Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02887:Golgb1'

363825

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Golgb1

Ensembl Gene

ENSMUSG00000034243

Gene Name

golgi autoantigen, golgin subfamily b, macrogolgin 1

Synonyms

Giantin, C130074L01Rik, F730017E11Rik, Gm6840, 6330407A06Rik

Accession Numbers

Essential gene?

Probably essential (E-score: 0.908) question?

Stock #

IGL02887

Quality Score

Status

Chromosome

Chromosomal Location

36875140-36933085 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 36925849 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Arginine at position 2930 (L2930R)

Ref Sequence

ENSEMBL: ENSMUSP00000110460 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039855] [ENSMUST00000114812]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000039855
AA Change: L2971R

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

SMART Domains

Protein: ENSMUSP00000045239
Gene: ENSMUSG00000034243
AA Change: L2971R

Domain	Start	End	E-Value	Type
internal_repeat_2	24	61	7.47e-6	PROSPERO
low complexity region	87	107	N/A	INTRINSIC
coiled coil region	130	219	N/A	INTRINSIC
low complexity region	491	512	N/A	INTRINSIC
internal_repeat_3	519	558	7.47e-6	PROSPERO
coiled coil region	563	594	N/A	INTRINSIC
internal_repeat_4	627	661	3.38e-5	PROSPERO
coiled coil region	679	1121	N/A	INTRINSIC
coiled coil region	1153	1240	N/A	INTRINSIC
internal_repeat_4	1253	1288	3.38e-5	PROSPERO
low complexity region	1300	1314	N/A	INTRINSIC
internal_repeat_1	1321	1352	3.51e-6	PROSPERO
low complexity region	1357	1369	N/A	INTRINSIC
coiled coil region	1402	1755	N/A	INTRINSIC
internal_repeat_2	1760	1798	7.47e-6	PROSPERO
internal_repeat_3	1761	1804	7.47e-6	PROSPERO
coiled coil region	1818	2034	N/A	INTRINSIC
low complexity region	2291	2306	N/A	INTRINSIC
internal_repeat_1	2351	2382	3.51e-6	PROSPERO
low complexity region	2400	2418	N/A	INTRINSIC
low complexity region	2538	2549	N/A	INTRINSIC
coiled coil region	2775	2827	N/A	INTRINSIC
coiled coil region	2854	2943	N/A	INTRINSIC
low complexity region	2964	2976	N/A	INTRINSIC
coiled coil region	3007	3057	N/A	INTRINSIC
coiled coil region	3117	3163	N/A	INTRINSIC
transmembrane domain	3215	3237	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000114812
AA Change: L2930R

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

SMART Domains

Protein: ENSMUSP00000110460
Gene: ENSMUSG00000034243
AA Change: L2930R

Domain	Start	End	E-Value	Type
internal_repeat_2	24	61	6.71e-6	PROSPERO
low complexity region	87	107	N/A	INTRINSIC
low complexity region	120	134	N/A	INTRINSIC
low complexity region	143	154	N/A	INTRINSIC
low complexity region	200	219	N/A	INTRINSIC
low complexity region	450	471	N/A	INTRINSIC
internal_repeat_3	478	517	6.71e-6	PROSPERO
coiled coil region	522	553	N/A	INTRINSIC
internal_repeat_4	586	620	3.05e-5	PROSPERO
coiled coil region	638	1080	N/A	INTRINSIC
coiled coil region	1112	1199	N/A	INTRINSIC
internal_repeat_4	1212	1247	3.05e-5	PROSPERO
low complexity region	1259	1273	N/A	INTRINSIC
internal_repeat_1	1280	1311	3.14e-6	PROSPERO
low complexity region	1316	1328	N/A	INTRINSIC
coiled coil region	1361	1714	N/A	INTRINSIC
internal_repeat_2	1719	1757	6.71e-6	PROSPERO
internal_repeat_3	1720	1763	6.71e-6	PROSPERO
coiled coil region	1777	1993	N/A	INTRINSIC
low complexity region	2250	2265	N/A	INTRINSIC
internal_repeat_1	2310	2341	3.14e-6	PROSPERO
low complexity region	2359	2377	N/A	INTRINSIC
low complexity region	2497	2508	N/A	INTRINSIC
coiled coil region	2734	2786	N/A	INTRINSIC
coiled coil region	2813	2902	N/A	INTRINSIC
low complexity region	2923	2935	N/A	INTRINSIC
coiled coil region	2966	3016	N/A	INTRINSIC
coiled coil region	3076	3122	N/A	INTRINSIC
transmembrane domain	3174	3196	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152864

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Homozygous knockout affects glycosylation of glycoproteins in the extra-cellular matrix of the palatal shelves, resulting in their failure to elevate and fuse, leading to cleft palate. [provided by MGI curators]

Allele List at MGI

All alleles(7) : Targeted, other(2) Gene trapped(5)

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017B05Rik	A	G	9: 57,258,885 (GRCm38)	Y69H	probably damaging	Het
Afap1l2	A	T	19: 56,920,563 (GRCm38)	S310R	probably damaging	Het
Aldh7a1	A	G	18: 56,542,216 (GRCm38)		probably benign	Het
Anxa8	T	A	14: 34,096,524 (GRCm38)		probably null	Het
Ap1ar	T	C	3: 127,808,543 (GRCm38)	E282G	probably damaging	Het
Arl6ip6	T	G	2: 53,202,927 (GRCm38)	S155A	probably benign	Het
Armc9	T	C	1: 86,164,835 (GRCm38)	F107S	probably damaging	Het
Ash1l	C	A	3: 88,984,181 (GRCm38)	D1122E	probably benign	Het
Atp2b4	T	A	1: 133,728,774 (GRCm38)	I713F	probably damaging	Het
BC005624	A	C	2: 30,973,305 (GRCm38)		probably benign	Het
Calcrl	T	C	2: 84,339,242 (GRCm38)	D365G	probably benign	Het
Ccdc110	A	G	8: 45,943,184 (GRCm38)	N704S	probably benign	Het
Ccr10	G	T	11: 101,174,666 (GRCm38)	L13I	probably benign	Het
Cfap52	A	G	11: 67,953,515 (GRCm38)	Y125H	probably damaging	Het
Cnr2	C	A	4: 135,917,625 (GRCm38)	T338K	possibly damaging	Het
Cntn2	T	A	1: 132,516,570 (GRCm38)	D935V	probably damaging	Het
Cog7	T	C	7: 121,943,844 (GRCm38)	K448R	possibly damaging	Het
Csnk1g2	G	A	10: 80,638,535 (GRCm38)	D197N	probably damaging	Het
Cyp2e1	T	A	7: 140,763,911 (GRCm38)	S21T	probably damaging	Het
Dcaf11	T	C	14: 55,564,135 (GRCm38)	F187L	probably damaging	Het
Dmd	T	A	X: 83,878,504 (GRCm38)	F1460Y	probably benign	Het
Dnah11	G	A	12: 117,911,040 (GRCm38)	A4030V	probably damaging	Het
Dnah7a	A	G	1: 53,522,360 (GRCm38)	V2046A	possibly damaging	Het
Dnajc6	T	C	4: 101,639,300 (GRCm38)	I820T	probably damaging	Het
Dsel	T	C	1: 111,860,732 (GRCm38)	D691G	possibly damaging	Het
Fbp1	T	A	13: 62,869,080 (GRCm38)	M203L	probably benign	Het
Fndc1	T	C	17: 7,773,638 (GRCm38)	T409A	unknown	Het
Htr2a	A	G	14: 74,645,143 (GRCm38)	T190A	probably benign	Het
Klra4	C	T	6: 130,044,070 (GRCm38)	C254Y	probably damaging	Het
Large1	A	T	8: 73,132,039 (GRCm38)	V67E	probably benign	Het
Lins1	T	C	7: 66,714,183 (GRCm38)	S609P	probably damaging	Het
Magi3	T	C	3: 104,095,157 (GRCm38)	E156G	probably damaging	Het
Mdh1b	A	G	1: 63,715,364 (GRCm38)		probably benign	Het
Mfsd6	T	C	1: 52,708,878 (GRCm38)	D276G	probably benign	Het
Myh9	T	A	15: 77,796,020 (GRCm38)	K185*	probably null	Het
Myof	T	C	19: 37,920,779 (GRCm38)		probably null	Het
Naip2	T	G	13: 100,161,512 (GRCm38)	Y672S	possibly damaging	Het
Nbeal1	A	G	1: 60,287,444 (GRCm38)		probably benign	Het
Nbeal2	T	A	9: 110,628,276 (GRCm38)	H2273L	probably damaging	Het
Neb	T	C	2: 52,200,721 (GRCm38)	K1346E	possibly damaging	Het
Nfatc2	T	C	2: 168,504,450 (GRCm38)	D908G	probably damaging	Het
Nlgn2	T	C	11: 69,827,254 (GRCm38)	N375S	probably benign	Het
Nova1	G	T	12: 46,720,722 (GRCm38)	Q139K	unknown	Het
Opa3	A	T	7: 19,228,582 (GRCm38)	Q47L	probably damaging	Het
Or10g7	T	A	9: 39,993,813 (GRCm38)	M1K	probably null	Het
Or2t47	A	G	11: 58,552,161 (GRCm38)	L26P	probably damaging	Het
Or6c205	T	A	10: 129,250,925 (GRCm38)	Y130*	probably null	Het
Pacs1	A	T	19: 5,135,110 (GRCm38)		probably benign	Het
Pappa2	T	A	1: 158,782,259 (GRCm38)	H1544L	probably damaging	Het
Pax8	A	G	2: 24,444,615 (GRCm38)	S48P	probably damaging	Het
Pdilt	T	C	7: 119,498,049 (GRCm38)	N70S	possibly damaging	Het
Poldip3	T	C	15: 83,129,268 (GRCm38)		probably benign	Het
Ppp6r1	T	A	7: 4,642,212 (GRCm38)	I80F	probably damaging	Het
Pycr2	T	A	1: 180,904,739 (GRCm38)		probably null	Het
Rapgef2	C	T	3: 79,068,880 (GRCm38)		probably benign	Het
Rbm44	T	A	1: 91,153,180 (GRCm38)	D363E	probably damaging	Het
Rnf213	A	T	11: 119,427,510 (GRCm38)	I1046F	probably damaging	Het
Ryr2	A	G	13: 11,591,269 (GRCm38)	S4476P	probably damaging	Het
Scara5	G	A	14: 65,762,829 (GRCm38)	D483N	unknown	Het
Scmh1	T	A	4: 120,468,389 (GRCm38)	F101Y	probably damaging	Het
Sgo2a	T	A	1: 58,016,352 (GRCm38)	V565E	probably damaging	Het
Simc1	T	C	13: 54,525,258 (GRCm38)	M473T	probably benign	Het
Skint6	T	A	4: 113,238,184 (GRCm38)	R93*	probably null	Het
Skint7	T	C	4: 111,982,178 (GRCm38)	V223A	possibly damaging	Het
Slc25a2	T	C	18: 37,637,886 (GRCm38)	I197V	probably benign	Het
Slit2	A	G	5: 48,217,474 (GRCm38)	T361A	probably benign	Het
Sugp1	G	A	8: 70,070,126 (GRCm38)	G492D	probably damaging	Het
Svep1	C	T	4: 58,145,301 (GRCm38)	G388D	probably damaging	Het
Tbpl2	G	T	2: 24,093,876 (GRCm38)	A183E	probably damaging	Het
Tcerg1l	G	T	7: 138,229,890 (GRCm38)	P453T	probably damaging	Het
Tdpoz2	T	C	3: 93,651,739 (GRCm38)	T309A	probably benign	Het
Thbs4	T	A	13: 92,790,798 (GRCm38)	Y61F	probably benign	Het
Tmem117	C	A	15: 95,094,775 (GRCm38)	P439T	probably damaging	Het
Tmem151a	A	G	19: 5,082,965 (GRCm38)	V71A	probably benign	Het
Tmem268	G	T	4: 63,568,454 (GRCm38)		probably benign	Het
Tmem43	T	A	6: 91,477,374 (GRCm38)	Y48N	possibly damaging	Het
Tmigd1	T	C	11: 76,913,986 (GRCm38)	V217A	probably benign	Het
Tmprss11g	A	T	5: 86,497,329 (GRCm38)		probably benign	Het
Tsn	T	C	1: 118,309,821 (GRCm38)	I38V	probably benign	Het
Ttc41	A	T	10: 86,733,654 (GRCm38)	Y632F	probably damaging	Het
Vmn2r117	C	T	17: 23,475,578 (GRCm38)		probably benign	Het
Vmn2r12	A	T	5: 109,090,485 (GRCm38)	I463N	probably benign	Het
Wdsub1	T	A	2: 59,852,832 (GRCm38)	N466I	probably damaging	Het
Zdhhc21	A	T	4: 82,844,190 (GRCm38)	I56N	probably benign	Het
Zfand4	A	G	6: 116,273,656 (GRCm38)	T16A	possibly damaging	Het
Zmym4	T	C	4: 126,948,475 (GRCm38)	E15G	probably damaging	Het

Other mutations in Golgb1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01394:Golgb1	APN	16	36,931,564 (GRCm38)	missense	probably damaging	1.00
IGL01717:Golgb1	APN	16	36,915,502 (GRCm38)	nonsense	probably null
IGL01965:Golgb1	APN	16	36,917,920 (GRCm38)	missense	probably damaging	1.00
IGL02128:Golgb1	APN	16	36,916,304 (GRCm38)	missense	probably damaging	1.00
IGL02268:Golgb1	APN	16	36,913,128 (GRCm38)	missense	probably benign	0.25
IGL02383:Golgb1	APN	16	36,886,200 (GRCm38)	missense	probably benign	0.01
IGL02444:Golgb1	APN	16	36,907,816 (GRCm38)	splice site	probably benign
IGL02635:Golgb1	APN	16	36,915,013 (GRCm38)	missense	probably benign	0.00
IGL02655:Golgb1	APN	16	36,918,080 (GRCm38)	missense	probably damaging	0.98
IGL02937:Golgb1	APN	16	36,916,210 (GRCm38)	missense	probably damaging	1.00
IGL02973:Golgb1	APN	16	36,912,080 (GRCm38)	missense	possibly damaging	0.92
IGL02982:Golgb1	APN	16	36,925,810 (GRCm38)	missense	probably damaging	0.98
IGL03065:Golgb1	APN	16	36,912,866 (GRCm38)	missense	probably benign	0.11
IGL03109:Golgb1	APN	16	36,915,611 (GRCm38)	missense	possibly damaging	0.93
IGL03323:Golgb1	APN	16	36,913,453 (GRCm38)	nonsense	probably null
I2288:Golgb1	UTSW	16	36,898,542 (GRCm38)	missense	probably benign	0.00
I2289:Golgb1	UTSW	16	36,898,542 (GRCm38)	missense	probably benign	0.00
R0071:Golgb1	UTSW	16	36,915,503 (GRCm38)	missense	probably benign	0.00
R0071:Golgb1	UTSW	16	36,915,503 (GRCm38)	missense	probably benign	0.00
R0080:Golgb1	UTSW	16	36,898,611 (GRCm38)	missense	probably damaging	1.00
R0102:Golgb1	UTSW	16	36,875,468 (GRCm38)	intron	probably benign
R0242:Golgb1	UTSW	16	36,875,630 (GRCm38)	nonsense	probably null
R0242:Golgb1	UTSW	16	36,875,630 (GRCm38)	nonsense	probably null
R0276:Golgb1	UTSW	16	36,913,876 (GRCm38)	missense	probably damaging	1.00
R0394:Golgb1	UTSW	16	36,875,579 (GRCm38)	intron	probably benign
R0469:Golgb1	UTSW	16	36,931,635 (GRCm38)	missense	probably benign	0.41
R0522:Golgb1	UTSW	16	36,915,205 (GRCm38)	frame shift	probably null
R0575:Golgb1	UTSW	16	36,918,809 (GRCm38)	missense	probably benign
R0600:Golgb1	UTSW	16	36,916,271 (GRCm38)	missense	probably damaging	1.00
R0608:Golgb1	UTSW	16	36,916,330 (GRCm38)	nonsense	probably null
R0711:Golgb1	UTSW	16	36,918,790 (GRCm38)	missense	probably damaging	1.00
R0785:Golgb1	UTSW	16	36,898,790 (GRCm38)	missense	possibly damaging	0.95
R0893:Golgb1	UTSW	16	36,912,277 (GRCm38)	missense	possibly damaging	0.64
R1163:Golgb1	UTSW	16	36,916,126 (GRCm38)	missense	possibly damaging	0.50
R1208:Golgb1	UTSW	16	36,915,205 (GRCm38)	frame shift	probably null
R1315:Golgb1	UTSW	16	36,914,900 (GRCm38)	missense	probably benign	0.40
R1429:Golgb1	UTSW	16	36,900,563 (GRCm38)	missense	possibly damaging	0.93
R1505:Golgb1	UTSW	16	36,919,643 (GRCm38)	missense	possibly damaging	0.79
R1537:Golgb1	UTSW	16	36,898,788 (GRCm38)	missense	possibly damaging	0.89
R1610:Golgb1	UTSW	16	36,926,101 (GRCm38)	missense	probably benign	0.25
R1659:Golgb1	UTSW	16	36,887,617 (GRCm38)	missense	probably benign	0.01
R1769:Golgb1	UTSW	16	36,916,001 (GRCm38)	missense	probably damaging	1.00
R2105:Golgb1	UTSW	16	36,914,664 (GRCm38)	missense	probably benign
R2212:Golgb1	UTSW	16	36,887,347 (GRCm38)	missense	probably damaging	1.00
R2261:Golgb1	UTSW	16	36,893,360 (GRCm38)	missense	probably damaging	1.00
R2352:Golgb1	UTSW	16	36,898,559 (GRCm38)	missense	probably damaging	0.99
R2357:Golgb1	UTSW	16	36,912,008 (GRCm38)	missense	probably damaging	1.00
R2400:Golgb1	UTSW	16	36,918,466 (GRCm38)	missense	possibly damaging	0.62
R2513:Golgb1	UTSW	16	36,915,151 (GRCm38)	missense	possibly damaging	0.73
R3103:Golgb1	UTSW	16	36,894,849 (GRCm38)	missense	probably damaging	1.00
R3413:Golgb1	UTSW	16	36,887,347 (GRCm38)	missense	probably damaging	1.00
R3748:Golgb1	UTSW	16	36,918,912 (GRCm38)	missense	probably benign	0.00
R3847:Golgb1	UTSW	16	36,898,733 (GRCm38)	missense	probably benign	0.00
R3850:Golgb1	UTSW	16	36,898,733 (GRCm38)	missense	probably benign	0.00
R3936:Golgb1	UTSW	16	36,914,056 (GRCm38)	nonsense	probably null
R3975:Golgb1	UTSW	16	36,918,571 (GRCm38)	missense	probably damaging	0.99
R4025:Golgb1	UTSW	16	36,915,344 (GRCm38)	missense	probably benign	0.00
R4369:Golgb1	UTSW	16	36,916,907 (GRCm38)	missense	probably damaging	1.00
R4518:Golgb1	UTSW	16	36,929,263 (GRCm38)	missense	probably damaging	0.98
R4600:Golgb1	UTSW	16	36,918,625 (GRCm38)	missense	probably damaging	1.00
R4610:Golgb1	UTSW	16	36,918,625 (GRCm38)	missense	probably damaging	1.00
R4660:Golgb1	UTSW	16	36,887,618 (GRCm38)	missense	probably damaging	0.99
R4811:Golgb1	UTSW	16	36,891,419 (GRCm38)	missense	probably damaging	1.00
R4815:Golgb1	UTSW	16	36,913,115 (GRCm38)	missense	possibly damaging	0.79
R4835:Golgb1	UTSW	16	36,891,407 (GRCm38)	missense	possibly damaging	0.86
R4904:Golgb1	UTSW	16	36,893,386 (GRCm38)	missense	probably damaging	1.00
R4916:Golgb1	UTSW	16	36,916,118 (GRCm38)	missense	probably benign	0.05
R5121:Golgb1	UTSW	16	36,919,258 (GRCm38)	missense	probably damaging	0.99
R5133:Golgb1	UTSW	16	36,891,457 (GRCm38)	missense	possibly damaging	0.75
R5143:Golgb1	UTSW	16	36,898,689 (GRCm38)	missense	probably benign	0.09
R5185:Golgb1	UTSW	16	36,875,141 (GRCm38)	unclassified	probably benign
R5188:Golgb1	UTSW	16	36,918,465 (GRCm38)	missense	probably benign	0.13
R5260:Golgb1	UTSW	16	36,913,141 (GRCm38)	missense	probably benign	0.00
R5297:Golgb1	UTSW	16	36,875,616 (GRCm38)	intron	probably benign
R5386:Golgb1	UTSW	16	36,912,315 (GRCm38)	nonsense	probably null
R5438:Golgb1	UTSW	16	36,900,508 (GRCm38)	missense	probably benign	0.15
R5439:Golgb1	UTSW	16	36,900,508 (GRCm38)	missense	probably benign	0.15
R5494:Golgb1	UTSW	16	36,928,683 (GRCm38)	missense	possibly damaging	0.67
R5592:Golgb1	UTSW	16	36,925,763 (GRCm38)	missense	probably benign	0.02
R5740:Golgb1	UTSW	16	36,919,000 (GRCm38)	missense	probably damaging	0.99
R5862:Golgb1	UTSW	16	36,926,091 (GRCm38)	splice site	silent
R5928:Golgb1	UTSW	16	36,911,987 (GRCm38)	missense	probably damaging	1.00
R6009:Golgb1	UTSW	16	36,914,959 (GRCm38)	missense	probably damaging	1.00
R6062:Golgb1	UTSW	16	36,914,671 (GRCm38)	missense	possibly damaging	0.89
R6102:Golgb1	UTSW	16	36,912,865 (GRCm38)	missense	probably damaging	1.00
R6198:Golgb1	UTSW	16	36,893,395 (GRCm38)	missense	probably damaging	1.00
R6253:Golgb1	UTSW	16	36,915,622 (GRCm38)	missense	possibly damaging	0.77
R6254:Golgb1	UTSW	16	36,913,978 (GRCm38)	missense	probably damaging	0.99
R6321:Golgb1	UTSW	16	36,918,197 (GRCm38)	nonsense	probably null
R6700:Golgb1	UTSW	16	36,875,584 (GRCm38)	intron	probably benign
R6870:Golgb1	UTSW	16	36,918,203 (GRCm38)	missense	probably damaging	1.00
R6882:Golgb1	UTSW	16	36,913,990 (GRCm38)	missense	probably benign
R6944:Golgb1	UTSW	16	36,912,113 (GRCm38)	missense	probably benign
R7108:Golgb1	UTSW	16	36,913,721 (GRCm38)	missense	probably benign	0.01
R7124:Golgb1	UTSW	16	36,913,673 (GRCm38)	missense	probably benign	0.01
R7125:Golgb1	UTSW	16	36,917,963 (GRCm38)	missense	possibly damaging	0.85
R7187:Golgb1	UTSW	16	36,916,150 (GRCm38)	missense	probably benign	0.43
R7205:Golgb1	UTSW	16	36,875,301 (GRCm38)	missense	unknown
R7206:Golgb1	UTSW	16	36,913,749 (GRCm38)	missense	probably benign	0.41
R7233:Golgb1	UTSW	16	36,914,758 (GRCm38)	missense	possibly damaging	0.91
R7320:Golgb1	UTSW	16	36,915,951 (GRCm38)	nonsense	probably null
R7367:Golgb1	UTSW	16	36,898,546 (GRCm38)	missense	probably benign	0.00
R7408:Golgb1	UTSW	16	36,898,547 (GRCm38)	missense	probably damaging	0.98
R7419:Golgb1	UTSW	16	36,912,919 (GRCm38)	missense	possibly damaging	0.95
R7556:Golgb1	UTSW	16	36,915,793 (GRCm38)	missense	probably benign	0.03
R7599:Golgb1	UTSW	16	36,875,396 (GRCm38)	missense	unknown
R7673:Golgb1	UTSW	16	36,913,669 (GRCm38)	missense	probably benign	0.05
R7789:Golgb1	UTSW	16	36,875,399 (GRCm38)	missense	unknown
R7792:Golgb1	UTSW	16	36,918,730 (GRCm38)	missense	probably benign	0.43
R7830:Golgb1	UTSW	16	36,898,721 (GRCm38)	missense	possibly damaging	0.93
R7847:Golgb1	UTSW	16	36,931,920 (GRCm38)	missense	probably damaging	1.00
R7905:Golgb1	UTSW	16	36,913,685 (GRCm38)	missense	probably benign
R7944:Golgb1	UTSW	16	36,914,104 (GRCm38)	missense	probably benign	0.02
R7945:Golgb1	UTSW	16	36,914,104 (GRCm38)	missense	probably benign	0.02
R7950:Golgb1	UTSW	16	36,915,424 (GRCm38)	missense	probably benign	0.13
R8040:Golgb1	UTSW	16	36,913,479 (GRCm38)	missense	possibly damaging	0.85
R8077:Golgb1	UTSW	16	36,918,633 (GRCm38)	missense	probably damaging	0.99
R8181:Golgb1	UTSW	16	36,916,830 (GRCm38)	missense	probably damaging	1.00
R8370:Golgb1	UTSW	16	36,912,317 (GRCm38)	missense	probably benign	0.00
R8684:Golgb1	UTSW	16	36,914,402 (GRCm38)	missense	possibly damaging	0.92
R8725:Golgb1	UTSW	16	36,919,201 (GRCm38)	missense	probably damaging	1.00
R8727:Golgb1	UTSW	16	36,919,201 (GRCm38)	missense	probably damaging	1.00
R8738:Golgb1	UTSW	16	36,916,313 (GRCm38)	missense	probably damaging	1.00
R8785:Golgb1	UTSW	16	36,919,744 (GRCm38)	missense	probably damaging	0.99
R8824:Golgb1	UTSW	16	36,915,689 (GRCm38)	missense	probably benign
R8825:Golgb1	UTSW	16	36,919,447 (GRCm38)	missense	probably benign	0.00
R8940:Golgb1	UTSW	16	36,916,397 (GRCm38)	missense	probably damaging	1.00
R8962:Golgb1	UTSW	16	36,913,616 (GRCm38)	missense	probably damaging	1.00
R9245:Golgb1	UTSW	16	36,918,819 (GRCm38)	nonsense	probably null
R9365:Golgb1	UTSW	16	36,915,762 (GRCm38)	missense	probably damaging	1.00
R9612:Golgb1	UTSW	16	36,919,605 (GRCm38)	missense	probably benign	0.41
R9620:Golgb1	UTSW	16	36,919,449 (GRCm38)	missense	probably benign
R9691:Golgb1	UTSW	16	36,898,634 (GRCm38)	missense	probably damaging	1.00
R9747:Golgb1	UTSW	16	36,893,407 (GRCm38)	missense	probably damaging	1.00
V1662:Golgb1	UTSW	16	36,898,542 (GRCm38)	missense	probably benign	0.00
X0067:Golgb1	UTSW	16	36,914,303 (GRCm38)	nonsense	probably null
Z1088:Golgb1	UTSW	16	36,919,742 (GRCm38)	missense	probably damaging	1.00

Posted On

2015-12-18