Incidental Mutation 'IGL01064:Gm13030'
ID50834
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm13030
Ensembl Gene ENSMUSG00000078518
Gene Namepredicted gene 13030
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.054) question?
Stock #IGL01064
Quality Score
Status
Chromosome4
Chromosomal Location138870992-138873964 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) G to A at 138873558 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101429 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030531] [ENSMUST00000105803] [ENSMUST00000105805]
Predicted Effect probably benign
Transcript: ENSMUST00000030531
SMART Domains Protein: ENSMUSP00000030531
Gene: ENSMUSG00000028751

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
PA2c 20 136 9.74e-55 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000105803
SMART Domains Protein: ENSMUSP00000101429
Gene: ENSMUSG00000028751

DomainStartEndE-ValueType
low complexity region 44 59 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000105805
AA Change: P12S
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A T 11: 9,483,855 T4137S probably benign Het
Abcb1a T C 5: 8,732,388 Y924H possibly damaging Het
Ash1l T G 3: 89,072,484 C2772G probably damaging Het
Cfap206 C T 4: 34,721,562 S162N probably damaging Het
Cpne6 T C 14: 55,512,730 F106S probably damaging Het
Cysltr1 A T X: 106,578,736 I48N probably damaging Het
Dsg1a A T 18: 20,340,206 I779F probably damaging Het
Fpr-rs4 T A 17: 18,022,517 L262H probably damaging Het
Gart G A 16: 91,623,007 R871C probably damaging Het
Get4 C T 5: 139,252,522 R20C probably damaging Het
Gm17654 A T 14: 43,578,998 H49Q unknown Het
Gpnmb A G 6: 49,055,659 I506V probably benign Het
Ist1 T C 8: 109,682,611 I86V probably damaging Het
Kcnip1 C T 11: 33,633,192 D198N probably damaging Het
Kif5c A G 2: 49,694,816 I184V possibly damaging Het
Mink1 A T 11: 70,603,481 M236L probably benign Het
Muc5ac A T 7: 141,807,473 N1507I probably benign Het
Nrxn2 G T 19: 6,517,053 E1326D probably damaging Het
Olfr1329 A T 4: 118,916,894 M191K possibly damaging Het
Olfr1469 T C 19: 13,411,226 I219T probably benign Het
Olfr635 A T 7: 103,979,792 Y200F probably benign Het
Patj T C 4: 98,496,973 S326P possibly damaging Het
Pdha2 T C 3: 141,211,015 H244R possibly damaging Het
Pkhd1 C T 1: 20,534,530 probably benign Het
Ptk7 A T 17: 46,573,566 L746* probably null Het
Rad54b G A 4: 11,604,866 G438D probably damaging Het
Rbm27 T C 18: 42,319,814 V536A possibly damaging Het
Rundc3b T A 5: 8,569,553 M135L probably damaging Het
Sorcs2 T C 5: 36,065,352 Y353C probably damaging Het
Srcap T C 7: 127,559,892 probably benign Het
Sytl5 A G X: 9,905,595 H66R probably benign Het
Tlr7 T A X: 167,308,211 E93V probably damaging Het
Tmem156 A G 5: 65,079,984 L76S probably damaging Het
Tmem246 C T 4: 49,586,860 V103M possibly damaging Het
Tomm70a T C 16: 57,152,612 F571S probably damaging Het
Trmt10b A G 4: 45,314,347 Y261C possibly damaging Het
Other mutations in Gm13030
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2080:Gm13030 UTSW 4 138873419 unclassified probably benign
R4915:Gm13030 UTSW 4 138873928 unclassified probably benign
R5454:Gm13030 UTSW 4 138873509 unclassified probably benign
R5933:Gm13030 UTSW 4 138871204 missense unknown
R6333:Gm13030 UTSW 4 138871397 splice site probably null
R7424:Gm13030 UTSW 4 138871266 missense unknown
R8166:Gm13030 UTSW 4 138871222 missense unknown
Posted On2013-06-21