGAAACGGTG -3'
(R):5'- CAGCTGGGGATGCTAAACTC -3'

Sequencing Primer
(F):5'- TGTGCAGGAGGAGCCAC -3'
(R):5'- GATGCTAAACTCTTCCTGTGTGGAC -3'

Posted On

2017-02-10