Mutagenetix > Incidental Mutation

Incidental Mutation 'R0639:Tg'

56958

Institutional Source

Beutler Lab

Gene Symbol

Ensembl Gene

ENSMUSG00000053469

Gene Name

thyroglobulin

Synonyms

Tgn

MMRRC Submission

038828-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.128) question?

Stock #

R0639 (G1)

Quality Score

194

Status

Not validated

Chromosome

Chromosomal Location

66670753-66850721 bp(+) (GRCm38)

Type of Mutation

critical splice acceptor site

DNA Base Change (assembly)

A to T at 66741484 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000126454 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000065916] [ENSMUST00000163495] [ENSMUST00000171045] [ENSMUST00000171045]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000065916

SMART Domains

Protein: ENSMUSP00000070239
Gene: ENSMUSG00000053469

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
TY	50	97	5.9e-16	SMART
TY	118	165	5.59e-17	SMART
Pfam:Thyroglobulin_1	174	252	4e-9	PFAM
TY	317	363	4.36e-19	SMART
low complexity region	495	504	N/A	INTRINSIC
TY	617	662	3.58e-15	SMART
TY	684	730	1.47e-16	SMART
TY	880	926	1.51e-4	SMART
TY	1029	1078	1.21e-12	SMART
TY	1106	1150	7.56e-5	SMART
TY	1167	1215	7.26e-16	SMART
low complexity region	1244	1255	N/A	INTRINSIC
Pfam:GCC2_GCC3	1464	1509	2.7e-16	PFAM
TY	1519	1568	9.81e-13	SMART
Pfam:COesterase	2181	2717	8.4e-140	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000163495

SMART Domains

Protein: ENSMUSP00000129868
Gene: ENSMUSG00000053469

Domain	Start	End	E-Value	Type
TY	14	63	1.21e-12	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000169163

Predicted Effect

probably null
Transcript: ENSMUST00000171045

SMART Domains

Protein: ENSMUSP00000126454
Gene: ENSMUSG00000053469

Domain	Start	End	E-Value	Type
internal_repeat_1	93	331	1.53e-6	PROSPERO
Pfam:COesterase	562	1098	2.1e-137	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000171045

SMART Domains

Protein: ENSMUSP00000126454
Gene: ENSMUSG00000053469

Domain	Start	End	E-Value	Type
internal_repeat_1	93	331	1.53e-6	PROSPERO
Pfam:COesterase	562	1098	2.1e-137	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000172153

SMART Domains

Protein: ENSMUSP00000128410
Gene: ENSMUSG00000053469

Domain	Start	End	E-Value	Type
Pfam:COesterase	313	849	6e-140	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000172153

SMART Domains

Protein: ENSMUSP00000128410
Gene: ENSMUSG00000053469

Domain	Start	End	E-Value	Type
Pfam:COesterase	313	849	6e-140	PFAM

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.7%
20x: 95.7%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Thyroglobulin (Tg) is a glycoprotein homodimer produced predominantly by the thryroid gland. It acts as a substrate for the synthesis of thyroxine and triiodothyronine as well as the storage of the inactive forms of thyroid hormone and iodine. Thyroglobulin is secreted from the endoplasmic reticulum to its site of iodination, and subsequent thyroxine biosynthesis, in the follicular lumen. Mutations in this gene cause thyroid dyshormonogenesis, manifested as goiter, and are associated with moderate to severe congenital hypothyroidism. Polymorphisms in this gene are associated with susceptibility to autoimmune thyroid diseases (AITD) such as Graves disease and Hashimoto thryoiditis. [provided by RefSeq, Nov 2009]
PHENOTYPE: Mice homozygous for a spontaneous mutation exhibit enlarged thyroid gland, hypothyroidism, abnormal thyroid gland morphology, and decreased body weight. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 104 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1600014C23Rik	C	T	17: 45,733,073 (GRCm38)	W86*	probably null	Het
Acadl	T	C	1: 66,857,408 (GRCm38)	H75R	probably benign	Het
Adamtsl1	T	C	4: 86,277,143 (GRCm38)	F599S	probably damaging	Het
Adrb3	T	C	8: 27,228,265 (GRCm38)	N52S	probably damaging	Het
Agbl3	T	A	6: 34,799,705 (GRCm38)	L377Q	probably damaging	Het
Akap9	T	C	5: 4,060,318 (GRCm38)	L3007P	probably damaging	Het
Amer3	T	A	1: 34,587,821 (GRCm38)	Y380*	probably null	Het
Ankrd13d	A	T	19: 4,273,019 (GRCm38)		probably null	Het
Ap4m1	T	A	5: 138,176,239 (GRCm38)	C235S	probably benign	Het
Arhgap29	T	C	3: 122,007,641 (GRCm38)	F675S	probably damaging	Het
Asah2	C	A	19: 32,008,639 (GRCm38)	V544F	probably damaging	Het
Ash2l	A	G	8: 25,823,291 (GRCm38)	I389T	possibly damaging	Het
Bend5	T	C	4: 111,433,298 (GRCm38)	S164P	probably benign	Het
Cacna1d	A	G	14: 30,171,294 (GRCm38)		probably null	Het
Cdc25b	A	G	2: 131,197,262 (GRCm38)	N516D	probably benign	Het
Cdc27	A	G	11: 104,531,734 (GRCm38)	Y125H	probably damaging	Het
Cdk5r2	C	T	1: 74,855,836 (GRCm38)	L247F	probably damaging	Het
Cenpf	C	A	1: 189,658,062 (GRCm38)	G1191V	probably benign	Het
Cops4	C	T	5: 100,537,460 (GRCm38)	T293I	possibly damaging	Het
Csmd3	A	G	15: 47,913,940 (GRCm38)	L1294P	probably damaging	Het
Dclre1a	T	C	19: 56,538,440 (GRCm38)	Y848C	probably damaging	Het
Disp2	A	T	2: 118,790,844 (GRCm38)	I686F	possibly damaging	Het
Dnah6	T	A	6: 73,022,412 (GRCm38)	Y4012F	probably benign	Het
Dnajc11	C	G	4: 151,969,936 (GRCm38)	R200G	probably damaging	Het
Dnhd1	A	T	7: 105,696,464 (GRCm38)	D2272V	possibly damaging	Het
Elane	A	C	10: 79,886,349 (GRCm38)	R5S	possibly damaging	Het
Entpd7	G	A	19: 43,691,094 (GRCm38)	V29M	probably benign	Het
Fanca	A	G	8: 123,289,359 (GRCm38)		probably null	Het
Fgl1	G	T	8: 41,191,624 (GRCm38)	T281K	probably benign	Het
Flii	T	C	11: 60,722,997 (GRCm38)		probably null	Het
Foxn1	T	C	11: 78,371,144 (GRCm38)	D133G	possibly damaging	Het
Fzd7	T	A	1: 59,484,560 (GRCm38)	M534K	probably damaging	Het
Galnt5	A	G	2: 57,999,395 (GRCm38)	T336A	probably benign	Het
Gli3	G	A	13: 15,724,715 (GRCm38)	D896N	probably damaging	Het
Gsx1	G	T	5: 147,189,946 (GRCm38)	W193L	probably damaging	Het
Gtpbp3	A	T	8: 71,492,735 (GRCm38)	I485F	probably damaging	Het
H2-M11	A	G	17: 36,547,391 (GRCm38)	T26A	probably benign	Het
Igfbp7	T	C	5: 77,351,980 (GRCm38)	D243G	probably damaging	Het
Il31ra	A	T	13: 112,525,843 (GRCm38)	D477E	possibly damaging	Het
Inmt	A	C	6: 55,171,227 (GRCm38)	V139G	probably damaging	Het
Inpp5j	T	A	11: 3,501,147 (GRCm38)	M501L	probably benign	Het
Itsn2	T	C	12: 4,712,556 (GRCm38)	F1579L	probably damaging	Het
Kat2b	C	A	17: 53,567,538 (GRCm38)	A70E	probably benign	Het
Klhl20	T	C	1: 161,093,711 (GRCm38)	E58G	probably damaging	Het
Krt79	A	T	15: 101,931,548 (GRCm38)	Y337*	probably null	Het
Krt81	C	A	15: 101,463,627 (GRCm38)	R24L	possibly damaging	Het
Letm1	T	C	5: 33,769,426 (GRCm38)	I176V	possibly damaging	Het
Lingo3	C	A	10: 80,835,784 (GRCm38)	R104L	probably benign	Het
Lrig3	T	G	10: 126,010,221 (GRCm38)	C840G	probably damaging	Het
Lrrc9	A	G	12: 72,486,288 (GRCm38)	N977S	probably damaging	Het
Lrrk2	T	A	15: 91,772,996 (GRCm38)	M1831K	probably benign	Het
Mn1	A	T	5: 111,419,316 (GRCm38)	D384V	probably damaging	Het
Morc3	C	A	16: 93,853,850 (GRCm38)	H319Q	probably damaging	Het
Morn1	T	C	4: 155,089,503 (GRCm38)	F56L	possibly damaging	Het
Mrpl53	G	T	6: 83,109,411 (GRCm38)	V64L	probably damaging	Het
Myo15a	T	A	11: 60,479,336 (GRCm38)	V974D	probably benign	Het
Neb	A	G	2: 52,256,124 (GRCm38)	V2947A	possibly damaging	Het
Nfasc	A	C	1: 132,603,816 (GRCm38)	N737K	probably damaging	Het
Nlk	T	C	11: 78,572,277 (GRCm38)	D464G	possibly damaging	Het
Nlrc4	C	T	17: 74,426,963 (GRCm38)	R985K	probably benign	Het
Nsun6	T	C	2: 14,996,336 (GRCm38)	K470E	probably benign	Het
Nup85	T	G	11: 115,564,531 (GRCm38)	M1R	probably null	Het
Or8b39	G	A	9: 38,085,370 (GRCm38)	C178Y	probably damaging	Het
Otop1	T	C	5: 38,287,948 (GRCm38)	V150A	possibly damaging	Het
Pclo	C	T	5: 14,681,749 (GRCm38)	R296*	probably null	Het
Pdzd2	A	T	15: 12,458,058 (GRCm38)	C240S	possibly damaging	Het
Plekhg5	A	G	4: 152,114,120 (GRCm38)	T922A	probably benign	Het
Plekhm2	A	C	4: 141,642,070 (GRCm38)	L101R	probably damaging	Het
Plscr3	T	A	11: 69,847,994 (GRCm38)	C161S	probably benign	Het
Prr14l	C	T	5: 32,828,915 (GRCm38)	D1079N	probably benign	Het
Ptpru	A	T	4: 131,771,179 (GRCm38)	V1377E	possibly damaging	Het
Rab37	C	A	11: 115,158,702 (GRCm38)	D112E	probably benign	Het
Raet1e	T	A	10: 22,174,375 (GRCm38)	I19N	probably damaging	Het
Rassf5	T	C	1: 131,245,066 (GRCm38)	Y22C	probably damaging	Het
Rp1	T	C	1: 4,346,498 (GRCm38)	T1464A	probably benign	Het
Safb	T	A	17: 56,601,092 (GRCm38)		probably benign	Het
Scarf2	A	G	16: 17,806,505 (GRCm38)		probably null	Het
Scart2	A	G	7: 140,247,959 (GRCm38)	N27D	probably benign	Het
Sh3d19	T	C	3: 86,106,973 (GRCm38)	S415P	probably benign	Het
Slc26a9	T	A	1: 131,763,804 (GRCm38)	L595Q	probably damaging	Het
Slc4a8	T	C	15: 100,796,550 (GRCm38)	Y470H	probably damaging	Het
Slitrk3	T	C	3: 73,049,649 (GRCm38)	N597D	probably benign	Het
Spata31	T	A	13: 64,922,213 (GRCm38)	V725E	probably benign	Het
Spink12	T	A	18: 44,107,764 (GRCm38)	C72*	probably null	Het
Spink5	T	A	18: 44,012,975 (GRCm38)		probably null	Het
Stk40	C	A	4: 126,118,332 (GRCm38)	S9*	probably null	Het
Sypl1	A	T	12: 32,965,421 (GRCm38)	T40S	probably damaging	Het
Tbc1d8	C	T	1: 39,391,209 (GRCm38)	E438K	probably benign	Het
Tdrd7	A	G	4: 45,989,102 (GRCm38)	T111A	probably benign	Het
Tlr5	T	A	1: 182,973,889 (GRCm38)	W253R	probably damaging	Het
Tmprss11c	C	T	5: 86,235,469 (GRCm38)	C353Y	probably damaging	Het
Tnfrsf8	T	A	4: 145,288,027 (GRCm38)	M271L	probably benign	Het
Toe1	T	C	4: 116,806,750 (GRCm38)	N21S	probably benign	Het
Tpp2	T	C	1: 43,975,447 (GRCm38)	F649L	probably benign	Het
Ttll1	G	A	15: 83,502,225 (GRCm38)	Q60*	probably null	Het
Vcp	C	T	4: 42,982,565 (GRCm38)	R709Q	probably benign	Het
Vmn1r119	T	A	7: 21,011,668 (GRCm38)	H263L	possibly damaging	Het
Vmn1r195	C	A	13: 22,278,941 (GRCm38)	Q194K	probably damaging	Het
Vmn1r33	T	C	6: 66,611,799 (GRCm38)	Y257C	probably damaging	Het
Vmn2r15	A	G	5: 109,293,015 (GRCm38)	F326L	probably benign	Het
Wbp11	A	T	6: 136,816,110 (GRCm38)		probably benign	Het
Wwp2	T	G	8: 107,517,946 (GRCm38)	V250G	probably benign	Het
Xpnpep3	T	C	15: 81,430,837 (GRCm38)	V246A	probably benign	Het
Zcchc14	G	A	8: 121,605,449 (GRCm38)	R419*	probably null	Het

Other mutations in Tg

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00157:Tg	APN	15	66,847,166 (GRCm38)	missense	probably damaging	1.00
IGL00230:Tg	APN	15	66,827,290 (GRCm38)	missense	probably benign	0.00
IGL00324:Tg	APN	15	66,693,424 (GRCm38)	missense	probably benign
IGL00428:Tg	APN	15	66,773,424 (GRCm38)	missense	probably benign	0.33
IGL00703:Tg	APN	15	66,696,489 (GRCm38)	missense	probably benign	0.34
IGL00808:Tg	APN	15	66,683,813 (GRCm38)	missense	probably damaging	1.00
IGL00833:Tg	APN	15	66,688,801 (GRCm38)	missense	probably benign	0.34
IGL00899:Tg	APN	15	66,674,073 (GRCm38)	critical splice donor site	probably null
IGL00921:Tg	APN	15	66,764,453 (GRCm38)	missense	probably benign	0.28
IGL00975:Tg	APN	15	66,681,882 (GRCm38)	missense	probably benign
IGL01288:Tg	APN	15	66,736,276 (GRCm38)	missense	possibly damaging	0.81
IGL01397:Tg	APN	15	66,696,092 (GRCm38)	splice site	probably benign
IGL01634:Tg	APN	15	66,729,566 (GRCm38)	missense	probably benign	0.34
IGL01646:Tg	APN	15	66,678,087 (GRCm38)	missense	probably damaging	1.00
IGL01704:Tg	APN	15	66,671,351 (GRCm38)	missense	probably damaging	0.98
IGL01958:Tg	APN	15	66,759,486 (GRCm38)	missense	probably benign	0.06
IGL02093:Tg	APN	15	66,692,374 (GRCm38)	missense	possibly damaging	0.83
IGL02113:Tg	APN	15	66,705,330 (GRCm38)	missense	probably benign	0.08
IGL02138:Tg	APN	15	66,717,233 (GRCm38)	missense	probably benign	0.01
IGL02156:Tg	APN	15	66,705,348 (GRCm38)	missense	probably benign	0.19
IGL02169:Tg	APN	15	66,757,943 (GRCm38)	missense	probably benign	0.04
IGL02342:Tg	APN	15	66,764,291 (GRCm38)	missense	probably benign
IGL02434:Tg	APN	15	66,764,342 (GRCm38)	missense	probably damaging	0.97
IGL02506:Tg	APN	15	66,741,594 (GRCm38)	missense	possibly damaging	0.71
IGL02513:Tg	APN	15	66,705,274 (GRCm38)	missense	probably benign
IGL02549:Tg	APN	15	66,839,361 (GRCm38)	missense	probably damaging	1.00
IGL02669:Tg	APN	15	66,748,726 (GRCm38)	splice site	probably benign
IGL02756:Tg	APN	15	66,734,586 (GRCm38)	missense	probably benign
IGL02800:Tg	APN	15	66,757,886 (GRCm38)	missense	probably damaging	1.00
IGL02828:Tg	APN	15	66,682,394 (GRCm38)	missense	probably damaging	1.00
IGL02927:Tg	APN	15	66,678,093 (GRCm38)	missense	probably damaging	1.00
IGL03061:Tg	APN	15	66,671,405 (GRCm38)	missense	probably damaging	1.00
IGL03105:Tg	APN	15	66,715,106 (GRCm38)	missense	probably benign	0.01
IGL03160:Tg	APN	15	66,839,303 (GRCm38)	nonsense	probably null
IGL03242:Tg	APN	15	66,683,798 (GRCm38)	missense	probably damaging	0.99
Also_ran	UTSW	15	66,678,839 (GRCm38)	missense	probably damaging	1.00
bedraggled	UTSW	15	66,740,714 (GRCm38)	missense	probably damaging	1.00
foster	UTSW	15	66,693,260 (GRCm38)	nonsense	probably null
hognose	UTSW	15	66,717,208 (GRCm38)	missense	probably damaging	0.99
ito	UTSW	15	66,766,162 (GRCm38)	nonsense	probably null
ito2	UTSW	15	66,671,396 (GRCm38)	missense	probably damaging	1.00
ito3	UTSW	15	66,773,474 (GRCm38)	missense	probably damaging	1.00
ito4	UTSW	15	66,696,520 (GRCm38)	missense	possibly damaging	0.47
Papua	UTSW	15	66,674,050 (GRCm38)	missense	probably damaging	1.00
Pipistrella	UTSW	15	66,696,135 (GRCm38)	missense	probably damaging	1.00
pluribus	UTSW	15	66,715,163 (GRCm38)	missense	probably damaging	0.98
samarai	UTSW	15	66,758,006 (GRCm38)	critical splice donor site	probably null
sariba	UTSW	15	66,694,870 (GRCm38)	missense	probably benign	0.01
ticker	UTSW	15	66,827,382 (GRCm38)	nonsense	probably null
Vampire	UTSW	15	66,682,827 (GRCm38)	missense	probably damaging	1.00
IGL03134:Tg	UTSW	15	66,740,718 (GRCm38)	missense	probably damaging	1.00
P0019:Tg	UTSW	15	66,688,863 (GRCm38)	missense	probably benign	0.01
R0121:Tg	UTSW	15	66,740,781 (GRCm38)	missense	probably benign	0.04
R0135:Tg	UTSW	15	66,694,870 (GRCm38)	missense	probably benign	0.01
R0227:Tg	UTSW	15	66,698,446 (GRCm38)	missense	possibly damaging	0.84
R0448:Tg	UTSW	15	66,764,442 (GRCm38)	missense	probably damaging	1.00
R0453:Tg	UTSW	15	66,828,533 (GRCm38)	missense	probably benign	0.09
R0504:Tg	UTSW	15	66,682,404 (GRCm38)	missense	probably damaging	0.97
R0543:Tg	UTSW	15	66,729,597 (GRCm38)	missense	probably benign	0.13
R0638:Tg	UTSW	15	66,717,208 (GRCm38)	missense	probably damaging	0.99
R0646:Tg	UTSW	15	66,729,626 (GRCm38)	missense	probably damaging	0.99
R0666:Tg	UTSW	15	66,737,521 (GRCm38)	missense	probably benign
R0673:Tg	UTSW	15	66,741,484 (GRCm38)	critical splice acceptor site	probably null
R0689:Tg	UTSW	15	66,839,404 (GRCm38)	splice site	probably benign
R0704:Tg	UTSW	15	66,757,880 (GRCm38)	missense	probably benign	0.02
R0730:Tg	UTSW	15	66,678,789 (GRCm38)	missense	probably damaging	1.00
R0830:Tg	UTSW	15	66,725,144 (GRCm38)	missense	probably damaging	1.00
R0959:Tg	UTSW	15	66,708,010 (GRCm38)	missense	probably damaging	0.98
R1027:Tg	UTSW	15	66,672,409 (GRCm38)	missense	possibly damaging	0.65
R1061:Tg	UTSW	15	66,698,559 (GRCm38)	missense	probably benign	0.09
R1086:Tg	UTSW	15	66,684,062 (GRCm38)	missense	probably benign
R1103:Tg	UTSW	15	66,719,655 (GRCm38)	missense	probably benign	0.45
R1240:Tg	UTSW	15	66,828,548 (GRCm38)	missense	probably benign	0.16
R1281:Tg	UTSW	15	66,696,489 (GRCm38)	missense	probably benign	0.34
R1470:Tg	UTSW	15	66,849,463 (GRCm38)	missense	possibly damaging	0.95
R1470:Tg	UTSW	15	66,849,463 (GRCm38)	missense	possibly damaging	0.95
R1531:Tg	UTSW	15	66,850,502 (GRCm38)	missense	probably benign	0.02
R1544:Tg	UTSW	15	66,705,232 (GRCm38)	missense	probably benign	0.04
R1550:Tg	UTSW	15	66,693,430 (GRCm38)	missense	possibly damaging	0.52
R1575:Tg	UTSW	15	66,729,685 (GRCm38)	critical splice donor site	probably null
R1638:Tg	UTSW	15	66,696,166 (GRCm38)	nonsense	probably null
R1655:Tg	UTSW	15	66,828,568 (GRCm38)	critical splice donor site	probably null
R1671:Tg	UTSW	15	66,692,387 (GRCm38)	missense	possibly damaging	0.89
R1789:Tg	UTSW	15	66,737,548 (GRCm38)	missense	probably benign	0.00
R1883:Tg	UTSW	15	66,671,309 (GRCm38)	missense	probably damaging	1.00
R1984:Tg	UTSW	15	66,682,842 (GRCm38)	missense	probably benign
R2063:Tg	UTSW	15	66,828,553 (GRCm38)	missense	probably damaging	1.00
R2092:Tg	UTSW	15	66,849,607 (GRCm38)	missense	probably null	0.26
R2109:Tg	UTSW	15	66,729,594 (GRCm38)	missense	probably benign	0.02
R2128:Tg	UTSW	15	66,694,894 (GRCm38)	missense	probably benign	0.10
R2129:Tg	UTSW	15	66,694,894 (GRCm38)	missense	probably benign	0.10
R2207:Tg	UTSW	15	66,681,939 (GRCm38)	missense	probably benign	0.15
R2219:Tg	UTSW	15	66,681,933 (GRCm38)	missense	probably benign	0.03
R2228:Tg	UTSW	15	66,674,011 (GRCm38)	missense	probably damaging	0.99
R2229:Tg	UTSW	15	66,674,011 (GRCm38)	missense	probably damaging	0.99
R2259:Tg	UTSW	15	66,683,898 (GRCm38)	missense	probably benign
R2994:Tg	UTSW	15	66,681,953 (GRCm38)	missense	probably benign
R3904:Tg	UTSW	15	66,766,162 (GRCm38)	nonsense	probably null
R3946:Tg	UTSW	15	66,674,023 (GRCm38)	missense	probably damaging	1.00
R3965:Tg	UTSW	15	66,684,190 (GRCm38)	missense	probably benign
R4245:Tg	UTSW	15	66,696,469 (GRCm38)	missense	possibly damaging	0.68
R4451:Tg	UTSW	15	66,766,147 (GRCm38)	missense	probably benign	0.01
R4487:Tg	UTSW	15	66,671,396 (GRCm38)	missense	probably damaging	1.00
R4489:Tg	UTSW	15	66,707,942 (GRCm38)	missense	probably damaging	1.00
R4623:Tg	UTSW	15	66,735,271 (GRCm38)	missense	probably benign	0.23
R4659:Tg	UTSW	15	66,673,920 (GRCm38)	missense	possibly damaging	0.67
R4728:Tg	UTSW	15	66,682,827 (GRCm38)	missense	probably damaging	1.00
R4760:Tg	UTSW	15	66,693,319 (GRCm38)	missense	probably damaging	1.00
R4797:Tg	UTSW	15	66,758,006 (GRCm38)	critical splice donor site	probably null
R4944:Tg	UTSW	15	66,764,337 (GRCm38)	missense	probably damaging	1.00
R4998:Tg	UTSW	15	66,674,050 (GRCm38)	missense	probably damaging	1.00
R5009:Tg	UTSW	15	66,696,586 (GRCm38)	missense	probably benign	0.01
R5025:Tg	UTSW	15	66,707,930 (GRCm38)	missense	probably damaging	1.00
R5035:Tg	UTSW	15	66,681,813 (GRCm38)	splice site	probably null
R5049:Tg	UTSW	15	66,827,382 (GRCm38)	nonsense	probably null
R5073:Tg	UTSW	15	66,735,252 (GRCm38)	missense	probably benign	0.05
R5169:Tg	UTSW	15	66,678,780 (GRCm38)	nonsense	probably null
R5185:Tg	UTSW	15	66,773,474 (GRCm38)	missense	probably damaging	1.00
R5227:Tg	UTSW	15	66,759,567 (GRCm38)	missense	possibly damaging	0.87
R5300:Tg	UTSW	15	66,678,855 (GRCm38)	missense	probably damaging	1.00
R5334:Tg	UTSW	15	66,678,055 (GRCm38)	missense	probably damaging	1.00
R5339:Tg	UTSW	15	66,678,093 (GRCm38)	missense	probably damaging	1.00
R5402:Tg	UTSW	15	66,739,168 (GRCm38)	missense	probably damaging	0.98
R5441:Tg	UTSW	15	66,696,520 (GRCm38)	missense	possibly damaging	0.47
R5509:Tg	UTSW	15	66,827,293 (GRCm38)	missense	probably benign	0.45
R5580:Tg	UTSW	15	66,685,300 (GRCm38)	missense	possibly damaging	0.66
R5582:Tg	UTSW	15	66,693,435 (GRCm38)	missense	probably damaging	1.00
R5624:Tg	UTSW	15	66,838,057 (GRCm38)	missense	probably benign	0.11
R5686:Tg	UTSW	15	66,688,889 (GRCm38)	missense	probably benign	0.28
R6042:Tg	UTSW	15	66,683,993 (GRCm38)	missense	probably benign	0.01
R6122:Tg	UTSW	15	66,828,457 (GRCm38)	missense	probably damaging	1.00
R6146:Tg	UTSW	15	66,673,367 (GRCm38)	splice site	probably null
R6159:Tg	UTSW	15	66,735,247 (GRCm38)	missense	possibly damaging	0.71
R6223:Tg	UTSW	15	66,707,922 (GRCm38)	missense	probably benign	0.15
R6480:Tg	UTSW	15	66,671,311 (GRCm38)	missense	probably damaging	1.00
R6505:Tg	UTSW	15	66,759,558 (GRCm38)	missense	probably damaging	0.99
R6531:Tg	UTSW	15	66,839,362 (GRCm38)	missense	probably damaging	0.99
R6614:Tg	UTSW	15	66,735,259 (GRCm38)	missense	probably damaging	0.99
R6698:Tg	UTSW	15	66,839,362 (GRCm38)	missense	probably damaging	1.00
R6798:Tg	UTSW	15	66,678,839 (GRCm38)	missense	probably damaging	1.00
R6837:Tg	UTSW	15	66,696,135 (GRCm38)	missense	probably damaging	1.00
R6861:Tg	UTSW	15	66,688,891 (GRCm38)	missense	probably benign	0.00
R6888:Tg	UTSW	15	66,696,246 (GRCm38)	missense	probably damaging	0.99
R6933:Tg	UTSW	15	66,764,309 (GRCm38)	missense	possibly damaging	0.73
R6983:Tg	UTSW	15	66,693,358 (GRCm38)	missense	probably benign	0.01
R7078:Tg	UTSW	15	66,673,543 (GRCm38)	missense	probably damaging	1.00
R7244:Tg	UTSW	15	66,740,714 (GRCm38)	missense	probably damaging	1.00
R7320:Tg	UTSW	15	66,694,784 (GRCm38)	missense	possibly damaging	0.71
R7334:Tg	UTSW	15	66,725,272 (GRCm38)	missense	probably benign	0.01
R7418:Tg	UTSW	15	66,696,583 (GRCm38)	missense	probably damaging	0.99
R7485:Tg	UTSW	15	66,696,588 (GRCm38)	missense	probably benign	0.04
R7524:Tg	UTSW	15	66,696,161 (GRCm38)	missense	probably benign	0.01
R7529:Tg	UTSW	15	66,694,768 (GRCm38)	missense	probably damaging	0.99
R7540:Tg	UTSW	15	66,689,927 (GRCm38)	missense	probably benign	0.16
R7583:Tg	UTSW	15	66,764,418 (GRCm38)	missense	probably damaging	1.00
R7594:Tg	UTSW	15	66,729,583 (GRCm38)	missense	probably benign	0.20
R7667:Tg	UTSW	15	66,715,163 (GRCm38)	missense	probably damaging	0.98
R7722:Tg	UTSW	15	66,764,309 (GRCm38)	missense	possibly damaging	0.73
R7790:Tg	UTSW	15	66,849,604 (GRCm38)	missense	probably damaging	0.99
R7838:Tg	UTSW	15	66,693,263 (GRCm38)	missense	probably benign	0.00
R7890:Tg	UTSW	15	66,683,814 (GRCm38)	missense	probably damaging	1.00
R7904:Tg	UTSW	15	66,705,279 (GRCm38)	missense	probably benign	0.08
R7919:Tg	UTSW	15	66,684,074 (GRCm38)	missense	possibly damaging	0.73
R7921:Tg	UTSW	15	66,683,793 (GRCm38)	missense	probably benign	0.08
R8037:Tg	UTSW	15	66,688,875 (GRCm38)	missense	probably benign	0.00
R8038:Tg	UTSW	15	66,688,875 (GRCm38)	missense	probably benign	0.00
R8214:Tg	UTSW	15	66,773,398 (GRCm38)	missense	probably damaging	1.00
R8304:Tg	UTSW	15	66,693,260 (GRCm38)	nonsense	probably null
R8688:Tg	UTSW	15	66,694,953 (GRCm38)	critical splice donor site	probably benign
R8709:Tg	UTSW	15	66,681,937 (GRCm38)	missense	probably benign	0.08
R8714:Tg	UTSW	15	66,684,042 (GRCm38)	missense	probably damaging	0.97
R8901:Tg	UTSW	15	66,685,335 (GRCm38)	missense	probably damaging	1.00
R8917:Tg	UTSW	15	66,773,483 (GRCm38)	critical splice donor site	probably null
R9023:Tg	UTSW	15	66,683,673 (GRCm38)	missense	probably damaging	1.00
R9232:Tg	UTSW	15	66,698,461 (GRCm38)	missense	probably benign	0.01
R9310:Tg	UTSW	15	66,827,269 (GRCm38)	missense	possibly damaging	0.69
R9361:Tg	UTSW	15	66,685,397 (GRCm38)	missense	possibly damaging	0.50
R9389:Tg	UTSW	15	66,689,324 (GRCm38)	missense	probably benign	0.04
R9501:Tg	UTSW	15	66,847,074 (GRCm38)	missense	possibly damaging	0.52
R9510:Tg	UTSW	15	66,674,064 (GRCm38)	missense	probably damaging	1.00
R9594:Tg	UTSW	15	66,735,260 (GRCm38)	nonsense	probably null
R9629:Tg	UTSW	15	66,683,738 (GRCm38)	missense	possibly damaging	0.95
R9701:Tg	UTSW	15	66,766,142 (GRCm38)	missense	probably benign	0.03
R9743:Tg	UTSW	15	66,689,990 (GRCm38)	missense	probably benign	0.18
R9748:Tg	UTSW	15	66,847,159 (GRCm38)	missense	possibly damaging	0.91
T0975:Tg	UTSW	15	66,688,863 (GRCm38)	missense	probably benign	0.01
X0005:Tg	UTSW	15	66,688,863 (GRCm38)	missense	probably benign	0.01
X0065:Tg	UTSW	15	66,682,454 (GRCm38)	missense	probably damaging	1.00
X0067:Tg	UTSW	15	66,748,743 (GRCm38)	missense	probably benign	0.10
Z1177:Tg	UTSW	15	66,849,547 (GRCm38)	missense	probably benign	0.02
Z1177:Tg	UTSW	15	66,685,310 (GRCm38)	missense	possibly damaging	0.49

Predicted Primers

PCR Primer
(F):5'- TGTCTGATCCCAAGGACTGTTCCTC -3'
(R):5'- ATGTGCCAGTAGCAGGTTCCTCAC -3'

Sequencing Primer
(F):5'- tgaacactcactcagtcacttac -3'
(R):5'- AGGTTCCTCACCAGGCTTC -3'

Posted On

2013-07-11