Mutagenetix > Incidental Mutations

Incidental Mutation 'R0197:Shank1'

60769

Institutional Source

Beutler Lab

Gene Symbol

Shank1

Ensembl Gene

ENSMUSG00000038738

Gene Name

SH3 and multiple ankyrin repeat domains 1

Synonyms

MMRRC Submission

038456-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.222) question?

Stock #

R0197 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

44310253-44360572 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 44352294 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Tryptophan at position 1146 (R1146W)

Ref Sequence

ENSEMBL: ENSMUSP00000103571 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000107934] [ENSMUST00000107935] [ENSMUST00000107938]

AlphaFold

D3YZU1

Predicted Effect

unknown
Transcript: ENSMUST00000107934
AA Change: R1137W

SMART Domains

Protein: ENSMUSP00000103567
Gene: ENSMUSG00000038738
AA Change: R1137W

Domain	Start	End	E-Value	Type
low complexity region	17	46	N/A	INTRINSIC
ANK	212	242	5.75e-1	SMART
ANK	246	275	3.6e-2	SMART
ANK	279	309	3.44e1	SMART
ANK	313	342	1.97e1	SMART
ANK	346	375	3.97e-4	SMART
ANK	379	407	5.69e2	SMART
low complexity region	452	479	N/A	INTRINSIC
low complexity region	487	504	N/A	INTRINSIC
low complexity region	521	548	N/A	INTRINSIC
SH3	557	612	3.73e-16	SMART
PDZ	663	752	2.12e-13	SMART
Blast:PDZ	795	830	5e-11	BLAST
low complexity region	920	941	N/A	INTRINSIC
low complexity region	955	982	N/A	INTRINSIC
low complexity region	993	1023	N/A	INTRINSIC
low complexity region	1051	1080	N/A	INTRINSIC
low complexity region	1123	1138	N/A	INTRINSIC
low complexity region	1162	1175	N/A	INTRINSIC
low complexity region	1179	1220	N/A	INTRINSIC
low complexity region	1256	1275	N/A	INTRINSIC
low complexity region	1298	1323	N/A	INTRINSIC
low complexity region	1348	1359	N/A	INTRINSIC
low complexity region	1369	1404	N/A	INTRINSIC
low complexity region	1450	1466	N/A	INTRINSIC
low complexity region	1512	1532	N/A	INTRINSIC
low complexity region	1539	1555	N/A	INTRINSIC
low complexity region	1557	1570	N/A	INTRINSIC
low complexity region	1580	1614	N/A	INTRINSIC
low complexity region	1633	1667	N/A	INTRINSIC
low complexity region	1685	1720	N/A	INTRINSIC
low complexity region	1735	1746	N/A	INTRINSIC
low complexity region	1776	1787	N/A	INTRINSIC
low complexity region	1806	1823	N/A	INTRINSIC
low complexity region	1834	1852	N/A	INTRINSIC
low complexity region	1893	1907	N/A	INTRINSIC
low complexity region	1925	1936	N/A	INTRINSIC
low complexity region	1942	1976	N/A	INTRINSIC
low complexity region	1988	2004	N/A	INTRINSIC
low complexity region	2009	2029	N/A	INTRINSIC
low complexity region	2059	2083	N/A	INTRINSIC
SAM	2092	2158	1.35e-14	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000107935
AA Change: R1138W

SMART Domains

Protein: ENSMUSP00000103568
Gene: ENSMUSG00000038738
AA Change: R1138W

Domain	Start	End	E-Value	Type
low complexity region	17	46	N/A	INTRINSIC
ANK	212	242	5.75e-1	SMART
ANK	246	275	3.6e-2	SMART
ANK	279	309	3.44e1	SMART
ANK	313	342	1.97e1	SMART
ANK	346	375	3.97e-4	SMART
ANK	379	407	5.69e2	SMART
low complexity region	452	479	N/A	INTRINSIC
low complexity region	487	504	N/A	INTRINSIC
low complexity region	521	548	N/A	INTRINSIC
SH3	557	612	3.73e-16	SMART
low complexity region	648	659	N/A	INTRINSIC
PDZ	672	761	2.12e-13	SMART
Blast:PDZ	796	831	1e-10	BLAST
low complexity region	921	942	N/A	INTRINSIC
low complexity region	956	983	N/A	INTRINSIC
low complexity region	994	1024	N/A	INTRINSIC
low complexity region	1052	1081	N/A	INTRINSIC
low complexity region	1124	1139	N/A	INTRINSIC
low complexity region	1163	1176	N/A	INTRINSIC
low complexity region	1180	1221	N/A	INTRINSIC
low complexity region	1257	1276	N/A	INTRINSIC
low complexity region	1299	1324	N/A	INTRINSIC
low complexity region	1349	1360	N/A	INTRINSIC
low complexity region	1370	1405	N/A	INTRINSIC
low complexity region	1451	1467	N/A	INTRINSIC
low complexity region	1513	1533	N/A	INTRINSIC
low complexity region	1540	1556	N/A	INTRINSIC
low complexity region	1558	1571	N/A	INTRINSIC
low complexity region	1581	1615	N/A	INTRINSIC
low complexity region	1634	1668	N/A	INTRINSIC
low complexity region	1686	1721	N/A	INTRINSIC
low complexity region	1736	1747	N/A	INTRINSIC
low complexity region	1777	1788	N/A	INTRINSIC
low complexity region	1807	1824	N/A	INTRINSIC
low complexity region	1835	1853	N/A	INTRINSIC
low complexity region	1894	1908	N/A	INTRINSIC
low complexity region	1926	1937	N/A	INTRINSIC
low complexity region	1943	1977	N/A	INTRINSIC
low complexity region	1989	2005	N/A	INTRINSIC
low complexity region	2010	2030	N/A	INTRINSIC
low complexity region	2060	2084	N/A	INTRINSIC
SAM	2093	2159	1.35e-14	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000107938
AA Change: R1146W

SMART Domains

Protein: ENSMUSP00000103571
Gene: ENSMUSG00000038738
AA Change: R1146W

Domain	Start	End	E-Value	Type
low complexity region	17	46	N/A	INTRINSIC
Pfam:FERM_f0	73	156	6.6e-17	PFAM
ANK	212	242	5.75e-1	SMART
ANK	246	275	3.6e-2	SMART
ANK	279	309	3.44e1	SMART
ANK	313	342	1.97e1	SMART
ANK	346	375	3.97e-4	SMART
ANK	379	407	5.69e2	SMART
low complexity region	452	479	N/A	INTRINSIC
low complexity region	487	504	N/A	INTRINSIC
low complexity region	521	548	N/A	INTRINSIC
SH3	557	612	3.73e-16	SMART
low complexity region	648	659	N/A	INTRINSIC
PDZ	672	761	2.12e-13	SMART
Blast:PDZ	804	839	5e-11	BLAST
low complexity region	929	950	N/A	INTRINSIC
low complexity region	964	991	N/A	INTRINSIC
low complexity region	1002	1032	N/A	INTRINSIC
low complexity region	1060	1089	N/A	INTRINSIC
low complexity region	1132	1147	N/A	INTRINSIC
low complexity region	1171	1184	N/A	INTRINSIC
low complexity region	1188	1229	N/A	INTRINSIC
low complexity region	1265	1284	N/A	INTRINSIC
low complexity region	1307	1332	N/A	INTRINSIC
low complexity region	1357	1368	N/A	INTRINSIC
low complexity region	1378	1413	N/A	INTRINSIC
low complexity region	1459	1475	N/A	INTRINSIC
low complexity region	1521	1541	N/A	INTRINSIC
low complexity region	1548	1564	N/A	INTRINSIC
low complexity region	1566	1579	N/A	INTRINSIC
low complexity region	1589	1623	N/A	INTRINSIC
low complexity region	1642	1676	N/A	INTRINSIC
low complexity region	1694	1729	N/A	INTRINSIC
low complexity region	1744	1755	N/A	INTRINSIC
low complexity region	1785	1796	N/A	INTRINSIC
low complexity region	1815	1832	N/A	INTRINSIC
low complexity region	1843	1861	N/A	INTRINSIC
low complexity region	1902	1916	N/A	INTRINSIC
low complexity region	1934	1945	N/A	INTRINSIC
low complexity region	1951	1985	N/A	INTRINSIC
low complexity region	1997	2013	N/A	INTRINSIC
low complexity region	2018	2038	N/A	INTRINSIC
low complexity region	2068	2092	N/A	INTRINSIC
SAM	2101	2167	1.35e-14	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127164

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154776

Meta Mutation Damage Score

0.0869

Coding Region Coverage

1x: 98.6%
3x: 97.3%
10x: 92.5%
20x: 75.9%

Validation Efficiency

97% (121/125)

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 SHANK (SH3 domain and ankyrin repeat containing) family of proteins. Members of this family act as scaffold proteins that are required for the development and function of neuronal synapses. Deletions in this gene may be associated with autism spectrum disorder in males. [provided by RefSeq, Apr 2016]
PHENOTYPE: Homozygous mutation of this gene results in smaller pyramidal neuron dendritic spines, smaller and thinner postsynaptic density of central excitatory synapses, weaker synaptic transmission, increased anxiety-related behavior, and impaired contextual fearmemory, but enhanced spatial learning. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	T	C	3: 138,069,871	L1607P	probably damaging	Het
1700016H13Rik	T	C	5: 103,648,821	*118W	probably null	Het
1700061G19Rik	A	T	17: 56,883,835	N468Y	probably benign	Het
2610507B11Rik	A	C	11: 78,269,704		probably benign	Het
4930452B06Rik	C	T	14: 8,518,695	G254R	probably damaging	Het
Abcc2	A	T	19: 43,826,614	R1147*	probably null	Het
Agap2	A	G	10: 127,091,702	T1131A	possibly damaging	Het
Aldh9a1	A	G	1: 167,361,847	D388G	probably damaging	Het
Ap3d1	G	T	10: 80,730,042	A97E	probably damaging	Het
Arhgef10	T	A	8: 14,962,636	V320E	probably damaging	Het
Baiap2l1	C	A	5: 144,266,010	V498L	probably damaging	Het
Ccdc189	T	C	7: 127,584,862	E261G	probably damaging	Het
Cdh2	T	C	18: 16,629,576	N437S	probably benign	Het
Chd1	C	A	17: 15,725,431	N72K	probably benign	Het
Col4a3bp	T	A	13: 96,549,287	Y63N	probably benign	Het
Cstf2t	A	T	19: 31,084,626	M521L	probably benign	Het
Dlx5	T	C	6: 6,881,619	K90E	possibly damaging	Het
Dmp1	A	G	5: 104,207,630	E32G	possibly damaging	Het
Espnl	T	G	1: 91,344,489	Y524D	probably damaging	Het
Fam20c	T	C	5: 138,755,724	L30P	probably damaging	Het
Fat1	G	T	8: 45,026,553	A2879S	probably benign	Het
Gabrg1	A	T	5: 70,774,389	V337D	probably damaging	Het
Gart	C	A	16: 91,623,403	D851Y	possibly damaging	Het
Gcc1	T	C	6: 28,420,616	H234R	probably damaging	Het
Gemin6	T	A	17: 80,228,095	H161Q	probably damaging	Het
Glt6d1	A	G	2: 25,794,070	I308T	probably benign	Het
Gm10320	T	C	13: 98,491,983	T7A	probably benign	Het
Gm10912	T	C	2: 104,066,530	S5P	probably benign	Het
Gm13088	C	T	4: 143,656,440	E70K	possibly damaging	Het
Gmpr2	T	A	14: 55,672,735	D7E	possibly damaging	Het
Hc	A	G	2: 34,984,750	Y1620H	probably damaging	Het
Hoxa3	T	C	6: 52,170,143		probably benign	Het
Ift140	A	G	17: 25,090,933	T1105A	probably benign	Het
Kdr	G	T	5: 75,968,422	T188N	possibly damaging	Het
Lepr	A	T	4: 101,752,152	D312V	possibly damaging	Het
Mcm3	A	G	1: 20,810,105	V501A	probably damaging	Het
Mcur1	T	C	13: 43,545,740	Y267C	probably damaging	Het
Med13	T	A	11: 86,307,038	T736S	probably benign	Het
Med13l	T	C	5: 118,671,002		probably benign	Het
Mroh2a	G	C	1: 88,246,042	A871P	probably damaging	Het
Ndrg2	T	A	14: 51,907,003		probably benign	Het
Oas3	G	A	5: 120,756,145	R39C	probably damaging	Het
Olfr1258	A	G	2: 89,930,201	T131A	probably benign	Het
Olfr1298	C	T	2: 111,645,791	V69I	probably benign	Het
Olfr272	G	A	4: 52,910,849	T315M	probably benign	Het
Olfr558	T	A	7: 102,709,995	H245Q	probably damaging	Het
Onecut2	T	A	18: 64,341,472	S365T	possibly damaging	Het
Pds5b	C	A	5: 150,754,431	Q505K	probably benign	Het
Rfx2	T	C	17: 56,803,722	Y88C	probably damaging	Het
Rpl6	T	C	5: 121,208,478	V214A	probably benign	Het
Samd3	T	A	10: 26,271,854	C476S	possibly damaging	Het
Sfi1	TCGC	TC	11: 3,146,254		probably null	Het
Smcr8	T	C	11: 60,778,115	Y30H	probably damaging	Het
Smpd4	T	A	16: 17,641,597		probably null	Het
Strip1	C	A	3: 107,614,613	D750Y	probably damaging	Het
Svep1	T	C	4: 58,070,851	K2312E	possibly damaging	Het
Taf1c	A	T	8: 119,599,983	I438N	probably damaging	Het
Tnfaip1	A	T	11: 78,530,014		probably benign	Het
Unc45b	T	A	11: 82,940,205	L797Q	possibly damaging	Het
Usp24	T	A	4: 106,407,133	W1754R	probably damaging	Het
Utp20	G	A	10: 88,777,516	P1301L	probably benign	Het
Vmn2r115	T	A	17: 23,359,781	S743T	probably damaging	Het
Vps41	T	G	13: 18,854,663		probably null	Het
Vps72	G	T	3: 95,122,583	L304F	probably damaging	Het
Wiz	A	T	17: 32,356,441	I907N	probably damaging	Het
Zfp521	T	C	18: 13,845,062	T765A	probably benign	Het
Zfp616	A	T	11: 74,085,674	H923L	probably damaging	Het
Zp2	A	T	7: 120,143,576		probably benign	Het

Other mutations in Shank1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00970:Shank1	APN	7	44354238	missense	possibly damaging	0.89
IGL01293:Shank1	APN	7	44354236	missense	possibly damaging	0.59
IGL01319:Shank1	APN	7	44353123	missense	possibly damaging	0.93
IGL01347:Shank1	APN	7	44342120	missense	unknown
IGL01621:Shank1	APN	7	44342465	missense	unknown
IGL01621:Shank1	APN	7	44351599	missense	unknown
IGL01964:Shank1	APN	7	44325678	missense	unknown
IGL02309:Shank1	APN	7	44312842	missense	unknown
IGL02325:Shank1	APN	7	44327080	nonsense	probably null
IGL02387:Shank1	APN	7	44356937	missense	possibly damaging	0.77
IGL02958:Shank1	APN	7	44354473	missense	possibly damaging	0.59
R0098:Shank1	UTSW	7	44313285	missense	unknown
R0098:Shank1	UTSW	7	44313285	missense	unknown
R0326:Shank1	UTSW	7	44319170	missense	unknown
R0365:Shank1	UTSW	7	44353977	missense	possibly damaging	0.89
R0883:Shank1	UTSW	7	44352294	missense	unknown
R1033:Shank1	UTSW	7	44356796	missense	possibly damaging	0.77
R1390:Shank1	UTSW	7	44357038	missense	probably damaging	1.00
R1453:Shank1	UTSW	7	44316075	missense	unknown
R1594:Shank1	UTSW	7	44327223	nonsense	probably null
R1713:Shank1	UTSW	7	44319737	missense	unknown
R1783:Shank1	UTSW	7	44352737	missense	possibly damaging	0.70
R1869:Shank1	UTSW	7	44342115	nonsense	probably null
R1870:Shank1	UTSW	7	44342115	nonsense	probably null
R1959:Shank1	UTSW	7	44325377	missense	unknown
R1962:Shank1	UTSW	7	44344323	critical splice donor site	probably null
R2406:Shank1	UTSW	7	44356952	missense	possibly damaging	0.94
R2509:Shank1	UTSW	7	44351724	missense	unknown
R2509:Shank1	UTSW	7	44352123	missense	unknown
R3877:Shank1	UTSW	7	44344992	missense	unknown
R4041:Shank1	UTSW	7	44342162	missense	unknown
R4249:Shank1	UTSW	7	44319736	missense	unknown
R4303:Shank1	UTSW	7	44342474	missense	unknown
R4431:Shank1	UTSW	7	44319652	nonsense	probably null
R4525:Shank1	UTSW	7	44354590	missense	possibly damaging	0.77
R4527:Shank1	UTSW	7	44354590	missense	possibly damaging	0.77
R4642:Shank1	UTSW	7	44313141	missense	unknown
R4722:Shank1	UTSW	7	44313214	nonsense	probably null
R4805:Shank1	UTSW	7	44343711	missense	unknown
R4874:Shank1	UTSW	7	44316073	missense	unknown
R4904:Shank1	UTSW	7	44334040	intron	probably benign
R4939:Shank1	UTSW	7	44326162	missense	unknown
R5394:Shank1	UTSW	7	44352651	missense	possibly damaging	0.85
R5410:Shank1	UTSW	7	44351822	missense	unknown
R5556:Shank1	UTSW	7	44344315	intron	probably benign
R5620:Shank1	UTSW	7	44312736	missense	unknown
R5656:Shank1	UTSW	7	44352886	missense	probably benign	0.33
R5688:Shank1	UTSW	7	44354487	missense	possibly damaging	0.77
R5740:Shank1	UTSW	7	44353740	missense	possibly damaging	0.89
R5801:Shank1	UTSW	7	44356816	missense	possibly damaging	0.77
R6179:Shank1	UTSW	7	44357206	missense	possibly damaging	0.58
R6186:Shank1	UTSW	7	44352566	missense	probably benign	0.18
R6245:Shank1	UTSW	7	44352253	missense	unknown
R6500:Shank1	UTSW	7	44327221	missense	unknown
R6602:Shank1	UTSW	7	44352336	missense	probably benign	0.03
R6655:Shank1	UTSW	7	44327220	missense	unknown
R6709:Shank1	UTSW	7	44354176	missense	probably benign	0.43
R6734:Shank1	UTSW	7	44353686	missense	probably benign	0.01
R6881:Shank1	UTSW	7	44351793	missense	unknown
R6902:Shank1	UTSW	7	44356815	missense	probably benign	0.39
R6975:Shank1	UTSW	7	44313106	splice site	probably null
R6985:Shank1	UTSW	7	44344913	missense	unknown
R7072:Shank1	UTSW	7	44344946	missense	unknown
R7116:Shank1	UTSW	7	44327161	missense	unknown
R7117:Shank1	UTSW	7	44327161	missense	unknown
R7199:Shank1	UTSW	7	44353140	missense	possibly damaging	0.86
R7249:Shank1	UTSW	7	44327161	missense	unknown
R7252:Shank1	UTSW	7	44327161	missense	unknown
R7552:Shank1	UTSW	7	44353028	missense	probably benign	0.00
R7653:Shank1	UTSW	7	44319669	missense	unknown
R7707:Shank1	UTSW	7	44344301	missense	unknown
R7801:Shank1	UTSW	7	44351598	missense	unknown
R7804:Shank1	UTSW	7	44312884	missense	unknown
R8122:Shank1	UTSW	7	44333591	missense	unknown
R8178:Shank1	UTSW	7	44313324	critical splice donor site	probably null
R8339:Shank1	UTSW	7	44326165	missense	unknown
R8463:Shank1	UTSW	7	44354181	missense	possibly damaging	0.77
R9005:Shank1	UTSW	7	44352985	missense	probably benign	0.00
R9023:Shank1	UTSW	7	44319107	missense	unknown
R9225:Shank1	UTSW	7	44334046	missense	unknown
R9234:Shank1	UTSW	7	44313155	missense	unknown
R9369:Shank1	UTSW	7	44352054	missense	unknown
R9432:Shank1	UTSW	7	44312918	missense	unknown
R9433:Shank1	UTSW	7	44312918	missense	unknown
R9434:Shank1	UTSW	7	44312918	missense	unknown
X0019:Shank1	UTSW	7	44356928	missense	probably damaging	1.00
X0065:Shank1	UTSW	7	44351929	missense	unknown
Z1088:Shank1	UTSW	7	44352166	missense	unknown
Z1177:Shank1	UTSW	7	44325644	missense	unknown

Predicted Primers

PCR Primer
(F):5'- GGGCCGAGAGAAGAGCCTATATCAC -3'
(R):5'- CCACTAGGGCTGCTCCAAACTG -3'

Sequencing Primer
(F):5'- ccaccaccacccacctc -3'
(R):5'- CTAGTGAAATCCAGGGTGGC -3'

Posted On

2013-07-24