Incidental Mutation 'R4738:Tspan17'
Institutional Source Beutler Lab
Gene Symbol Tspan17
Ensembl Gene ENSMUSG00000025875
Gene Nametetraspanin 17
Synonyms2210021G21Rik, Fbxo23, Tm4sf17
MMRRC Submission 041964-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R4738 (G1)
Quality Score225
Status Not validated
Chromosomal Location54789377-54796776 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 54795064 bp
Amino Acid Change Cysteine to Stop codon at position 116 (C116*)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026993] [ENSMUST00000099503] [ENSMUST00000130568] [ENSMUST00000131692] [ENSMUST00000163796] [ENSMUST00000163915]
Predicted Effect probably null
Transcript: ENSMUST00000026993
AA Change: C156*
SMART Domains Protein: ENSMUSP00000026993
Gene: ENSMUSG00000025875
AA Change: C156*

Pfam:Tetraspannin 16 263 6.9e-49 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000099503
AA Change: C156*
SMART Domains Protein: ENSMUSP00000097102
Gene: ENSMUSG00000025875
AA Change: C156*

Pfam:Tetraspannin 16 266 1.3e-49 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000130568
AA Change: C110*
SMART Domains Protein: ENSMUSP00000123607
Gene: ENSMUSG00000025875
AA Change: C110*

Pfam:Tetraspannin 3 174 1.2e-31 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000131692
AA Change: C156*
SMART Domains Protein: ENSMUSP00000115287
Gene: ENSMUSG00000025875
AA Change: C156*

Pfam:Tetraspannin 15 263 8.9e-58 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139574
Predicted Effect probably null
Transcript: ENSMUST00000145574
AA Change: C66*
SMART Domains Protein: ENSMUSP00000119687
Gene: ENSMUSG00000025875
AA Change: C66*

Pfam:Tetraspannin 1 174 8.2e-38 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000163796
AA Change: C90*
SMART Domains Protein: ENSMUSP00000131671
Gene: ENSMUSG00000025875
AA Change: C90*

Pfam:Tetraspannin 13 193 4.3e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000163915
SMART Domains Protein: ENSMUSP00000130765
Gene: ENSMUSG00000025875

Pfam:Tetraspannin 13 143 5e-15 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000171859
AA Change: C116*
SMART Domains Protein: ENSMUSP00000128568
Gene: ENSMUSG00000025875
AA Change: C116*

Pfam:Tetraspannin 1 79 3.6e-17 PFAM
Pfam:Tetraspannin 78 144 1.5e-13 PFAM
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.9%
  • 20x: 94.3%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the transmembrane 4 superfamily. It is characterized by four tetraspanin transmembrane segments. The function of this gene has not yet been determined. [provided by RefSeq, Mar 2014]
Allele List at MGI
Other mutations in this stock
Total: 81 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg3 A G 5: 104,973,983 I176T probably benign Het
Angpt2 C T 8: 18,741,059 D74N probably benign Het
Apol10a C T 15: 77,488,641 T159I possibly damaging Het
Areg T C 5: 91,146,724 I247T possibly damaging Het
Atg16l2 A G 7: 101,297,178 L129P probably damaging Het
Atp6v1b2 T A 8: 69,103,410 S246T probably benign Het
Atp8b1 T C 18: 64,545,180 R882G probably benign Het
Atp9a A G 2: 168,668,181 V444A probably benign Het
Babam2 T A 5: 31,901,142 Y211N probably damaging Het
Btbd11 C T 10: 85,627,248 Q626* probably null Het
Ccdc127 T G 13: 74,357,068 probably benign Het
Cep192 A T 18: 67,884,830 K2500* probably null Het
Cnot4 T C 6: 35,051,376 N435S probably benign Het
Col12a1 T C 9: 79,699,282 I620V probably damaging Het
Cyth4 G A 15: 78,605,874 M62I probably benign Het
Dbt T C 3: 116,539,132 I200T probably damaging Het
Dchs1 C T 7: 105,758,673 R1984Q probably damaging Het
Depdc5 A G 5: 32,975,322 M1237V probably benign Het
Disp2 A G 2: 118,790,326 Y513C probably damaging Het
Dph7 T C 2: 24,963,131 S86P possibly damaging Het
Eif3b T A 5: 140,430,078 M384K probably benign Het
Emc1 G T 4: 139,362,202 G227V possibly damaging Het
Eri2 A G 7: 119,787,732 probably null Het
Frzb A G 2: 80,424,597 probably null Het
Ganc T A 2: 120,452,594 V743D probably damaging Het
Gfpt1 C A 6: 87,054,747 probably benign Het
Gm3086 A T 12: 69,969,381 probably benign Het
Gsdmc2 A T 15: 63,826,801 Y315* probably null Het
Haus6 A G 4: 86,600,749 probably null Het
Hhip C T 8: 79,992,570 D443N probably damaging Het
Isg15 T C 4: 156,199,862 M70V probably benign Het
Kank2 T C 9: 21,774,619 N653S probably damaging Het
Klhdc1 G T 12: 69,283,133 R345S probably benign Het
Larp7 A G 3: 127,546,045 probably null Het
Lgals12 A G 19: 7,604,099 V81A probably benign Het
Lhx9 A G 1: 138,832,748 L288P probably damaging Het
Mcpt9 T A 14: 56,026,999 H213L probably damaging Het
Met T C 6: 17,491,541 C101R probably damaging Het
Myo16 G T 8: 10,373,527 G288W probably damaging Het
Neb A C 2: 52,187,482 S1846A probably damaging Het
Nr3c2 T C 8: 76,909,307 S346P possibly damaging Het
Olfr1564 A G 17: 33,215,810 F178S probably benign Het
Olfr187 T C 16: 59,036,195 I181V probably benign Het
Olfr376 G T 11: 73,375,350 L200F possibly damaging Het
Olfr487 A T 7: 108,211,994 N178K probably damaging Het
Olfr558 T A 7: 102,710,171 I304N probably damaging Het
Osbpl10 A G 9: 115,216,574 E426G probably damaging Het
Ovgp1 T C 3: 105,979,918 V210A probably damaging Het
Pam A T 1: 97,923,132 V167D probably damaging Het
Pappa2 T C 1: 158,957,012 R143G probably benign Het
Pbx4 C T 8: 69,864,969 T201M probably damaging Het
Pcdhb9 T C 18: 37,403,415 C821R probably benign Het
Plekhg3 T C 12: 76,576,914 I976T probably damaging Het
Pold1 G A 7: 44,541,329 R304C probably damaging Het
Prss38 T C 11: 59,372,945 T314A probably benign Het
Psph T C 5: 129,769,386 probably null Het
Ptprj G A 2: 90,440,643 P1247L probably damaging Het
Rab3gap1 A G 1: 127,934,436 E648G probably damaging Het
Ralgds A G 2: 28,545,416 E465G probably damaging Het
Rfng T C 11: 120,783,964 T67A probably damaging Het
Rnf219 C T 14: 104,510,383 D43N probably damaging Het
Rps6kl1 G T 12: 85,140,387 F181L probably benign Het
Spata46 G A 1: 170,311,886 M151I possibly damaging Het
Ssbp1 T A 6: 40,477,980 N124K probably damaging Het
Sspo C T 6: 48,478,396 A3064V possibly damaging Het
Tbc1d8 G A 1: 39,402,878 T211I possibly damaging Het
Tdpoz4 T C 3: 93,797,089 I231T probably damaging Het
Tff3 G A 17: 31,127,509 P30S probably benign Het
Thg1l C T 11: 45,954,191 R18Q probably damaging Het
Tlk2 T A 11: 105,256,882 H369Q probably benign Het
Tnfaip8 A G 18: 50,090,502 T14A probably damaging Het
Ttn T C 2: 76,880,546 probably benign Het
Tyr T C 7: 87,492,647 Y158C probably null Het
U2af1l4 G T 7: 30,563,348 probably benign Het
Ubqlnl C T 7: 104,149,718 V191M probably benign Het
Vmn2r86 T A 10: 130,447,070 D559V probably damaging Het
Wfikkn2 T A 11: 94,239,076 T80S probably benign Het
Zdhhc2 T A 8: 40,464,142 probably null Het
Zfp521 T C 18: 13,844,054 K1101E possibly damaging Het
Zfp595 A T 13: 67,317,165 F345I probably benign Het
Zswim2 T A 2: 83,915,395 R566S probably benign Het
Other mutations in Tspan17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02681:Tspan17 APN 13 54789629 missense probably damaging 0.99
R0745:Tspan17 UTSW 13 54789674 missense possibly damaging 0.45
R1128:Tspan17 UTSW 13 54795171 missense probably damaging 1.00
R5905:Tspan17 UTSW 13 54793298 missense probably damaging 0.98
R6028:Tspan17 UTSW 13 54793298 missense probably damaging 0.98
R6389:Tspan17 UTSW 13 54795616 splice site probably null
R6919:Tspan17 UTSW 13 54796033 missense probably damaging 1.00
R7050:Tspan17 UTSW 13 54796063 missense probably benign 0.39
R7346:Tspan17 UTSW 13 54792621 missense probably benign 0.01
R7408:Tspan17 UTSW 13 54789653 missense probably benign 0.15
R7429:Tspan17 UTSW 13 54795972 missense probably benign 0.03
R7430:Tspan17 UTSW 13 54795972 missense probably benign 0.03
Z1177:Tspan17 UTSW 13 54792778 frame shift probably null
Z1177:Tspan17 UTSW 13 54796221 makesense probably null
Predicted Primers PCR Primer

Sequencing Primer
Posted On2015-11-11