Mutagenetix > Incidental Mutation

Incidental Mutation 'R7124:Pard6g'

552241

Institutional Source

Beutler Lab

Gene Symbol

Pard6g

Ensembl Gene

ENSMUSG00000056214

Gene Name

par-6 family cell polarity regulator gamma

Synonyms

2410049N21Rik

MMRRC Submission

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.345) question?

Stock #

R7124 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

80046895-80119640 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 80117125 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 151 (I151T)

Ref Sequence

ENSEMBL: ENSMUSP00000069182 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000070219]

AlphaFold

Q9JK84

Predicted Effect

possibly damaging
Transcript: ENSMUST00000070219
AA Change: I151T

PolyPhen 2 Score 0.698 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000069182
Gene: ENSMUSG00000056214
AA Change: I151T

Domain	Start	End	E-Value	Type
PB1	18	98	1.16e-16	SMART
PDZ	168	251	8.6e-14	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

97% (72/74)

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700006A11Rik	A	C	3: 124,414,393	S212R	probably benign	Het
4930562C15Rik	T	C	16: 4,864,332	S170P	probably benign	Het
9330182O14Rik	G	A	15: 40,144,907	C59Y	unknown	Het
AA986860	A	G	1: 130,742,887	E282G	possibly damaging	Het
Adam1a	G	T	5: 121,519,334	T632K	probably benign	Het
Aspg	G	T	12: 112,122,983	A402S	probably damaging	Het
Capn7	C	T	14: 31,336,685		probably benign	Het
Card9	C	T	2: 26,356,884		probably null	Het
Cdh13	T	C	8: 118,968,173	V254A	probably damaging	Het
Colec10	T	C	15: 54,462,371	V199A	probably damaging	Het
Copb2	T	C	9: 98,577,053	S283P	probably damaging	Het
Csmd1	G	T	8: 15,903,202	S3426R	probably damaging	Het
Cyp4f14	A	G	17: 32,914,588	V98A	probably benign	Het
Disp1	C	A	1: 183,087,466	R1130L	probably damaging	Het
Dysf	A	G	6: 84,190,901		probably null	Het
Eif4ebp1	T	C	8: 27,273,419	V80A	probably damaging	Het
Eloa	T	A	4: 136,009,141	I565F	probably damaging	Het
Espn	G	T	4: 152,131,264	H513N	probably benign	Het
Fam83c	C	T	2: 155,829,571	S648N	probably benign	Het
Fdxr	C	T	11: 115,269,577	V351M	probably benign	Het
Fras1	A	T	5: 96,714,401	D2213V	probably damaging	Het
Gbp4	T	A	5: 105,119,959	I474F	possibly damaging	Het
Gm11639	T	C	11: 104,738,274	F926S	probably benign	Het
Golgb1	T	C	16: 36,913,673	V1135A	probably benign	Het
Gpt2	G	A	8: 85,518,052	E325K	probably benign	Het
Hipk2	A	T	6: 38,818,478	Y285*	probably null	Het
Ifi27l2b	T	C	12: 103,451,320	I203V	probably damaging	Het
Itga10	T	A	3: 96,651,765	M390K	probably damaging	Het
Itgb8	G	T	12: 119,202,424	S124*	probably null	Het
Klhdc10	T	A	6: 30,441,827	F173I	probably damaging	Het
Kng2	T	G	16: 23,012,055	N168T	probably damaging	Het
Krtap24-1	T	C	16: 88,611,546	T231A	probably damaging	Het
Lbx2	A	T	6: 83,088,064	D194V	probably damaging	Het
Lrrc39	C	A	3: 116,565,913	Q36K	probably benign	Het
Madd	T	C	2: 91,162,048	E1093G	possibly damaging	Het
Mfap3l	A	G	8: 60,671,269	T182A	probably damaging	Het
Myo9b	T	A	8: 71,333,701	Y670*	probably null	Het
Nbea	A	G	3: 55,992,444	L1428P	probably damaging	Het
Nkx2-3	T	C	19: 43,614,806	Y284H	possibly damaging	Het
Nphp4	A	G	4: 152,555,684	D1009G	probably benign	Het
Npy2r	G	A	3: 82,541,183	A95V	probably damaging	Het
Nuggc	A	G	14: 65,608,802	E70G	probably damaging	Het
Olfr1020	T	C	2: 85,849,910	S153P	probably benign	Het
Olfr1028	T	A	2: 85,951,473	S137T	possibly damaging	Het
Palld	A	T	8: 61,516,645	V1215D	unknown	Het
Parp12	T	C	6: 39,111,736	I189V	probably benign	Het
Parp4	A	G	14: 56,602,799	I554V	probably benign	Het
Pcnx2	G	A	8: 125,753,617	P1984S	probably damaging	Het
Piwil4	T	C	9: 14,736,900	M128V	probably benign	Het
Polr2a	C	A	11: 69,737,462	E1302*	probably null	Het
Psg17	C	A	7: 18,814,496	G450V	probably damaging	Het
Psg17	C	G	7: 18,814,497	G450R	probably damaging	Het
Rag1	T	C	2: 101,643,783	E338G	probably damaging	Het
Rev3l	A	T	10: 39,822,167	K887*	probably null	Het
Rragd	T	C	4: 32,996,027	F124S	possibly damaging	Het
Scube1	A	T	15: 83,629,511		probably null	Het
Sfpq	A	T	4: 127,025,932	D490V	possibly damaging	Het
Smc1b	G	T	15: 85,071,597	Q1034K	probably damaging	Het
Smg7	T	C	1: 152,878,080	N5S	probably benign	Het
Spata31d1a	A	C	13: 59,702,487	L609R	probably damaging	Het
Ssh2	A	G	11: 77,454,338	K1050E	probably benign	Het
Stab1	G	A	14: 31,160,867	T393I	possibly damaging	Het
Sult2a4	C	T	7: 13,988,395	W49*	probably null	Het
Thrap3	A	T	4: 126,180,438	S172T	unknown	Het
Tmem130	A	G	5: 144,750,911	V205A	probably damaging	Het
Ube2d2b	A	G	5: 107,830,851	I123V	probably benign	Het
Unc79	G	T	12: 103,061,393	L414F	probably damaging	Het
Vmn2r30	C	T	7: 7,334,184	S151N	probably benign	Het
Vmn2r54	T	A	7: 12,622,151	T443S	probably benign	Het
Zfp229	T	A	17: 21,742,616	S51T	probably damaging	Het
Zfp617	T	C	8: 71,932,540	L238P	probably damaging	Het
Zfp707	T	A	15: 75,973,549	C87*	probably null	Het
Zfp853	T	C	5: 143,289,607	K101R	unknown	Het

Other mutations in Pard6g

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01024:Pard6g	APN	18	80079822	splice site	probably benign
IGL01514:Pard6g	APN	18	80117446	missense	probably damaging	1.00
IGL01519:Pard6g	APN	18	80079856	missense	probably benign	0.34
IGL02305:Pard6g	APN	18	80117770	missense	probably damaging	1.00
IGL03115:Pard6g	APN	18	80079853	missense	probably damaging	1.00
R0411:Pard6g	UTSW	18	80117122	missense	probably damaging	1.00
R0604:Pard6g	UTSW	18	80117208	missense	probably damaging	1.00
R0938:Pard6g	UTSW	18	80080044	nonsense	probably null
R1730:Pard6g	UTSW	18	80079825	missense	probably damaging	0.97
R1783:Pard6g	UTSW	18	80079825	missense	probably damaging	0.97
R1785:Pard6g	UTSW	18	80117308	missense	probably damaging	0.96
R1786:Pard6g	UTSW	18	80117308	missense	probably damaging	0.96
R1851:Pard6g	UTSW	18	80117142	missense	probably damaging	1.00
R2070:Pard6g	UTSW	18	80117725	missense	probably benign	0.00
R2132:Pard6g	UTSW	18	80117308	missense	probably damaging	0.96
R2133:Pard6g	UTSW	18	80117308	missense	probably damaging	0.96
R3778:Pard6g	UTSW	18	80079823	critical splice acceptor site	probably null
R5282:Pard6g	UTSW	18	80079901	missense	probably benign	0.01
R6084:Pard6g	UTSW	18	80117205	missense	possibly damaging	0.73
R6913:Pard6g	UTSW	18	80117319	missense	possibly damaging	0.94
R8109:Pard6g	UTSW	18	80117443	missense	possibly damaging	0.65
R8469:Pard6g	UTSW	18	80047132	missense	possibly damaging	0.81
R8903:Pard6g	UTSW	18	80117196	nonsense	probably null
R8915:Pard6g	UTSW	18	80117742	missense	probably damaging	0.99
R9077:Pard6g	UTSW	18	80117557	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TTTCTGCCCATGTATGGCGTAC -3'
(R):5'- TCATTCACAGCCAGTAGCCC -3'

Sequencing Primer
(F):5'- ATGTATGGCGTACACCTCTCAC -3'
(R):5'- ACAGCCAGTAGCCCAGTGC -3'

Posted On

2019-05-15