Mutagenetix > Incidental Mutation

Incidental Mutation 'R7775:Gm14226'

598815

Institutional Source

Beutler Lab

Gene Symbol

Gm14226

Ensembl Gene

ENSMUSG00000084897

Gene Name

predicted gene 14226

Synonyms

MMRRC Submission

045831-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.192) question?

Stock #

R7775 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

154860186-154869024 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 154866630 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 196 (C196S)

Ref Sequence

ENSEMBL: ENSMUSP00000122157 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000029123] [ENSMUST00000109697] [ENSMUST00000130870] [ENSMUST00000137333] [ENSMUST00000148402]

AlphaFold

Q3TZL0

Predicted Effect

probably benign
Transcript: ENSMUST00000029123

SMART Domains

Protein: ENSMUSP00000029123
Gene: ENSMUSG00000027596

Domain	Start	End	E-Value	Type
Agouti	6	127	3.98e-69	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000109697

SMART Domains

Protein: ENSMUSP00000105319
Gene: ENSMUSG00000027596

Domain	Start	End	E-Value	Type
Agouti	6	127	3.98e-69	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000130870
AA Change: C196S

PolyPhen 2 Score 0.711 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000122157
Gene: ENSMUSG00000084897
AA Change: C196S

Domain	Start	End	E-Value	Type
Pfam:TLV_coat	14	627	1.4e-139	PFAM
low complexity region	649	662	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000137333

SMART Domains

Protein: ENSMUSP00000122261
Gene: ENSMUSG00000027596

Domain	Start	End	E-Value	Type
Agouti	6	70	2.53e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000148402

SMART Domains

Protein: ENSMUSP00000121072
Gene: ENSMUSG00000027596

Domain	Start	End	E-Value	Type
Agouti	6	75	2.32e-6	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (64/64)

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgap35	T	C	7: 16,296,573 (GRCm39)	K831E	probably benign	Het
Arpc1a	C	T	5: 145,041,622 (GRCm39)	R302C	probably benign	Het
Asb5	A	C	8: 55,037,827 (GRCm39)	H173P		Het
Atp6v0a2	A	G	5: 124,779,443 (GRCm39)	E186G	probably damaging	Het
Bbs2	A	T	8: 94,816,388 (GRCm39)		probably null	Het
Capn7	A	G	14: 31,074,367 (GRCm39)	T257A	probably benign	Het
Car4	T	C	11: 84,856,449 (GRCm39)	S246P	probably damaging	Het
Chrm5	A	G	2: 112,310,301 (GRCm39)	S272P	probably benign	Het
Chrna6	T	C	8: 27,897,392 (GRCm39)	I162V	probably damaging	Het
Chst12	T	A	5: 140,509,376 (GRCm39)	M1K	probably null	Het
Cldn6	T	A	17: 23,900,581 (GRCm39)	C182S	probably damaging	Het
Coro6	T	G	11: 77,356,599 (GRCm39)	D102E	probably benign	Het
Cysltr2	A	G	14: 73,267,203 (GRCm39)	I169T	probably benign	Het
Dtx4	G	T	19: 12,469,374 (GRCm39)	P251Q	probably benign	Het
Dyrk3	C	T	1: 131,057,364 (GRCm39)	V270I	possibly damaging	Het
Efhc1	A	T	1: 21,049,685 (GRCm39)	Y515F	probably damaging	Het
Ep300	T	C	15: 81,470,887 (GRCm39)	S20P	unknown	Het
Fmnl2	C	T	2: 52,963,692 (GRCm39)	L275F	unknown	Het
Fstl4	C	T	11: 53,067,798 (GRCm39)	Q554*	probably null	Het
Gal3st2b	G	T	1: 93,868,506 (GRCm39)	D246Y	probably damaging	Het
Gkap1	A	T	13: 58,398,966 (GRCm39)	D188E	probably benign	Het
Gm8297	A	G	14: 16,167,939 (GRCm39)	N193S	possibly damaging	Het
Grm8	T	C	6: 27,363,671 (GRCm39)	R615G	possibly damaging	Het
Ing1	A	G	8: 11,611,814 (GRCm39)	E178G	probably benign	Het
Kansl3	A	T	1: 36,387,758 (GRCm39)	L530H	probably damaging	Het
Kcna5	A	T	6: 126,511,768 (GRCm39)	L120*	probably null	Het
Kif26b	T	A	1: 178,692,441 (GRCm39)	S461T	probably benign	Het
L3mbtl3	A	T	10: 26,228,215 (GRCm39)	V15E	unknown	Het
Lama4	A	T	10: 38,954,843 (GRCm39)	H1132L	probably damaging	Het
Ldlrad4	G	T	18: 68,368,740 (GRCm39)	A66S	possibly damaging	Het
Ldlrad4	T	C	18: 68,368,827 (GRCm39)	S95P	probably damaging	Het
Liph	G	T	16: 21,777,664 (GRCm39)	L379I	probably damaging	Het
Lrp2	T	A	2: 69,331,883 (GRCm39)	E1624V	possibly damaging	Het
Matn2	A	T	15: 34,399,223 (GRCm39)	H370L	possibly damaging	Het
Mettl23	T	G	11: 116,740,096 (GRCm39)	V189G	probably benign	Het
Mpp4	G	A	1: 59,162,672 (GRCm39)	T543M	not run	Het
Mrps15	A	T	4: 125,945,170 (GRCm39)	N119I	probably damaging	Het
Or10d4	C	A	9: 39,580,534 (GRCm39)	F60L	possibly damaging	Het
Or5ac21	A	T	16: 59,123,614 (GRCm39)	I33F	probably damaging	Het
Or7d9	A	G	9: 20,193,708 (GRCm39)		probably benign	Het
Or8b36	T	A	9: 37,937,963 (GRCm39)	I287N	probably damaging	Het
Or8g21	T	A	9: 38,906,203 (GRCm39)	H176L	probably damaging	Het
Pax8	A	G	2: 24,325,913 (GRCm39)	S324P	possibly damaging	Het
Pcdha11	A	T	18: 37,145,733 (GRCm39)	Y608F	possibly damaging	Het
Pcdhga5	A	G	18: 37,828,578 (GRCm39)	D342G	probably damaging	Het
Pde6d	A	G	1: 86,471,250 (GRCm39)	S143P	probably damaging	Het
Plau	A	G	14: 20,892,393 (GRCm39)	S393G	probably benign	Het
Plec	A	T	15: 76,061,135 (GRCm39)	I2934N	probably damaging	Het
Primpol	G	T	8: 47,039,459 (GRCm39)	P387Q	probably damaging	Het
Prph2	T	C	17: 47,221,732 (GRCm39)	L37S	possibly damaging	Het
Prrt4	A	G	6: 29,177,718 (GRCm39)	L17P	probably damaging	Het
Pycr3	T	C	15: 75,790,138 (GRCm39)	D171G	probably damaging	Het
Rapgefl1	A	G	11: 98,741,980 (GRCm39)	N648S	probably damaging	Het
Rapsn	A	G	2: 90,875,293 (GRCm39)	T359A	probably benign	Het
Sap25	C	T	5: 137,640,186 (GRCm39)	R66W	probably benign	Het
Setd6	A	T	8: 96,442,866 (GRCm39)	H101L	probably benign	Het
Slc22a3	G	T	17: 12,683,350 (GRCm39)	A171E	probably damaging	Het
Tbc1d2	C	T	4: 46,637,746 (GRCm39)		probably null	Het
Tfap2b	G	A	1: 19,304,531 (GRCm39)	G447D	probably damaging	Het
Txndc2	A	G	17: 65,945,238 (GRCm39)	V313A	probably benign	Het
Uevld	A	T	7: 46,576,100 (GRCm39)	I462N	probably damaging	Het
Vmn2r120	T	C	17: 57,832,942 (GRCm39)	Y79C	probably damaging	Het
Vwa8	T	C	14: 79,275,587 (GRCm39)	V790A	probably benign	Het
Zfp936	A	G	7: 42,839,720 (GRCm39)	T396A	possibly damaging	Het

Other mutations in Gm14226

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00402:Gm14226	APN	2	154,867,078 (GRCm39)	missense	probably damaging	1.00
IGL02852:Gm14226	APN	2	154,866,841 (GRCm39)	missense	possibly damaging	0.91
R0279:Gm14226	UTSW	2	154,867,372 (GRCm39)	missense	possibly damaging	0.82
R1393:Gm14226	UTSW	2	154,866,111 (GRCm39)	missense	probably damaging	1.00
R1740:Gm14226	UTSW	2	154,866,851 (GRCm39)	intron	probably benign
R1758:Gm14226	UTSW	2	154,867,378 (GRCm39)	missense	probably damaging	1.00
R1816:Gm14226	UTSW	2	154,867,549 (GRCm39)	missense	probably damaging	1.00
R1837:Gm14226	UTSW	2	154,866,930 (GRCm39)	missense	probably benign	0.31
R1951:Gm14226	UTSW	2	154,866,255 (GRCm39)	missense	possibly damaging	0.92
R4485:Gm14226	UTSW	2	154,867,191 (GRCm39)	missense	probably benign	0.18
R4947:Gm14226	UTSW	2	154,866,879 (GRCm39)	missense	probably benign	0.21
R5061:Gm14226	UTSW	2	154,867,106 (GRCm39)	missense	probably benign	0.13
R5673:Gm14226	UTSW	2	154,866,842 (GRCm39)	missense	possibly damaging	0.81
R5863:Gm14226	UTSW	2	154,866,211 (GRCm39)	missense	probably benign	0.19
R6525:Gm14226	UTSW	2	154,867,003 (GRCm39)	missense	possibly damaging	0.67
R6996:Gm14226	UTSW	2	154,866,357 (GRCm39)	missense	probably benign	0.00
R7546:Gm14226	UTSW	2	154,867,131 (GRCm39)	missense	probably damaging	0.96
R7593:Gm14226	UTSW	2	154,866,114 (GRCm39)	missense	unknown
R7778:Gm14226	UTSW	2	154,866,630 (GRCm39)	missense	possibly damaging	0.71
R8254:Gm14226	UTSW	2	154,866,646 (GRCm39)	missense	possibly damaging	0.52
R8558:Gm14226	UTSW	2	154,866,909 (GRCm39)	missense	probably benign	0.03
R8712:Gm14226	UTSW	2	154,866,094 (GRCm39)	missense	unknown
R8815:Gm14226	UTSW	2	154,866,538 (GRCm39)	nonsense	probably null
R9149:Gm14226	UTSW	2	154,866,843 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GAGGTCATAATGACTGGGGAACTC -3'
(R):5'- TCCCGGGTAGGCCTAAGGT -3'

Sequencing Primer
(F):5'- TTGACGATCCTAGACAAGTTGCC -3'
(R):5'- TAACAGTCTGTGGAATACTCGGC -3'

Posted On

2019-11-26