Mutagenetix > Incidental Mutation

Incidental Mutation 'R4942:Fam184b'

383178

Institutional Source

Beutler Lab

Gene Symbol

Fam184b

Ensembl Gene

ENSMUSG00000015879

Gene Name

family with sequence similarity 184, member B

Synonyms

9630031F12Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4942 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

45687047-45796843 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 45730649 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 461 (E461G)

Ref Sequence

ENSEMBL: ENSMUSP00000016023 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000016023]

AlphaFold

Q0KK56

Predicted Effect

probably damaging
Transcript: ENSMUST00000016023
AA Change: E461G

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

SMART Domains

Protein: ENSMUSP00000016023
Gene: ENSMUSG00000015879
AA Change: E461G

Domain	Start	End	E-Value	Type
Pfam:FAM184	50	248	7.7e-28	PFAM
coiled coil region	284	337	N/A	INTRINSIC
coiled coil region	387	495	N/A	INTRINSIC
low complexity region	515	525	N/A	INTRINSIC
coiled coil region	575	620	N/A	INTRINSIC
coiled coil region	686	775	N/A	INTRINSIC

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 96.0%
20x: 91.6%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele are viable and exhibit no overt phenotypic abnormalities. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5730522E02Rik	A	G	11: 25,720,472 (GRCm39)		probably null	Het
Adamts7	T	C	9: 90,045,364 (GRCm39)	S23P	probably benign	Het
Adamtsl1	T	A	4: 86,259,451 (GRCm39)	C824*	probably null	Het
Adgre1	A	G	17: 57,713,903 (GRCm39)	Y196C	probably damaging	Het
Arap1	A	G	7: 101,051,009 (GRCm39)	D542G	possibly damaging	Het
B3gat1	A	G	9: 26,666,894 (GRCm39)	D42G	probably benign	Het
Birc6	G	A	17: 74,930,045 (GRCm39)	A2412T	probably damaging	Het
Bnip5	T	C	17: 29,122,232 (GRCm39)	R420G	probably benign	Het
Bsn	A	G	9: 107,983,678 (GRCm39)	Y3459H	unknown	Het
Cacnb1	T	C	11: 97,893,809 (GRCm39)	Y571C	probably damaging	Het
Cdk2ap2	G	A	19: 4,147,508 (GRCm39)		probably null	Het
Cep57	A	G	9: 13,724,723 (GRCm39)	S265P	probably damaging	Het
Clca3a1	A	G	3: 144,710,524 (GRCm39)	I893T	probably benign	Het
Clca3a2	T	A	3: 144,512,263 (GRCm39)	E491V	probably damaging	Het
Cldn10	G	A	14: 119,025,725 (GRCm39)	G53S	possibly damaging	Het
Cobl	A	T	11: 12,204,185 (GRCm39)	I832N	probably damaging	Het
Col9a2	T	C	4: 120,910,316 (GRCm39)	V487A	possibly damaging	Het
Cse1l	C	T	2: 166,771,714 (GRCm39)	T325I	probably damaging	Het
Dlx6	A	G	6: 6,863,468 (GRCm39)	Q30R	probably benign	Het
Dnah8	T	C	17: 30,948,116 (GRCm39)	V1902A	probably benign	Het
Dusp8	A	G	7: 141,635,965 (GRCm39)	F542L	possibly damaging	Het
Emid1	T	G	11: 5,079,430 (GRCm39)	M323L	probably benign	Het
Ercc5	A	G	1: 44,215,125 (GRCm39)	D886G	probably benign	Het
Fbn1	C	A	2: 125,225,536 (GRCm39)	C572F	possibly damaging	Het
Gigyf1	G	T	5: 137,523,952 (GRCm39)	V1041L	possibly damaging	Het
Grin3b	A	G	10: 79,811,556 (GRCm39)	H714R	probably damaging	Het
Heatr1	A	G	13: 12,428,391 (GRCm39)		probably null	Het
Klk14	G	A	7: 43,341,501 (GRCm39)	C51Y	probably damaging	Het
Llgl1	C	T	11: 60,600,394 (GRCm39)	P581L	probably benign	Het
Lypd6b	C	A	2: 49,836,132 (GRCm39)	H104Q	probably benign	Het
Man1a	A	T	10: 53,809,586 (GRCm39)		probably null	Het
Megf6	A	T	4: 154,338,277 (GRCm39)	D449V	probably damaging	Het
Mtor	T	C	4: 148,556,599 (GRCm39)	V1003A	probably benign	Het
Ncan	C	A	8: 70,552,944 (GRCm39)	W1096L	probably damaging	Het
Ndor1	C	T	2: 25,138,133 (GRCm39)		probably null	Het
Ndufaf1	T	C	2: 119,490,547 (GRCm39)	E171G	possibly damaging	Het
Nell1	T	C	7: 49,770,397 (GRCm39)	V152A	possibly damaging	Het
Nherf4	C	A	9: 44,159,915 (GRCm39)	G402*	probably null	Het
Nt5dc1	A	T	10: 34,198,673 (GRCm39)	V255E	probably damaging	Het
Or2a20	T	A	6: 43,193,928 (GRCm39)	F27Y	probably damaging	Het
Or2y1b	A	T	11: 49,208,375 (GRCm39)	M1L	probably null	Het
Or52h7	A	G	7: 104,214,212 (GRCm39)	I261M	probably benign	Het
Or52z14	G	A	7: 103,253,401 (GRCm39)	R180H	probably benign	Het
Otud7a	T	C	7: 63,407,171 (GRCm39)	I50T	probably damaging	Het
P2ry13	G	A	3: 59,116,983 (GRCm39)	T265I	probably benign	Het
Pde4d	A	G	13: 108,996,733 (GRCm39)	S12G	probably benign	Het
Pigk	C	A	3: 152,450,154 (GRCm39)	N219K	probably damaging	Het
Plcg1	T	A	2: 160,595,509 (GRCm39)		probably null	Het
Psd2	A	T	18: 36,111,717 (GRCm39)	D114V	probably damaging	Het
Ptch1	A	T	13: 63,672,884 (GRCm39)	I770N	probably benign	Het
Ptprq	A	T	10: 107,524,290 (GRCm39)	M481K	probably benign	Het
Rnf216	A	C	5: 143,078,814 (GRCm39)	M45R	probably damaging	Het
Rpsa	T	A	9: 119,960,129 (GRCm39)	W231R	probably benign	Het
Ryr1	G	T	7: 28,768,998 (GRCm39)	T2797N	probably damaging	Het
Ryr3	A	T	2: 112,666,602 (GRCm39)	M1468K	probably damaging	Het
Slc6a7	A	G	18: 61,137,589 (GRCm39)	Y244H	probably damaging	Het
Slco6c1	T	A	1: 97,009,049 (GRCm39)	D462V	probably damaging	Het
Spata31d1b	A	T	13: 59,864,917 (GRCm39)	E688D	possibly damaging	Het
Srpra	G	A	9: 35,126,766 (GRCm39)	R508H	probably benign	Het
Tnrc18	A	T	5: 142,773,737 (GRCm39)	I181N	unknown	Het
Tnrc6a	T	C	7: 122,791,836 (GRCm39)	F1785L	probably damaging	Het
Trio	A	T	15: 27,752,811 (GRCm39)	D2174E	probably benign	Het
Ttn	C	T	2: 76,623,600 (GRCm39)	V15326I	probably damaging	Het
Ubap2	T	A	4: 41,245,461 (GRCm39)		probably benign	Het
Vmn2r113	C	T	17: 23,177,321 (GRCm39)	P702S	probably damaging	Het
Vmn2r66	A	T	7: 84,656,980 (GRCm39)	W142R	probably damaging	Het
Vmn2r73	A	G	7: 85,519,582 (GRCm39)	Y459H	probably damaging	Het
Wsb2	C	T	5: 117,515,550 (GRCm39)	T385M	probably damaging	Het

Other mutations in Fam184b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00163:Fam184b	APN	5	45,697,091 (GRCm39)	missense	probably benign	0.17
IGL00781:Fam184b	APN	5	45,712,534 (GRCm39)	splice site	probably null
IGL01636:Fam184b	APN	5	45,741,637 (GRCm39)	missense	probably benign	0.00
IGL02008:Fam184b	APN	5	45,690,165 (GRCm39)	missense	possibly damaging	0.75
IGL02123:Fam184b	APN	5	45,796,493 (GRCm39)	missense	possibly damaging	0.92
IGL02177:Fam184b	APN	5	45,690,157 (GRCm39)	nonsense	probably null
IGL02192:Fam184b	APN	5	45,695,062 (GRCm39)	missense	probably benign	0.00
IGL02478:Fam184b	APN	5	45,695,039 (GRCm39)	missense	probably damaging	0.99
IGL03368:Fam184b	APN	5	45,689,166 (GRCm39)	missense	possibly damaging	0.91
R0003:Fam184b	UTSW	5	45,712,536 (GRCm39)	splice site	probably benign
R0129:Fam184b	UTSW	5	45,690,120 (GRCm39)	missense	probably damaging	1.00
R0420:Fam184b	UTSW	5	45,741,854 (GRCm39)	missense	probably damaging	1.00
R0647:Fam184b	UTSW	5	45,741,932 (GRCm39)	missense	probably benign
R1215:Fam184b	UTSW	5	45,741,520 (GRCm39)	missense	probably damaging	1.00
R1374:Fam184b	UTSW	5	45,712,485 (GRCm39)	missense	probably benign
R1466:Fam184b	UTSW	5	45,737,851 (GRCm39)	splice site	probably benign
R1773:Fam184b	UTSW	5	45,741,676 (GRCm39)	missense	possibly damaging	0.60
R1865:Fam184b	UTSW	5	45,689,231 (GRCm39)	missense	possibly damaging	0.91
R3615:Fam184b	UTSW	5	45,740,157 (GRCm39)	missense	possibly damaging	0.56
R3616:Fam184b	UTSW	5	45,740,157 (GRCm39)	missense	possibly damaging	0.56
R4180:Fam184b	UTSW	5	45,697,106 (GRCm39)	missense	probably benign	0.00
R4375:Fam184b	UTSW	5	45,699,685 (GRCm39)	missense	probably benign
R4674:Fam184b	UTSW	5	45,740,230 (GRCm39)	nonsense	probably null
R5021:Fam184b	UTSW	5	45,730,604 (GRCm39)	missense	probably benign	0.01
R5450:Fam184b	UTSW	5	45,697,143 (GRCm39)	missense	probably benign
R5731:Fam184b	UTSW	5	45,710,471 (GRCm39)	missense	probably benign	0.00
R5858:Fam184b	UTSW	5	45,796,461 (GRCm39)	missense	probably damaging	0.99
R6032:Fam184b	UTSW	5	45,740,238 (GRCm39)	missense	probably benign	0.01
R6032:Fam184b	UTSW	5	45,740,238 (GRCm39)	missense	probably benign	0.01
R6060:Fam184b	UTSW	5	45,710,489 (GRCm39)	missense	probably damaging	0.99
R6088:Fam184b	UTSW	5	45,741,354 (GRCm39)	missense	probably damaging	1.00
R6416:Fam184b	UTSW	5	45,694,995 (GRCm39)	missense	probably benign	0.04
R6932:Fam184b	UTSW	5	45,690,243 (GRCm39)	splice site	probably null
R6956:Fam184b	UTSW	5	45,688,099 (GRCm39)	missense	probably damaging	0.97
R6965:Fam184b	UTSW	5	45,712,477 (GRCm39)	missense	probably benign
R7229:Fam184b	UTSW	5	45,741,517 (GRCm39)	missense	probably damaging	1.00
R7303:Fam184b	UTSW	5	45,699,568 (GRCm39)	critical splice donor site	probably null
R7429:Fam184b	UTSW	5	45,698,230 (GRCm39)	missense	probably benign
R7522:Fam184b	UTSW	5	45,688,093 (GRCm39)	missense	probably damaging	1.00
R7541:Fam184b	UTSW	5	45,699,574 (GRCm39)	missense	probably damaging	0.99
R7942:Fam184b	UTSW	5	45,741,595 (GRCm39)	missense	probably benign	0.16
R8172:Fam184b	UTSW	5	45,741,709 (GRCm39)	missense	possibly damaging	0.86
R9470:Fam184b	UTSW	5	45,741,854 (GRCm39)	missense	probably damaging	1.00
R9649:Fam184b	UTSW	5	45,796,484 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTTGTGCAGAGGACACAGGG -3'
(R):5'- TGTGCTCCAGGCTATATAACATG -3'

Sequencing Primer
(F):5'- GGTGAACCTCCGGATCCCATTTAG -3'
(R):5'- GGATTTAACACTTGTTTTCTCTTGAC -3'

Posted On

2016-04-27