Incidental Mutation 'R9694:Ergic1'
ID 735987
Institutional Source Beutler Lab
Gene Symbol Ergic1
Ensembl Gene ENSMUSG00000001576
Gene Name endoplasmic reticulum-golgi intermediate compartment 1
Synonyms 1200007D18Rik
MMRRC Submission
Accession Numbers
Essential gene? Probably essential (E-score: 0.851) question?
Stock # R9694 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 26780463-26875908 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 26843585 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 59 (D59E)
Ref Sequence ENSEMBL: ENSMUSP00000132922 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167662] [ENSMUST00000170640]
AlphaFold Q9DC16
Predicted Effect probably benign
Transcript: ENSMUST00000167662
AA Change: D59E

PolyPhen 2 Score 0.255 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000132922
Gene: ENSMUSG00000001576
AA Change: D59E

DomainStartEndE-ValueType
Pfam:ERGIC_N 5 98 1.1e-39 PFAM
Pfam:COPIIcoated_ERV 95 271 1.2e-38 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000170640
AA Change: D18E

PolyPhen 2 Score 0.150 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000126282
Gene: ENSMUSG00000001576
AA Change: D18E

DomainStartEndE-ValueType
Pfam:ERGIC_N 1 62 1.1e-13 PFAM
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.7%
  • 10x: 99.3%
  • 20x: 98.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a cycling membrane protein which is an endoplasmic reticulum-golgi intermediate compartment (ERGIC) protein which interacts with other members of this protein family to increase their turnover. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb1b T A 5: 8,899,573 (GRCm39) Y948N probably damaging Het
Adamts2 A G 11: 50,558,972 (GRCm39) D229G probably benign Het
Adamts4 T C 1: 171,081,530 (GRCm39) S395P probably benign Het
Adcy1 T C 11: 7,094,774 (GRCm39) Y567H probably damaging Het
Agap3 A G 5: 24,682,139 (GRCm39) N212D probably benign Het
Atp2a2 A G 5: 122,597,708 (GRCm39) F775S probably damaging Het
Baz1b A T 5: 135,273,094 (GRCm39) Q1406L probably benign Het
C030006K11Rik A T 15: 76,607,928 (GRCm39) V30D possibly damaging Het
Cep170b T A 12: 112,701,993 (GRCm39) V262E probably damaging Het
Cgnl1 C T 9: 71,632,803 (GRCm39) G183R probably benign Het
Chd8 A G 14: 52,441,341 (GRCm39) I2257T possibly damaging Het
Chrna7 A G 7: 62,754,809 (GRCm39) I266T probably damaging Het
Cyp3a25 A T 5: 145,923,685 (GRCm39) Y319* probably null Het
Dcdc2a A T 13: 25,286,340 (GRCm39) I125F probably benign Het
Dcdc2c A T 12: 28,585,553 (GRCm39) I80N Het
Dmtn T C 14: 70,852,732 (GRCm39) probably null Het
Dock2 T C 11: 34,218,054 (GRCm39) N1172S probably benign Het
Dock9 A G 14: 121,818,791 (GRCm39) S1564P probably damaging Het
Ecel1 T C 1: 87,080,853 (GRCm39) I350V possibly damaging Het
Eif4enif1 C T 11: 3,170,384 (GRCm39) L146F probably damaging Het
F2rl2 A T 13: 95,838,050 (GRCm39) D365V possibly damaging Het
Fbxl16 C T 17: 26,036,813 (GRCm39) Q265* probably null Het
Fbxw26 T C 9: 109,575,135 (GRCm39) probably benign Het
Fras1 A T 5: 96,929,545 (GRCm39) Y3983F probably benign Het
G6pd2 T A 5: 61,966,460 (GRCm39) D78E probably benign Het
Gas2l2 A C 11: 83,314,170 (GRCm39) S381A possibly damaging Het
Gm57858 A G 3: 36,073,092 (GRCm39) S397P possibly damaging Het
Grk2 G A 19: 4,338,511 (GRCm39) R474C probably damaging Het
Gxylt2 T A 6: 100,710,174 (GRCm39) V105E probably benign Het
Hexd T C 11: 121,107,813 (GRCm39) V181A probably damaging Het
Ift70a2 T C 2: 75,807,691 (GRCm39) T274A probably benign Het
Ik T A 18: 36,877,840 (GRCm39) D5E probably benign Het
Ilkap A G 1: 91,303,973 (GRCm39) C163R Het
Itpr3 C T 17: 27,334,927 (GRCm39) T2147I probably damaging Het
Kif1a A T 1: 92,950,173 (GRCm39) V1418E probably benign Het
Kif26b T C 1: 178,743,815 (GRCm39) C1304R probably benign Het
Lmna CAGCACGGTGCGTGAGC CAGC 3: 88,389,857 (GRCm39) probably null Het
Lvrn A T 18: 47,033,609 (GRCm39) D940V probably damaging Het
Mill1 G A 7: 17,997,027 (GRCm39) R206H probably benign Het
Mrgpra1 A T 7: 46,985,268 (GRCm39) L137Q probably damaging Het
Npc2 C A 12: 84,807,638 (GRCm39) L73F probably benign Het
Or11g26 A G 14: 50,752,669 (GRCm39) T3A probably benign Het
Or52i2 A T 7: 102,320,011 (GRCm39) I295F possibly damaging Het
Or5al1 T C 2: 85,990,681 (GRCm39) E11G probably benign Het
Or5b97 A T 19: 12,879,021 (GRCm39) V41E probably damaging Het
Or5j3 T C 2: 86,128,718 (GRCm39) I186T probably benign Het
Osbpl1a T C 18: 12,952,565 (GRCm39) H533R probably benign Het
Pax7 G A 4: 139,556,819 (GRCm39) T147M probably benign Het
Pdik1l A T 4: 134,006,711 (GRCm39) S143T unknown Het
Prkg1 T G 19: 30,764,371 (GRCm39) T255P possibly damaging Het
Prmt2 A T 10: 76,061,213 (GRCm39) I91N probably damaging Het
Ptprm A G 17: 67,116,484 (GRCm39) Y932H probably damaging Het
Ptprz1 A T 6: 22,959,694 (GRCm39) I64F probably damaging Het
Qrich2 T C 11: 116,337,946 (GRCm39) K154R probably damaging Het
Rab8b T C 9: 66,826,824 (GRCm39) D31G probably benign Het
Radil A G 5: 142,473,378 (GRCm39) S768P probably damaging Het
Rbm5 A T 9: 107,622,152 (GRCm39) D607E probably benign Het
Reep6 T A 10: 80,169,393 (GRCm39) V131E probably damaging Het
Rrbp1 T A 2: 143,832,099 (GRCm39) I23F probably damaging Het
Rubcn A T 16: 32,663,481 (GRCm39) V385D probably benign Het
Sall2 C T 14: 52,552,124 (GRCm39) G357D possibly damaging Het
Slc12a6 T A 2: 112,174,881 (GRCm39) L547H probably damaging Het
Slc16a6 T C 11: 109,354,322 (GRCm39) T100A probably benign Het
Sptbn2 T C 19: 4,800,535 (GRCm39) L2250P probably damaging Het
Stab1 C T 14: 30,876,901 (GRCm39) A808T probably benign Het
Stag1 A G 9: 100,810,151 (GRCm39) T785A probably benign Het
Stambpl1 T G 19: 34,211,535 (GRCm39) S199A probably benign Het
Styxl2 A T 1: 165,928,654 (GRCm39) S319R probably damaging Het
Supt20 C T 3: 54,623,015 (GRCm39) S496L probably benign Het
Tanc1 T C 2: 59,626,196 (GRCm39) F518L probably damaging Het
Tdpoz3 T A 3: 93,734,156 (GRCm39) V277D probably benign Het
Unc45a A C 7: 79,975,403 (GRCm39) Y934D probably damaging Het
Vmn1r192 G A 13: 22,372,119 (GRCm39) P34S probably benign Het
Wipf3 T C 6: 54,466,004 (GRCm39) S421P possibly damaging Het
Zfp296 A G 7: 19,314,227 (GRCm39) K361E possibly damaging Het
Zfp882 T A 8: 72,667,915 (GRCm39) N247K probably benign Het
Zfpm2 A G 15: 40,965,710 (GRCm39) T732A possibly damaging Het
Other mutations in Ergic1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02312:Ergic1 APN 17 26,848,601 (GRCm39) missense probably damaging 0.96
R1157:Ergic1 UTSW 17 26,833,369 (GRCm39) missense probably damaging 1.00
R1536:Ergic1 UTSW 17 26,860,680 (GRCm39) critical splice donor site probably null
R2147:Ergic1 UTSW 17 26,855,024 (GRCm39) splice site probably null
R2200:Ergic1 UTSW 17 26,860,566 (GRCm39) missense possibly damaging 0.82
R4721:Ergic1 UTSW 17 26,857,750 (GRCm39) missense probably damaging 1.00
R4897:Ergic1 UTSW 17 26,848,597 (GRCm39) missense probably benign 0.00
R5523:Ergic1 UTSW 17 26,843,580 (GRCm39) missense probably damaging 1.00
R5526:Ergic1 UTSW 17 26,843,652 (GRCm39) missense probably damaging 1.00
R5646:Ergic1 UTSW 17 26,833,332 (GRCm39) missense probably damaging 1.00
R7015:Ergic1 UTSW 17 26,873,853 (GRCm39) intron probably benign
R7182:Ergic1 UTSW 17 26,873,856 (GRCm39) missense
R7323:Ergic1 UTSW 17 26,860,644 (GRCm39) missense probably damaging 1.00
R7763:Ergic1 UTSW 17 26,857,801 (GRCm39) missense possibly damaging 0.88
R7832:Ergic1 UTSW 17 26,853,449 (GRCm39) missense probably damaging 1.00
R8405:Ergic1 UTSW 17 26,874,096 (GRCm39) missense probably damaging 1.00
R9618:Ergic1 UTSW 17 26,827,619 (GRCm39) missense probably damaging 1.00
Z1177:Ergic1 UTSW 17 26,873,861 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- CTGGACATGTGCACACTGTTG -3'
(R):5'- CTATGATTCCAGAAAACAGGTGGG -3'

Sequencing Primer
(F):5'- GTACCCACATGGATATCTGGATC -3'
(R):5'- TATGTATATTTACACACGCACACAC -3'
Posted On 2022-11-14