Mutagenetix > Incidental Mutation

Incidental Mutation 'R7491:Naip5'

580789

Institutional Source

Beutler Lab

Gene Symbol

Naip5

Ensembl Gene

ENSMUSG00000071203

Gene Name

NLR family, apoptosis inhibitory protein 5

Synonyms

Birc1e, Lgn1, Naip-rs3

MMRRC Submission

045565-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.101) question?

Stock #

R7491 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

100211739-100246323 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 100217071 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Valine at position 1227 (F1227V)

Ref Sequence

ENSEMBL: ENSMUSP00000058611 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049789]

AlphaFold

Q9R016

Predicted Effect

probably benign
Transcript: ENSMUST00000049789
AA Change: F1227V

PolyPhen 2 Score 0.184 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000058611
Gene: ENSMUSG00000071203
AA Change: F1227V

Domain	Start	End	E-Value	Type
low complexity region	36	51	N/A	INTRINSIC
BIR	58	129	1.08e-19	SMART
BIR	157	229	1.06e-36	SMART
BIR	276	347	2.14e-32	SMART
Pfam:NACHT	464	618	1.7e-36	PFAM
low complexity region	851	862	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

MGI Phenotype

PHENOTYPE: This locus controls resistance to Legionella pneumophila, the organism responsible for Legionnaire's disease. Cultured peritoneal macrophages from A/J mice are susceptible, supporting bacterial proliferation; other strains, e.g., C57BL/6 are resistant. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 90 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933409G03Rik	G	T	2: 68,614,755 (GRCm38)		probably null	Het
5730522E02Rik	A	T	11: 25,769,014 (GRCm38)	V44E	unknown	Het
Adcy9	A	G	16: 4,418,809 (GRCm38)	L246S	possibly damaging	Het
Adk	C	T	14: 21,234,929 (GRCm38)	H123Y	probably damaging	Het
Adra1b	T	A	11: 43,835,967 (GRCm38)	D41V	probably benign	Het
Ankib1	T	G	5: 3,701,911 (GRCm38)	K710Q	probably damaging	Het
Aoc2	T	A	11: 101,328,377 (GRCm38)	V542D	probably benign	Het
Arhgef28	T	C	13: 97,944,686 (GRCm38)	N1221S	probably benign	Het
Arntl	T	C	7: 113,299,424 (GRCm38)	V353A	probably benign	Het
BC028528	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	3: 95,888,136 (GRCm38)		probably benign	Het
BC028528	CACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGT	CACTGGTTCTGTGGTTACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGT	3: 95,888,138 (GRCm38)		probably benign	Het
Cacna1a	C	A	8: 84,559,293 (GRCm38)	R856S	possibly damaging	Het
Cacna1c	T	C	6: 118,613,343 (GRCm38)	M1559V		Het
Cdh10	G	C	15: 19,013,359 (GRCm38)	E682Q	probably damaging	Het
Celsr1	T	C	15: 86,032,518 (GRCm38)	D418G	possibly damaging	Het
Cfap44	T	C	16: 44,470,748 (GRCm38)	L1537P	probably damaging	Het
Clca3a2	A	G	3: 144,813,579 (GRCm38)	S279P	probably damaging	Het
Col2a1	C	T	15: 97,976,159 (GRCm38)	V1449I	not run	Het
Cpt2	A	G	4: 107,907,142 (GRCm38)	F475S	probably damaging	Het
Cpxm1	T	C	2: 130,393,567 (GRCm38)	T502A	probably benign	Het
Creb3l2	G	T	6: 37,379,859 (GRCm38)	T91N	probably benign	Het
D630045J12Rik	A	T	6: 38,142,666 (GRCm38)	S1714T	possibly damaging	Het
Dennd1c	C	A	17: 57,072,379 (GRCm38)	V246F	probably damaging	Het
Dse	A	G	10: 34,152,565 (GRCm38)	V843A	probably benign	Het
Ern2	C	A	7: 122,170,533 (GRCm38)	W810L	probably damaging	Het
Fer1l6	G	A	15: 58,600,432 (GRCm38)	D906N	probably damaging	Het
Fry	A	G	5: 150,466,326 (GRCm38)	E140G		Het
Galnt7	A	G	8: 57,552,518 (GRCm38)	V227A	probably damaging	Het
Gas2l3	A	G	10: 89,413,901 (GRCm38)	S452P	probably benign	Het
Gm40460	ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG	7: 142,240,713 (GRCm38)		probably benign	Het
Gm826	A	T	2: 160,312,022 (GRCm38)	S34T	unknown	Het
Gzmk	A	T	13: 113,172,001 (GRCm38)	I222N	probably benign	Het
Hivep3	A	T	4: 120,098,830 (GRCm38)	T1448S	probably benign	Het
Hk1	T	C	10: 62,295,745 (GRCm38)	D278G	probably damaging	Het
Ipo7	C	A	7: 110,039,194 (GRCm38)	Q223K	possibly damaging	Het
Itga9	T	A	9: 118,769,111 (GRCm38)	I571N	probably damaging	Het
Itgb6	T	C	2: 60,620,376 (GRCm38)	Y573C	probably damaging	Het
Kmt2c	T	A	5: 25,284,564 (GRCm38)	H4459L	probably damaging	Het
Limch1	T	G	5: 67,054,237 (GRCm38)	S894R	probably damaging	Het
Lrit2	A	T	14: 37,068,910 (GRCm38)	Q182L	possibly damaging	Het
Mlph	A	T	1: 90,939,378 (GRCm38)	H374L	possibly damaging	Het
Mmrn2	A	G	14: 34,399,417 (GRCm38)	H748R	probably damaging	Het
Mrpl58	T	C	11: 115,410,266 (GRCm38)	V134A	possibly damaging	Het
Nae1	A	T	8: 104,518,239 (GRCm38)	D353E	probably benign	Het
Nln	A	T	13: 104,069,323 (GRCm38)	F108I	probably damaging	Het
Nop16	C	T	13: 54,588,604 (GRCm38)	V94I	probably benign	Het
Nt5c1b	A	T	12: 10,374,903 (GRCm38)	T150S	probably benign	Het
Olfr960	T	G	9: 39,623,972 (GRCm38)	I281S	possibly damaging	Het
Pcdha4	T	C	18: 36,954,636 (GRCm38)	V624A	probably damaging	Het
Pcdhga8	T	C	18: 37,727,430 (GRCm38)	I513T	probably benign	Het
Prc1	A	T	7: 80,309,491 (GRCm38)		probably null	Het
Prpf4	T	A	4: 62,417,876 (GRCm38)	F280Y	probably damaging	Het
Ptprd	T	C	4: 76,133,155 (GRCm38)	E43G	probably benign	Het
Pum1	T	A	4: 130,719,174 (GRCm38)	D181E	probably benign	Het
Rab7	A	G	6: 88,013,642 (GRCm38)	S17P	probably damaging	Het
Rgs1	T	C	1: 144,245,396 (GRCm38)	Y179C	probably damaging	Het
Rrm1	T	C	7: 102,454,557 (GRCm38)	C238R	probably damaging	Het
Rusc2	T	A	4: 43,426,528 (GRCm38)	L1484Q	probably damaging	Het
Sall3	C	T	18: 80,972,705 (GRCm38)	M669I	probably benign	Het
Saxo1	A	C	4: 86,445,407 (GRCm38)	F280V	probably benign	Het
Scn2a	T	C	2: 65,702,008 (GRCm38)	S655P	probably damaging	Het
Senp6	G	T	9: 80,123,728 (GRCm38)	E571*	probably null	Het
Sin3b	C	G	8: 72,746,441 (GRCm38)	T463S	probably damaging	Het
Sirt7	C	A	11: 120,619,011 (GRCm38)	R349L	probably benign	Het
Skor1	T	C	9: 63,146,448 (GRCm38)	T80A	probably damaging	Het
Slc12a9	C	A	5: 137,322,820 (GRCm38)	A478S	probably damaging	Het
Slc25a23	T	A	17: 57,052,822 (GRCm38)	R310*	probably null	Het
Slco6c1	A	T	1: 97,127,854 (GRCm38)	H107Q	probably benign	Het
Slit2	A	G	5: 48,219,994 (GRCm38)	E455G	probably benign	Het
Smo	G	C	6: 29,736,120 (GRCm38)	G37A	probably damaging	Het
St6galnac1	T	C	11: 116,769,184 (GRCm38)	K101R	probably benign	Het
Stat1	C	A	1: 52,152,371 (GRCm38)	N628K	probably benign	Het
Syn2	A	T	6: 115,254,654 (GRCm38)	Y302F	probably benign	Het
Tapt1	T	G	5: 44,188,636 (GRCm38)	Q324P	probably damaging	Het
Tcrg-V3	T	A	13: 19,242,846 (GRCm38)	M1K	probably null	Het
Tgoln1	C	T	6: 72,616,420 (GRCm38)	A26T	unknown	Het
Timm13	T	A	10: 80,900,544 (GRCm38)	T43S	probably benign	Het
Tnfrsf19	G	A	14: 61,005,205 (GRCm38)	P77S	possibly damaging	Het
Trem3	T	G	17: 48,257,941 (GRCm38)	F157V	probably benign	Het
Trim33	T	A	3: 103,326,148 (GRCm38)	S420T	probably benign	Het
Trip11	T	C	12: 101,885,435 (GRCm38)	K790R	probably damaging	Het
Trnt1	A	G	6: 106,778,904 (GRCm38)	T307A	probably benign	Het
Tshz1	T	C	18: 84,015,641 (GRCm38)	Y214C	probably damaging	Het
Vmn2r105	T	A	17: 20,228,565 (GRCm38)	T117S	probably benign	Het
Vmn2r45	A	G	7: 8,481,343 (GRCm38)	Y488H	probably benign	Het
Vwa8	A	T	14: 79,082,814 (GRCm38)	K1088N	probably benign	Het
Wdr35	T	C	12: 8,986,000 (GRCm38)	V257A	probably benign	Het
Zfp189	T	A	4: 49,521,569 (GRCm38)	S3T	probably benign	Het
Zscan22	G	A	7: 12,906,906 (GRCm38)	C359Y	probably damaging	Het
Zscan4-ps2	A	T	7: 11,517,885 (GRCm38)	R283*	probably null	Het

Other mutations in Naip5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00096:Naip5	APN	13	100,246,175 (GRCm38)	nonsense	probably null
IGL00493:Naip5	APN	13	100,230,771 (GRCm38)	missense	probably damaging	0.96
IGL01294:Naip5	APN	13	100,217,080 (GRCm38)	missense	probably damaging	0.99
IGL01405:Naip5	APN	13	100,221,945 (GRCm38)	missense	probably benign	0.11
IGL01568:Naip5	APN	13	100,217,101 (GRCm38)	missense	probably benign	0.26
IGL01804:Naip5	APN	13	100,221,584 (GRCm38)	missense	probably damaging	1.00
IGL02012:Naip5	APN	13	100,223,339 (GRCm38)	missense	probably benign	0.01
IGL02183:Naip5	APN	13	100,221,642 (GRCm38)	missense	probably benign	0.41
IGL02449:Naip5	APN	13	100,222,175 (GRCm38)	missense	probably benign	0.34
IGL02815:Naip5	APN	13	100,222,731 (GRCm38)	missense	probably benign
IGL02992:Naip5	APN	13	100,223,028 (GRCm38)	missense	probably damaging	1.00
IGL03027:Naip5	APN	13	100,223,016 (GRCm38)	missense	probably benign	0.00
IGL03234:Naip5	APN	13	100,212,627 (GRCm38)	missense	probably damaging	1.00
inwood2	UTSW	13	100,223,014 (GRCm38)	nonsense	probably null
inwood3	UTSW	13	100,221,903 (GRCm38)	nonsense	probably null
Nuchal	UTSW	13	100,214,663 (GRCm38)	missense	possibly damaging	0.82
PIT4131001:Naip5	UTSW	13	100,219,760 (GRCm38)	missense	probably benign	0.00
PIT4131001:Naip5	UTSW	13	100,219,739 (GRCm38)	missense	probably benign
R0001:Naip5	UTSW	13	100,223,114 (GRCm38)	missense	probably benign
R0001:Naip5	UTSW	13	100,214,650 (GRCm38)	critical splice donor site	probably null
R0462:Naip5	UTSW	13	100,221,732 (GRCm38)	missense	probably damaging	1.00
R0636:Naip5	UTSW	13	100,219,688 (GRCm38)	missense	probably benign
R0674:Naip5	UTSW	13	100,223,199 (GRCm38)	missense	probably benign	0.04
R0764:Naip5	UTSW	13	100,217,105 (GRCm38)	missense	probably benign	0.03
R0837:Naip5	UTSW	13	100,230,743 (GRCm38)	missense	probably benign
R1179:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R1302:Naip5	UTSW	13	100,221,591 (GRCm38)	missense	possibly damaging	0.91
R1441:Naip5	UTSW	13	100,219,717 (GRCm38)	missense	possibly damaging	0.95
R1513:Naip5	UTSW	13	100,222,206 (GRCm38)	missense	probably benign
R1638:Naip5	UTSW	13	100,212,669 (GRCm38)	missense	probably damaging	1.00
R1651:Naip5	UTSW	13	100,221,911 (GRCm38)	missense	probably benign	0.41
R1707:Naip5	UTSW	13	100,242,855 (GRCm38)	missense	probably damaging	1.00
R1835:Naip5	UTSW	13	100,223,218 (GRCm38)	nonsense	probably null
R1836:Naip5	UTSW	13	100,219,687 (GRCm38)	missense	probably benign	0.18
R1972:Naip5	UTSW	13	100,212,770 (GRCm38)	missense	probably damaging	0.98
R2080:Naip5	UTSW	13	100,221,533 (GRCm38)	missense	probably damaging	1.00
R2333:Naip5	UTSW	13	100,223,171 (GRCm38)	missense	probably damaging	1.00
R2348:Naip5	UTSW	13	100,219,738 (GRCm38)	missense	probably benign	0.01
R3055:Naip5	UTSW	13	100,221,878 (GRCm38)	missense	probably benign	0.23
R3401:Naip5	UTSW	13	100,221,903 (GRCm38)	nonsense	probably null
R3723:Naip5	UTSW	13	100,223,014 (GRCm38)	nonsense	probably null
R3775:Naip5	UTSW	13	100,223,394 (GRCm38)	missense	probably benign	0.00
R3775:Naip5	UTSW	13	100,223,375 (GRCm38)	missense	probably benign	0.00
R4019:Naip5	UTSW	13	100,223,375 (GRCm38)	missense	probably benign	0.00
R4019:Naip5	UTSW	13	100,223,394 (GRCm38)	missense	probably benign	0.00
R4020:Naip5	UTSW	13	100,223,394 (GRCm38)	missense	probably benign	0.00
R4020:Naip5	UTSW	13	100,223,375 (GRCm38)	missense	probably benign	0.00
R4074:Naip5	UTSW	13	100,246,064 (GRCm38)	missense	probably damaging	1.00
R4082:Naip5	UTSW	13	100,245,830 (GRCm38)	missense	probably damaging	1.00
R4105:Naip5	UTSW	13	100,219,739 (GRCm38)	missense	probably benign
R4227:Naip5	UTSW	13	100,212,768 (GRCm38)	missense	probably damaging	0.99
R4639:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R4640:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R4641:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R4644:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R4645:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R4700:Naip5	UTSW	13	100,223,414 (GRCm38)	missense	possibly damaging	0.62
R4727:Naip5	UTSW	13	100,221,870 (GRCm38)	missense	possibly damaging	0.81
R4729:Naip5	UTSW	13	100,222,131 (GRCm38)	missense	possibly damaging	0.75
R4816:Naip5	UTSW	13	100,219,681 (GRCm38)	missense	probably benign	0.32
R4816:Naip5	UTSW	13	100,219,687 (GRCm38)	missense	probably benign	0.01
R4816:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R4869:Naip5	UTSW	13	100,245,131 (GRCm38)	missense	probably damaging	1.00
R5162:Naip5	UTSW	13	100,223,406 (GRCm38)	missense	possibly damaging	0.78
R5244:Naip5	UTSW	13	100,245,662 (GRCm38)	missense	probably benign	0.08
R5411:Naip5	UTSW	13	100,245,746 (GRCm38)	missense	possibly damaging	0.54
R5632:Naip5	UTSW	13	100,230,662 (GRCm38)	splice site	probably null
R5760:Naip5	UTSW	13	100,242,838 (GRCm38)	missense	probably damaging	1.00
R5916:Naip5	UTSW	13	100,222,701 (GRCm38)	missense	probably benign	0.02
R6302:Naip5	UTSW	13	100,223,166 (GRCm38)	missense	possibly damaging	0.76
R6304:Naip5	UTSW	13	100,223,166 (GRCm38)	missense	possibly damaging	0.76
R6411:Naip5	UTSW	13	100,223,405 (GRCm38)	missense	probably benign	0.01
R6474:Naip5	UTSW	13	100,214,663 (GRCm38)	missense	possibly damaging	0.82
R6499:Naip5	UTSW	13	100,221,594 (GRCm38)	missense	probably benign
R6544:Naip5	UTSW	13	100,223,144 (GRCm38)	missense	possibly damaging	0.50
R6827:Naip5	UTSW	13	100,245,929 (GRCm38)	missense	possibly damaging	0.48
R6954:Naip5	UTSW	13	100,223,414 (GRCm38)	missense	probably damaging	0.99
R7052:Naip5	UTSW	13	100,222,347 (GRCm38)	missense	probably benign	0.01
R7138:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R7141:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R7375:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R7375:Naip5	UTSW	13	100,219,697 (GRCm38)	missense	not run
R7401:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R7401:Naip5	UTSW	13	100,219,697 (GRCm38)	missense	not run
R7447:Naip5	UTSW	13	100,219,697 (GRCm38)	missense	not run
R7447:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R7466:Naip5	UTSW	13	100,221,986 (GRCm38)	nonsense	probably null
R7559:Naip5	UTSW	13	100,219,697 (GRCm38)	missense	not run
R7559:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R7562:Naip5	UTSW	13	100,219,697 (GRCm38)	missense	not run
R7562:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R7588:Naip5	UTSW	13	100,219,697 (GRCm38)	missense	not run
R7588:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R7589:Naip5	UTSW	13	100,219,697 (GRCm38)	missense	not run
R7589:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R7590:Naip5	UTSW	13	100,219,697 (GRCm38)	missense	not run
R7590:Naip5	UTSW	13	100,219,696 (GRCm38)	missense	probably benign	0.00
R7742:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R7886:Naip5	UTSW	13	100,246,181 (GRCm38)	missense	probably benign	0.28
R7996:Naip5	UTSW	13	100,221,656 (GRCm38)	missense	probably damaging	1.00
R8026:Naip5	UTSW	13	100,245,898 (GRCm38)	missense	probably damaging	1.00
R8046:Naip5	UTSW	13	100,222,233 (GRCm38)	missense	probably benign
R8319:Naip5	UTSW	13	100,221,659 (GRCm38)	missense	probably benign	0.12
R8471:Naip5	UTSW	13	100,221,645 (GRCm38)	missense	probably damaging	0.99
R8480:Naip5	UTSW	13	100,222,235 (GRCm38)	missense	probably damaging	1.00
R8496:Naip5	UTSW	13	100,212,739 (GRCm38)	missense	probably benign	0.00
R8500:Naip5	UTSW	13	100,222,712 (GRCm38)	missense	probably damaging	0.98
R8712:Naip5	UTSW	13	100,223,096 (GRCm38)	missense	possibly damaging	0.61
R8780:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R8781:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R8788:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R8817:Naip5	UTSW	13	100,212,699 (GRCm38)	missense	probably benign	0.01
R8833:Naip5	UTSW	13	100,222,934 (GRCm38)	missense	probably damaging	0.97
R8835:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R8958:Naip5	UTSW	13	100,217,609 (GRCm38)	nonsense	probably null
R9031:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R9032:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R9074:Naip5	UTSW	13	100,221,756 (GRCm38)	missense	possibly damaging	0.92
R9098:Naip5	UTSW	13	100,229,619 (GRCm38)	missense	possibly damaging	0.67
R9204:Naip5	UTSW	13	100,222,500 (GRCm38)	missense	probably damaging	1.00
R9223:Naip5	UTSW	13	100,227,676 (GRCm38)	missense	probably benign	0.05
R9358:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R9389:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R9403:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R9518:Naip5	UTSW	13	100,221,859 (GRCm38)	missense	probably benign
R9568:Naip5	UTSW	13	100,223,313 (GRCm38)	missense	probably benign	0.00
R9568:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R9569:Naip5	UTSW	13	100,223,313 (GRCm38)	missense	probably benign	0.00
R9569:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R9570:Naip5	UTSW	13	100,223,313 (GRCm38)	missense	probably benign	0.00
R9572:Naip5	UTSW	13	100,223,313 (GRCm38)	missense	probably benign	0.00
R9581:Naip5	UTSW	13	100,214,686 (GRCm38)	missense	probably benign	0.11
R9627:Naip5	UTSW	13	100,219,830 (GRCm38)	missense	probably benign
R9725:Naip5	UTSW	13	100,222,276 (GRCm38)	missense	possibly damaging	0.94
R9763:Naip5	UTSW	13	100,230,761 (GRCm38)	missense	probably damaging	0.99
R9764:Naip5	UTSW	13	100,230,761 (GRCm38)	missense	probably damaging	0.99
R9765:Naip5	UTSW	13	100,230,761 (GRCm38)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- CAAGGTGATGGAGTGTTACCTG -3'
(R):5'- CAGTCTGAATGTCATATCACCTTTG -3'

Sequencing Primer
(F):5'- GAGTGTTACCTGAGATCTGTAACCTC -3'
(R):5'- CAATGGTTTTCCCATGTCA -3'

Posted On

2019-10-17