Incidental Mutation 'IGL01451:Treml4'
ID 84651
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Treml4
Ensembl Gene ENSMUSG00000051682
Gene Name triggering receptor expressed on myeloid cells-like 4
Synonyms 5031403H21Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # IGL01451
Quality Score
Status
Chromosome 17
Chromosomal Location 48571323-48582388 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 48572023 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000118772 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059873] [ENSMUST00000125426] [ENSMUST00000136272] [ENSMUST00000153420] [ENSMUST00000154335]
AlphaFold Q3LRV9
Predicted Effect probably benign
Transcript: ENSMUST00000059873
SMART Domains Protein: ENSMUSP00000054121
Gene: ENSMUSG00000051682

DomainStartEndE-ValueType
low complexity region 7 18 N/A INTRINSIC
IG 32 137 6.51e-3 SMART
transmembrane domain 200 222 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000125426
SMART Domains Protein: ENSMUSP00000119177
Gene: ENSMUSG00000051682

DomainStartEndE-ValueType
low complexity region 7 18 N/A INTRINSIC
IG 28 133 6.51e-3 SMART
transmembrane domain 196 218 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000136272
SMART Domains Protein: ENSMUSP00000120550
Gene: ENSMUSG00000051682

DomainStartEndE-ValueType
low complexity region 7 18 N/A INTRINSIC
IG 32 137 6.51e-3 SMART
transmembrane domain 192 214 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000153420
SMART Domains Protein: ENSMUSP00000115290
Gene: ENSMUSG00000051682

DomainStartEndE-ValueType
low complexity region 7 18 N/A INTRINSIC
IG 32 137 6.51e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000154335
SMART Domains Protein: ENSMUSP00000118772
Gene: ENSMUSG00000051682

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
IG 32 137 6.51e-3 SMART
transmembrane domain 201 223 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele do not exhibit any significant alterations in the uptake and cross-presentation of dying cells. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700003H04Rik A G 3: 124,373,527 (GRCm39) S23P possibly damaging Het
Adam1a T C 5: 121,657,439 (GRCm39) Y618C probably benign Het
Amigo2 A C 15: 97,143,107 (GRCm39) S438R probably benign Het
Atp5me T C 5: 108,581,922 (GRCm39) I21V probably benign Het
Dnah2 T C 11: 69,365,017 (GRCm39) probably benign Het
Dock2 A G 11: 34,260,390 (GRCm39) Y984H probably damaging Het
Dpysl2 T A 14: 67,045,367 (GRCm39) I469F possibly damaging Het
Edem3 C T 1: 151,694,379 (GRCm39) T886I probably benign Het
Gart T C 16: 91,422,400 (GRCm39) T706A probably benign Het
Gfpt2 A T 11: 49,698,517 (GRCm39) probably benign Het
Gm11541 T G 11: 94,586,495 (GRCm39) D84A unknown Het
Gne T C 4: 44,041,860 (GRCm39) probably null Het
Gria4 A T 9: 4,503,652 (GRCm39) D321E probably benign Het
Ift122 T G 6: 115,889,565 (GRCm39) probably null Het
Lcp2 A T 11: 33,997,345 (GRCm39) probably benign Het
Mcm2 C T 6: 88,868,948 (GRCm39) probably benign Het
Or8b54 A G 9: 38,687,225 (GRCm39) I225V probably benign Het
Ptpru C A 4: 131,496,803 (GRCm39) probably benign Het
Rpap2 T C 5: 107,751,492 (GRCm39) probably null Het
Slc25a39 T C 11: 102,295,726 (GRCm39) T138A probably damaging Het
St6galnac1 A C 11: 116,660,165 (GRCm39) S49R probably benign Het
Stat1 T C 1: 52,178,502 (GRCm39) L312P probably damaging Het
Tmem198 T C 1: 75,461,014 (GRCm39) probably benign Het
Top2a A T 11: 98,901,856 (GRCm39) L458Q probably damaging Het
Trpm6 A G 19: 18,786,933 (GRCm39) D503G probably damaging Het
Ttn C A 2: 76,775,617 (GRCm39) E1854D unknown Het
Ubqln3 A T 7: 103,791,403 (GRCm39) M229K possibly damaging Het
Zfyve9 T C 4: 108,539,457 (GRCm39) T939A probably damaging Het
Other mutations in Treml4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01407:Treml4 APN 17 48,571,877 (GRCm39) missense possibly damaging 0.82
IGL01787:Treml4 APN 17 48,571,732 (GRCm39) missense probably damaging 1.00
R0027:Treml4 UTSW 17 48,571,962 (GRCm39) missense possibly damaging 0.82
R1975:Treml4 UTSW 17 48,579,821 (GRCm39) missense probably damaging 1.00
R4013:Treml4 UTSW 17 48,571,837 (GRCm39) missense probably benign 0.09
R4327:Treml4 UTSW 17 48,581,417 (GRCm39) missense probably damaging 0.98
R5586:Treml4 UTSW 17 48,571,927 (GRCm39) missense probably damaging 1.00
R6220:Treml4 UTSW 17 48,571,876 (GRCm39) missense possibly damaging 0.91
R6510:Treml4 UTSW 17 48,581,472 (GRCm39) missense probably benign
R6964:Treml4 UTSW 17 48,579,847 (GRCm39) critical splice donor site probably null
R8136:Treml4 UTSW 17 48,571,745 (GRCm39) nonsense probably null
R8289:Treml4 UTSW 17 48,581,456 (GRCm39) missense probably benign 0.23
R9070:Treml4 UTSW 17 48,576,781 (GRCm39) missense probably damaging 1.00
R9574:Treml4 UTSW 17 48,571,672 (GRCm39) missense probably damaging 1.00
Posted On 2013-11-11