Mutagenetix > Incidental Mutation

Incidental Mutation 'R2878:Accsl'

260161

Institutional Source

Beutler Lab

Gene Symbol

Accsl

Ensembl Gene

ENSMUSG00000075023

Gene Name

1-aminocyclopropane-1-carboxylate synthase (inactive)-like

Synonyms

MMRRC Submission

040466-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

R2878 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

93685706-93699502 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 93689755 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 384 (M384K)

Ref Sequence

ENSEMBL: ENSMUSP00000097281 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099690]

AlphaFold

Q3UX83

Predicted Effect

probably damaging
Transcript: ENSMUST00000099690
AA Change: M384K

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000097281
Gene: ENSMUSG00000075023
AA Change: M384K

Domain	Start	End	E-Value	Type
low complexity region	37	48	N/A	INTRINSIC
Pfam:Aminotran_1_2	190	568	6.9e-53	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129248

Predicted Effect

probably benign
Transcript: ENSMUST00000132722

SMART Domains

Protein: ENSMUSP00000121623
Gene: ENSMUSG00000075023

Domain	Start	End	E-Value	Type
SCOP:d1gdea_	2	79	4e-10	SMART
PDB:1IAY\|A	16	58	3e-6	PDB

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141561

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151579

Meta Mutation Damage Score

0.3568

Coding Region Coverage

1x: 99.1%
3x: 98.6%
10x: 97.3%
20x: 95.2%

Validation Efficiency

92% (58/63)

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	C	T	11: 9,241,889 (GRCm39)	L1251F	possibly damaging	Het
Adgrg7	A	G	16: 56,570,817 (GRCm39)	F404L	probably benign	Het
Akr1c20	G	A	13: 4,557,774 (GRCm39)	T251M	probably damaging	Het
Amph	G	A	13: 19,288,437 (GRCm39)	V309I	possibly damaging	Het
Ano2	T	G	6: 125,840,481 (GRCm39)	F384C	probably damaging	Het
Aplf	G	A	6: 87,645,409 (GRCm39)	R32*	probably null	Het
Arhgef18	A	G	8: 3,482,759 (GRCm39)	M155V	probably benign	Het
Atg2b	A	T	12: 105,630,268 (GRCm39)	Y374*	probably null	Het
Camkmt	T	C	17: 85,738,979 (GRCm39)		probably benign	Het
Capn2	T	A	1: 182,344,798 (GRCm39)	E41V	probably benign	Het
Cd53	T	C	3: 106,674,732 (GRCm39)	T112A	probably benign	Het
Cyp2a4	G	A	7: 26,011,612 (GRCm39)	E278K	possibly damaging	Het
Dact2	A	T	17: 14,416,176 (GRCm39)	S675T	probably damaging	Het
Dync1li2	A	C	8: 105,156,047 (GRCm39)	Y265D	probably damaging	Het
Eml4	T	A	17: 83,717,603 (GRCm39)	H58Q	probably benign	Het
F13b	T	C	1: 139,429,485 (GRCm39)	M1T	probably null	Het
Fam83b	A	G	9: 76,398,092 (GRCm39)	F1004L	probably damaging	Het
Fbxo48	A	G	11: 16,903,382 (GRCm39)	K3E	possibly damaging	Het
Fbxw13	A	G	9: 109,010,534 (GRCm39)	F368S	probably damaging	Het
Fbxw19	A	T	9: 109,315,038 (GRCm39)	W175R	probably damaging	Het
Fibcd1	G	A	2: 31,728,678 (GRCm39)	P60S	probably benign	Het
Fscb	A	T	12: 64,519,348 (GRCm39)	V706E	unknown	Het
Gfm2	A	G	13: 97,289,757 (GRCm39)	R181G	possibly damaging	Het
Gm17546	A	T	15: 95,727,805 (GRCm39)		probably benign	Het
Grin1	A	G	2: 25,187,641 (GRCm39)	V594A	probably damaging	Het
Itpripl1	A	G	2: 126,983,534 (GRCm39)	V196A	probably benign	Het
Kcns1	A	G	2: 164,006,682 (GRCm39)	I427T	probably damaging	Het
Map3k19	T	A	1: 127,751,530 (GRCm39)	E607V	possibly damaging	Het
Map3k4	T	C	17: 12,482,954 (GRCm39)	S588G	probably benign	Het
Mslnl	G	A	17: 25,961,908 (GRCm39)	V128M	probably damaging	Het
Naa80	A	T	9: 107,460,367 (GRCm39)	E87D	possibly damaging	Het
Nebl	C	A	2: 17,439,740 (GRCm39)	D178Y	probably damaging	Het
Nfatc3	C	A	8: 106,818,776 (GRCm39)	T498K	probably damaging	Het
Nfkb2	G	A	19: 46,295,880 (GRCm39)	R158H	possibly damaging	Het
Obscn	T	C	11: 58,947,014 (GRCm39)	E4337G	possibly damaging	Het
Or5b106	A	G	19: 13,123,771 (GRCm39)	L84P	probably benign	Het
Palb2	A	G	7: 121,713,652 (GRCm39)	V877A	probably damaging	Het
Rbm6	T	C	9: 107,729,649 (GRCm39)	E333G	probably damaging	Het
Rem2	A	G	14: 54,713,819 (GRCm39)	T31A	possibly damaging	Het
Ric1	A	G	19: 29,579,730 (GRCm39)	D1224G	possibly damaging	Het
Rp1	A	G	1: 4,418,362 (GRCm39)	S917P	probably damaging	Het
Scn2a	G	A	2: 65,518,715 (GRCm39)	G363D	probably damaging	Het
Shcbp1l	A	T	1: 153,313,264 (GRCm39)		probably benign	Het
Skor2	G	T	18: 76,948,419 (GRCm39)	E714*	probably null	Het
Slc15a1	T	A	14: 121,703,345 (GRCm39)	K545N	probably benign	Het
Slc1a2	T	A	2: 102,591,512 (GRCm39)	M414K	probably damaging	Het
Slc7a8	A	G	14: 54,997,143 (GRCm39)	S70P	probably damaging	Het
Spopfm1	G	T	3: 94,173,787 (GRCm39)	C265F	possibly damaging	Het
Taf1a	A	G	1: 183,179,173 (GRCm39)	E117G	probably damaging	Het
Trem2	A	G	17: 48,658,141 (GRCm39)	D135G	probably benign	Het
Ttn	T	C	2: 76,567,409 (GRCm39)	D27828G	probably damaging	Het
Ulk4	T	C	9: 121,089,105 (GRCm39)	D258G	probably benign	Het
Unc80	TGTATTCCAGGCG	TG	1: 66,710,735 (GRCm39)		probably benign	Het
Vmn2r56	A	C	7: 12,444,954 (GRCm39)	M433R	probably benign	Het
Wdr45	C	T	X: 7,593,611 (GRCm39)	P271S	probably damaging	Het
Zfp410	A	C	12: 84,378,411 (GRCm39)	N245T	probably damaging	Het

Other mutations in Accsl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02336:Accsl	APN	2	93,696,253 (GRCm39)	missense	possibly damaging	0.46
IGL02511:Accsl	APN	2	93,692,111 (GRCm39)	unclassified	probably benign
IGL03248:Accsl	APN	2	93,693,129 (GRCm39)	unclassified	probably benign
IGL03338:Accsl	APN	2	93,686,092 (GRCm39)	missense	probably benign	0.34
R0323:Accsl	UTSW	2	93,691,425 (GRCm39)	missense	probably benign	0.27
R0449:Accsl	UTSW	2	93,696,419 (GRCm39)	missense	probably benign	0.00
R1172:Accsl	UTSW	2	93,696,589 (GRCm39)	splice site	probably benign
R1173:Accsl	UTSW	2	93,696,589 (GRCm39)	splice site	probably benign
R1175:Accsl	UTSW	2	93,696,589 (GRCm39)	splice site	probably benign
R1752:Accsl	UTSW	2	93,688,375 (GRCm39)	missense	probably damaging	1.00
R1952:Accsl	UTSW	2	93,689,778 (GRCm39)	missense	probably damaging	1.00
R2877:Accsl	UTSW	2	93,689,755 (GRCm39)	missense	probably damaging	0.99
R4472:Accsl	UTSW	2	93,694,337 (GRCm39)	splice site	probably null
R4472:Accsl	UTSW	2	93,694,336 (GRCm39)	critical splice acceptor site	probably null
R5400:Accsl	UTSW	2	93,689,767 (GRCm39)	missense	probably damaging	0.99
R5502:Accsl	UTSW	2	93,687,289 (GRCm39)	critical splice donor site	probably null
R5610:Accsl	UTSW	2	93,692,118 (GRCm39)	critical splice donor site	probably null
R5636:Accsl	UTSW	2	93,699,370 (GRCm39)	missense	probably benign	0.41
R5799:Accsl	UTSW	2	93,694,748 (GRCm39)	splice site	probably null
R6376:Accsl	UTSW	2	93,687,343 (GRCm39)	missense	probably damaging	1.00
R6913:Accsl	UTSW	2	93,696,488 (GRCm39)	missense	possibly damaging	0.66
R7311:Accsl	UTSW	2	93,696,160 (GRCm39)	missense	possibly damaging	0.51
R7564:Accsl	UTSW	2	93,688,501 (GRCm39)	missense	possibly damaging	0.83
R7731:Accsl	UTSW	2	93,691,363 (GRCm39)	missense	probably benign	0.01
R7835:Accsl	UTSW	2	93,696,329 (GRCm39)	nonsense	probably null
R8184:Accsl	UTSW	2	93,686,086 (GRCm39)	missense	probably benign	0.19
R8305:Accsl	UTSW	2	93,696,423 (GRCm39)	missense	probably benign	0.00
R8824:Accsl	UTSW	2	93,693,195 (GRCm39)	missense	probably damaging	1.00
R8868:Accsl	UTSW	2	93,696,490 (GRCm39)	missense	probably benign	0.00
R8954:Accsl	UTSW	2	93,688,299 (GRCm39)	missense	probably benign	0.06
R9172:Accsl	UTSW	2	93,691,833 (GRCm39)	missense	probably damaging	1.00
R9473:Accsl	UTSW	2	93,686,092 (GRCm39)	missense	probably benign	0.03
R9513:Accsl	UTSW	2	93,699,498 (GRCm39)	unclassified	probably benign
Z1088:Accsl	UTSW	2	93,696,293 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ACTTGGACTCCACACTCTCG -3'
(R):5'- ACCATGCAGAGAGTGTAAGC -3'

Sequencing Primer
(F):5'- TCCACACTCTCGAGAGCAGTG -3'
(R):5'- CATAGGCTTGGGCTCACAGAC -3'

Posted On

2015-01-23