Mutagenetix > Incidental Mutation

Incidental Mutation 'R4690:Sh3rf3'

354853

Institutional Source

Beutler Lab

Gene Symbol

Sh3rf3

Ensembl Gene

ENSMUSG00000037990

Gene Name

SH3 domain containing ring finger 3

Synonyms

Sh3md4, 4831416G18Rik

MMRRC Submission

041941-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.121) question?

Stock #

R4690 (G1)

Quality Score

202

Status

Validated

Chromosome

Chromosomal Location

58649181-58974738 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 58649526 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 44 (S44P)

Ref Sequence

ENSEMBL: ENSMUSP00000120938 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000135526] [ENSMUST00000153031]

AlphaFold

Q8C120

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000069768

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133151

Predicted Effect

possibly damaging
Transcript: ENSMUST00000135526
AA Change: S44P

PolyPhen 2 Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000114368
Gene: ENSMUSG00000037990
AA Change: S44P

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
RING	52	92	2.76e-7	SMART
low complexity region	119	152	N/A	INTRINSIC
low complexity region	161	170	N/A	INTRINSIC
SH3	190	245	8.24e-18	SMART
SH3	252	311	5.56e-15	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000153031
AA Change: S44P

PolyPhen 2 Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000120938
Gene: ENSMUSG00000037990
AA Change: S44P

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
RING	52	92	2.76e-7	SMART
low complexity region	119	152	N/A	INTRINSIC
low complexity region	161	170	N/A	INTRINSIC
SH3	190	245	8.24e-18	SMART
SH3	252	311	5.56e-15	SMART
SH3	461	518	1.43e-17	SMART
low complexity region	707	739	N/A	INTRINSIC
SH3	822	878	5.19e-15	SMART

Meta Mutation Damage Score

0.0698

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.9%
20x: 94.5%

Validation Efficiency

98% (89/91)

Allele List at MGI

Other mutations in this stock

Total: 85 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	A	G	11: 110,039,706 (GRCm39)	F436L	probably damaging	Het
Adam28	G	T	14: 68,879,497 (GRCm39)	Q184K	probably benign	Het
Adh6a	A	G	3: 138,031,932 (GRCm39)	T275A	possibly damaging	Het
Agap2	A	G	10: 126,927,244 (GRCm39)	D1082G	possibly damaging	Het
Alox5	A	T	6: 116,400,150 (GRCm39)	V263E	probably damaging	Het
Arhgef16	C	T	4: 154,372,420 (GRCm39)		probably null	Het
Bspry	G	A	4: 62,404,762 (GRCm39)	R186Q	probably damaging	Het
Ccdc188	T	A	16: 18,036,159 (GRCm39)	H111Q	probably damaging	Het
Cd40	T	C	2: 164,911,615 (GRCm39)	F209S	possibly damaging	Het
Cfap43	C	A	19: 47,736,298 (GRCm39)	V1398L	probably benign	Het
Cln3	A	T	7: 126,174,565 (GRCm39)	I286N	possibly damaging	Het
Col9a1	T	C	1: 24,263,787 (GRCm39)		probably null	Het
Cpne9	A	G	6: 113,279,016 (GRCm39)	E470G	probably damaging	Het
Cul5	A	T	9: 53,534,171 (GRCm39)	W654R	probably damaging	Het
Cyp2a22	T	A	7: 26,638,634 (GRCm39)	K51*	probably null	Het
Dcaf10	G	A	4: 45,372,769 (GRCm39)	R394Q	possibly damaging	Het
Dot1l	C	A	10: 80,622,016 (GRCm39)	S556*	probably null	Het
Eif3d	A	T	15: 77,851,516 (GRCm39)	M98K	probably benign	Het
Fiz1	A	G	7: 5,012,167 (GRCm39)	V117A	probably benign	Het
Fryl	A	G	5: 73,257,636 (GRCm39)	V722A	probably benign	Het
Ftdc1	G	A	16: 58,434,333 (GRCm39)	T128I	probably benign	Het
Gm3095	G	T	14: 3,964,471 (GRCm38)	R63I	probably benign	Het
Gm7133	A	T	1: 97,197,224 (GRCm39)		noncoding transcript	Het
Hoxb8	A	T	11: 96,175,286 (GRCm39)	D241V	probably benign	Het
Hrnr	A	G	3: 93,230,959 (GRCm39)	Q399R	unknown	Het
Itpk1	A	T	12: 102,572,434 (GRCm39)	V93D	probably damaging	Het
Kars1	C	T	8: 112,729,216 (GRCm39)	A164T	probably benign	Het
Kcnq4	A	T	4: 120,574,208 (GRCm39)	I150N	probably damaging	Het
Kcnrg	A	T	14: 61,849,176 (GRCm39)	L212F	probably damaging	Het
Kif5b	A	T	18: 6,216,759 (GRCm39)	D521E	probably benign	Het
Klf11	C	T	12: 24,705,071 (GRCm39)	T158M	probably damaging	Het
Klhl6	T	C	16: 19,776,034 (GRCm39)	I175V	probably benign	Het
Lsm1	A	G	8: 26,283,708 (GRCm39)	N40S	probably damaging	Het
Map1b	T	C	13: 99,567,576 (GRCm39)	E1715G	unknown	Het
Mecom	C	A	3: 30,292,459 (GRCm39)	A4S	probably benign	Het
Muc5b	G	A	7: 141,396,031 (GRCm39)	V96M	unknown	Het
Mug2	A	T	6: 122,013,255 (GRCm39)	I341L	probably benign	Het
Mxra7	A	T	11: 116,707,078 (GRCm39)		probably null	Het
Myo5a	T	C	9: 75,061,105 (GRCm39)	L537P	probably damaging	Het
Myo5b	A	T	18: 74,855,533 (GRCm39)	N1241Y	probably damaging	Het
Naa16	T	C	14: 79,582,497 (GRCm39)	R531G	probably damaging	Het
Neb	T	A	2: 52,134,087 (GRCm39)	M3299L	probably benign	Het
Nlrp4b	T	A	7: 10,453,130 (GRCm39)	Y76N	probably benign	Het
Nmral1	T	C	16: 4,534,205 (GRCm39)	T79A	probably damaging	Het
Noct	C	T	3: 51,155,300 (GRCm39)	Q23*	probably null	Het
Nrxn1	A	T	17: 90,344,509 (GRCm39)	V438D	probably damaging	Het
Or5b109	A	C	19: 13,212,132 (GRCm39)	N173H	possibly damaging	Het
Or5m9	T	A	2: 85,877,242 (GRCm39)	C139S	probably damaging	Het
Oxct2a	T	C	4: 123,216,836 (GRCm39)	T182A	probably benign	Het
Pank2	T	C	2: 131,115,945 (GRCm39)	I121T	probably damaging	Het
Pcdh1	T	A	18: 38,336,528 (GRCm39)	T36S	probably benign	Het
Pfdn1	A	T	18: 36,584,133 (GRCm39)	M67K	possibly damaging	Het
Plec	T	C	15: 76,058,456 (GRCm39)	E3849G	probably damaging	Het
Polr3a	A	T	14: 24,514,349 (GRCm39)	S817T	possibly damaging	Het
Pomgnt1	T	A	4: 116,012,707 (GRCm39)	D401E	probably damaging	Het
Ppp1r13b	T	A	12: 111,798,992 (GRCm39)	D891V	probably damaging	Het
Prr14l	A	G	5: 33,001,500 (GRCm39)		probably benign	Het
Ptk2b	A	G	14: 66,410,749 (GRCm39)		probably null	Het
Rab13	G	C	3: 90,128,330 (GRCm39)		probably null	Het
Rexo1	C	T	10: 80,382,255 (GRCm39)	A751T	probably benign	Het
Rfx1	T	C	8: 84,809,374 (GRCm39)	V233A	possibly damaging	Het
Rnf149	C	T	1: 39,616,295 (GRCm39)		probably benign	Het
Rrm1	A	G	7: 102,097,086 (GRCm39)	D122G	probably benign	Het
Serpina1b	A	G	12: 103,698,639 (GRCm39)	F70S	probably damaging	Het
Serpinb13	C	T	1: 106,910,574 (GRCm39)	S66L	probably damaging	Het
Shroom1	A	G	11: 53,356,549 (GRCm39)	T471A	possibly damaging	Het
Slc6a1	A	G	6: 114,279,792 (GRCm39)	Y152C	probably damaging	Het
Spata31f3	T	A	4: 42,873,032 (GRCm39)		probably null	Het
Spata6	A	T	4: 111,632,023 (GRCm39)	T145S	probably damaging	Het
Srcap	G	A	7: 127,137,186 (GRCm39)	G956D	probably damaging	Het
Ssh2	A	T	11: 77,346,031 (GRCm39)	I1339F	possibly damaging	Het
Tardbp	A	T	4: 148,697,078 (GRCm39)	*99K	probably null	Het
Tbc1d22a	A	G	15: 86,196,037 (GRCm39)	Y336C	probably damaging	Het
Tmcc3	G	A	10: 94,381,419 (GRCm39)		probably benign	Het
Tmem178b	T	G	6: 40,222,547 (GRCm39)	D87E	probably benign	Het
Tmem184a	A	C	5: 139,791,377 (GRCm39)	S380A	probably benign	Het
Tnfaip2	A	G	12: 111,411,682 (GRCm39)	K84R	possibly damaging	Het
Tpgs1	A	G	10: 79,511,235 (GRCm39)	T126A	probably benign	Het
Traf3ip1	A	G	1: 91,447,834 (GRCm39)	E437G	possibly damaging	Het
Trpc4ap	C	T	2: 155,477,053 (GRCm39)	C755Y	probably damaging	Het
Tsfm	A	G	10: 126,866,547 (GRCm39)		probably benign	Het
Tulp1	A	C	17: 28,570,811 (GRCm39)		probably benign	Het
Vmn1r23	A	T	6: 57,903,010 (GRCm39)	M256K	probably benign	Het
Zdhhc8	T	C	16: 18,044,605 (GRCm39)	D305G	probably damaging	Het
Zfp326	G	A	5: 106,054,942 (GRCm39)	R282H	probably damaging	Het

Other mutations in Sh3rf3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00596:Sh3rf3	APN	10	58,885,178 (GRCm39)	missense	probably benign	0.06
IGL01898:Sh3rf3	APN	10	58,885,352 (GRCm39)	missense	probably damaging	0.99
IGL02108:Sh3rf3	APN	10	58,971,650 (GRCm39)	missense	probably damaging	1.00
IGL02148:Sh3rf3	APN	10	58,922,562 (GRCm39)	missense	probably benign	0.02
exasperated	UTSW	10	58,922,646 (GRCm39)	missense	probably benign	0.06
strained	UTSW	10	58,842,925 (GRCm39)	missense	probably damaging	1.00
R0421:Sh3rf3	UTSW	10	58,819,897 (GRCm39)	missense	probably damaging	1.00
R1056:Sh3rf3	UTSW	10	58,842,904 (GRCm39)	missense	probably damaging	1.00
R1313:Sh3rf3	UTSW	10	58,907,821 (GRCm39)	missense	possibly damaging	0.92
R1313:Sh3rf3	UTSW	10	58,907,821 (GRCm39)	missense	possibly damaging	0.92
R1615:Sh3rf3	UTSW	10	58,966,899 (GRCm39)	missense	probably benign	0.02
R1797:Sh3rf3	UTSW	10	58,922,489 (GRCm39)	nonsense	probably null
R1869:Sh3rf3	UTSW	10	58,919,335 (GRCm39)	missense	probably damaging	1.00
R1924:Sh3rf3	UTSW	10	58,939,989 (GRCm39)	splice site	probably benign
R1968:Sh3rf3	UTSW	10	58,649,809 (GRCm39)	missense	probably benign	0.32
R2353:Sh3rf3	UTSW	10	58,842,895 (GRCm39)	missense	probably damaging	1.00
R3617:Sh3rf3	UTSW	10	58,922,685 (GRCm39)	missense	possibly damaging	0.83
R3769:Sh3rf3	UTSW	10	58,820,013 (GRCm39)	missense	probably benign	0.07
R4059:Sh3rf3	UTSW	10	58,919,355 (GRCm39)	missense	probably damaging	1.00
R4425:Sh3rf3	UTSW	10	58,919,398 (GRCm39)	missense	probably benign	0.00
R4832:Sh3rf3	UTSW	10	58,649,905 (GRCm39)	missense	probably benign	0.19
R4853:Sh3rf3	UTSW	10	58,919,341 (GRCm39)	missense	probably damaging	1.00
R4854:Sh3rf3	UTSW	10	58,649,545 (GRCm39)	missense	possibly damaging	0.93
R4917:Sh3rf3	UTSW	10	58,842,925 (GRCm39)	missense	probably damaging	1.00
R4918:Sh3rf3	UTSW	10	58,842,925 (GRCm39)	missense	probably damaging	1.00
R4995:Sh3rf3	UTSW	10	58,922,646 (GRCm39)	missense	probably benign	0.06
R5125:Sh3rf3	UTSW	10	58,967,012 (GRCm39)	missense	probably benign	0.14
R5640:Sh3rf3	UTSW	10	58,649,769 (GRCm39)	missense	probably benign
R5716:Sh3rf3	UTSW	10	58,967,105 (GRCm39)	missense	probably benign	0.03
R5756:Sh3rf3	UTSW	10	58,940,204 (GRCm39)	missense	probably damaging	0.98
R5848:Sh3rf3	UTSW	10	58,819,975 (GRCm39)	missense	possibly damaging	0.54
R5908:Sh3rf3	UTSW	10	58,885,270 (GRCm39)	missense	probably benign	0.32
R5930:Sh3rf3	UTSW	10	58,966,808 (GRCm39)	missense	probably damaging	1.00
R6036:Sh3rf3	UTSW	10	58,649,806 (GRCm39)	missense	probably benign	0.19
R6036:Sh3rf3	UTSW	10	58,649,806 (GRCm39)	missense	probably benign	0.19
R6392:Sh3rf3	UTSW	10	58,842,898 (GRCm39)	missense	probably damaging	0.97
R6450:Sh3rf3	UTSW	10	58,819,966 (GRCm39)	missense	probably damaging	1.00
R6470:Sh3rf3	UTSW	10	58,819,791 (GRCm39)	missense	probably damaging	1.00
R6639:Sh3rf3	UTSW	10	58,919,289 (GRCm39)	missense	probably damaging	1.00
R6685:Sh3rf3	UTSW	10	58,922,663 (GRCm39)	missense	possibly damaging	0.95
R7292:Sh3rf3	UTSW	10	58,907,795 (GRCm39)	missense	probably damaging	1.00
R7789:Sh3rf3	UTSW	10	58,922,637 (GRCm39)	missense	probably benign	0.01
R7941:Sh3rf3	UTSW	10	58,842,883 (GRCm39)	missense	probably damaging	0.99
R7959:Sh3rf3	UTSW	10	58,842,925 (GRCm39)	missense	probably damaging	1.00
R8140:Sh3rf3	UTSW	10	58,885,177 (GRCm39)	missense	possibly damaging	0.88
R8142:Sh3rf3	UTSW	10	58,885,205 (GRCm39)	nonsense	probably null
R8241:Sh3rf3	UTSW	10	58,940,242 (GRCm39)	missense	probably benign	0.11
R8406:Sh3rf3	UTSW	10	58,919,407 (GRCm39)	missense	probably damaging	1.00
R8725:Sh3rf3	UTSW	10	58,939,992 (GRCm39)	critical splice acceptor site	probably null
R8727:Sh3rf3	UTSW	10	58,939,992 (GRCm39)	critical splice acceptor site	probably null
R9341:Sh3rf3	UTSW	10	58,966,802 (GRCm39)	missense	probably damaging	0.99
R9343:Sh3rf3	UTSW	10	58,966,802 (GRCm39)	missense	probably damaging	0.99
RF020:Sh3rf3	UTSW	10	58,649,590 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GTTTATTGACGGCGACTGC -3'
(R):5'- GCACTAGCAGTATGTTGGCG -3'

Sequencing Primer
(F):5'- CTCTGGCTGCTAGACTTAGGC -3'
(R):5'- CAGTATGTTGGCGGGCAG -3'

Posted On

2015-10-21