Incidental Mutation 'R9764:1700029F12Rik'
ID 733165
Institutional Source Beutler Lab
Gene Symbol 1700029F12Rik
Ensembl Gene ENSMUSG00000052075
Gene Name RIKEN cDNA 1700029F12 gene
Synonyms
MMRRC Submission
Accession Numbers
Essential gene? Not available question?
Stock # R9764 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 97158372-97170870 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 97166738 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 93 (T93A)
Ref Sequence ENSEMBL: ENSMUSP00000088938 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091377]
AlphaFold Q9CRB4
Predicted Effect unknown
Transcript: ENSMUST00000091377
AA Change: T93A
SMART Domains Protein: ENSMUSP00000088938
Gene: ENSMUSG00000052075
AA Change: T93A

DomainStartEndE-ValueType
low complexity region 86 95 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 99.3%
  • 20x: 98.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrg6 T A 10: 14,302,515 (GRCm39) H938L probably benign Het
Aff1 A G 5: 103,997,365 (GRCm39) Y1153C probably damaging Het
Akr1c20 T A 13: 4,564,388 (GRCm39) I42L probably benign Het
Atad2b T A 12: 5,082,064 (GRCm39) N1324K probably benign Het
Aurka T A 2: 172,201,760 (GRCm39) I270F probably damaging Het
Camk2g A T 14: 20,815,498 (GRCm39) D189E probably damaging Het
Cc2d2b A G 19: 40,804,299 (GRCm39) D942G unknown Het
Ccnd1 A C 7: 144,491,770 (GRCm39) S90A probably benign Het
Cfap77 G T 2: 28,852,741 (GRCm39) T177K probably damaging Het
Chd9 A G 8: 91,721,220 (GRCm39) N1003D unknown Het
Chga C G 12: 102,525,613 (GRCm39) Q85E possibly damaging Het
Cnot1 T C 8: 96,496,209 (GRCm39) S322G probably benign Het
Cyp8b1 C A 9: 121,744,294 (GRCm39) S346I probably benign Het
Cysltr2 T A 14: 73,266,906 (GRCm39) H268L probably damaging Het
Dnah11 T C 12: 117,884,704 (GRCm39) T3783A probably benign Het
Dock3 C T 9: 106,959,713 (GRCm39) V109I probably benign Het
Dscc1 A G 15: 54,953,674 (GRCm39) C50R probably benign Het
Dtx3l T A 16: 35,753,277 (GRCm39) D443V probably damaging Het
Ephb6 A G 6: 41,592,911 (GRCm39) H383R probably benign Het
Fdft1 A G 14: 63,400,869 (GRCm39) I88T probably damaging Het
Fmo3 C A 1: 162,794,524 (GRCm39) W182L probably benign Het
Folh1 T A 7: 86,406,158 (GRCm39) Q305L probably benign Het
Gale C T 4: 135,692,975 (GRCm39) Q73* probably null Het
Gm9195 T C 14: 72,699,885 (GRCm39) M1154V unknown Het
Grip1 G A 10: 119,874,569 (GRCm39) E778K possibly damaging Het
Gtsf1l T C 2: 162,929,052 (GRCm39) T144A probably benign Het
Itpkc T C 7: 26,927,222 (GRCm39) T231A probably benign Het
Kng2 C A 16: 22,822,737 (GRCm39) C205F probably damaging Het
Ldlrap1 T G 4: 134,476,661 (GRCm39) N244T probably benign Het
Lingo2 A G 4: 35,709,750 (GRCm39) F77L possibly damaging Het
Lpcat2b A T 5: 107,581,438 (GRCm39) T256S possibly damaging Het
Lrit2 A G 14: 36,790,936 (GRCm39) D205G probably damaging Het
Lrrc34 T C 3: 30,697,467 (GRCm39) D88G probably damaging Het
Macf1 T C 4: 123,366,136 (GRCm39) E2875G probably benign Het
Med13 G T 11: 86,177,345 (GRCm39) Q1584K possibly damaging Het
Naip5 C G 13: 100,367,269 (GRCm39) A276P probably damaging Het
Ndufv2 A G 17: 66,394,503 (GRCm39) Y121H probably damaging Het
Or4f52 T A 2: 111,061,521 (GRCm39) I206F probably damaging Het
Peg12 T C 7: 62,113,297 (GRCm39) T267A unknown Het
Pkig A G 2: 163,567,375 (GRCm39) probably null Het
Prkch C G 12: 73,747,078 (GRCm39) T319S probably benign Het
Rhobtb1 T C 10: 69,115,202 (GRCm39) S534P probably damaging Het
Riok2 A G 17: 17,607,814 (GRCm39) N454S probably benign Het
Ryr2 T A 13: 11,701,935 (GRCm39) K2907N possibly damaging Het
Sdc3 C T 4: 130,546,048 (GRCm39) P136S unknown Het
Slc37a3 G A 6: 39,322,844 (GRCm39) L371F probably damaging Het
Slc3a1 A T 17: 85,371,419 (GRCm39) H657L probably damaging Het
Slc7a13 T A 4: 19,819,033 (GRCm39) Y78N probably benign Het
Slfn8 G T 11: 82,907,838 (GRCm39) A235E probably damaging Het
Snap91 T A 9: 86,707,094 (GRCm39) D232V possibly damaging Het
Stap2 C A 17: 56,309,914 (GRCm39) S79I probably damaging Het
Stra6l T C 4: 45,884,602 (GRCm39) V544A probably damaging Het
Syn2 T C 6: 115,251,219 (GRCm39) probably null Het
Tctn1 G A 5: 122,388,527 (GRCm39) P284S possibly damaging Het
Terb2 G A 2: 122,018,475 (GRCm39) M77I probably benign Het
Trim80 G T 11: 115,338,757 (GRCm39) R529L possibly damaging Het
Washc2 T C 6: 116,186,048 (GRCm39) L86P possibly damaging Het
Zfp74 A T 7: 29,631,845 (GRCm39) F133Y probably benign Het
Zfp987 T A 4: 146,060,752 (GRCm39) N61K probably benign Het
Other mutations in 1700029F12Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02121:1700029F12Rik APN 13 97,159,038 (GRCm39) missense unknown
R1194:1700029F12Rik UTSW 13 97,166,873 (GRCm39) missense unknown
R1246:1700029F12Rik UTSW 13 97,166,803 (GRCm39) missense unknown
R9792:1700029F12Rik UTSW 13 97,166,719 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- CTCTATCTTGGGAATTAGGGGCC -3'
(R):5'- ATTATGCAGGACAGCTGTGGAG -3'

Sequencing Primer
(F):5'- AATTAGGGGCCCTCCTGCTG -3'
(R):5'- GCTCAAGCGGCACCCAG -3'
Posted On 2022-11-14