Mutagenetix > Incidental Mutation

Incidental Mutation 'R4166:Trank1'

320588

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

041639-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4166 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

111140807-111224843 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to A at 111202592 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 1652 (Y1652*)

Ref Sequence

ENSEMBL: ENSMUSP00000077697 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000078626
AA Change: Y1652*

SMART Domains

Protein: ENSMUSP00000077697
Gene: ENSMUSG00000062296
AA Change: Y1652*

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000196945

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198890

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000200272

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.8%

Validation Efficiency

100% (56/56)

Allele List at MGI

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

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	T	C	14: 32,382,912 (GRCm39)	T1018A	possibly damaging	Het
Aak1	T	A	6: 86,827,044 (GRCm39)	F4I	probably damaging	Het
Adamts8	G	T	9: 30,862,684 (GRCm39)	E296D	probably benign	Het
Ankrd35	T	A	3: 96,586,471 (GRCm39)		probably null	Het
Arhgap20	G	A	9: 51,738,135 (GRCm39)		probably null	Het
Bhmt	T	A	13: 93,762,007 (GRCm39)		probably benign	Het
Cacna1b	C	A	2: 24,567,923 (GRCm39)	R1055L	probably benign	Het
Cdk5r1	A	G	11: 80,369,035 (GRCm39)	Y234C	probably damaging	Het
Cdx2	G	T	5: 147,243,539 (GRCm39)	A85D	possibly damaging	Het
Cenpe	G	A	3: 134,949,479 (GRCm39)	G88D	probably damaging	Het
Cfap300	A	T	9: 8,026,071 (GRCm39)	L167Q	probably damaging	Het
Dennd5a	A	C	7: 109,526,032 (GRCm39)		probably null	Het
Erich6	G	A	3: 58,526,229 (GRCm39)	A591V	probably damaging	Het
Espl1	A	G	15: 102,221,424 (GRCm39)	I944V	probably damaging	Het
Fbln5	A	G	12: 101,723,618 (GRCm39)	V374A	probably damaging	Het
Fmn1	G	A	2: 113,467,080 (GRCm39)	S1327N	probably benign	Het
Fnip2	A	T	3: 79,369,442 (GRCm39)	V1081E	probably damaging	Het
Gm5174	A	G	10: 86,492,797 (GRCm39)		noncoding transcript	Het
Gpaa1	A	C	15: 76,216,667 (GRCm39)		probably benign	Het
Grina	T	A	15: 76,133,529 (GRCm39)	L334Q	probably damaging	Het
Gulp1	T	A	1: 44,747,829 (GRCm39)	Y27*	probably null	Het
Kdm3b	A	T	18: 34,928,797 (GRCm39)	I183F	probably benign	Het
Loxhd1	A	T	18: 77,460,025 (GRCm39)	I758F	probably damaging	Het
Msi2	T	C	11: 88,237,914 (GRCm39)	H346R	probably benign	Het
Naip6	T	A	13: 100,452,657 (GRCm39)	I135F	probably benign	Het
Npr3	T	G	15: 11,848,599 (GRCm39)	E202A	probably benign	Het
Nsun4	A	T	4: 115,891,248 (GRCm39)	L377Q	probably damaging	Het
Oog2	A	C	4: 143,921,411 (GRCm39)	H107P	probably damaging	Het
Or14c40	C	A	7: 86,313,602 (GRCm39)	T244N	probably damaging	Het
Otof	A	G	5: 30,539,762 (GRCm39)	L1032P	probably damaging	Het
Pcdh9	T	A	14: 94,124,956 (GRCm39)	R405*	probably null	Het
Pcdhb19	T	A	18: 37,632,243 (GRCm39)	N679K	probably benign	Het
Pigr	G	A	1: 130,769,554 (GRCm39)	D122N	probably benign	Het
Prol1	A	T	5: 88,476,530 (GRCm39)	I307F	unknown	Het
Pycr1	T	C	11: 120,532,949 (GRCm39)	I104V	probably benign	Het
Ralgapa1	C	T	12: 55,687,429 (GRCm39)	R2019Q	probably damaging	Het
Rb1cc1	T	C	1: 6,335,887 (GRCm39)		probably benign	Het
Skint11	C	A	4: 114,101,856 (GRCm39)	Q99K	probably benign	Het
Skint3	A	G	4: 112,112,832 (GRCm39)	I147M	possibly damaging	Het
Slc22a14	T	G	9: 119,007,498 (GRCm39)	M304L	probably benign	Het
Slc22a14	T	C	9: 119,008,934 (GRCm39)	N178S	possibly damaging	Het
Slc2a1	T	G	4: 118,990,313 (GRCm39)	I179S	probably damaging	Het
Slco2b1	G	T	7: 99,309,333 (GRCm39)	T666N	probably benign	Het
Smap1	T	C	1: 23,887,506 (GRCm39)	M258V	probably benign	Het
Smr3a	A	T	5: 88,156,013 (GRCm39)		probably benign	Het
Stt3b	T	A	9: 115,083,969 (GRCm39)	E402D	probably damaging	Het
Sync	T	C	4: 129,200,535 (GRCm39)		probably benign	Het
Tbx20	T	A	9: 24,681,040 (GRCm39)	I151F	probably damaging	Het
Tomm22	C	A	15: 79,555,206 (GRCm39)		probably benign	Het
Trim34a	T	A	7: 103,910,223 (GRCm39)	C342S	probably benign	Het
Txnl4a	T	A	18: 80,265,471 (GRCm39)	M112K	probably benign	Het
Zfp146	A	G	7: 29,861,865 (GRCm39)	V59A	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
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
R5878:Trank1	UTSW	9	111,195,753 (GRCm39)	missense	possibly damaging	0.93
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'- TGGCCAGTTCTCTTTAGAGCC -3'
(R):5'- GCTCAGAGCTATTCTCGACC -3'

Sequencing Primer
(F):5'- AGAGCCATTACTTGTTTTACAGGG -3'
(R):5'- GAGCTATTCTCGACCCCCAC -3'

Posted On

2015-06-12