Incidental Mutation 'R5440:Itgb4'
ID 428598
Institutional Source Beutler Lab
Gene Symbol Itgb4
Ensembl Gene ENSMUSG00000020758
Gene Name integrin beta 4
Synonyms CD104
MMRRC Submission 043005-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5440 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 115865556-115899238 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 115874983 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Tryptophan at position 447 (R447W)
Ref Sequence ENSEMBL: ENSMUSP00000127604 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021107] [ENSMUST00000068981] [ENSMUST00000106458] [ENSMUST00000106460] [ENSMUST00000106461] [ENSMUST00000169928]
AlphaFold A2A863
Predicted Effect probably benign
Transcript: ENSMUST00000021107
AA Change: R447W

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000021107
Gene: ENSMUSG00000020758
AA Change: R447W

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
PSI 30 74 3.89e-1 SMART
INB 38 457 4.23e-213 SMART
VWA 130 361 8.29e-1 SMART
EGF_like 544 576 3.23e1 SMART
Integrin_B_tail 628 712 1.32e-28 SMART
low complexity region 715 732 N/A INTRINSIC
transmembrane domain 737 756 N/A INTRINSIC
Calx_beta 980 1085 3.13e-35 SMART
FN3 1125 1203 3.15e-8 SMART
FN3 1218 1305 6.29e-8 SMART
low complexity region 1324 1332 N/A INTRINSIC
FN3 1508 1589 1.79e-12 SMART
FN3 1621 1705 1.7e-13 SMART
low complexity region 1738 1751 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000068981
AA Change: R447W

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000070811
Gene: ENSMUSG00000020758
AA Change: R447W

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
PSI 30 74 3.89e-1 SMART
INB 38 457 4.23e-213 SMART
VWA 130 361 8.29e-1 SMART
EGF_like 544 576 3.23e1 SMART
Integrin_B_tail 628 713 7.06e-29 SMART
low complexity region 716 733 N/A INTRINSIC
transmembrane domain 738 757 N/A INTRINSIC
Calx_beta 981 1086 3.13e-35 SMART
FN3 1129 1207 3.15e-8 SMART
FN3 1222 1309 6.29e-8 SMART
low complexity region 1328 1336 N/A INTRINSIC
FN3 1459 1540 1.79e-12 SMART
FN3 1572 1656 1.7e-13 SMART
low complexity region 1689 1702 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000106458
AA Change: R447W

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000102066
Gene: ENSMUSG00000020758
AA Change: R447W

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
PSI 30 74 3.89e-1 SMART
INB 38 457 4.23e-213 SMART
VWA 130 361 8.29e-1 SMART
EGF_like 544 576 3.23e1 SMART
Integrin_B_tail 628 713 7.06e-29 SMART
low complexity region 716 733 N/A INTRINSIC
transmembrane domain 738 757 N/A INTRINSIC
Calx_beta 981 1086 3.13e-35 SMART
FN3 1129 1207 3.15e-8 SMART
FN3 1222 1309 6.29e-8 SMART
low complexity region 1328 1336 N/A INTRINSIC
low complexity region 1413 1425 N/A INTRINSIC
FN3 1524 1605 1.79e-12 SMART
FN3 1637 1721 1.7e-13 SMART
low complexity region 1754 1767 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000106460
AA Change: R447W

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000102068
Gene: ENSMUSG00000020758
AA Change: R447W

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
PSI 30 74 3.89e-1 SMART
INB 38 457 4.23e-213 SMART
VWA 130 361 8.29e-1 SMART
EGF_like 544 576 3.23e1 SMART
Integrin_B_tail 628 713 7.06e-29 SMART
low complexity region 716 733 N/A INTRINSIC
transmembrane domain 738 757 N/A INTRINSIC
Calx_beta 981 1086 3.13e-35 SMART
FN3 1129 1207 3.15e-8 SMART
FN3 1222 1309 6.29e-8 SMART
low complexity region 1328 1336 N/A INTRINSIC
FN3 1512 1593 1.79e-12 SMART
FN3 1625 1709 1.7e-13 SMART
low complexity region 1742 1755 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000106461
AA Change: R447W

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000102069
Gene: ENSMUSG00000020758
AA Change: R447W

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
PSI 30 74 3.89e-1 SMART
INB 38 457 4.23e-213 SMART
VWA 130 361 8.29e-1 SMART
EGF_like 544 576 3.23e1 SMART
Integrin_B_tail 628 713 7.06e-29 SMART
low complexity region 716 733 N/A INTRINSIC
transmembrane domain 738 757 N/A INTRINSIC
Calx_beta 981 1086 3.13e-35 SMART
FN3 1129 1207 3.15e-8 SMART
FN3 1222 1309 6.29e-8 SMART
low complexity region 1328 1336 N/A INTRINSIC
low complexity region 1413 1425 N/A INTRINSIC
FN3 1524 1605 1.79e-12 SMART
FN3 1637 1721 1.7e-13 SMART
low complexity region 1754 1767 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000151691
Predicted Effect probably benign
Transcript: ENSMUST00000169928
AA Change: R447W

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000127604
Gene: ENSMUSG00000020758
AA Change: R447W

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
PSI 30 74 3.89e-1 SMART
INB 38 457 4.23e-213 SMART
VWA 130 361 8.29e-1 SMART
EGF_like 544 576 3.23e1 SMART
Integrin_B_tail 628 712 1.32e-28 SMART
low complexity region 715 732 N/A INTRINSIC
transmembrane domain 737 756 N/A INTRINSIC
Calx_beta 980 1085 3.13e-35 SMART
FN3 1125 1203 3.15e-8 SMART
FN3 1218 1305 6.29e-8 SMART
low complexity region 1324 1332 N/A INTRINSIC
FN3 1508 1589 1.79e-12 SMART
FN3 1621 1705 1.7e-13 SMART
low complexity region 1738 1751 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180782
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency
MGI Phenotype FUNCTION: Integrins are heterodimers comprised of alpha and beta subunits, that are noncovalently associated transmembrane glycoprotein receptors. Different combinations of alpha and beta polypeptides form complexes that vary in their ligand-binding specificities. Integrins mediate cell-matrix or cell-cell adhesion, and transduced signals that regulate gene expression and cell growth. This gene encodes the integrin beta 4 subunit, a receptor for the laminins. This subunit tends to associate with alpha 6 subunit and is likely to play a pivotal role in the biology of invasive carcinoma. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for targeted null mutations die shortly after birth with extensive detachment of the epidermis and other squamus epithelia. Stratified tissues lack hemidesmosomes and simple epithelia are also defective in adherence. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Apc G T 18: 34,354,213 (GRCm39) probably benign Het
Apol11b T A 15: 77,519,793 (GRCm39) K96* probably null Het
Arhgap35 C T 7: 16,296,849 (GRCm39) G739S probably damaging Het
Atp6v0a4 A C 6: 38,069,752 (GRCm39) F47V probably damaging Het
Bcl9 G A 3: 97,117,881 (GRCm39) P271L probably benign Het
Cd109 T C 9: 78,587,446 (GRCm39) probably null Het
Col12a1 T A 9: 79,521,645 (GRCm39) I2771F probably benign Het
Col6a1 A G 10: 76,559,288 (GRCm39) V116A probably damaging Het
Cpsf2 C G 12: 101,963,138 (GRCm39) L401V probably benign Het
Cwf19l2 G A 9: 3,475,549 (GRCm39) E829K probably damaging Het
D7Ertd443e G A 7: 133,951,004 (GRCm39) T223I probably damaging Het
Dtx4 G A 19: 12,469,681 (GRCm39) R149C probably damaging Het
Fam186b C T 15: 99,171,734 (GRCm39) A838T possibly damaging Het
Fzd4 G T 7: 89,057,326 (GRCm39) E458* probably null Het
Gm17669 C T 18: 67,695,526 (GRCm39) P24S possibly damaging Het
Grin2b C T 6: 135,713,304 (GRCm39) G859D probably damaging Het
Gucy2e T C 11: 69,114,472 (GRCm39) Y1019C probably damaging Het
Gzme T A 14: 56,355,910 (GRCm39) N134I possibly damaging Het
Havcr1 A T 11: 46,643,197 (GRCm39) Y39F probably damaging Het
Hint3 A T 10: 30,494,347 (GRCm39) M1K probably null Het
Hspa4l A G 3: 40,736,008 (GRCm39) K543R probably damaging Het
Ifna9 A G 4: 88,510,048 (GRCm39) probably null Het
Lipo2 A G 19: 33,698,258 (GRCm39) I373T probably benign Het
Myo5c T A 9: 75,165,407 (GRCm39) I405N possibly damaging Het
Or10a49 T C 7: 108,467,833 (GRCm39) H176R probably damaging Het
P2rx1 A G 11: 72,899,329 (GRCm39) M108V probably benign Het
Pcsk2 T A 2: 143,388,463 (GRCm39) V18E probably benign Het
Pigr A T 1: 130,777,359 (GRCm39) probably null Het
Pkp1 A T 1: 135,810,230 (GRCm39) C447S probably benign Het
Prom1 T A 5: 44,215,988 (GRCm39) I96F probably benign Het
Prpf4b T C 13: 35,068,076 (GRCm39) probably benign Het
Ropn1 C A 16: 34,491,542 (GRCm39) D102E probably benign Het
Slc35e2 C T 4: 155,694,483 (GRCm39) P10L probably benign Het
Sphk1 T G 11: 116,425,714 (GRCm39) V17G possibly damaging Het
Syngr1 A G 15: 79,982,219 (GRCm39) N2S probably benign Het
Syt9 T G 7: 107,101,330 (GRCm39) S359A possibly damaging Het
Terb1 T C 8: 105,215,131 (GRCm39) I282V probably damaging Het
Ttn T A 2: 76,585,168 (GRCm39) I22042F probably damaging Het
Ttn A T 2: 76,739,600 (GRCm39) D3646E probably benign Het
Ube2d1 A G 10: 71,091,682 (GRCm39) W141R probably damaging Het
Vmn2r41 T A 7: 8,141,362 (GRCm39) I701F probably damaging Het
Zfp770 T C 2: 114,026,596 (GRCm39) D491G probably benign Het
Other mutations in Itgb4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01360:Itgb4 APN 11 115,881,766 (GRCm39) missense probably damaging 1.00
IGL01391:Itgb4 APN 11 115,881,746 (GRCm39) missense probably damaging 1.00
IGL01431:Itgb4 APN 11 115,897,283 (GRCm39) splice site probably benign
IGL01750:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL01752:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL01756:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL01766:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL01769:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL02188:Itgb4 APN 11 115,894,213 (GRCm39) missense probably benign 0.08
IGL02262:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL02293:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL02318:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL02319:Itgb4 APN 11 115,879,752 (GRCm39) missense probably damaging 0.99
IGL02338:Itgb4 APN 11 115,898,795 (GRCm39) missense probably damaging 1.00
IGL02734:Itgb4 APN 11 115,896,792 (GRCm39) missense probably benign
IGL02879:Itgb4 APN 11 115,885,178 (GRCm39) missense probably benign 0.05
IGL02889:Itgb4 APN 11 115,879,731 (GRCm39) missense probably damaging 1.00
IGL03183:Itgb4 APN 11 115,879,550 (GRCm39) missense probably damaging 1.00
IGL03054:Itgb4 UTSW 11 115,891,166 (GRCm39) nonsense probably null
R0021:Itgb4 UTSW 11 115,870,453 (GRCm39) missense possibly damaging 0.95
R0092:Itgb4 UTSW 11 115,869,950 (GRCm39) missense probably damaging 1.00
R0305:Itgb4 UTSW 11 115,870,238 (GRCm39) missense probably damaging 1.00
R0408:Itgb4 UTSW 11 115,898,428 (GRCm39) missense probably damaging 0.99
R0465:Itgb4 UTSW 11 115,870,582 (GRCm39) missense probably damaging 1.00
R0499:Itgb4 UTSW 11 115,870,521 (GRCm39) missense probably benign 0.00
R0535:Itgb4 UTSW 11 115,881,835 (GRCm39) missense possibly damaging 0.86
R0571:Itgb4 UTSW 11 115,870,594 (GRCm39) missense possibly damaging 0.94
R0613:Itgb4 UTSW 11 115,884,168 (GRCm39) missense probably damaging 0.98
R0838:Itgb4 UTSW 11 115,888,988 (GRCm39) intron probably benign
R1381:Itgb4 UTSW 11 115,885,163 (GRCm39) missense probably benign 0.00
R1451:Itgb4 UTSW 11 115,881,710 (GRCm39) missense probably damaging 1.00
R1459:Itgb4 UTSW 11 115,869,937 (GRCm39) missense probably benign 0.42
R1460:Itgb4 UTSW 11 115,874,990 (GRCm39) missense probably damaging 0.96
R1473:Itgb4 UTSW 11 115,874,873 (GRCm39) missense probably benign 0.01
R1484:Itgb4 UTSW 11 115,890,625 (GRCm39) missense probably benign 0.01
R1593:Itgb4 UTSW 11 115,871,817 (GRCm39) missense probably damaging 1.00
R1623:Itgb4 UTSW 11 115,882,142 (GRCm39) nonsense probably null
R1633:Itgb4 UTSW 11 115,898,586 (GRCm39) missense probably damaging 1.00
R1642:Itgb4 UTSW 11 115,898,183 (GRCm39) missense probably damaging 1.00
R1669:Itgb4 UTSW 11 115,882,156 (GRCm39) missense probably benign 0.07
R1713:Itgb4 UTSW 11 115,894,315 (GRCm39) missense probably damaging 1.00
R1732:Itgb4 UTSW 11 115,879,744 (GRCm39) missense probably damaging 1.00
R1791:Itgb4 UTSW 11 115,879,346 (GRCm39) missense probably damaging 1.00
R1847:Itgb4 UTSW 11 115,874,590 (GRCm39) missense probably benign 0.31
R1902:Itgb4 UTSW 11 115,871,564 (GRCm39) missense probably damaging 0.98
R1945:Itgb4 UTSW 11 115,884,279 (GRCm39) nonsense probably null
R2102:Itgb4 UTSW 11 115,896,561 (GRCm39) missense probably benign 0.23
R2184:Itgb4 UTSW 11 115,870,450 (GRCm39) missense probably damaging 0.96
R2334:Itgb4 UTSW 11 115,884,261 (GRCm39) missense probably damaging 1.00
R2401:Itgb4 UTSW 11 115,897,389 (GRCm39) missense possibly damaging 0.67
R3743:Itgb4 UTSW 11 115,894,496 (GRCm39) missense probably damaging 1.00
R3938:Itgb4 UTSW 11 115,896,752 (GRCm39) missense possibly damaging 0.92
R4134:Itgb4 UTSW 11 115,897,296 (GRCm39) missense probably benign 0.03
R4280:Itgb4 UTSW 11 115,881,761 (GRCm39) missense probably damaging 1.00
R4342:Itgb4 UTSW 11 115,879,555 (GRCm39) missense probably benign 0.01
R4434:Itgb4 UTSW 11 115,890,640 (GRCm39) missense probably benign 0.10
R4505:Itgb4 UTSW 11 115,874,087 (GRCm39) splice site silent
R4585:Itgb4 UTSW 11 115,884,151 (GRCm39) missense probably damaging 1.00
R4586:Itgb4 UTSW 11 115,884,151 (GRCm39) missense probably damaging 1.00
R4601:Itgb4 UTSW 11 115,896,548 (GRCm39) missense probably damaging 1.00
R4921:Itgb4 UTSW 11 115,897,431 (GRCm39) missense probably benign 0.12
R4962:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5027:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5029:Itgb4 UTSW 11 115,879,417 (GRCm39) intron probably benign
R5084:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5085:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5124:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5125:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5150:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5175:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5176:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5179:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5207:Itgb4 UTSW 11 115,897,365 (GRCm39) missense probably damaging 1.00
R5263:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5264:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5334:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5337:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5344:Itgb4 UTSW 11 115,880,575 (GRCm39) missense probably null 0.92
R5391:Itgb4 UTSW 11 115,875,894 (GRCm39) missense probably benign 0.05
R5437:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5653:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5654:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5655:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5772:Itgb4 UTSW 11 115,879,258 (GRCm39) intron probably benign
R5812:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5813:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5814:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5863:Itgb4 UTSW 11 115,881,748 (GRCm39) missense probably damaging 1.00
R5864:Itgb4 UTSW 11 115,881,748 (GRCm39) missense probably damaging 1.00
R5865:Itgb4 UTSW 11 115,881,748 (GRCm39) missense probably damaging 1.00
R5951:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5954:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R5982:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R6043:Itgb4 UTSW 11 115,870,212 (GRCm39) missense probably benign 0.30
R6133:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R6134:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R6135:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R6169:Itgb4 UTSW 11 115,885,102 (GRCm39) missense probably damaging 0.98
R6172:Itgb4 UTSW 11 115,891,237 (GRCm39) missense probably benign 0.23
R6255:Itgb4 UTSW 11 115,888,963 (GRCm39) missense possibly damaging 0.83
R6258:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R6259:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R6260:Itgb4 UTSW 11 115,874,983 (GRCm39) missense probably benign 0.00
R6612:Itgb4 UTSW 11 115,874,897 (GRCm39) missense probably benign 0.00
R7037:Itgb4 UTSW 11 115,896,391 (GRCm39) nonsense probably null
R7371:Itgb4 UTSW 11 115,888,906 (GRCm39) missense probably benign 0.29
R7605:Itgb4 UTSW 11 115,897,302 (GRCm39) missense probably benign 0.01
R7659:Itgb4 UTSW 11 115,870,557 (GRCm39) missense probably damaging 1.00
R7759:Itgb4 UTSW 11 115,894,536 (GRCm39) missense possibly damaging 0.92
R7804:Itgb4 UTSW 11 115,894,510 (GRCm39) missense probably damaging 1.00
R7832:Itgb4 UTSW 11 115,891,087 (GRCm39) missense probably damaging 1.00
R7842:Itgb4 UTSW 11 115,873,531 (GRCm39) missense probably benign 0.18
R7923:Itgb4 UTSW 11 115,873,525 (GRCm39) critical splice acceptor site probably null
R8004:Itgb4 UTSW 11 115,873,531 (GRCm39) missense probably benign 0.00
R8143:Itgb4 UTSW 11 115,884,255 (GRCm39) missense probably damaging 1.00
R8427:Itgb4 UTSW 11 115,882,544 (GRCm39) critical splice donor site probably null
R8857:Itgb4 UTSW 11 115,871,853 (GRCm39) missense probably benign 0.04
R8863:Itgb4 UTSW 11 115,875,898 (GRCm39) nonsense probably null
R8932:Itgb4 UTSW 11 115,879,295 (GRCm39) missense probably benign 0.01
R9153:Itgb4 UTSW 11 115,874,879 (GRCm39) missense probably benign 0.00
R9207:Itgb4 UTSW 11 115,897,923 (GRCm39) missense probably damaging 1.00
R9239:Itgb4 UTSW 11 115,898,130 (GRCm39) missense probably damaging 1.00
R9267:Itgb4 UTSW 11 115,870,465 (GRCm39) missense probably benign
R9289:Itgb4 UTSW 11 115,885,187 (GRCm39) missense probably benign 0.01
R9328:Itgb4 UTSW 11 115,880,625 (GRCm39) missense probably benign 0.00
R9435:Itgb4 UTSW 11 115,895,855 (GRCm39) missense probably benign 0.01
R9450:Itgb4 UTSW 11 115,874,097 (GRCm39) missense probably damaging 1.00
R9649:Itgb4 UTSW 11 115,885,171 (GRCm39) missense possibly damaging 0.78
R9779:Itgb4 UTSW 11 115,882,485 (GRCm39) missense probably damaging 1.00
X0062:Itgb4 UTSW 11 115,884,278 (GRCm39) missense probably damaging 1.00
Z1176:Itgb4 UTSW 11 115,897,346 (GRCm39) missense probably damaging 1.00
Z1177:Itgb4 UTSW 11 115,888,884 (GRCm39) missense probably benign 0.00
Z1177:Itgb4 UTSW 11 115,877,637 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- CAAGTCCCTGTCCATACACTG -3'
(R):5'- TCTCTGTGACTTGGGACAGC -3'

Sequencing Primer
(F):5'- TGAGCGAACAGGCTAATGTC -3'
(R):5'- TTTTACCCAGGGTCCTAG -3'
Posted On 2016-09-01