Incidental Mutation 'R2212:Golgb1'
ID 239477
Institutional Source Beutler Lab
Gene Symbol Golgb1
Ensembl Gene ENSMUSG00000034243
Gene Name golgi autoantigen, golgin subfamily b, macrogolgin 1
Synonyms Giantin, C130074L01Rik, F730017E11Rik, Gm6840, 6330407A06Rik
MMRRC Submission 040214-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.911) question?
Stock # R2212 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 36875140-36933085 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 36887347 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 68 (K68E)
Ref Sequence ENSEMBL: ENSMUSP00000116503 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039855] [ENSMUST00000114812] [ENSMUST00000134616] [ENSMUST00000135406]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000039855
AA Change: K68E

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000045239
Gene: ENSMUSG00000034243
AA Change: K68E

DomainStartEndE-ValueType
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: K68E

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000110460
Gene: ENSMUSG00000034243
AA Change: K68E

DomainStartEndE-ValueType
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 probably damaging
Transcript: ENSMUST00000134616
AA Change: K68E

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000116503
Gene: ENSMUSG00000034243
AA Change: K68E

DomainStartEndE-ValueType
coiled coil region 42 107 N/A INTRINSIC
low complexity region 120 134 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000135406
AA Change: K68E

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000115848
Gene: ENSMUSG00000034243
AA Change: K68E

DomainStartEndE-ValueType
coiled coil region 42 107 N/A INTRINSIC
low complexity region 120 134 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135800
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153572
Meta Mutation Damage Score 0.1630 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 94.9%
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: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700062C07Rik A G 18: 24,470,920 (GRCm38) Y6C probably damaging Het
3425401B19Rik T A 14: 32,661,602 (GRCm38) Q802L probably benign Het
Adarb2 T C 13: 8,752,618 (GRCm38) F643S probably damaging Het
Angptl4 A G 17: 33,775,418 (GRCm38) I401T probably damaging Het
Ap2a2 T A 7: 141,598,776 (GRCm38) N105K probably benign Het
Atp8b4 C A 2: 126,375,757 (GRCm38) W613L probably damaging Het
Coq10a A G 10: 128,365,129 (GRCm38) V93A possibly damaging Het
Cyp4f39 A T 17: 32,487,063 (GRCm38) E376V possibly damaging Het
Deup1 A T 9: 15,599,843 (GRCm38) D213E probably benign Het
Ehmt2 A G 17: 34,899,365 (GRCm38) S39G probably benign Het
Eya1 T A 1: 14,274,209 (GRCm38) probably null Het
Fam92a A G 4: 12,171,696 (GRCm38) probably null Het
Fcna G C 2: 25,627,493 (GRCm38) P49A probably damaging Het
Flnb AAGGAG AAG 14: 7,881,652 (GRCm38) probably benign Het
Fscn2 G T 11: 120,361,591 (GRCm38) probably benign Het
Gckr T A 5: 31,300,867 (GRCm38) probably null Het
H2-M11 G A 17: 36,548,930 (GRCm38) V272M probably damaging Het
Hace1 T A 10: 45,648,675 (GRCm38) D234E possibly damaging Het
Il18r1 A T 1: 40,491,067 (GRCm38) D318V probably damaging Het
Il4i1 T C 7: 44,836,658 (GRCm38) L22P probably damaging Het
Kcnq3 A T 15: 66,020,293 (GRCm38) F411Y probably benign Het
Kcnt2 A G 1: 140,530,800 (GRCm38) Y775C probably damaging Het
Krt84 A C 15: 101,532,538 (GRCm38) V73G probably benign Het
Lcp2 A C 11: 34,070,995 (GRCm38) D117A probably benign Het
Lemd1 C A 1: 132,228,286 (GRCm38) T22K probably benign Het
Mdm4 T C 1: 132,994,522 (GRCm38) D294G probably damaging Het
Mep1a G A 17: 43,477,263 (GRCm38) A634V probably benign Het
Myh15 A G 16: 49,138,732 (GRCm38) D989G probably benign Het
Myo1g G T 11: 6,517,870 (GRCm38) H188Q possibly damaging Het
Nsmaf C A 4: 6,396,732 (GRCm38) L918F probably damaging Het
Olfr1396 C T 11: 49,113,216 (GRCm38) C170Y probably damaging Het
Olfr561 T C 7: 102,774,755 (GRCm38) L77P possibly damaging Het
Olfr635 T C 7: 103,979,402 (GRCm38) L76P probably damaging Het
Olfr963 T A 9: 39,669,228 (GRCm38) M57K probably damaging Het
Pfkfb2 A T 1: 130,707,532 (GRCm38) N97K probably damaging Het
Phlda1 A T 10: 111,507,168 (GRCm38) E255V probably damaging Het
Pla2g4f T C 2: 120,303,106 (GRCm38) S579G probably benign Het
Plcz1 C T 6: 140,002,081 (GRCm38) R525Q probably damaging Het
Ppargc1b G A 18: 61,311,220 (GRCm38) Q291* probably null Het
Ppef2 T G 5: 92,228,722 (GRCm38) S649R probably damaging Het
Ppp1r3b A G 8: 35,384,225 (GRCm38) T73A possibly damaging Het
Prss43 G C 9: 110,829,464 (GRCm38) Q277H probably damaging Het
Rusc2 T G 4: 43,415,935 (GRCm38) S414A probably damaging Het
Serpina3j G A 12: 104,314,726 (GRCm38) D53N probably damaging Het
Sez6l A G 5: 112,475,361 (GRCm38) L108P possibly damaging Het
Slc1a7 A G 4: 108,010,994 (GRCm38) E497G probably benign Het
Spag8 T A 4: 43,651,606 (GRCm38) S423C probably damaging Het
Spata13 A G 14: 60,706,723 (GRCm38) T522A probably benign Het
Spryd3 A G 15: 102,130,276 (GRCm38) probably null Het
Sry T A Y: 2,663,339 (GRCm38) N107I probably damaging Het
St6galnac1 A G 11: 116,765,856 (GRCm38) W486R probably damaging Het
Syt1 G T 10: 108,504,414 (GRCm38) P348T possibly damaging Het
Taok2 T C 7: 126,870,858 (GRCm38) I933V possibly damaging Het
Tex9 C A 9: 72,477,758 (GRCm38) Q265H possibly damaging Het
Tmem63a G A 1: 180,963,114 (GRCm38) D446N possibly damaging Het
Trim59 T C 3: 69,037,543 (GRCm38) T155A probably benign Het
Trim69 T C 2: 122,178,644 (GRCm38) V395A probably benign Het
Tusc1 C A 4: 93,334,936 (GRCm38) R162L probably damaging Het
Ubash3a A T 17: 31,218,034 (GRCm38) Q208H probably damaging Het
Ubn2 A G 6: 38,498,739 (GRCm38) T1211A probably benign Het
Vmn2r110 A T 17: 20,573,947 (GRCm38) probably null Het
Vrk3 C T 7: 44,775,442 (GRCm38) T427M probably benign Het
Zfyve28 C T 5: 34,199,684 (GRCm38) M723I probably benign Het
Zmynd8 A T 2: 165,815,451 (GRCm38) M533K probably damaging Het
Other mutations in Golgb1
AlleleSourceChrCoordTypePredicted EffectPPH 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
IGL02887:Golgb1 APN 16 36,925,849 (GRCm38) missense probably damaging 0.99
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
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
Predicted Primers PCR Primer
(F):5'- CAGTTTCTAAAGAAAGGAGTTGGGC -3'
(R):5'- CCTGCCATGGAGCAAAGAAG -3'

Sequencing Primer
(F):5'- CAAAAGATGGGGCAGGTTGTG -3'
(R):5'- GTGAATTCACCGGTTATCTAGCACAC -3'
Posted On 2014-10-15