Incidental Mutation 'R6340:Ogfrl1'
ID 513863
Institutional Source Beutler Lab
Gene Symbol Ogfrl1
Ensembl Gene ENSMUSG00000026158
Gene Name opioid growth factor receptor-like 1
Synonyms 2210417C17Rik
MMRRC Submission 044494-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.096) question?
Stock # R6340 (G1)
Quality Score 225.009
Status Validated
Chromosome 1
Chromosomal Location 23405505-23422282 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 23408944 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Asparagine at position 427 (K427N)
Ref Sequence ENSEMBL: ENSMUSP00000027343 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000027343] [ENSMUST00000188677]
AlphaFold Q8VE52
Predicted Effect probably benign
Transcript: ENSMUST00000027343
AA Change: K427N

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000027343
Gene: ENSMUSG00000026158
AA Change: K427N

DomainStartEndE-ValueType
low complexity region 28 44 N/A INTRINSIC
low complexity region 72 86 N/A INTRINSIC
Pfam:OGFr_N 114 320 1.7e-104 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186064
Predicted Effect probably benign
Transcript: ENSMUST00000188677
SMART Domains Protein: ENSMUSP00000139453
Gene: ENSMUSG00000026158

DomainStartEndE-ValueType
Pfam:OGFr_N 1 92 1.6e-38 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 93.7%
Validation Efficiency 98% (41/42)
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgef4 C T 1: 34,771,304 (GRCm39) L1204F probably damaging Het
Atp9b T C 18: 80,822,115 (GRCm39) D495G probably benign Het
B020011L13Rik G A 1: 117,729,614 (GRCm39) V374I probably benign Het
Babam1 T A 8: 71,855,449 (GRCm39) V214D probably damaging Het
Chpf2 T C 5: 24,796,773 (GRCm39) V573A probably damaging Het
Elmo3 T A 8: 106,033,379 (GRCm39) I115N probably damaging Het
Emc1 T A 4: 139,092,874 (GRCm39) Y564N probably damaging Het
Fam180a A C 6: 35,292,322 (GRCm39) L28R probably damaging Het
Fiz1 C T 7: 5,011,400 (GRCm39) A373T possibly damaging Het
Fnip2 A G 3: 79,415,152 (GRCm39) F243L probably damaging Het
Gabra5 A T 7: 57,063,496 (GRCm39) N309K probably damaging Het
Gm17654 A G 14: 43,815,534 (GRCm39) L91P unknown Het
Gm19684 G A 17: 36,438,402 (GRCm39) probably null Het
Gm9376 A T 14: 118,504,669 (GRCm39) M34L unknown Het
Hmgcr A G 13: 96,802,366 (GRCm39) F106S probably damaging Het
Hydin T G 8: 111,081,574 (GRCm39) probably null Het
Igf2bp3 A G 6: 49,191,393 (GRCm39) Y5H probably damaging Het
Igsf11 A G 16: 38,829,336 (GRCm39) T77A probably benign Het
Il20 A G 1: 130,836,118 (GRCm39) Y142H probably benign Het
Macf1 A T 4: 123,342,042 (GRCm39) D2160E probably benign Het
Melk A G 4: 44,340,633 (GRCm39) Y310C probably damaging Het
Mep1a C T 17: 43,789,949 (GRCm39) V454M probably benign Het
Mep1a A T 17: 43,790,124 (GRCm39) N395K probably benign Het
Mnt A G 11: 74,727,242 (GRCm39) K43E probably damaging Het
Nrap A G 19: 56,335,616 (GRCm39) I853T probably damaging Het
Or1j13 T C 2: 36,370,032 (GRCm39) T37A probably benign Het
Or8d1b T G 9: 38,887,062 (GRCm39) L30R probably damaging Het
Pdia4 A G 6: 47,777,952 (GRCm39) S347P probably benign Het
Pkd1l1 T G 11: 8,794,649 (GRCm39) Q1837H probably benign Het
Pramel11 T C 4: 143,623,877 (GRCm39) N99S possibly damaging Het
Pygo1 T A 9: 72,852,711 (GRCm39) N299K probably damaging Het
Sirpb1b A T 3: 15,613,725 (GRCm39) V52E probably damaging Het
Tdrd7 T A 4: 45,994,517 (GRCm39) I305N probably damaging Het
Trav14-1 T C 14: 53,791,955 (GRCm39) S102P probably damaging Het
Tsga10 C A 1: 37,874,266 (GRCm39) probably benign Het
Uso1 T A 5: 92,347,711 (GRCm39) H837Q probably benign Het
Vmn2r82 A T 10: 79,231,727 (GRCm39) R575S probably benign Het
Yae1d1 C A 13: 18,167,861 (GRCm39) A11S probably benign Het
Zfp277 A G 12: 40,368,548 (GRCm39) I459T possibly damaging Het
Other mutations in Ogfrl1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00913:Ogfrl1 APN 1 23,409,171 (GRCm39) missense probably benign
IGL02200:Ogfrl1 APN 1 23,409,150 (GRCm39) missense probably benign 0.00
PIT4508001:Ogfrl1 UTSW 1 23,409,351 (GRCm39) nonsense probably null
R0012:Ogfrl1 UTSW 1 23,409,206 (GRCm39) missense possibly damaging 0.83
R0735:Ogfrl1 UTSW 1 23,414,835 (GRCm39) missense possibly damaging 0.76
R1474:Ogfrl1 UTSW 1 23,414,890 (GRCm39) missense probably damaging 1.00
R3837:Ogfrl1 UTSW 1 23,409,041 (GRCm39) missense probably benign 0.03
R4037:Ogfrl1 UTSW 1 23,418,045 (GRCm39) splice site probably benign
R4039:Ogfrl1 UTSW 1 23,418,045 (GRCm39) splice site probably benign
R4332:Ogfrl1 UTSW 1 23,414,910 (GRCm39) missense probably damaging 1.00
R4780:Ogfrl1 UTSW 1 23,409,402 (GRCm39) missense probably damaging 1.00
R5056:Ogfrl1 UTSW 1 23,418,130 (GRCm39) missense probably damaging 0.97
R5994:Ogfrl1 UTSW 1 23,418,070 (GRCm39) missense probably damaging 1.00
R6167:Ogfrl1 UTSW 1 23,415,309 (GRCm39) missense probably damaging 1.00
R6341:Ogfrl1 UTSW 1 23,408,944 (GRCm39) missense probably benign 0.04
R6342:Ogfrl1 UTSW 1 23,408,944 (GRCm39) missense probably benign 0.04
R6343:Ogfrl1 UTSW 1 23,408,944 (GRCm39) missense probably benign 0.04
R6363:Ogfrl1 UTSW 1 23,409,194 (GRCm39) missense probably benign 0.01
R6584:Ogfrl1 UTSW 1 23,408,944 (GRCm39) missense probably benign 0.04
R6586:Ogfrl1 UTSW 1 23,408,944 (GRCm39) missense probably benign 0.04
R7419:Ogfrl1 UTSW 1 23,422,063 (GRCm39) nonsense probably null
R8364:Ogfrl1 UTSW 1 23,414,824 (GRCm39) nonsense probably null
R8749:Ogfrl1 UTSW 1 23,409,399 (GRCm39) missense probably damaging 1.00
R9539:Ogfrl1 UTSW 1 23,415,322 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GTTCTTCAGGACACATTAGAAAGC -3'
(R):5'- TTTCCCCAGGAGCTAGTCAC -3'

Sequencing Primer
(F):5'- CATTTTGCTGTGCCACTAC -3'
(R):5'- CCCAGGAGCTAGTCACGTAAATAG -3'
Posted On 2018-04-27