Incidental Mutation 'R8004:Tmem184b'
ID616538
Institutional Source Beutler Lab
Gene Symbol Tmem184b
Ensembl Gene ENSMUSG00000009035
Gene Nametransmembrane protein 184b
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.280) question?
Stock #R8004 (G1)
Quality Score225.009
Status Not validated
Chromosome15
Chromosomal Location79360684-79403569 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 79362766 bp
ZygosityHeterozygous
Amino Acid Change Serine to Proline at position 368 (S368P)
Ref Sequence ENSEMBL: ENSMUSP00000074518 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074991] [ENSMUST00000096350] [ENSMUST00000163691] [ENSMUST00000178522] [ENSMUST00000228002] [ENSMUST00000229130] [ENSMUST00000231076]
Predicted Effect probably damaging
Transcript: ENSMUST00000074991
AA Change: S368P

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000074518
Gene: ENSMUSG00000009035
AA Change: S368P

DomainStartEndE-ValueType
low complexity region 6 28 N/A INTRINSIC
Pfam:Solute_trans_a 46 319 2.9e-94 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000096350
SMART Domains Protein: ENSMUSP00000094076
Gene: ENSMUSG00000042622

DomainStartEndE-ValueType
BRLZ 49 113 5.09e-7 SMART
low complexity region 118 135 N/A INTRINSIC
low complexity region 143 154 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000163691
SMART Domains Protein: ENSMUSP00000131628
Gene: ENSMUSG00000042622

DomainStartEndE-ValueType
BRLZ 49 113 5.09e-7 SMART
low complexity region 118 135 N/A INTRINSIC
low complexity region 143 154 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000178522
AA Change: S368P

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000136416
Gene: ENSMUSG00000009035
AA Change: S368P

DomainStartEndE-ValueType
low complexity region 6 28 N/A INTRINSIC
Pfam:Solute_trans_a 43 319 1.9e-101 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000228002
AA Change: S375P

PolyPhen 2 Score 0.936 (Sensitivity: 0.80; Specificity: 0.94)
Predicted Effect probably benign
Transcript: ENSMUST00000229130
Predicted Effect probably benign
Transcript: ENSMUST00000231076
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a gene-trapped allele exhibit delayed axon degeneration following peripheral nerve injury, progressive structural abnormalities at neuromuscular synapses, swellings within sensory terminals, sensory-motor dysfunction, and abnormal autophagy. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 T A 2: 69,257,210 K1070N possibly damaging Het
Ankrd24 T A 10: 81,638,357 N179K unknown Het
Atp6v0a4 A T 6: 38,050,549 F775L possibly damaging Het
Bbs2 A G 8: 94,082,490 V269A possibly damaging Het
Bpifc T G 10: 85,979,284 S273R probably benign Het
Cdan1 C T 2: 120,731,443 R20Q unknown Het
Chrm2 T A 6: 36,523,286 I26N probably damaging Het
Cngb3 A G 4: 19,505,273 K669E possibly damaging Het
Cnot1 T C 8: 95,752,752 I876V probably benign Het
Col12a1 T A 9: 79,684,401 T926S probably damaging Het
Cyp2b23 G T 7: 26,679,466 T191K probably benign Het
Dpp4 A G 2: 62,358,828 V453A probably benign Het
Eif2ak4 T C 2: 118,417,294 S271P possibly damaging Het
Fam69a T C 5: 107,909,666 D342G probably damaging Het
Fbxw20 G T 9: 109,221,381 P392H probably damaging Het
Fcho2 T A 13: 98,789,505 E118V possibly damaging Het
Gm2042 C G 12: 87,960,151 Q413E possibly damaging Het
Gm904 G A 13: 50,645,307 probably null Het
H2-D1 A G 17: 35,266,696 S352G probably benign Het
Igf2bp3 C A 6: 49,091,020 V451L probably benign Het
Igkv1-99 T C 6: 68,542,128 V23A Het
Igsf10 A G 3: 59,329,709 I1017T probably benign Het
Il18r1 G A 1: 40,474,757 C41Y probably damaging Het
Itgb4 A G 11: 115,982,705 D249G probably benign Het
Ldlrad1 G A 4: 107,209,491 A8T probably benign Het
Lrrn2 T A 1: 132,937,751 F185I probably damaging Het
Mllt6 G T 11: 97,676,140 E635D possibly damaging Het
Msh6 A G 17: 87,986,787 E990G probably damaging Het
Myo1h A T 5: 114,320,708 D184V Het
Nfatc2ip A G 7: 126,390,405 V269A possibly damaging Het
Nol12 A T 15: 78,940,517 K181N probably damaging Het
Npl T A 1: 153,503,540 T266S probably benign Het
Olfr195 T A 16: 59,148,988 V46E probably damaging Het
Olfr863-ps1 A T 9: 19,942,112 D109E possibly damaging Het
Oog2 A T 4: 144,194,251 I85L probably benign Het
Parm1 A C 5: 91,594,273 S167R probably benign Het
Pcsk4 T C 10: 80,322,840 D526G probably damaging Het
Plscr4 C T 9: 92,490,790 R322* probably null Het
Psmd9 T C 5: 123,241,935 probably null Het
Ralgapa1 A G 12: 55,702,457 V1220A probably damaging Het
Rbm25 A T 12: 83,674,392 E577D possibly damaging Het
S100a6 T C 3: 90,613,812 F16L probably benign Het
Sar1a C A 10: 61,685,166 H53Q probably benign Het
Setd2 G A 9: 110,592,545 A282T Het
Slc35f5 A T 1: 125,589,887 H474L probably damaging Het
Slc4a3 T C 1: 75,549,067 probably null Het
Smc1b G A 15: 85,097,614 S735F probably damaging Het
Sp3 A T 2: 72,970,208 I531K possibly damaging Het
St6galnac5 A T 3: 152,840,165 M252K probably damaging Het
Tas2r120 T A 6: 132,657,427 H157Q possibly damaging Het
Tbc1d10b T A 7: 127,199,011 S653C probably damaging Het
Tex10 T C 4: 48,452,047 E693G possibly damaging Het
Thada A G 17: 84,192,205 S1855P probably benign Het
Tjp2 G A 19: 24,114,120 P559L probably damaging Het
Tnc G A 4: 63,984,657 S1461L probably benign Het
Tnpo2 T C 8: 85,044,699 F177S probably benign Het
Vmn1r58 A T 7: 5,410,507 Y241* probably null Het
Wdr66 T C 5: 123,254,450 W216R unknown Het
Other mutations in Tmem184b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01696:Tmem184b APN 15 79378529 missense possibly damaging 0.94
IGL02544:Tmem184b APN 15 79365807 missense probably damaging 1.00
IGL03330:Tmem184b APN 15 79369979 unclassified probably null
R0172:Tmem184b UTSW 15 79378540 missense possibly damaging 0.56
R1938:Tmem184b UTSW 15 79365814 missense probably damaging 1.00
R2340:Tmem184b UTSW 15 79378532 missense probably benign 0.00
R2418:Tmem184b UTSW 15 79365943 missense possibly damaging 0.78
R4771:Tmem184b UTSW 15 79377177 missense probably benign 0.03
R5945:Tmem184b UTSW 15 79365481 critical splice acceptor site probably null
R6996:Tmem184b UTSW 15 79362759 missense probably benign 0.01
R7823:Tmem184b UTSW 15 79365291 missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- CCTCTGGAAGTGATATGCGAG -3'
(R):5'- CTTTCATGTCCCAGGAGCAC -3'

Sequencing Primer
(F):5'- TTCTGGTCCAATAAATAAAAGGGCAG -3'
(R):5'- TCTGTCCCAGGAGTAGGGG -3'
Posted On2020-01-23