Mutagenetix > Incidental Mutation

Incidental Mutation 'R7514:Trank1'

582318

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

045587-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7514 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

111311739-111395775 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 111364756 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 616 (N616S)

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: N616S

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

SMART Domains

Protein: ENSMUSP00000077697
Gene: ENSMUSG00000062296
AA Change: N616S

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: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

Allele List at MGI

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

Other mutations in this stock

Total: 103 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933427D14Rik	A	G	11: 72,195,802 (GRCm38)	L261P	probably damaging	Het
A4gnt	A	G	9: 99,620,545 (GRCm38)	I253V	probably benign	Het
AAdacl4fm3	A	T	4: 144,703,228 (GRCm38)	V397D	possibly damaging	Het
Acap2	A	T	16: 31,154,567 (GRCm38)		probably null	Het
Adora2b	G	T	11: 62,265,320 (GRCm38)	M198I	probably damaging	Het
Akap5	C	A	12: 76,328,529 (GRCm38)	T245K	probably benign	Het
Aldh1a2	T	C	9: 71,284,963 (GRCm38)	I399T	probably damaging	Het
Ank2	G	A	3: 127,025,603 (GRCm38)	S473L	probably benign	Het
Anln	A	T	9: 22,360,857 (GRCm38)	D655E	probably damaging	Het
Arhgef10	T	C	8: 14,975,956 (GRCm38)	V820A	probably benign	Het
Arid1b	A	G	17: 5,341,714 (GRCm38)	K1787E	probably benign	Het
Art4	T	C	6: 136,854,741 (GRCm38)	H134R	probably benign	Het
Borcs6	G	A	11: 69,060,584 (GRCm38)	V263M	probably damaging	Het
C8a	A	T	4: 104,846,050 (GRCm38)	M314K	possibly damaging	Het
Cbfa2t3	T	G	8: 122,635,126 (GRCm38)	M386L	probably damaging	Het
Ccdc170	T	A	10: 4,546,839 (GRCm38)	V459E	probably benign	Het
Cdh4	T	A	2: 179,890,843 (GRCm38)	N699K	possibly damaging	Het
Cdk12	T	C	11: 98,222,658 (GRCm38)	L756P	unknown	Het
Chsy1	A	G	7: 66,172,120 (GRCm38)	D701G	probably damaging	Het
Cnot9	A	G	1: 74,528,762 (GRCm38)	T270A	probably benign	Het
Crat	C	T	2: 30,404,565 (GRCm38)	R497Q	probably benign	Het
Cyb5r1	A	G	1: 134,410,530 (GRCm38)	E228G	probably damaging	Het
D630003M21Rik	A	G	2: 158,217,353 (GRCm38)	L209P	probably damaging	Het
Dennd2c	T	A	3: 103,163,062 (GRCm38)	D791E	probably benign	Het
Dnah14	T	C	1: 181,628,067 (GRCm38)	I919T	probably damaging	Het
Dpp8	T	C	9: 65,078,754 (GRCm38)	L842S	probably damaging	Het
Ern1	A	G	11: 106,409,893 (GRCm38)		probably null	Het
Exo1	T	C	1: 175,906,666 (GRCm38)		probably null	Het
Fam161b	T	G	12: 84,357,738 (GRCm38)	E56A	possibly damaging	Het
Fbrsl1	T	C	5: 110,432,933 (GRCm38)	T153A	probably benign	Het
Fcgr3	T	G	1: 171,059,343 (GRCm38)	D4A	probably benign	Het
Gltp	C	T	5: 114,670,460 (GRCm38)	A193T	probably benign	Het
Gm10031	A	G	1: 156,524,754 (GRCm38)	D175G	probably benign	Het
Gm3159	A	T	14: 4,399,690 (GRCm38)	S142C	probably damaging	Het
Gphn	T	C	12: 78,626,165 (GRCm38)	V485A	probably damaging	Het
Grik2	A	T	10: 49,523,808 (GRCm38)	N275K	probably damaging	Het
Gstt3	G	T	10: 75,776,791 (GRCm38)	Q102K	probably damaging	Het
Hivep3	T	A	4: 120,096,855 (GRCm38)	F789L	possibly damaging	Het
Ing5	A	G	1: 93,816,442 (GRCm38)	N157D	possibly damaging	Het
Itga3	C	T	11: 95,065,896 (GRCm38)	W177*	probably null	Het
Jag2	T	C	12: 112,929,052 (GRCm38)	T83A	probably benign	Het
Krt90	G	A	15: 101,553,170 (GRCm38)	T532I	unknown	Het
Lcn2	A	G	2: 32,387,849 (GRCm38)		probably null	Het
Lrig2	A	G	3: 104,465,760 (GRCm38)	S602P	probably damaging	Het
Lsm1	A	C	8: 25,792,209 (GRCm38)	R33S	probably damaging	Het
Mast4	A	T	13: 102,787,426 (GRCm38)	Y492*	probably null	Het
Mcm3	A	T	1: 20,805,896 (GRCm38)	L658Q	probably benign	Het
Myh4	G	A	11: 67,243,322 (GRCm38)		probably null	Het
Nck2	T	C	1: 43,569,221 (GRCm38)	V341A	probably benign	Het
Nucb1	T	C	7: 45,501,718 (GRCm38)		probably null	Het
Nup210l	G	C	3: 90,210,459 (GRCm38)		probably null	Het
Or1j1	A	G	2: 36,812,639 (GRCm38)	I151T	probably benign	Het
Or5al5	A	T	2: 86,131,628 (GRCm38)	F12I	probably damaging	Het
Or7g22	A	T	9: 19,137,865 (GRCm38)	S291C	possibly damaging	Het
Or8b48	T	A	9: 38,582,051 (GRCm38)	M258K	probably damaging	Het
Or8b54	G	A	9: 38,775,678 (GRCm38)	C141Y	probably damaging	Het
Pla2g4a	G	A	1: 149,851,362 (GRCm38)	P556S	probably damaging	Het
Plat	T	C	8: 22,775,642 (GRCm38)	C234R	probably damaging	Het
Ppfia1	T	C	7: 144,517,713 (GRCm38)	I321V	probably benign	Het
Prrc1	T	A	18: 57,363,253 (GRCm38)	V92E	probably benign	Het
Prss3	A	G	6: 41,373,914 (GRCm38)	V214A	probably damaging	Het
Ptprg	G	T	14: 12,179,342 (GRCm38)	K786N	possibly damaging	Het
Rabgap1	G	T	2: 37,537,342 (GRCm38)	G645V	probably damaging	Het
Rfx4	T	C	10: 84,880,226 (GRCm38)	S470P	probably damaging	Het
Rin3	C	T	12: 102,369,650 (GRCm38)	Q607*	probably null	Het
Sema3a	A	G	5: 13,523,126 (GRCm38)	H207R	probably benign	Het
Serpinb12	G	A	1: 106,950,804 (GRCm38)	E181K	probably damaging	Het
Serpinb6c	G	A	13: 33,897,403 (GRCm38)	Q88*	probably null	Het
Shmt1	A	C	11: 60,801,986 (GRCm38)	C90W	probably damaging	Het
Slc16a13	C	T	11: 70,218,884 (GRCm38)	V264M	probably damaging	Het
Slc17a8	G	T	10: 89,592,107 (GRCm38)	P286Q	probably damaging	Het
Slc27a6	C	T	18: 58,612,221 (GRCm38)	Q576*	probably null	Het
Slc30a9	T	C	5: 67,348,078 (GRCm38)	S470P	possibly damaging	Het
Slc44a2	G	T	9: 21,342,472 (GRCm38)	K136N	possibly damaging	Het
Smarca5	A	T	8: 80,717,534 (GRCm38)	H534Q	probably damaging	Het
Son	T	G	16: 91,654,860 (GRCm38)	L165R	probably damaging	Het
Sox10	G	A	15: 79,156,221 (GRCm38)	P373L	probably benign	Het
Sp100	C	T	1: 85,681,139 (GRCm38)	R330*	probably null	Het
Srrm4	A	G	5: 116,446,511 (GRCm38)	L500P	probably damaging	Het
Tap1	T	C	17: 34,196,665 (GRCm38)	L689P	probably damaging	Het
Tfg	A	G	16: 56,705,609 (GRCm38)		probably null	Het
Tjp2	C	T	19: 24,111,522 (GRCm38)	V677I	probably benign	Het
Tmprss11g	T	G	5: 86,497,317 (GRCm38)	D85A	probably damaging	Het
Tnfsf9	T	C	17: 57,107,238 (GRCm38)	S222P	probably damaging	Het
Tubgcp6	C	A	15: 89,120,525 (GRCm38)	W297L	probably damaging	Het
Twist1	T	C	12: 33,958,356 (GRCm38)	S127P	probably damaging	Het
Ubr4	T	C	4: 139,452,655 (GRCm38)	I247T	unknown	Het
Ubr5	G	A	15: 37,988,237 (GRCm38)	T2153M		Het
Utrn	A	G	10: 12,698,089 (GRCm38)	V1079A	probably benign	Het
Vcan	T	C	13: 89,704,118 (GRCm38)	T908A	probably damaging	Het
Vmn2r104	A	G	17: 20,029,529 (GRCm38)	F827L	probably damaging	Het
Vmn2r111	T	A	17: 22,548,399 (GRCm38)	T706S	probably benign	Het
Vmn2r114	T	C	17: 23,308,061 (GRCm38)	D499G	probably null	Het
Vmn2r92	T	C	17: 18,171,271 (GRCm38)	S512P	probably damaging	Het
Vps4b	A	T	1: 106,780,502 (GRCm38)		probably null	Het
Vwa8	A	C	14: 78,982,234 (GRCm38)		probably null	Het
Wnt10b	T	C	15: 98,774,164 (GRCm38)	Q224R	probably benign	Het
Ylpm1	C	T	12: 85,030,494 (GRCm38)	P1331L	possibly damaging	Het
Zfhx4	G	A	3: 5,242,207 (GRCm38)	M164I	possibly damaging	Het
Zfp51	A	G	17: 21,463,500 (GRCm38)	T126A	probably benign	Het
Zfp609	A	G	9: 65,706,136 (GRCm38)	V339A	probably benign	Het
Zfp687	C	T	3: 95,007,530 (GRCm38)	R1220H	probably damaging	Het
Zfyve21	C	T	12: 111,823,815 (GRCm38)	L84F	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
R6724:Trank1	UTSW	9	111,365,916 (GRCm38)	missense	probably damaging	1.00
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
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'- TGTGCATCATCACGTCTTTGGAG -3'
(R):5'- TGTCAGCGCTTTGTTCCAAG -3'

Sequencing Primer
(F):5'- AAAGAAGGTCAGTGTTGTATGATGCC -3'
(R):5'- GCGCTTTGTTCCAAGCCAAAAG -3'

Posted On

2019-10-17