Mutagenetix > Incidental Mutation

Incidental Mutation 'R4657:Pkhd1l1'

352555

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

041917-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4657 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

44457494-44601369 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 44547347 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Tyrosine at position 2750 (C2750Y)

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 damaging
Transcript: ENSMUST00000038336
AA Change: C2750Y

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

SMART Domains

Protein: ENSMUSP00000036988
Gene: ENSMUSG00000038725
AA Change: C2750Y

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 damaging
Transcript: ENSMUST00000166957
AA Change: C2750Y

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000129522
Gene: ENSMUSG00000038725
AA Change: C2750Y

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 damaging
Transcript: ENSMUST00000209244
AA Change: C2750Y

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

Meta Mutation Damage Score

0.6774

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.6%

Validation Efficiency

98% (105/107)

Allele List at MGI

Other mutations in this stock

Total: 102 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aatk	A	T	11: 120,013,478 (GRCm38)	V264E	possibly damaging	Het
Abcg1	T	A	17: 31,108,434 (GRCm38)	W368R	probably benign	Het
Acin1	A	G	14: 54,643,047 (GRCm38)	I476T	possibly damaging	Het
Acsm1	T	A	7: 119,640,694 (GRCm38)	I287N	possibly damaging	Het
Adgrv1	C	T	13: 81,405,364 (GRCm38)	V5464I	probably benign	Het
AI429214	T	A	8: 36,994,391 (GRCm38)	L231Q	probably damaging	Het
Akp3	A	G	1: 87,125,834 (GRCm38)		probably benign	Het
Amy2b	C	T	3: 113,153,477 (GRCm38)		noncoding transcript	Het
Apoa5	A	G	9: 46,269,872 (GRCm38)	Q82R	probably benign	Het
Arhgap44	A	G	11: 65,005,452 (GRCm38)		probably null	Het
Arhgef38	C	A	3: 133,234,681 (GRCm38)	G48V	probably damaging	Het
Bltp3a	T	A	17: 27,890,105 (GRCm38)	F1099L	probably benign	Het
Bod1l	G	T	5: 41,818,612 (GRCm38)	N1786K	probably benign	Het
Cav2	A	T	6: 17,281,410 (GRCm38)	D17V	probably null	Het
Ccdc148	G	T	2: 59,001,888 (GRCm38)	N238K	probably benign	Het
Ccin	A	T	4: 43,984,981 (GRCm38)	I463F	probably damaging	Het
Cd8b1	C	T	6: 71,329,774 (GRCm38)	H162Y	possibly damaging	Het
Cdh16	T	A	8: 104,615,226 (GRCm38)		probably null	Het
Cfap65	T	A	1: 74,925,354 (GRCm38)		probably benign	Het
Clec4n	T	C	6: 123,232,196 (GRCm38)		probably null	Het
Cpne7	T	A	8: 123,134,575 (GRCm38)	*558R	probably null	Het
Cs	A	G	10: 128,353,137 (GRCm38)	I172V	probably benign	Het
Cyp2ab1	A	T	16: 20,313,072 (GRCm38)	L306Q	probably damaging	Het
D16Ertd472e	A	T	16: 78,547,926 (GRCm38)	V98E	probably damaging	Het
Dcaf15	A	C	8: 84,102,838 (GRCm38)	S92A	probably damaging	Het
Dkk3	T	C	7: 112,149,046 (GRCm38)		probably null	Het
Dnah11	A	T	12: 118,192,427 (GRCm38)	C163S	probably benign	Het
Eda2r	T	A	X: 97,341,633 (GRCm38)	Q171L	probably damaging	Het
Eml4	A	T	17: 83,450,948 (GRCm38)	K397*	probably null	Het
Eml6	A	T	11: 29,805,108 (GRCm38)	I889N	possibly damaging	Het
Etaa1	A	T	11: 17,946,964 (GRCm38)	D384E	possibly damaging	Het
Fzr1	T	A	10: 81,367,552 (GRCm38)		probably null	Het
Gm13889	G	T	2: 93,956,576 (GRCm38)	F61L	probably damaging	Het
Gm14149	A	T	2: 151,230,764 (GRCm38)		noncoding transcript	Het
Gm5828	T	A	1: 16,769,418 (GRCm38)		noncoding transcript	Het
Gm5866	G	A	5: 52,582,920 (GRCm38)		noncoding transcript	Het
Gp2	T	C	7: 119,457,168 (GRCm38)	I27M	probably benign	Het
Gpr83	G	A	9: 14,866,983 (GRCm38)		probably null	Het
Gucd1	T	C	10: 75,511,125 (GRCm38)	N97S	probably benign	Het
H2-Q7	T	A	17: 35,442,759 (GRCm38)	V326E	possibly damaging	Het
Haao	A	T	17: 83,832,345 (GRCm38)	D227E	possibly damaging	Het
Hipk3	C	T	2: 104,433,759 (GRCm38)	S819N	probably benign	Het
Hist3h2ba	C	T	11: 58,948,971 (GRCm38)	P11L	probably benign	Het
Hlcs	A	G	16: 94,262,698 (GRCm38)	V501A	probably benign	Het
Hmcn1	A	G	1: 150,624,550 (GRCm38)	Y3964H	probably damaging	Het
Ifi204	C	A	1: 173,760,361 (GRCm38)		probably benign	Het
Ifi211	A	G	1: 173,907,660 (GRCm38)	F68L	probably benign	Het
Ift57	A	G	16: 49,762,594 (GRCm38)		probably null	Het
Ighv5-12-4	A	T	12: 113,762,267 (GRCm38)	L112*	probably null	Het
Il1f6	T	A	2: 24,224,404 (GRCm38)	M97K	possibly damaging	Het
Il1rl2	CTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATT	CTTTATTTTATTTTATTTTATTTTATTTTATTTTATT	1: 40,327,310 (GRCm38)		probably benign	Het
Itsn2	A	G	12: 4,713,197 (GRCm38)	*1686W	probably null	Het
Jkamp	G	T	12: 72,094,049 (GRCm38)	V123F	probably damaging	Het
Kat7	C	A	11: 95,277,598 (GRCm38)	V411L	probably damaging	Het
Kcnj5	A	G	9: 32,322,677 (GRCm38)	V114A	probably benign	Het
Krtap5-4	T	A	7: 142,303,754 (GRCm38)	C54S	unknown	Het
Lats1	T	A	10: 7,705,684 (GRCm38)	N744K	possibly damaging	Het
Lpo	T	C	11: 87,814,347 (GRCm38)	E387G	probably damaging	Het
Lrba	T	G	3: 86,737,164 (GRCm38)	M388R	probably damaging	Het
Lrp2	C	A	2: 69,466,993 (GRCm38)	R3208L	probably damaging	Het
Mterf1b	T	A	5: 4,197,176 (GRCm38)	C272*	probably null	Het
Myh15	A	T	16: 49,172,058 (GRCm38)	R1632*	probably null	Het
Myo3b	T	C	2: 70,238,899 (GRCm38)	V494A	possibly damaging	Het
Myo9a	T	C	9: 59,875,416 (GRCm38)		probably null	Het
Nelfa	T	G	5: 33,901,813 (GRCm38)	S233R	probably benign	Het
Nr4a3	A	T	4: 48,051,522 (GRCm38)	E121V	probably damaging	Het
Obscn	T	A	11: 59,042,290 (GRCm38)	E5406D	probably damaging	Het
Ofcc1	G	A	13: 40,015,388 (GRCm38)	T841I	probably damaging	Het
Or1j18	T	A	2: 36,734,403 (GRCm38)	Y27*	probably null	Het
Or7e177	A	C	9: 20,300,623 (GRCm38)	H142P	probably damaging	Het
Oxct2b	T	C	4: 123,117,133 (GRCm38)	L282P	probably damaging	Het
Pappa	G	A	4: 65,314,796 (GRCm38)		probably null	Het
Pcdhb14	A	G	18: 37,448,847 (GRCm38)	I335M	possibly damaging	Het
Pcsk1	T	A	13: 75,132,235 (GRCm38)	D726E	probably damaging	Het
Pkhd1	T	A	1: 20,364,167 (GRCm38)	Q2349L	possibly damaging	Het
Ppp2r3d	A	G	9: 124,476,821 (GRCm38)	C26R	unknown	Het
Prex2	T	A	1: 11,065,825 (GRCm38)	I74N	probably benign	Het
Ptgir	A	G	7: 16,907,146 (GRCm38)	D121G	probably benign	Het
Pwwp3a	T	A	10: 80,233,014 (GRCm38)	C331S	probably benign	Het
Ralbp1	T	C	17: 65,852,691 (GRCm38)	S526G	probably null	Het
Ric8b	T	C	10: 84,992,137 (GRCm38)	Y442H	probably damaging	Het
Rpap1	C	T	2: 119,775,006 (GRCm38)	D385N	probably benign	Het
Sash1	T	C	10: 8,725,660 (GRCm38)	Y1177C	probably damaging	Het
Shroom1	T	C	11: 53,465,588 (GRCm38)	I363T	possibly damaging	Het
Slc26a9	T	C	1: 131,753,138 (GRCm38)	L95P	probably damaging	Het
Slc44a5	A	G	3: 154,256,584 (GRCm38)	T385A	possibly damaging	Het
Slc5a9	C	A	4: 111,891,744 (GRCm38)		probably null	Het
Slc7a1	T	A	5: 148,352,399 (GRCm38)	M13L	probably benign	Het
Snrpb2	A	G	2: 143,070,973 (GRCm38)	N172S	possibly damaging	Het
Spns1	G	T	7: 126,374,302 (GRCm38)		probably benign	Het
Srsf6	T	A	2: 162,933,427 (GRCm38)	S86R	probably benign	Het
Stk25	A	T	1: 93,625,656 (GRCm38)		probably benign	Het
Szt2	A	T	4: 118,397,669 (GRCm38)	C275S	probably benign	Het
Tcp10b	T	A	17: 13,073,617 (GRCm38)		probably null	Het
Tmem248	T	A	5: 130,231,774 (GRCm38)	L60H	probably damaging	Het
Trim27	T	C	13: 21,183,760 (GRCm38)	I182T	probably damaging	Het
Tspan10	A	G	11: 120,444,498 (GRCm38)	N145D	probably damaging	Het
Vps13d	A	G	4: 145,074,842 (GRCm38)	F487S	probably damaging	Het
Wdr86	A	T	5: 24,718,231 (GRCm38)	D154E	probably benign	Het
Wfdc18	C	A	11: 83,709,869 (GRCm38)	A32D	possibly damaging	Het
Wrn	A	T	8: 33,335,991 (GRCm38)		probably null	Het
Zfp811	C	A	17: 32,800,923 (GRCm38)	E7*	probably null	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	44,528,247 (GRCm38)	missense	probably damaging	1.00
P4717OSA:Pkhd1l1	UTSW	15	44,523,499 (GRCm38)	missense	probably benign	0.17
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
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
R7475:Pkhd1l1	UTSW	15	44,505,185 (GRCm38)	nonsense	probably null
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'- ATCCTGGCTCCCTATGTTGG -3'
(R):5'- ACTGGTGAATCAGCCTTAACC -3'

Sequencing Primer
(F):5'- CTCCCTATGTTGGAGGATGGG -3'
(R):5'- CTGGGATTGAATGCATGCATCACC -3'

Posted On

2015-10-08