Mutagenetix > Incidental Mutation

Incidental Mutation 'R0707:Scfd1'

63184

Institutional Source

Beutler Lab

Gene Symbol

Scfd1

Ensembl Gene

ENSMUSG00000020952

Gene Name

Sec1 family domain containing 1

Synonyms

RA410, STXBP1L2, 3110021P21Rik

MMRRC Submission

038890-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.960) question?

Stock #

R0707 (G1)

Quality Score

112

Status

Validated

Chromosome

Chromosomal Location

51424296-51496887 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 51459360 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Methionine at position 307 (K307M)

Ref Sequence

ENSEMBL: ENSMUSP00000151347 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021335] [ENSMUST00000219434]

AlphaFold

Q8BRF7

Predicted Effect

probably damaging
Transcript: ENSMUST00000021335
AA Change: K307M

PolyPhen 2 Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000021335
Gene: ENSMUSG00000020952
AA Change: K307M

Domain	Start	End	E-Value	Type
Pfam:Sec1	41	632	1.6e-109	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000219434
AA Change: K307M

PolyPhen 2 Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)

Meta Mutation Damage Score

0.3023

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.7%
20x: 96.1%

Validation Efficiency

100% (74/74)

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acot11	A	G	4: 106,617,329 (GRCm39)	F259S	probably damaging	Het
Aldh16a1	T	A	7: 44,793,931 (GRCm39)		probably benign	Het
Ankrd24	A	T	10: 81,478,547 (GRCm39)		probably benign	Het
Arhgap5	T	C	12: 52,564,951 (GRCm39)	S641P	probably damaging	Het
Arpp21	A	C	9: 111,986,824 (GRCm39)	S242R	probably benign	Het
Bpifb5	A	G	2: 154,070,820 (GRCm39)	T204A	probably benign	Het
Bud31	A	G	5: 145,083,265 (GRCm39)	Y77C	probably damaging	Het
Ccdc65	G	A	15: 98,607,095 (GRCm39)	V101I	possibly damaging	Het
Ccr7	T	A	11: 99,036,809 (GRCm39)	T38S	probably damaging	Het
Cdc14a	T	C	3: 116,087,362 (GRCm39)		probably benign	Het
Ces2f	C	T	8: 105,677,618 (GRCm39)	H208Y	possibly damaging	Het
Chst1	C	A	2: 92,443,964 (GRCm39)	N145K	possibly damaging	Het
Clock	A	G	5: 76,374,976 (GRCm39)	V731A	possibly damaging	Het
Cog6	C	T	3: 52,921,283 (GRCm39)	V108I	possibly damaging	Het
Cplane1	T	A	15: 8,287,805 (GRCm39)	N2881K	unknown	Het
Crtc2	T	A	3: 90,170,804 (GRCm39)	F626I	probably damaging	Het
Dicer1	A	T	12: 104,673,144 (GRCm39)	F792I	probably damaging	Het
Dnajc13	T	C	9: 104,049,781 (GRCm39)	K1780R	probably benign	Het
Dph5	A	C	3: 115,708,782 (GRCm39)	N155H	probably benign	Het
Dscam	T	C	16: 96,626,982 (GRCm39)		probably null	Het
Etl4	C	A	2: 20,810,382 (GRCm39)		probably benign	Het
Flt3l	T	C	7: 44,785,450 (GRCm39)	S9G	probably benign	Het
Fmnl2	A	G	2: 52,944,498 (GRCm39)	E159G	possibly damaging	Het
Fryl	A	G	5: 73,240,715 (GRCm39)	I1295T	probably benign	Het
G530012D18Rik	CAGAGAGA	CAGAGAGAGA	1: 85,504,945 (GRCm39)		probably null	Het
Gatad2b	T	A	3: 90,263,489 (GRCm39)	S529T	probably benign	Het
Herc6	G	A	6: 57,639,347 (GRCm39)	G905E	possibly damaging	Het
Hhip	T	A	8: 80,724,884 (GRCm39)	N296I	probably damaging	Het
Hmgcr	A	T	13: 96,787,151 (GRCm39)		probably benign	Het
Kalrn	T	G	16: 33,830,951 (GRCm39)	N723H	possibly damaging	Het
Mroh5	T	A	15: 73,662,588 (GRCm39)	Y242F	possibly damaging	Het
Msh3	T	A	13: 92,483,848 (GRCm39)	K258*	probably null	Het
Myo1a	T	C	10: 127,555,732 (GRCm39)		probably benign	Het
Nlrp4f	C	T	13: 65,342,317 (GRCm39)	E443K	probably benign	Het
Nupr2	A	G	5: 129,937,533 (GRCm39)	Y34C	probably damaging	Het
Ociad1	T	C	5: 73,452,255 (GRCm39)		probably benign	Het
Or1af1	A	T	2: 37,110,208 (GRCm39)	K236*	probably null	Het
Or5af2	T	A	11: 58,708,577 (GRCm39)	L248M	probably damaging	Het
Or5b3	A	T	19: 13,388,784 (GRCm39)	M284L	probably benign	Het
Or5p5	A	G	7: 107,414,331 (GRCm39)	D182G	probably damaging	Het
Or6ae1	T	C	7: 139,742,002 (GRCm39)	N287S	probably damaging	Het
P2ry12	C	A	3: 59,124,908 (GRCm39)	V256F	probably damaging	Het
Pcdhb22	T	A	18: 37,651,904 (GRCm39)	I124N	probably damaging	Het
Pcnt	A	G	10: 76,256,375 (GRCm39)	F622L	probably damaging	Het
Pfas	A	T	11: 68,888,863 (GRCm39)	N361K	probably benign	Het
Plod2	T	G	9: 92,487,480 (GRCm39)	L600V	possibly damaging	Het
Pole	T	C	5: 110,446,854 (GRCm39)	Y631H	probably damaging	Het
Proser1	T	C	3: 53,386,197 (GRCm39)	L693P	probably damaging	Het
Ptprd	A	G	4: 75,875,476 (GRCm39)	Y1195H	probably damaging	Het
Rbm27	T	A	18: 42,459,091 (GRCm39)		probably null	Het
Ric8a	A	G	7: 140,437,886 (GRCm39)		probably benign	Het
Rif1	GCCACCA	GCCA	2: 52,000,336 (GRCm39)		probably benign	Het
Rimkla	C	T	4: 119,335,177 (GRCm39)	V69M	probably damaging	Het
Sh2b2	A	G	5: 136,261,117 (GRCm39)	F33S	probably damaging	Het
Smg7	T	G	1: 152,746,508 (GRCm39)		probably null	Het
Srebf1	T	C	11: 60,094,942 (GRCm39)	T486A	probably benign	Het
Strn3	G	A	12: 51,657,187 (GRCm39)	T642I	probably damaging	Het
Syne2	T	C	12: 76,028,837 (GRCm39)		probably null	Het
Syne3	A	G	12: 104,935,619 (GRCm39)	L53P	probably damaging	Het
Tcea1	T	A	1: 4,950,569 (GRCm39)		probably benign	Het
Tmem30b	T	C	12: 73,592,942 (GRCm39)	N58D	probably benign	Het
Tnpo1	A	G	13: 98,991,954 (GRCm39)	Y641H	probably damaging	Het
Trim25	A	T	11: 88,890,564 (GRCm39)	T84S	probably benign	Het
Trip4	A	T	9: 65,746,286 (GRCm39)	F537I	possibly damaging	Het
Uaca	G	A	9: 60,755,900 (GRCm39)		probably benign	Het
Ugt2b34	T	A	5: 87,040,758 (GRCm39)	Y388F	possibly damaging	Het
Vmn2r71	T	C	7: 85,268,640 (GRCm39)	V281A	probably benign	Het
Vps13d	A	T	4: 144,882,502 (GRCm39)	D1030E	probably damaging	Het
Vps8	C	A	16: 21,261,107 (GRCm39)	F82L	probably damaging	Het
Zfp296	A	G	7: 19,313,661 (GRCm39)	D172G	probably benign	Het
Zfp977	C	A	7: 42,229,958 (GRCm39)	C189F	probably damaging	Het

Other mutations in Scfd1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00497:Scfd1	APN	12	51,474,652 (GRCm39)	missense	probably benign	0.01
IGL00640:Scfd1	APN	12	51,436,098 (GRCm39)	missense	probably benign	0.12
IGL01481:Scfd1	APN	12	51,430,903 (GRCm39)	missense	probably damaging	0.99
IGL01585:Scfd1	APN	12	51,462,336 (GRCm39)	missense	probably damaging	1.00
IGL01862:Scfd1	APN	12	51,492,494 (GRCm39)	missense	probably damaging	1.00
IGL02000:Scfd1	APN	12	51,460,900 (GRCm39)	missense	probably benign	0.03
IGL02226:Scfd1	APN	12	51,436,164 (GRCm39)	splice site	probably benign
IGL02327:Scfd1	APN	12	51,436,100 (GRCm39)	missense	possibly damaging	0.81
IGL02503:Scfd1	APN	12	51,469,704 (GRCm39)	missense	possibly damaging	0.90
IGL02585:Scfd1	APN	12	51,433,890 (GRCm39)	missense	probably damaging	0.97
IGL02732:Scfd1	APN	12	51,469,756 (GRCm39)	missense	probably benign	0.01
R0671:Scfd1	UTSW	12	51,459,411 (GRCm39)	missense	probably benign	0.01
R1467:Scfd1	UTSW	12	51,478,281 (GRCm39)	missense	possibly damaging	0.49
R1467:Scfd1	UTSW	12	51,478,281 (GRCm39)	missense	possibly damaging	0.49
R1962:Scfd1	UTSW	12	51,469,769 (GRCm39)	missense	probably benign	0.00
R2173:Scfd1	UTSW	12	51,433,862 (GRCm39)	missense	probably benign	0.22
R2249:Scfd1	UTSW	12	51,462,299 (GRCm39)	missense	possibly damaging	0.48
R3872:Scfd1	UTSW	12	51,438,979 (GRCm39)	missense	probably damaging	0.98
R4080:Scfd1	UTSW	12	51,478,302 (GRCm39)	missense	probably benign
R4356:Scfd1	UTSW	12	51,486,068 (GRCm39)	missense	probably benign	0.00
R4841:Scfd1	UTSW	12	51,436,109 (GRCm39)	missense	probably damaging	0.96
R4842:Scfd1	UTSW	12	51,436,109 (GRCm39)	missense	probably damaging	0.96
R4909:Scfd1	UTSW	12	51,437,195 (GRCm39)	missense	probably benign	0.00
R5004:Scfd1	UTSW	12	51,491,777 (GRCm39)	missense	probably benign	0.03
R5275:Scfd1	UTSW	12	51,462,372 (GRCm39)	missense	probably benign	0.19
R5494:Scfd1	UTSW	12	51,443,522 (GRCm39)	splice site	probably null
R5779:Scfd1	UTSW	12	51,478,312 (GRCm39)	missense	probably benign
R6000:Scfd1	UTSW	12	51,492,457 (GRCm39)	missense	possibly damaging	0.55
R6017:Scfd1	UTSW	12	51,492,461 (GRCm39)	missense	probably damaging	1.00
R6522:Scfd1	UTSW	12	51,478,324 (GRCm39)	missense	probably benign	0.04
R6954:Scfd1	UTSW	12	51,474,729 (GRCm39)	critical splice donor site	probably null
R7748:Scfd1	UTSW	12	51,436,140 (GRCm39)	missense	probably benign	0.21
R7993:Scfd1	UTSW	12	51,492,490 (GRCm39)	missense	probably damaging	1.00
R8122:Scfd1	UTSW	12	51,480,052 (GRCm39)	missense	possibly damaging	0.95
R8353:Scfd1	UTSW	12	51,459,374 (GRCm39)	missense	possibly damaging	0.91
R8453:Scfd1	UTSW	12	51,459,374 (GRCm39)	missense	possibly damaging	0.91
R8890:Scfd1	UTSW	12	51,474,678 (GRCm39)	missense	probably benign
R9284:Scfd1	UTSW	12	51,439,024 (GRCm39)	missense	probably benign	0.00
R9294:Scfd1	UTSW	12	51,440,649 (GRCm39)	missense	possibly damaging	0.76
RF007:Scfd1	UTSW	12	51,469,756 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AGAGATGGGTAGCCACTGCTAGTC -3'
(R):5'- CTTGGGTCACTCAATGACCTCTGTG -3'

Sequencing Primer
(F):5'- GCACAATGAGAGCACGTTTATG -3'
(R):5'- ACTCAATGACCTCTGTGTTGTG -3'

Posted On

2013-07-30