Mutagenetix > Incidental Mutation

Incidental Mutation 'R0635:Pcnt'

56617

Institutional Source

Beutler Lab

Gene Symbol

Pcnt

Ensembl Gene

ENSMUSG00000001151

Gene Name

pericentrin (kendrin)

Synonyms

m239Asp, m275Asp, Pcnt2

MMRRC Submission

038824-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0635 (G1)

Quality Score

177

Status

Validated

Chromosome

Chromosomal Location

76351263-76442786 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 76404585 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 1205 (D1205G)

Ref Sequence

ENSEMBL: ENSMUSP00000151534 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000001179] [ENSMUST00000217838]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000001179
AA Change: D1205G

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

SMART Domains

Protein: ENSMUSP00000001179
Gene: ENSMUSG00000001151
AA Change: D1205G

Domain	Start	End	E-Value	Type
internal_repeat_1	7	78	2.47e-5	PROSPERO
low complexity region	104	114	N/A	INTRINSIC
coiled coil region	131	229	N/A	INTRINSIC
internal_repeat_3	241	259	6.69e-5	PROSPERO
low complexity region	313	325	N/A	INTRINSIC
internal_repeat_3	391	409	6.69e-5	PROSPERO
low complexity region	456	467	N/A	INTRINSIC
coiled coil region	468	520	N/A	INTRINSIC
coiled coil region	554	581	N/A	INTRINSIC
low complexity region	652	666	N/A	INTRINSIC
coiled coil region	727	787	N/A	INTRINSIC
coiled coil region	871	916	N/A	INTRINSIC
low complexity region	931	942	N/A	INTRINSIC
low complexity region	969	985	N/A	INTRINSIC
coiled coil region	1055	1383	N/A	INTRINSIC
coiled coil region	1429	1481	N/A	INTRINSIC
coiled coil region	1529	1567	N/A	INTRINSIC
low complexity region	1614	1624	N/A	INTRINSIC
internal_repeat_2	1916	1964	2.47e-5	PROSPERO
coiled coil region	2158	2178	N/A	INTRINSIC
coiled coil region	2211	2279	N/A	INTRINSIC
coiled coil region	2300	2421	N/A	INTRINSIC
coiled coil region	2447	2526	N/A	INTRINSIC
Pfam:PACT_coil_coil	2718	2797	5.8e-29	PFAM
internal_repeat_1	2820	2885	2.47e-5	PROSPERO
internal_repeat_2	2844	2891	2.47e-5	PROSPERO

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000190491

Predicted Effect

probably damaging
Transcript: ENSMUST00000217838
AA Change: D1205G

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000219701

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220395

Meta Mutation Damage Score

0.0966

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.4%
20x: 94.9%

Validation Efficiency

99% (68/69)

MGI Phenotype

PHENOTYPE: Mice homozygous for a gene trapped allele display mitotic spindle misorientation, microcephaly, craniofacial developmental anomalies, such as cleft palate and eye defects, variable structural kidney and cardiovascular defects, and altered hemodynamics leading to heart failure and prenatal lethality. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3632451O06Rik	A	G	14: 49,773,143 (GRCm38)	L369S	probably benign	Het
4932429P05Rik	T	C	X: 89,752,522 (GRCm38)		probably benign	Het
5730455P16Rik	A	T	11: 80,374,065 (GRCm38)		probably benign	Het
Adamts15	A	G	9: 30,904,770 (GRCm38)	L631P	probably damaging	Het
Adamts17	T	C	7: 66,908,605 (GRCm38)	F266L	probably damaging	Het
Adgrb1	C	A	15: 74,540,892 (GRCm38)	Q488K	possibly damaging	Het
Cep290	A	G	10: 100,492,676 (GRCm38)	D109G	probably damaging	Het
Chil5	A	T	3: 106,017,203 (GRCm38)	Y229N	possibly damaging	Het
Cntnap1	A	G	11: 101,183,459 (GRCm38)	T742A	probably benign	Het
Col6a3	A	T	1: 90,808,086 (GRCm38)		probably null	Het
Col6a5	G	A	9: 105,928,606 (GRCm38)	P1034S	unknown	Het
Daxx	T	A	17: 33,912,644 (GRCm38)	D442E	probably benign	Het
Dmxl1	T	C	18: 49,851,423 (GRCm38)		probably benign	Het
Dnah11	A	G	12: 118,007,996 (GRCm38)	F2942S	probably damaging	Het
Fam71a	T	C	1: 191,163,727 (GRCm38)	T240A	probably benign	Het
Glg1	A	G	8: 111,163,764 (GRCm38)		probably benign	Het
Gm10272	G	A	10: 77,706,701 (GRCm38)		probably benign	Het
Gm17333	AAGAAGAGAAGAGAAGAGAAGAGAAGAGAAGAGAA	AAGAAGAGAAGAGAAGAGAAGAGAAGAGAAGAGAAGAGAA	16: 77,852,878 (GRCm38)		noncoding transcript	Het
Haao	A	G	17: 83,838,574 (GRCm38)	F83S	probably damaging	Het
Hdgfl2	T	A	17: 56,096,057 (GRCm38)	L177Q	probably damaging	Het
Hrh1	T	C	6: 114,480,145 (GRCm38)	V129A	probably damaging	Het
Ift43	T	A	12: 86,085,081 (GRCm38)		probably benign	Het
Il21r	T	C	7: 125,632,506 (GRCm38)	Y369H	probably damaging	Het
Il2ra	C	T	2: 11,680,366 (GRCm38)	T171M	probably benign	Het
Lao1	C	T	4: 118,968,296 (GRCm38)	R438C	probably benign	Het
Lrrcc1	G	A	3: 14,559,228 (GRCm38)	S350N	probably benign	Het
Mageb5	T	A	X: 91,779,993 (GRCm38)	Y260F	probably benign	Het
March5	A	T	19: 37,220,408 (GRCm38)	I159F	possibly damaging	Het
Mgat4a	G	A	1: 37,452,294 (GRCm38)	A282V	probably benign	Het
Mipep	G	A	14: 60,829,390 (GRCm38)	V420I	probably damaging	Het
Morc2b	A	T	17: 33,137,687 (GRCm38)	F370L	possibly damaging	Het
Mt1	A	T	8: 94,179,821 (GRCm38)		probably null	Het
Ncapd2	A	G	6: 125,173,036 (GRCm38)	V943A	probably benign	Het
Nkd2	T	C	13: 73,826,894 (GRCm38)	D58G	probably benign	Het
Nol8	C	G	13: 49,676,758 (GRCm38)	S1106C	probably benign	Het
Nrm	C	A	17: 35,864,264 (GRCm38)	Y61*	probably null	Het
Nusap1	A	G	2: 119,627,667 (GRCm38)	T95A	probably damaging	Het
Ocln	T	A	13: 100,506,236 (GRCm38)	Q197L	probably damaging	Het
Olfr495	T	A	7: 108,395,764 (GRCm38)	F215I	probably benign	Het
Oxtr	A	G	6: 112,489,200 (GRCm38)	Y200H	probably damaging	Het
Paip2b	T	C	6: 83,809,909 (GRCm38)	E115G	possibly damaging	Het
Pcm1	T	A	8: 41,267,179 (GRCm38)		probably benign	Het
Phka1	G	A	X: 102,621,400 (GRCm38)	R186C	probably damaging	Het
Pik3cb	A	G	9: 99,064,218 (GRCm38)		probably benign	Het
Pik3r1	C	T	13: 101,757,418 (GRCm38)	R81K	probably benign	Het
Ppa1	A	G	10: 61,666,970 (GRCm38)	R191G	probably damaging	Het
Ppa1	A	G	10: 61,665,440 (GRCm38)	D162G	probably benign	Het
Prss22	T	A	17: 23,996,688 (GRCm38)	T87S	probably benign	Het
Rgr	T	A	14: 37,038,947 (GRCm38)	R218*	probably null	Het
Rreb1	A	T	13: 37,941,564 (GRCm38)	Q1282L	possibly damaging	Het
Scel	T	A	14: 103,583,139 (GRCm38)		probably null	Het
Sema6b	A	G	17: 56,129,971 (GRCm38)		probably null	Het
Slc4a1	T	C	11: 102,352,672 (GRCm38)	E711G	possibly damaging	Het
Snx19	T	G	9: 30,428,811 (GRCm38)	L415R	probably damaging	Het
Snx19	C	A	9: 30,428,810 (GRCm38)	L415M	probably damaging	Het
Specc1	G	A	11: 62,118,903 (GRCm38)	R495Q	probably damaging	Het
Tead1	T	C	7: 112,891,706 (GRCm38)		probably benign	Het
Timm10b	A	C	7: 105,640,688 (GRCm38)		probably benign	Het
Ubxn7	T	A	16: 32,367,417 (GRCm38)		probably benign	Het
Vmn2r116	T	A	17: 23,386,887 (GRCm38)	Y258N	possibly damaging	Het
Vmn2r77	T	A	7: 86,811,175 (GRCm38)	F570I	probably benign	Het
Vmn2r98	T	C	17: 19,080,497 (GRCm38)	V587A	probably benign	Het
Zfp398	T	C	6: 47,863,140 (GRCm38)	I101T	probably damaging	Het
Zfp808	T	A	13: 62,172,419 (GRCm38)	H487Q	probably damaging	Het

Other mutations in Pcnt

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01075:Pcnt	APN	10	76,422,904 (GRCm38)	nonsense	probably null
IGL01307:Pcnt	APN	10	76,411,588 (GRCm38)	missense	probably damaging	1.00
IGL01549:Pcnt	APN	10	76,367,486 (GRCm38)	splice site	probably null
IGL01576:Pcnt	APN	10	76,368,822 (GRCm38)	missense	probably damaging	0.99
IGL01611:Pcnt	APN	10	76,436,424 (GRCm38)	critical splice donor site	probably null
IGL01630:Pcnt	APN	10	76,420,246 (GRCm38)	missense	probably damaging	0.99
IGL01647:Pcnt	APN	10	76,370,001 (GRCm38)	nonsense	probably null
IGL01689:Pcnt	APN	10	76,411,653 (GRCm38)	missense	probably damaging	1.00
IGL01690:Pcnt	APN	10	76,392,775 (GRCm38)	missense	probably damaging	1.00
IGL01723:Pcnt	APN	10	76,418,499 (GRCm38)	missense	possibly damaging	0.63
IGL01920:Pcnt	APN	10	76,404,528 (GRCm38)	missense	probably damaging	1.00
IGL01958:Pcnt	APN	10	76,433,679 (GRCm38)	missense	probably damaging	0.96
IGL02210:Pcnt	APN	10	76,389,219 (GRCm38)	missense	possibly damaging	0.95
IGL02225:Pcnt	APN	10	76,389,474 (GRCm38)	missense	probably benign	0.00
IGL02228:Pcnt	APN	10	76,389,474 (GRCm38)	missense	probably benign	0.00
IGL02237:Pcnt	APN	10	76,352,984 (GRCm38)	missense	probably damaging	1.00
IGL02279:Pcnt	APN	10	76,403,765 (GRCm38)	missense	probably damaging	1.00
IGL02303:Pcnt	APN	10	76,442,559 (GRCm38)	splice site	probably benign
IGL02355:Pcnt	APN	10	76,375,162 (GRCm38)	nonsense	probably null
IGL02362:Pcnt	APN	10	76,375,162 (GRCm38)	nonsense	probably null
IGL02428:Pcnt	APN	10	76,429,256 (GRCm38)	missense	probably damaging	0.99
IGL02536:Pcnt	APN	10	76,380,229 (GRCm38)	missense	possibly damaging	0.68
IGL02715:Pcnt	APN	10	76,368,722 (GRCm38)	splice site	probably benign
IGL02800:Pcnt	APN	10	76,412,583 (GRCm38)	nonsense	probably null
IGL03395:Pcnt	APN	10	76,436,491 (GRCm38)	missense	possibly damaging	0.95
IGL02799:Pcnt	UTSW	10	76,412,583 (GRCm38)	nonsense	probably null
PIT4520001:Pcnt	UTSW	10	76,420,235 (GRCm38)	missense	probably damaging	0.99
R0049:Pcnt	UTSW	10	76,369,821 (GRCm38)	unclassified	probably benign
R0049:Pcnt	UTSW	10	76,369,821 (GRCm38)	unclassified	probably benign
R0109:Pcnt	UTSW	10	76,389,196 (GRCm38)	missense	probably benign	0.00
R0117:Pcnt	UTSW	10	76,408,727 (GRCm38)	nonsense	probably null
R0254:Pcnt	UTSW	10	76,392,580 (GRCm38)	missense	probably benign	0.10
R0392:Pcnt	UTSW	10	76,384,826 (GRCm38)	missense	probably benign
R0511:Pcnt	UTSW	10	76,404,595 (GRCm38)	missense	possibly damaging	0.66
R0570:Pcnt	UTSW	10	76,412,107 (GRCm38)	missense	probably damaging	1.00
R0614:Pcnt	UTSW	10	76,420,316 (GRCm38)	missense	probably damaging	1.00
R0707:Pcnt	UTSW	10	76,420,541 (GRCm38)	missense	probably damaging	1.00
R0749:Pcnt	UTSW	10	76,381,364 (GRCm38)	missense	probably damaging	1.00
R0969:Pcnt	UTSW	10	76,427,951 (GRCm38)	missense	probably damaging	1.00
R1172:Pcnt	UTSW	10	76,393,044 (GRCm38)	splice site	probably null
R1174:Pcnt	UTSW	10	76,393,044 (GRCm38)	splice site	probably null
R1175:Pcnt	UTSW	10	76,393,044 (GRCm38)	splice site	probably null
R1512:Pcnt	UTSW	10	76,404,662 (GRCm38)	splice site	probably null
R1542:Pcnt	UTSW	10	76,401,386 (GRCm38)	missense	probably benign	0.02
R1542:Pcnt	UTSW	10	76,389,387 (GRCm38)	missense	probably benign	0.08
R1558:Pcnt	UTSW	10	76,422,922 (GRCm38)	missense	possibly damaging	0.53
R1562:Pcnt	UTSW	10	76,367,330 (GRCm38)	missense	probably benign	0.02
R1762:Pcnt	UTSW	10	76,355,137 (GRCm38)	critical splice acceptor site	probably null
R1779:Pcnt	UTSW	10	76,408,796 (GRCm38)	missense	probably damaging	0.99
R1869:Pcnt	UTSW	10	76,379,906 (GRCm38)	missense	probably null	0.94
R1911:Pcnt	UTSW	10	76,368,816 (GRCm38)	missense	possibly damaging	0.94
R1985:Pcnt	UTSW	10	76,380,337 (GRCm38)	missense	possibly damaging	0.95
R1995:Pcnt	UTSW	10	76,392,799 (GRCm38)	nonsense	probably null
R2073:Pcnt	UTSW	10	76,380,380 (GRCm38)	missense	possibly damaging	0.92
R2111:Pcnt	UTSW	10	76,420,526 (GRCm38)	missense	probably damaging	0.99
R2112:Pcnt	UTSW	10	76,420,526 (GRCm38)	missense	probably damaging	0.99
R2309:Pcnt	UTSW	10	76,442,626 (GRCm38)	start gained	probably benign
R2902:Pcnt	UTSW	10	76,375,230 (GRCm38)	missense	probably damaging	0.98
R3623:Pcnt	UTSW	10	76,433,750 (GRCm38)	missense	probably benign	0.23
R4088:Pcnt	UTSW	10	76,428,014 (GRCm38)	missense	probably damaging	1.00
R4300:Pcnt	UTSW	10	76,367,391 (GRCm38)	missense	probably benign	0.40
R4402:Pcnt	UTSW	10	76,392,393 (GRCm38)	missense	probably benign	0.00
R4407:Pcnt	UTSW	10	76,374,870 (GRCm38)	missense	possibly damaging	0.90
R4483:Pcnt	UTSW	10	76,401,483 (GRCm38)	missense	probably damaging	1.00
R4647:Pcnt	UTSW	10	76,354,213 (GRCm38)	missense	probably benign	0.01
R4734:Pcnt	UTSW	10	76,437,206 (GRCm38)	missense	probably benign	0.25
R4747:Pcnt	UTSW	10	76,436,465 (GRCm38)	missense	possibly damaging	0.91
R4782:Pcnt	UTSW	10	76,409,577 (GRCm38)	missense	possibly damaging	0.62
R4795:Pcnt	UTSW	10	76,370,024 (GRCm38)	missense	probably benign	0.21
R4831:Pcnt	UTSW	10	76,412,501 (GRCm38)	missense	probably damaging	0.96
R4873:Pcnt	UTSW	10	76,369,854 (GRCm38)	missense	probably benign	0.03
R4875:Pcnt	UTSW	10	76,369,854 (GRCm38)	missense	probably benign	0.03
R4946:Pcnt	UTSW	10	76,356,185 (GRCm38)	missense	probably damaging	1.00
R5032:Pcnt	UTSW	10	76,355,077 (GRCm38)	missense	probably benign	0.00
R5033:Pcnt	UTSW	10	76,399,945 (GRCm38)	missense	possibly damaging	0.95
R5106:Pcnt	UTSW	10	76,401,444 (GRCm38)	missense	probably damaging	1.00
R5118:Pcnt	UTSW	10	76,412,168 (GRCm38)	missense	probably damaging	0.98
R5167:Pcnt	UTSW	10	76,420,424 (GRCm38)	missense	probably damaging	0.97
R5199:Pcnt	UTSW	10	76,418,544 (GRCm38)	missense	probably benign	0.09
R5223:Pcnt	UTSW	10	76,380,272 (GRCm38)	missense	probably damaging	0.99
R5241:Pcnt	UTSW	10	76,433,617 (GRCm38)	missense	probably benign	0.26
R5308:Pcnt	UTSW	10	76,356,325 (GRCm38)	nonsense	probably null
R5328:Pcnt	UTSW	10	76,411,719 (GRCm38)	missense	probably damaging	1.00
R5454:Pcnt	UTSW	10	76,389,547 (GRCm38)	splice site	probably null
R5543:Pcnt	UTSW	10	76,412,052 (GRCm38)	missense	probably benign	0.01
R5588:Pcnt	UTSW	10	76,442,611 (GRCm38)	missense	possibly damaging	0.74
R5647:Pcnt	UTSW	10	76,385,841 (GRCm38)	missense	probably benign	0.17
R5668:Pcnt	UTSW	10	76,409,500 (GRCm38)	missense	probably benign	0.16
R5712:Pcnt	UTSW	10	76,429,271 (GRCm38)	missense	probably damaging	0.96
R5714:Pcnt	UTSW	10	76,420,491 (GRCm38)	missense	probably damaging	1.00
R5797:Pcnt	UTSW	10	76,392,756 (GRCm38)	missense	probably benign	0.00
R5946:Pcnt	UTSW	10	76,382,063 (GRCm38)	missense	possibly damaging	0.91
R5955:Pcnt	UTSW	10	76,411,622 (GRCm38)	missense	possibly damaging	0.45
R6024:Pcnt	UTSW	10	76,420,037 (GRCm38)	missense	possibly damaging	0.87
R6267:Pcnt	UTSW	10	76,385,798 (GRCm38)	missense	probably benign	0.02
R6485:Pcnt	UTSW	10	76,389,330 (GRCm38)	nonsense	probably null
R6605:Pcnt	UTSW	10	76,429,198 (GRCm38)	critical splice donor site	probably null
R6877:Pcnt	UTSW	10	76,434,017 (GRCm38)	missense	possibly damaging	0.94
R6882:Pcnt	UTSW	10	76,427,828 (GRCm38)	missense	probably benign	0.00
R6919:Pcnt	UTSW	10	76,385,798 (GRCm38)	missense	probably benign	0.02
R7025:Pcnt	UTSW	10	76,403,835 (GRCm38)	missense	probably damaging	1.00
R7098:Pcnt	UTSW	10	76,384,839 (GRCm38)	missense	probably benign
R7109:Pcnt	UTSW	10	76,369,904 (GRCm38)	missense	probably damaging	1.00
R7121:Pcnt	UTSW	10	76,427,927 (GRCm38)	missense	possibly damaging	0.73
R7143:Pcnt	UTSW	10	76,389,060 (GRCm38)	missense	possibly damaging	0.47
R7152:Pcnt	UTSW	10	76,411,360 (GRCm38)	splice site	probably null
R7213:Pcnt	UTSW	10	76,408,904 (GRCm38)	missense	probably damaging	1.00
R7368:Pcnt	UTSW	10	76,400,001 (GRCm38)	missense	probably benign
R7453:Pcnt	UTSW	10	76,389,450 (GRCm38)	missense	probably benign
R7486:Pcnt	UTSW	10	76,418,437 (GRCm38)	missense	probably benign
R7486:Pcnt	UTSW	10	76,418,436 (GRCm38)	missense	probably benign	0.03
R7538:Pcnt	UTSW	10	76,399,939 (GRCm38)	missense	probably benign
R7575:Pcnt	UTSW	10	76,389,252 (GRCm38)	missense	probably benign	0.32
R7662:Pcnt	UTSW	10	76,387,522 (GRCm38)	missense	probably benign	0.27
R7685:Pcnt	UTSW	10	76,422,808 (GRCm38)	missense	probably benign	0.14
R7764:Pcnt	UTSW	10	76,354,248 (GRCm38)	missense	probably benign	0.33
R7802:Pcnt	UTSW	10	76,375,303 (GRCm38)	splice site	probably null
R8432:Pcnt	UTSW	10	76,420,205 (GRCm38)	missense	probably damaging	1.00
R8439:Pcnt	UTSW	10	76,420,205 (GRCm38)	missense	probably damaging	1.00
R8493:Pcnt	UTSW	10	76,403,623 (GRCm38)	critical splice donor site	probably null
R8530:Pcnt	UTSW	10	76,420,205 (GRCm38)	missense	probably damaging	1.00
R8535:Pcnt	UTSW	10	76,420,205 (GRCm38)	missense	probably damaging	1.00
R8830:Pcnt	UTSW	10	76,382,174 (GRCm38)	missense	probably benign	0.03
R8878:Pcnt	UTSW	10	76,408,841 (GRCm38)	missense	probably damaging	1.00
R8911:Pcnt	UTSW	10	76,387,525 (GRCm38)	missense	probably damaging	0.98
R8988:Pcnt	UTSW	10	76,409,573 (GRCm38)	nonsense	probably null
R9084:Pcnt	UTSW	10	76,399,992 (GRCm38)	missense	probably benign	0.09
R9169:Pcnt	UTSW	10	76,385,738 (GRCm38)	missense	possibly damaging	0.95
R9372:Pcnt	UTSW	10	76,423,126 (GRCm38)	missense	probably damaging	1.00
R9411:Pcnt	UTSW	10	76,423,062 (GRCm38)	missense	probably damaging	0.96
R9448:Pcnt	UTSW	10	76,420,526 (GRCm38)	missense	probably damaging	0.99
R9459:Pcnt	UTSW	10	76,392,738 (GRCm38)	missense	probably damaging	1.00
R9479:Pcnt	UTSW	10	76,382,129 (GRCm38)	missense	probably benign	0.00
R9503:Pcnt	UTSW	10	76,428,048 (GRCm38)	missense	possibly damaging	0.59
R9561:Pcnt	UTSW	10	76,381,294 (GRCm38)	nonsense	probably null
R9618:Pcnt	UTSW	10	76,352,960 (GRCm38)	missense	probably damaging	1.00
R9648:Pcnt	UTSW	10	76,354,255 (GRCm38)	missense	probably benign	0.32
R9733:Pcnt	UTSW	10	76,401,480 (GRCm38)	missense	probably benign	0.01
Z1176:Pcnt	UTSW	10	76,382,157 (GRCm38)	nonsense	probably null
Z1177:Pcnt	UTSW	10	76,399,968 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CCTCCTTACATCCATGAACTGACGC -3'
(R):5'- GCTTGAATCTCACGCCAGCCATAG -3'

Sequencing Primer
(F):5'- ATGAACTGACGCTGGCTAC -3'
(R):5'- ACGGTTGTCTCCTAAGCG -3'

Posted On

2013-07-11