Mutagenetix > Incidental Mutation

Incidental Mutation 'R8794:Poln'

671100

Institutional Source

Beutler Lab

Gene Symbol

Poln

Ensembl Gene

ENSMUSG00000045102

Gene Name

DNA polymerase N

Synonyms

POL4P

MMRRC Submission

068723-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8794 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

34164523-34326792 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 34286871 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 99 (T99I)

Ref Sequence

ENSEMBL: ENSMUSP00000036110 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042954] [ENSMUST00000202409] [ENSMUST00000202638]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000042954
AA Change: T99I

PolyPhen 2 Score 0.847 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000036110
Gene: ENSMUSG00000045102
AA Change: T99I

Domain	Start	End	E-Value	Type
low complexity region	110	121	N/A	INTRINSIC
POLAc	605	814	7.88e-67	SMART
low complexity region	829	843	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000202409
AA Change: T99I

PolyPhen 2 Score 0.847 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000144578
Gene: ENSMUSG00000045102
AA Change: T99I

Domain	Start	End	E-Value	Type
low complexity region	110	121	N/A	INTRINSIC
coiled coil region	448	471	N/A	INTRINSIC
POLAc	587	796	2.6e-69	SMART
low complexity region	811	825	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000202638
AA Change: T99I

PolyPhen 2 Score 0.662 (Sensitivity: 0.86; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000143793
Gene: ENSMUSG00000045102
AA Change: T99I

Domain	Start	End	E-Value	Type
low complexity region	110	121	N/A	INTRINSIC
coiled coil region	448	471	N/A	INTRINSIC
POLAc	605	770	3e-37	SMART
low complexity region	785	799	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.9%
20x: 99.6%

Validation Efficiency

100% (86/86)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced meiotic double-strand breaks at a meiotic recombination hot spot harboring insertion/deletion polymorphisms, but are otherwise normal. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700010I14Rik	T	A	17: 9,226,939 (GRCm39)	V498D	unknown	Het
Actn1	C	T	12: 80,245,754 (GRCm39)		probably benign	Het
Actrt2	T	C	4: 154,751,176 (GRCm39)	E320G	probably damaging	Het
Adamts7	C	T	9: 90,076,239 (GRCm39)	Q1265*	probably null	Het
Adra1a	A	G	14: 66,875,064 (GRCm39)	N13S	probably benign	Het
Alpk3	G	T	7: 80,707,403 (GRCm39)	R9L	unknown	Het
Ankrd42	A	G	7: 92,263,674 (GRCm39)	F225L	probably benign	Het
C3	T	C	17: 57,528,011 (GRCm39)	E736G	probably benign	Het
Ccng1	A	G	11: 40,644,826 (GRCm39)	S24P	probably benign	Het
Cdc42bpa	A	T	1: 179,894,816 (GRCm39)	N332I	probably damaging	Het
Cep131	G	A	11: 119,972,074 (GRCm39)	P90S	probably benign	Het
Chd8	A	G	14: 52,441,904 (GRCm39)	S2154P	probably damaging	Het
Cilp	A	G	9: 65,186,535 (GRCm39)	S877G	probably benign	Het
Clic6	T	A	16: 92,324,987 (GRCm39)	S382T	possibly damaging	Het
Coq8a	G	T	1: 180,006,773 (GRCm39)	P85Q	probably benign	Het
Creb3l4	A	G	3: 90,145,225 (GRCm39)	I309T	probably benign	Het
Cux2	T	C	5: 122,007,306 (GRCm39)	E785G	probably benign	Het
Cyfip2	A	G	11: 46,144,800 (GRCm39)	F685L	possibly damaging	Het
Epha6	T	C	16: 60,026,035 (GRCm39)	D469G	probably benign	Het
Erc1	A	T	6: 119,607,616 (GRCm39)	V962E	probably damaging	Het
Esrrb	A	T	12: 86,517,038 (GRCm39)	S57C	probably damaging	Het
Fam169a	A	G	13: 97,250,628 (GRCm39)	T320A	possibly damaging	Het
Farsb	C	T	1: 78,401,678 (GRCm39)		probably benign	Het
Frem3	T	C	8: 81,338,907 (GRCm39)	V400A	probably damaging	Het
Frem3	A	T	8: 81,342,851 (GRCm39)	M1715L	probably benign	Het
Frmpd1	A	G	4: 45,279,632 (GRCm39)	T786A	probably benign	Het
Gapvd1	A	T	2: 34,594,330 (GRCm39)	S886T	possibly damaging	Het
Gba2	A	G	4: 43,568,077 (GRCm39)	S737P	probably damaging	Het
Gm525	A	G	11: 88,979,479 (GRCm39)	N85S	probably damaging	Het
Gnpda1	T	A	18: 38,465,091 (GRCm39)	D175V	probably benign	Het
Heatr5b	T	C	17: 79,123,015 (GRCm39)	I655V	probably benign	Het
Hmcn1	G	A	1: 150,591,469 (GRCm39)	T1910I	probably benign	Het
Idh1	CA	CAA	1: 65,204,347 (GRCm39)		probably null	Het
Ier2	A	T	8: 85,389,096 (GRCm39)	D95E	probably damaging	Het
Ifi208	A	G	1: 173,523,370 (GRCm39)	R547G	possibly damaging	Het
Itih3	T	A	14: 30,634,854 (GRCm39)	S639C	possibly damaging	Het
Kif19b	A	G	5: 140,461,785 (GRCm39)	E529G	probably damaging	Het
Marchf7	G	A	2: 60,074,015 (GRCm39)		probably null	Het
Mep1b	A	C	18: 21,224,325 (GRCm39)	T373P	probably damaging	Het
Mlh3	G	A	12: 85,282,497 (GRCm39)	P1379S	probably damaging	Het
Nav3	T	A	10: 109,605,032 (GRCm39)	K1014*	probably null	Het
Nme1	A	T	11: 93,851,658 (GRCm39)	F78I	probably benign	Het
Nos3	T	A	5: 24,576,745 (GRCm39)	V458D	probably damaging	Het
Noxa1	A	G	2: 24,984,852 (GRCm39)	F29L	probably benign	Het
Nrcam	G	A	12: 44,624,958 (GRCm39)	G1055D	probably benign	Het
Nutf2	A	T	8: 106,602,171 (GRCm39)		probably benign	Het
Oog3	A	G	4: 143,884,556 (GRCm39)	I460T	probably benign	Het
Or4b1b	A	T	2: 90,112,150 (GRCm39)	Y256*	probably null	Het
Or4c113	T	C	2: 88,885,477 (GRCm39)	M98V	probably benign	Het
Or5p78	A	T	7: 108,211,580 (GRCm39)	D22V	probably benign	Het
Or7e175	A	T	9: 20,048,630 (GRCm39)	M73L	possibly damaging	Het
Pde2a	A	T	7: 101,155,136 (GRCm39)	Y559F	possibly damaging	Het
Pde6d	G	A	1: 86,475,209 (GRCm39)	Q61*	probably null	Het
Pdpr	A	G	8: 111,852,240 (GRCm39)	T536A	possibly damaging	Het
Pias4	T	A	10: 80,999,846 (GRCm39)	K69M	probably damaging	Het
Pigo	A	T	4: 43,023,787 (GRCm39)	D188E	possibly damaging	Het
Pik3r2	A	G	8: 71,224,007 (GRCm39)	V270A	probably benign	Het
Plod2	T	A	9: 92,482,801 (GRCm39)	W456R	probably damaging	Het
Pmpcb	T	C	5: 21,961,832 (GRCm39)	V450A	probably benign	Het
Prg2	A	G	2: 84,812,404 (GRCm39)	D38G	possibly damaging	Het
Psmd7	A	C	8: 108,310,831 (GRCm39)	Y138D	probably damaging	Het
Ptprk	T	A	10: 28,139,504 (GRCm39)	Y76*	probably null	Het
Ranbp2	T	A	10: 58,328,414 (GRCm39)	V2810E	probably damaging	Het
Rgma	A	T	7: 73,067,648 (GRCm39)	H411L	probably damaging	Het
Sapcd1	T	C	17: 35,246,814 (GRCm39)	T25A	probably damaging	Het
Serpinb6e	T	C	13: 34,024,977 (GRCm39)	I105V	possibly damaging	Het
Serpinb9f	A	T	13: 33,513,396 (GRCm39)	T158S	probably benign	Het
Sirpb1b	T	A	3: 15,613,843 (GRCm39)	T80S	probably benign	Het
Skint6	A	T	4: 113,049,869 (GRCm39)	S265R	possibly damaging	Het
Slc23a2	A	T	2: 131,902,629 (GRCm39)	F524L	probably benign	Het
Slc2a13	C	A	15: 91,234,302 (GRCm39)	G345C	probably damaging	Het
Sp110	A	G	1: 85,511,231 (GRCm39)		probably null	Het
Srcin1	A	G	11: 97,439,803 (GRCm39)	V109A	probably benign	Het
Tfcp2l1	A	G	1: 118,560,118 (GRCm39)	N70S	probably damaging	Het
Tmem30c	T	A	16: 57,090,553 (GRCm39)	H218L	probably benign	Het
Tmprss11d	G	A	5: 86,486,680 (GRCm39)	T70I	probably damaging	Het
Tnpo2	A	T	8: 85,765,114 (GRCm39)	Q32L	probably benign	Het
Trav16n	A	C	14: 53,588,867 (GRCm39)	T48P	probably damaging	Het
Ufc1	A	G	1: 171,117,095 (GRCm39)	Y110H	probably damaging	Het
Wars2	A	G	3: 99,123,888 (GRCm39)	K250E	probably damaging	Het
Wdfy4	G	T	14: 32,869,049 (GRCm39)	N326K	probably benign	Het
Xirp2	A	T	2: 67,341,557 (GRCm39)	E1266V	probably damaging	Het
Zfp423	A	C	8: 88,507,857 (GRCm39)	L829R	probably damaging	Het
Zfp735	A	G	11: 73,603,029 (GRCm39)	K658E	possibly damaging	Het
Zscan12	T	A	13: 21,547,847 (GRCm39)	C10S	possibly damaging	Het
Zswim3	T	A	2: 164,662,687 (GRCm39)	M389K	probably damaging	Het

Other mutations in Poln

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00803:Poln	APN	5	34,280,104 (GRCm39)	missense	probably benign	0.17
IGL00938:Poln	APN	5	34,286,568 (GRCm39)	missense	probably damaging	1.00
IGL02081:Poln	APN	5	34,286,483 (GRCm39)	missense	probably benign
IGL02411:Poln	APN	5	34,270,666 (GRCm39)	nonsense	probably null
IGL02440:Poln	APN	5	34,286,474 (GRCm39)	missense	probably damaging	1.00
IGL02484:Poln	APN	5	34,286,721 (GRCm39)	missense	probably damaging	1.00
IGL02577:Poln	APN	5	34,270,679 (GRCm39)	missense	probably benign	0.03
IGL03113:Poln	APN	5	34,274,206 (GRCm39)	missense	probably benign	0.01
R0034:Poln	UTSW	5	34,272,762 (GRCm39)	missense	possibly damaging	0.78
R0034:Poln	UTSW	5	34,272,762 (GRCm39)	missense	possibly damaging	0.78
R0068:Poln	UTSW	5	34,234,432 (GRCm39)	splice site	probably benign
R0068:Poln	UTSW	5	34,234,432 (GRCm39)	splice site	probably benign
R0325:Poln	UTSW	5	34,307,108 (GRCm39)	missense	probably benign	0.00
R0578:Poln	UTSW	5	34,171,682 (GRCm39)	missense	probably damaging	1.00
R0631:Poln	UTSW	5	34,276,302 (GRCm39)	missense	possibly damaging	0.93
R1171:Poln	UTSW	5	34,261,284 (GRCm39)	missense	probably damaging	1.00
R1266:Poln	UTSW	5	34,290,453 (GRCm39)	critical splice donor site	probably null
R1418:Poln	UTSW	5	34,236,319 (GRCm39)	missense	probably benign	0.00
R1449:Poln	UTSW	5	34,171,682 (GRCm39)	missense	probably damaging	1.00
R1558:Poln	UTSW	5	34,190,143 (GRCm39)	missense	probably benign	0.04
R1723:Poln	UTSW	5	34,280,016 (GRCm39)	missense	probably benign	0.16
R1806:Poln	UTSW	5	34,264,494 (GRCm39)	splice site	probably benign
R4124:Poln	UTSW	5	34,261,295 (GRCm39)	missense	probably benign	0.32
R4125:Poln	UTSW	5	34,261,295 (GRCm39)	missense	probably benign	0.32
R4128:Poln	UTSW	5	34,261,295 (GRCm39)	missense	probably benign	0.32
R4155:Poln	UTSW	5	34,166,993 (GRCm39)	missense	possibly damaging	0.90
R4353:Poln	UTSW	5	34,286,796 (GRCm39)	missense	probably benign	0.00
R4717:Poln	UTSW	5	34,286,792 (GRCm39)	missense	possibly damaging	0.46
R4788:Poln	UTSW	5	34,286,675 (GRCm39)	missense	probably benign	0.30
R4981:Poln	UTSW	5	34,264,429 (GRCm39)	critical splice donor site	probably null
R5456:Poln	UTSW	5	34,164,786 (GRCm39)	missense	possibly damaging	0.95
R6020:Poln	UTSW	5	34,266,775 (GRCm39)	missense	probably damaging	0.99
R6484:Poln	UTSW	5	34,286,857 (GRCm39)	missense	probably benign	0.01
R7134:Poln	UTSW	5	34,276,340 (GRCm39)	missense	possibly damaging	0.86
R7639:Poln	UTSW	5	34,290,495 (GRCm39)	missense	possibly damaging	0.77
R7764:Poln	UTSW	5	34,274,151 (GRCm39)	critical splice donor site	probably null
R7874:Poln	UTSW	5	34,181,694 (GRCm39)	missense	probably damaging	1.00
R8039:Poln	UTSW	5	34,280,016 (GRCm39)	missense	probably benign	0.16
R8315:Poln	UTSW	5	34,266,717 (GRCm39)	missense	probably benign	0.00
R8320:Poln	UTSW	5	34,307,171 (GRCm39)	missense	possibly damaging	0.70
R8340:Poln	UTSW	5	34,307,118 (GRCm39)	missense	probably damaging	0.99
R8926:Poln	UTSW	5	34,286,769 (GRCm39)	missense	probably benign	0.24
R9021:Poln	UTSW	5	34,286,485 (GRCm39)	missense	probably benign	0.00
R9128:Poln	UTSW	5	34,171,658 (GRCm39)	missense	probably damaging	1.00
R9382:Poln	UTSW	5	34,164,842 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- CCAGAGCTGTGTGTTTACTTGC -3'
(R):5'- GCTCTCGTTATCTTTGAGAAGCTG -3'

Sequencing Primer
(F):5'- ATTTTCTTTTAAGACTCGAGTTGTCC -3'
(R):5'- GAAGCTGTATCAAAAATGCACTTGG -3'

Posted On

2021-04-30