Incidental Mutation 'R0614:Hif1a'
| ID |
54967 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Hif1a
|
| Ensembl Gene |
ENSMUSG00000021109 |
| Gene Name |
hypoxia inducible factor 1, alpha subunit |
| Synonyms |
bHLHe78, MOP1, HIF-1alpha, HIF1alpha |
| MMRRC Submission |
038803-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R0614 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
12 |
| Chromosomal Location |
73948149-73994304 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 73992405 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Lysine
at position 787
(N787K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000106088
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021530]
[ENSMUST00000110461]
|
| AlphaFold |
Q61221 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000021530
AA Change: N813K
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000021530
Gene: ENSMUSG00000021109
AA Change: N813K
| Domain | Start | End | E-Value | Type |
|---|
|
HLH
|
23 |
78 |
1.29e-8 |
SMART |
|
PAS
|
87 |
153 |
1.05e-9 |
SMART |
|
PAS
|
230 |
296 |
2.08e-8 |
SMART |
|
PAC
|
302 |
345 |
6.85e-9 |
SMART |
|
low complexity region
|
416 |
427 |
N/A |
INTRINSIC |
|
Pfam:HIF-1
|
564 |
594 |
5.4e-18 |
PFAM |
|
low complexity region
|
621 |
645 |
N/A |
INTRINSIC |
|
Pfam:HIF-1a_CTAD
|
799 |
835 |
3.9e-25 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000110461
AA Change: N787K
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000106088
Gene: ENSMUSG00000021109
AA Change: N787K
| Domain | Start | End | E-Value | Type |
|---|
|
HLH
|
11 |
66 |
1.29e-8 |
SMART |
|
PAS
|
75 |
141 |
1.05e-9 |
SMART |
|
PAS
|
218 |
284 |
2.08e-8 |
SMART |
|
PAC
|
290 |
333 |
6.85e-9 |
SMART |
|
low complexity region
|
404 |
415 |
N/A |
INTRINSIC |
|
Pfam:HIF-1
|
536 |
569 |
6e-19 |
PFAM |
|
low complexity region
|
595 |
619 |
N/A |
INTRINSIC |
|
Pfam:HIF-1a_CTAD
|
771 |
810 |
1.2e-25 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125308
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000221427
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000221833
|
| Meta Mutation Damage Score |
0.8395 |
| Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.4%
- 20x: 94.9%
|
| Validation Efficiency |
97% (61/63) |
| MGI Phenotype |
FUNCTION: This gene encodes the alpha subunit which, along with the beta subunit, forms a heterodimeric transcription factor that regulates the cellular and developmental response to reduced oxygen tension. The transcription factor has been shown to regulate genes involved in several biological processes, including erythropoiesis and angiogenesis which aid in increased delivery of oxygen to hypoxic regions. The transcription factor also plays a role in the induction of genes involved in cell proliferation and survival, energy metabolism, apoptosis, and glucose and iron metabolism. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015]
PHENOTYPE: Homozygous null mutants die during embryonic development with severe cardiovascular malformations, neural tube defects, cephalic defects, reduced somite number and increased hypoxia. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 61 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2210408I21Rik |
C |
T |
13: 77,340,782 (GRCm39) |
T137I |
probably benign |
Het |
| 3110082I17Rik |
C |
T |
5: 139,349,786 (GRCm39) |
V88I |
possibly damaging |
Het |
| 4930453N24Rik |
T |
A |
16: 64,586,977 (GRCm39) |
Q249L |
probably damaging |
Het |
| Ap1g2 |
C |
T |
14: 55,337,230 (GRCm39) |
V702I |
probably benign |
Het |
| Armcx5 |
G |
A |
X: 134,647,564 (GRCm39) |
E547K |
probably damaging |
Het |
| Asah2 |
C |
A |
19: 31,994,128 (GRCm39) |
V406L |
probably damaging |
Het |
| Atp8b1 |
T |
C |
18: 64,666,658 (GRCm39) |
|
probably benign |
Het |
| Axl |
C |
A |
7: 25,473,588 (GRCm39) |
R346L |
probably benign |
Het |
| Baz1a |
G |
A |
12: 54,988,304 (GRCm39) |
R282* |
probably null |
Het |
| Card14 |
A |
G |
11: 119,213,653 (GRCm39) |
N200S |
probably benign |
Het |
| Cdt1 |
A |
G |
8: 123,294,876 (GRCm39) |
T28A |
probably benign |
Het |
| Cep250 |
C |
T |
2: 155,812,017 (GRCm39) |
Q438* |
probably null |
Het |
| Dapk1 |
C |
A |
13: 60,865,946 (GRCm39) |
P181Q |
probably damaging |
Het |
| Dnah17 |
C |
T |
11: 117,961,394 (GRCm39) |
|
probably benign |
Het |
| Dph7 |
T |
C |
2: 24,858,968 (GRCm39) |
|
probably null |
Het |
| Edc4 |
A |
T |
8: 106,616,028 (GRCm39) |
D801V |
possibly damaging |
Het |
| Eif4g2 |
A |
G |
7: 110,676,430 (GRCm39) |
|
probably null |
Het |
| Eml2 |
T |
C |
7: 18,936,516 (GRCm39) |
L531P |
probably damaging |
Het |
| Ephb2 |
T |
C |
4: 136,400,676 (GRCm39) |
Y533C |
probably benign |
Het |
| Fcho1 |
C |
T |
8: 72,165,204 (GRCm39) |
A418T |
probably benign |
Het |
| Fsip2 |
A |
G |
2: 82,807,877 (GRCm39) |
K1399E |
probably benign |
Het |
| Hcls1 |
A |
G |
16: 36,782,987 (GRCm39) |
D446G |
probably damaging |
Het |
| Ints14 |
T |
C |
9: 64,871,715 (GRCm39) |
S18P |
probably benign |
Het |
| Kalrn |
A |
T |
16: 33,814,040 (GRCm39) |
|
probably benign |
Het |
| Llgl2 |
T |
A |
11: 115,741,093 (GRCm39) |
D502E |
probably damaging |
Het |
| Lrwd1 |
A |
G |
5: 136,152,354 (GRCm39) |
V570A |
probably damaging |
Het |
| Mga |
C |
G |
2: 119,794,947 (GRCm39) |
P2877R |
probably damaging |
Het |
| Mvd |
T |
C |
8: 123,163,292 (GRCm39) |
I313V |
probably benign |
Het |
| Myo15b |
C |
A |
11: 115,773,739 (GRCm39) |
P270T |
probably damaging |
Het |
| Naip1 |
C |
A |
13: 100,580,708 (GRCm39) |
V180L |
probably benign |
Het |
| Ofd1 |
T |
C |
X: 165,218,536 (GRCm39) |
|
probably benign |
Het |
| Or1j19 |
T |
A |
2: 36,676,705 (GRCm39) |
L56H |
probably damaging |
Het |
| Or4c125 |
T |
A |
2: 89,170,329 (GRCm39) |
I106F |
probably damaging |
Het |
| Or4d11 |
A |
T |
19: 12,013,929 (GRCm39) |
M59K |
possibly damaging |
Het |
| Otogl |
G |
A |
10: 107,634,216 (GRCm39) |
P1420S |
probably benign |
Het |
| Pakap |
C |
A |
4: 57,856,720 (GRCm39) |
A926E |
probably benign |
Het |
| Pcnt |
C |
T |
10: 76,256,150 (GRCm39) |
V697M |
probably damaging |
Het |
| Plekha7 |
A |
T |
7: 115,753,880 (GRCm39) |
Y702* |
probably null |
Het |
| Plxnb3 |
A |
G |
X: 72,807,964 (GRCm39) |
|
probably benign |
Het |
| Ptgis |
A |
G |
2: 167,048,802 (GRCm39) |
F405L |
probably damaging |
Het |
| Ptprk |
C |
T |
10: 27,951,132 (GRCm39) |
P19L |
probably damaging |
Het |
| Ptprt |
A |
G |
2: 161,654,040 (GRCm39) |
V530A |
possibly damaging |
Het |
| Rasgrp4 |
A |
T |
7: 28,845,276 (GRCm39) |
Y299F |
probably damaging |
Het |
| Slc39a11 |
T |
A |
11: 113,414,452 (GRCm39) |
|
probably null |
Het |
| Slc6a15 |
T |
A |
10: 103,240,213 (GRCm39) |
L312* |
probably null |
Het |
| Slf1 |
T |
A |
13: 77,197,233 (GRCm39) |
M794L |
probably benign |
Het |
| Sntg2 |
G |
A |
12: 30,307,977 (GRCm39) |
T236I |
possibly damaging |
Het |
| Stau1 |
T |
C |
2: 166,792,726 (GRCm39) |
Y413C |
probably damaging |
Het |
| Syne2 |
T |
G |
12: 75,959,127 (GRCm39) |
|
probably null |
Het |
| Tas2r104 |
A |
T |
6: 131,662,165 (GRCm39) |
N181K |
probably damaging |
Het |
| Tmem81 |
G |
A |
1: 132,435,469 (GRCm39) |
V92I |
probably benign |
Het |
| Trap1 |
A |
G |
16: 3,878,615 (GRCm39) |
|
probably benign |
Het |
| Trip12 |
T |
C |
1: 84,735,482 (GRCm39) |
E905G |
probably damaging |
Het |
| Usp2 |
C |
T |
9: 44,003,789 (GRCm39) |
R494* |
probably null |
Het |
| Vps13a |
G |
T |
19: 16,630,058 (GRCm39) |
R2692S |
probably damaging |
Het |
| Zfhx3 |
T |
C |
8: 109,675,171 (GRCm39) |
S2074P |
probably benign |
Het |
| Zfhx3 |
C |
G |
8: 109,675,599 (GRCm39) |
Y2216* |
probably null |
Het |
| Zfp423 |
A |
G |
8: 88,508,742 (GRCm39) |
F409S |
probably damaging |
Het |
| Zfp472 |
G |
A |
17: 33,196,908 (GRCm39) |
E328K |
possibly damaging |
Het |
| Zfp619 |
T |
A |
7: 39,187,099 (GRCm39) |
M1043K |
possibly damaging |
Het |
| Zfp940 |
T |
C |
7: 29,545,671 (GRCm39) |
I79V |
probably benign |
Het |
|
| Other mutations in Hif1a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00979:Hif1a
|
APN |
12 |
73,988,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01396:Hif1a
|
APN |
12 |
73,987,307 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02230:Hif1a
|
APN |
12 |
73,979,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02561:Hif1a
|
APN |
12 |
73,988,980 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
IGL02698:Hif1a
|
APN |
12 |
73,977,545 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03027:Hif1a
|
APN |
12 |
73,987,251 (GRCm39) |
missense |
probably benign |
0.03 |
|
lightweight
|
UTSW |
12 |
73,988,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0597:Hif1a
|
UTSW |
12 |
73,989,049 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0678:Hif1a
|
UTSW |
12 |
73,990,965 (GRCm39) |
splice site |
probably null |
|
|
R0967:Hif1a
|
UTSW |
12 |
73,984,444 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1351:Hif1a
|
UTSW |
12 |
73,987,235 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1387:Hif1a
|
UTSW |
12 |
73,989,066 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1858:Hif1a
|
UTSW |
12 |
73,990,929 (GRCm39) |
missense |
probably benign |
|
|
R2105:Hif1a
|
UTSW |
12 |
73,984,519 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2194:Hif1a
|
UTSW |
12 |
73,977,521 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4825:Hif1a
|
UTSW |
12 |
73,979,175 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4924:Hif1a
|
UTSW |
12 |
73,986,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5386:Hif1a
|
UTSW |
12 |
73,990,867 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5594:Hif1a
|
UTSW |
12 |
73,984,566 (GRCm39) |
nonsense |
probably null |
|
|
R5722:Hif1a
|
UTSW |
12 |
73,988,533 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5818:Hif1a
|
UTSW |
12 |
73,986,338 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R5831:Hif1a
|
UTSW |
12 |
73,988,918 (GRCm39) |
missense |
probably benign |
|
|
R6026:Hif1a
|
UTSW |
12 |
73,979,055 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6059:Hif1a
|
UTSW |
12 |
73,988,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6084:Hif1a
|
UTSW |
12 |
73,988,616 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6818:Hif1a
|
UTSW |
12 |
73,992,337 (GRCm39) |
nonsense |
probably null |
|
|
R6878:Hif1a
|
UTSW |
12 |
73,975,055 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R8028:Hif1a
|
UTSW |
12 |
73,988,801 (GRCm39) |
missense |
probably benign |
0.27 |
|
R8286:Hif1a
|
UTSW |
12 |
73,992,022 (GRCm39) |
intron |
probably benign |
|
|
R8322:Hif1a
|
UTSW |
12 |
73,986,373 (GRCm39) |
missense |
probably benign |
|
|
R8414:Hif1a
|
UTSW |
12 |
73,984,428 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8729:Hif1a
|
UTSW |
12 |
73,990,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9030:Hif1a
|
UTSW |
12 |
73,983,010 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9087:Hif1a
|
UTSW |
12 |
73,989,099 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9093:Hif1a
|
UTSW |
12 |
73,979,111 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9300:Hif1a
|
UTSW |
12 |
73,987,302 (GRCm39) |
missense |
probably benign |
0.04 |
|
| Predicted Primers |
PCR Primer
(F):5'- TAGGGTTTGCCCAGGGGACTAAAG -3'
(R):5'- TGGCTACCATGTACTGCTGACAAAG -3'
Sequencing Primer
(F):5'- CAGGGGACTAAAGCCCTTC -3'
(R):5'- TAGACTGCTGAGCCACCAG -3'
|
| Posted On |
2013-07-11 |
Incidental Mutation