Incidental Mutation 'R3791:Cnrip1'
Institutional Source Beutler Lab
Gene Symbol Cnrip1
Ensembl Gene ENSMUSG00000044629
Gene Namecannabinoid receptor interacting protein 1
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.072) question?
Stock #R3791 (G1)
Quality Score225
Status Not validated
Chromosomal Location17051586-17079371 bp(+) (GRCm38)
Type of Mutationintron
DNA Base Change (assembly) C to T at 17054845 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000050036 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020321] [ENSMUST00000058159] [ENSMUST00000131515]
Predicted Effect probably benign
Transcript: ENSMUST00000020321
SMART Domains Protein: ENSMUSP00000020321
Gene: ENSMUSG00000020120

PH 1 80 1.12e-2 SMART
DEP 113 198 2.53e-16 SMART
PH 222 326 5.96e-21 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000058159
SMART Domains Protein: ENSMUSP00000050036
Gene: ENSMUSG00000044629

Pfam:CNRIP1 1 164 2.3e-80 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000131515
AA Change: H132Y
SMART Domains Protein: ENSMUSP00000122150
Gene: ENSMUSG00000044629
AA Change: H132Y

Pfam:CNRIP1 4 171 5.6e-57 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135637
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 93.9%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that interacts with the C-terminal tail of cannabinoid receptor 1. Two transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2013]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A930009A15Rik A T 10: 115,578,289 probably benign Het
Adgrv1 T C 13: 81,593,102 Y81C probably damaging Het
Alx3 A T 3: 107,600,706 Y177F probably damaging Het
C6 A G 15: 4,735,235 T138A probably benign Het
Cacna2d3 T C 14: 29,183,581 M410V probably benign Het
Celsr3 G A 9: 108,842,552 R2450H probably benign Het
Col6a5 A C 9: 105,864,669 D2350E probably damaging Het
Cyp4a12b A G 4: 115,434,970 I407V probably benign Het
Gpx4 A G 10: 80,056,189 I245V probably benign Het
H2-K1 A G 17: 33,999,525 I139T probably benign Het
Hmgcl A G 4: 135,959,987 K191R probably benign Het
Hpdl A G 4: 116,820,532 V244A possibly damaging Het
Hpse A G 5: 100,692,238 S338P probably damaging Het
Ifi203 T C 1: 173,935,080 K162R possibly damaging Het
Kit A G 5: 75,639,150 N514S probably damaging Het
Kmt2d G A 15: 98,844,149 probably benign Het
Limd1 T A 9: 123,480,374 S379R possibly damaging Het
Llph A G 10: 120,228,155 K59E probably benign Het
Lrrc7 T A 3: 158,163,956 M709L probably benign Het
Muc5ac A G 7: 141,798,501 S665G probably benign Het
Ncapd3 C T 9: 27,052,635 H524Y probably benign Het
Nfix CAAAAA CAAAA 8: 84,716,247 probably null Het
Olfr571 T C 7: 102,909,032 D269G probably benign Het
Papd5 G A 8: 88,243,329 E210K probably damaging Het
Phtf2 T C 5: 20,782,298 E400G probably damaging Het
Pkd1l3 T C 8: 109,636,317 V1080A probably damaging Het
Plch1 A T 3: 63,699,523 H1007Q probably benign Het
Prr5 T C 15: 84,681,216 S3P probably damaging Het
Qtrt1 G A 9: 21,419,340 D279N probably damaging Het
Rundc1 G A 11: 101,434,201 A578T probably damaging Het
Shc4 A T 2: 125,723,331 V16E probably damaging Het
Sik3 A T 9: 46,194,822 L329F possibly damaging Het
Slc36a3 A G 11: 55,125,156 S391P possibly damaging Het
Smad1 C A 8: 79,339,770 R426L probably damaging Het
Thrap3 A T 4: 126,167,500 N820K possibly damaging Het
Tnrc6b T C 15: 80,923,640 S1598P probably damaging Het
Ttn T C 2: 76,714,824 I32645V probably damaging Het
Wisp1 A G 15: 66,919,288 Y313C probably damaging Het
Zfp266 A C 9: 20,499,481 Y467D probably damaging Het
Zfp526 T A 7: 25,226,203 M629K probably damaging Het
Zfp788 A T 7: 41,649,728 H596L probably damaging Het
Zhx3 A G 2: 160,780,448 W600R possibly damaging Het
Other mutations in Cnrip1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02188:Cnrip1 APN 11 17078398 critical splice acceptor site probably null
IGL02584:Cnrip1 APN 11 17078536 missense probably damaging 0.99
IGL02701:Cnrip1 APN 11 17078415 missense probably benign 0.00
R2093:Cnrip1 UTSW 11 17052237 missense probably damaging 0.99
R4960:Cnrip1 UTSW 11 17052228 missense probably damaging 1.00
R5068:Cnrip1 UTSW 11 17054687 missense probably damaging 0.98
R6169:Cnrip1 UTSW 11 17054731 missense probably null 0.99
R6423:Cnrip1 UTSW 11 17052350 critical splice donor site probably null
R6520:Cnrip1 UTSW 11 17078536 missense probably damaging 0.99
R6562:Cnrip1 UTSW 11 17078539 nonsense probably null
R6897:Cnrip1 UTSW 11 17054705 missense probably damaging 1.00
Predicted Primers PCR Primer

Sequencing Primer
Posted On2015-03-25