Incidental Mutation 'IGL02945:Zfp319'
ID364675
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp319
Ensembl Gene ENSMUSG00000046556
Gene Namezinc finger protein 319
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.149) question?
Stock #IGL02945
Quality Score
Status
Chromosome8
Chromosomal Location95323011-95331950 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to T at 95323818 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148526 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057717] [ENSMUST00000098480] [ENSMUST00000135142] [ENSMUST00000161029] [ENSMUST00000162294] [ENSMUST00000212056]
Predicted Effect probably benign
Transcript: ENSMUST00000057717
SMART Domains Protein: ENSMUSP00000053397
Gene: ENSMUSG00000046556

DomainStartEndE-ValueType
low complexity region 6 29 N/A INTRINSIC
low complexity region 53 64 N/A INTRINSIC
Blast:ZnF_C2H2 75 99 6e-7 BLAST
ZnF_C2H2 103 123 7.57e1 SMART
ZnF_C2H2 131 153 8.67e-1 SMART
low complexity region 168 189 N/A INTRINSIC
ZnF_C2H2 201 223 9.73e-4 SMART
ZnF_C2H2 229 251 1.47e-3 SMART
ZnF_C2H2 257 279 1.12e-3 SMART
ZnF_C2H2 314 336 6.42e-4 SMART
ZnF_C2H2 342 364 1.2e-3 SMART
ZnF_C2H2 370 392 8.81e-2 SMART
ZnF_C2H2 398 418 2.75e1 SMART
ZnF_C2H2 427 449 1.84e-4 SMART
ZnF_C2H2 457 477 1.27e2 SMART
ZnF_C2H2 485 507 2.79e-4 SMART
ZnF_C2H2 513 535 6.42e-4 SMART
ZnF_C2H2 541 563 4.11e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000098480
Predicted Effect probably benign
Transcript: ENSMUST00000135142
Predicted Effect probably benign
Transcript: ENSMUST00000153991
Predicted Effect probably benign
Transcript: ENSMUST00000161029
Predicted Effect probably benign
Transcript: ENSMUST00000162294
Predicted Effect probably benign
Transcript: ENSMUST00000212056
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933411G06Rik A T 10: 51,756,999 noncoding transcript Het
Adgrf4 T C 17: 42,667,366 Q362R probably benign Het
Akap6 A G 12: 52,880,837 N177D probably damaging Het
Alms1 A G 6: 85,620,933 I914V probably damaging Het
Arhgap11a A T 2: 113,837,473 S394R possibly damaging Het
Cacna1h C T 17: 25,388,059 V962I probably damaging Het
Calr3 A T 8: 72,438,557 L91Q probably damaging Het
Ccnf T C 17: 24,224,916 E626G probably damaging Het
Clec10a A T 11: 70,170,542 I295F possibly damaging Het
Cop1 A T 1: 159,306,689 N167I probably benign Het
Csmd1 G T 8: 16,271,570 Q505K possibly damaging Het
Ctrc A C 4: 141,846,252 V6G possibly damaging Het
Cyp2c69 T C 19: 39,886,647 R21G possibly damaging Het
Dnah5 A G 15: 28,270,426 H958R probably benign Het
Egfr T A 11: 16,752,514 L11Q probably damaging Het
Erich2 A G 2: 70,534,394 T371A probably damaging Het
Fbxl21 T A 13: 56,527,170 F111L probably damaging Het
Grik4 G T 9: 42,597,879 T416N possibly damaging Het
Grin3a A G 4: 49,792,971 V254A possibly damaging Het
Hat1 G A 2: 71,420,693 R195K probably benign Het
Hmgb4 A C 4: 128,260,594 Y60* probably null Het
Ighv12-3 A G 12: 114,366,717 W53R probably damaging Het
Irs2 C A 8: 11,007,781 C217F probably damaging Het
Kcnb1 T C 2: 167,188,388 E79G probably benign Het
Lingo3 A G 10: 80,834,698 I466T probably damaging Het
Lyst T C 13: 13,761,198 S3665P possibly damaging Het
Myh9 A T 15: 77,762,005 L1926Q probably benign Het
Myom1 A G 17: 71,092,093 probably benign Het
Nbeal1 T C 1: 60,206,410 F198L probably damaging Het
Nktr A G 9: 121,728,631 T63A probably damaging Het
Nle1 A T 11: 82,904,084 probably benign Het
Nr3c2 A T 8: 76,909,659 D463V probably damaging Het
Olfr181 A T 16: 58,926,340 I77N probably damaging Het
Olfr902 A G 9: 38,449,516 I215V probably benign Het
Pcdhb18 T C 18: 37,489,995 I126T probably benign Het
Pgm2 A G 4: 99,961,534 I127V probably benign Het
Rai14 A G 15: 10,574,709 I721T probably benign Het
Rps6ka1 A G 4: 133,867,199 Y57H probably damaging Het
Scara3 T A 14: 65,931,211 D319V probably damaging Het
Selp G A 1: 164,133,929 G404S probably damaging Het
Serinc3 A G 2: 163,630,916 probably benign Het
Slc4a8 A G 15: 100,807,199 probably null Het
Spen G T 4: 141,494,313 L325I unknown Het
Sphkap A T 1: 83,276,831 S779T probably damaging Het
Stxbp2 A T 8: 3,641,971 I538F probably benign Het
Thumpd1 A T 7: 119,716,747 S326R possibly damaging Het
Tmem255b T C 8: 13,455,141 S149P probably damaging Het
Tnni3k A T 3: 155,037,438 S95T possibly damaging Het
Trim66 G A 7: 109,460,176 Q954* probably null Het
Ttn A T 2: 76,751,972 I22859N probably damaging Het
Other mutations in Zfp319
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01611:Zfp319 APN 8 95328912 missense probably benign 0.11
IGL02478:Zfp319 APN 8 95329093 missense possibly damaging 0.95
IGL02563:Zfp319 APN 8 95323734 unclassified probably benign
IGL02622:Zfp319 APN 8 95328961 missense probably damaging 0.97
Lanky UTSW 8 95328105 frame shift probably null
R0894:Zfp319 UTSW 8 95329622 unclassified probably benign
R1898:Zfp319 UTSW 8 95328789 missense probably damaging 1.00
R1937:Zfp319 UTSW 8 95328571 missense probably damaging 1.00
R2127:Zfp319 UTSW 8 95323763 unclassified probably benign
R2157:Zfp319 UTSW 8 95328031 missense probably damaging 1.00
R2256:Zfp319 UTSW 8 95328501 missense possibly damaging 0.47
R3547:Zfp319 UTSW 8 95328817 missense probably damaging 0.96
R4665:Zfp319 UTSW 8 95325573 unclassified probably benign
R5174:Zfp319 UTSW 8 95328169 unclassified probably null
R5249:Zfp319 UTSW 8 95328471 missense probably benign 0.00
R5478:Zfp319 UTSW 8 95325565 unclassified probably benign
R5623:Zfp319 UTSW 8 95325571 unclassified probably benign
R6165:Zfp319 UTSW 8 95328105 frame shift probably null
R7175:Zfp319 UTSW 8 95328782 missense probably damaging 1.00
R7271:Zfp319 UTSW 8 95331843 unclassified probably benign
Posted On2015-12-18