Incidental Mutation 'R0497:Dirc2'
ID 40564
Institutional Source Beutler Lab
Gene Symbol Dirc2
Ensembl Gene ENSMUSG00000022848
Gene Name disrupted in renal carcinoma 2 (human)
Synonyms RCC4
MMRRC Submission 038693-MU
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.905) question?
Stock # R0497 (G1)
Quality Score 133
Status Validated
Chromosome 16
Chromosomal Location 35694062-35769356 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 35735604 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Aspartic acid at position 162 (V162D)
Ref Sequence ENSEMBL: ENSMUSP00000023554 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023554] [ENSMUST00000149892]
AlphaFold Q8BFQ6
Predicted Effect probably benign
Transcript: ENSMUST00000023554
AA Change: V162D

PolyPhen 2 Score 0.403 (Sensitivity: 0.89; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000023554
Gene: ENSMUSG00000022848
AA Change: V162D

DomainStartEndE-ValueType
low complexity region 8 33 N/A INTRINSIC
transmembrane domain 53 75 N/A INTRINSIC
transmembrane domain 90 111 N/A INTRINSIC
transmembrane domain 116 138 N/A INTRINSIC
transmembrane domain 148 170 N/A INTRINSIC
transmembrane domain 183 205 N/A INTRINSIC
transmembrane domain 231 250 N/A INTRINSIC
low complexity region 251 258 N/A INTRINSIC
transmembrane domain 280 302 N/A INTRINSIC
transmembrane domain 317 339 N/A INTRINSIC
transmembrane domain 344 366 N/A INTRINSIC
transmembrane domain 381 403 N/A INTRINSIC
transmembrane domain 415 437 N/A INTRINSIC
transmembrane domain 441 463 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000149892
SMART Domains Protein: ENSMUSP00000120775
Gene: ENSMUSG00000022848

DomainStartEndE-ValueType
low complexity region 8 33 N/A INTRINSIC
transmembrane domain 53 75 N/A INTRINSIC
transmembrane domain 90 111 N/A INTRINSIC
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.6%
  • 3x: 98.7%
  • 10x: 96.6%
  • 20x: 93.1%
Validation Efficiency 100% (68/68)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a membrane-bound protein from the major facilitator superfamily of transporters. Disruption of this gene by translocation has been associated with haplo-insufficiency and renal cell carcinomas. Alternatively spliced transcript variants have been described, but their biological validity has not yet been determined. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530053A07Rik T A 7: 28,147,465 C1158S probably damaging Het
Aatk A C 11: 120,018,780 V110G probably damaging Het
Adcy6 A C 15: 98,597,725 probably null Het
Adm A G 7: 110,629,121 T170A probably benign Het
Afap1l2 G T 19: 56,930,209 N171K probably benign Het
Aph1b G T 9: 66,790,618 S112* probably null Het
Arhgap23 A G 11: 97,452,163 S424G probably damaging Het
Asah2 T A 19: 32,054,631 N46I probably benign Het
Braf G A 6: 39,640,549 probably benign Het
Brd2 C T 17: 34,114,360 R47Q probably damaging Het
C2cd5 A G 6: 143,012,093 V972A probably benign Het
Car9 T A 4: 43,511,881 L300H probably damaging Het
Chmp3 T C 6: 71,552,411 S20P probably damaging Het
Chp1 A G 2: 119,571,782 N79S possibly damaging Het
Cnot2 A T 10: 116,498,355 I335N probably damaging Het
Cntnap4 T C 8: 112,570,151 V6A probably benign Het
Ctcf T A 8: 105,675,040 probably benign Het
Dennd1b A G 1: 139,039,986 probably benign Het
Dnmbp A G 19: 43,856,640 probably benign Het
Eef2 T C 10: 81,181,586 F782L probably benign Het
Eogt T A 6: 97,135,233 Y153F probably benign Het
Fam81a G T 9: 70,096,119 Q237K possibly damaging Het
Fat2 T A 11: 55,283,402 T2162S probably benign Het
Gas6 T C 8: 13,470,387 I434V possibly damaging Het
Gm42417 A T 1: 36,532,167 L77Q probably damaging Het
Grik3 A T 4: 125,623,510 N49Y possibly damaging Het
Gucy2e A T 11: 69,224,159 V974E probably damaging Het
Helz2 A G 2: 181,229,656 V2721A probably damaging Het
Klhl6 GT G 16: 19,956,966 279 probably null Het
Krt73 A G 15: 101,802,230 L23P probably damaging Het
L3mbtl3 T C 10: 26,282,874 probably benign Het
Lrrc15 A T 16: 30,272,892 V543E probably damaging Het
Med13 G A 11: 86,276,983 probably benign Het
Med25 T C 7: 44,892,100 D60G probably damaging Het
Mgam T A 6: 40,664,892 Y560N probably damaging Het
Mlkl A G 8: 111,327,873 Y211H probably damaging Het
Msl2 A G 9: 101,101,294 N289S probably benign Het
Nwd2 G T 5: 63,806,343 W1090L probably damaging Het
Olfr1281 A G 2: 111,328,830 D137G probably benign Het
Omt2b T C 9: 78,328,231 probably benign Het
Pald1 A G 10: 61,341,315 L652P probably damaging Het
Pard3b T A 1: 62,440,008 probably null Het
Prdm15 G A 16: 97,794,334 T1098I possibly damaging Het
Rock2 A G 12: 16,954,953 T436A probably benign Het
Sema4c A T 1: 36,549,608 D812E probably benign Het
Sla A T 15: 66,792,249 I91K probably benign Het
Slc22a16 T G 10: 40,584,967 M255R probably damaging Het
Smg8 C T 11: 87,086,084 D224N possibly damaging Het
Spdef A T 17: 27,718,058 D190E probably benign Het
Taok1 A G 11: 77,573,804 I152T probably damaging Het
Tmem220 A G 11: 67,025,922 D36G probably damaging Het
Tmem235 A C 11: 117,864,351 I210L probably benign Het
Tmem266 C T 9: 55,380,884 probably null Het
Tmprss12 A G 15: 100,281,039 probably benign Het
Trim32 G A 4: 65,613,254 R16Q probably damaging Het
Usp38 T A 8: 80,984,424 probably benign Het
Usp44 C T 10: 93,846,806 P373S possibly damaging Het
Vmn1r209 G T 13: 22,805,948 Q191K probably damaging Het
Vmn1r70 T C 7: 10,634,026 I147T probably benign Het
Vmn2r107 T A 17: 20,375,132 I649N probably damaging Het
Vmn2r12 A T 5: 109,091,889 Y269* probably null Het
Zan C T 5: 137,412,676 probably benign Het
Zfp616 G T 11: 74,083,480 V192L probably benign Het
Zfp644 A T 5: 106,638,333 V116D probably damaging Het
Zgrf1 T C 3: 127,584,650 probably benign Het
Zhx3 A T 2: 160,779,994 L751* probably null Het
Znfx1 T A 2: 167,055,411 Q531L probably benign Het
Other mutations in Dirc2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02505:Dirc2 APN 16 35735558 missense probably benign 0.01
IGL02990:Dirc2 APN 16 35735491 missense possibly damaging 0.68
R0166:Dirc2 UTSW 16 35719314 missense possibly damaging 0.49
R0319:Dirc2 UTSW 16 35750514 missense probably benign 0.01
R0323:Dirc2 UTSW 16 35719360 frame shift probably null
R1240:Dirc2 UTSW 16 35698009 missense probably benign 0.00
R1460:Dirc2 UTSW 16 35719366 missense probably benign 0.25
R2115:Dirc2 UTSW 16 35697939 missense probably benign 0.17
R4502:Dirc2 UTSW 16 35719417 missense probably benign 0.00
R4503:Dirc2 UTSW 16 35719417 missense probably benign 0.00
R4563:Dirc2 UTSW 16 35697942 missense probably damaging 1.00
R4834:Dirc2 UTSW 16 35735575 missense probably benign 0.08
R5278:Dirc2 UTSW 16 35697988 missense probably damaging 1.00
R5651:Dirc2 UTSW 16 35735616 missense probably benign 0.25
R5717:Dirc2 UTSW 16 35719429 missense probably benign 0.00
R5947:Dirc2 UTSW 16 35730306 missense probably benign 0.14
R6176:Dirc2 UTSW 16 35704797 missense probably benign
R7155:Dirc2 UTSW 16 35735577 missense probably benign 0.02
R7450:Dirc2 UTSW 16 35768974 missense possibly damaging 0.76
R7645:Dirc2 UTSW 16 35734068 critical splice acceptor site probably null
R7905:Dirc2 UTSW 16 35768950 missense probably benign 0.33
R8425:Dirc2 UTSW 16 35735597 missense probably benign 0.01
R8670:Dirc2 UTSW 16 35735635 missense possibly damaging 0.76
R8827:Dirc2 UTSW 16 35733950 missense probably benign 0.01
R9022:Dirc2 UTSW 16 35750542 missense probably benign 0.00
R9421:Dirc2 UTSW 16 35698002 missense
Predicted Primers PCR Primer
(F):5'- ACCTGCATACAACACGGTCTCG -3'
(R):5'- TCGGTCAGCTCACCTTTTCAGAATG -3'

Sequencing Primer
(F):5'- TACAACACGGTCTCGATTCG -3'
(R):5'- AATGCTTGCTTCAAATGTCTCA -3'
Posted On 2013-05-23