Mutagenetix > Incidental Mutation

Incidental Mutation 'R1642:Ablim3'

173646

Institutional Source

Beutler Lab

Gene Symbol

Ablim3

Ensembl Gene

ENSMUSG00000032735

Gene Name

actin binding LIM protein family, member 3

Synonyms

D930036B08Rik

MMRRC Submission

039678-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.099) question?

Stock #

R1642 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

61932463-62044895 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 61947382 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Arginine at position 457 (K457R)

Ref Sequence

ENSEMBL: ENSMUSP00000125836 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049378] [ENSMUST00000166783]

AlphaFold

Q69ZX8

Predicted Effect

probably benign
Transcript: ENSMUST00000049378
AA Change: K457R

PolyPhen 2 Score 0.264 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000041243
Gene: ENSMUSG00000032735
AA Change: K457R

Domain	Start	End	E-Value	Type
LIM	22	73	4.19e-8	SMART
LIM	81	133	2.31e-10	SMART
LIM	150	201	2.4e-17	SMART
LIM	209	261	1.12e-8	SMART
Pfam:AbLIM_anchor	273	646	6.5e-154	PFAM
VHP	647	682	1.66e-19	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000166783
AA Change: K457R

PolyPhen 2 Score 0.264 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000125836
Gene: ENSMUSG00000032735
AA Change: K457R

Domain	Start	End	E-Value	Type
LIM	22	73	4.19e-8	SMART
LIM	81	133	2.31e-10	SMART
LIM	150	201	2.4e-17	SMART
LIM	209	261	1.12e-8	SMART
Pfam:AbLIM_anchor	273	646	6.5e-154	PFAM
VHP	647	682	1.66e-19	SMART

Coding Region Coverage

1x: 99.0%
3x: 98.1%
10x: 95.4%
20x: 89.7%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the actin-binding LIM (abLIM) family of proteins. These proteins are characterized by an N-terminal LIM domain and a C-terminal dematin-like domain. The encoded protein interacts with actin filaments and may be a component of adherens junctions in several cell types. A variant of this gene may be associated with pain sensitivity in male human patients. [provided by RefSeq, Sep 2016]

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310057J18Rik	A	G	10: 28,862,233 (GRCm39)	V19A	probably benign	Het
6820408C15Rik	T	C	2: 152,282,774 (GRCm39)	Y210H	probably damaging	Het
Aars1	T	A	8: 111,769,882 (GRCm39)	I327N	possibly damaging	Het
Abca6	T	A	11: 110,109,107 (GRCm39)	N688Y	possibly damaging	Het
Acsm2	A	T	7: 119,162,860 (GRCm39)	N45Y	probably damaging	Het
Agxt2	T	C	15: 10,373,917 (GRCm39)	S108P	probably damaging	Het
Akr1cl	A	T	1: 65,060,588 (GRCm39)	M174K	probably benign	Het
Armh4	T	C	14: 50,005,867 (GRCm39)		probably null	Het
Bfsp1	G	A	2: 143,683,683 (GRCm39)	R214W	probably damaging	Het
Cby3	A	G	11: 50,250,343 (GRCm39)	D183G	probably damaging	Het
Clip2	T	C	5: 134,532,107 (GRCm39)	D566G	possibly damaging	Het
Colgalt1	A	G	8: 72,073,401 (GRCm39)	I341V	probably benign	Het
Cyp2c38	T	A	19: 39,390,153 (GRCm39)	D349V	probably damaging	Het
Cyp3a16	T	A	5: 145,406,399 (GRCm39)	I18F	unknown	Het
Degs2	C	T	12: 108,658,451 (GRCm39)	C176Y	probably benign	Het
Dhx16	A	T	17: 36,201,957 (GRCm39)	T995S	probably damaging	Het
Dicer1	A	T	12: 104,679,415 (GRCm39)	C521S	probably damaging	Het
Dop1b	T	C	16: 93,559,203 (GRCm39)	S532P	probably benign	Het
Dpysl4	T	G	7: 138,670,254 (GRCm39)	M124R	probably damaging	Het
Eml6	A	G	11: 29,727,001 (GRCm39)		probably null	Het
Erbb4	A	T	1: 68,370,393 (GRCm39)	V395D	probably damaging	Het
Esf1	T	C	2: 140,000,406 (GRCm39)	D460G	possibly damaging	Het
F830045P16Rik	G	A	2: 129,305,634 (GRCm39)	H247Y	probably benign	Het
Fsbp	T	A	4: 11,583,965 (GRCm39)	S221R	probably benign	Het
Fstl5	T	A	3: 76,317,929 (GRCm39)	N198K	possibly damaging	Het
Gemin5	G	T	11: 58,029,906 (GRCm39)	H855Q	probably damaging	Het
Gjd3	T	C	11: 98,873,535 (GRCm39)	E103G	probably benign	Het
I0C0044D17Rik	A	G	4: 98,708,471 (GRCm39)		probably benign	Het
Iqca1l	C	A	5: 24,757,686 (GRCm39)	R177L	probably damaging	Het
Itgb4	A	T	11: 115,898,183 (GRCm39)	R1646W	probably damaging	Het
Klri2	A	T	6: 129,715,837 (GRCm39)	C121S	probably benign	Het
Lamc3	A	G	2: 31,806,008 (GRCm39)	Y703C	probably damaging	Het
Lrrc10	A	G	10: 116,881,788 (GRCm39)	N154S	probably damaging	Het
Lrriq1	A	G	10: 103,050,317 (GRCm39)	F812L	probably benign	Het
Naip2	C	T	13: 100,298,489 (GRCm39)	A516T	possibly damaging	Het
Nav1	T	C	1: 135,380,010 (GRCm39)	Y1564C	probably damaging	Het
Ndufc1	T	C	3: 51,315,664 (GRCm39)	T25A	probably benign	Het
Neurl4	A	G	11: 69,794,485 (GRCm39)	M23V	probably benign	Het
Nnt	A	G	13: 119,541,086 (GRCm39)		probably null	Het
Nolc1	G	C	19: 46,067,461 (GRCm39)		probably null	Het
Nrg1	A	T	8: 32,314,536 (GRCm39)	M289K	probably benign	Het
Oas3	G	T	5: 120,915,639 (GRCm39)	H17Q	possibly damaging	Het
Or10h1	A	G	17: 33,418,430 (GRCm39)	Y132C	probably damaging	Het
Or2z2	A	G	11: 58,346,664 (GRCm39)	I37T	probably benign	Het
Or5m5	A	G	2: 85,814,201 (GRCm39)	K6E	probably benign	Het
Or8g36	C	T	9: 39,422,650 (GRCm39)	R122H	possibly damaging	Het
Parp9	T	C	16: 35,788,067 (GRCm39)	Y612H	probably benign	Het
Pcdh1	A	T	18: 38,332,283 (GRCm39)	M240K	possibly damaging	Het
Pcdhb9	A	G	18: 37,533,987 (GRCm39)		probably benign	Het
Plpp2	A	G	10: 79,366,518 (GRCm39)	V42A	probably damaging	Het
Ppic	C	T	18: 53,540,134 (GRCm39)	V172M	probably damaging	Het
Ppp1r9b	A	G	11: 94,892,150 (GRCm39)		silent	Het
Prop1	A	G	11: 50,844,152 (GRCm39)	V27A	possibly damaging	Het
Psmc5	A	G	11: 106,153,242 (GRCm39)	T295A	probably benign	Het
Rpa1	A	G	11: 75,203,517 (GRCm39)		probably null	Het
Rrp12	A	G	19: 41,860,176 (GRCm39)	F1016L	probably damaging	Het
Scn2a	A	T	2: 65,514,041 (GRCm39)	I242F	probably damaging	Het
Slco1a6	T	A	6: 142,032,160 (GRCm39)	H655L	probably benign	Het
Sp140	G	A	1: 85,538,545 (GRCm39)		probably null	Het
Syne1	A	G	10: 5,298,694 (GRCm39)	I1071T	possibly damaging	Het
Tbc1d9b	A	G	11: 50,040,659 (GRCm39)	D392G	probably damaging	Het
Tcaim	G	A	9: 122,647,838 (GRCm39)		probably null	Het
Tgm3	T	A	2: 129,889,702 (GRCm39)	V632E	probably damaging	Het
Triobp	C	A	15: 78,886,348 (GRCm39)	R1830S	probably damaging	Het
Ttn	A	T	2: 76,641,587 (GRCm39)	L5176Q	possibly damaging	Het
Vps8	A	G	16: 21,400,329 (GRCm39)	T1266A	probably benign	Het
Znfx1	T	C	2: 166,880,930 (GRCm39)	I285V	possibly damaging	Het

Other mutations in Ablim3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00928:Ablim3	APN	18	61,982,477 (GRCm39)	missense	possibly damaging	0.83
IGL00954:Ablim3	APN	18	61,972,756 (GRCm39)	splice site	probably benign
IGL01012:Ablim3	APN	18	61,972,772 (GRCm39)	missense	possibly damaging	0.91
IGL01402:Ablim3	APN	18	62,004,754 (GRCm39)	missense	probably damaging	0.99
IGL01404:Ablim3	APN	18	62,004,754 (GRCm39)	missense	probably damaging	0.99
IGL01609:Ablim3	APN	18	61,955,092 (GRCm39)	missense	probably benign	0.05
IGL01710:Ablim3	APN	18	62,004,645 (GRCm39)	missense	probably damaging	1.00
IGL01775:Ablim3	APN	18	61,949,989 (GRCm39)	splice site	probably benign
IGL02967:Ablim3	APN	18	61,959,574 (GRCm39)	nonsense	probably null
IGL03409:Ablim3	APN	18	61,978,922 (GRCm39)	missense	probably damaging	1.00
R0143:Ablim3	UTSW	18	61,988,288 (GRCm39)	missense	probably benign	0.20
R0601:Ablim3	UTSW	18	61,982,441 (GRCm39)	missense	probably benign	0.19
R1067:Ablim3	UTSW	18	61,957,018 (GRCm39)	splice site	probably benign
R1851:Ablim3	UTSW	18	61,982,466 (GRCm39)	missense	probably benign	0.33
R1852:Ablim3	UTSW	18	61,982,466 (GRCm39)	missense	probably benign	0.33
R2072:Ablim3	UTSW	18	61,990,159 (GRCm39)	missense	possibly damaging	0.74
R2763:Ablim3	UTSW	18	61,946,615 (GRCm39)	nonsense	probably null
R4865:Ablim3	UTSW	18	61,938,157 (GRCm39)	missense	probably damaging	1.00
R5190:Ablim3	UTSW	18	61,952,982 (GRCm39)	missense	probably benign	0.00
R5353:Ablim3	UTSW	18	61,934,470 (GRCm39)	missense	probably damaging	1.00
R5442:Ablim3	UTSW	18	61,990,296 (GRCm39)	splice site	probably null
R5835:Ablim3	UTSW	18	61,956,993 (GRCm39)	missense	probably damaging	1.00
R6547:Ablim3	UTSW	18	61,957,000 (GRCm39)	missense	probably benign	0.01
R7231:Ablim3	UTSW	18	61,938,135 (GRCm39)	critical splice donor site	probably null
R7386:Ablim3	UTSW	18	61,955,065 (GRCm39)	missense	probably damaging	1.00
R7404:Ablim3	UTSW	18	61,955,099 (GRCm39)	missense	probably damaging	0.99
R7529:Ablim3	UTSW	18	61,955,039 (GRCm39)	missense	probably benign
R8979:Ablim3	UTSW	18	61,982,397 (GRCm39)	missense	probably benign
R9037:Ablim3	UTSW	18	61,952,066 (GRCm39)	missense	probably benign	0.10
R9095:Ablim3	UTSW	18	61,953,463 (GRCm39)	missense	probably benign	0.01
R9250:Ablim3	UTSW	18	61,944,501 (GRCm39)	missense	probably damaging	1.00
R9320:Ablim3	UTSW	18	61,972,805 (GRCm39)	missense	probably damaging	1.00
R9454:Ablim3	UTSW	18	61,952,067 (GRCm39)	missense	possibly damaging	0.79
R9457:Ablim3	UTSW	18	61,978,920 (GRCm39)	missense	probably benign	0.06
R9591:Ablim3	UTSW	18	61,954,984 (GRCm39)	missense	probably benign	0.15
R9761:Ablim3	UTSW	18	61,952,885 (GRCm39)	missense	possibly damaging	0.82
X0028:Ablim3	UTSW	18	61,938,183 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AATCTCAGTGATAGCCCCTCCCAG -3'
(R):5'- GAAGAAGCCCAAGTCGAGTTAGTCC -3'

Sequencing Primer
(F):5'- CCCAGCATTCTCTGTGAAGTG -3'
(R):5'- ctctttcccttctcttccctc -3'

Posted On

2014-04-24