Mutagenetix > Incidental Mutation

Incidental Mutation 'R7206:Trank1'

560630

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

045284-MU

Accession Numbers

Genbank: NM_001164659.1; Ensembl: ENSMUST00000078626

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7206 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

111311739-111395775 bp(+) (GRCm38)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

T to C at 111345515 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000077697 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078626] [ENSMUST00000197049]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000078626

SMART Domains

Protein: ENSMUSP00000077697
Gene: ENSMUSG00000062296

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

probably benign
Transcript: ENSMUST00000197049

SMART Domains

Protein: ENSMUSP00000143534
Gene: ENSMUSG00000062296

Domain	Start	End	E-Value	Type
Blast:TPR	15	48	3e-17	BLAST
SCOP:d1ihga1	15	84	8e-10	SMART
Blast:TPR	49	82	4e-14	BLAST

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 98.9%

Validation Efficiency

99% (87/88)

Allele List at MGI

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

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl2	G	A	3: 60,025,241 (GRCm38)	M392I	probably benign	Het
Acr	T	C	15: 89,574,171 (GRCm38)	S352P	probably benign	Het
Adam6a	T	C	12: 113,546,034 (GRCm38)	C676R	probably damaging	Het
Adgra3	T	C	5: 50,006,896 (GRCm38)	D247G	probably damaging	Het
Agxt2	A	T	15: 10,377,456 (GRCm38)	E147D	probably damaging	Het
Atp2a1	T	C	7: 126,447,972 (GRCm38)	T805A	probably benign	Het
Atp8b4	T	C	2: 126,458,292 (GRCm38)	S106G	probably damaging	Het
Ccdc170	T	A	10: 4,514,120 (GRCm38)	M87K	possibly damaging	Het
Ccnl2	T	G	4: 155,820,974 (GRCm38)	V287G	possibly damaging	Het
Ccr6	A	T	17: 8,256,949 (GRCm38)	M329L	probably benign	Het
Cflar	G	T	1: 58,740,991 (GRCm38)	M248I		Het
Cib4	A	T	5: 30,545,766 (GRCm38)	L5*	probably null	Het
Col27a1	A	T	4: 63,235,346 (GRCm38)	Y645F	probably benign	Het
Cxcr2	A	G	1: 74,159,054 (GRCm38)	T236A	possibly damaging	Het
Dnah12	G	A	14: 26,778,912 (GRCm38)		probably null	Het
Dnah7a	A	T	1: 53,698,633 (GRCm38)	L47*	probably null	Het
Dnajb6	A	C	5: 29,781,337 (GRCm38)	K301T	possibly damaging	Het
Dpf2	T	A	19: 5,904,543 (GRCm38)	I157F	possibly damaging	Het
Drd4	G	A	7: 141,292,119 (GRCm38)	G28R	probably damaging	Het
Dupd1	A	G	14: 21,677,034 (GRCm38)	V182A	probably damaging	Het
Dus3l	A	T	17: 56,767,807 (GRCm38)	I310F	probably damaging	Het
Eef1akmt3	A	G	10: 127,040,993 (GRCm38)	L95P	probably damaging	Het
Fabp7	C	T	10: 57,784,991 (GRCm38)		probably benign	Het
Fam135a	T	C	1: 24,030,273 (GRCm38)	N505S	probably benign	Het
Fam213a	T	A	14: 41,004,185 (GRCm38)	M12L	probably benign	Het
Fam216b	C	A	14: 78,085,127 (GRCm38)	D46Y	probably damaging	Het
Gata6	C	T	18: 11,054,850 (GRCm38)	R260C	probably damaging	Het
Gm10800	A	AC	2: 98,667,033 (GRCm38)		probably null	Het
Gm13124	T	A	4: 144,558,641 (GRCm38)	D142V	probably damaging	Het
Golgb1	A	G	16: 36,913,749 (GRCm38)	I1160M	probably benign	Het
Hfe2	A	T	3: 96,528,128 (GRCm38)	D234V	probably damaging	Het
Kiss1	A	G	1: 133,327,325 (GRCm38)	K26E	probably benign	Het
Knl1	T	A	2: 119,069,299 (GRCm38)	F494I	probably benign	Het
Ktn1	T	C	14: 47,695,528 (GRCm38)	L713S	probably damaging	Het
Loxhd1	A	G	18: 77,441,817 (GRCm38)	D2052G	probably damaging	Het
Lpo	A	C	11: 87,807,423 (GRCm38)	L582R	probably damaging	Het
Map2k3	A	G	11: 60,943,580 (GRCm38)	T125A		Het
Matn3	T	A	12: 8,961,170 (GRCm38)	N360K	probably benign	Het
Mlip	A	T	9: 77,164,862 (GRCm38)	V237E	probably damaging	Het
Mms22l	T	C	4: 24,591,146 (GRCm38)	V999A	probably benign	Het
Mn1	A	G	5: 111,420,512 (GRCm38)	K783E	possibly damaging	Het
Myo1h	A	T	5: 114,319,775 (GRCm38)	K132*	probably null	Het
Nle1	A	G	11: 82,904,931 (GRCm38)	V230A	probably benign	Het
Olfr1240	T	C	2: 89,440,457 (GRCm38)		probably benign	Het
Olfr1318	T	G	2: 112,156,459 (GRCm38)	C169W	probably damaging	Het
Olfr22-ps1	A	T	11: 73,954,821 (GRCm38)	I44F	probably benign	Het
Olfr356	T	A	2: 36,937,772 (GRCm38)	Y218N	probably damaging	Het
Olfr564	T	C	7: 102,803,684 (GRCm38)	S69P	probably damaging	Het
Olfr860	C	T	9: 19,846,560 (GRCm38)	D20N	probably damaging	Het
Ormdl2	T	A	10: 128,820,415 (GRCm38)	H7L	possibly damaging	Het
Pam	A	G	1: 97,896,032 (GRCm38)	S225P	probably damaging	Het
Pan2	C	A	10: 128,314,545 (GRCm38)	Y719*	probably null	Het
Ppfia4	T	C	1: 134,327,389 (GRCm38)	S243G	probably benign	Het
Ppig	T	G	2: 69,741,566 (GRCm38)	S210A	unknown	Het
Ppwd1	A	T	13: 104,213,598 (GRCm38)	N426K	probably damaging	Het
Rnf10	T	G	5: 115,244,121 (GRCm38)	D675A	probably benign	Het
Rrp12	A	T	19: 41,878,039 (GRCm38)	L619H	probably damaging	Het
Rsph10b	C	T	5: 143,961,192 (GRCm38)	T497I	possibly damaging	Het
Scnm1	A	T	3: 95,133,894 (GRCm38)	M1K	probably null	Het
Scp2	G	T	4: 108,074,441 (GRCm38)	D332E	probably benign	Het
Senp3	T	C	11: 69,678,731 (GRCm38)	I314V	probably benign	Het
Sfmbt1	T	A	14: 30,811,373 (GRCm38)		probably null	Het
Slc44a2	T	C	9: 21,346,807 (GRCm38)	F451S	probably damaging	Het
Slfn1	A	T	11: 83,122,011 (GRCm38)	M318L	probably benign	Het
Syne2	C	T	12: 76,004,757 (GRCm38)	S4087L	probably benign	Het
Syt7	A	G	19: 10,417,973 (GRCm38)	Y49C	probably damaging	Het
Tas2r134	T	C	2: 51,628,108 (GRCm38)	Y200H	probably benign	Het
Tgfbr1	A	T	4: 47,402,941 (GRCm38)	H315L	probably damaging	Het
Tmem184c	A	G	8: 77,596,577 (GRCm38)	V552A	possibly damaging	Het
Tnxb	A	G	17: 34,704,101 (GRCm38)	R2553G	possibly damaging	Het
Tomm40	C	G	7: 19,710,936 (GRCm38)	R173S	probably benign	Het
Tonsl	T	C	15: 76,633,651 (GRCm38)	D650G	probably damaging	Het
Tpo	G	C	12: 30,103,134 (GRCm38)	S407W	possibly damaging	Het
Trp53tg5	T	C	2: 164,471,458 (GRCm38)	E99G	probably damaging	Het
Tubb2a	C	A	13: 34,075,522 (GRCm38)	S95I	possibly damaging	Het
Vav2	C	A	2: 27,336,719 (GRCm38)	R114L	probably benign	Het
Vmn1r172	A	T	7: 23,660,157 (GRCm38)	I156L	possibly damaging	Het
Vmn1r238	A	G	18: 3,122,623 (GRCm38)	Y264H	possibly damaging	Het
Vmn2r26	T	A	6: 124,039,768 (GRCm38)	M397K	probably benign	Het
Vmn2r73	T	C	7: 85,872,867 (GRCm38)	N88S	probably benign	Het
Vps13a	T	C	19: 16,754,298 (GRCm38)	N150S	probably damaging	Het
Vps35	A	T	8: 85,287,721 (GRCm38)	Y100N	probably damaging	Het
Vps8	A	C	16: 21,457,421 (GRCm38)	I235L	probably damaging	Het
Yipf2	T	A	9: 21,590,361 (GRCm38)	H157L	probably damaging	Het
Zfp354a	A	T	11: 51,070,246 (GRCm38)	H426L	probably damaging	Het
Zfp503	G	T	14: 21,985,485 (GRCm38)	S454R	possibly damaging	Het
Zfp619	C	T	7: 39,535,400 (GRCm38)	R285C	probably benign	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
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'- GGAGTCGTTCTTCAGGCTTC -3'
(R):5'- AGCCCTAGTTGTCCTCAAAC -3'

Sequencing Primer
(F):5'- AGGCTTCCCTCACTTGAAAG -3'
(R):5'- GTTGTCCTCAAACTCAGAAATCTGC -3'

Posted On

2019-06-26