Incidental Mutation 'R1117:Muc21'
ID 97460
Institutional Source Beutler Lab
Gene Symbol Muc21
Ensembl Gene ENSMUSG00000090588
Gene Name mucin 21
Synonyms epiglycanin, Gm9573
MMRRC Submission 039190-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.097) question?
Stock # R1117 (G1)
Quality Score 221
Status Not validated
Chromosome 17
Chromosomal Location 35928815-35937529 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 35930920 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: T1089A
SMART Domains Protein: ENSMUSP00000130987
Gene: ENSMUSG00000090588
AA Change: T1089A

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: 99.0%
  • 3x: 98.1%
  • 10x: 95.6%
  • 20x: 90.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh1l2 G A 10: 83,344,487 (GRCm39) T353I probably benign Het
Arpc1b T C 5: 145,062,564 (GRCm39) V226A possibly damaging Het
Casz1 C A 4: 149,019,052 (GRCm39) T451K probably damaging Het
Ccr4 C T 9: 114,321,085 (GRCm39) V327M probably benign Het
Cntrl A G 2: 35,017,985 (GRCm39) E465G probably damaging Het
Cpa1 A G 6: 30,645,260 (GRCm39) D412G probably benign Het
Crispld1 T A 1: 17,819,846 (GRCm39) N281K probably benign Het
Cul3 T C 1: 80,258,641 (GRCm39) Q465R probably damaging Het
Cyp2c68 G A 19: 39,700,903 (GRCm39) T305M probably damaging Het
Elp4 T C 2: 105,672,656 (GRCm39) D143G probably benign Het
Etnppl A G 3: 130,428,212 (GRCm39) I462M probably benign Het
Fmo4 A G 1: 162,631,232 (GRCm39) V245A probably benign Het
Gm4076 A G 13: 85,275,437 (GRCm39) noncoding transcript Het
Gtf3c3 C T 1: 54,456,937 (GRCm39) A488T probably damaging Het
Kcnj15 G A 16: 95,096,484 (GRCm39) M8I probably benign Het
Klk1b22 A T 7: 43,766,283 (GRCm39) M255L probably benign Het
Mmrn1 T A 6: 60,953,309 (GRCm39) I530K possibly damaging Het
Nid2 A C 14: 19,813,732 (GRCm39) probably null Het
Or10g6 T C 9: 39,934,058 (GRCm39) F123S probably damaging Het
Or10h28 C T 17: 33,487,940 (GRCm39) R81* probably null Het
Or9e1 A G 11: 58,732,641 (GRCm39) K234E possibly damaging Het
Peak1 G A 9: 56,165,702 (GRCm39) T742M probably benign Het
Sel1l3 T A 5: 53,329,949 (GRCm39) T469S probably benign Het
Sez6 A G 11: 77,865,340 (GRCm39) Y659C probably damaging Het
Slc19a2 A T 1: 164,091,025 (GRCm39) I278F possibly damaging Het
Slc36a3 T C 11: 55,037,006 (GRCm39) I100V possibly damaging Het
Tcerg1 A G 18: 42,707,717 (GRCm39) D1079G probably damaging Het
Trim43c T C 9: 88,727,030 (GRCm39) S286P probably benign Het
Umod T C 7: 119,076,529 (GRCm39) N79S possibly damaging Het
Wdr43 A G 17: 71,923,382 (GRCm39) T43A probably benign 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
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
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'- GTAGATCCTGAGGCAGAGCTGGATG -3'
(R):5'- TCAGGCTCTACACCTACCTGGACC -3'

Sequencing Primer
(F):5'- TAGAGCCTGAGCCACTCCTG -3'
(R):5'- TGGACCACCACTACATCCAG -3'
Posted On 2014-01-05