Incidental Mutation 'R8988:Efcab3'
ID 684245
Institutional Source Beutler Lab
Gene Symbol Efcab3
Ensembl Gene ENSMUSG00000020690
Gene Name EF-hand calcium binding domain 3
Synonyms Gm11639, Efcab13, 4921510J17Rik, Efcab15, Gm11639
MMRRC Submission 068820-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8988 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 104954418-105008363 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 104911352 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 4544 (V4544G)
Ref Sequence ENSEMBL: ENSMUSP00000148433 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000212287]
AlphaFold Q80X60
Predicted Effect probably benign
Transcript: ENSMUST00000212287
AA Change: V4544G

PolyPhen 2 Score 0.073 (Sensitivity: 0.93; Specificity: 0.84)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.3%
Validation Efficiency 96% (81/84)
Allele List at MGI
Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abi2 C T 1: 60,489,251 (GRCm39) T291I probably benign Het
Aox1 A C 1: 58,088,625 (GRCm39) D137A possibly damaging Het
Apbb2 T C 5: 66,609,444 (GRCm39) K68E probably damaging Het
Arf3 A T 15: 98,638,933 (GRCm39) M108K probably benign Het
Atg2b T A 12: 105,583,388 (GRCm39) I2058F probably damaging Het
Bhlhe40 C T 6: 108,639,518 (GRCm39) L99F probably damaging Het
Cd200l1 T C 16: 45,238,271 (GRCm39) H294R probably benign Het
Cyp2b10 G A 7: 25,625,670 (GRCm39) R500H probably damaging Het
Dlc1 C T 8: 37,039,997 (GRCm39) E937K probably damaging Het
Dll3 A T 7: 27,995,793 (GRCm39) V336D possibly damaging Het
Dync2h1 A G 9: 7,037,727 (GRCm39) F3377L probably benign Het
Eef1d A G 15: 75,768,160 (GRCm39) Y561H probably damaging Het
Epb41l1 C A 2: 156,363,591 (GRCm39) T700K probably benign Het
Epha8 G T 4: 136,665,897 (GRCm39) L420M probably damaging Het
Ephb2 C A 4: 136,402,769 (GRCm39) G501C probably benign Het
Erbb3 T C 10: 128,406,030 (GRCm39) Y1129C probably damaging Het
Fbn1 C T 2: 125,212,726 (GRCm39) V799M possibly damaging Het
Fbxo9 G A 9: 77,991,933 (GRCm39) P353S probably benign Het
Ggt1 T G 10: 75,412,056 (GRCm39) V100G probably benign Het
Gm45861 T C 8: 28,032,531 (GRCm39) M885T unknown Het
Grin2d A T 7: 45,483,425 (GRCm39) Y917* probably null Het
Hectd4 T A 5: 121,415,819 (GRCm39) V540D possibly damaging Het
Helz T A 11: 107,495,079 (GRCm39) I351K probably damaging Het
Ighv2-6-8 A G 12: 113,759,980 (GRCm39) V43A probably damaging Het
Igkv9-129 T A 6: 67,817,106 (GRCm39) I70N probably damaging Het
Il18 A T 9: 50,489,178 (GRCm39) D69V probably damaging Het
Kcnh7 T A 2: 62,552,209 (GRCm39) E927D Het
Kcnt2 T A 1: 140,356,587 (GRCm39) V342E probably benign Het
Khdc4 A G 3: 88,607,286 (GRCm39) N330S probably benign Het
Krt1 AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC 15: 101,758,813 (GRCm39) probably benign Het
Krt18 C G 15: 101,937,962 (GRCm39) A153G probably damaging Het
Lmntd2 A T 7: 140,791,977 (GRCm39) probably benign Het
Lrrc26 G T 2: 25,180,286 (GRCm39) A96S probably benign Het
Map3k11 A T 19: 5,752,166 (GRCm39) S783C probably damaging Het
Mib2 G A 4: 155,740,729 (GRCm39) L632F possibly damaging Het
Mical2 A C 7: 111,910,661 (GRCm39) D277A possibly damaging Het
Mtr A T 13: 12,250,365 (GRCm39) F339L probably benign Het
Musk T C 4: 58,354,032 (GRCm39) F362L probably benign Het
Ncor1 G A 11: 62,233,871 (GRCm39) Q444* probably null Het
Nek4 T C 14: 30,685,924 (GRCm39) S279P Het
Nell1 C T 7: 50,210,543 (GRCm39) T348I unknown Het
Nicn1 C T 9: 108,171,708 (GRCm39) R163C possibly damaging Het
Nrip1 T C 16: 76,088,902 (GRCm39) H885R probably damaging Het
Or13a19 G A 7: 139,902,938 (GRCm39) G109R possibly damaging Het
Or2a5 T A 6: 42,874,201 (GRCm39) V272D Het
Or2y12 C A 11: 49,426,028 (GRCm39) N5K probably damaging Het
Or6c208 T C 10: 129,224,240 (GRCm39) V246A probably damaging Het
Or6c69c T A 10: 129,910,522 (GRCm39) V81D possibly damaging Het
Or6d14 A G 6: 116,534,255 (GRCm39) T290A possibly damaging Het
Otog A G 7: 45,959,571 (GRCm39) D720G probably damaging Het
P3h3 C A 6: 124,834,564 (GRCm39) Q29H possibly damaging Het
Parn A G 16: 13,466,281 (GRCm39) probably null Het
Pcnt C A 10: 76,245,407 (GRCm39) E1077* probably null Het
Peg10 CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG CCACATCAGGATCCACATCAGGATGCACATCAG 6: 4,756,398 (GRCm39) probably benign Het
Pigb A G 9: 72,929,576 (GRCm39) W336R probably damaging Het
Pkdrej A T 15: 85,700,538 (GRCm39) S1799R probably damaging Het
Pnpla6 G T 8: 3,567,401 (GRCm39) M86I possibly damaging Het
Prickle2 T C 6: 92,435,620 (GRCm39) K50E possibly damaging Het
Psg21 A G 7: 18,386,389 (GRCm39) V199A probably benign Het
Reep3 T C 10: 66,871,786 (GRCm39) probably null Het
Reln T C 5: 22,104,155 (GRCm39) D3272G probably damaging Het
Rps6ka4 A G 19: 6,808,667 (GRCm39) V526A possibly damaging Het
Sel1l3 T C 5: 53,280,771 (GRCm39) E911G probably damaging Het
Serpinb6b C A 13: 33,162,125 (GRCm39) A308E probably benign Het
Slc26a4 A G 12: 31,572,523 (GRCm39) V746A probably benign Het
Slc4a3 T G 1: 75,527,957 (GRCm39) M402R probably damaging Het
Slc9b1 A T 3: 135,078,900 (GRCm39) T186S possibly damaging Het
Slk A G 19: 47,608,712 (GRCm39) Q555R probably benign Het
Smc2 T A 4: 52,475,100 (GRCm39) D925E probably benign Het
Stat5a A T 11: 100,774,764 (GRCm39) T758S unknown Het
Sulf1 A G 1: 12,906,499 (GRCm39) S514G probably benign Het
Tcp11l1 T A 2: 104,536,853 (GRCm39) N4I probably damaging Het
Tex2 A T 11: 106,402,731 (GRCm39) I1047K unknown Het
Tmem184b A G 15: 79,261,264 (GRCm39) V114A possibly damaging Het
Trmt11 A G 10: 30,467,027 (GRCm39) V95A probably benign Het
Trp53bp2 A G 1: 182,268,433 (GRCm39) D169G possibly damaging Het
Ttc41 T A 10: 86,549,599 (GRCm39) N264K possibly damaging Het
Uba2 A C 7: 33,853,987 (GRCm39) S318R probably benign Het
Wapl T A 14: 34,451,139 (GRCm39) N724K probably damaging Het
Wfdc9 T A 2: 164,493,671 (GRCm39) I5F probably damaging Het
Zan C T 5: 137,406,563 (GRCm39) D3686N unknown Het
Zfp618 A T 4: 63,012,708 (GRCm39) Y140F probably benign Het
Zfp790 A G 7: 29,527,593 (GRCm39) T93A probably benign Het
Zfp979 A C 4: 147,697,984 (GRCm39) F242V probably benign Het
Other mutations in Efcab3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00897:Efcab3 APN 11 104,990,847 (GRCm39) missense probably damaging 1.00
IGL01308:Efcab3 APN 11 104,611,523 (GRCm39) missense probably benign 0.03
IGL01483:Efcab3 APN 11 104,630,173 (GRCm39) missense probably benign 0.03
IGL01695:Efcab3 APN 11 104,626,889 (GRCm39) missense probably damaging 1.00
IGL01860:Efcab3 APN 11 104,581,747 (GRCm39) missense probably benign 0.16
IGL01981:Efcab3 APN 11 104,612,258 (GRCm39) intron probably benign
IGL01984:Efcab3 APN 11 104,629,134 (GRCm39) missense probably benign 0.20
IGL02023:Efcab3 APN 11 104,612,258 (GRCm39) intron probably benign
IGL02252:Efcab3 APN 11 104,644,753 (GRCm39) missense possibly damaging 0.68
IGL02886:Efcab3 APN 11 104,986,700 (GRCm39) missense possibly damaging 0.95
IGL03116:Efcab3 APN 11 104,612,359 (GRCm39) missense probably benign 0.02
IGL03141:Efcab3 APN 11 104,986,696 (GRCm39) missense probably damaging 0.99
IGL03242:Efcab3 APN 11 104,997,230 (GRCm39) missense probably damaging 1.00
IGL03274:Efcab3 APN 11 104,611,919 (GRCm39) missense probably benign 0.03
IGL03408:Efcab3 APN 11 104,601,447 (GRCm39) missense probably benign 0.03
PIT4812001:Efcab3 UTSW 11 104,990,805 (GRCm39) missense probably null 0.00
R0018:Efcab3 UTSW 11 104,612,378 (GRCm39) critical splice donor site probably null
R0068:Efcab3 UTSW 11 104,611,648 (GRCm39) missense probably benign 0.29
R0350:Efcab3 UTSW 11 104,581,706 (GRCm39) missense probably benign 0.03
R0388:Efcab3 UTSW 11 105,000,227 (GRCm39) missense possibly damaging 0.61
R0646:Efcab3 UTSW 11 104,611,327 (GRCm39) missense probably benign 0.03
R0668:Efcab3 UTSW 11 104,611,318 (GRCm39) missense probably benign 0.16
R0715:Efcab3 UTSW 11 104,611,706 (GRCm39) missense possibly damaging 0.90
R0944:Efcab3 UTSW 11 104,601,556 (GRCm39) splice site probably null
R1330:Efcab3 UTSW 11 104,637,116 (GRCm39) missense possibly damaging 0.84
R1440:Efcab3 UTSW 11 104,999,581 (GRCm39) splice site probably benign
R1508:Efcab3 UTSW 11 104,601,503 (GRCm39) missense probably benign 0.03
R1540:Efcab3 UTSW 11 104,999,726 (GRCm39) missense probably benign 0.07
R1643:Efcab3 UTSW 11 104,589,804 (GRCm39) missense probably benign 0.16
R1651:Efcab3 UTSW 11 104,611,492 (GRCm39) missense probably benign 0.03
R1665:Efcab3 UTSW 11 104,611,940 (GRCm39) missense probably benign 0.07
R1702:Efcab3 UTSW 11 104,581,832 (GRCm39) missense probably benign 0.03
R1711:Efcab3 UTSW 11 104,611,514 (GRCm39) missense probably benign 0.07
R1779:Efcab3 UTSW 11 104,611,765 (GRCm39) missense probably benign 0.15
R1813:Efcab3 UTSW 11 104,611,514 (GRCm39) missense probably benign 0.07
R1818:Efcab3 UTSW 11 104,612,333 (GRCm39) missense probably benign 0.10
R1896:Efcab3 UTSW 11 104,611,514 (GRCm39) missense probably benign 0.07
R1969:Efcab3 UTSW 11 104,637,090 (GRCm39) missense probably damaging 1.00
R2029:Efcab3 UTSW 11 104,990,851 (GRCm39) missense probably damaging 0.99
R2139:Efcab3 UTSW 11 104,642,737 (GRCm39) missense possibly damaging 0.53
R2165:Efcab3 UTSW 11 104,642,688 (GRCm39) missense possibly damaging 0.93
R2359:Efcab3 UTSW 11 104,630,106 (GRCm39) missense possibly damaging 0.80
R2394:Efcab3 UTSW 11 104,629,121 (GRCm39) missense probably benign 0.17
R2401:Efcab3 UTSW 11 104,963,144 (GRCm39) critical splice donor site probably null
R2406:Efcab3 UTSW 11 104,611,457 (GRCm39) missense probably benign 0.03
R2570:Efcab3 UTSW 11 104,624,490 (GRCm39) missense probably damaging 1.00
R3795:Efcab3 UTSW 11 104,624,501 (GRCm39) missense possibly damaging 0.94
R3901:Efcab3 UTSW 11 104,974,713 (GRCm39) missense possibly damaging 0.68
R4244:Efcab3 UTSW 11 105,002,629 (GRCm39) missense probably damaging 1.00
R4352:Efcab3 UTSW 11 104,630,140 (GRCm39) missense probably null 0.25
R4359:Efcab3 UTSW 11 104,624,547 (GRCm39) splice site probably null
R4424:Efcab3 UTSW 11 104,626,940 (GRCm39) critical splice donor site probably null
R4895:Efcab3 UTSW 11 105,008,227 (GRCm39) unclassified probably benign
R4895:Efcab3 UTSW 11 104,640,496 (GRCm39) missense probably damaging 1.00
R4895:Efcab3 UTSW 11 104,611,112 (GRCm39) missense probably benign 0.16
R5006:Efcab3 UTSW 11 104,620,503 (GRCm39) splice site probably null
R5066:Efcab3 UTSW 11 104,611,490 (GRCm39) missense probably benign 0.03
R5316:Efcab3 UTSW 11 104,967,286 (GRCm39) missense possibly damaging 0.80
R5329:Efcab3 UTSW 11 104,644,632 (GRCm39) splice site probably null
R5405:Efcab3 UTSW 11 104,612,018 (GRCm39) missense probably benign 0.07
R5814:Efcab3 UTSW 11 104,626,940 (GRCm39) critical splice donor site probably benign
R5888:Efcab3 UTSW 11 104,612,227 (GRCm39) splice site probably benign
R5910:Efcab3 UTSW 11 104,581,760 (GRCm39) missense probably benign 0.01
R5975:Efcab3 UTSW 11 104,578,375 (GRCm39) start gained probably benign
R6019:Efcab3 UTSW 11 104,933,728 (GRCm39) critical splice donor site probably null
R6028:Efcab3 UTSW 11 104,660,481 (GRCm39) critical splice donor site probably null
R6048:Efcab3 UTSW 11 104,835,259 (GRCm39) missense unknown
R6059:Efcab3 UTSW 11 104,927,595 (GRCm39) missense probably benign 0.03
R6147:Efcab3 UTSW 11 104,858,566 (GRCm39) missense unknown
R6176:Efcab3 UTSW 11 104,683,383 (GRCm39) missense probably benign 0.16
R6181:Efcab3 UTSW 11 104,722,159 (GRCm39) missense probably benign 0.25
R6196:Efcab3 UTSW 11 104,746,386 (GRCm39) missense probably benign 0.07
R6245:Efcab3 UTSW 11 104,675,834 (GRCm39) missense probably benign 0.03
R6262:Efcab3 UTSW 11 104,784,579 (GRCm39) missense probably benign 0.24
R6263:Efcab3 UTSW 11 104,810,312 (GRCm39) missense unknown
R6277:Efcab3 UTSW 11 104,901,148 (GRCm39) missense possibly damaging 0.49
R6338:Efcab3 UTSW 11 104,734,034 (GRCm39) nonsense probably null
R6355:Efcab3 UTSW 11 104,896,511 (GRCm39) missense probably benign 0.29
R6356:Efcab3 UTSW 11 104,784,533 (GRCm39) missense probably benign 0.19
R6365:Efcab3 UTSW 11 104,815,412 (GRCm39) missense unknown
R6378:Efcab3 UTSW 11 104,999,620 (GRCm39) missense possibly damaging 0.83
R6391:Efcab3 UTSW 11 104,885,143 (GRCm39) missense possibly damaging 0.92
R6494:Efcab3 UTSW 11 104,990,845 (GRCm39) missense possibly damaging 0.93
R6556:Efcab3 UTSW 11 104,899,077 (GRCm39) missense probably null 0.03
R6573:Efcab3 UTSW 11 104,971,461 (GRCm39) missense possibly damaging 0.91
R6604:Efcab3 UTSW 11 104,589,772 (GRCm39) nonsense probably null
R6605:Efcab3 UTSW 11 104,890,107 (GRCm39) splice site probably null
R6634:Efcab3 UTSW 11 104,784,609 (GRCm39) missense probably benign 0.17
R6723:Efcab3 UTSW 11 105,007,906 (GRCm39) missense possibly damaging 0.95
R6851:Efcab3 UTSW 11 104,896,521 (GRCm39) missense probably benign 0.03
R6862:Efcab3 UTSW 11 104,612,284 (GRCm39) nonsense probably null
R6949:Efcab3 UTSW 11 104,799,896 (GRCm39) missense probably damaging 1.00
R6970:Efcab3 UTSW 11 104,667,182 (GRCm39) missense probably benign 0.03
R7014:Efcab3 UTSW 11 104,584,248 (GRCm39) missense probably benign 0.03
R7097:Efcab3 UTSW 11 104,899,787 (GRCm39) missense possibly damaging 0.68
R7122:Efcab3 UTSW 11 104,899,787 (GRCm39) missense possibly damaging 0.68
R7124:Efcab3 UTSW 11 104,629,100 (GRCm39) missense probably benign 0.17
R7146:Efcab3 UTSW 11 104,913,764 (GRCm39) missense probably benign 0.03
R7146:Efcab3 UTSW 11 104,858,578 (GRCm39) missense unknown
R7154:Efcab3 UTSW 11 104,589,966 (GRCm39) splice site probably null
R7175:Efcab3 UTSW 11 104,838,237 (GRCm39) missense unknown
R7189:Efcab3 UTSW 11 104,986,690 (GRCm39) missense probably benign
R7198:Efcab3 UTSW 11 104,642,711 (GRCm39) missense probably benign 0.15
R7211:Efcab3 UTSW 11 104,601,539 (GRCm39) missense probably benign 0.01
R7211:Efcab3 UTSW 11 104,615,435 (GRCm39) critical splice donor site probably null
R7216:Efcab3 UTSW 11 104,771,375 (GRCm39) missense possibly damaging 0.49
R7221:Efcab3 UTSW 11 104,791,432 (GRCm39) missense probably benign 0.36
R7233:Efcab3 UTSW 11 104,730,669 (GRCm39) missense possibly damaging 0.69
R7236:Efcab3 UTSW 11 104,790,093 (GRCm39) missense probably benign 0.10
R7262:Efcab3 UTSW 11 104,745,432 (GRCm39) critical splice donor site probably null
R7289:Efcab3 UTSW 11 104,929,184 (GRCm39) missense probably benign 0.24
R7323:Efcab3 UTSW 11 104,920,837 (GRCm39) missense probably benign 0.07
R7378:Efcab3 UTSW 11 104,605,528 (GRCm39) missense probably benign 0.03
R7388:Efcab3 UTSW 11 104,611,871 (GRCm39) missense probably damaging 0.97
R7390:Efcab3 UTSW 11 104,615,411 (GRCm39) missense possibly damaging 0.46
R7411:Efcab3 UTSW 11 104,890,549 (GRCm39) missense probably benign 0.10
R7468:Efcab3 UTSW 11 104,640,526 (GRCm39) missense probably benign 0.17
R7483:Efcab3 UTSW 11 105,000,112 (GRCm39) missense probably benign 0.39
R7497:Efcab3 UTSW 11 104,653,516 (GRCm39) critical splice donor site probably null
R7612:Efcab3 UTSW 11 104,999,647 (GRCm39) missense possibly damaging 0.80
R7620:Efcab3 UTSW 11 104,722,969 (GRCm39) missense possibly damaging 0.95
R7638:Efcab3 UTSW 11 104,927,625 (GRCm39) missense probably benign 0.03
R7661:Efcab3 UTSW 11 104,617,503 (GRCm39) missense probably benign 0.03
R7667:Efcab3 UTSW 11 104,642,737 (GRCm39) missense possibly damaging 0.53
R7682:Efcab3 UTSW 11 104,855,174 (GRCm39) splice site probably null
R7708:Efcab3 UTSW 11 104,855,397 (GRCm39) missense unknown
R7719:Efcab3 UTSW 11 105,002,674 (GRCm39) missense probably benign 0.14
R7721:Efcab3 UTSW 11 104,615,366 (GRCm39) nonsense probably null
R7735:Efcab3 UTSW 11 104,962,465 (GRCm39) missense probably benign
R7747:Efcab3 UTSW 11 104,733,429 (GRCm39) missense probably damaging 0.96
R7840:Efcab3 UTSW 11 104,624,539 (GRCm39) missense probably benign 0.07
R7846:Efcab3 UTSW 11 104,605,571 (GRCm39) critical splice donor site probably null
R7893:Efcab3 UTSW 11 104,870,186 (GRCm39) missense unknown
R7895:Efcab3 UTSW 11 105,008,150 (GRCm39) missense probably benign 0.29
R7897:Efcab3 UTSW 11 104,889,061 (GRCm39) missense probably benign 0.24
R7936:Efcab3 UTSW 11 104,890,524 (GRCm39) missense possibly damaging 0.89
R7936:Efcab3 UTSW 11 104,937,385 (GRCm39) critical splice donor site probably null
R7959:Efcab3 UTSW 11 104,933,627 (GRCm39) missense probably damaging 0.96
R8031:Efcab3 UTSW 11 104,772,295 (GRCm39) missense possibly damaging 0.49
R8041:Efcab3 UTSW 11 104,810,305 (GRCm39) missense unknown
R8054:Efcab3 UTSW 11 104,621,226 (GRCm39) missense probably benign 0.07
R8056:Efcab3 UTSW 11 104,799,896 (GRCm39) missense probably damaging 0.98
R8061:Efcab3 UTSW 11 104,997,275 (GRCm39) missense probably benign 0.00
R8088:Efcab3 UTSW 11 104,889,072 (GRCm39) missense probably benign 0.10
R8112:Efcab3 UTSW 11 104,841,026 (GRCm39) missense unknown
R8116:Efcab3 UTSW 11 105,002,677 (GRCm39) missense possibly damaging 0.65
R8340:Efcab3 UTSW 11 104,876,856 (GRCm39) missense unknown
R8405:Efcab3 UTSW 11 104,612,024 (GRCm39) missense probably benign 0.02
R8413:Efcab3 UTSW 11 104,811,135 (GRCm39) missense unknown
R8472:Efcab3 UTSW 11 104,709,463 (GRCm39) missense probably benign 0.07
R8549:Efcab3 UTSW 11 104,890,521 (GRCm39) missense probably damaging 0.99
R8699:Efcab3 UTSW 11 104,672,072 (GRCm39) missense probably benign 0.03
R8711:Efcab3 UTSW 11 104,743,371 (GRCm39) missense probably benign 0.03
R8732:Efcab3 UTSW 11 104,695,100 (GRCm39) missense probably benign 0.03
R8745:Efcab3 UTSW 11 104,749,304 (GRCm39) missense possibly damaging 0.57
R8806:Efcab3 UTSW 11 104,928,695 (GRCm39) missense probably benign 0.07
R8810:Efcab3 UTSW 11 104,805,721 (GRCm39) missense unknown
R8845:Efcab3 UTSW 11 104,899,787 (GRCm39) missense possibly damaging 0.68
R8870:Efcab3 UTSW 11 104,791,500 (GRCm39) missense probably benign 0.07
R8872:Efcab3 UTSW 11 104,760,880 (GRCm39) missense probably benign 0.19
R8879:Efcab3 UTSW 11 104,581,781 (GRCm39) missense probably benign 0.03
R8924:Efcab3 UTSW 11 104,806,253 (GRCm39) frame shift probably null
R8954:Efcab3 UTSW 11 104,909,525 (GRCm39) critical splice donor site probably null
R8960:Efcab3 UTSW 11 104,820,772 (GRCm39) splice site probably benign
R8975:Efcab3 UTSW 11 104,954,415 (GRCm39) missense probably benign 0.17
R8998:Efcab3 UTSW 11 104,640,477 (GRCm39) missense probably benign 0.09
R8999:Efcab3 UTSW 11 104,640,477 (GRCm39) missense probably benign 0.09
R9002:Efcab3 UTSW 11 104,920,822 (GRCm39) missense probably damaging 0.99
R9012:Efcab3 UTSW 11 104,711,347 (GRCm39) critical splice donor site probably null
R9036:Efcab3 UTSW 11 104,927,601 (GRCm39) missense probably benign 0.03
R9037:Efcab3 UTSW 11 104,803,791 (GRCm39) missense unknown
R9059:Efcab3 UTSW 11 104,642,689 (GRCm39) missense possibly damaging 0.73
R9066:Efcab3 UTSW 11 104,631,688 (GRCm39) intron probably benign
R9122:Efcab3 UTSW 11 104,856,605 (GRCm39) missense unknown
R9125:Efcab3 UTSW 11 104,736,360 (GRCm39) missense probably damaging 1.00
R9127:Efcab3 UTSW 11 104,741,407 (GRCm39) missense probably benign 0.07
R9171:Efcab3 UTSW 11 104,800,708 (GRCm39) missense probably benign 0.36
R9219:Efcab3 UTSW 11 104,836,691 (GRCm39) missense unknown
R9224:Efcab3 UTSW 11 104,661,801 (GRCm39) missense probably benign 0.07
R9235:Efcab3 UTSW 11 104,907,987 (GRCm39) missense probably benign 0.19
R9294:Efcab3 UTSW 11 104,722,126 (GRCm39) missense probably benign 0.24
R9318:Efcab3 UTSW 11 104,856,648 (GRCm39) critical splice donor site probably null
R9322:Efcab3 UTSW 11 104,765,199 (GRCm39) missense probably benign 0.36
R9361:Efcab3 UTSW 11 104,896,524 (GRCm39) missense probably benign 0.03
R9408:Efcab3 UTSW 11 104,621,255 (GRCm39) critical splice donor site probably null
R9434:Efcab3 UTSW 11 104,899,863 (GRCm39) missense probably benign 0.24
R9477:Efcab3 UTSW 11 104,836,698 (GRCm39) missense unknown
R9658:Efcab3 UTSW 11 104,611,120 (GRCm39) missense probably benign 0.03
R9719:Efcab3 UTSW 11 104,867,912 (GRCm39) missense unknown
R9751:Efcab3 UTSW 11 104,783,911 (GRCm39) missense probably benign 0.19
R9763:Efcab3 UTSW 11 104,890,485 (GRCm39) missense possibly damaging 0.89
X0026:Efcab3 UTSW 11 105,007,937 (GRCm39) missense probably benign 0.03
X0026:Efcab3 UTSW 11 104,611,801 (GRCm39) missense probably benign 0.07
Z1088:Efcab3 UTSW 11 104,642,728 (GRCm39) missense probably damaging 0.96
Z1176:Efcab3 UTSW 11 104,990,872 (GRCm39) missense probably damaging 1.00
Z1176:Efcab3 UTSW 11 104,892,793 (GRCm39) missense probably benign 0.29
Z1176:Efcab3 UTSW 11 104,999,598 (GRCm39) nonsense probably null
Z1177:Efcab3 UTSW 11 104,711,344 (GRCm39) missense probably benign 0.03
Z1177:Efcab3 UTSW 11 104,630,164 (GRCm39) nonsense probably null
Z1177:Efcab3 UTSW 11 104,814,845 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AGTTTTCAAGTCCGTGTTCATCTG -3'
(R):5'- AGTGTCTCTACCTATTGAGCCATC -3'

Sequencing Primer
(F):5'- CAAGTCCGTGTTCATCTGGGAAAG -3'
(R):5'- CCATCTCACAGAGATGCAT -3'
Posted On 2021-10-11