Mutagenetix > Incidental Mutation

Incidental Mutation 'R5092:Slmap'

387865

Institutional Source

Beutler Lab

Gene Symbol

Slmap

Ensembl Gene

ENSMUSG00000021870

Gene Name

sarcolemma associated protein

Synonyms

Slap, D330001L02Rik, Miranda

MMRRC Submission

042681-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R5092 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

26134323-26256086 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 26184744 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Arginine at position 272 (L272R)

Ref Sequence

ENSEMBL: ENSMUSP00000107949 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038522] [ENSMUST00000090359] [ENSMUST00000102956] [ENSMUST00000112330] [ENSMUST00000112331] [ENSMUST00000139075]

AlphaFold

Q3URD3

Predicted Effect

probably damaging
Transcript: ENSMUST00000038522
AA Change: L272R

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

SMART Domains

Protein: ENSMUSP00000046956
Gene: ENSMUSG00000021870
AA Change: L272R

Domain	Start	End	E-Value	Type
FHA	27	85	1.05e-8	SMART
coiled coil region	167	199	N/A	INTRINSIC
coiled coil region	230	390	N/A	INTRINSIC
coiled coil region	486	568	N/A	INTRINSIC
coiled coil region	595	794	N/A	INTRINSIC
transmembrane domain	796	818	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000090359
AA Change: L272R

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000087836
Gene: ENSMUSG00000021870
AA Change: L272R

Domain	Start	End	E-Value	Type
FHA	27	85	1.05e-8	SMART
coiled coil region	167	199	N/A	INTRINSIC
coiled coil region	230	390	N/A	INTRINSIC
coiled coil region	490	572	N/A	INTRINSIC
coiled coil region	599	799	N/A	INTRINSIC
transmembrane domain	801	823	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000102956
AA Change: L272R

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

SMART Domains

Protein: ENSMUSP00000100021
Gene: ENSMUSG00000021870
AA Change: L272R

Domain	Start	End	E-Value	Type
FHA	27	85	1.05e-8	SMART
coiled coil region	167	199	N/A	INTRINSIC
coiled coil region	230	390	N/A	INTRINSIC
coiled coil region	486	568	N/A	INTRINSIC
coiled coil region	595	794	N/A	INTRINSIC
transmembrane domain	796	818	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000112330
AA Change: L272R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000107949
Gene: ENSMUSG00000021870
AA Change: L272R

Domain	Start	End	E-Value	Type
FHA	27	85	1.05e-8	SMART
coiled coil region	167	199	N/A	INTRINSIC
coiled coil region	230	383	N/A	INTRINSIC
coiled coil region	452	534	N/A	INTRINSIC
coiled coil region	561	761	N/A	INTRINSIC
transmembrane domain	763	785	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000112331
AA Change: L151R

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000107950
Gene: ENSMUSG00000021870
AA Change: L151R

Domain	Start	End	E-Value	Type
coiled coil region	46	78	N/A	INTRINSIC
coiled coil region	109	260	N/A	INTRINSIC
coiled coil region	352	434	N/A	INTRINSIC
coiled coil region	461	661	N/A	INTRINSIC
transmembrane domain	663	685	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000139075
AA Change: L272R

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

SMART Domains

Protein: ENSMUSP00000117816
Gene: ENSMUSG00000021870
AA Change: L272R

Domain	Start	End	E-Value	Type
FHA	27	85	1.05e-8	SMART
coiled coil region	167	199	N/A	INTRINSIC
coiled coil region	230	390	N/A	INTRINSIC
coiled coil region	507	589	N/A	INTRINSIC
coiled coil region	616	816	N/A	INTRINSIC
transmembrane domain	818	840	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000142679

SMART Domains

Protein: ENSMUSP00000123072
Gene: ENSMUSG00000021870

Domain	Start	End	E-Value	Type
coiled coil region	1	52	N/A	INTRINSIC
coiled coil region	97	179	N/A	INTRINSIC
coiled coil region	206	405	N/A	INTRINSIC
transmembrane domain	408	430	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144737

Predicted Effect

unknown
Transcript: ENSMUST00000146438
AA Change: L35R

SMART Domains

Protein: ENSMUSP00000123344
Gene: ENSMUSG00000021870
AA Change: L35R

Domain	Start	End	E-Value	Type
coiled coil region	17	142	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000145738

SMART Domains

Protein: ENSMUSP00000117276
Gene: ENSMUSG00000021870

Domain	Start	End	E-Value	Type
coiled coil region	1	59	N/A	INTRINSIC
coiled coil region	138	220	N/A	INTRINSIC
coiled coil region	247	447	N/A	INTRINSIC
transmembrane domain	450	472	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 93.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
PHENOTYPE: Homozygous inactivation in this locus affects T cell development. Mice homozygous for a transposon induced allele exhibit cleft palate. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930433I11Rik	C	T	7: 40,637,091 (GRCm39)		probably benign	Het
Abca13	T	A	11: 9,208,535 (GRCm39)	L236Q	probably damaging	Het
Acp2	A	T	2: 91,038,391 (GRCm39)	T255S	probably benign	Het
Acsf3	A	C	8: 123,544,131 (GRCm39)	R536S	probably benign	Het
Adgrb1	T	G	15: 74,401,664 (GRCm39)	V220G	probably benign	Het
Anks6	C	T	4: 47,030,795 (GRCm39)	G601S	probably damaging	Het
Atp5f1b	A	G	10: 127,919,854 (GRCm39)	Q74R	probably benign	Het
Bltp1	A	T	3: 37,054,234 (GRCm39)	M3118L	probably benign	Het
Brf1	G	A	12: 112,943,352 (GRCm39)	T166M	probably damaging	Het
Capn9	A	G	8: 125,324,264 (GRCm39)	K188R	probably damaging	Het
Casp8	A	T	1: 58,883,835 (GRCm39)	N381Y	possibly damaging	Het
Ccdc88b	A	G	19: 6,825,600 (GRCm39)	S1218P	probably damaging	Het
Cdc42bpg	C	T	19: 6,363,250 (GRCm39)	P403S	probably benign	Het
Cdkal1	T	A	13: 30,030,222 (GRCm39)	Y91F	probably damaging	Het
Cdyl2	T	C	8: 117,350,679 (GRCm39)	N151D	possibly damaging	Het
Cnot1	T	A	8: 96,479,396 (GRCm39)	R875S	possibly damaging	Het
Cpd	A	G	11: 76,702,530 (GRCm39)	S613P	possibly damaging	Het
Cyp2e1	G	T	7: 140,354,648 (GRCm39)	R492L	probably damaging	Het
D5Ertd579e	G	A	5: 36,760,047 (GRCm39)	T1371M	probably benign	Het
Dcaf8	A	G	1: 172,014,476 (GRCm39)	T394A	probably benign	Het
Dgka	T	C	10: 128,571,702 (GRCm39)	E117G	probably damaging	Het
Dock4	G	A	12: 40,894,440 (GRCm39)	V1867I	probably benign	Het
E2f2	G	T	4: 135,914,248 (GRCm39)	A333S	probably benign	Het
Eif3l	T	C	15: 78,968,354 (GRCm39)	S208P	probably benign	Het
Elovl3	A	T	19: 46,122,961 (GRCm39)	H179L	probably damaging	Het
Eml5	T	C	12: 98,758,875 (GRCm39)	D1766G	probably damaging	Het
Eno4	A	G	19: 58,934,023 (GRCm39)	T75A	probably benign	Het
Fam135a	C	T	1: 24,067,888 (GRCm39)	D94N	probably benign	Het
Fasn	G	T	11: 120,705,862 (GRCm39)	Q1136K	probably benign	Het
Fcer1a	T	G	1: 173,053,022 (GRCm39)	N58T	probably damaging	Het
Frmd4b	T	A	6: 97,272,941 (GRCm39)	D763V	probably damaging	Het
Gm43518	A	G	5: 124,076,297 (GRCm39)	T115A	probably damaging	Het
Gria4	C	T	9: 4,472,176 (GRCm39)	E438K	probably benign	Het
Grin2d	T	C	7: 45,503,692 (GRCm39)	E681G	probably damaging	Het
Gtf3c5	G	T	2: 28,472,885 (GRCm39)	N35K	possibly damaging	Het
Hydin	A	G	8: 111,309,300 (GRCm39)	T4031A	probably benign	Het
Igfn1	G	T	1: 135,892,564 (GRCm39)	N2185K	probably benign	Het
Il17rb	T	C	14: 29,724,333 (GRCm39)	T174A	probably benign	Het
Kdm3b	T	A	18: 34,946,515 (GRCm39)	C835S	probably benign	Het
Lgi2	A	T	5: 52,695,429 (GRCm39)	I510N	probably damaging	Het
Map3k6	A	G	4: 132,979,054 (GRCm39)	E1164G	probably benign	Het
Mpv17l	T	A	16: 13,758,537 (GRCm39)	M1K	probably null	Het
Myoc	T	A	1: 162,467,203 (GRCm39)	L124Q	probably damaging	Het
Nbeal2	C	A	9: 110,455,796 (GRCm39)		probably null	Het
Nek10	A	G	14: 14,820,851 (GRCm38)	K13E	possibly damaging	Het
Nt5dc2	A	G	14: 30,860,989 (GRCm39)	H491R	possibly damaging	Het
Or4f61	A	C	2: 111,922,452 (GRCm39)	M198R	possibly damaging	Het
Or51b6	T	A	7: 103,556,406 (GRCm39)	Y250*	probably null	Het
Or8k21	T	C	2: 86,144,706 (GRCm39)	Q308R	probably benign	Het
Pclo	T	A	5: 14,727,322 (GRCm39)		probably benign	Het
Pgm2	A	T	5: 64,265,092 (GRCm39)	N371I	possibly damaging	Het
Phf20l1	T	A	15: 66,508,762 (GRCm39)	S873T	possibly damaging	Het
Plch1	T	C	3: 63,606,131 (GRCm39)	T1249A	probably benign	Het
Plekhn1	A	T	4: 156,309,222 (GRCm39)	I228N	possibly damaging	Het
Ppp1r12a	A	T	10: 108,103,263 (GRCm39)		probably null	Het
Ptchd3	T	C	11: 121,721,972 (GRCm39)	Y282H	probably damaging	Het
Ptprk	T	A	10: 28,468,769 (GRCm39)	N1396K	probably damaging	Het
Rap1gap2	T	C	11: 74,329,121 (GRCm39)	E81G	probably damaging	Het
Rpf2	T	C	10: 40,122,971 (GRCm39)	M1V	probably null	Het
Rpgrip1l	G	A	8: 91,948,012 (GRCm39)	Q1224*	probably null	Het
Rreb1	A	G	13: 38,112,254 (GRCm39)	D286G	probably benign	Het
Rufy4	T	C	1: 74,186,822 (GRCm39)	C537R	probably damaging	Het
Senp5	A	T	16: 31,807,960 (GRCm39)	N431K	probably benign	Het
Serpina1f	A	C	12: 103,659,809 (GRCm39)	S158A	probably damaging	Het
Sertad3	T	A	7: 27,176,145 (GRCm39)	I193N	probably damaging	Het
Slc22a8	T	A	19: 8,571,528 (GRCm39)	N86K	probably damaging	Het
Slc6a2	T	C	8: 93,721,347 (GRCm39)	V492A	possibly damaging	Het
Slf2	T	A	19: 44,940,523 (GRCm39)	D773E	probably benign	Het
Smyd5	T	C	6: 85,422,185 (GRCm39)		probably benign	Het
Snx21	G	T	2: 164,628,666 (GRCm39)	R103L	probably damaging	Het
Sphk2	T	A	7: 45,361,777 (GRCm39)		probably null	Het
Stab1	T	C	14: 30,867,812 (GRCm39)	K1653E	probably benign	Het
Syde1	A	G	10: 78,425,252 (GRCm39)	V253A	probably benign	Het
Sympk	G	T	7: 18,776,584 (GRCm39)	R492L	probably benign	Het
Taar7f	T	C	10: 23,925,451 (GRCm39)	I15T	probably benign	Het
Tas2r140	A	G	6: 40,468,200 (GRCm39)	D10G	probably benign	Het
Tbcc	A	G	17: 47,202,600 (GRCm39)	S329G	probably benign	Het
Teddm3	G	A	16: 20,971,900 (GRCm39)	T223M	probably benign	Het
Tex14	G	T	11: 87,405,668 (GRCm39)	C860F	probably benign	Het
Thada	A	T	17: 84,751,896 (GRCm39)	L360Q	probably damaging	Het
Thop1	C	A	10: 80,916,412 (GRCm39)	H473Q	probably damaging	Het
Tln2	T	C	9: 67,163,310 (GRCm39)	D1075G	probably benign	Het
Tmem130	G	A	5: 144,680,528 (GRCm39)	T292I	probably benign	Het
Tmem198b	T	C	10: 128,637,305 (GRCm39)	N278S	probably benign	Het
Ttc21a	A	T	9: 119,771,731 (GRCm39)	T177S	probably benign	Het
Ubr2	A	T	17: 47,280,173 (GRCm39)	C659S	probably damaging	Het
Vmn2r4	T	C	3: 64,298,373 (GRCm39)	K585R	probably benign	Het
Vmn2r86	A	G	10: 130,282,456 (GRCm39)	I720T	probably damaging	Het
Wdr35	G	T	12: 9,037,327 (GRCm39)	W311L	probably damaging	Het
Zfp39	A	T	11: 58,782,028 (GRCm39)	F245I	possibly damaging	Het
Zftraf1	A	T	15: 76,530,512 (GRCm39)	F269L	probably benign	Het
Zmym5	G	A	14: 57,034,236 (GRCm39)	T325I	probably benign	Het
Zng1	A	T	19: 24,898,383 (GRCm39)		probably null	Het

Other mutations in Slmap

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02402:Slmap	APN	14	26,184,865 (GRCm39)	missense	probably damaging	0.97
IGL02612:Slmap	APN	14	26,180,621 (GRCm39)	splice site	probably benign
IGL02630:Slmap	APN	14	26,143,586 (GRCm39)	missense	possibly damaging	0.93
IGL02798:Slmap	APN	14	26,191,533 (GRCm39)	missense	possibly damaging	0.88
PIT4382001:Slmap	UTSW	14	26,254,586 (GRCm39)	missense	probably damaging	1.00
R0433:Slmap	UTSW	14	26,174,749 (GRCm39)	nonsense	probably null
R0963:Slmap	UTSW	14	26,189,675 (GRCm39)	missense	probably damaging	1.00
R1721:Slmap	UTSW	14	26,181,373 (GRCm39)	splice site	probably benign
R1848:Slmap	UTSW	14	26,143,729 (GRCm39)	missense	probably benign
R2151:Slmap	UTSW	14	26,139,402 (GRCm39)	missense	probably damaging	1.00
R2152:Slmap	UTSW	14	26,139,402 (GRCm39)	missense	probably damaging	1.00
R2153:Slmap	UTSW	14	26,139,402 (GRCm39)	missense	probably damaging	1.00
R2154:Slmap	UTSW	14	26,139,402 (GRCm39)	missense	probably damaging	1.00
R3725:Slmap	UTSW	14	26,148,397 (GRCm39)	missense	probably damaging	0.99
R3726:Slmap	UTSW	14	26,148,397 (GRCm39)	missense	probably damaging	0.99
R3935:Slmap	UTSW	14	26,180,570 (GRCm39)	missense	probably benign
R4118:Slmap	UTSW	14	26,204,027 (GRCm39)	missense	probably damaging	0.99
R4594:Slmap	UTSW	14	26,186,772 (GRCm39)	missense	probably damaging	1.00
R4731:Slmap	UTSW	14	26,189,690 (GRCm39)	missense	probably damaging	0.97
R4732:Slmap	UTSW	14	26,189,690 (GRCm39)	missense	probably damaging	0.97
R4733:Slmap	UTSW	14	26,189,690 (GRCm39)	missense	probably damaging	0.97
R4817:Slmap	UTSW	14	26,183,507 (GRCm39)	missense	probably damaging	0.97
R4847:Slmap	UTSW	14	26,147,763 (GRCm39)	missense	possibly damaging	0.90
R4860:Slmap	UTSW	14	26,181,364 (GRCm39)	missense	probably benign	0.22
R4860:Slmap	UTSW	14	26,181,364 (GRCm39)	missense	probably benign	0.22
R5211:Slmap	UTSW	14	26,204,117 (GRCm39)	missense	probably damaging	1.00
R5387:Slmap	UTSW	14	26,181,088 (GRCm39)	missense	probably benign	0.22
R5821:Slmap	UTSW	14	26,183,435 (GRCm39)	missense	probably damaging	1.00
R6404:Slmap	UTSW	14	26,143,566 (GRCm39)	splice site	probably null
R6856:Slmap	UTSW	14	26,151,247 (GRCm39)	splice site	probably null
R6977:Slmap	UTSW	14	26,254,574 (GRCm39)	missense	probably damaging	1.00
R7108:Slmap	UTSW	14	26,143,676 (GRCm39)	missense	probably benign	0.04
R7320:Slmap	UTSW	14	26,181,227 (GRCm39)	missense	possibly damaging	0.53
R7470:Slmap	UTSW	14	26,148,575 (GRCm39)	missense	probably benign
R7520:Slmap	UTSW	14	26,148,575 (GRCm39)	missense	probably benign
R7540:Slmap	UTSW	14	26,181,346 (GRCm39)	missense	probably damaging	0.99
R7544:Slmap	UTSW	14	26,151,003 (GRCm39)	missense	probably damaging	0.99
R7544:Slmap	UTSW	14	26,151,001 (GRCm39)	missense	probably damaging	0.99
R8112:Slmap	UTSW	14	26,143,703 (GRCm39)	missense	probably damaging	1.00
R8153:Slmap	UTSW	14	26,254,488 (GRCm39)	missense	probably benign
R8196:Slmap	UTSW	14	26,189,646 (GRCm39)	missense	probably damaging	1.00
R8300:Slmap	UTSW	14	26,139,374 (GRCm39)	missense	possibly damaging	0.62
R8523:Slmap	UTSW	14	26,150,965 (GRCm39)	missense	probably damaging	0.99
R9039:Slmap	UTSW	14	26,254,519 (GRCm39)	missense	probably benign	0.08
R9094:Slmap	UTSW	14	26,137,355 (GRCm39)	intron	probably benign
R9504:Slmap	UTSW	14	26,136,133 (GRCm39)	missense	probably damaging	1.00
R9657:Slmap	UTSW	14	26,151,013 (GRCm39)	missense	probably benign	0.19
R9695:Slmap	UTSW	14	26,183,496 (GRCm39)	missense	probably damaging	0.97
R9763:Slmap	UTSW	14	26,204,118 (GRCm39)	missense	probably damaging	1.00
R9801:Slmap	UTSW	14	26,143,595 (GRCm39)	missense	probably damaging	1.00
Z1177:Slmap	UTSW	14	26,254,605 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- CTCAGCCTTATGTGACCATCG -3'
(R):5'- TCACAGAAAAGTGACTTGGGTG -3'

Sequencing Primer
(F):5'- GGCAATGATAGCTCAGTTCCCAG -3'
(R):5'- CACAGAAAAGTGACTTGGGTGTGATG -3'

Posted On

2016-06-06