Mutagenetix > Incidental Mutation

Incidental Mutation 'R4811:Fam46b'

369413

Institutional Source

Beutler Lab

Gene Symbol

Fam46b

Ensembl Gene

ENSMUSG00000046694

Gene Name

family with sequence similarity 46, member B

Synonyms

MMRRC Submission

042430-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.201) question?

Stock #

R4811 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

133480132-133487938 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 133486370 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 184 (L184P)

Ref Sequence

ENSEMBL: ENSMUSP00000056015 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051676] [ENSMUST00000125541]

AlphaFold

Q8C152

Predicted Effect

probably benign
Transcript: ENSMUST00000051676
AA Change: L184P

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000056015
Gene: ENSMUSG00000046694
AA Change: L184P

Domain	Start	End	E-Value	Type
low complexity region	15	44	N/A	INTRINSIC
DUF1693	52	372	2.52e-218	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000123169

Predicted Effect

probably benign
Transcript: ENSMUST00000125541

SMART Domains

Protein: ENSMUSP00000129613
Gene: ENSMUSG00000056596

Domain	Start	End	E-Value	Type
low complexity region	20	54	N/A	INTRINSIC
low complexity region	72	124	N/A	INTRINSIC
low complexity region	131	144	N/A	INTRINSIC
low complexity region	164	189	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132840

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 93.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930447A16Rik	G	A	15: 37,425,708 (GRCm38)		probably benign	Het
Adam3	C	T	8: 24,711,724 (GRCm38)	G208R	probably benign	Het
AI481877	T	C	4: 59,082,404 (GRCm38)	N408S	probably benign	Het
Arsg	G	T	11: 109,534,072 (GRCm38)	V290L	probably benign	Het
Cad	A	G	5: 31,074,690 (GRCm38)	T104A	probably benign	Het
Ccdc180	A	G	4: 45,928,020 (GRCm38)	N1185S	probably damaging	Het
Cdh18	A	G	15: 23,226,791 (GRCm38)	T113A	probably benign	Het
Crocc2	G	A	1: 93,205,896 (GRCm38)	A967T	probably damaging	Het
Cyp4f16	A	G	17: 32,545,106 (GRCm38)	T291A	probably benign	Het
Dcc	T	A	18: 71,299,483 (GRCm38)	H1300L	probably benign	Het
Ddx23	T	A	15: 98,647,471 (GRCm38)		probably null	Het
Dnhd1	T	G	7: 105,714,281 (GRCm38)	S4017A	probably damaging	Het
Erbb4	A	T	1: 68,254,544 (GRCm38)	F729L	probably damaging	Het
Ercc6	G	T	14: 32,574,929 (GRCm38)	R1292L	probably benign	Het
Fam186b	C	T	15: 99,280,237 (GRCm38)	V403M	probably benign	Het
Fam227a	T	C	15: 79,615,427 (GRCm38)	N576D	possibly damaging	Het
Fbln1	A	G	15: 85,226,966 (GRCm38)		probably null	Het
Fbxw17	T	C	13: 50,425,633 (GRCm38)	V162A	probably benign	Het
Gas2l1	A	C	11: 5,064,436 (GRCm38)	I8S	probably damaging	Het
Gm7030	A	G	17: 36,127,776 (GRCm38)	L241S	probably damaging	Het
Golgb1	T	C	16: 36,891,419 (GRCm38)	L195P	probably damaging	Het
Gps2	A	T	11: 69,915,928 (GRCm38)	H233L	probably damaging	Het
Guf1	T	G	5: 69,564,509 (GRCm38)		probably null	Het
Il1rap	T	A	16: 26,701,238 (GRCm38)		probably null	Het
Ints14	A	G	9: 64,964,518 (GRCm38)	Y46C	probably damaging	Het
Kalrn	T	G	16: 34,356,969 (GRCm38)	Q293H	probably damaging	Het
Kank2	A	G	9: 21,775,747 (GRCm38)	L593P	probably damaging	Het
Krt19	T	C	11: 100,141,348 (GRCm38)	T297A	possibly damaging	Het
Lcp1	T	C	14: 75,200,408 (GRCm38)	V86A	probably damaging	Het
Lins1	T	A	7: 66,708,150 (GRCm38)	I11K	probably benign	Het
Lrba	T	C	3: 86,776,141 (GRCm38)	F2757L	probably damaging	Het
Lyst	T	C	13: 13,777,100 (GRCm38)	I3762T	probably benign	Het
Lyzl6	A	G	11: 103,635,025 (GRCm38)	S90P	possibly damaging	Het
Mfsd2a	T	A	4: 122,959,382 (GRCm38)	Q38L	probably benign	Het
Mtss1	A	G	15: 58,944,073 (GRCm38)	F546S	probably damaging	Het
Myo5a	G	A	9: 75,141,543 (GRCm38)		probably null	Het
Naip6	C	A	13: 100,285,791 (GRCm38)	G1245W	probably damaging	Het
Ndfip1	C	T	18: 38,451,592 (GRCm38)	T107I	probably benign	Het
Nek8	C	T	11: 78,167,718 (GRCm38)		probably null	Het
Nphs1	T	C	7: 30,460,429 (GRCm38)	V55A	probably damaging	Het
Nrp2	C	A	1: 62,719,081 (GRCm38)	H75Q	probably damaging	Het
Oas1e	C	T	5: 120,795,383 (GRCm38)	S39N	probably damaging	Het
Olfr1164	A	G	2: 88,093,532 (GRCm38)	F135L	probably benign	Het
Olfr1391	T	G	11: 49,327,748 (GRCm38)	S112R	possibly damaging	Het
Olfr309	T	C	7: 86,306,958 (GRCm38)	T52A	probably benign	Het
Olfr871	A	T	9: 20,212,753 (GRCm38)	I135F	probably damaging	Het
Pan3	T	A	5: 147,530,058 (GRCm38)	H632Q	probably damaging	Het
Paqr3	A	C	5: 97,095,983 (GRCm38)	S291A	probably benign	Het
Pcdh17	A	C	14: 84,447,935 (GRCm38)	D614A	probably damaging	Het
Pcyox1l	T	C	18: 61,697,535 (GRCm38)	E422G	possibly damaging	Het
Pgr	G	T	9: 8,900,843 (GRCm38)	E126*	probably null	Het
Pik3ap1	A	G	19: 41,302,497 (GRCm38)	V532A	possibly damaging	Het
Pla2g4c	T	C	7: 13,337,813 (GRCm38)	I186T	probably damaging	Het
Pnkd	G	A	1: 74,349,405 (GRCm38)		probably null	Het
Poc1a	A	G	9: 106,349,709 (GRCm38)	T334A	probably damaging	Het
Pou2f2	T	A	7: 25,097,686 (GRCm38)	K211*	probably null	Het
Rdh13	T	C	7: 4,442,653 (GRCm38)	E94G	probably benign	Het
Rnf186	A	G	4: 138,967,187 (GRCm38)	S13G	probably benign	Het
Ryr2	T	C	13: 11,655,698 (GRCm38)	R3471G	probably damaging	Het
Sbf2	T	C	7: 110,372,535 (GRCm38)	T831A	probably damaging	Het
Sh3gl2	A	G	4: 85,398,166 (GRCm38)		probably benign	Het
Snn	T	C	16: 11,072,533 (GRCm38)	V72A	probably benign	Het
Sys1	T	A	2: 164,464,424 (GRCm38)	H99Q	possibly damaging	Het
Syt7	A	G	19: 10,435,567 (GRCm38)	K122R	probably damaging	Het
Tas1r2	T	A	4: 139,669,000 (GRCm38)	L550Q	probably damaging	Het
Thoc1	T	C	18: 9,993,438 (GRCm38)	I599T	probably damaging	Het
Tle3	C	T	9: 61,373,997 (GRCm38)		probably benign	Het
Tll1	A	C	8: 64,085,473 (GRCm38)	V379G	possibly damaging	Het
Tnfrsf21	G	A	17: 43,037,730 (GRCm38)	E78K	probably benign	Het
Tpgs2	A	G	18: 25,129,840 (GRCm38)		probably benign	Het
Trpm1	T	C	7: 64,208,306 (GRCm38)	L165P	probably damaging	Het
Trpm5	T	C	7: 143,080,219 (GRCm38)	Y750C	probably damaging	Het
Ttbk2	A	C	2: 120,740,070 (GRCm38)	S1201A	possibly damaging	Het
Ust	T	A	10: 8,245,941 (GRCm38)	H301L	probably damaging	Het
Vwa5a	T	C	9: 38,735,953 (GRCm38)	F543L	probably benign	Het
Yeats2	T	A	16: 20,152,895 (GRCm38)		probably null	Het
Zfp85	T	C	13: 67,749,626 (GRCm38)	Y109C	probably damaging	Het
Zfr2	T	A	10: 81,243,713 (GRCm38)	V362E	probably benign	Het
Znrf3	A	T	11: 5,287,420 (GRCm38)	C134S	probably benign	Het

Other mutations in Fam46b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01730:Fam46b	APN	4	133,486,522 (GRCm38)	splice site	probably null
IGL01871:Fam46b	APN	4	133,486,309 (GRCm38)	missense	possibly damaging	0.89
IGL02218:Fam46b	APN	4	133,486,151 (GRCm38)	missense	probably damaging	1.00
IGL02222:Fam46b	APN	4	133,486,553 (GRCm38)	missense	probably damaging	0.99
R0345:Fam46b	UTSW	4	133,486,211 (GRCm38)	missense	probably benign	0.01
R0515:Fam46b	UTSW	4	133,486,139 (GRCm38)	missense	possibly damaging	0.92
R0843:Fam46b	UTSW	4	133,486,531 (GRCm38)	missense	probably damaging	1.00
R1240:Fam46b	UTSW	4	133,486,504 (GRCm38)	missense	probably benign	0.01
R2042:Fam46b	UTSW	4	133,486,613 (GRCm38)	missense	possibly damaging	0.82
R4328:Fam46b	UTSW	4	133,486,603 (GRCm38)	nonsense	probably null
R4868:Fam46b	UTSW	4	133,486,082 (GRCm38)	critical splice acceptor site	probably null
R5056:Fam46b	UTSW	4	133,480,438 (GRCm38)	missense	possibly damaging	0.91
R6360:Fam46b	UTSW	4	133,486,756 (GRCm38)	missense	probably damaging	0.99
R6454:Fam46b	UTSW	4	133,480,409 (GRCm38)	missense	probably damaging	1.00
R7017:Fam46b	UTSW	4	133,486,234 (GRCm38)	missense	possibly damaging	0.95
R7186:Fam46b	UTSW	4	133,486,207 (GRCm38)	missense	probably damaging	1.00
R7315:Fam46b	UTSW	4	133,487,084 (GRCm38)	missense	probably damaging	1.00
R8410:Fam46b	UTSW	4	133,487,051 (GRCm38)	missense	possibly damaging	0.95
R9093:Fam46b	UTSW	4	133,487,041 (GRCm38)	missense	probably damaging	0.99
R9361:Fam46b	UTSW	4	133,486,150 (GRCm38)	missense	probably damaging	1.00
Z1176:Fam46b	UTSW	4	133,486,682 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTACAAGGACCTGGACTTGG -3'
(R):5'- TCAGCGAAGTCCCCATAGAG -3'

Sequencing Primer
(F):5'- CTACAAGGACCTGGACTTGGTGTTC -3'
(R):5'- GAAGTCCCCATAGAGGCTCTC -3'

Posted On

2016-02-04