Incidental Mutation 'R5173:Muc21'
ID 398945
Institutional Source Beutler Lab
Gene Symbol Muc21
Ensembl Gene ENSMUSG00000090588
Gene Name mucin 21
Synonyms epiglycanin, Gm9573
MMRRC Submission 042753-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.097) question?
Stock # R5173 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 35928815-35937529 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) G to T at 35931633 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 unknown
Transcript: ENSMUST00000164502
AA Change: T851N
SMART Domains Protein: ENSMUSP00000130987
Gene: ENSMUSG00000090588
AA Change: T851N

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 noncoding transcript
Transcript: ENSMUST00000173759
Predicted Effect probably benign
Transcript: ENSMUST00000174521
SMART Domains Protein: ENSMUSP00000134221
Gene: ENSMUSG00000090509

DomainStartEndE-ValueType
Pfam:SFTA2 80 117 9.2e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000174534
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 95.5%
Validation Efficiency 100% (50/50)
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 AC A 11: 9,632,032 (GRCm39) probably null Het
Abca6 A T 11: 110,082,546 (GRCm39) F1142L probably benign Het
Ap1g1 T A 8: 110,577,764 (GRCm39) probably null Het
Apob T C 12: 8,058,238 (GRCm39) V2207A probably benign Het
Cenpp CAAACCTGAAAA CAAA 13: 49,618,258 (GRCm39) probably null Het
Chd3 A G 11: 69,260,069 (GRCm39) probably benign Het
Coch C A 12: 51,643,290 (GRCm39) Y103* probably null Het
Cul3 A T 1: 80,259,133 (GRCm39) D382E possibly damaging Het
Cul5 T C 9: 53,554,034 (GRCm39) T291A probably benign Het
Dab1 T C 4: 104,545,645 (GRCm39) probably null Het
Dmtf1 A G 5: 9,190,356 (GRCm39) probably benign Het
Dpp4 T C 2: 62,217,474 (GRCm39) Y41C probably damaging Het
Eif2ak4 A G 2: 118,238,841 (GRCm39) I45M probably damaging Het
Epn3 T C 11: 94,386,923 (GRCm39) K149R probably damaging Het
Flnc A G 6: 29,455,537 (GRCm39) E2029G probably damaging Het
Gm5799 A G 14: 43,782,116 (GRCm39) N96S probably damaging Het
Gprc5c G T 11: 114,755,093 (GRCm39) V257L possibly damaging Het
Grik5 T C 7: 24,762,319 (GRCm39) H224R possibly damaging Het
Lpar6 A T 14: 73,476,537 (GRCm39) E166V probably benign Het
Mical1 T C 10: 41,360,985 (GRCm39) L683P probably damaging Het
Mis18bp1 T C 12: 65,196,149 (GRCm39) I538M possibly damaging Het
Mobp A G 9: 119,997,311 (GRCm39) R77G possibly damaging Het
Mylk A G 16: 34,797,383 (GRCm39) H1614R probably benign Het
Or2y16 T C 11: 49,334,713 (GRCm39) F12L probably benign Het
Or4p18 G A 2: 88,233,266 (GRCm39) T4I probably benign Het
Or7c19 T C 8: 85,957,205 (GRCm39) L27P probably damaging Het
Osbpl1a C T 18: 12,895,697 (GRCm39) V390I probably benign Het
Pcdha7 C A 18: 37,107,705 (GRCm39) D243E probably benign Het
Pi4ka A T 16: 17,168,770 (GRCm39) N653K possibly damaging Het
Plin5 T G 17: 56,422,548 (GRCm39) probably null Het
Plod1 A G 4: 148,000,758 (GRCm39) probably benign Het
Psd3 T C 8: 68,149,641 (GRCm39) K372E probably damaging Het
Psmd11 C T 11: 80,351,566 (GRCm39) T263I probably benign Het
Ptprt A T 2: 161,769,676 (GRCm39) N396K probably benign Het
Rab39 T C 9: 53,597,800 (GRCm39) E155G probably damaging Het
Rimbp2 T C 5: 128,874,712 (GRCm39) D293G probably benign Het
Rnf220 T C 4: 117,146,471 (GRCm39) probably benign Het
Rnmt C T 18: 68,454,430 (GRCm39) probably benign Het
Slc10a1 T A 12: 81,002,802 (GRCm39) I279F probably damaging Het
Sp140l1 G A 1: 85,078,288 (GRCm39) R54* probably null Het
Taar6 A G 10: 23,861,250 (GRCm39) Y99H probably damaging Het
Tas2r144 T A 6: 42,193,048 (GRCm39) F263I probably benign Het
Tex15 T A 8: 34,061,768 (GRCm39) N399K possibly damaging Het
Tlr9 T A 9: 106,103,151 (GRCm39) V814D possibly damaging Het
Tmem53 T A 4: 117,122,908 (GRCm39) probably benign Het
Ubap2l T C 3: 89,928,337 (GRCm39) I511V possibly damaging Het
Vmn2r60 T C 7: 41,844,935 (GRCm39) M766T probably damaging Het
Zfp462 T C 4: 55,011,115 (GRCm39) V1027A 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
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
R7139:Muc21 UTSW 17 35,933,525 (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'- CATAGATCCTGAGGCAGAGCTG -3'
(R):5'- AGCACTGCCTCAAGATCTAC -3'

Sequencing Primer
(F):5'- CTGAGGCAGAGCTGGATGC -3'
(R):5'- ACTCCTACCACCACTGCATCTAG -3'
Posted On 2016-07-06