Mutagenetix > Incidental Mutation

Incidental Mutation 'R4697:Fam161b'

355792

Institutional Source

Beutler Lab

Gene Symbol

Fam161b

Ensembl Gene

ENSMUSG00000021234

Gene Name

family with sequence similarity 161, member B

Synonyms

MMRRC Submission

041947-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.069) question?

Stock #

R4697 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

84345309-84361833 bp(-) (GRCm38)

Type of Mutation

unclassified

DNA Base Change (assembly)

G to A at 84348558 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000152160 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021659] [ENSMUST00000045931] [ENSMUST00000065536] [ENSMUST00000222606]

AlphaFold

Q8CB59

Predicted Effect

probably benign
Transcript: ENSMUST00000021659

SMART Domains

Protein: ENSMUSP00000021659
Gene: ENSMUSG00000021234

Domain	Start	End	E-Value	Type
low complexity region	57	65	N/A	INTRINSIC
low complexity region	93	107	N/A	INTRINSIC
Pfam:UPF0564	168	535	5.3e-100	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000045931

SMART Domains

Protein: ENSMUSP00000045550
Gene: ENSMUSG00000042472

Domain	Start	End	E-Value	Type
ZnF_C2H2	219	243	1.04e-3	SMART
ZnF_C2H2	249	273	6.88e-4	SMART
ZnF_C2H2	279	303	1.13e-4	SMART
ZnF_C2H2	309	333	1.45e-2	SMART
ZnF_C2H2	339	361	5.59e-4	SMART
low complexity region	400	417	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000065536

SMART Domains

Protein: ENSMUSP00000070407
Gene: ENSMUSG00000021234

Domain	Start	End	E-Value	Type
low complexity region	57	65	N/A	INTRINSIC
low complexity region	93	107	N/A	INTRINSIC
Pfam:UPF0564	168	535	8.3e-112	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126752

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133230

Predicted Effect

probably benign
Transcript: ENSMUST00000222606

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.0%
20x: 94.5%

Validation Efficiency

96% (75/78)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9030624J02Rik	T	A	7: 118,791,448	I455N	probably damaging	Het
A2m	T	C	6: 121,638,284	M1T	probably null	Het
Aatf	T	A	11: 84,449,138	D449V	probably damaging	Het
Acbd3	T	A	1: 180,721,944		probably benign	Het
BC005561	A	G	5: 104,522,240	K1543E	probably benign	Het
Bicc1	T	A	10: 70,953,484	I366F	possibly damaging	Het
Ccdc74a	T	C	16: 17,649,749	S184P	possibly damaging	Het
Cntn4	T	C	6: 106,525,485	V401A	probably damaging	Het
Cux2	T	C	5: 121,873,753	T540A	probably damaging	Het
Disp2	G	T	2: 118,791,684	E966*	probably null	Het
Dpp7	A	G	2: 25,354,919	Y209H	probably benign	Het
Dstyk	T	A	1: 132,449,487	F277Y	probably damaging	Het
Dtx1	A	T	5: 120,694,408		probably null	Het
Ear-ps2	G	A	14: 44,047,060		noncoding transcript	Het
Ednra	T	C	8: 77,664,995	H422R	probably benign	Het
Erlec1	T	A	11: 30,952,640	I67F	probably benign	Het
Gata5	A	T	2: 180,327,379	C345*	probably null	Het
Glmp	T	C	3: 88,328,274	V47A	probably damaging	Het
Gm9762	T	A	3: 78,966,550		noncoding transcript	Het
Gnas	A	T	2: 174,298,080	D14V	probably damaging	Het
Gnl3	T	C	14: 31,017,329	S53G	probably damaging	Het
Grhl3	C	T	4: 135,548,466	V527M	probably damaging	Het
Hoxd10	T	A	2: 74,694,187	L281*	probably null	Het
Kif16b	T	G	2: 142,690,694	Y1175S	probably benign	Het
Kif2b	A	G	11: 91,576,846	S204P	probably benign	Het
Klhl40	T	A	9: 121,778,734	I320N	probably damaging	Het
Ksr2	G	A	5: 117,708,147	R693Q	probably damaging	Het
Mis12	A	G	11: 71,025,326	K62E	possibly damaging	Het
Mlc1	A	G	15: 88,974,777	C102R	probably damaging	Het
Muc5b	T	C	7: 141,857,361	I1348T	unknown	Het
Myh7b	A	G	2: 155,629,322	E1130G	probably damaging	Het
Nat8f4	T	C	6: 85,901,386	T52A	probably benign	Het
Nxpe2	C	A	9: 48,320,521	V379L	probably benign	Het
Olfr1231	C	A	2: 89,302,902	S230I	possibly damaging	Het
Olfr1231	T	A	2: 89,302,903	S230C	probably damaging	Het
Olfr1448	C	T	19: 12,919,934	C125Y	probably damaging	Het
Olfr1465	A	T	19: 13,313,717	D189E	probably benign	Het
Olfr288	G	A	15: 98,186,868	R310W	probably damaging	Het
Pcdhga7	A	T	18: 37,717,208	Y756F	probably damaging	Het
Pcsk6	T	A	7: 65,959,241	Y284N	probably damaging	Het
Pdcd11	T	C	19: 47,126,347	V1367A	possibly damaging	Het
Postn	T	A	3: 54,375,071	N484K	probably damaging	Het
Prkd3	C	T	17: 78,961,171	V572I	probably benign	Het
Qser1	T	C	2: 104,787,183	S1005G	probably benign	Het
Radil	G	T	5: 142,486,801	D951E	probably benign	Het
Ripk1	C	T	13: 34,027,942	R352*	probably null	Het
Sacs	T	C	14: 61,212,747	F4081L	probably benign	Het
Sbf1	A	G	15: 89,315,085	V11A	possibly damaging	Het
Sgip1	T	A	4: 102,934,587	F536I	probably damaging	Het
Slc45a1	A	G	4: 150,638,284	L381P	probably damaging	Het
Smarcad1	C	T	6: 65,052,641	P71L	probably benign	Het
Spns1	T	A	7: 126,377,037	D14V	probably damaging	Het
Sv2c	T	A	13: 95,986,018	I417F	possibly damaging	Het
Tas2r113	T	A	6: 132,893,516	M169K	probably benign	Het
Tgm1	A	T	14: 55,705,681	N567K	probably benign	Het
Tln2	C	T	9: 67,395,461	R76Q	probably damaging	Het
Trpm6	T	C	19: 18,853,791	V1340A	probably benign	Het
Tspan18	A	T	2: 93,312,030		probably null	Het
Txndc11	C	T	16: 11,084,314	V679I	probably damaging	Het
Usf1	G	T	1: 171,416,964	G144V	possibly damaging	Het
Vmn1r59	T	C	7: 5,454,452	Y103C	probably damaging	Het
Vmn2r23	A	T	6: 123,741,826	I713F	probably damaging	Het
Vmn2r79	A	T	7: 87,037,960	I850F	probably damaging	Het
Wdr90	C	T	17: 25,855,363	R676H	probably benign	Het
Zfp867	G	A	11: 59,463,661	R281W	probably damaging	Het
Zfp939	T	C	7: 39,472,942		noncoding transcript	Het

Other mutations in Fam161b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00540:Fam161b	APN	12	84361751	unclassified	probably benign
IGL00900:Fam161b	APN	12	84355969	missense	probably benign	0.05
IGL00905:Fam161b	APN	12	84357685	missense	probably benign	0.00
IGL01123:Fam161b	APN	12	84357664	missense	probably benign	0.00
IGL02156:Fam161b	APN	12	84354753	missense	probably benign	0.00
IGL02630:Fam161b	APN	12	84353914	missense	probably benign	0.03
IGL02670:Fam161b	APN	12	84357594	missense	probably benign	0.00
IGL03160:Fam161b	APN	12	84353825	missense	probably benign	0.05
R0560:Fam161b	UTSW	12	84357718	missense	probably damaging	0.96
R0569:Fam161b	UTSW	12	84348639	missense	probably damaging	1.00
R1834:Fam161b	UTSW	12	84348778	splice site	probably benign
R2070:Fam161b	UTSW	12	84356428	missense	probably benign	0.00
R3784:Fam161b	UTSW	12	84361690	critical splice donor site	probably null
R3786:Fam161b	UTSW	12	84361690	critical splice donor site	probably null
R5247:Fam161b	UTSW	12	84357750	missense	probably damaging	1.00
R5390:Fam161b	UTSW	12	84348634	missense	probably damaging	0.99
R5668:Fam161b	UTSW	12	84356350	missense	probably damaging	0.96
R6891:Fam161b	UTSW	12	84354780	missense	probably damaging	1.00
R7189:Fam161b	UTSW	12	84348646	missense	probably damaging	1.00
R7410:Fam161b	UTSW	12	84357801	missense	probably benign	0.04
R7514:Fam161b	UTSW	12	84357738	missense	possibly damaging	0.76
R8035:Fam161b	UTSW	12	84348656	missense	probably damaging	1.00
R8219:Fam161b	UTSW	12	84346874	missense	probably benign	0.00
R8428:Fam161b	UTSW	12	84357595	missense	probably benign	0.00
R8921:Fam161b	UTSW	12	84348282	missense	probably benign	0.02
R9638:Fam161b	UTSW	12	84356413	missense	probably benign	0.00
X0019:Fam161b	UTSW	12	84354973	missense	probably benign	0.30
Z1176:Fam161b	UTSW	12	84356053	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TGCTCCTGGAATTAACAAGGTTTC -3'
(R):5'- ATGCATGTGCCCAGGTCATC -3'

Sequencing Primer
(F):5'- GGTTTCTAGAAGCAACCAATCTC -3'
(R):5'- ATCAGACATGAGCATTCAGTGGTTG -3'

Posted On

2015-10-21