Mutagenetix > Incidental Mutation

Incidental Mutation 'R6377:Scai'

515024

Institutional Source

Beutler Lab

Gene Symbol

Scai

Ensembl Gene

ENSMUSG00000035236

Gene Name

suppressor of cancer cell invasion

Synonyms

A930041I02Rik

MMRRC Submission

044527-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.533) question?

Stock #

R6377 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

38956226-39080746 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 38992340 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 379 (D379E)

Ref Sequence

ENSEMBL: ENSMUSP00000145133 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038874] [ENSMUST00000147433] [ENSMUST00000204093] [ENSMUST00000204500] [ENSMUST00000204404]

AlphaFold

Q8C8N2

Predicted Effect

probably benign
Transcript: ENSMUST00000038874
AA Change: D379E

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

SMART Domains

Protein: ENSMUSP00000037194
Gene: ENSMUSG00000035236
AA Change: D379E

Domain	Start	End	E-Value	Type
Pfam:DUF3550	64	557	6.1e-216	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000131225

Predicted Effect

probably benign
Transcript: ENSMUST00000147433

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000157038

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000203399

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000203872

Predicted Effect

probably benign
Transcript: ENSMUST00000204093
AA Change: D379E

PolyPhen 2 Score 0.024 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000145133
Gene: ENSMUSG00000035236
AA Change: D379E

Domain	Start	End	E-Value	Type
Pfam:DUF3550	64	480	2.5e-177	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000204500

SMART Domains

Protein: ENSMUSP00000144844
Gene: ENSMUSG00000035236

Domain	Start	End	E-Value	Type
Pfam:DUF3550	1	77	3.2e-23	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000204404

Meta Mutation Damage Score

0.0692

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 97.8%

Validation Efficiency

94% (59/63)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a regulator of cell migration. The encoded protein appears to function in the RhoA (ras homolog gene family, member A)-Dia1 (diaphanous homolog 1) signal transduction pathway. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2010]
PHENOTYPE: Homozygous mice of both sexes are sub-fertile owing to compromised meiotic synapsis and homologous recombination-mediated double-strand break DNA repair. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ankib1	A	G	5: 3,743,855 (GRCm39)	S812P	possibly damaging	Het
Atp2c2	A	G	8: 120,453,093 (GRCm39)	E159G	probably benign	Het
Atrn	A	G	2: 130,821,889 (GRCm39)	I861V	probably damaging	Het
Clip1	A	G	5: 123,741,717 (GRCm39)	V1053A	possibly damaging	Het
Cngb1	C	A	8: 95,975,608 (GRCm39)	G629C	probably damaging	Het
Cntn5	A	T	9: 9,743,657 (GRCm39)	F540Y	probably damaging	Het
Cpb1	A	C	3: 20,329,748 (GRCm39)		probably null	Het
Cyp4a14	A	G	4: 115,353,280 (GRCm39)	Y11H	probably benign	Het
Dact2	A	G	17: 14,419,450 (GRCm39)	S103P	probably damaging	Het
Dcstamp	A	T	15: 39,618,317 (GRCm39)	Y242F	probably benign	Het
Drd3	G	T	16: 43,641,670 (GRCm39)	G329*	probably null	Het
Duxf1	T	C	10: 58,059,494 (GRCm39)		probably benign	Het
Dysf	T	A	6: 83,985,945 (GRCm39)	S17T	probably benign	Het
Eno1	A	T	4: 150,333,009 (GRCm39)	K366N	possibly damaging	Het
Ffar2	C	T	7: 30,518,971 (GRCm39)	V190I	probably benign	Het
Fkbp15	T	C	4: 62,242,429 (GRCm39)	T508A	probably damaging	Het
Fndc1	A	G	17: 7,988,567 (GRCm39)	V1165A	unknown	Het
Foxj3	A	T	4: 119,430,945 (GRCm39)		probably null	Het
Gabarap	T	C	11: 69,882,630 (GRCm39)		probably null	Het
Gm19410	T	A	8: 36,270,736 (GRCm39)	L1221*	probably null	Het
Gpat2	G	C	2: 127,273,838 (GRCm39)	G294R	possibly damaging	Het
Igf1r	A	T	7: 67,850,998 (GRCm39)	Y931F	probably benign	Het
Il23r	A	T	6: 67,400,636 (GRCm39)	S565T	probably damaging	Het
Ipo8	A	T	6: 148,717,995 (GRCm39)	Y209*	probably null	Het
Jph2	C	T	2: 163,181,632 (GRCm39)	G511R	probably benign	Het
Khdrbs1	C	A	4: 129,635,890 (GRCm39)	D22Y	probably damaging	Het
Kif5b	A	T	18: 6,212,562 (GRCm39)	L754Q	probably damaging	Het
Ksr1	C	T	11: 78,927,320 (GRCm39)		probably null	Het
L3mbtl4	G	T	17: 69,084,918 (GRCm39)	V610F	probably benign	Het
Lars2	A	G	9: 123,283,825 (GRCm39)	T698A	probably benign	Het
Lonp1	A	G	17: 56,928,961 (GRCm39)	V267A	possibly damaging	Het
Loxhd1	T	A	18: 77,468,128 (GRCm39)	D925E	probably damaging	Het
Lsg1	A	G	16: 30,393,386 (GRCm39)	L187P	possibly damaging	Het
Mki67	A	T	7: 135,298,050 (GRCm39)	V2328E	possibly damaging	Het
Mlh3	A	G	12: 85,315,271 (GRCm39)	I305T	probably damaging	Het
Mtbp	A	G	15: 55,421,016 (GRCm39)	M1V	probably null	Het
Myadml2	C	A	11: 120,538,538 (GRCm39)	C99F	probably benign	Het
Ncbp1	A	G	4: 46,150,703 (GRCm39)	Y185C	probably damaging	Het
Ndufaf7	A	T	17: 79,250,739 (GRCm39)	Q222L	probably null	Het
Nlrp4b	A	T	7: 10,449,339 (GRCm39)	Y147F	probably benign	Het
Or4c11c	C	T	2: 88,661,613 (GRCm39)	R51*	probably null	Het
Pet100	T	C	8: 3,672,370 (GRCm39)	V15A	probably benign	Het
Pot1a	A	G	6: 25,778,869 (GRCm39)	V75A	probably benign	Het
Ptprs	A	T	17: 56,725,935 (GRCm39)	M1043K	probably damaging	Het
Rnf31	A	G	14: 55,832,984 (GRCm39)	T413A	probably damaging	Het
Rsf1	ATGGCG	ATGGCGACGGTGGCG	7: 97,229,111 (GRCm39)		probably benign	Homo
Rsf1	CG	CGACGGCGGTG	7: 97,229,115 (GRCm39)		probably benign	Het
Rubcnl	A	T	14: 75,287,635 (GRCm39)		probably null	Het
Ryr3	A	T	2: 112,462,530 (GRCm39)	C4839S	probably damaging	Het
Scd2	G	T	19: 44,288,198 (GRCm39)	G197*	probably null	Het
Sdr39u1	A	C	14: 56,135,166 (GRCm39)	I259S	probably benign	Het
Slco1a5	A	T	6: 142,187,906 (GRCm39)		probably null	Het
Sp1	A	T	15: 102,339,318 (GRCm39)	T733S	probably benign	Het
Tecta	A	G	9: 42,255,051 (GRCm39)	S1711P	probably damaging	Het
Tedc1	G	T	12: 113,124,975 (GRCm39)	W240L	probably damaging	Het
Trarg1	T	C	11: 76,571,355 (GRCm39)	S124P	probably damaging	Het
Trim50	A	G	5: 135,382,454 (GRCm39)	K102R	probably benign	Het
Utrn	A	G	10: 12,619,827 (GRCm39)	Y278H	probably damaging	Het
Vinac1	T	A	2: 128,878,731 (GRCm39)	D1065V	unknown	Het
Vmn2r109	A	C	17: 20,784,796 (GRCm39)		probably null	Het
Zbed5	T	C	5: 129,932,210 (GRCm39)	S720P	possibly damaging	Het
Zc3h3	A	G	15: 75,711,304 (GRCm39)	S386P	probably damaging	Het
Zscan4-ps1	C	T	7: 10,802,418 (GRCm39)		probably null	Het

Other mutations in Scai

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00434:Scai	APN	2	38,998,406 (GRCm39)	missense	probably damaging	1.00
IGL01366:Scai	APN	2	38,996,973 (GRCm39)	missense	probably benign	0.36
IGL01739:Scai	APN	2	38,984,803 (GRCm39)	splice site	probably benign
IGL02251:Scai	APN	2	38,989,429 (GRCm39)	missense	probably benign	0.01
IGL02274:Scai	APN	2	38,992,329 (GRCm39)	unclassified	probably benign
R0239:Scai	UTSW	2	38,965,054 (GRCm39)	missense	probably benign	0.00
R0239:Scai	UTSW	2	38,965,054 (GRCm39)	missense	probably benign	0.00
R0685:Scai	UTSW	2	38,993,749 (GRCm39)	missense	probably damaging	0.96
R0904:Scai	UTSW	2	38,965,164 (GRCm39)	missense	possibly damaging	0.90
R1655:Scai	UTSW	2	38,970,129 (GRCm39)	missense	possibly damaging	0.79
R1820:Scai	UTSW	2	38,996,990 (GRCm39)	missense	possibly damaging	0.82
R1913:Scai	UTSW	2	38,970,093 (GRCm39)	missense	probably damaging	1.00
R2068:Scai	UTSW	2	39,013,025 (GRCm39)	missense	probably damaging	1.00
R2183:Scai	UTSW	2	38,970,138 (GRCm39)	missense	probably benign	0.00
R3237:Scai	UTSW	2	39,040,326 (GRCm39)	splice site	probably benign
R3933:Scai	UTSW	2	38,965,064 (GRCm39)	missense	probably benign	0.44
R5460:Scai	UTSW	2	38,973,586 (GRCm39)	missense	probably damaging	1.00
R5460:Scai	UTSW	2	38,973,585 (GRCm39)	missense	probably damaging	1.00
R6089:Scai	UTSW	2	38,973,566 (GRCm39)	nonsense	probably null
R6606:Scai	UTSW	2	38,965,147 (GRCm39)	missense	probably benign	0.00
R7034:Scai	UTSW	2	39,011,147 (GRCm39)	missense	probably damaging	1.00
R7037:Scai	UTSW	2	39,080,633 (GRCm39)	missense	probably benign	0.04
R7171:Scai	UTSW	2	38,996,948 (GRCm39)	missense	possibly damaging	0.48
R7451:Scai	UTSW	2	39,015,148 (GRCm39)	missense	probably damaging	1.00
R7737:Scai	UTSW	2	39,013,034 (GRCm39)	missense	probably damaging	0.96
R8856:Scai	UTSW	2	38,996,978 (GRCm39)	missense	probably benign	0.01
R8890:Scai	UTSW	2	39,040,400 (GRCm39)	intron	probably benign
R9040:Scai	UTSW	2	38,965,164 (GRCm39)	missense	probably benign	0.30

Predicted Primers

PCR Primer
(F):5'- CTGATTTCTACAAAGACTTTCAGCC -3'
(R):5'- AAAGACATCGGTGTTCCCC -3'

Sequencing Primer
(F):5'- CGACACATTTGACAAATATGATAGGG -3'
(R):5'- ACATCGGTGTTCCCCCACAG -3'

Posted On

2018-05-04