Mutagenetix > Incidental Mutation

Incidental Mutation 'R7475:Pkhd1l1'

579446

Institutional Source

Beutler Lab

Gene Symbol

Pkhd1l1

Ensembl Gene

ENSMUSG00000038725

Gene Name

polycystic kidney and hepatic disease 1-like 1

Synonyms

PKHDL1, D86 mRNA, fibrocystin L

MMRRC Submission

045549-MU

Accession Numbers

Genbank: NM_138674; MGI: 2183153

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7475 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

44457494-44601369 bp(+) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to T at 44505185 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 800 (Q800*)

Ref Sequence

ENSEMBL: ENSMUSP00000036988 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038336] [ENSMUST00000166957] [ENSMUST00000209244]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000038336
AA Change: Q800*

SMART Domains

Protein: ENSMUSP00000036988
Gene: ENSMUSG00000038725
AA Change: Q800*

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
IPT	30	141	9.02e-3	SMART
Pfam:TIG	146	255	1.6e-16	PFAM
IPT	269	362	2.27e-8	SMART
PbH1	398	420	2.98e3	SMART
IPT	1066	1154	5.34e-5	SMART
IPT	1156	1235	1.44e-1	SMART
Pfam:TIG	1240	1322	1.1e-13	PFAM
IPT	1328	1407	7.06e0	SMART
Pfam:TIG	1565	1645	5.1e-11	PFAM
IPT	1657	1743	1.89e-5	SMART
Pfam:TIG	1748	1828	2.1e-10	PFAM
IPT	1829	1910	4.87e-8	SMART
IPT	1914	1997	6.84e-3	SMART
IPT	1998	2085	9.86e-1	SMART
IPT	2089	2176	7.21e-11	SMART
PbH1	2105	2126	1.56e3	SMART
G8	2183	2303	2.37e-59	SMART
PbH1	2484	2506	9.48e3	SMART
PbH1	2507	2529	8.45e2	SMART
PbH1	2565	2587	4.11e3	SMART
PbH1	2664	2686	3.5e3	SMART
PbH1	2732	2755	2.7e3	SMART
Blast:G8	2949	2979	1e-5	BLAST
low complexity region	3014	3025	N/A	INTRINSIC
G8	3035	3173	6.5e-57	SMART
PbH1	3292	3314	1.96e3	SMART
PbH1	3354	3376	3.79e1	SMART
PbH1	3415	3437	4.87e2	SMART
PbH1	3470	3492	8.34e3	SMART
PbH1	3493	3514	5.86e3	SMART
low complexity region	3563	3574	N/A	INTRINSIC
low complexity region	4076	4103	N/A	INTRINSIC
low complexity region	4184	4212	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000166957
AA Change: Q800*

SMART Domains

Protein: ENSMUSP00000129522
Gene: ENSMUSG00000038725
AA Change: Q800*

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
IPT	30	141	9.02e-3	SMART
Pfam:TIG	146	255	9.4e-18	PFAM
IPT	269	362	2.27e-8	SMART
PbH1	398	420	2.98e3	SMART
IPT	1066	1154	5.34e-5	SMART
IPT	1156	1235	1.44e-1	SMART
Pfam:TIG	1240	1323	3e-13	PFAM
IPT	1328	1407	7.06e0	SMART
Pfam:TIG	1565	1645	3.7e-11	PFAM
IPT	1657	1743	1.89e-5	SMART
Pfam:TIG	1748	1828	9.7e-12	PFAM
IPT	1829	1910	4.87e-8	SMART
IPT	1914	1997	6.84e-3	SMART
IPT	1998	2085	9.86e-1	SMART
IPT	2089	2176	7.21e-11	SMART
PbH1	2105	2126	1.56e3	SMART
G8	2183	2303	2.37e-59	SMART
PbH1	2484	2506	9.48e3	SMART
PbH1	2507	2529	8.45e2	SMART
PbH1	2565	2587	4.11e3	SMART
PbH1	2664	2686	3.5e3	SMART
PbH1	2732	2755	2.7e3	SMART
Blast:G8	2949	2979	1e-5	BLAST
low complexity region	3014	3025	N/A	INTRINSIC
G8	3035	3173	6.5e-57	SMART
PbH1	3292	3314	1.96e3	SMART
PbH1	3354	3376	3.79e1	SMART
PbH1	3415	3437	4.87e2	SMART
PbH1	3470	3492	8.34e3	SMART
PbH1	3493	3514	5.86e3	SMART
low complexity region	3563	3574	N/A	INTRINSIC
low complexity region	4076	4103	N/A	INTRINSIC
low complexity region	4184	4212	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000209244
AA Change: Q800*

Coding Region Coverage

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

Validation Efficiency

99% (77/78)

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc5	G	T	16: 20,399,989 (GRCm38)	N214K	probably benign	Het
Abcf1	A	G	17: 35,963,567 (GRCm38)		probably null	Het
Agxt2	A	T	15: 10,409,537 (GRCm38)	M508L	probably benign	Het
Akr1c21	A	T	13: 4,576,319 (GRCm38)	Y114F	probably benign	Het
Amz1	T	C	5: 140,744,186 (GRCm38)		probably null	Het
Ank1	G	T	8: 23,132,630 (GRCm38)	A1732S	probably benign	Het
Atg16l1	T	C	1: 87,760,083 (GRCm38)	S50P	possibly damaging	Het
AW551984	A	G	9: 39,597,940 (GRCm38)	S302P	probably damaging	Het
Ces3a	T	A	8: 105,053,690 (GRCm38)		probably null	Het
Dedd	C	A	1: 171,340,313 (GRCm38)	P185Q	probably benign	Het
Fam186a	A	T	15: 99,947,514 (GRCm38)	V283E	unknown	Het
Fat2	C	A	11: 55,303,653 (GRCm38)	V1187F	probably benign	Het
Fbxw11	T	C	11: 32,711,999 (GRCm38)		probably null	Het
Fcgbp	C	T	7: 28,102,976 (GRCm38)	T1443I	probably damaging	Het
Foxj2	A	G	6: 122,837,842 (GRCm38)	D279G	probably benign	Het
Gbp5	A	G	3: 142,501,361 (GRCm38)	D97G	probably damaging	Het
Gm49368	A	T	7: 128,107,982 (GRCm38)	T661S	possibly damaging	Het
Gria4	T	G	9: 4,513,330 (GRCm38)	T260P	probably damaging	Het
Gtf2ird2	T	A	5: 134,201,426 (GRCm38)	D195E	possibly damaging	Het
Hectd4	T	A	5: 121,358,133 (GRCm38)		probably null	Het
Ifngr2	G	A	16: 91,557,909 (GRCm38)	C32Y	unknown	Het
Ikzf5	A	T	7: 131,392,059 (GRCm38)	C280S	probably benign	Het
Ints9	G	T	14: 65,026,465 (GRCm38)	E395D	probably null	Het
Isoc2b	T	C	7: 4,851,085 (GRCm38)	D96G	probably benign	Het
Jmjd1c	T	G	10: 67,225,313 (GRCm38)	S967R	probably benign	Het
Kcnj3	A	T	2: 55,437,326 (GRCm38)	K42N	probably benign	Het
Kiz	T	C	2: 146,891,086 (GRCm38)	V394A	possibly damaging	Het
Knl1	A	T	2: 119,087,546 (GRCm38)	H1795L	probably damaging	Het
Lmntd2	A	G	7: 141,210,689 (GRCm38)		probably null	Het
Loxhd1	C	A	18: 77,412,305 (GRCm38)	D1690E	possibly damaging	Het
Lrp1b	T	C	2: 41,344,576 (GRCm38)	D1121G		Het
Map3k2	T	C	18: 32,199,962 (GRCm38)	V63A	possibly damaging	Het
Mcc	G	T	18: 44,476,236 (GRCm38)	A499D	probably damaging	Het
Mcpt9	T	A	14: 56,026,943 (GRCm38)	I232F	probably damaging	Het
Meltf	A	G	16: 31,881,938 (GRCm38)	K92R	probably benign	Het
Mff	T	A	1: 82,745,438 (GRCm38)		probably null	Het
Mrgpra3	T	A	7: 47,589,947 (GRCm38)	Y77F	probably damaging	Het
Mylk	G	A	16: 34,914,076 (GRCm38)		probably null	Het
Ndufv2	A	G	17: 66,087,537 (GRCm38)	V111A	possibly damaging	Het
Nkd2	T	C	13: 73,825,742 (GRCm38)	E99G	probably damaging	Het
Nlk	C	A	11: 78,583,399 (GRCm38)	G358V	probably damaging	Het
Nnmt	A	T	9: 48,592,232 (GRCm38)	C165S	probably damaging	Het
Nxpe4	T	A	9: 48,393,340 (GRCm38)	C242*	probably null	Het
Oas1b	A	T	5: 120,817,640 (GRCm38)	N162I	probably damaging	Het
Olfr1191-ps1	A	G	2: 88,643,210 (GRCm38)	I148V	probably benign	Het
Otog	A	G	7: 46,267,276 (GRCm38)	N879S	probably damaging	Het
Park2	A	G	17: 11,434,614 (GRCm38)	D199G	probably benign	Het
Pcsk7	T	A	9: 45,927,625 (GRCm38)	Y612N	probably damaging	Het
Peg10	CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG	CCACATCAGGATCCACATCAGGATGCACATCAG	6: 4,756,398 (GRCm38)		probably benign	Het
Pgbd5	T	C	8: 124,434,011 (GRCm38)	D39G	probably benign	Het
Pkn3	T	C	2: 30,087,110 (GRCm38)	S621P	probably benign	Het
Polr3c	T	C	3: 96,715,185 (GRCm38)	I385V	probably benign	Het
Ppp1r21	G	T	17: 88,555,603 (GRCm38)	G257W	probably benign	Het
Pxylp1	C	T	9: 96,856,367 (GRCm38)		probably null	Het
Rasgrp1	T	C	2: 117,286,108 (GRCm38)	T613A	probably benign	Het
Robo3	C	T	9: 37,425,378 (GRCm38)	V387I	probably benign	Het
Rxfp2	T	A	5: 150,049,581 (GRCm38)	Y174N	possibly damaging	Het
Sec24a	T	C	11: 51,713,552 (GRCm38)	M746V	probably damaging	Het
Sema4f	T	A	6: 82,914,374 (GRCm38)	E571D	possibly damaging	Het
Sept3	T	C	15: 82,286,456 (GRCm38)	V217A	probably benign	Het
Serpinb1b	A	C	13: 33,093,565 (GRCm38)	K260N	probably benign	Het
Sin3b	A	G	8: 72,749,872 (GRCm38)	T645A	possibly damaging	Het
Sobp	C	T	10: 43,021,834 (GRCm38)	R585Q	probably damaging	Het
Specc1l	T	A	10: 75,246,447 (GRCm38)	L559Q	possibly damaging	Het
Srxn1	C	T	2: 152,105,653 (GRCm38)		probably benign	Het
Sspo	G	A	6: 48,455,860 (GRCm38)	R890Q	probably benign	Het
Stard9	A	G	2: 120,688,110 (GRCm38)	D505G	probably damaging	Het
Tjp1	A	T	7: 65,322,339 (GRCm38)	I653K	probably damaging	Het
Tnks	C	T	8: 34,831,712 (GRCm38)	E1296K	probably damaging	Het
Ttbk2	A	T	2: 120,748,640 (GRCm38)	I667N	probably benign	Het
Usp24	T	C	4: 106,342,353 (GRCm38)	S165P	possibly damaging	Het
Usp46	T	A	5: 74,028,937 (GRCm38)	K109*	probably null	Het
Vmn1r191	A	G	13: 22,178,772 (GRCm38)	C271R	probably benign	Het
Wisp3	T	A	10: 39,158,300 (GRCm38)	Y102F	probably damaging	Het
Zfp592	T	C	7: 81,023,452 (GRCm38)	S55P	probably damaging	Het
Zmynd15	T	C	11: 70,461,041 (GRCm38)	S158P	probably benign	Het
Zscan22	T	G	7: 12,906,737 (GRCm38)	C303G	probably damaging	Het

Other mutations in Pkhd1l1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00233:Pkhd1l1	APN	15	44,477,586 (GRCm38)	missense	probably damaging	1.00
IGL00235:Pkhd1l1	APN	15	44,556,019 (GRCm38)	missense	probably damaging	1.00
IGL00264:Pkhd1l1	APN	15	44,491,029 (GRCm38)	missense	possibly damaging	0.67
IGL00537:Pkhd1l1	APN	15	44,591,992 (GRCm38)	missense	possibly damaging	0.88
IGL00537:Pkhd1l1	APN	15	44,500,047 (GRCm38)	missense	probably benign	0.42
IGL00580:Pkhd1l1	APN	15	44,586,474 (GRCm38)	missense	probably damaging	0.98
IGL01085:Pkhd1l1	APN	15	44,562,752 (GRCm38)	splice site	probably null
IGL01089:Pkhd1l1	APN	15	44,483,869 (GRCm38)	splice site	probably benign
IGL01094:Pkhd1l1	APN	15	44,546,929 (GRCm38)	missense	probably benign	0.09
IGL01120:Pkhd1l1	APN	15	44,505,312 (GRCm38)	critical splice donor site	probably null
IGL01307:Pkhd1l1	APN	15	44,530,029 (GRCm38)	missense	possibly damaging	0.82
IGL01362:Pkhd1l1	APN	15	44,532,982 (GRCm38)	missense	probably benign	0.00
IGL01403:Pkhd1l1	APN	15	44,483,833 (GRCm38)	nonsense	probably null
IGL01546:Pkhd1l1	APN	15	44,566,316 (GRCm38)	missense	probably damaging	1.00
IGL01596:Pkhd1l1	APN	15	44,529,410 (GRCm38)	missense	possibly damaging	0.50
IGL01696:Pkhd1l1	APN	15	44,529,351 (GRCm38)	missense	possibly damaging	0.79
IGL01844:Pkhd1l1	APN	15	44,499,400 (GRCm38)	splice site	probably benign
IGL02007:Pkhd1l1	APN	15	44,533,733 (GRCm38)	splice site	probably benign
IGL02041:Pkhd1l1	APN	15	44,493,056 (GRCm38)	splice site	probably null
IGL02171:Pkhd1l1	APN	15	44,516,146 (GRCm38)	missense	possibly damaging	0.80
IGL02206:Pkhd1l1	APN	15	44,512,849 (GRCm38)	missense	probably benign	0.08
IGL02266:Pkhd1l1	APN	15	44,573,614 (GRCm38)	missense	probably damaging	1.00
IGL02487:Pkhd1l1	APN	15	44,459,426 (GRCm38)	missense	possibly damaging	0.65
IGL02488:Pkhd1l1	APN	15	44,558,597 (GRCm38)	missense	probably benign
IGL02522:Pkhd1l1	APN	15	44,555,902 (GRCm38)	missense	possibly damaging	0.71
IGL02554:Pkhd1l1	APN	15	44,578,500 (GRCm38)	missense	probably damaging	1.00
IGL02566:Pkhd1l1	APN	15	44,526,054 (GRCm38)	splice site	probably null
IGL02602:Pkhd1l1	APN	15	44,557,931 (GRCm38)	missense	probably damaging	1.00
IGL02606:Pkhd1l1	APN	15	44,589,456 (GRCm38)	missense	probably benign	0.00
IGL02623:Pkhd1l1	APN	15	44,584,873 (GRCm38)	missense	probably damaging	1.00
IGL02634:Pkhd1l1	APN	15	44,539,667 (GRCm38)	missense	probably damaging	1.00
IGL02637:Pkhd1l1	APN	15	44,564,324 (GRCm38)	missense	probably damaging	1.00
IGL02651:Pkhd1l1	APN	15	44,483,814 (GRCm38)	missense	probably damaging	1.00
IGL02679:Pkhd1l1	APN	15	44,530,045 (GRCm38)	critical splice donor site	probably null
IGL02684:Pkhd1l1	APN	15	44,516,209 (GRCm38)	critical splice donor site	probably null
IGL02739:Pkhd1l1	APN	15	44,540,950 (GRCm38)	missense	probably benign	0.11
IGL02831:Pkhd1l1	APN	15	44,501,493 (GRCm38)	missense	probably benign	0.18
IGL02839:Pkhd1l1	APN	15	44,529,543 (GRCm38)	missense	probably damaging	0.98
IGL02944:Pkhd1l1	APN	15	44,501,531 (GRCm38)	missense	probably damaging	1.00
IGL02957:Pkhd1l1	APN	15	44,512,908 (GRCm38)	missense	probably damaging	1.00
IGL03001:Pkhd1l1	APN	15	44,558,004 (GRCm38)	missense	probably damaging	1.00
IGL03030:Pkhd1l1	APN	15	44,596,902 (GRCm38)	missense	probably benign	0.41
IGL03030:Pkhd1l1	APN	15	44,591,976 (GRCm38)	missense	probably benign	0.00
IGL03132:Pkhd1l1	APN	15	44,574,617 (GRCm38)	missense	probably damaging	1.00
IGL03194:Pkhd1l1	APN	15	44,518,135 (GRCm38)	missense	probably damaging	1.00
IGL03219:Pkhd1l1	APN	15	44,596,895 (GRCm38)	missense	possibly damaging	0.62
IGL03236:Pkhd1l1	APN	15	44,581,826 (GRCm38)	missense	probably damaging	1.00
IGL03266:Pkhd1l1	APN	15	44,538,952 (GRCm38)	missense	probably damaging	1.00
IGL03276:Pkhd1l1	APN	15	44,594,584 (GRCm38)	missense	possibly damaging	0.77
IGL03284:Pkhd1l1	APN	15	44,547,518 (GRCm38)	splice site	probably benign
IGL03377:Pkhd1l1	APN	15	44,484,351 (GRCm38)	splice site	probably null
R0310_Pkhd1l1_251	UTSW	15	44,522,738 (GRCm38)	splice site	probably benign
R0344_Pkhd1l1_462	UTSW	15	44,597,011 (GRCm38)	missense	probably benign	0.15
R1737_Pkhd1l1_815	UTSW	15	44,547,509 (GRCm38)	critical splice donor site	probably null
R5049_Pkhd1l1_556	UTSW	15	44,457,616 (GRCm38)	missense	probably benign	0.00
K7371:Pkhd1l1	UTSW	15	44,500,067 (GRCm38)	missense	possibly damaging	0.94
K7371:Pkhd1l1	UTSW	15	44,537,442 (GRCm38)	missense	possibly damaging	0.67
N/A - 287:Pkhd1l1	UTSW	15	44,582,258 (GRCm38)	missense	probably damaging	0.98
P4717OSA:Pkhd1l1	UTSW	15	44,523,499 (GRCm38)	missense	probably benign	0.17
P4717OSA:Pkhd1l1	UTSW	15	44,528,247 (GRCm38)	missense	probably damaging	1.00
R0007:Pkhd1l1	UTSW	15	44,574,398 (GRCm38)	splice site	probably benign
R0020:Pkhd1l1	UTSW	15	44,556,872 (GRCm38)	missense	probably damaging	1.00
R0034:Pkhd1l1	UTSW	15	44,504,009 (GRCm38)	missense	probably benign	0.00
R0040:Pkhd1l1	UTSW	15	44,573,625 (GRCm38)	missense	probably damaging	1.00
R0050:Pkhd1l1	UTSW	15	44,573,807 (GRCm38)	missense	possibly damaging	0.79
R0050:Pkhd1l1	UTSW	15	44,573,807 (GRCm38)	missense	possibly damaging	0.79
R0063:Pkhd1l1	UTSW	15	44,529,237 (GRCm38)	missense	probably damaging	1.00
R0063:Pkhd1l1	UTSW	15	44,529,237 (GRCm38)	missense	probably damaging	1.00
R0086:Pkhd1l1	UTSW	15	44,556,008 (GRCm38)	missense	possibly damaging	0.94
R0103:Pkhd1l1	UTSW	15	44,597,141 (GRCm38)	missense	probably benign
R0103:Pkhd1l1	UTSW	15	44,597,141 (GRCm38)	missense	probably benign
R0127:Pkhd1l1	UTSW	15	44,554,605 (GRCm38)	missense	probably damaging	0.99
R0226:Pkhd1l1	UTSW	15	44,526,784 (GRCm38)	missense	possibly damaging	0.65
R0268:Pkhd1l1	UTSW	15	44,597,011 (GRCm38)	missense	probably benign	0.15
R0294:Pkhd1l1	UTSW	15	44,560,435 (GRCm38)	missense	probably benign	0.05
R0310:Pkhd1l1	UTSW	15	44,522,738 (GRCm38)	splice site	probably benign
R0344:Pkhd1l1	UTSW	15	44,597,011 (GRCm38)	missense	probably benign	0.15
R0449:Pkhd1l1	UTSW	15	44,501,519 (GRCm38)	missense	probably damaging	1.00
R0492:Pkhd1l1	UTSW	15	44,519,690 (GRCm38)	missense	probably benign	0.03
R0505:Pkhd1l1	UTSW	15	44,589,418 (GRCm38)	missense	probably damaging	1.00
R0529:Pkhd1l1	UTSW	15	44,526,754 (GRCm38)	missense	possibly damaging	0.62
R0543:Pkhd1l1	UTSW	15	44,523,491 (GRCm38)	critical splice acceptor site	probably null
R0552:Pkhd1l1	UTSW	15	44,489,546 (GRCm38)	missense	probably damaging	0.98
R0558:Pkhd1l1	UTSW	15	44,484,424 (GRCm38)	missense	probably damaging	0.97
R0609:Pkhd1l1	UTSW	15	44,467,424 (GRCm38)	missense	possibly damaging	0.48
R0619:Pkhd1l1	UTSW	15	44,483,838 (GRCm38)	missense	probably damaging	1.00
R0727:Pkhd1l1	UTSW	15	44,535,788 (GRCm38)	missense	possibly damaging	0.80
R0787:Pkhd1l1	UTSW	15	44,529,264 (GRCm38)	missense	probably damaging	1.00
R0846:Pkhd1l1	UTSW	15	44,495,597 (GRCm38)	missense	probably damaging	1.00
R0909:Pkhd1l1	UTSW	15	44,538,883 (GRCm38)	splice site	probably null
R0942:Pkhd1l1	UTSW	15	44,532,959 (GRCm38)	missense	probably benign	0.01
R1056:Pkhd1l1	UTSW	15	44,591,964 (GRCm38)	missense	probably damaging	1.00
R1147:Pkhd1l1	UTSW	15	44,537,441 (GRCm38)	missense	probably null	0.15
R1147:Pkhd1l1	UTSW	15	44,537,441 (GRCm38)	missense	probably null	0.15
R1187:Pkhd1l1	UTSW	15	44,498,051 (GRCm38)	missense	possibly damaging	0.65
R1328:Pkhd1l1	UTSW	15	44,497,996 (GRCm38)	missense	probably benign	0.01
R1331:Pkhd1l1	UTSW	15	44,589,597 (GRCm38)	missense	probably damaging	1.00
R1331:Pkhd1l1	UTSW	15	44,505,547 (GRCm38)	missense	probably damaging	1.00
R1332:Pkhd1l1	UTSW	15	44,505,547 (GRCm38)	missense	probably damaging	1.00
R1335:Pkhd1l1	UTSW	15	44,505,547 (GRCm38)	missense	probably damaging	1.00
R1338:Pkhd1l1	UTSW	15	44,526,724 (GRCm38)	missense	probably damaging	1.00
R1440:Pkhd1l1	UTSW	15	44,540,988 (GRCm38)	splice site	probably benign
R1445:Pkhd1l1	UTSW	15	44,505,644 (GRCm38)	missense	probably benign	0.32
R1458:Pkhd1l1	UTSW	15	44,516,115 (GRCm38)	missense	probably benign	0.01
R1469:Pkhd1l1	UTSW	15	44,536,886 (GRCm38)	missense	probably benign	0.45
R1469:Pkhd1l1	UTSW	15	44,536,886 (GRCm38)	missense	probably benign	0.45
R1500:Pkhd1l1	UTSW	15	44,545,494 (GRCm38)	missense	probably damaging	1.00
R1528:Pkhd1l1	UTSW	15	44,526,724 (GRCm38)	missense	probably damaging	1.00
R1542:Pkhd1l1	UTSW	15	44,528,191 (GRCm38)	missense	probably benign	0.44
R1568:Pkhd1l1	UTSW	15	44,545,501 (GRCm38)	splice site	probably null
R1571:Pkhd1l1	UTSW	15	44,526,841 (GRCm38)	missense	probably benign
R1572:Pkhd1l1	UTSW	15	44,543,473 (GRCm38)	missense	probably benign	0.01
R1604:Pkhd1l1	UTSW	15	44,467,367 (GRCm38)	nonsense	probably null
R1638:Pkhd1l1	UTSW	15	44,597,117 (GRCm38)	missense	probably benign	0.06
R1639:Pkhd1l1	UTSW	15	44,540,955 (GRCm38)	missense	probably damaging	0.99
R1737:Pkhd1l1	UTSW	15	44,547,509 (GRCm38)	critical splice donor site	probably null
R1816:Pkhd1l1	UTSW	15	44,528,239 (GRCm38)	missense	possibly damaging	0.91
R1826:Pkhd1l1	UTSW	15	44,503,345 (GRCm38)	missense	possibly damaging	0.75
R1880:Pkhd1l1	UTSW	15	44,525,242 (GRCm38)	missense	probably benign	0.13
R1930:Pkhd1l1	UTSW	15	44,503,337 (GRCm38)	missense	possibly damaging	0.69
R1933:Pkhd1l1	UTSW	15	44,540,884 (GRCm38)	missense	possibly damaging	0.48
R1938:Pkhd1l1	UTSW	15	44,500,038 (GRCm38)	missense	probably benign
R1975:Pkhd1l1	UTSW	15	44,529,713 (GRCm38)	missense	probably damaging	1.00
R1999:Pkhd1l1	UTSW	15	44,499,982 (GRCm38)	splice site	probably null
R2037:Pkhd1l1	UTSW	15	44,568,221 (GRCm38)	splice site	probably null
R2045:Pkhd1l1	UTSW	15	44,479,654 (GRCm38)	missense	probably damaging	1.00
R2049:Pkhd1l1	UTSW	15	44,581,741 (GRCm38)	missense	probably damaging	1.00
R2049:Pkhd1l1	UTSW	15	44,547,513 (GRCm38)	splice site	probably benign
R2063:Pkhd1l1	UTSW	15	44,550,752 (GRCm38)	missense	possibly damaging	0.69
R2072:Pkhd1l1	UTSW	15	44,558,639 (GRCm38)	missense	probably damaging	1.00
R2073:Pkhd1l1	UTSW	15	44,558,639 (GRCm38)	missense	probably damaging	1.00
R2075:Pkhd1l1	UTSW	15	44,558,639 (GRCm38)	missense	probably damaging	1.00
R2078:Pkhd1l1	UTSW	15	44,527,767 (GRCm38)	missense	probably benign	0.08
R2116:Pkhd1l1	UTSW	15	44,569,482 (GRCm38)	missense	probably damaging	0.97
R2133:Pkhd1l1	UTSW	15	44,516,185 (GRCm38)	missense	possibly damaging	0.91
R2138:Pkhd1l1	UTSW	15	44,501,457 (GRCm38)	missense	probably damaging	1.00
R2139:Pkhd1l1	UTSW	15	44,529,818 (GRCm38)	missense	possibly damaging	0.46
R2145:Pkhd1l1	UTSW	15	44,512,877 (GRCm38)	splice site	probably null
R2150:Pkhd1l1	UTSW	15	44,499,982 (GRCm38)	splice site	probably null
R2177:Pkhd1l1	UTSW	15	44,459,395 (GRCm38)	missense	probably benign
R2184:Pkhd1l1	UTSW	15	44,499,296 (GRCm38)	missense	possibly damaging	0.89
R2216:Pkhd1l1	UTSW	15	44,573,895 (GRCm38)	missense	probably damaging	1.00
R2226:Pkhd1l1	UTSW	15	44,512,792 (GRCm38)	missense	possibly damaging	0.79
R2227:Pkhd1l1	UTSW	15	44,512,792 (GRCm38)	missense	possibly damaging	0.79
R2243:Pkhd1l1	UTSW	15	44,546,927 (GRCm38)	missense	probably damaging	1.00
R2290:Pkhd1l1	UTSW	15	44,528,250 (GRCm38)	missense	probably benign	0.03
R2294:Pkhd1l1	UTSW	15	44,479,607 (GRCm38)	missense	probably damaging	0.99
R2346:Pkhd1l1	UTSW	15	44,560,506 (GRCm38)	missense	possibly damaging	0.82
R2356:Pkhd1l1	UTSW	15	44,533,019 (GRCm38)	missense	probably benign	0.00
R2386:Pkhd1l1	UTSW	15	44,528,178 (GRCm38)	missense	probably benign	0.00
R2404:Pkhd1l1	UTSW	15	44,550,820 (GRCm38)	missense	probably damaging	1.00
R2504:Pkhd1l1	UTSW	15	44,485,428 (GRCm38)	missense	probably damaging	0.97
R2679:Pkhd1l1	UTSW	15	44,545,386 (GRCm38)	missense	probably damaging	0.99
R2860:Pkhd1l1	UTSW	15	44,540,871 (GRCm38)	missense	probably damaging	1.00
R2861:Pkhd1l1	UTSW	15	44,540,871 (GRCm38)	missense	probably damaging	1.00
R2862:Pkhd1l1	UTSW	15	44,540,871 (GRCm38)	missense	probably damaging	1.00
R2972:Pkhd1l1	UTSW	15	44,547,248 (GRCm38)	missense	possibly damaging	0.65
R3016:Pkhd1l1	UTSW	15	44,545,370 (GRCm38)	missense	probably benign	0.02
R3162:Pkhd1l1	UTSW	15	44,505,528 (GRCm38)	missense	probably damaging	1.00
R3162:Pkhd1l1	UTSW	15	44,505,528 (GRCm38)	missense	probably damaging	1.00
R3416:Pkhd1l1	UTSW	15	44,547,364 (GRCm38)	missense	probably damaging	1.00
R3623:Pkhd1l1	UTSW	15	44,526,869 (GRCm38)	missense	probably damaging	1.00
R3687:Pkhd1l1	UTSW	15	44,546,587 (GRCm38)	missense	probably benign	0.17
R3755:Pkhd1l1	UTSW	15	44,589,406 (GRCm38)	missense	probably damaging	1.00
R3776:Pkhd1l1	UTSW	15	44,514,975 (GRCm38)	critical splice donor site	probably null
R3803:Pkhd1l1	UTSW	15	44,493,135 (GRCm38)	missense	probably benign	0.25
R3942:Pkhd1l1	UTSW	15	44,592,026 (GRCm38)	critical splice donor site	probably null
R4010:Pkhd1l1	UTSW	15	44,529,100 (GRCm38)	missense	possibly damaging	0.80
R4049:Pkhd1l1	UTSW	15	44,498,557 (GRCm38)	missense	probably damaging	1.00
R4059:Pkhd1l1	UTSW	15	44,550,760 (GRCm38)	missense	probably benign	0.01
R4179:Pkhd1l1	UTSW	15	44,523,649 (GRCm38)	missense	probably benign	0.45
R4184:Pkhd1l1	UTSW	15	44,591,906 (GRCm38)	missense	probably benign	0.00
R4369:Pkhd1l1	UTSW	15	44,505,553 (GRCm38)	missense	probably benign	0.00
R4462:Pkhd1l1	UTSW	15	44,581,804 (GRCm38)	missense	probably damaging	1.00
R4551:Pkhd1l1	UTSW	15	44,550,885 (GRCm38)	missense	probably damaging	1.00
R4618:Pkhd1l1	UTSW	15	44,539,682 (GRCm38)	missense	probably damaging	1.00
R4632:Pkhd1l1	UTSW	15	44,484,400 (GRCm38)	missense	probably benign	0.07
R4657:Pkhd1l1	UTSW	15	44,547,347 (GRCm38)	missense	probably damaging	1.00
R4716:Pkhd1l1	UTSW	15	44,556,032 (GRCm38)	missense	probably damaging	1.00
R4788:Pkhd1l1	UTSW	15	44,498,021 (GRCm38)	missense	probably damaging	0.99
R4828:Pkhd1l1	UTSW	15	44,529,405 (GRCm38)	missense	possibly damaging	0.55
R4858:Pkhd1l1	UTSW	15	44,491,101 (GRCm38)	missense	probably damaging	0.99
R4860:Pkhd1l1	UTSW	15	44,537,378 (GRCm38)	missense	possibly damaging	0.77
R4860:Pkhd1l1	UTSW	15	44,537,378 (GRCm38)	missense	possibly damaging	0.77
R4951:Pkhd1l1	UTSW	15	44,533,891 (GRCm38)	missense	possibly damaging	0.82
R4963:Pkhd1l1	UTSW	15	44,504,025 (GRCm38)	missense	probably benign	0.00
R5023:Pkhd1l1	UTSW	15	44,528,191 (GRCm38)	missense	probably benign	0.44
R5023:Pkhd1l1	UTSW	15	44,582,227 (GRCm38)	missense	probably benign	0.00
R5035:Pkhd1l1	UTSW	15	44,568,324 (GRCm38)	missense	probably damaging	1.00
R5049:Pkhd1l1	UTSW	15	44,457,616 (GRCm38)	missense	probably benign	0.00
R5065:Pkhd1l1	UTSW	15	44,582,293 (GRCm38)	missense	possibly damaging	0.68
R5089:Pkhd1l1	UTSW	15	44,591,887 (GRCm38)	missense	probably benign	0.01
R5151:Pkhd1l1	UTSW	15	44,505,309 (GRCm38)	missense	probably benign	0.00
R5153:Pkhd1l1	UTSW	15	44,505,309 (GRCm38)	missense	probably benign	0.00
R5189:Pkhd1l1	UTSW	15	44,547,148 (GRCm38)	missense	probably damaging	1.00
R5204:Pkhd1l1	UTSW	15	44,547,041 (GRCm38)	missense	possibly damaging	0.51
R5216:Pkhd1l1	UTSW	15	44,495,647 (GRCm38)	nonsense	probably null
R5286:Pkhd1l1	UTSW	15	44,514,972 (GRCm38)	nonsense	probably null
R5292:Pkhd1l1	UTSW	15	44,529,566 (GRCm38)	missense	probably damaging	1.00
R5293:Pkhd1l1	UTSW	15	44,535,750 (GRCm38)	missense	probably benign	0.01
R5298:Pkhd1l1	UTSW	15	44,504,046 (GRCm38)	missense	probably benign	0.00
R5327:Pkhd1l1	UTSW	15	44,546,862 (GRCm38)	missense	probably damaging	1.00
R5346:Pkhd1l1	UTSW	15	44,540,967 (GRCm38)	missense	probably damaging	1.00
R5481:Pkhd1l1	UTSW	15	44,558,646 (GRCm38)	missense	probably damaging	1.00
R5645:Pkhd1l1	UTSW	15	44,532,992 (GRCm38)	missense	probably benign	0.18
R5718:Pkhd1l1	UTSW	15	44,545,417 (GRCm38)	missense	probably damaging	1.00
R5809:Pkhd1l1	UTSW	15	44,519,707 (GRCm38)	missense	probably benign	0.03
R5816:Pkhd1l1	UTSW	15	44,566,322 (GRCm38)	missense	probably benign	0.01
R5854:Pkhd1l1	UTSW	15	44,581,790 (GRCm38)	missense	probably damaging	1.00
R5876:Pkhd1l1	UTSW	15	44,578,588 (GRCm38)	missense	possibly damaging	0.51
R5909:Pkhd1l1	UTSW	15	44,526,763 (GRCm38)	missense	probably damaging	1.00
R5950:Pkhd1l1	UTSW	15	44,532,965 (GRCm38)	missense	probably benign	0.00
R5961:Pkhd1l1	UTSW	15	44,459,463 (GRCm38)	missense	probably damaging	1.00
R5972:Pkhd1l1	UTSW	15	44,545,416 (GRCm38)	missense	probably damaging	1.00
R5975:Pkhd1l1	UTSW	15	44,525,988 (GRCm38)	missense	probably damaging	1.00
R5982:Pkhd1l1	UTSW	15	44,489,504 (GRCm38)	splice site	probably null
R6066:Pkhd1l1	UTSW	15	44,528,129 (GRCm38)	missense	probably damaging	0.99
R6122:Pkhd1l1	UTSW	15	44,557,940 (GRCm38)	missense	probably damaging	1.00
R6248:Pkhd1l1	UTSW	15	44,529,559 (GRCm38)	missense	probably benign
R6294:Pkhd1l1	UTSW	15	44,570,028 (GRCm38)	missense	probably damaging	1.00
R6301:Pkhd1l1	UTSW	15	44,589,525 (GRCm38)	missense	probably damaging	0.99
R6526:Pkhd1l1	UTSW	15	44,498,089 (GRCm38)	critical splice donor site	probably null
R6707:Pkhd1l1	UTSW	15	44,529,143 (GRCm38)	missense	probably benign
R6736:Pkhd1l1	UTSW	15	44,557,940 (GRCm38)	missense	probably damaging	1.00
R6753:Pkhd1l1	UTSW	15	44,589,663 (GRCm38)	missense	probably benign	0.45
R6815:Pkhd1l1	UTSW	15	44,562,655 (GRCm38)	missense	probably damaging	1.00
R6874:Pkhd1l1	UTSW	15	44,589,527 (GRCm38)	missense	probably benign	0.06
R6942:Pkhd1l1	UTSW	15	44,522,629 (GRCm38)	missense	probably damaging	1.00
R6970:Pkhd1l1	UTSW	15	44,511,674 (GRCm38)	missense	possibly damaging	0.61
R6982:Pkhd1l1	UTSW	15	44,566,268 (GRCm38)	missense	probably damaging	0.97
R7103:Pkhd1l1	UTSW	15	44,573,631 (GRCm38)	missense	probably benign	0.02
R7116:Pkhd1l1	UTSW	15	44,557,976 (GRCm38)	missense	probably benign	0.00
R7135:Pkhd1l1	UTSW	15	44,584,978 (GRCm38)	critical splice donor site	probably null
R7143:Pkhd1l1	UTSW	15	44,573,637 (GRCm38)	missense	possibly damaging	0.93
R7177:Pkhd1l1	UTSW	15	44,467,404 (GRCm38)	missense	probably damaging	1.00
R7194:Pkhd1l1	UTSW	15	44,529,116 (GRCm38)	missense	probably damaging	1.00
R7204:Pkhd1l1	UTSW	15	44,523,553 (GRCm38)	missense	possibly damaging	0.90
R7215:Pkhd1l1	UTSW	15	44,528,163 (GRCm38)	missense	possibly damaging	0.78
R7218:Pkhd1l1	UTSW	15	44,522,695 (GRCm38)	missense	possibly damaging	0.49
R7225:Pkhd1l1	UTSW	15	44,546,941 (GRCm38)	missense	probably damaging	1.00
R7283:Pkhd1l1	UTSW	15	44,503,280 (GRCm38)	missense	probably benign	0.10
R7292:Pkhd1l1	UTSW	15	44,498,590 (GRCm38)	missense	probably benign
R7304:Pkhd1l1	UTSW	15	44,498,482 (GRCm38)	missense	possibly damaging	0.94
R7349:Pkhd1l1	UTSW	15	44,514,954 (GRCm38)	missense	probably damaging	1.00
R7359:Pkhd1l1	UTSW	15	44,589,486 (GRCm38)	missense	probably damaging	1.00
R7407:Pkhd1l1	UTSW	15	44,595,011 (GRCm38)	missense	possibly damaging	0.75
R7481:Pkhd1l1	UTSW	15	44,512,911 (GRCm38)	missense	probably benign
R7554:Pkhd1l1	UTSW	15	44,495,470 (GRCm38)	missense	probably damaging	1.00
R7555:Pkhd1l1	UTSW	15	44,550,761 (GRCm38)	missense	possibly damaging	0.51
R7562:Pkhd1l1	UTSW	15	44,514,930 (GRCm38)	missense	possibly damaging	0.68
R7583:Pkhd1l1	UTSW	15	44,568,364 (GRCm38)	critical splice donor site	probably null
R7595:Pkhd1l1	UTSW	15	44,495,521 (GRCm38)	missense	probably damaging	1.00
R7749:Pkhd1l1	UTSW	15	44,527,737 (GRCm38)	missense	probably benign	0.00
R7754:Pkhd1l1	UTSW	15	44,586,408 (GRCm38)	missense	possibly damaging	0.94
R7761:Pkhd1l1	UTSW	15	44,529,884 (GRCm38)	missense	probably benign	0.00
R7774:Pkhd1l1	UTSW	15	44,540,907 (GRCm38)	missense	probably benign	0.03
R7785:Pkhd1l1	UTSW	15	44,543,569 (GRCm38)	missense	probably damaging	1.00
R7790:Pkhd1l1	UTSW	15	44,578,581 (GRCm38)	missense	probably damaging	1.00
R7804:Pkhd1l1	UTSW	15	44,597,138 (GRCm38)	nonsense	probably null
R7864:Pkhd1l1	UTSW	15	44,526,053 (GRCm38)	critical splice donor site	probably null
R7883:Pkhd1l1	UTSW	15	44,529,126 (GRCm38)	missense	probably damaging	1.00
R8031:Pkhd1l1	UTSW	15	44,512,834 (GRCm38)	missense	probably damaging	1.00
R8128:Pkhd1l1	UTSW	15	44,498,053 (GRCm38)	missense	possibly damaging	0.94
R8142:Pkhd1l1	UTSW	15	44,514,931 (GRCm38)	missense	probably benign	0.00
R8150:Pkhd1l1	UTSW	15	44,546,659 (GRCm38)	missense	possibly damaging	0.68
R8209:Pkhd1l1	UTSW	15	44,574,407 (GRCm38)	missense	possibly damaging	0.46
R8212:Pkhd1l1	UTSW	15	44,499,300 (GRCm38)	missense	probably benign	0.12
R8226:Pkhd1l1	UTSW	15	44,574,407 (GRCm38)	missense	possibly damaging	0.46
R8248:Pkhd1l1	UTSW	15	44,543,546 (GRCm38)	missense	probably damaging	0.99
R8299:Pkhd1l1	UTSW	15	44,581,934 (GRCm38)	missense	probably benign	0.26
R8425:Pkhd1l1	UTSW	15	44,574,515 (GRCm38)	missense	probably benign	0.01
R8485:Pkhd1l1	UTSW	15	44,560,400 (GRCm38)	missense	probably damaging	0.98
R8486:Pkhd1l1	UTSW	15	44,547,416 (GRCm38)	missense	probably damaging	1.00
R8701:Pkhd1l1	UTSW	15	44,574,683 (GRCm38)	missense	probably damaging	1.00
R8709:Pkhd1l1	UTSW	15	44,518,174 (GRCm38)	missense	probably benign	0.01
R8777:Pkhd1l1	UTSW	15	44,498,571 (GRCm38)	missense	probably damaging	1.00
R8777-TAIL:Pkhd1l1	UTSW	15	44,498,571 (GRCm38)	missense	probably damaging	1.00
R8845:Pkhd1l1	UTSW	15	44,505,254 (GRCm38)	missense	probably benign	0.30
R8846:Pkhd1l1	UTSW	15	44,546,962 (GRCm38)	nonsense	probably null
R8863:Pkhd1l1	UTSW	15	44,569,986 (GRCm38)	nonsense	probably null
R8917:Pkhd1l1	UTSW	15	44,533,007 (GRCm38)	missense	probably benign	0.04
R8936:Pkhd1l1	UTSW	15	44,538,916 (GRCm38)	missense	possibly damaging	0.94
R8962:Pkhd1l1	UTSW	15	44,536,895 (GRCm38)	missense	probably damaging	1.00
R8971:Pkhd1l1	UTSW	15	44,529,519 (GRCm38)	missense	possibly damaging	0.68
R8973:Pkhd1l1	UTSW	15	44,586,437 (GRCm38)	missense	probably damaging	1.00
R8982:Pkhd1l1	UTSW	15	44,523,673 (GRCm38)	nonsense	probably null
R8994:Pkhd1l1	UTSW	15	44,547,103 (GRCm38)	missense	probably damaging	0.99
R9004:Pkhd1l1	UTSW	15	44,543,372 (GRCm38)	missense	probably benign	0.16
R9064:Pkhd1l1	UTSW	15	44,562,642 (GRCm38)	missense	possibly damaging	0.93
R9173:Pkhd1l1	UTSW	15	44,520,756 (GRCm38)	missense	probably benign	0.09
R9185:Pkhd1l1	UTSW	15	44,589,623 (GRCm38)	missense	probably benign	0.01
R9213:Pkhd1l1	UTSW	15	44,495,478 (GRCm38)	missense	probably damaging	1.00
R9218:Pkhd1l1	UTSW	15	44,520,726 (GRCm38)	missense	possibly damaging	0.90
R9256:Pkhd1l1	UTSW	15	44,533,894 (GRCm38)	critical splice donor site	probably null
R9291:Pkhd1l1	UTSW	15	44,569,976 (GRCm38)	missense	probably damaging	1.00
R9309:Pkhd1l1	UTSW	15	44,536,893 (GRCm38)	missense	probably benign	0.00
R9319:Pkhd1l1	UTSW	15	44,529,578 (GRCm38)	missense	possibly damaging	0.46
R9339:Pkhd1l1	UTSW	15	44,589,553 (GRCm38)	missense	probably damaging	1.00
R9366:Pkhd1l1	UTSW	15	44,546,912 (GRCm38)	missense	probably benign	0.03
R9444:Pkhd1l1	UTSW	15	44,554,657 (GRCm38)	missense	probably benign	0.00
R9464:Pkhd1l1	UTSW	15	44,479,613 (GRCm38)	missense	probably damaging	1.00
R9525:Pkhd1l1	UTSW	15	44,584,926 (GRCm38)	missense	possibly damaging	0.88
R9542:Pkhd1l1	UTSW	15	44,546,888 (GRCm38)	missense	probably benign	0.12
R9544:Pkhd1l1	UTSW	15	44,546,843 (GRCm38)	missense	probably damaging	1.00
R9608:Pkhd1l1	UTSW	15	44,578,633 (GRCm38)	missense	possibly damaging	0.65
R9673:Pkhd1l1	UTSW	15	44,523,505 (GRCm38)	missense	probably benign	0.22
R9771:Pkhd1l1	UTSW	15	44,495,487 (GRCm38)	missense	probably benign
R9792:Pkhd1l1	UTSW	15	44,543,587 (GRCm38)	missense	probably benign	0.00
R9793:Pkhd1l1	UTSW	15	44,543,587 (GRCm38)	missense	probably benign	0.00
R9795:Pkhd1l1	UTSW	15	44,543,587 (GRCm38)	missense	probably benign	0.00
RF006:Pkhd1l1	UTSW	15	44,558,507 (GRCm38)	critical splice acceptor site	probably benign
RF006:Pkhd1l1	UTSW	15	44,503,238 (GRCm38)	missense	probably benign	0.03
RF008:Pkhd1l1	UTSW	15	44,558,505 (GRCm38)	critical splice acceptor site	probably benign
RF012:Pkhd1l1	UTSW	15	44,558,505 (GRCm38)	critical splice acceptor site	probably benign
RF019:Pkhd1l1	UTSW	15	44,558,507 (GRCm38)	critical splice acceptor site	probably benign
RF030:Pkhd1l1	UTSW	15	44,558,502 (GRCm38)	critical splice acceptor site	probably benign
RF033:Pkhd1l1	UTSW	15	44,558,506 (GRCm38)	critical splice acceptor site	probably benign
RF038:Pkhd1l1	UTSW	15	44,558,503 (GRCm38)	critical splice acceptor site	probably benign
RF046:Pkhd1l1	UTSW	15	44,558,495 (GRCm38)	critical splice acceptor site	probably benign
X0027:Pkhd1l1	UTSW	15	44,591,966 (GRCm38)	missense	probably damaging	0.99
Z1177:Pkhd1l1	UTSW	15	44,578,578 (GRCm38)	missense	probably damaging	0.99
Z1177:Pkhd1l1	UTSW	15	44,573,576 (GRCm38)	missense	probably damaging	0.97

Predicted Primers

PCR Primer
(F):5'- ATATTTGTGTACATGTGCCCGT -3'
(R):5'- TGGATAAACGATGCTATGACATAGA -3'

Sequencing Primer
(F):5'- ACCTTAAGTTCACCAGGTGG -3'
(R):5'- AGACTGTAGGTGTCTGTC -3'

Posted On

2019-10-07