Mutagenetix > Incidental Mutation

Incidental Mutation 'R1875:Armh4'

211175

Institutional Source

Beutler Lab

Gene Symbol

Armh4

Ensembl Gene

ENSMUSG00000036242

Gene Name

armadillo-like helical domain containing 4

Synonyms

3632451O06Rik

MMRRC Submission

039897-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1875 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

49919017-50020843 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 49919815 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 772 (D772G)

Ref Sequence

ENSEMBL: ENSMUSP00000113609 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000036972] [ENSMUST00000118129]

AlphaFold

Q8BT18

Predicted Effect

probably damaging
Transcript: ENSMUST00000036972
AA Change: D773G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000036220
Gene: ENSMUSG00000036242
AA Change: D773G

Domain	Start	End	E-Value	Type
Pfam:DUF4696	48	609	3.8e-224	PFAM
transmembrane domain	714	736	N/A	INTRINSIC
low complexity region	741	753	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000118129
AA Change: D772G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000113609
Gene: ENSMUSG00000036242
AA Change: D772G

Domain	Start	End	E-Value	Type
coiled coil region	603	644	N/A	INTRINSIC
transmembrane domain	714	736	N/A	INTRINSIC
low complexity region	741	754	N/A	INTRINSIC

Meta Mutation Damage Score

0.3739

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.1%
20x: 92.1%

Validation Efficiency

98% (85/87)

Allele List at MGI

Other mutations in this stock

Total: 80 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca14	A	T	7: 119,847,190 (GRCm39)	M685L	possibly damaging	Het
Abi3bp	A	G	16: 56,394,862 (GRCm39)	Y190C	probably damaging	Het
Adam26a	C	A	8: 44,022,888 (GRCm39)	V201L	probably benign	Het
Adamts20	G	T	15: 94,229,277 (GRCm39)	D947E	probably benign	Het
Ankrd26	A	G	6: 118,517,410 (GRCm39)		probably null	Het
Apol11a	C	A	15: 77,397,766 (GRCm39)	T39N	possibly damaging	Het
Arhgef38	T	A	3: 132,839,501 (GRCm39)		probably null	Het
Atp11b	T	C	3: 35,893,296 (GRCm39)	L883P	probably damaging	Het
Btnl10	T	A	11: 58,814,586 (GRCm39)	I422N	probably damaging	Het
C2cd3	A	G	7: 100,056,232 (GRCm39)	K547E	possibly damaging	Het
Cdh2	T	A	18: 16,757,934 (GRCm39)	L549F	probably benign	Het
Celsr3	T	C	9: 108,713,037 (GRCm39)	V1825A	probably benign	Het
Cfap221	T	C	1: 119,881,389 (GRCm39)	I358V	probably benign	Het
Cimap2	G	A	4: 106,470,453 (GRCm39)		probably benign	Het
Csmd1	T	C	8: 15,979,101 (GRCm39)	K2828E	probably damaging	Het
Ddah2	T	C	17: 35,279,821 (GRCm39)	F137S	probably damaging	Het
Ddx21	A	G	10: 62,429,847 (GRCm39)	I299T	probably damaging	Het
Dnah7a	A	T	1: 53,495,691 (GRCm39)		probably benign	Het
Elmod1	A	G	9: 53,843,151 (GRCm39)	I9T	probably benign	Het
Epha2	A	G	4: 141,036,290 (GRCm39)	E242G	probably benign	Het
Erbb3	T	C	10: 128,410,335 (GRCm39)	H641R	possibly damaging	Het
Fbxl18	G	A	5: 142,871,978 (GRCm39)	A419V	probably damaging	Het
Fli1	T	C	9: 32,335,209 (GRCm39)	M408V	probably benign	Het
Fmo4	T	C	1: 162,631,187 (GRCm39)	N260S	possibly damaging	Het
Fry	A	G	5: 150,249,597 (GRCm39)	E136G	probably damaging	Het
Gm10477	T	A	X: 55,570,127 (GRCm39)	F9Y	probably damaging	Het
Gm8258	A	G	5: 104,924,320 (GRCm39)		noncoding transcript	Het
Gpr68	T	A	12: 100,845,049 (GRCm39)	D165V	probably damaging	Het
Htt	T	A	5: 34,951,456 (GRCm39)	M139K	probably benign	Het
Jup	A	G	11: 100,263,120 (GRCm39)		probably null	Het
Kifc5b	G	A	17: 27,136,264 (GRCm39)		probably null	Het
Krba1	T	A	6: 48,390,983 (GRCm39)		probably null	Het
Lamp1	G	A	8: 13,217,257 (GRCm39)	G89R	probably damaging	Het
Lrrc17	C	T	5: 21,765,650 (GRCm39)	S44F	possibly damaging	Het
Mdga1	T	C	17: 30,071,581 (GRCm39)	T347A	probably damaging	Het
Mical3	A	T	6: 121,019,025 (GRCm39)	W66R	probably damaging	Het
Mpl	A	G	4: 118,314,026 (GRCm39)	Y73H	probably benign	Het
Mterf1b	T	A	5: 4,247,364 (GRCm39)	I335N	possibly damaging	Het
Mylk3	A	G	8: 86,079,494 (GRCm39)	I388T	probably damaging	Het
Myo15a	C	T	11: 60,398,354 (GRCm39)	R2775W	probably damaging	Het
Myoz2	A	T	3: 122,819,765 (GRCm39)	S65T	probably damaging	Het
Ndrg1	T	C	15: 66,802,940 (GRCm39)	T137A	possibly damaging	Het
Neil3	G	T	8: 54,052,454 (GRCm39)	N381K	probably damaging	Het
Obsl1	T	C	1: 75,474,877 (GRCm39)	Y841C	probably damaging	Het
Or2b4	A	G	17: 38,115,996 (GRCm39)		probably benign	Het
Or6b6	G	A	7: 106,571,389 (GRCm39)	S54F	possibly damaging	Het
Otogl	T	C	10: 107,735,451 (GRCm39)	D111G	probably damaging	Het
Parp10	T	C	15: 76,127,051 (GRCm39)	E103G	probably damaging	Het
Pars2	T	C	4: 106,510,913 (GRCm39)	F232L	possibly damaging	Het
Pcdh18	A	T	3: 49,709,154 (GRCm39)	F720L	probably damaging	Het
Phf3	T	C	1: 30,869,704 (GRCm39)	E448G	possibly damaging	Het
Pigc	A	G	1: 161,798,516 (GRCm39)	Y166C	probably damaging	Het
Pik3c2a	A	T	7: 116,017,206 (GRCm39)	S184T	probably benign	Het
Pkd1l1	A	G	11: 8,794,670 (GRCm39)		probably benign	Het
Plch2	G	A	4: 155,082,965 (GRCm39)	S485F	probably damaging	Het
Plxnd1	G	T	6: 115,955,045 (GRCm39)		probably null	Het
Pnliprp2	G	T	19: 58,751,821 (GRCm39)	V189L	probably benign	Het
Prl8a2	T	C	13: 27,535,037 (GRCm39)	V103A	probably benign	Het
Psg23	G	A	7: 18,344,375 (GRCm39)	T360I	probably benign	Het
Rad51c	A	T	11: 87,279,469 (GRCm39)	I323N	probably damaging	Het
Rsbn1l	C	T	5: 21,156,696 (GRCm39)	E30K	probably benign	Het
Serpina3c	C	A	12: 104,118,145 (GRCm39)	L64F	probably damaging	Het
Shroom1	A	G	11: 53,356,502 (GRCm39)	D392G	probably damaging	Het
Slc26a5	T	A	5: 22,020,725 (GRCm39)	I540L	probably benign	Het
Slc37a4	A	G	9: 44,312,808 (GRCm39)	T321A	probably damaging	Het
Slc41a2	A	G	10: 83,091,949 (GRCm39)	L438S	probably damaging	Het
Spef2	C	T	15: 9,584,194 (GRCm39)	E1624K	probably damaging	Het
Spef2	C	T	15: 9,597,487 (GRCm39)	G1390R	possibly damaging	Het
Spmap2l	A	T	5: 77,202,431 (GRCm39)	K284M	probably benign	Het
Synj2	G	T	17: 6,078,825 (GRCm39)	A740S	possibly damaging	Het
Tigd4	A	C	3: 84,502,394 (GRCm39)	D437A	probably benign	Het
Timm21	G	C	18: 84,967,387 (GRCm39)	L130V	probably damaging	Het
Tmem106a	CAGCTCAACACGACGGTA	CAGCTCAACACGACGGTAAGCTCAACACGACGGTA	11: 101,477,204 (GRCm39)		probably benign	Het
Tmem131l	A	T	3: 83,812,383 (GRCm39)	C1313*	probably null	Het
Tmem86b	A	T	7: 4,632,698 (GRCm39)	I47N	possibly damaging	Het
Tspan13	T	C	12: 36,070,550 (GRCm39)		probably null	Het
Vps54	A	G	11: 21,250,251 (GRCm39)	T396A	probably benign	Het
Zfp106	A	T	2: 120,344,096 (GRCm39)		probably null	Het
Zfp668	T	C	7: 127,465,654 (GRCm39)		probably null	Het
Zfp809	A	T	9: 22,150,027 (GRCm39)	R175*	probably null	Het

Other mutations in Armh4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00470:Armh4	APN	14	50,010,460 (GRCm39)	missense	probably damaging	1.00
IGL00981:Armh4	APN	14	50,010,447 (GRCm39)	missense	probably damaging	1.00
IGL01447:Armh4	APN	14	50,005,923 (GRCm39)	missense	probably damaging	0.99
IGL01645:Armh4	APN	14	50,011,011 (GRCm39)	missense	probably damaging	1.00
IGL02135:Armh4	APN	14	50,011,386 (GRCm39)	missense	probably damaging	0.99
IGL02154:Armh4	APN	14	50,010,399 (GRCm39)	missense	possibly damaging	0.58
IGL02163:Armh4	APN	14	50,011,614 (GRCm39)	missense	possibly damaging	0.61
IGL03234:Armh4	APN	14	50,005,973 (GRCm39)	missense	probably damaging	1.00
P0014:Armh4	UTSW	14	49,989,116 (GRCm39)	missense	probably damaging	1.00
R0165:Armh4	UTSW	14	50,011,243 (GRCm39)	missense	probably benign
R0240:Armh4	UTSW	14	50,005,859 (GRCm39)	splice site	probably benign
R0553:Armh4	UTSW	14	49,920,143 (GRCm39)	missense	probably damaging	0.99
R0616:Armh4	UTSW	14	50,011,113 (GRCm39)	missense	possibly damaging	0.74
R0635:Armh4	UTSW	14	50,010,600 (GRCm39)	missense	probably benign	0.00
R1423:Armh4	UTSW	14	49,988,896 (GRCm39)	missense	probably damaging	1.00
R1547:Armh4	UTSW	14	50,010,953 (GRCm39)	missense	probably benign	0.01
R1642:Armh4	UTSW	14	50,005,867 (GRCm39)	splice site	probably null
R1657:Armh4	UTSW	14	50,011,017 (GRCm39)	missense	probably damaging	0.99
R1717:Armh4	UTSW	14	49,989,121 (GRCm39)	missense	probably damaging	0.99
R1900:Armh4	UTSW	14	50,008,040 (GRCm39)	missense	probably damaging	1.00
R1916:Armh4	UTSW	14	50,005,932 (GRCm39)	missense	probably damaging	1.00
R1945:Armh4	UTSW	14	50,005,940 (GRCm39)	missense	probably damaging	1.00
R2102:Armh4	UTSW	14	50,011,459 (GRCm39)	missense	probably damaging	0.98
R2147:Armh4	UTSW	14	49,989,028 (GRCm39)	missense	probably benign	0.31
R2149:Armh4	UTSW	14	49,989,028 (GRCm39)	missense	probably benign	0.31
R3921:Armh4	UTSW	14	50,011,659 (GRCm39)	missense	probably benign	0.13
R4063:Armh4	UTSW	14	50,011,444 (GRCm39)	missense	probably benign	0.02
R4373:Armh4	UTSW	14	50,007,893 (GRCm39)	missense	probably damaging	1.00
R4374:Armh4	UTSW	14	50,007,893 (GRCm39)	missense	probably damaging	1.00
R4377:Armh4	UTSW	14	50,007,893 (GRCm39)	missense	probably damaging	1.00
R4589:Armh4	UTSW	14	50,011,039 (GRCm39)	missense	probably damaging	1.00
R4940:Armh4	UTSW	14	50,010,939 (GRCm39)	missense	probably benign	0.15
R4986:Armh4	UTSW	14	49,989,111 (GRCm39)	missense	probably damaging	0.97
R5047:Armh4	UTSW	14	50,007,895 (GRCm39)	missense	probably damaging	1.00
R5104:Armh4	UTSW	14	50,010,929 (GRCm39)	missense	possibly damaging	0.77
R5682:Armh4	UTSW	14	49,989,043 (GRCm39)	missense	probably damaging	1.00
R6357:Armh4	UTSW	14	50,010,769 (GRCm39)	missense	probably benign	0.10
R6478:Armh4	UTSW	14	50,010,789 (GRCm39)	missense	possibly damaging	0.61
R6673:Armh4	UTSW	14	50,008,049 (GRCm39)	missense	probably benign	0.00
R7035:Armh4	UTSW	14	50,010,507 (GRCm39)	missense	possibly damaging	0.77
R7054:Armh4	UTSW	14	50,011,155 (GRCm39)	missense	probably damaging	1.00
R7458:Armh4	UTSW	14	49,920,196 (GRCm39)	missense	probably damaging	1.00
R7536:Armh4	UTSW	14	50,011,703 (GRCm39)	splice site	probably null
R7944:Armh4	UTSW	14	50,010,670 (GRCm39)	missense	probably benign	0.25
R7945:Armh4	UTSW	14	50,010,670 (GRCm39)	missense	probably benign	0.25
R8049:Armh4	UTSW	14	50,010,993 (GRCm39)	missense	probably damaging	0.97
R8066:Armh4	UTSW	14	50,005,980 (GRCm39)	missense	possibly damaging	0.83
R8519:Armh4	UTSW	14	50,010,693 (GRCm39)	missense	probably damaging	1.00
R8765:Armh4	UTSW	14	49,920,100 (GRCm39)	missense	probably damaging	1.00
R8766:Armh4	UTSW	14	50,011,497 (GRCm39)	missense	probably damaging	1.00
R8833:Armh4	UTSW	14	50,011,318 (GRCm39)	missense	probably benign	0.17
R8936:Armh4	UTSW	14	50,008,024 (GRCm39)	missense	probably damaging	0.98
R9007:Armh4	UTSW	14	50,011,695 (GRCm39)	missense	probably damaging	0.99
R9122:Armh4	UTSW	14	50,011,459 (GRCm39)	missense	possibly damaging	0.64
R9406:Armh4	UTSW	14	50,010,945 (GRCm39)	missense	possibly damaging	0.93
R9741:Armh4	UTSW	14	50,008,081 (GRCm39)	missense	probably benign	0.06
X0026:Armh4	UTSW	14	49,920,193 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TAGCCAAACACTGCATGCTG -3'
(R):5'- GAGCAAGAAAGACTCCTGTTCAAG -3'

Sequencing Primer
(F):5'- CATGCTGCATTTTTAGGGTACAGC -3'
(R):5'- CAAGGTGCTTTGTATTAGCTGCTCC -3'

Posted On

2014-06-30