Mutagenetix > Incidental Mutation

Incidental Mutation 'R9257:Als2cl'

701956

Institutional Source

Beutler Lab

Gene Symbol

Als2cl

Ensembl Gene

ENSMUSG00000044037

Gene Name

ALS2 C-terminal like

Synonyms

D930044G19Rik, mRn.49018

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.106) question?

Stock #

R9257 (G1)

Quality Score

112.008

Status

Not validated

Chromosome

Chromosomal Location

110709203-110729598 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 110723755 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 717 (V717E)

Ref Sequence

ENSEMBL: ENSMUSP00000081989 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000084926] [ENSMUST00000130386] [ENSMUST00000155014]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000084926
AA Change: V717E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000081989
Gene: ENSMUSG00000044037
AA Change: V717E

Domain	Start	End	E-Value	Type
SCOP:d1by1a_	8	215	2e-3	SMART
Blast:PH	220	318	8e-7	BLAST
MORN	356	377	1.83e-3	SMART
Pfam:MORN	381	397	4.5e-4	PFAM
MORN	407	428	1.2e1	SMART
MORN	430	451	3.71e-1	SMART
MORN	457	478	4.33e-1	SMART
MORN	481	502	3.18e-1	SMART
MORN	504	525	1.68e0	SMART
MORN	527	549	3.63e1	SMART
Pfam:VPS9	833	937	1.3e-20	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000130386
AA Change: V717E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000123304
Gene: ENSMUSG00000044037
AA Change: V717E

Domain	Start	End	E-Value	Type
SCOP:d1by1a_	8	215	2e-3	SMART
Blast:PH	220	318	8e-7	BLAST
MORN	356	377	1.83e-3	SMART
Pfam:MORN	381	397	4.5e-4	PFAM
MORN	407	428	1.2e1	SMART
MORN	430	451	3.71e-1	SMART
MORN	457	478	4.33e-1	SMART
MORN	481	502	3.18e-1	SMART
MORN	504	525	1.68e0	SMART
MORN	527	549	3.63e1	SMART
Pfam:VPS9	833	937	1.3e-20	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000155014
AA Change: V717E

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000115718
Gene: ENSMUSG00000044037
AA Change: V717E

Domain	Start	End	E-Value	Type
SCOP:d1by1a_	8	215	2e-3	SMART
Blast:PH	220	318	8e-7	BLAST
MORN	356	377	1.83e-3	SMART
Pfam:MORN	381	399	5.6e-4	PFAM
MORN	407	428	1.2e1	SMART
MORN	430	451	3.71e-1	SMART
MORN	457	478	4.33e-1	SMART
MORN	481	502	3.18e-1	SMART
MORN	504	525	1.68e0	SMART
MORN	527	549	3.63e1	SMART
Pfam:VPS9	833	937	1.7e-22	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 97.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921509C19Rik	T	A	2: 151,315,627 (GRCm39)	D17V	probably benign	Het
9130401M01Rik	A	C	15: 57,892,414 (GRCm39)	H128Q	possibly damaging	Het
Abcd2	T	C	15: 91,075,315 (GRCm39)	Y166C	possibly damaging	Het
Adamtsl4	C	A	3: 95,588,575 (GRCm39)	V546F	probably damaging	Het
Atm	A	G	9: 53,407,150 (GRCm39)		probably null	Het
Atp2c1	C	A	9: 105,291,851 (GRCm39)	E904*	probably null	Het
Ccdc88c	G	A	12: 100,889,474 (GRCm39)	S1523F	possibly damaging	Het
Cds1	A	T	5: 101,963,751 (GRCm39)	I357F	probably benign	Het
Cilp	T	A	9: 65,174,451 (GRCm39)	V13D	possibly damaging	Het
Copz2	A	G	11: 96,748,386 (GRCm39)	D180G	possibly damaging	Het
Cpsf1	C	T	15: 76,484,992 (GRCm39)	E546K	probably benign	Het
Ctsm	T	C	13: 61,684,413 (GRCm39)	N320D	probably damaging	Het
Fat3	G	A	9: 15,907,863 (GRCm39)	T2713I	probably benign	Het
Fcrl5	T	A	3: 87,343,195 (GRCm39)	S2T	probably benign	Het
Fgfr4	T	C	13: 55,315,974 (GRCm39)	S796P	unknown	Het
Flrt3	A	G	2: 140,502,159 (GRCm39)	F490L	probably benign	Het
Fras1	A	T	5: 96,910,359 (GRCm39)	I3263F	probably damaging	Het
Hydin	A	T	8: 111,301,648 (GRCm39)	D3793V	probably damaging	Het
Kif5c	T	A	2: 49,590,604 (GRCm39)	L269*	probably null	Het
Klhl32	A	G	4: 24,649,608 (GRCm39)	V396A	probably benign	Het
Krt1c	C	T	15: 101,724,926 (GRCm39)	R228Q	probably benign	Het
Lcn9	T	C	2: 25,714,784 (GRCm39)		probably null	Het
Lingo4	A	C	3: 94,310,676 (GRCm39)	D538A	probably benign	Het
Lonp1	G	T	17: 56,927,516 (GRCm39)	Y299*	probably null	Het
Mettl16	T	A	11: 74,708,127 (GRCm39)	V442D	possibly damaging	Het
Mettl25b	G	T	3: 87,831,768 (GRCm39)	Q397K	probably benign	Het
Mis18bp1	A	G	12: 65,180,631 (GRCm39)	V950A	probably benign	Het
Mndal	A	T	1: 173,690,274 (GRCm39)	V352E	probably damaging	Het
Mrpl55	T	C	11: 59,096,578 (GRCm39)	V117A	probably benign	Het
Muc6	T	A	7: 141,226,738 (GRCm39)	S1430C	unknown	Het
Myh11	C	A	16: 14,087,120 (GRCm39)	G119C		Het
Myorg	T	C	4: 41,499,030 (GRCm39)	D200G	probably benign	Het
Neu1	A	G	17: 35,150,396 (GRCm39)	D5G	probably benign	Het
Nrcam	T	A	12: 44,610,837 (GRCm39)	D512E	probably benign	Het
Nup214	T	G	2: 31,923,347 (GRCm39)	V1292G	possibly damaging	Het
Nwd1	T	A	8: 73,397,566 (GRCm39)	L602M	probably damaging	Het
Or6c3b	C	A	10: 129,527,003 (GRCm39)	L302F	probably benign	Het
Pck2	G	T	14: 55,782,702 (GRCm39)	G379W	probably damaging	Het
Per2	C	T	1: 91,376,445 (GRCm39)	V143M	probably damaging	Het
Pfkl	A	T	10: 77,825,489 (GRCm39)	Y634N	probably damaging	Het
Phlpp1	A	G	1: 106,100,281 (GRCm39)	D183G	possibly damaging	Het
Pkdrej	T	A	15: 85,700,098 (GRCm39)	Y1946F	probably damaging	Het
Plxna4	C	T	6: 32,139,018 (GRCm39)	D1717N	probably damaging	Het
Ppp1r14bl	G	T	1: 23,141,275 (GRCm39)	T13N	probably benign	Het
Pramel23	T	A	4: 143,425,685 (GRCm39)	D86V	probably damaging	Het
Prdm16	A	T	4: 154,422,155 (GRCm39)	V879E	probably damaging	Het
Prr23a3	T	C	9: 98,747,298 (GRCm39)	V84A	probably benign	Het
Ptp4a1	A	G	1: 30,985,346 (GRCm39)		probably benign	Het
Rhbdf1	T	C	11: 32,160,754 (GRCm39)	H634R	probably benign	Het
Rmi2	T	C	16: 10,653,089 (GRCm39)	S46P	probably benign	Het
Rsf1	A	T	7: 97,334,918 (GRCm39)	E1350D		Het
Slc6a6	T	A	6: 91,716,952 (GRCm39)	F276Y	possibly damaging	Het
Sppl3	A	G	5: 115,221,532 (GRCm39)	Y120C	probably benign	Het
Stard13	G	T	5: 150,985,956 (GRCm39)	A518E	probably benign	Het
Taf2	A	T	15: 54,929,409 (GRCm39)	V49E	possibly damaging	Het
Tas2r140	T	A	6: 40,468,592 (GRCm39)	W141R	probably damaging	Het
Tlx2	T	A	6: 83,047,035 (GRCm39)	H9L	unknown	Het
Tmco1	C	T	1: 167,136,132 (GRCm39)		probably benign	Het
Tmem132d	G	A	5: 127,861,491 (GRCm39)	Q877*	probably null	Het
Unc5d	A	T	8: 29,215,174 (GRCm39)		probably null	Het
Upp1	A	T	11: 9,075,661 (GRCm39)	T4S	probably benign	Het
Uros	A	T	7: 133,292,853 (GRCm39)	I146N	probably damaging	Het
Vsig10	A	T	5: 117,463,131 (GRCm39)	D119V	probably benign	Het
Washc2	C	A	6: 116,193,069 (GRCm39)	Y138*	probably null	Het
Ywhah	T	A	5: 33,184,095 (GRCm39)	D99E	probably benign	Het
Zdbf2	G	A	1: 63,345,400 (GRCm39)	G1260R	probably damaging	Het
Zfp663	T	C	2: 165,195,974 (GRCm39)	T82A	probably benign	Het
Zfp831	T	A	2: 174,488,156 (GRCm39)	C944S	possibly damaging	Het

Other mutations in Als2cl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00424:Als2cl	APN	9	110,715,607 (GRCm39)	critical splice donor site	probably null
IGL00743:Als2cl	APN	9	110,718,227 (GRCm39)	missense	possibly damaging	0.88
IGL01504:Als2cl	APN	9	110,718,351 (GRCm39)	missense	probably benign	0.05
IGL01991:Als2cl	APN	9	110,721,985 (GRCm39)	missense	probably benign	0.00
IGL02073:Als2cl	APN	9	110,723,407 (GRCm39)	missense	probably benign
IGL02407:Als2cl	APN	9	110,718,295 (GRCm39)	nonsense	probably null
IGL03266:Als2cl	APN	9	110,719,924 (GRCm39)	missense	possibly damaging	0.74
R0006:Als2cl	UTSW	9	110,723,686 (GRCm39)	missense	possibly damaging	0.93
R0127:Als2cl	UTSW	9	110,720,935 (GRCm39)	missense	probably damaging	1.00
R0395:Als2cl	UTSW	9	110,727,152 (GRCm39)	missense	probably damaging	1.00
R0490:Als2cl	UTSW	9	110,724,414 (GRCm39)	missense	probably benign	0.04
R0540:Als2cl	UTSW	9	110,724,852 (GRCm39)	nonsense	probably null
R0900:Als2cl	UTSW	9	110,719,496 (GRCm39)	missense	possibly damaging	0.94
R1542:Als2cl	UTSW	9	110,723,102 (GRCm39)	missense	probably benign	0.36
R1574:Als2cl	UTSW	9	110,713,128 (GRCm39)	missense	probably damaging	1.00
R1574:Als2cl	UTSW	9	110,713,128 (GRCm39)	missense	probably damaging	1.00
R2059:Als2cl	UTSW	9	110,714,506 (GRCm39)	missense	probably benign	0.00
R2168:Als2cl	UTSW	9	110,717,810 (GRCm39)	missense	probably damaging	1.00
R2851:Als2cl	UTSW	9	110,723,203 (GRCm39)	missense	probably damaging	0.99
R2853:Als2cl	UTSW	9	110,723,203 (GRCm39)	missense	probably damaging	0.99
R2919:Als2cl	UTSW	9	110,726,567 (GRCm39)	critical splice acceptor site	probably null
R3761:Als2cl	UTSW	9	110,727,202 (GRCm39)	missense	probably damaging	1.00
R3848:Als2cl	UTSW	9	110,718,377 (GRCm39)	splice site	probably benign
R3850:Als2cl	UTSW	9	110,718,377 (GRCm39)	splice site	probably benign
R4110:Als2cl	UTSW	9	110,713,115 (GRCm39)	missense	probably benign	0.18
R4438:Als2cl	UTSW	9	110,714,466 (GRCm39)	missense	probably damaging	0.98
R4732:Als2cl	UTSW	9	110,718,204 (GRCm39)	missense	probably damaging	0.99
R4733:Als2cl	UTSW	9	110,718,204 (GRCm39)	missense	probably damaging	0.99
R5060:Als2cl	UTSW	9	110,713,205 (GRCm39)	missense	probably damaging	0.99
R5119:Als2cl	UTSW	9	110,719,887 (GRCm39)	missense	probably damaging	1.00
R5905:Als2cl	UTSW	9	110,727,152 (GRCm39)	missense	probably damaging	1.00
R5913:Als2cl	UTSW	9	110,718,773 (GRCm39)	critical splice acceptor site	probably null
R5930:Als2cl	UTSW	9	110,716,432 (GRCm39)	missense	probably damaging	1.00
R6197:Als2cl	UTSW	9	110,724,952 (GRCm39)	missense	probably damaging	1.00
R6362:Als2cl	UTSW	9	110,724,514 (GRCm39)	splice site	probably null
R7052:Als2cl	UTSW	9	110,727,151 (GRCm39)	missense	probably damaging	1.00
R7081:Als2cl	UTSW	9	110,723,650 (GRCm39)	missense	possibly damaging	0.66
R7472:Als2cl	UTSW	9	110,727,174 (GRCm39)	missense	probably benign	0.05
R7854:Als2cl	UTSW	9	110,727,564 (GRCm39)	makesense	probably null
R8120:Als2cl	UTSW	9	110,714,460 (GRCm39)	missense	possibly damaging	0.57
R8279:Als2cl	UTSW	9	110,723,653 (GRCm39)	missense	probably damaging	1.00
R8458:Als2cl	UTSW	9	110,714,025 (GRCm39)	missense	probably damaging	0.98
R8475:Als2cl	UTSW	9	110,715,484 (GRCm39)	missense	possibly damaging	0.46
R8808:Als2cl	UTSW	9	110,718,282 (GRCm39)	missense	possibly damaging	0.87
R8819:Als2cl	UTSW	9	110,714,855 (GRCm39)	missense	probably benign	0.07
R8820:Als2cl	UTSW	9	110,714,855 (GRCm39)	missense	probably benign	0.07
R9070:Als2cl	UTSW	9	110,718,288 (GRCm39)	missense	probably benign
R9149:Als2cl	UTSW	9	110,718,191 (GRCm39)	missense	probably benign	0.42
X0011:Als2cl	UTSW	9	110,714,079 (GRCm39)	missense	probably damaging	1.00
Z1177:Als2cl	UTSW	9	110,724,885 (GRCm39)	nonsense	probably null
Z1177:Als2cl	UTSW	9	110,717,596 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TTGGAGCTCCTGGTTCTCAGAG -3'
(R):5'- ACTGACCAAGCTCTGATCCTG -3'

Sequencing Primer
(F):5'- GGGCTTCTTGTGCTCCAGAC -3'
(R):5'- TCTGATCCTGTACCAAACAAGACTTG -3'

Posted On

2022-03-25