Incidental Mutation 'R7204:Pax5'
| ID |
560429 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Pax5
|
| Ensembl Gene |
ENSMUSG00000014030 |
| Gene Name |
paired box 5 |
| Synonyms |
EBB-1, Pax-5 |
| MMRRC Submission |
045282-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7204 (G1)
|
| Quality Score |
175.009 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
44524757-44710487 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 44679485 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 187
(I187F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000014174
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000014174]
[ENSMUST00000102932]
[ENSMUST00000107825]
[ENSMUST00000107826]
[ENSMUST00000107827]
[ENSMUST00000134968]
[ENSMUST00000143235]
[ENSMUST00000146335]
[ENSMUST00000165417]
[ENSMUST00000173733]
[ENSMUST00000173821]
[ENSMUST00000174242]
[ENSMUST00000186542]
|
| AlphaFold |
Q02650 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000014174
AA Change: I187F
PolyPhen 2
Score 0.933 (Sensitivity: 0.80; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000014174
Gene: ENSMUSG00000014030
AA Change: I187F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
low complexity region
|
157 |
189 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
220 |
254 |
1e-4 |
SMART |
|
Pfam:Pax2_C
|
279 |
390 |
6e-53 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000102932
AA Change: I187F
PolyPhen 2
Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)
|
| SMART Domains |
Protein: ENSMUSP00000099996
Gene: ENSMUSG00000014030
AA Change: I187F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
low complexity region
|
157 |
189 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
220 |
254 |
1e-4 |
SMART |
|
Pfam:Pax2_C
|
276 |
341 |
1.1e-25 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000107825
AA Change: I187F
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000103455
Gene: ENSMUSG00000014030
AA Change: I187F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
low complexity region
|
157 |
189 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
220 |
254 |
2e-4 |
SMART |
|
Pfam:Pax2_C
|
279 |
356 |
5.7e-28 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000107826
AA Change: I187F
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000103457
Gene: ENSMUSG00000014030
AA Change: I187F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
low complexity region
|
157 |
189 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
220 |
254 |
7e-4 |
SMART |
|
low complexity region
|
269 |
281 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000107827
AA Change: I187F
PolyPhen 2
Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000103458
Gene: ENSMUSG00000014030
AA Change: I187F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
low complexity region
|
157 |
189 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
220 |
254 |
4e-4 |
SMART |
|
low complexity region
|
298 |
310 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000134968
|
| SMART Domains |
Protein: ENSMUSP00000133540
Gene: ENSMUSG00000014030
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
SCOP:d1ftt__
|
177 |
211 |
1e-4 |
SMART |
|
Pfam:Pax2_C
|
233 |
298 |
2.4e-25 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000143235
AA Change: I187F
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000134370
Gene: ENSMUSG00000014030
AA Change: I187F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
low complexity region
|
157 |
189 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
220 |
254 |
1e-3 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000146335
AA Change: I186F
PolyPhen 2
Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000139296
Gene: ENSMUSG00000014030
AA Change: I186F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
15 |
139 |
8e-96 |
SMART |
|
low complexity region
|
156 |
188 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000165417
|
| SMART Domains |
Protein: ENSMUSP00000128880
Gene: ENSMUSG00000014030
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
SCOP:d1ftt__
|
177 |
211 |
1e-4 |
SMART |
|
Pfam:Pax2_C
|
233 |
347 |
7.3e-55 |
PFAM |
|
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000134119
Gene: ENSMUSG00000014030
AA Change: I131F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
85 |
2.44e-27 |
SMART |
|
low complexity region
|
102 |
134 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
165 |
199 |
7e-5 |
SMART |
|
Pfam:Pax2_C
|
224 |
335 |
2.3e-53 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173733
AA Change: I121F
PolyPhen 2
Score 0.141 (Sensitivity: 0.92; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000133671
Gene: ENSMUSG00000014030
AA Change: I121F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
120 |
2.93e-30 |
SMART |
|
SCOP:d1ftt__
|
154 |
188 |
1e-4 |
SMART |
|
Pfam:Pax2_C
|
212 |
290 |
8.7e-28 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000173821
AA Change: I187F
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000134712
Gene: ENSMUSG00000014030
AA Change: I187F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
low complexity region
|
157 |
189 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
220 |
254 |
2e-4 |
SMART |
|
low complexity region
|
306 |
325 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174242
AA Change: I187F
PolyPhen 2
Score 0.073 (Sensitivity: 0.93; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000134391
Gene: ENSMUSG00000014030
AA Change: I187F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
16 |
140 |
4.92e-96 |
SMART |
|
low complexity region
|
157 |
189 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
220 |
254 |
2e-3 |
SMART |
|
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000133978
Gene: ENSMUSG00000014030
AA Change: I131F
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
4 |
85 |
2.44e-27 |
SMART |
|
low complexity region
|
102 |
134 |
N/A |
INTRINSIC |
|
SCOP:d1ftt__
|
165 |
199 |
2e-4 |
SMART |
|
low complexity region
|
251 |
270 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000186542
AA Change: H98L
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000141186
Gene: ENSMUSG00000014030
AA Change: H98L
| Domain | Start | End | E-Value | Type |
|---|
|
PAX
|
15 |
108 |
1.2e-22 |
SMART |
|
| Meta Mutation Damage Score |
0.0862 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.6%
|
| Validation Efficiency |
99% (75/76) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the paired box (PAX) family of transcription factors. The central feature of this gene family is a novel, highly conserved DNA-binding motif, known as the paired box. Paired box transcription factors are important regulators in early development, and alterations in the expression of their genes are thought to contribute to neoplastic transformation. This gene encodes the B-cell lineage specific activator protein that is expressed at early, but not late stages of B-cell differentiation. Its expression has also been detected in developing CNS and testis and so the encoded protein may also play a role in neural development and spermatogenesis. This gene is located at 9p13, which is involved in t(9;14)(p13;q32) translocations recurring in small lymphocytic lymphomas of the plasmacytoid subtype, and in derived large-cell lymphomas. This translocation brings the potent E-mu enhancer of the IgH gene into close proximity of the PAX5 promoter, suggesting that the deregulation of transcription of this gene contributes to the pathogenesis of these lymphomas. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
PHENOTYPE: Null mutants exhibit impaired development of the midbrain resulting in a reduced inferior colliculus and an altered cerebellar folial pattern, failure of B cell differentiation, runting, and high postnatal mortality with few survivors. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 75 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700067K01Rik |
T |
C |
8: 84,730,636 (GRCm39) |
S227P |
probably damaging |
Het |
| Acot6 |
A |
G |
12: 84,153,301 (GRCm39) |
H181R |
probably benign |
Het |
| Adam15 |
A |
T |
3: 89,254,244 (GRCm39) |
H184Q |
probably benign |
Het |
| Agl |
A |
G |
3: 116,587,469 (GRCm39) |
F29L |
probably benign |
Het |
| Ak7 |
A |
G |
12: 105,708,502 (GRCm39) |
Y319C |
probably benign |
Het |
| Ano8 |
C |
A |
8: 71,931,669 (GRCm39) |
V813L |
probably benign |
Het |
| Apbb2 |
T |
G |
5: 66,608,946 (GRCm39) |
K234Q |
probably damaging |
Het |
| Arfgef3 |
A |
T |
10: 18,522,210 (GRCm39) |
D605E |
probably damaging |
Het |
| Bfsp2 |
C |
A |
9: 103,309,865 (GRCm39) |
R340L |
probably damaging |
Het |
| Birc6 |
C |
A |
17: 74,947,103 (GRCm39) |
P2956T |
probably damaging |
Het |
| C1rb |
T |
C |
6: 124,554,386 (GRCm39) |
I389T |
probably benign |
Het |
| Ccdc146 |
A |
G |
5: 21,513,624 (GRCm39) |
F498S |
probably benign |
Het |
| Cdc14b |
A |
C |
13: 64,358,012 (GRCm39) |
V361G |
possibly damaging |
Het |
| Cdc25b |
A |
T |
2: 131,033,552 (GRCm39) |
I164F |
probably damaging |
Het |
| Col18a1 |
A |
G |
10: 76,921,110 (GRCm39) |
S297P |
unknown |
Het |
| Col3a1 |
A |
T |
1: 45,361,578 (GRCm39) |
I117F |
unknown |
Het |
| Cox4i2 |
AG |
A |
2: 152,602,618 (GRCm39) |
|
probably null |
Het |
| Crybg3 |
C |
A |
16: 59,379,253 (GRCm39) |
G667V |
probably benign |
Het |
| Ctc1 |
A |
G |
11: 68,920,567 (GRCm39) |
D623G |
probably damaging |
Het |
| Dennd1a |
A |
T |
2: 37,929,215 (GRCm39) |
H152Q |
probably damaging |
Het |
| Dgke |
G |
A |
11: 88,932,306 (GRCm39) |
P495S |
probably damaging |
Het |
| Dll3 |
A |
T |
7: 27,998,330 (GRCm39) |
C212S |
possibly damaging |
Het |
| Dll4 |
A |
T |
2: 119,159,054 (GRCm39) |
S235C |
probably damaging |
Het |
| Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
| Dnah12 |
A |
T |
14: 26,503,442 (GRCm39) |
T1599S |
probably damaging |
Het |
| Elavl1 |
G |
A |
8: 4,361,712 (GRCm39) |
T20M |
probably damaging |
Het |
| Epha3 |
T |
C |
16: 63,472,695 (GRCm39) |
T397A |
probably benign |
Het |
| Fanca |
A |
T |
8: 124,013,216 (GRCm39) |
I859N |
probably damaging |
Het |
| Fzd1 |
A |
T |
5: 4,805,980 (GRCm39) |
V534D |
probably damaging |
Het |
| Glmp |
A |
G |
3: 88,233,917 (GRCm39) |
Y258C |
probably damaging |
Het |
| Gm9195 |
G |
A |
14: 72,711,626 (GRCm39) |
P329S |
probably damaging |
Het |
| Gpt |
A |
G |
15: 76,583,199 (GRCm39) |
R379G |
probably benign |
Het |
| Gsdmc2 |
T |
C |
15: 63,696,903 (GRCm39) |
T423A |
probably damaging |
Het |
| Hemgn |
T |
C |
4: 46,397,054 (GRCm39) |
K61E |
possibly damaging |
Het |
| Ikzf4 |
A |
T |
10: 128,479,759 (GRCm39) |
S56T |
possibly damaging |
Het |
| Jak1 |
T |
C |
4: 101,032,332 (GRCm39) |
T425A |
probably benign |
Het |
| Jsrp1 |
T |
C |
10: 80,646,319 (GRCm39) |
T80A |
probably benign |
Het |
| Klra9 |
T |
A |
6: 130,165,643 (GRCm39) |
D124V |
possibly damaging |
Het |
| Lama5 |
A |
T |
2: 179,843,970 (GRCm39) |
V397D |
probably damaging |
Het |
| Lrp2 |
A |
G |
2: 69,302,877 (GRCm39) |
S2951P |
probably benign |
Het |
| Map7d1 |
A |
G |
4: 126,149,808 (GRCm39) |
|
probably null |
Het |
| Mcm6 |
A |
T |
1: 128,265,864 (GRCm39) |
C636S |
probably damaging |
Het |
| Mia |
T |
C |
7: 26,880,358 (GRCm39) |
E39G |
possibly damaging |
Het |
| Mpeg1 |
T |
A |
19: 12,440,258 (GRCm39) |
I572N |
probably damaging |
Het |
| Muc21 |
AGCTGGATGCAGTGGTGGTCAGGGTGGGTGTAGAGCCTGAGCCAGTGCTGGATACAGTGGTGGTC |
AGCTGGATACAGTGGTGGTC |
17: 35,932,105 (GRCm39) |
|
probably benign |
Het |
| Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
| Mup5 |
A |
G |
4: 61,751,992 (GRCm39) |
Y86H |
probably damaging |
Het |
| Nckap5 |
A |
T |
1: 125,954,104 (GRCm39) |
V816D |
probably benign |
Het |
| Nfib |
T |
C |
4: 82,215,052 (GRCm39) |
|
probably null |
Het |
| Nlrc5 |
T |
A |
8: 95,218,153 (GRCm39) |
V1056D |
possibly damaging |
Het |
| Nynrin |
G |
C |
14: 56,110,190 (GRCm39) |
E1766Q |
probably damaging |
Het |
| Or7d9 |
A |
T |
9: 20,197,100 (GRCm39) |
Y43F |
probably benign |
Het |
| Oxct1 |
T |
A |
15: 4,123,524 (GRCm39) |
L328Q |
probably damaging |
Het |
| Pcdhb4 |
A |
T |
18: 37,442,292 (GRCm39) |
D534V |
probably damaging |
Het |
| Pebp4 |
C |
T |
14: 70,085,046 (GRCm39) |
P35S |
probably benign |
Het |
| Pkhd1l1 |
T |
A |
15: 44,386,949 (GRCm39) |
V1274E |
possibly damaging |
Het |
| Plcz1 |
A |
T |
6: 139,956,150 (GRCm39) |
V373D |
probably benign |
Het |
| Plxnb1 |
C |
T |
9: 108,929,243 (GRCm39) |
T33I |
probably damaging |
Het |
| Prag1 |
T |
C |
8: 36,613,915 (GRCm39) |
C1156R |
probably benign |
Het |
| Ptprc |
T |
A |
1: 138,045,600 (GRCm39) |
I87F |
probably benign |
Het |
| Rbp4 |
G |
A |
19: 38,112,551 (GRCm39) |
T138I |
possibly damaging |
Het |
| Semp2l2b |
A |
G |
10: 21,943,785 (GRCm39) |
L65P |
probably damaging |
Het |
| Slc12a1 |
A |
T |
2: 125,042,542 (GRCm39) |
N733Y |
possibly damaging |
Het |
| Slc27a3 |
A |
G |
3: 90,297,033 (GRCm39) |
V22A |
probably benign |
Het |
| Tcaf1 |
T |
C |
6: 42,651,973 (GRCm39) |
|
probably null |
Het |
| Tnc |
T |
C |
4: 63,889,392 (GRCm39) |
|
probably null |
Het |
| Tspan31 |
A |
T |
10: 126,903,987 (GRCm39) |
*211R |
probably null |
Het |
| Ttc17 |
A |
T |
2: 94,192,773 (GRCm39) |
V86D |
possibly damaging |
Het |
| Ubr1 |
T |
A |
2: 120,734,558 (GRCm39) |
N1114I |
possibly damaging |
Het |
| Ulk2 |
C |
T |
11: 61,674,457 (GRCm39) |
G850R |
probably benign |
Het |
| Vmn1r13 |
T |
A |
6: 57,187,141 (GRCm39) |
I100N |
probably benign |
Het |
| Zan |
T |
C |
5: 137,426,240 (GRCm39) |
D2512G |
unknown |
Het |
| Zc3h14 |
A |
T |
12: 98,737,615 (GRCm39) |
N34I |
probably damaging |
Het |
| Zcwpw1 |
T |
G |
5: 137,810,346 (GRCm39) |
L374R |
probably damaging |
Het |
| Zfp747l1 |
A |
T |
7: 126,983,518 (GRCm39) |
I528K |
possibly damaging |
Het |
|
| Other mutations in Pax5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02369:Pax5
|
APN |
4 |
44,691,919 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02700:Pax5
|
APN |
4 |
44,682,722 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02754:Pax5
|
APN |
4 |
44,570,059 (GRCm39) |
missense |
probably damaging |
0.96 |
|
apple
|
UTSW |
4 |
0 () |
unclassified |
|
|
|
Denim
|
UTSW |
4 |
44,645,661 (GRCm39) |
nonsense |
probably null |
|
|
Glacier
|
UTSW |
4 |
44,679,494 (GRCm39) |
missense |
probably damaging |
1.00 |
|
glacier2
|
UTSW |
4 |
44,710,407 (GRCm39) |
start codon destroyed |
probably null |
0.96 |
|
Glacier3
|
UTSW |
4 |
44,679,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
jeans
|
UTSW |
4 |
44,645,621 (GRCm39) |
missense |
probably benign |
0.03 |
|
k2
|
UTSW |
4 |
44,697,630 (GRCm39) |
missense |
probably damaging |
1.00 |
|
menshevik
|
UTSW |
4 |
44,570,071 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Son_of_apple
|
UTSW |
4 |
44,710,583 (GRCm39) |
unclassified |
probably benign |
|
|
R0411:Pax5
|
UTSW |
4 |
44,609,783 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0415:Pax5
|
UTSW |
4 |
44,691,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0655:Pax5
|
UTSW |
4 |
44,537,462 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1146:Pax5
|
UTSW |
4 |
44,697,512 (GRCm39) |
splice site |
probably benign |
|
|
R1752:Pax5
|
UTSW |
4 |
44,609,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1891:Pax5
|
UTSW |
4 |
44,691,859 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4766:Pax5
|
UTSW |
4 |
44,679,494 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4783:Pax5
|
UTSW |
4 |
44,570,086 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5134:Pax5
|
UTSW |
4 |
44,710,407 (GRCm39) |
start codon destroyed |
probably null |
0.96 |
|
R5341:Pax5
|
UTSW |
4 |
44,697,630 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5458:Pax5
|
UTSW |
4 |
44,679,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6281:Pax5
|
UTSW |
4 |
44,691,955 (GRCm39) |
missense |
probably benign |
0.37 |
|
R6871:Pax5
|
UTSW |
4 |
44,710,583 (GRCm39) |
unclassified |
probably benign |
|
|
R7025:Pax5
|
UTSW |
4 |
44,679,501 (GRCm39) |
nonsense |
probably null |
|
|
R7975:Pax5
|
UTSW |
4 |
44,537,465 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8246:Pax5
|
UTSW |
4 |
44,570,027 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8527:Pax5
|
UTSW |
4 |
44,570,071 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8542:Pax5
|
UTSW |
4 |
44,570,071 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8836:Pax5
|
UTSW |
4 |
44,645,621 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8847:Pax5
|
UTSW |
4 |
44,691,865 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8987:Pax5
|
UTSW |
4 |
44,645,661 (GRCm39) |
nonsense |
probably null |
|
|
R9404:Pax5
|
UTSW |
4 |
44,645,565 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
S24628:Pax5
|
UTSW |
4 |
44,691,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0018:Pax5
|
UTSW |
4 |
44,691,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Pax5
|
UTSW |
4 |
44,697,678 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Pax5
|
UTSW |
4 |
44,697,558 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTCTCACCCAAGGAGTAAAGATGG -3'
(R):5'- TTGCCCTTCTGCAGCAGTTG -3'
Sequencing Primer
(F):5'- CTGTCTCAGGAAAGGCTAGGACC -3'
(R):5'- AGTTGTACCCAGCCCAGTATATCTAG -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation