Mutagenetix > Incidental Mutation

Incidental Mutation 'R1835:Fam135b'

205220

Institutional Source

Beutler Lab

Gene Symbol

Fam135b

Ensembl Gene

ENSMUSG00000036800

Gene Name

family with sequence similarity 135, member B

Synonyms

1700010C24Rik, A830008O07Rik

MMRRC Submission

039862-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1835 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

71431609-71727838 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 71490711 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Methionine at position 274 (L274M)

Ref Sequence

ENSEMBL: ENSMUSP00000022953 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000022953]

AlphaFold

Q9DAI6

Predicted Effect

probably damaging
Transcript: ENSMUST00000022953
AA Change: L274M

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000022953
Gene: ENSMUSG00000036800
AA Change: L274M

Domain	Start	End	E-Value	Type
Pfam:DUF3657	111	172	1.9e-19	PFAM
low complexity region	744	757	N/A	INTRINSIC
low complexity region	1124	1130	N/A	INTRINSIC
Pfam:DUF676	1132	1328	2.7e-60	PFAM
Pfam:PGAP1	1135	1309	3.2e-9	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230569

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 94.9%
20x: 91.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 97 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610507B11Rik	G	T	11: 78,287,750	V1993F	probably damaging	Het
4933425L06Rik	C	A	13: 105,082,194	A12E	unknown	Het
Acss2	T	A	2: 155,558,630	Y530N	probably damaging	Het
Adam4	T	C	12: 81,419,559	I763V	probably benign	Het
Aipl1	T	G	11: 72,030,499	K190T	possibly damaging	Het
Alms1	T	A	6: 85,678,503	S3344T	possibly damaging	Het
Alpi	A	G	1: 87,099,414	V381A	possibly damaging	Het
Ankfn1	A	T	11: 89,447,618	S365R	probably benign	Het
Aox2	G	A	1: 58,308,991	A623T	probably benign	Het
Apc	T	A	18: 34,317,077	L2308Q	probably damaging	Het
Atp9b	C	T	18: 80,778,883	V501I	probably benign	Het
Baz2b	T	C	2: 59,901,819	E1994G	probably benign	Het
Cacna1a	T	C	8: 84,581,357		probably null	Het
Cacna1h	C	A	17: 25,392,076	V583L	probably benign	Het
Cd55	T	C	1: 130,447,609		probably benign	Het
Cep192	T	A	18: 67,804,424	S75T	possibly damaging	Het
Cfap54	T	A	10: 92,962,375	D1674V	probably benign	Het
Churc1	T	C	12: 76,773,297	F27L	possibly damaging	Het
Coro1c	A	G	5: 113,848,543	I280T	probably benign	Het
Creb1	C	T	1: 64,550,950	Q32*	probably null	Het
Cyp2b9	A	G	7: 26,200,783	T339A	probably benign	Het
Dctn3	T	C	4: 41,720,813	R51G	probably damaging	Het
Ddb1	T	C	19: 10,626,593	V888A	probably damaging	Het
Disp1	A	G	1: 183,089,000	Y619H	probably damaging	Het
Dnajc9	T	C	14: 20,388,334	D96G	possibly damaging	Het
Eepd1	A	G	9: 25,482,868	T143A	possibly damaging	Het
Eps8	T	A	6: 137,522,279	K204*	probably null	Het
Ercc5	T	A	1: 44,180,875	S1102R	probably benign	Het
Ergic2	T	A	6: 148,189,581	Y211F	possibly damaging	Het
Fat3	G	A	9: 15,998,088	T2206I	probably damaging	Het
Fat4	A	G	3: 38,983,571	I3791V	probably benign	Het
Gemin4	A	G	11: 76,213,296	M213T	possibly damaging	Het
Gnai3	T	C	3: 108,118,407	M119V	probably benign	Het
Heatr5b	A	T	17: 78,773,563	L1420Q	probably damaging	Het
Herc2	G	T	7: 56,206,765	G3918*	probably null	Het
Ints9	A	G	14: 65,032,256	Y465C	probably damaging	Het
Ist1	A	G	8: 109,678,883	V175A	probably damaging	Het
Kcnj12	T	C	11: 61,069,557	L227P	possibly damaging	Het
Kcnq5	T	C	1: 21,466,387	S416G	probably benign	Het
Kdm3a	T	A	6: 71,613,956	T295S	probably benign	Het
Kif1c	T	A	11: 70,708,971	M479K	probably damaging	Het
Kif20b	T	C	19: 34,956,038	L83P	probably damaging	Het
Kndc1	A	G	7: 139,927,711	E1194G	probably damaging	Het
Llgl1	A	G	11: 60,704,730	M81V	probably benign	Het
Map4k5	C	A	12: 69,824,662	M495I	probably damaging	Het
Mest	C	T	6: 30,742,791	R146C	probably benign	Het
Mettl24	T	A	10: 40,737,816		probably null	Het
Mical1	T	C	10: 41,483,535	S586P	probably benign	Het
Mrgpra3	G	T	7: 47,589,946	Y77*	probably null	Het
Mss51	A	T	14: 20,483,178	C408*	probably null	Het
Myh6	T	C	14: 54,957,401	T666A	probably benign	Het
Myo10	T	C	15: 25,805,587	C1685R	possibly damaging	Het
Naip5	A	T	13: 100,223,218	Y503*	probably null	Het
Neil1	A	C	9: 57,146,604	F144C	probably damaging	Het
Nipbl	T	A	15: 8,343,517	I1082F	possibly damaging	Het
Nkiras1	T	C	14: 18,276,732	V7A	probably damaging	Het
Ntng2	G	A	2: 29,197,057	Q384*	probably null	Het
Ocrl	T	A	X: 47,962,116	I74N	probably damaging	Het
Olfr137	A	T	17: 38,305,312	S50T	probably benign	Het
Olfr1385	A	T	11: 49,494,670	I46F	probably damaging	Het
Olfr1408	A	G	1: 173,130,815	V134A	probably benign	Het
Olfr381	A	C	11: 73,486,374	V150G	probably benign	Het
Olfr535	A	G	7: 140,492,709	S24G	probably benign	Het
Olfr761	C	T	17: 37,952,385	G213E	possibly damaging	Het
Patj	A	G	4: 98,491,590	D151G	probably benign	Het
Plpbp	T	C	8: 27,049,231	V126A	probably damaging	Het
Pold2	A	G	11: 5,873,454	L325P	possibly damaging	Het
Ppp1r12c	A	C	7: 4,483,651	S480A	probably damaging	Het
Pum1	T	C	4: 130,701,048	S124P	possibly damaging	Het
Pwp2	C	G	10: 78,179,091	G353A	probably damaging	Het
Reln	C	A	5: 21,979,002	Q1666H	probably damaging	Het
Rnf19a	T	C	15: 36,265,925	I9V	probably benign	Het
Ryr2	T	C	13: 11,769,878	H1063R	probably benign	Het
Samd14	C	G	11: 95,023,600	D361E	probably damaging	Het
Samd15	A	T	12: 87,201,843	N365I	probably damaging	Het
Sec16b	A	G	1: 157,531,312	H105R	probably benign	Het
Sez6	T	C	11: 77,953,503	S51P	probably benign	Het
Sh3bp1	T	A	15: 78,905,150	L236Q	probably damaging	Het
Sspo	C	T	6: 48,457,340	T991I	probably damaging	Het
Suco	A	T	1: 161,859,500	L97*	probably null	Het
Tab1	C	A	15: 80,148,296	R35S	probably benign	Het
Tet3	C	A	6: 83,404,163	S341I	possibly damaging	Het
Tlr1	A	T	5: 64,925,700	D511E	probably benign	Het
Tmem132b	A	C	5: 125,785,899	D656A	probably damaging	Het
Tmtc4	T	A	14: 122,941,988		probably null	Het
Trmo	T	C	4: 46,380,158	T404A	probably damaging	Het
Trpm1	A	G	7: 64,230,268	K790E	probably damaging	Het
Ulk4	C	A	9: 121,168,184	R774M	probably null	Het
Ush2a	C	T	1: 188,451,818	L1440F	probably benign	Het
Usp16	A	G	16: 87,480,907	K682E	probably damaging	Het
Virma	T	C	4: 11,540,511	S1471P	probably benign	Het
Vmn1r177	A	T	7: 23,865,686	I255N	probably damaging	Het
Vmn2r61	A	T	7: 42,266,652	R230*	probably null	Het
Vps13c	T	A	9: 67,993,013	F3671L	probably benign	Het
Washc5	T	C	15: 59,359,340	N358S	possibly damaging	Het
Wdr72	A	G	9: 74,151,617	K331E	probably damaging	Het
Zfp986	A	T	4: 145,899,235	K155I	probably benign	Het

Other mutations in Fam135b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00088:Fam135b	APN	15	71450494	missense	probably damaging	1.00
IGL00565:Fam135b	APN	15	71471512	missense	probably benign
IGL00645:Fam135b	APN	15	71462546	missense	probably damaging	1.00
IGL00686:Fam135b	APN	15	71462319	missense	probably benign	0.00
IGL00857:Fam135b	APN	15	71463616	missense	probably benign	0.16
IGL01443:Fam135b	APN	15	71463364	missense	probably benign	0.02
IGL01690:Fam135b	APN	15	71456935	missense	probably benign	0.19
IGL01920:Fam135b	APN	15	71622036	missense	possibly damaging	0.94
IGL01987:Fam135b	APN	15	71462115	missense	probably benign
IGL02154:Fam135b	APN	15	71448710	missense	probably benign	0.12
IGL03107:Fam135b	APN	15	71463561	missense	probably benign
IGL03264:Fam135b	APN	15	71462788	missense	probably benign
IGL03055:Fam135b	UTSW	15	71622034	missense	possibly damaging	0.51
R0010:Fam135b	UTSW	15	71622032	missense	probably damaging	1.00
R0010:Fam135b	UTSW	15	71622032	missense	probably damaging	1.00
R0230:Fam135b	UTSW	15	71446037	missense	probably benign	0.02
R0413:Fam135b	UTSW	15	71463821	missense	probably benign	0.45
R0524:Fam135b	UTSW	15	71462284	missense	probably benign	0.00
R0565:Fam135b	UTSW	15	71490837	missense	possibly damaging	0.88
R0628:Fam135b	UTSW	15	71448656	splice site	probably benign
R1415:Fam135b	UTSW	15	71456928	missense	probably damaging	0.99
R1462:Fam135b	UTSW	15	71621996	splice site	probably benign
R1701:Fam135b	UTSW	15	71459729	missense	probably damaging	1.00
R1797:Fam135b	UTSW	15	71452441	missense	probably benign	0.41
R1807:Fam135b	UTSW	15	71463912	missense	probably benign
R1905:Fam135b	UTSW	15	71532987	missense	probably damaging	1.00
R1937:Fam135b	UTSW	15	71622014	missense	probably damaging	1.00
R1998:Fam135b	UTSW	15	71452404	missense	probably damaging	0.98
R2076:Fam135b	UTSW	15	71478243	missense	probably damaging	0.99
R2518:Fam135b	UTSW	15	71463911	missense	probably benign	0.00
R3110:Fam135b	UTSW	15	71464030	missense	probably benign	0.05
R3112:Fam135b	UTSW	15	71464030	missense	probably benign	0.05
R3932:Fam135b	UTSW	15	71450431	missense	probably benign	0.29
R4361:Fam135b	UTSW	15	71490827	missense	probably damaging	1.00
R4397:Fam135b	UTSW	15	71448676	missense	probably benign	0.17
R4435:Fam135b	UTSW	15	71448739	missense	probably damaging	1.00
R4645:Fam135b	UTSW	15	71462340	missense	probably benign
R4740:Fam135b	UTSW	15	71464071	missense	probably benign	0.01
R4748:Fam135b	UTSW	15	71464055	missense	probably benign	0.00
R4754:Fam135b	UTSW	15	71462951	missense	probably benign	0.01
R5044:Fam135b	UTSW	15	71462711	missense	probably benign	0.02
R5469:Fam135b	UTSW	15	71446043	missense	probably benign	0.16
R5617:Fam135b	UTSW	15	71622016	missense	probably damaging	1.00
R5642:Fam135b	UTSW	15	71462136	missense	probably damaging	1.00
R5778:Fam135b	UTSW	15	71479032	missense	probably damaging	1.00
R5891:Fam135b	UTSW	15	71525803	missense	probably damaging	1.00
R5958:Fam135b	UTSW	15	71462895	missense
R5982:Fam135b	UTSW	15	71448669	critical splice donor site	probably null
R5987:Fam135b	UTSW	15	71490848	missense	probably benign	0.00
R6535:Fam135b	UTSW	15	71622075	missense	probably damaging	0.99
R6734:Fam135b	UTSW	15	71462780	missense	probably benign	0.02
R6887:Fam135b	UTSW	15	71463315	missense	probably damaging	1.00
R7028:Fam135b	UTSW	15	71471563	missense	probably damaging	1.00
R7035:Fam135b	UTSW	15	71462253	missense	possibly damaging	0.77
R7097:Fam135b	UTSW	15	71622068	missense	possibly damaging	0.92
R7143:Fam135b	UTSW	15	71479151	missense	probably benign	0.44
R7414:Fam135b	UTSW	15	71478256	missense	probably damaging	0.97
R7439:Fam135b	UTSW	15	71463680	missense	probably damaging	0.98
R7441:Fam135b	UTSW	15	71463680	missense	probably damaging	0.98
R7545:Fam135b	UTSW	15	71450510	missense	possibly damaging	0.95
R7615:Fam135b	UTSW	15	71463323	missense	probably damaging	1.00
R7642:Fam135b	UTSW	15	71479142	missense	possibly damaging	0.51
R7649:Fam135b	UTSW	15	71462580	missense	probably benign	0.00
R7686:Fam135b	UTSW	15	71463384	missense	possibly damaging	0.68
R7866:Fam135b	UTSW	15	71462076	missense	probably benign	0.00
R8006:Fam135b	UTSW	15	71462334	missense	probably benign	0.00
R8068:Fam135b	UTSW	15	71532978	missense	probably damaging	1.00
R8167:Fam135b	UTSW	15	71532991	missense	probably null	1.00
R8252:Fam135b	UTSW	15	71533023	missense	probably benign	0.10
R8548:Fam135b	UTSW	15	71462810	missense	probably damaging	0.99
R8833:Fam135b	UTSW	15	71462934	missense	probably benign	0.04
R8955:Fam135b	UTSW	15	71462214	missense	possibly damaging	0.85
R8961:Fam135b	UTSW	15	71532963	missense	probably damaging	1.00
R8987:Fam135b	UTSW	15	71462340	missense	probably benign	0.00
R9149:Fam135b	UTSW	15	71462895	missense
R9161:Fam135b	UTSW	15	71462568	missense	possibly damaging	0.91
R9227:Fam135b	UTSW	15	71464007	missense	probably benign	0.28
R9230:Fam135b	UTSW	15	71464007	missense	probably benign	0.28
R9365:Fam135b	UTSW	15	71462964	missense	probably benign	0.00
R9622:Fam135b	UTSW	15	71525837	missense	probably damaging	0.98
R9758:Fam135b	UTSW	15	71452350	missense	probably benign	0.28
R9759:Fam135b	UTSW	15	71463840	missense	probably benign	0.44
T0722:Fam135b	UTSW	15	71463885	missense	probably damaging	1.00
T0975:Fam135b	UTSW	15	71463885	missense	probably damaging	1.00
Z1177:Fam135b	UTSW	15	71622076	start codon destroyed	probably null	0.06

Predicted Primers

PCR Primer
(F):5'- TGGGTGTCTTGGAGTACTCATATAC -3'
(R):5'- TCTGTGACTCCAGGATAAGGC -3'

Sequencing Primer
(F):5'- ATACATTCTCAATTCGTTTGTCCTTC -3'
(R):5'- CAGGATAAGGCATATATTCCTCAGC -3'

Posted On

2014-06-23