Incidental Mutation 'R7139:Muc21'
ID 553312
Institutional Source Beutler Lab
Gene Symbol Muc21
Ensembl Gene ENSMUSG00000090588
Gene Name mucin 21
Synonyms epiglycanin, Gm9573
Accession Numbers
Essential gene? Probably non essential (E-score: 0.097) question?
Stock # R7139 (G1)
Quality Score 180.468
Status Not validated
Chromosome 17
Chromosomal Location 35928815-35937529 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) TCCTGAGGCAGTGCTGGATACAGGGGTGGTTGGGGTGGGTGAAGAGCCTGAGGCAGTGCTGGAT to TCCTGAGGCAGTGCTGGAT at 35933525 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000134221 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164502] [ENSMUST00000174521]
AlphaFold F7C950
Predicted Effect probably benign
Transcript: ENSMUST00000164502
SMART Domains Protein: ENSMUSP00000130987
Gene: ENSMUSG00000090588

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
low complexity region 26 39 N/A INTRINSIC
low complexity region 42 59 N/A INTRINSIC
low complexity region 76 144 N/A INTRINSIC
low complexity region 149 578 N/A INTRINSIC
low complexity region 580 653 N/A INTRINSIC
low complexity region 655 1179 N/A INTRINSIC
low complexity region 1183 1373 N/A INTRINSIC
low complexity region 1383 1436 N/A INTRINSIC
low complexity region 1438 1479 N/A INTRINSIC
Pfam:Epiglycanin_C 1518 1605 3.8e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000174521
SMART Domains Protein: ENSMUSP00000134221
Gene: ENSMUSG00000090509

DomainStartEndE-ValueType
Pfam:SFTA2 80 117 9.2e-18 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 79 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2510039O18Rik A G 4: 148,026,295 (GRCm39) R272G possibly damaging Het
4930512M02Rik T A 11: 11,540,078 (GRCm39) N179Y unknown Het
4930562C15Rik A T 16: 4,668,048 (GRCm39) M480L probably benign Het
Abcd4 A G 12: 84,653,072 (GRCm39) C377R probably benign Het
Adam23 C A 1: 63,584,736 (GRCm39) D381E probably damaging Het
Angpt1 T A 15: 42,539,747 (GRCm39) Q37H probably damaging Het
Apeh A T 9: 107,969,345 (GRCm39) F260I probably damaging Het
Cadps2 T C 6: 23,410,888 (GRCm39) Y681C probably damaging Het
Ccdc162 T C 10: 41,542,717 (GRCm39) M386V possibly damaging Het
Celsr2 T C 3: 108,322,675 (GRCm39) S46G unknown Het
Cfc1 T C 1: 34,575,560 (GRCm39) L78P probably benign Het
Chd7 T C 4: 8,865,865 (GRCm39) V2724A probably benign Het
Clca3a1 A T 3: 144,461,063 (GRCm39) V196E possibly damaging Het
Cma1 T C 14: 56,181,273 (GRCm39) H44R probably damaging Het
Cnot2 T C 10: 116,330,924 (GRCm39) N394S probably benign Het
Cplx3 A T 9: 57,522,879 (GRCm39) H160Q probably benign Het
Cstf3 A T 2: 104,483,409 (GRCm39) I372F possibly damaging Het
Cyb5rl A C 4: 106,928,208 (GRCm39) I115L probably benign Het
D5Ertd579e A G 5: 36,771,320 (GRCm39) L1025P probably damaging Het
Dmtn T C 14: 70,854,867 (GRCm39) N36S probably benign Het
Dnah6 A G 6: 73,112,663 (GRCm39) V1647A probably damaging Het
Dock6 T C 9: 21,712,572 (GRCm39) Y2063C probably damaging Het
Dst T A 1: 34,338,888 (GRCm39) D5149E probably damaging Het
Fancl A G 11: 26,353,358 (GRCm39) M85V probably benign Het
Fgd2 T A 17: 29,592,229 (GRCm39) F387Y probably damaging Het
Fshr A T 17: 89,293,589 (GRCm39) I363N possibly damaging Het
Glce G T 9: 61,977,716 (GRCm39) S56* probably null Het
Gm26727 A T 2: 67,263,381 (GRCm39) S49T unknown Het
Gm36210 T A 7: 4,902,277 (GRCm39) D131V probably damaging Het
Gm5089 T C 14: 122,673,403 (GRCm39) D106G unknown Het
Gm5622 G T 14: 51,893,339 (GRCm39) E89* probably null Het
H2-Eb2 C T 17: 34,553,395 (GRCm39) R194W probably benign Het
Hivep1 A T 13: 42,313,430 (GRCm39) E1890V probably benign Het
Ighv1-53 A T 12: 115,122,441 (GRCm39) C5* probably null Het
Ighv2-5 T A 12: 113,649,219 (GRCm39) Y78F probably benign Het
Il9 C T 13: 56,628,426 (GRCm39) V88I probably benign Het
Kidins220 A G 12: 25,044,820 (GRCm39) T163A probably damaging Het
Lama4 G T 10: 38,951,491 (GRCm39) D1079Y probably damaging Het
Lrrc34 T C 3: 30,679,036 (GRCm39) I354V probably benign Het
Macroh2a2 T A 10: 61,593,674 (GRCm39) M1L unknown Het
Mpeg1 A T 19: 12,439,078 (GRCm39) T179S probably benign Het
Mrgpra2a A T 7: 47,076,337 (GRCm39) L307H probably damaging Het
Mst1 G A 9: 107,960,027 (GRCm39) R328H probably damaging Het
Nav3 C A 10: 109,689,338 (GRCm39) S313I probably benign Het
Nmt2 T G 2: 3,285,352 (GRCm39) S7A probably benign Het
Nsmce1 T C 7: 125,068,254 (GRCm39) S197G probably benign Het
Ociad2 A G 5: 73,493,218 (GRCm39) V4A probably benign Het
Or56a41 G T 7: 104,742,005 (GRCm39) T7K probably benign Het
Osmr T C 15: 6,850,569 (GRCm39) D679G possibly damaging Het
Pappa T A 4: 65,107,687 (GRCm39) F699L probably benign Het
Parp8 T A 13: 117,161,802 (GRCm39) M40L probably benign Het
Pcyox1 A T 6: 86,371,519 (GRCm39) N122K possibly damaging Het
Pkd1l1 T C 11: 8,840,737 (GRCm39) S1224G Het
Pkd1l3 T A 8: 110,362,972 (GRCm39) S1088T probably damaging Het
Prrt1 T C 17: 34,850,051 (GRCm39) V155A probably benign Het
Rbm6 A C 9: 107,730,410 (GRCm39) D79E probably damaging Het
Sec31b A T 19: 44,507,375 (GRCm39) S819T probably benign Het
Slc22a27 A T 19: 7,903,912 (GRCm39) I75N probably damaging Het
Slc25a54 G A 3: 109,005,905 (GRCm39) G138R probably damaging Het
Slc6a12 T C 6: 121,342,278 (GRCm39) S612P probably benign Het
Slc7a2 A T 8: 41,368,050 (GRCm39) I605F probably benign Het
Slit2 A G 5: 48,402,025 (GRCm39) T805A probably benign Het
Strbp A T 2: 37,514,514 (GRCm39) H308Q probably benign Het
Stxbp4 G A 11: 90,497,835 (GRCm39) Q155* probably null Het
Sybu A T 15: 44,541,110 (GRCm39) N317K possibly damaging Het
Taok1 G A 11: 77,462,459 (GRCm39) S210F probably damaging Het
Tapbp A G 17: 34,139,022 (GRCm39) D72G possibly damaging Het
Thbd G T 2: 148,248,461 (GRCm39) T469K probably benign Het
Tia1 T C 6: 86,404,670 (GRCm39) Y302H possibly damaging Het
Tlr4 T C 4: 66,758,520 (GRCm39) F438L probably benign Het
Tmem235 C T 11: 117,751,723 (GRCm39) S49L probably damaging Het
Trip4 A G 9: 65,792,503 (GRCm39) probably benign Het
Trrap C A 5: 144,739,988 (GRCm39) L1137I possibly damaging Het
Vmo1 T C 11: 70,404,674 (GRCm39) E109G probably benign Het
Wdfy4 T C 14: 32,873,535 (GRCm39) Y258C Het
Wdr91 T G 6: 34,885,198 (GRCm39) N121T possibly damaging Het
Zfp39 T C 11: 58,781,385 (GRCm39) H459R probably damaging Het
Zfp936 T A 7: 42,839,715 (GRCm39) I394K possibly damaging Het
Zpr1 G A 9: 46,192,357 (GRCm39) D423N probably damaging Het
Other mutations in Muc21
AlleleSourceChrCoordTypePredicted EffectPPH Score
BB009:Muc21 UTSW 17 35,933,525 (GRCm39) intron probably benign
FR4304:Muc21 UTSW 17 35,933,013 (GRCm39) intron probably benign
R0334:Muc21 UTSW 17 35,933,614 (GRCm39) intron probably benign
R0946:Muc21 UTSW 17 35,929,105 (GRCm39) missense probably benign 0.32
R1117:Muc21 UTSW 17 35,930,920 (GRCm39) intron probably benign
R1345:Muc21 UTSW 17 35,932,489 (GRCm39) intron probably benign
R1697:Muc21 UTSW 17 35,931,540 (GRCm39) intron probably benign
R1750:Muc21 UTSW 17 35,931,940 (GRCm39) intron probably benign
R1756:Muc21 UTSW 17 35,930,131 (GRCm39) intron probably benign
R1946:Muc21 UTSW 17 35,933,416 (GRCm39) intron probably benign
R1978:Muc21 UTSW 17 35,933,857 (GRCm39) intron probably benign
R1991:Muc21 UTSW 17 35,929,600 (GRCm39) missense probably benign 0.32
R1992:Muc21 UTSW 17 35,929,600 (GRCm39) missense probably benign 0.32
R2063:Muc21 UTSW 17 35,932,297 (GRCm39) intron probably benign
R2356:Muc21 UTSW 17 35,932,563 (GRCm39) intron probably benign
R2866:Muc21 UTSW 17 35,930,599 (GRCm39) intron probably benign
R3826:Muc21 UTSW 17 35,932,504 (GRCm39) intron probably benign
R4020:Muc21 UTSW 17 35,930,953 (GRCm39) intron probably benign
R4474:Muc21 UTSW 17 35,931,496 (GRCm39) intron probably benign
R4677:Muc21 UTSW 17 35,930,599 (GRCm39) intron probably benign
R4786:Muc21 UTSW 17 35,930,221 (GRCm39) intron probably benign
R5071:Muc21 UTSW 17 35,931,444 (GRCm39) intron probably benign
R5173:Muc21 UTSW 17 35,931,633 (GRCm39) intron probably benign
R5283:Muc21 UTSW 17 35,932,224 (GRCm39) intron probably benign
R5446:Muc21 UTSW 17 35,933,395 (GRCm39) intron probably benign
R5542:Muc21 UTSW 17 35,933,395 (GRCm39) intron probably benign
R5716:Muc21 UTSW 17 35,931,675 (GRCm39) intron probably benign
R5913:Muc21 UTSW 17 35,934,123 (GRCm39) intron probably benign
R6011:Muc21 UTSW 17 35,933,074 (GRCm39) intron probably benign
R6198:Muc21 UTSW 17 35,931,808 (GRCm39) intron probably benign
R6394:Muc21 UTSW 17 35,931,058 (GRCm39) intron probably benign
R6786:Muc21 UTSW 17 35,934,057 (GRCm39) intron probably benign
R6940:Muc21 UTSW 17 35,934,118 (GRCm39) intron probably benign
R7082:Muc21 UTSW 17 35,932,093 (GRCm39) missense unknown
R7103:Muc21 UTSW 17 35,932,432 (GRCm39) missense unknown
R7110:Muc21 UTSW 17 35,933,510 (GRCm39) intron probably benign
R7165:Muc21 UTSW 17 35,932,870 (GRCm39) missense unknown
R7200:Muc21 UTSW 17 35,933,525 (GRCm39) intron probably benign
R7204:Muc21 UTSW 17 35,932,105 (GRCm39) intron probably benign
R7289:Muc21 UTSW 17 35,929,761 (GRCm39) missense unknown
R7290:Muc21 UTSW 17 35,929,761 (GRCm39) missense unknown
R7295:Muc21 UTSW 17 35,929,761 (GRCm39) missense unknown
R7319:Muc21 UTSW 17 35,932,935 (GRCm39) intron probably benign
R7462:Muc21 UTSW 17 35,931,568 (GRCm39) missense unknown
R7529:Muc21 UTSW 17 35,930,123 (GRCm39) missense unknown
R7718:Muc21 UTSW 17 35,933,728 (GRCm39) missense unknown
R7762:Muc21 UTSW 17 35,932,977 (GRCm39) missense unknown
R7788:Muc21 UTSW 17 35,929,798 (GRCm39) missense unknown
R7798:Muc21 UTSW 17 35,932,146 (GRCm39) missense unknown
R7831:Muc21 UTSW 17 35,929,651 (GRCm39) missense unknown
R7896:Muc21 UTSW 17 35,930,917 (GRCm39) missense unknown
R7899:Muc21 UTSW 17 35,931,493 (GRCm39) intron probably benign
R7932:Muc21 UTSW 17 35,933,525 (GRCm39) intron probably benign
R8025:Muc21 UTSW 17 35,931,879 (GRCm39) intron probably benign
R8077:Muc21 UTSW 17 35,930,628 (GRCm39) intron probably benign
R8090:Muc21 UTSW 17 35,932,617 (GRCm39) missense unknown
R8169:Muc21 UTSW 17 35,932,072 (GRCm39) missense unknown
R8184:Muc21 UTSW 17 35,933,722 (GRCm39) missense unknown
R8209:Muc21 UTSW 17 35,930,599 (GRCm39) intron probably benign
R8226:Muc21 UTSW 17 35,930,599 (GRCm39) intron probably benign
R8464:Muc21 UTSW 17 35,933,098 (GRCm39) intron probably benign
R8670:Muc21 UTSW 17 35,932,540 (GRCm39) missense unknown
R8783:Muc21 UTSW 17 35,930,875 (GRCm39) missense unknown
R8856:Muc21 UTSW 17 35,931,865 (GRCm39) missense unknown
R9155:Muc21 UTSW 17 35,932,131 (GRCm39) missense unknown
R9214:Muc21 UTSW 17 35,931,838 (GRCm39) missense unknown
R9353:Muc21 UTSW 17 35,930,545 (GRCm39) missense unknown
R9618:Muc21 UTSW 17 35,932,935 (GRCm39) intron probably benign
R9621:Muc21 UTSW 17 35,932,720 (GRCm39) missense unknown
R9679:Muc21 UTSW 17 35,930,491 (GRCm39) missense unknown
RF025:Muc21 UTSW 17 35,933,771 (GRCm39) intron probably benign
Z1176:Muc21 UTSW 17 35,932,137 (GRCm39) missense unknown
Z1177:Muc21 UTSW 17 35,931,951 (GRCm39) missense unknown
Z1177:Muc21 UTSW 17 35,931,817 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- ATCCTGAGGCAGTGCTAGATG -3'
(R):5'- CACCACTGTATCCAGCACTG -3'

Sequencing Primer
(F):5'- TGGGTGCTGATCCTGAGGC -3'
(R):5'- ACTGGCTCAGGCTCTACAC -3'
Posted On 2019-05-15