Incidental Mutation 'IGL01524:Zfp623'
ID 89518
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp623
Ensembl Gene ENSMUSG00000050846
Gene Name zinc finger protein 623
Synonyms 2610029D06Rik
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.368) question?
Stock # IGL01524
Quality Score
Status
Chromosome 15
Chromosomal Location 75812801-75821249 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 75819528 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Arginine at position 161 (S161R)
Ref Sequence ENSEMBL: ENSMUSP00000036049 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037260]
AlphaFold Q9CY99
Predicted Effect probably benign
Transcript: ENSMUST00000037260
AA Change: S161R

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000036049
Gene: ENSMUSG00000050846
AA Change: S161R

DomainStartEndE-ValueType
ZnF_C2H2 119 141 5.59e-4 SMART
ZnF_C2H2 147 169 9.96e-1 SMART
ZnF_C2H2 175 197 2.4e-3 SMART
ZnF_C2H2 203 225 6.42e-4 SMART
ZnF_C2H2 231 253 1.3e-4 SMART
ZnF_C2H2 259 281 1.3e-4 SMART
ZnF_C2H2 287 309 1.28e-3 SMART
ZnF_C2H2 315 337 3.21e-4 SMART
ZnF_C2H2 343 365 3.39e-3 SMART
ZnF_C2H2 371 393 4.87e-4 SMART
ZnF_C2H2 399 421 2.53e-2 SMART
ZnF_C2H2 427 449 3.95e-4 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadat A T 8: 60,969,106 (GRCm39) D117V probably damaging Het
Abca14 T C 7: 119,852,644 (GRCm39) Y870H possibly damaging Het
Ankrd36 T C 11: 5,585,092 (GRCm39) I301T probably benign Het
Atp10b T A 11: 43,150,672 (GRCm39) S1457T probably benign Het
Bltp1 A G 3: 36,996,531 (GRCm39) D1081G possibly damaging Het
Ccdc175 G A 12: 72,177,916 (GRCm39) probably benign Het
Ccdc93 A G 1: 121,389,628 (GRCm39) K224E probably benign Het
Cep131 C T 11: 119,956,786 (GRCm39) A886T probably damaging Het
Clip1 A C 5: 123,717,442 (GRCm39) H1282Q probably damaging Het
Ctcfl T G 2: 172,959,177 (GRCm39) D183A probably benign Het
Cyp17a1 C T 19: 46,659,495 (GRCm39) V112I probably benign Het
Fhod3 T C 18: 25,263,659 (GRCm39) I1521T probably damaging Het
Gipc2 A G 3: 151,843,214 (GRCm39) I141T probably damaging Het
Glo1 T C 17: 30,815,393 (GRCm39) R141G possibly damaging Het
Ipmk C A 10: 71,208,631 (GRCm39) A140E probably damaging Het
Kynu A G 2: 43,561,394 (GRCm39) D310G possibly damaging Het
Myo1f T A 17: 33,798,857 (GRCm39) I174N probably damaging Het
Nat10 T A 2: 103,588,102 (GRCm39) N8Y probably damaging Het
Nhlrc2 A G 19: 56,564,587 (GRCm39) I304V probably benign Het
Pdk4 T C 6: 5,491,979 (GRCm39) H31R probably damaging Het
Sema6d T C 2: 124,505,995 (GRCm39) V644A possibly damaging Het
Slc30a4 T A 2: 122,544,308 (GRCm39) K11N possibly damaging Het
Slc6a3 T C 13: 73,686,668 (GRCm39) S12P probably benign Het
Spats2 C T 15: 99,110,127 (GRCm39) A508V probably benign Het
Tinag A G 9: 76,952,820 (GRCm39) Y55H probably damaging Het
Topbp1 T C 9: 103,188,844 (GRCm39) I172T possibly damaging Het
Trim17 A G 11: 58,861,423 (GRCm39) T279A probably damaging Het
Vmn1r216 C A 13: 23,283,519 (GRCm39) N67K probably benign Het
Washc4 T C 10: 83,411,996 (GRCm39) L709P probably benign Het
Xdh T C 17: 74,230,132 (GRCm39) probably null Het
Zfhx4 C T 3: 5,309,036 (GRCm39) P754L probably damaging Het
Zfp267 T C 3: 36,218,729 (GRCm39) Y251H possibly damaging Het
Zmat3 G A 3: 32,395,827 (GRCm39) R227C possibly damaging Het
Other mutations in Zfp623
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00226:Zfp623 APN 15 75,820,052 (GRCm39) missense probably damaging 1.00
IGL01927:Zfp623 APN 15 75,819,354 (GRCm39) missense possibly damaging 0.57
IGL03199:Zfp623 APN 15 75,819,119 (GRCm39) missense probably benign 0.40
R0076:Zfp623 UTSW 15 75,819,058 (GRCm39) missense probably benign
R0352:Zfp623 UTSW 15 75,820,433 (GRCm39) missense probably benign 0.00
R0360:Zfp623 UTSW 15 75,820,510 (GRCm39) missense probably benign
R0364:Zfp623 UTSW 15 75,820,510 (GRCm39) missense probably benign
R1783:Zfp623 UTSW 15 75,819,760 (GRCm39) missense probably damaging 0.99
R2219:Zfp623 UTSW 15 75,819,379 (GRCm39) missense possibly damaging 0.90
R5975:Zfp623 UTSW 15 75,820,012 (GRCm39) missense probably benign 0.43
R6161:Zfp623 UTSW 15 75,820,470 (GRCm39) missense probably benign 0.22
R6342:Zfp623 UTSW 15 75,819,837 (GRCm39) nonsense probably null
R6490:Zfp623 UTSW 15 75,820,308 (GRCm39) missense probably damaging 1.00
R6513:Zfp623 UTSW 15 75,819,317 (GRCm39) missense probably benign
R7028:Zfp623 UTSW 15 75,820,154 (GRCm39) missense probably damaging 0.99
R7399:Zfp623 UTSW 15 75,819,247 (GRCm39) missense probably damaging 0.98
R7716:Zfp623 UTSW 15 75,820,271 (GRCm39) missense probably damaging 1.00
R8362:Zfp623 UTSW 15 75,819,488 (GRCm39) missense probably damaging 1.00
R8445:Zfp623 UTSW 15 75,819,402 (GRCm39) nonsense probably null
R9028:Zfp623 UTSW 15 75,819,349 (GRCm39) missense probably damaging 0.97
R9035:Zfp623 UTSW 15 75,820,162 (GRCm39) missense possibly damaging 0.93
R9310:Zfp623 UTSW 15 75,819,949 (GRCm39) missense probably damaging 1.00
Posted On 2013-12-03