Incidental Mutation 'IGL00966:Cnbd1'
ID 306618
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cnbd1
Ensembl Gene ENSMUSG00000073991
Gene Name cyclic nucleotide binding domain containing 1
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00966
Quality Score
Status
Chromosome 4
Chromosomal Location 18860454-19122526 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 18906988 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000121576 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000137780]
AlphaFold B1AWM0
Predicted Effect probably benign
Transcript: ENSMUST00000137780
SMART Domains Protein: ENSMUSP00000121576
Gene: ENSMUSG00000073991

DomainStartEndE-ValueType
low complexity region 21 34 N/A INTRINSIC
Blast:cNMP 166 225 6e-6 BLAST
SCOP:d1cx4a1 296 430 3e-13 SMART
Blast:cNMP 318 429 2e-60 BLAST
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acad11 A G 9: 104,003,855 (GRCm39) E649G probably damaging Het
Adgre1 C A 17: 57,726,335 (GRCm39) T402K probably benign Het
Agap3 A G 5: 24,706,000 (GRCm39) probably benign Het
Amy1 T C 3: 113,349,689 (GRCm39) I494V probably benign Het
Arhgef40 G A 14: 52,229,155 (GRCm39) probably null Het
Atp2c2 T C 8: 120,472,329 (GRCm39) V461A probably benign Het
Bub1 A G 2: 127,652,583 (GRCm39) S595P probably damaging Het
Cdcp3 T A 7: 130,844,836 (GRCm39) Y692* probably null Het
Cmya5 C T 13: 93,234,414 (GRCm39) V225I probably benign Het
Cux1 A T 5: 136,340,345 (GRCm39) probably benign Het
Dsg3 T A 18: 20,656,664 (GRCm39) I178N probably benign Het
Dus2 T A 8: 106,752,533 (GRCm39) probably null Het
Enpp1 G A 10: 24,529,929 (GRCm39) H570Y probably damaging Het
Ephb3 A C 16: 21,036,044 (GRCm39) T57P probably benign Het
Fat3 C A 9: 15,910,390 (GRCm39) V1871F possibly damaging Het
Fbll1 T C 11: 35,688,874 (GRCm39) T130A probably benign Het
Fbxl20 C T 11: 98,001,800 (GRCm39) S99N probably damaging Het
Folr2 T C 7: 101,489,593 (GRCm39) E182G probably damaging Het
Fras1 A G 5: 96,703,080 (GRCm39) D281G probably benign Het
Gm17175 G T 14: 51,810,526 (GRCm39) Q34K possibly damaging Het
Gm5592 T A 7: 40,938,519 (GRCm39) D600E probably damaging Het
Gtf2e1 T C 16: 37,336,092 (GRCm39) E294G probably benign Het
Gtf3c2 A G 5: 31,327,517 (GRCm39) probably benign Het
Heg1 T C 16: 33,530,977 (GRCm39) L151P probably damaging Het
Hmcn2 T G 2: 31,319,006 (GRCm39) V3902G probably damaging Het
Ift140 A G 17: 25,237,776 (GRCm39) Y4C probably damaging Het
Ighv1-19 A C 12: 114,672,569 (GRCm39) V17G possibly damaging Het
Iqca1 T A 1: 89,973,379 (GRCm39) I770F probably benign Het
Jak3 T A 8: 72,131,656 (GRCm39) C115S probably benign Het
Kif18b A T 11: 102,805,501 (GRCm39) M252K probably damaging Het
Klhdc7a A T 4: 139,694,236 (GRCm39) V237D probably benign Het
Klhl11 C T 11: 100,354,031 (GRCm39) V597I possibly damaging Het
Krt72 T A 15: 101,689,396 (GRCm39) Y312F probably damaging Het
Lonp2 T A 8: 87,360,600 (GRCm39) I191N probably damaging Het
Npc2 A T 12: 84,819,619 (GRCm39) I8N possibly damaging Het
Nr4a1 T C 15: 101,170,669 (GRCm39) L413P probably damaging Het
Nup133 T C 8: 124,638,645 (GRCm39) N895S probably damaging Het
Or7e175 T C 9: 20,048,531 (GRCm39) F40L probably benign Het
Ppef1 A G X: 159,468,290 (GRCm39) I94T probably benign Het
Prrt4 G A 6: 29,176,455 (GRCm39) T290I probably benign Het
Ptpru A T 4: 131,499,927 (GRCm39) V1239E probably damaging Het
Rab8b T G 9: 66,760,274 (GRCm39) M117L probably benign Het
S1pr5 T A 9: 21,155,512 (GRCm39) I305F possibly damaging Het
Sdr39u1 A G 14: 56,135,463 (GRCm39) V160A probably damaging Het
Slc6a21 C T 7: 44,937,668 (GRCm39) T653M probably benign Het
Stk39 T A 2: 68,042,302 (GRCm39) E544D probably benign Het
Tgfbr3 T C 5: 107,290,367 (GRCm39) T313A probably benign Het
Tle6 A T 10: 81,430,292 (GRCm39) L287M probably damaging Het
Tmc2 A G 2: 130,105,932 (GRCm39) H821R probably benign Het
Tmem230 G T 2: 132,087,897 (GRCm39) D26E probably benign Het
Tnfaip3 A G 10: 18,880,885 (GRCm39) F394S probably damaging Het
Ttn T A 2: 76,641,721 (GRCm39) L13458F probably damaging Het
Vwa5a A T 9: 38,634,675 (GRCm39) N161I probably benign Het
Wdr87-ps C A 7: 29,236,888 (GRCm39) noncoding transcript Het
Other mutations in Cnbd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01101:Cnbd1 APN 4 18,907,098 (GRCm39) missense probably benign 0.30
IGL01365:Cnbd1 APN 4 18,860,576 (GRCm39) missense probably damaging 1.00
IGL01646:Cnbd1 APN 4 18,895,141 (GRCm39) nonsense probably null
IGL02106:Cnbd1 APN 4 18,894,993 (GRCm39) missense possibly damaging 0.55
IGL02218:Cnbd1 APN 4 18,887,739 (GRCm39) missense probably benign 0.00
IGL02335:Cnbd1 APN 4 19,055,095 (GRCm39) missense possibly damaging 0.87
IGL02380:Cnbd1 APN 4 18,887,749 (GRCm39) critical splice acceptor site probably null
IGL02380:Cnbd1 APN 4 18,887,748 (GRCm39) critical splice acceptor site probably null
IGL02404:Cnbd1 APN 4 18,895,047 (GRCm39) missense possibly damaging 0.64
IGL03293:Cnbd1 APN 4 18,860,565 (GRCm39) missense possibly damaging 0.65
IGL03301:Cnbd1 APN 4 19,055,039 (GRCm39) missense probably benign 0.00
IGL03342:Cnbd1 APN 4 19,098,264 (GRCm39) splice site probably benign
IGL03392:Cnbd1 APN 4 18,862,111 (GRCm39) missense probably damaging 1.00
R0062:Cnbd1 UTSW 4 18,860,504 (GRCm39) missense possibly damaging 0.65
R0062:Cnbd1 UTSW 4 18,860,504 (GRCm39) missense possibly damaging 0.65
R0195:Cnbd1 UTSW 4 18,906,988 (GRCm39) splice site probably benign
R0462:Cnbd1 UTSW 4 18,895,044 (GRCm39) missense probably benign 0.01
R0909:Cnbd1 UTSW 4 19,122,444 (GRCm39) missense probably benign
R1435:Cnbd1 UTSW 4 18,907,026 (GRCm39) missense probably benign 0.00
R1995:Cnbd1 UTSW 4 19,055,112 (GRCm39) missense possibly damaging 0.55
R2495:Cnbd1 UTSW 4 18,860,579 (GRCm39) missense probably damaging 1.00
R3974:Cnbd1 UTSW 4 18,887,693 (GRCm39) missense probably benign 0.00
R4083:Cnbd1 UTSW 4 18,886,042 (GRCm39) missense possibly damaging 0.88
R4494:Cnbd1 UTSW 4 19,098,150 (GRCm39) missense probably benign 0.34
R4558:Cnbd1 UTSW 4 19,055,095 (GRCm39) missense possibly damaging 0.87
R4833:Cnbd1 UTSW 4 18,862,120 (GRCm39) missense probably damaging 0.97
R5326:Cnbd1 UTSW 4 18,860,517 (GRCm39) missense possibly damaging 0.67
R5542:Cnbd1 UTSW 4 18,860,517 (GRCm39) missense possibly damaging 0.67
R5930:Cnbd1 UTSW 4 18,886,119 (GRCm39) missense probably benign 0.14
R5958:Cnbd1 UTSW 4 18,862,056 (GRCm39) missense probably benign 0.31
R6064:Cnbd1 UTSW 4 18,895,084 (GRCm39) missense probably benign 0.14
R6250:Cnbd1 UTSW 4 19,098,255 (GRCm39) missense probably benign 0.00
R6348:Cnbd1 UTSW 4 18,860,462 (GRCm39) missense probably damaging 0.99
R7027:Cnbd1 UTSW 4 18,862,063 (GRCm39) missense probably benign 0.01
R7905:Cnbd1 UTSW 4 18,907,100 (GRCm39) missense possibly damaging 0.81
R8434:Cnbd1 UTSW 4 19,055,045 (GRCm39) missense probably benign 0.00
R9066:Cnbd1 UTSW 4 19,098,181 (GRCm39) missense probably benign 0.35
R9098:Cnbd1 UTSW 4 18,886,061 (GRCm39) nonsense probably null
R9225:Cnbd1 UTSW 4 18,907,010 (GRCm39) missense probably benign 0.08
R9248:Cnbd1 UTSW 4 18,862,113 (GRCm39) missense possibly damaging 0.48
R9307:Cnbd1 UTSW 4 18,887,647 (GRCm39) missense probably damaging 1.00
R9419:Cnbd1 UTSW 4 19,098,156 (GRCm39) missense probably benign 0.11
R9648:Cnbd1 UTSW 4 19,098,142 (GRCm39) critical splice donor site probably null
Posted On 2015-04-16