Mutagenetix > Incidental Mutation

Incidental Mutation 'R4989:Pakap'

386018

Institutional Source

Beutler Lab

Gene Symbol

Pakap

Ensembl Gene

ENSMUSG00000089945

Gene Name

paralemmin A kinase anchor protein

Synonyms

Palm2-Akap2, Akap2, AKAP-KL, Palm2Akap2, Gm20459, AF064781, B230340M18Rik, 53-H12, pEN70, Palm2

MMRRC Submission

042583-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.107) question?

Stock #

R4989 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

57434475-57896984 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 57856552 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 668 (V668E)

Ref Sequence

ENSEMBL: ENSMUSP00000103226 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000043456] [ENSMUST00000098064] [ENSMUST00000098066] [ENSMUST00000102902] [ENSMUST00000102903] [ENSMUST00000107598] [ENSMUST00000107600] [ENSMUST00000124581] [ENSMUST00000132497] [ENSMUST00000126465]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000043456
AA Change: V627E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000048678
Gene: ENSMUSG00000038729
AA Change: V627E

Domain	Start	End	E-Value	Type
low complexity region	152	163	N/A	INTRINSIC
low complexity region	213	227	N/A	INTRINSIC
coiled coil region	256	314	N/A	INTRINSIC
Pfam:AKAP2_C	568	885	2.5e-17	PFAM
Pfam:RII_binding_1	585	602	1.6e-5	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000098064
AA Change: V627E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000095672
Gene: ENSMUSG00000038729
AA Change: V627E

Domain	Start	End	E-Value	Type
low complexity region	152	163	N/A	INTRINSIC
low complexity region	213	227	N/A	INTRINSIC
coiled coil region	256	314	N/A	INTRINSIC
Pfam:AKAP2_C	569	872	4e-13	PFAM
Pfam:RII_binding_1	585	602	2.9e-5	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000098065

Predicted Effect

probably benign
Transcript: ENSMUST00000098066

SMART Domains

Protein: ENSMUSP00000095674
Gene: ENSMUSG00000089945

Domain	Start	End	E-Value	Type
Pfam:Paralemmin	67	138	6.3e-23	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000102902
AA Change: V627E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000099966
Gene: ENSMUSG00000038729
AA Change: V627E

Domain	Start	End	E-Value	Type
low complexity region	152	163	N/A	INTRINSIC
low complexity region	213	227	N/A	INTRINSIC
coiled coil region	256	314	N/A	INTRINSIC
Pfam:RII_binding_1	585	602	3.5e-5	PFAM
coiled coil region	730	766	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000102903
AA Change: V627E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000099967
Gene: ENSMUSG00000038729
AA Change: V627E

Domain	Start	End	E-Value	Type
low complexity region	152	163	N/A	INTRINSIC
low complexity region	213	227	N/A	INTRINSIC
coiled coil region	256	314	N/A	INTRINSIC
Pfam:RII_binding_1	585	602	3.5e-5	PFAM
coiled coil region	730	766	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000107598
AA Change: V627E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000103224
Gene: ENSMUSG00000038729
AA Change: V627E

Domain	Start	End	E-Value	Type
low complexity region	152	163	N/A	INTRINSIC
low complexity region	213	227	N/A	INTRINSIC
coiled coil region	256	314	N/A	INTRINSIC
Pfam:AKAP2_C	569	872	4e-13	PFAM
Pfam:RII_binding_1	585	602	2.9e-5	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000107600
AA Change: V668E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000103226
Gene: ENSMUSG00000038729
AA Change: V668E

Domain	Start	End	E-Value	Type
low complexity region	193	204	N/A	INTRINSIC
low complexity region	254	268	N/A	INTRINSIC
coiled coil region	297	355	N/A	INTRINSIC
Pfam:AKAP2_C	636	913	2.8e-12	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000150412
AA Change: V870E

SMART Domains

Protein: ENSMUSP00000117466
Gene: ENSMUSG00000089945
AA Change: V870E

Domain	Start	End	E-Value	Type
low complexity region	15	28	N/A	INTRINSIC
low complexity region	35	59	N/A	INTRINSIC
Pfam:Paralemmin	115	269	6.5e-23	PFAM
low complexity region	396	407	N/A	INTRINSIC
low complexity region	457	471	N/A	INTRINSIC
coiled coil region	499	557	N/A	INTRINSIC
Pfam:AKAP2_C	847	1129	1.9e-17	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000124581

SMART Domains

Protein: ENSMUSP00000119742
Gene: ENSMUSG00000038729

Domain	Start	End	E-Value	Type
low complexity region	152	163	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000132497

Predicted Effect

probably benign
Transcript: ENSMUST00000126465

SMART Domains

Protein: ENSMUSP00000130230
Gene: ENSMUSG00000089945

Domain	Start	End	E-Value	Type
Pfam:Paralemmin	67	138	6.3e-23	PFAM

Meta Mutation Damage Score

0.0689

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.0%
20x: 94.4%

Validation Efficiency

100% (115/115)

MGI Phenotype

FUNCTION: This locus represents naturally occurring readthrough transcription between the neighboring Palm2 (paralemmin 2) and Akap2 (A kinase (PRKA) anchor protein 2) genes on chromosome 4. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. Similar readthrough transcription has also been observed in human, as described in PMID: 11478809. [provided by RefSeq, Feb 2015]

Allele List at MGI

Other mutations in this stock

Total: 114 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	G	T	12: 71,211,320 (GRCm39)	E685*	probably null	Het
2700049A03Rik	A	T	12: 71,211,321 (GRCm39)	E685V	possibly damaging	Het
Acot6	A	G	12: 84,155,789 (GRCm39)	K246E	probably benign	Het
Actl11	T	A	9: 107,808,615 (GRCm39)	H979Q	probably damaging	Het
Adal	T	A	2: 120,986,030 (GRCm39)		probably benign	Het
Add2	G	A	6: 86,087,840 (GRCm39)	V596I	probably benign	Het
Adrb3	A	C	8: 27,717,798 (GRCm39)	M217R	probably damaging	Het
Ank1	T	C	8: 23,631,134 (GRCm39)		probably benign	Het
Ank2	A	T	3: 126,757,094 (GRCm39)	N1054K	possibly damaging	Het
Ankib1	T	C	5: 3,763,217 (GRCm39)	Y504C	probably damaging	Het
Ankrd29	T	C	18: 12,395,242 (GRCm39)	K217R	probably damaging	Het
Ankrd45	T	C	1: 160,982,876 (GRCm39)	V129A	probably damaging	Het
Aox4	A	T	1: 58,275,835 (GRCm39)	D389V	probably benign	Het
Aph1a	G	T	3: 95,802,843 (GRCm39)	G148W	probably damaging	Het
Arhgef26	G	A	3: 62,247,806 (GRCm39)	D297N	possibly damaging	Het
Atxn7l3b	C	A	10: 112,764,649 (GRCm39)		probably benign	Het
Auh	A	G	13: 52,995,065 (GRCm39)	S167P	probably damaging	Het
Bach1	A	T	16: 87,515,888 (GRCm39)	K143I	possibly damaging	Het
Bbx	T	A	16: 50,045,101 (GRCm39)	T487S	probably damaging	Het
Bche	T	G	3: 73,609,177 (GRCm39)	D83A	probably benign	Het
Bri3bp	G	T	5: 125,518,760 (GRCm39)		probably benign	Het
Cd3d	A	T	9: 44,896,296 (GRCm39)	E28D	probably damaging	Het
Cdc42bpa	A	G	1: 179,965,366 (GRCm39)	T1028A	probably damaging	Het
Ceacam23	A	G	7: 17,639,143 (GRCm39)		probably null	Het
Celsr2	T	C	3: 108,319,945 (GRCm39)	I956V	possibly damaging	Het
Cep95	A	T	11: 106,707,480 (GRCm39)		probably null	Het
Cic	G	T	7: 24,986,535 (GRCm39)	G1289C	probably damaging	Het
Cndp1	A	G	18: 84,650,025 (GRCm39)	Y223H	probably damaging	Het
Cops8	A	G	1: 90,538,724 (GRCm39)	D51G	probably damaging	Het
Csgalnact1	T	C	8: 68,913,623 (GRCm39)	E194G	probably benign	Het
Ctsm	A	G	13: 61,686,776 (GRCm39)	Y39H	probably damaging	Het
Dhrs2	T	C	14: 55,474,722 (GRCm39)	V119A	probably damaging	Het
Drosha	T	A	15: 12,935,093 (GRCm39)	M1336K	probably benign	Het
Dsp	G	A	13: 38,381,678 (GRCm39)	D2808N	possibly damaging	Het
Ehmt1	G	T	2: 24,767,509 (GRCm39)	P135T	probably damaging	Het
Epas1	A	G	17: 87,116,882 (GRCm39)	N184S	probably damaging	Het
Erich3	C	T	3: 154,454,025 (GRCm39)	T597I	possibly damaging	Het
F10	T	C	8: 13,105,698 (GRCm39)	V421A	probably damaging	Het
Fabp3	C	T	4: 130,206,180 (GRCm39)	T57I	probably benign	Het
Fam227b	G	A	2: 125,958,043 (GRCm39)	P241S	probably damaging	Het
Fcgrt	C	T	7: 44,751,372 (GRCm39)	G192D	probably benign	Het
Fras1	A	G	5: 96,798,541 (GRCm39)	E1184G	possibly damaging	Het
Garre1	A	C	7: 33,945,225 (GRCm39)	Y552D	probably damaging	Het
Grn	C	A	11: 102,321,380 (GRCm39)		probably benign	Het
Gvin-ps5	A	T	7: 105,928,664 (GRCm39)		noncoding transcript	Het
Hadh	A	T	3: 131,029,197 (GRCm39)	L274*	probably null	Het
Hus1	T	C	11: 8,956,027 (GRCm39)	S169G	probably damaging	Het
Hydin	A	T	8: 111,290,554 (GRCm39)	I3338F	possibly damaging	Het
Ighv11-1	T	G	12: 113,945,768 (GRCm39)	E28D	probably benign	Het
Kctd9	C	T	14: 67,966,805 (GRCm39)	T106I	probably damaging	Het
Krit1	A	T	5: 3,872,238 (GRCm39)	N421I	probably damaging	Het
Lamb1	A	G	12: 31,376,677 (GRCm39)	D1619G	probably damaging	Het
Lpar6	G	A	14: 73,476,147 (GRCm39)	C36Y	probably damaging	Het
Lrrc37a	G	C	11: 103,347,565 (GRCm39)	F3043L	unknown	Het
Lrrc46	A	T	11: 96,931,765 (GRCm39)	V19D	probably damaging	Het
Mapkap1	G	T	2: 34,471,303 (GRCm39)	S197I	probably damaging	Het
Mrps35	A	C	6: 146,961,645 (GRCm39)	K173N	possibly damaging	Het
Mtf2	A	G	5: 108,220,894 (GRCm39)		probably benign	Het
Ncf1	A	C	5: 134,252,267 (GRCm39)	D261E	probably damaging	Het
Notch1	C	T	2: 26,371,193 (GRCm39)	E298K	probably damaging	Het
Nrxn1	A	T	17: 90,928,274 (GRCm39)		probably benign	Het
Or13a18	C	A	7: 140,190,304 (GRCm39)	A75E	possibly damaging	Het
Or4x13	T	A	2: 90,231,107 (GRCm39)	M34K	probably benign	Het
Or52a33	A	G	7: 103,289,308 (GRCm39)	F13S	probably damaging	Het
Or5k3	T	C	16: 58,969,981 (GRCm39)	L256P	probably damaging	Het
Or5v1	G	T	17: 37,810,017 (GRCm39)	L158F	probably benign	Het
Otud4	G	A	8: 80,382,318 (GRCm39)	V176I	probably damaging	Het
Papolg	T	C	11: 23,823,919 (GRCm39)		probably null	Het
Pgk2	A	G	17: 40,518,402 (GRCm39)	V342A	probably damaging	Het
Phf2	G	A	13: 48,961,320 (GRCm39)	A790V	unknown	Het
Prkdc	T	C	16: 15,491,861 (GRCm39)	I602T	possibly damaging	Het
Prl3d3	T	C	13: 27,343,072 (GRCm39)	I86T	possibly damaging	Het
Prss8	G	T	7: 127,525,635 (GRCm39)	Q295K	probably benign	Het
Ptpre	C	T	7: 135,270,861 (GRCm39)	H346Y	probably benign	Het
Ptpro	T	A	6: 137,420,592 (GRCm39)	V1007D	probably damaging	Het
Pwwp3a	T	C	10: 80,068,702 (GRCm39)	L282P	probably benign	Het
Qrfpr	A	G	3: 36,276,285 (GRCm39)	V35A	probably damaging	Het
Rpf1	A	G	3: 146,212,293 (GRCm39)	L349S	probably damaging	Het
Rpl41	G	T	10: 128,384,652 (GRCm39)		probably null	Het
Rprd2	G	C	3: 95,672,632 (GRCm39)	R924G	probably benign	Het
Serpini1	T	A	3: 75,521,795 (GRCm39)	N95K	probably benign	Het
Sfxn1	A	T	13: 54,242,933 (GRCm39)	T64S	probably benign	Het
Siae	T	G	9: 37,557,816 (GRCm39)	I541S	possibly damaging	Het
Slc25a4	T	A	8: 46,660,509 (GRCm39)	K296N	probably benign	Het
Slc37a1	A	G	17: 31,541,120 (GRCm39)	N204S	probably damaging	Het
Slc9c1	A	G	16: 45,413,800 (GRCm39)	N976S	probably benign	Het
Smarcal1	T	C	1: 72,672,019 (GRCm39)	S847P	possibly damaging	Het
Smg1	A	T	7: 117,757,323 (GRCm39)		probably benign	Het
Smg1	C	T	7: 117,807,274 (GRCm39)	A168T	probably benign	Het
Sptlc1	A	G	13: 53,505,692 (GRCm39)	I242T	probably damaging	Het
St8sia2	T	C	7: 73,616,709 (GRCm39)	I89V	possibly damaging	Het
Supt20	A	T	3: 54,602,555 (GRCm39)		probably benign	Het
Tep1	T	C	14: 51,076,457 (GRCm39)	D1659G	probably benign	Het
Tex10	C	A	4: 48,458,525 (GRCm39)		probably benign	Het
Thbs3	CAGAAG	CAG	3: 89,130,409 (GRCm39)		probably benign	Het
Tmbim6	C	A	15: 99,299,950 (GRCm39)	S22*	probably null	Het
Tmc2	A	T	2: 130,043,961 (GRCm39)	K65M	possibly damaging	Het
Tmod1	A	G	4: 46,090,872 (GRCm39)	S142G	probably damaging	Het
Tns2	C	T	15: 102,017,369 (GRCm39)	R281C	probably damaging	Het
Trmt6	T	C	2: 132,650,191 (GRCm39)	R349G	possibly damaging	Het
Ttn	T	A	2: 76,537,586 (GRCm39)	T26454S	possibly damaging	Het
Ttn	C	T	2: 76,605,122 (GRCm39)	V16555I	probably benign	Het
Tut4	T	A	4: 108,384,042 (GRCm39)		probably benign	Het
Ubr3	T	C	2: 69,850,790 (GRCm39)		probably benign	Het
Vmn1r17	A	C	6: 57,337,460 (GRCm39)	F253V	possibly damaging	Het
Vmn1r201	G	T	13: 22,659,622 (GRCm39)	A279S	possibly damaging	Het
Vmn2r17	A	T	5: 109,575,739 (GRCm39)	R203S	probably benign	Het
Vwa5a	A	G	9: 38,633,926 (GRCm39)	E43G	probably benign	Het
Wdr86	C	T	5: 24,917,843 (GRCm39)		probably null	Het
Wdsub1	A	T	2: 59,700,758 (GRCm39)		probably benign	Het
Zcchc7	T	C	4: 44,931,039 (GRCm39)	L76P	probably damaging	Het
Zfp108	G	T	7: 23,960,163 (GRCm39)	K251N	probably benign	Het
Zfp263	T	C	16: 3,566,992 (GRCm39)	C148R	probably damaging	Het
Zfp687	A	C	3: 94,917,697 (GRCm39)	F692V	probably damaging	Het

Other mutations in Pakap

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01123:Pakap	APN	4	57,757,627 (GRCm39)	nonsense	probably null
IGL01371:Pakap	APN	4	57,856,325 (GRCm39)	missense	probably benign	0.03
IGL01647:Pakap	APN	4	57,688,477 (GRCm39)	missense	possibly damaging	0.82
IGL01733:Pakap	APN	4	57,856,488 (GRCm39)	missense	probably benign	0.01
IGL02677:Pakap	APN	4	57,856,263 (GRCm39)	missense	probably benign	0.01
IGL02696:Pakap	APN	4	57,854,663 (GRCm39)	missense	probably damaging	0.97
IGL02736:Pakap	APN	4	57,709,721 (GRCm39)	missense	probably damaging	0.96
IGL03067:Pakap	APN	4	57,648,038 (GRCm39)	missense	probably benign	0.02
IGL03343:Pakap	APN	4	57,688,502 (GRCm39)	missense	probably damaging	1.00
A9681:Pakap	UTSW	4	57,855,358 (GRCm39)	missense	probably damaging	1.00
IGL02835:Pakap	UTSW	4	57,883,044 (GRCm39)	missense	probably damaging	1.00
PIT4305001:Pakap	UTSW	4	57,638,029 (GRCm39)	missense	possibly damaging	0.94
R0158:Pakap	UTSW	4	57,709,649 (GRCm39)	missense	possibly damaging	0.96
R0244:Pakap	UTSW	4	57,710,177 (GRCm39)	missense	possibly damaging	0.74
R0284:Pakap	UTSW	4	57,855,207 (GRCm39)	missense	probably damaging	1.00
R0356:Pakap	UTSW	4	57,855,628 (GRCm39)	missense	possibly damaging	0.48
R0594:Pakap	UTSW	4	57,856,752 (GRCm39)	missense	probably benign	0.00
R0614:Pakap	UTSW	4	57,856,720 (GRCm39)	missense	probably benign	0.41
R0617:Pakap	UTSW	4	57,829,434 (GRCm39)	intron	probably benign
R0763:Pakap	UTSW	4	57,688,441 (GRCm39)	missense	probably damaging	1.00
R0800:Pakap	UTSW	4	57,709,650 (GRCm39)	missense	probably benign	0.06
R1228:Pakap	UTSW	4	57,856,909 (GRCm39)	missense	probably damaging	1.00
R1861:Pakap	UTSW	4	57,709,468 (GRCm39)	missense	probably damaging	0.97
R1895:Pakap	UTSW	4	57,638,068 (GRCm39)	missense	probably benign	0.01
R1913:Pakap	UTSW	4	57,892,963 (GRCm39)	missense	probably damaging	1.00
R2081:Pakap	UTSW	4	57,855,927 (GRCm39)	missense	possibly damaging	0.49
R2128:Pakap	UTSW	4	57,854,890 (GRCm39)	missense	probably benign	0.40
R2339:Pakap	UTSW	4	57,883,180 (GRCm39)	missense	probably damaging	1.00
R4600:Pakap	UTSW	4	57,709,954 (GRCm39)	missense	probably benign	0.26
R4667:Pakap	UTSW	4	57,855,655 (GRCm39)	missense	possibly damaging	0.80
R4804:Pakap	UTSW	4	57,854,688 (GRCm39)	missense	probably benign	0.05
R5135:Pakap	UTSW	4	57,855,912 (GRCm39)	missense	probably benign	0.00
R5292:Pakap	UTSW	4	57,855,356 (GRCm39)	missense	probably damaging	0.98
R5420:Pakap	UTSW	4	57,856,434 (GRCm39)	missense	probably damaging	1.00
R5420:Pakap	UTSW	4	57,856,062 (GRCm39)	missense	probably benign	0.08
R5442:Pakap	UTSW	4	57,637,876 (GRCm39)	missense	probably null
R5517:Pakap	UTSW	4	57,855,987 (GRCm39)	missense	probably damaging	0.99
R5648:Pakap	UTSW	4	57,854,848 (GRCm39)	missense	probably damaging	1.00
R5886:Pakap	UTSW	4	57,856,295 (GRCm39)	missense	probably damaging	1.00
R5993:Pakap	UTSW	4	57,855,273 (GRCm39)	missense	possibly damaging	0.86
R6133:Pakap	UTSW	4	57,855,516 (GRCm39)	nonsense	probably null
R6189:Pakap	UTSW	4	57,855,928 (GRCm39)	missense	probably benign	0.00
R6221:Pakap	UTSW	4	57,855,618 (GRCm39)	nonsense	probably null
R6320:Pakap	UTSW	4	57,710,173 (GRCm39)	missense	probably damaging	1.00
R6365:Pakap	UTSW	4	57,709,675 (GRCm39)	nonsense	probably null
R6532:Pakap	UTSW	4	57,855,174 (GRCm39)	missense	probably benign	0.00
R6760:Pakap	UTSW	4	57,856,026 (GRCm39)	missense	probably damaging	1.00
R6792:Pakap	UTSW	4	57,855,880 (GRCm39)	missense	possibly damaging	0.90
R6983:Pakap	UTSW	4	57,709,973 (GRCm39)	missense	probably damaging	1.00
R7090:Pakap	UTSW	4	57,648,042 (GRCm39)	missense	probably benign	0.00
R7128:Pakap	UTSW	4	57,855,816 (GRCm39)	missense	probably benign	0.03
R7269:Pakap	UTSW	4	57,855,217 (GRCm39)	missense	probably damaging	1.00
R7726:Pakap	UTSW	4	57,709,876 (GRCm39)	missense	probably damaging	1.00
R7744:Pakap	UTSW	4	57,709,519 (GRCm39)	missense	probably damaging	0.97
R7837:Pakap	UTSW	4	57,855,262 (GRCm39)	missense	probably damaging	1.00
R7940:Pakap	UTSW	4	57,883,026 (GRCm39)	missense	probably damaging	0.98
R7946:Pakap	UTSW	4	57,710,045 (GRCm39)	missense	probably damaging	1.00
R8094:Pakap	UTSW	4	57,886,319 (GRCm39)	missense	possibly damaging	0.81
R8275:Pakap	UTSW	4	57,886,329 (GRCm39)	critical splice donor site	probably null
R8702:Pakap	UTSW	4	57,709,489 (GRCm39)	nonsense	probably null
R8836:Pakap	UTSW	4	57,709,916 (GRCm39)	missense	probably benign	0.01
R9010:Pakap	UTSW	4	57,883,192 (GRCm39)	missense	probably damaging	1.00
R9016:Pakap	UTSW	4	57,637,857 (GRCm39)	missense	unknown
R9060:Pakap	UTSW	4	57,855,412 (GRCm39)	missense	probably damaging	1.00
R9215:Pakap	UTSW	4	57,709,595 (GRCm39)	missense	probably damaging	0.97
R9652:Pakap	UTSW	4	57,710,125 (GRCm39)	missense	possibly damaging	0.51
X0065:Pakap	UTSW	4	57,709,805 (GRCm39)	missense	probably benign
Z1177:Pakap	UTSW	4	57,856,348 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCCTTCCTCCACATTGGGAG -3'
(R):5'- AATACTTGCTGAAGTACCCTCCTTC -3'

Sequencing Primer
(F):5'- GAGATTCTCCGTCCGTTGATGAC -3'
(R):5'- TCCATGTTGACTGGACCGCTG -3'

Posted On

2016-05-10