Mutagenetix > Incidental Mutation

Incidental Mutation 'R1991:Armc3'

225060

Institutional Source

Beutler Lab

Gene Symbol

Armc3

Ensembl Gene

ENSMUSG00000037683

Gene Name

armadillo repeat containing 3

Synonyms

4921513G22Rik

MMRRC Submission

040002-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.074) question?

Stock #

R1991 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

19199302-19310241 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 19293142 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 575 (Y575H)

Ref Sequence

ENSEMBL: ENSMUSP00000110287 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049255] [ENSMUST00000114640]

AlphaFold

A2AU72

Predicted Effect

probably damaging
Transcript: ENSMUST00000049255
AA Change: Y575H

PolyPhen 2 Score 0.961 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000048784
Gene: ENSMUSG00000037683
AA Change: Y575H

Domain	Start	End	E-Value	Type
low complexity region	3	14	N/A	INTRINSIC
ARM	56	96	2.07e-2	SMART
ARM	97	138	9.84e1	SMART
ARM	139	179	7.86e-3	SMART
ARM	180	220	7.63e0	SMART
ARM	221	262	7.76e1	SMART
low complexity region	293	303	N/A	INTRINSIC
ARM	305	345	3.91e1	SMART
ARM	346	385	2.93e-2	SMART
ARM	387	427	7.74e-2	SMART
Blast:ARM	428	468	3e-11	BLAST
ARM	469	509	1.45e-1	SMART
low complexity region	544	557	N/A	INTRINSIC
low complexity region	583	595	N/A	INTRINSIC
low complexity region	620	639	N/A	INTRINSIC
low complexity region	675	696	N/A	INTRINSIC
Pfam:EDR1	723	857	3.1e-28	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000114640
AA Change: Y575H

PolyPhen 2 Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000110287
Gene: ENSMUSG00000037683
AA Change: Y575H

Domain	Start	End	E-Value	Type
low complexity region	3	14	N/A	INTRINSIC
ARM	56	96	2.07e-2	SMART
ARM	97	138	9.84e1	SMART
ARM	139	179	7.86e-3	SMART
ARM	180	220	7.63e0	SMART
ARM	221	262	7.76e1	SMART
low complexity region	293	303	N/A	INTRINSIC
ARM	305	345	3.91e1	SMART
ARM	346	385	2.93e-2	SMART
ARM	387	427	7.74e-2	SMART
Blast:ARM	428	468	3e-11	BLAST
ARM	469	509	1.45e-1	SMART
Pfam:EDR1	549	868	1.4e-41	PFAM

Meta Mutation Damage Score

0.1858

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.0%
20x: 94.3%

Validation Efficiency

100% (124/124)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Armadillo/beta-catenin (CTNNB1; MIM 116806)-like (ARM) domains are imperfect 45-amino acid repeats involved in protein-protein interactions. ARM domain-containing proteins, such as ARMC3, function in signal transduction, development, cell adhesion and mobility, and tumor initiation and metastasis (Li et al., 2006 [PubMed 16915934]).[supplied by OMIM, Mar 2008]

Allele List at MGI

All alleles(2) : Targeted(2)

Other mutations in this stock

Total: 123 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	C	T	3: 138,065,658 (GRCm38)	R203*	probably null	Het
Abcc2	A	T	19: 43,807,142 (GRCm38)	I446F	probably damaging	Het
Afap1l2	A	T	19: 57,002,267 (GRCm38)	I18N	possibly damaging	Het
Aida	A	T	1: 183,313,692 (GRCm38)	E107D	probably benign	Het
Amer2	A	G	14: 60,379,820 (GRCm38)	Y362C	probably damaging	Het
Amigo1	T	C	3: 108,187,328 (GRCm38)	S48P	probably benign	Het
Ano5	A	G	7: 51,537,813 (GRCm38)	K50R	possibly damaging	Het
Anxa2	A	T	9: 69,483,816 (GRCm38)	D95V	probably damaging	Het
Arhgap22	A	G	14: 33,366,959 (GRCm38)	N466D	probably damaging	Het
Ascc2	A	G	11: 4,679,257 (GRCm38)	E523G	probably benign	Het
B3galt5	A	T	16: 96,316,025 (GRCm38)	K286M	probably damaging	Het
Bag3	C	T	7: 128,545,683 (GRCm38)	H341Y	probably benign	Het
Blm	G	T	7: 80,505,949 (GRCm38)		probably null	Het
Cacna1b	G	A	2: 24,732,306 (GRCm38)	P222L	probably damaging	Het
Cap2	T	A	13: 46,637,881 (GRCm38)	Y175N	possibly damaging	Het
Cd81	G	T	7: 143,067,201 (GRCm38)	G206*	probably null	Het
Cep290	T	A	10: 100,531,184 (GRCm38)	S1132R	possibly damaging	Het
Cluh	C	A	11: 74,659,529 (GRCm38)	C222*	probably null	Het
Col14a1	A	T	15: 55,449,940 (GRCm38)	D1320V	unknown	Het
Col18a1	T	C	10: 77,081,154 (GRCm38)	I114V	unknown	Het
Cped1	A	G	6: 22,233,927 (GRCm38)	T847A	probably damaging	Het
Cpne7	A	G	8: 123,127,437 (GRCm38)	K288E	possibly damaging	Het
Cr2	G	A	1: 195,154,150 (GRCm38)	P1278S	possibly damaging	Het
Creb3	C	A	4: 43,565,327 (GRCm38)	R202S	probably damaging	Het
Cyp2j9	T	A	4: 96,571,964 (GRCm38)	K434M	probably damaging	Het
Dpp10	A	T	1: 123,905,106 (GRCm38)	V48E	probably null	Het
Dsg2	A	G	18: 20,601,473 (GRCm38)	K836R	probably damaging	Het
Dst	A	G	1: 34,190,258 (GRCm38)	T1986A	probably benign	Het
Dvl1	G	A	4: 155,847,816 (GRCm38)	V28I	possibly damaging	Het
Ecm2	A	G	13: 49,530,256 (GRCm38)	D570G	probably benign	Het
Efhc1	T	A	1: 20,989,560 (GRCm38)	C611*	probably null	Het
Epop	T	C	11: 97,628,654 (GRCm38)	T210A	probably benign	Het
Erc2	A	G	14: 28,011,636 (GRCm38)	I556V	probably benign	Het
Fdxacb1	A	T	9: 50,771,646 (GRCm38)	N101I	probably benign	Het
Fhad1	T	C	4: 141,982,162 (GRCm38)	S294G	possibly damaging	Het
Galnt16	A	G	12: 80,583,656 (GRCm38)	D262G	probably damaging	Het
Gm9573	A	T	17: 35,618,708 (GRCm38)	S1529T	probably benign	Het
Gorab	A	G	1: 163,397,056 (GRCm38)	S59P	probably damaging	Het
Gpr161	G	T	1: 165,306,563 (GRCm38)	M131I	probably damaging	Het
Gpr22	T	A	12: 31,709,203 (GRCm38)	M270L	probably benign	Het
Grin3b	C	A	10: 79,970,912 (GRCm38)	Q5K	probably benign	Het
Grin3b	C	T	10: 79,974,646 (GRCm38)	A662V	probably damaging	Het
Gsdmc	A	G	15: 63,801,899 (GRCm38)	I179T	probably benign	Het
Gsdmc2	T	A	15: 63,828,237 (GRCm38)	M229L	probably benign	Het
H2-Eb2	A	G	17: 34,334,304 (GRCm38)	I155V	probably benign	Het
Hoga1	A	C	19: 42,060,020 (GRCm38)		probably null	Het
Hs3st5	A	G	10: 36,832,886 (GRCm38)	Y139C	probably damaging	Het
Il10ra	C	A	9: 45,255,811 (GRCm38)	A481S	probably benign	Het
Ints2	T	A	11: 86,248,934 (GRCm38)	H278L	possibly damaging	Het
Kalrn	T	G	16: 33,975,738 (GRCm38)	L1222F	probably damaging	Het
Klhl25	T	A	7: 75,866,732 (GRCm38)	V157D	probably damaging	Het
Klk1b26	A	T	7: 44,016,900 (GRCm38)	T256S	probably damaging	Het
Krt81	T	C	15: 101,462,554 (GRCm38)	Q184R	probably benign	Het
Lce1k	A	T	3: 92,806,818 (GRCm38)	C20S	unknown	Het
Letm1	A	AG	5: 33,769,515 (GRCm38)		probably null	Het
Lin54	A	G	5: 100,485,801 (GRCm38)		probably null	Het
Lrrc37a	T	C	11: 103,500,261 (GRCm38)	E1446G	probably benign	Het
Macf1	A	G	4: 123,456,695 (GRCm38)	S3792P	probably damaging	Het
Manba	T	A	3: 135,551,191 (GRCm38)	D538E	probably benign	Het
Mcc	C	A	18: 44,491,315 (GRCm38)	E213*	probably null	Het
Mfap4	T	C	11: 61,485,807 (GRCm38)		probably null	Het
Nebl	T	A	2: 17,452,510 (GRCm38)	I80F	probably damaging	Het
Nek4	A	G	14: 30,956,953 (GRCm38)	I145V	probably damaging	Het
Nlrp14	T	C	7: 107,196,200 (GRCm38)	V230A	probably benign	Het
Nxf3	G	A	X: 136,075,834 (GRCm38)	P380S	possibly damaging	Het
Olfr1451	T	C	19: 12,999,502 (GRCm38)	V172A	possibly damaging	Het
Olfr403	T	C	11: 74,196,163 (GRCm38)	V220A	probably damaging	Het
Olfr421-ps1	C	T	1: 174,152,121 (GRCm38)	H202Y	probably damaging	Het
Olfr490	C	A	7: 108,286,359 (GRCm38)	G256*	probably null	Het
Olfr745	G	A	14: 50,642,866 (GRCm38)	C195Y	possibly damaging	Het
Pcdhb13	C	T	18: 37,443,859 (GRCm38)	T430I	possibly damaging	Het
Piezo2	A	T	18: 63,074,662 (GRCm38)	L1426Q	probably null	Het
Pigk	T	A	3: 152,744,494 (GRCm38)	Y212N	probably damaging	Het
Pigm	T	G	1: 172,377,261 (GRCm38)	L188R	probably damaging	Het
Plce1	T	C	19: 38,777,924 (GRCm38)	F2117S	probably damaging	Het
Plec	A	G	15: 76,173,543 (GRCm38)	F4055L	probably damaging	Het
Plk5	C	T	10: 80,363,102 (GRCm38)	S435L	possibly damaging	Het
Pms1	G	A	1: 53,282,042 (GRCm38)	L11F	probably damaging	Het
Prl3b1	C	T	13: 27,247,912 (GRCm38)	T140I	possibly damaging	Het
Prl7a1	T	G	13: 27,633,672 (GRCm38)	D203A	probably damaging	Het
Psg17	A	G	7: 18,814,652 (GRCm38)	V398A	probably benign	Het
Pum1	T	A	4: 130,718,218 (GRCm38)	I166K	possibly damaging	Het
R3hdm1	T	A	1: 128,169,016 (GRCm38)	D108E	probably damaging	Het
Reln	A	T	5: 21,969,360 (GRCm38)	D1948E	possibly damaging	Het
Rnf112	C	T	11: 61,452,426 (GRCm38)	R141Q	probably damaging	Het
Rnf145	T	C	11: 44,561,466 (GRCm38)	V424A	possibly damaging	Het
Serpina3m	C	A	12: 104,389,699 (GRCm38)	Y208*	probably null	Het
Serpind1	T	C	16: 17,342,944 (GRCm38)	V446A	probably benign	Het
Shc3	T	A	13: 51,442,836 (GRCm38)	M384L	probably benign	Het
Slc38a11	A	G	2: 65,330,339 (GRCm38)	F304L	probably benign	Het
Slpi	C	T	2: 164,355,543 (GRCm38)	C28Y	probably damaging	Het
Specc1	C	A	11: 62,029,294 (GRCm38)	P7T	possibly damaging	Het
Spib	T	C	7: 44,528,857 (GRCm38)	E180G	probably benign	Het
Spint5	T	C	2: 164,716,983 (GRCm38)		probably benign	Het
Ssr2	T	A	3: 88,576,867 (GRCm38)		probably benign	Het
Tbrg1	T	C	9: 37,649,419 (GRCm38)	D387G	probably benign	Het
Tex14	T	G	11: 87,549,470 (GRCm38)	L1367R	probably damaging	Het
Tfpi	A	C	2: 84,458,016 (GRCm38)		probably benign	Het
Tlr5	T	A	1: 182,974,347 (GRCm38)	D405E	probably damaging	Het
Tnnt3	C	T	7: 142,511,525 (GRCm38)	R131C	possibly damaging	Het
Tnxb	T	C	17: 34,671,904 (GRCm38)	V407A	probably damaging	Het
Tnxb	A	G	17: 34,682,251 (GRCm38)	Y1013C	probably damaging	Het
Tpx2	T	A	2: 152,890,624 (GRCm38)	M606K	probably benign	Het
Trim30a	T	A	7: 104,430,230 (GRCm38)		probably benign	Het
Trim46	A	T	3: 89,237,701 (GRCm38)	Y489N	probably damaging	Het
Trpm6	A	T	19: 18,796,284 (GRCm38)	H380L	probably benign	Het
Tstd2	A	G	4: 46,120,563 (GRCm38)	I279T	probably benign	Het
Ttn	C	T	2: 76,946,391 (GRCm38)		probably null	Het
Txnl1	T	C	18: 63,679,514 (GRCm38)	T70A	probably benign	Het
Ush2a	C	T	1: 188,578,532 (GRCm38)		probably benign	Het
Usp1	A	G	4: 98,934,294 (GRCm38)	D615G	probably benign	Het
Virma	T	A	4: 11,519,242 (GRCm38)	C830S	probably benign	Het
Vmn1r7	A	T	6: 57,024,868 (GRCm38)	S136T	probably benign	Het
Vmn2r9	A	G	5: 108,846,439 (GRCm38)	V448A	probably damaging	Het
Vps11	G	A	9: 44,359,227 (GRCm38)	H183Y	probably damaging	Het
Vsig10l	A	G	7: 43,467,468 (GRCm38)	T476A	possibly damaging	Het
Wdr63	G	T	3: 146,063,480 (GRCm38)	T522K	possibly damaging	Het
Whamm	C	T	7: 81,591,771 (GRCm38)	R277*	probably null	Het
Wnt8a	A	G	18: 34,544,884 (GRCm38)	D115G	probably damaging	Het
Xndc1	T	A	7: 102,073,191 (GRCm38)	V21E	probably damaging	Het
Zc3hav1	C	A	6: 38,336,517 (GRCm38)	V198L	probably damaging	Het
Zfp874a	T	A	13: 67,442,504 (GRCm38)	I354F	probably benign	Het
Zfr2	A	T	10: 81,242,852 (GRCm38)	D306V	possibly damaging	Het

Other mutations in Armc3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00535:Armc3	APN	2	19,303,858 (GRCm38)	missense	possibly damaging	0.48
IGL01123:Armc3	APN	2	19,201,805 (GRCm38)	missense	possibly damaging	0.87
IGL01142:Armc3	APN	2	19,297,898 (GRCm38)	splice site	probably benign
IGL01556:Armc3	APN	2	19,269,146 (GRCm38)	missense	probably damaging	1.00
IGL02145:Armc3	APN	2	19,286,137 (GRCm38)	critical splice donor site	probably null
IGL02145:Armc3	APN	2	19,296,860 (GRCm38)	missense	possibly damaging	0.81
IGL02152:Armc3	APN	2	19,286,137 (GRCm38)	critical splice donor site	probably null
IGL02154:Armc3	APN	2	19,286,137 (GRCm38)	critical splice donor site	probably null
IGL02243:Armc3	APN	2	19,286,137 (GRCm38)	critical splice donor site	probably null
IGL02244:Armc3	APN	2	19,286,137 (GRCm38)	critical splice donor site	probably null
IGL02516:Armc3	APN	2	19,300,506 (GRCm38)	missense	possibly damaging	0.94
IGL02691:Armc3	APN	2	19,235,484 (GRCm38)	missense	probably damaging	1.00
IGL03151:Armc3	APN	2	19,238,698 (GRCm38)	missense	probably damaging	1.00
IGL03190:Armc3	APN	2	19,288,950 (GRCm38)	missense	probably damaging	0.99
IGL03288:Armc3	APN	2	19,235,482 (GRCm38)	missense	probably damaging	1.00
IGL03338:Armc3	APN	2	19,248,701 (GRCm38)	missense	possibly damaging	0.88
R0015:Armc3	UTSW	2	19,296,321 (GRCm38)	critical splice acceptor site	probably null
R0015:Armc3	UTSW	2	19,296,321 (GRCm38)	critical splice acceptor site	probably null
R0256:Armc3	UTSW	2	19,269,216 (GRCm38)	missense	probably damaging	1.00
R0621:Armc3	UTSW	2	19,295,393 (GRCm38)	missense	probably damaging	0.96
R1326:Armc3	UTSW	2	19,310,124 (GRCm38)	makesense	probably null
R1470:Armc3	UTSW	2	19,238,736 (GRCm38)	missense	probably benign
R1470:Armc3	UTSW	2	19,238,736 (GRCm38)	missense	probably benign
R1489:Armc3	UTSW	2	19,310,047 (GRCm38)	missense	probably benign	0.01
R1990:Armc3	UTSW	2	19,293,142 (GRCm38)	missense	probably damaging	0.97
R1992:Armc3	UTSW	2	19,293,142 (GRCm38)	missense	probably damaging	0.97
R2002:Armc3	UTSW	2	19,288,936 (GRCm38)	missense	probably benign	0.01
R2095:Armc3	UTSW	2	19,288,929 (GRCm38)	missense	possibly damaging	0.65
R2127:Armc3	UTSW	2	19,201,811 (GRCm38)	missense	probably damaging	1.00
R2158:Armc3	UTSW	2	19,248,633 (GRCm38)	missense	probably damaging	0.99
R2697:Armc3	UTSW	2	19,303,935 (GRCm38)	missense	probably damaging	1.00
R3809:Armc3	UTSW	2	19,300,665 (GRCm38)	missense	probably damaging	1.00
R3897:Armc3	UTSW	2	19,269,177 (GRCm38)	missense	probably damaging	1.00
R4107:Armc3	UTSW	2	19,288,909 (GRCm38)	missense	probably benign	0.13
R4326:Armc3	UTSW	2	19,300,473 (GRCm38)	missense	probably damaging	0.97
R4464:Armc3	UTSW	2	19,248,659 (GRCm38)	missense	probably damaging	0.99
R4702:Armc3	UTSW	2	19,309,981 (GRCm38)	missense	probably damaging	1.00
R4923:Armc3	UTSW	2	19,292,980 (GRCm38)	critical splice acceptor site	probably null
R5370:Armc3	UTSW	2	19,286,062 (GRCm38)	missense	probably benign	0.00
R5518:Armc3	UTSW	2	19,297,928 (GRCm38)	missense	probably benign	0.28
R5718:Armc3	UTSW	2	19,303,799 (GRCm38)	nonsense	probably null
R5739:Armc3	UTSW	2	19,253,917 (GRCm38)	missense	possibly damaging	0.67
R5913:Armc3	UTSW	2	19,310,047 (GRCm38)	missense	possibly damaging	0.65
R6211:Armc3	UTSW	2	19,296,803 (GRCm38)	critical splice acceptor site	probably null
R6245:Armc3	UTSW	2	19,248,705 (GRCm38)	missense	probably damaging	1.00
R6841:Armc3	UTSW	2	19,201,819 (GRCm38)	splice site	probably null
R7003:Armc3	UTSW	2	19,270,028 (GRCm38)	missense	probably damaging	1.00
R7190:Armc3	UTSW	2	19,293,136 (GRCm38)	missense	probably damaging	1.00
R7499:Armc3	UTSW	2	19,285,979 (GRCm38)	missense	probably benign	0.03
R7738:Armc3	UTSW	2	19,288,950 (GRCm38)	missense	probably damaging	0.99
R7844:Armc3	UTSW	2	19,254,018 (GRCm38)	missense	possibly damaging	0.90
R7919:Armc3	UTSW	2	19,286,095 (GRCm38)	missense	probably benign	0.00
R8060:Armc3	UTSW	2	19,288,909 (GRCm38)	missense	probably benign	0.08
R8111:Armc3	UTSW	2	19,296,863 (GRCm38)	missense	probably benign
R8406:Armc3	UTSW	2	19,235,554 (GRCm38)	missense	probably damaging	0.98
R8485:Armc3	UTSW	2	19,293,134 (GRCm38)	missense	probably damaging	1.00
R8773:Armc3	UTSW	2	19,288,856 (GRCm38)	missense	probably benign	0.01
R8940:Armc3	UTSW	2	19,235,582 (GRCm38)	missense	probably damaging	1.00
R9441:Armc3	UTSW	2	19,248,615 (GRCm38)	missense	possibly damaging	0.89
Z1177:Armc3	UTSW	2	19,285,991 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TCGACAGGGCCCTAAATATCC -3'
(R):5'- AAATGAGCTTTTGTGGAGGAGC -3'

Sequencing Primer
(F):5'- AGGGCCCTAAATATCCTTGAAG -3'
(R):5'- CTGAGACTGTGATTAATAAGCTGAC -3'

Posted On

2014-08-25